Search the web
Sign In
New User? Sign Up
PozHealth
? Already a member? Sign in to Yahoo!

Yahoo! Groups Tips

Did you know...
Hear how Yahoo! Groups has changed the lives of others. Take me there.

Best of Y! Groups

   Check them out and nominate your group.
Having problems with message search? Fill out this form to ensure your group is one of the first to be migrated to the new message search system.

Messages

  Messages Help
Advanced
Messages 11421 - 11450 of 31349   Newest  |  < Newer  |  Older >  |  Oldest
Messages: Show Message Summaries   (Group by Topic) Sort by Date v  
#11450 From: PoWeRTX@...
Date: Mon Apr 4, 2005 2:26 pm
Subject: Fwd: Insurance coverage for Sculptra- LETTER TO INS COs
nelsonvergel
Offline Offline
Send Email Send Email
 
In a message dated 4/4/2005 1:03:51 P.M. Central Standard Time, Blm566 writes:
Hi Nelson:
 
             I am HIV+ and have had sculptra injections in my face due to the lipodystrophy.
             I am happy with the results and am pleased that the FDA finally approved it.
             I submitted a claim late last year to my insurance company from a visit to my
             plastic surgeon for an injection. Well, I just got back a letter denying my claim.
             I was wondering how successful other people were in getting their insurance
             company to cover the claim. My insurance is with Blue Shield.
 
             I understand , through my primary doc, that Kaiser is covering the treatment.
             Any advice as to how I can pursue this with my insurance co.?
 
             Thanks for your time and I really do enjoy  and benefit from reading all the emails
             from the group!
 
Sincerely,
 
Brian
*******************
Brian
 
 
I have posted a letter that your doctor can sign and send it to your insurance company here to try to get reimbursement. Let me know what happens
 
 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.
Hi Nelson:
 
             I am HIV+ and have had sculptra injections in my face due to the lipodystrophy.
             I am happy with the results and am pleased that the FDA finally approved it.
             I submitted a claim late last year to my insurance company from a visit to my
             plastic surgeon for an injection. Well, I just got back a letter denying my claim.
             I was wondering how successful other people were in getting their insurance
             company to cover the claim. My insurance is with Blue Shield.
 
             I understand , through my primary doc, that Kaiser is covering the treatment.
             Any advice as to how I can pursue this with my insurance co.?
 
             Thanks for your time and I really do enjoy  and benefit from reading all the emails
             from the group!
 
Sincerely,
 
Brian

#11449 From: Sotoway@...
Date: Mon Apr 4, 2005 10:59 am
Subject: HIV and Law
Sotoway@...
Send Email Send Email
 
Hi:
 
I am in desperate need of an attorney familiar with HIV and Divorce.
 
 
Nancy

#11448 From: PoWeRTX@...
Date: Mon Apr 4, 2005 12:24 pm
Subject: Management of Hypertension in HIV-Infected Patients
nelsonvergel
Offline Offline
Send Email Send Email
 
Management of Hypertension in HIV-Infected Patients

Laura P. Svetkey, MD
Professor of Medicine, Division of Nephrology
Director, Duke Hypertension Center
Duke University Medical Center
Durham, North Carolina

William L. Fan, MD
Duke University Medical Center
Durham, North Carolina


Introduction

The advent of highly active antiretroviral therapy (HAART) in the treatment of HIV disease has revolutionized the care of HIV-infected patients. Encouraging outcomes such as increasing CD4+ cell counts and decreasing incidences of opportunistic infections are more common today than before the introduction of HAART. With the reductions in HIV-related morbidity and mortality brought on by HAART, patients with HIV are living longer, and their clinicians are having to focus on diseases and conditions that typically affect the middle-aged, non-HIV-infected population, such as hypertension, hyperlipidemia, diabetes mellitus, and visceral fat accumulation, all considered risk factors for cardiovascular disease (CVD).

Burden of Hypertension and Other CVD Risk Factors

In the general population, 50 million Americans (1 in 4 adults) are estimated to have hypertension.[1] Hypertension is the most common primary diagnosis in the United States, accounting for 35 million office visits each year, and is the most common risk factor for both cardiovascular and renal disease.[2]

The prevalence of hypertension in the HIV-infected population remains unclear. Estimates suggest that the prevalence of hypertension in the HIV-infected population before the introduction of HAART was similar to that of the general population (between 20% and 25%).[3] The Data Collection on Adverse Events of Anti-HIV Drugs (DAD) study evaluated baseline data from 17,852 subjects in the HAART era and observed that more than 8% of the study population had hypertension.[4] Other results from this cross-sectional, multicenter study revealed that traditional cardiovascular risk factors, such as tobacco use, dyslipidemia, and family history of coronary heart disease, are prevalent among patients on HAART. The presence of these powerful cardiac risk factors further emphasizes the importance of treating hypertension in HIV-infected patients. Clinicians who assume responsibility for the primary care of their HIV-infected patients must now address issues related to the reduction of cardiac risk factors, in addition to managing the patient's HIV disease.

The relationship between HAART and blood pressure has not been carefully studied, and existing data do not consistently demonstrate that HAART routinely raises blood pressure. Nonetheless, clinicians must recognize the growing consensus that the very drugs used to treat HIV may exacerbate cardiac risk factors such as hyperlipidemia, insulin resistance, and increased visceral fat.

Why Treat Hypertension?

As mentioned, hypertension is the most prevalent risk factor for cardiovascular and renal disease in the general population and accounts for approximately 35% of atherosclerotic disease.[5] The magnitude of CVD risk that is attributed to hypertension is comparable to the risk from a low-density lipoprotein (LDL) cholesterol reading of > 160 mg/dL.[6] In addition, hypertension increases the risk of peripheral vascular disease and congestive heart failure by more than 2-fold and the risk of end-stage renal disease by more than 4-fold.[7-9]

Fortunately, treatment of hypertension can reduce its associated risks. Antihypertensive therapy reduces the risk of stroke by approximately 35%, congestive heart failure by 42%, and coronary heart disease by 28%.[10-13] Since renal diseases such as HIV-associated neuropathy (HIVAN) are prevalent in the HIV-infected population, it is important to note that adequate control of high blood pressure can delay progression of kidney dysfunction. Therefore, an important key to reducing the burden of hypertension-related CVD and chronic kidney disease is to increase the proportion of HIV-infected patients who achieve adequate control of their blood pressure—an important goal for HIV-infected patients, who are now living much longer than ever before.

Classification of Hypertension

The 2003 Joint National Committee on Prevention, Detection, Evaluation, and the Treatment of High Blood Pressure (JNC 7) guidelines classify blood pressure by stage and provide recommendations for treatment and follow-up.[14] The JNC 7 classification system consists of 3 main blood pressure categories: normal, prehypertension, and hypertension, which are shown in Table 1. In general, normal blood pressure for adults consists of a systolic blood pressure (SBP) reading of < 120 mm Hg and a diastolic blood pressure (DBP) reading of < 80 mm Hg, or 120/80 mm Hg.

Table 1. JNC 7 Blood Pressure Classification for Adults[14]

Classification Systolic and Diastolic Blood Pressure
Normal SBP < 120 and DBP < 80 mm Hg
Prehypertension SBP 120-139 or DBP 80-89 mm Hg
Stage 1 hypertension SBP 140-159 or DBP 90-99 mm Hg
Stage 2 hypertension SBP ≥ 160 or DBP ≥ 100 mm Hg

DBP, diastolic blood pressure; SBP, systolic blood pressure

Prehypertension is a new category derived from the previous guidelines, that includes patients with ranges of SBP from 120 to 139 mm Hg and/or of DBP from 80 to 89 mm Hg. Note that prehypertension is not a disease category; rather, it is a guideline for identifying individuals at high risk of developing hypertension to alert both patients and clinicians of this risk so that they can consider appropriate interventions for preventing or delaying development of the disease. Careful attention to patients in the prehypertension category is important because several studies indicate that mortality rates for myocardial infarctions (MIs), strokes, and other vascular diseases increase progressively with a rise in blood pressure and can begin at levels as low as 115/75 mm Hg.[15]

As shown in Table 1, hypertension is subdivided into 2 stages: stage 1 includes SBP ranges between 140 and 159 mm Hg or DBP ranges between 90 and 99 mm Hg, and stage 2 hypertension consists of SBP > 160 or DBP > 100 mm Hg.[14]

Management of Hypertension

The medical literature gives no indication that HIV-infected patients with hypertension or prehypertension should be managed in a way other than that recommended in the JNC 7 guidelines. For patients with stage 1 or 2 uncomplicated hypertension, the target blood pressure level is < 140/90 mm Hg. In HIV-positive patients with comorbidities such as diabetes or chronic kidney disease, a target blood pressure level of < 130/80 mm Hg is recommended.[14]

Lifestyle modification, an indispensable part of hypertension management that is recommended for all hypertensive patients, is the only intervention recommended for prehypertension. As shown in Table 2, appropriate lifestyle modification includes adoption of the Dietary Approaches to Stop Hypertension (DASH) eating plan,[16] which includes a diet rich in fruits, vegetables, and low-fat dairy products with a reduced content of dietary cholesterol and saturated and total fat. DASH also contains abundant levels of potassium and calcium. Lifestyle modification intervention also urges patients to engage in regular aerobic activity and to limit alcohol intake to no more than 2 drinks per day for men and 1 drink per day for women.

Table 2. Management of Hypertension: Lifestyle Modifications*

Modification Recommendation Estimated SBP Reduction (mm Hg)†
Reduce weight Maintain normal body weight (BMI, 18.5-24.9 kg/m2) 5-20 per 10-kg weight loss
Adopt DASH eating plan Consume a diet rich in fruits, vegetables, and low-fat dairy products with reduced saturated and total fat 8-14
Reduce dietary sodium intake Reduce intake to ≤ 100 mEq/L (2.4 g sodium or 6 g NaCl) 2-8
Increase physical activity Engage in regular aerobic physical activity (≥30 min/day, most days) 4-9
Limit alcohol consumption Limit consumption to ≤ 2 drinks/day (1 oz or 30 mL ethanol) for most men or ≤ 1 drink/day for women and lighter-weight people 2-4

BMI, body mass index; DASH, Dietary Approaches to Stop Hypertension; SBP, systolic blood pressure.
* Smoking cessation decreases overall cardiovascular risk.
†Effects are dose and time dependent and may be higher in some individuals.

If a patient continues to be hypertensive after a trial of lifestyle modification, a thiazide diuretic is the preferred agent for initial treatment. The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT), which involved more than 40,000 hypertensive individuals, found no differences in primary coronary heart disease (CHD) outcome or mortality between thiazide-type diuretics, the angiotensin-converting enzyme inhibitor (ACEI) lisinopril, or the calcium channel blocker (CCB) amlodipine.[13] Although thiazides are typically recommended for the treatment of hypertension because of their low cost, ACEIs, angiotensin II receptor blockers (ARBs), beta-blockers (BBs), CCBs, or a combination may be considered. ALLHAT also showed that effective treatment of two-thirds of patients requires 2 or more antihypertensive drugs. As shown in Figure 1, recommended treatment for patients with stage 2 hypertension includes a 2-drug regimen consisting of a thiazide and 1 other antihypertensive agent.[14] For patients with stage 1 hypertension thiazide-type diuretics are typically used, though some physicians may consider one of the other antihypertensive agents or a combination. Compelling indications for individual drug classes are listed in Table 3.

Figure 1. Recommendations for the treatment of hypertension

Figure 1

Table 3. Compelling Indications for Specific Drug Classes

Indication Recommended Drugs
Heart failure Diuretic, BB, ACEI, ARB, aldosterone antagonist
Post-myocardial infarction BB, ACEI, aldosterone antagonist
High coronary disease risk Diuretic, BB, ACEI, CCB
Diabetes mellitus Diuretic, BB, ACEI, ARB, CCB
Chronic kidney disease ACEI, ARB
Recurrent-stroke prevention Diuretic, ACEI

ACEI, angiotensin-converting enzyme inhibitor; ARB, angiotensin II receptor blocker; BB, beta-blocker; CCB, calcium channel blocker

Clinicians should consider individual patients' comorbid conditions when selecting classes of antihypertensive drugs for treatment. HIVAN is a notable comorbid condition for this patient population. Because HIVAN is characterized by proteinuria, clinicians are urged to use urinalysis to screen high-risk patients for proteinuria. Patients with evidence of kidney disease should have a blood pressure goal of < 130/80 mm Hg. Given the efficacy of ACEIs, clinicians may consider using one as a first-line agent when a patient's plasma creatinine is less than 2 mg/dL or there is no evidence of hyperkalemia.

HAART and Hypertension Medications

Currently, no contraindications exist regarding the use of any class of antihypertensive agents in the treatment of HIV-infected patients receiving HAART. However, the clinician must be aware of some pitfalls when treating hypertension in these patients.

Since several antihypertensive medications are on the market, CCBs should be avoided because they have been reported to interact with protease inhibitors (PIs). For example, the potential increase in serum concentrations of a CCB during concomitant use of ritonavir or atazanavir could lead to hypotension and bradycardia.[17] On the other hand, when serum concentrations of a CCB are decreased by a drug such as nevirapine, the clinician may be unable to effectively control the patient's blood pressure or heart rate,[18] both of which must be carefully monitored if this antihypertensive drug class is used.

Beta-blocker serum levels have also been known to be altered in patients receiving PIs. For example, atenolol levels are increased in patients taking atazanavir, and the beta-blocker effects of metoprolol may be enhanced in those receiving ritonavir.[17,19]

Nephrolithiasis is a well-established complication of indinavir therapy. Since volume depletion is a known risk factor for the development of kidney stones, diuretics should be used with extreme caution in patients receiving indinavir. To avoid volume depletion, clinicians should recommend that such patients drink at least 48 oz of water each day.[20]

Conclusion

The great strides made in developing effective antiretroviral therapy have substantially reduced the burden of HIV disease; consequently, HIV-infected patients are living longer. Clinicians who treat HIV-infected patients now have additional responsibilities for long-term primary care, including the management of cardiovascular disease risk factors. Proper management of hypertension has become an important component in the care of some HIV-infected patients. Fortunately, well-researched antihypertensive lifestyle interventions and pharmacologic therapies have been developed to help the clinician deal with this emerging issue in the HIV-infected population.

References

1. Burt VL, Whelton P, Roccella E, et al. Prevalence of hypertension in the US adult population. Results from the Third National Health and Nutrition Examination Survey, 1988-1991. Hypertension. 1995;25:305-313.

2. Hypertension Working Group. Working Group Report on Primary Prevention of Hypertension. National High Blood Pressure Education Program. National Heart, Lung, and Blood Institute document. 2000; Bethesda, Maryland: National Institutes of Health.

3. Aoun S, Ramos E. Hypertension in the HIV-infected patient. Curr Hypertens Rep. 2000;2:478-481.

4. Friis-Moller N, Weber R, Reiss P, et al. Cardiovascular disease risk factors in HIV patients--association with antiretroviral therapy: results from the DAD study. AIDS. 2003;17:1179-1193.

5. Kannel WB. Blood pressure as a cardiovascular risk factor: prevention and treatment. JAMA. 1996;275:1571-1576.

6. Wilson PW, C'Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB. Prediction of coronary heart disease using risk factor categories. Circulation. 1998;97:1837-1847.

7. Levy D, Larson MG, Vasan RS, Kamek WB, Ho KK, et al. The progression from hypertension to congestive heart failure. JAMA. 1996;275:1557-1562.

8. Klag MJ, Whelton PK, Randall BL, et al. Blood pressure and end-stage renal disease in men. N Engl J Med. 1996;334:13-18.

9. Smith SR, Svetkey LP, Dennis VW. Racial differences in the incidence and progression of renal diseases. Kidney Int. 1991;40:815-822.

10. Psaty BM, Smith NL, Siscovick DS, et al. Health outcomes associated with antihypertensive therapies used as first-line agents. A systematic review and meta-analysis. JAMA. 1997;277:739-745.

11. SHEP Cooperative Research Group. Prevention of stroke by antihypertensive drug treatment in older persons with isolated systolic hypertension: final results of the Systolic Hypertension in the Elderly Program (SHEP). JAMA. 1991;265:3255-3264.

12. Gueyffier F, Froment A, Gouton M. New meta-analysis of treatment trials of hypertension: improving the estimate of therapeutic benefit. J Hum Hypertens. 1996;10:1-8.

13. Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA. 2002;288:2981-2997.

14. Chobanian AV, Bakris GL, Black HR, et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension. 2003;42:1206-1252.

15. Lewington S, Clark R, Qizilbash N, Peto R, Collins R. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet. 2002;360:1903-1913.

16. Appel LJ, Moore TJ, Obarzanek E, et al. A clinical trial of the effects of dietary patterns on blood pressure. DASH Collaborative Research Group. N Engl J Med. 1997;336:1117-1124.

17. Reyataz [package insert]. Princeton, New Jersey: Bristol-Myers Squibb Company; 2004.

18. Viramune [package insert]. Ridgefield, Connecticut: Boehringer Ingelheim; 2004.

19. Norvir [package insert]. North Chicago, Illinois: Abbott Laboratories; 2003.

20. Crixivan [package insert]. Whitehouse Station, New Jersey: Merck & Co., Inc.; 2004.


 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.

#11447 From: PoWeRTX@...
Date: Mon Apr 4, 2005 12:02 pm
Subject: Fwd: Two good suggestions from a member
nelsonvergel
Offline Offline
Send Email Send Email
 
In a message dated 4/4/2005 10:52:44 A.M. Central Standard Time, Mikefitz1965 writes:
Good Morning!  Comments listed below.  Hope all is well! 
Mike Fitz


PoWeRTX@... wrote:
  • Rather than copy a whole article onto this yahoo group if you could give the name of the article (and topic if not evident in the name), what you found interesting and the URL where to find the complete article along with the source information.
Disagree because sometimes the "poster(s)" modify or change the original subject so one still re-views the original article from organizations such as NATAP. 
Also, these posts serve one in a manner to join other mailing lists to stay informed/updated on latest/most recent news.
  • When replying to a message delete everything below the first line of the message you are replying to, as it shows up numerous times for the person who has subscribed to this group to receive the emails in digest form.  If you leave the sender, subject and first line of the message almost anyone would understand what message you are responding to.
Disagree once again.  Some people have issues with short term memory and to have to divert back to the group web site and research the original posting.  This suggestion also impacts new "members" negatively because they would start receiving posts in the middle of discussion and not know what was originally said.
 
I apologize for being blunt but please suggest to the person who made the suggestion to utilize the "delete" and "scroll" options which every MAC and PC have.
 
 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.
Good Morning!  Comments listed below.  Hope all is well! 
Mike Fitz


PoWeRTX@... wrote:
  • Rather than copy a whole article onto this yahoo group if you could give the name of the article (and topic if not evident in the name), what you found interesting and the URL where to find the complete article along with the source information.
Disagree because sometimes the "poster(s)" modify or change the original subject so one still re-views the original article from organizations such as NATAP. 
Also, these posts serve one in a manner to join other mailing lists to stay informed/updated on latest/most recent news.
  • When replying to a message delete everything below the first line of the message you are replying to, as it shows up numerous times for the person who has subscribed to this group to receive the emails in digest form.  If you leave the sender, subject and first line of the message almost anyone would understand what message you are responding to.
Disagree once again.  Some people have issues with short term memory and to have to divert back to the group web site and research the original posting.  This suggestion also impacts new "members" negatively because they would start receiving posts in the middle of discussion and not know what was originally said.
 
I apologize for being blunt but please suggest to the person who made the suggestion to utilize the "delete" and "scroll" options which every MAC and PC have.
 
Luv ya man!   

#11446 From: PoWeRTX@...
Date: Mon Apr 4, 2005 12:11 pm
Subject: Lipodystrophy: What’s Going On?
nelsonvergel
Offline Offline
Send Email Send Email
 
 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.

#11445 From: "markboothan" <markboothan@...>
Date: Sun Apr 3, 2005 9:45 pm
Subject: Re: Sculpra and Dr. Frechette
markboothan
Offline Offline
Send Email Send Email
 
I have no doubt what so ever that sculptra had nothing to do with your face
swelling.
You see sculptra is slowly digested by the body in less then one year, as such
it would be
impossible for you to have an allergic reaction to something that is no longer
in your body.
The most comon misconception is that sculptra is a filler, it is not, sculptra
stimulate ones
body to produce collagen.
Polylactic acid (sculptra has been used now for 40 years world wide to both
correct
unwanted side effects from surgery and to make dissolving stitches used after
minor
surgeries, to my knoledge there have never been any cases of relevant side
effects
including allergies to polylactic acid.
In fact it was the above that made me choose sculptra 4 years ago to correct my
face,
it is as safe as it can be and it gave me back my own face, no filler, my own
nerves and
veins running in my own face, it simply doesn't get any better then that.



--- In PozHealth@yahoogroups.com, "t a" <tarantxx@m...> wrote:
> I had my face treated in November of 2001 by Dr. Frechette.  He massaged my
face and
so did I as he had told me to do.  Suddenly, in February of 2003, my face swell
up.  If
someone would have seen me for the first time, they probably would not have
noticed it
but people who knew me, saw the difference.  I went back to Dr. Frechette who
gave me
some injections of cortison and that took care of the swelling. He or I had no
idea why I
had this late reaction such a long time after the treatments (I had 2)  but
could not think of
anything else that could have caused it.  Scultra or Newfill as it was called
then lasted well
over 2 years.  If I were willing to spend money again, I would still use
sculptra, even after
the "allergic" reaction I had.  My opinion is that the lumping has less to do
with the doctor
and more with the individual patient's tolerance.
> Brigitte
>
>   ----- Original Message -----
>   From: PozHealth@yahoogroups.com<mailto:PozHealth@yahoogroups.com>
>   To: PozHealth@yahoogroups.com<mailto:PozHealth@yahoogroups.com>
>   Sent: Saturday, April 02, 2005 12:32 PM
>   Subject: [PozHealth] Digest Number 974
>
>
>
>
>   There are 10 messages in this issue.
>
>   Topics in this digest:
>
>         1. Avascular Necrosis Risk Factors-steroids, alcohol
>              From: JuLev@a...<mailto:JuLev@a...>
>         2. Re: More on abacavir-induced neuropsychiatric reactions
>              From: Mike DC <mikedcguy@y...<mailto:mikedcguy@y...>>
>         3. Sculptra and Dr. Frechette
>              From: Sotoway@a...<mailto:Sotoway@a...>
>         4. Re: cheekbone implants
>              From: Fit4fundc@a...<mailto:Fit4fundc@a...>
>         5. Two good suggestions from a member
>              From: PoWeRTX@a...<mailto:PoWeRTX@a...>
>         6. Abdominal Adiposity the Best Predictor of Type 2 Diabetes in Men
>              From: beefymusclebud@a...<mailto:beefymusclebud@a...>
>         7. One stop patient assistence, this is important
>              From: beefymusclebud@a...<mailto:beefymusclebud@a...>
>         8. Assessing the Relationship Between Fatigue and Mitochondrial
Toxicity in Patient
>              From: PoWeRTX@a...<mailto:PoWeRTX@a...>
>         9. MRI to assess facial wasting and AVN
>              From: PoWeRTX@a...<mailto:PoWeRTX@a...>
>        10. HIV Transplant study website
>              From: PoWeRTX@a...<mailto:PoWeRTX@a...>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 1
>      Date: Thu, 31 Mar 2005 17:00:37 EST
>      From: JuLev@a...<mailto:JuLev@a...>
>   Subject: Avascular Necrosis Risk Factors-steroids, alcohol
>
>   NATAP - www.natap.org<http://www.natap.org/>
>
>   Avascular Necrosis in HIV-Infected Patients:
>   A Case-Control Study from the Aquitaine Cohort, 1997-2002, France
>
>   “…… This comparative analysis (CID 4/2005) investigating a wide range
of
>   factors revealed that current alcohol use and a history of steroid use were
>   strongly associated with the occurrence of AN….history of steroid use was
>   independently associated with a high risk of AN…...even short courses of
steroid
>   treatment increased this risk substantially….the first line of prevention
of this
>   bone disorder in HIV-infected patients should be the cessation of alcohol
>   consumption and the limitation of steroid prescription….Although it has
been
>   speculated that receipt of HAART is associated with the occurrence of AN, no
>   association between this bone disorder and the receipt or duration of
antiretroviral
>   therapy has been observed in the present comparative
study…….Hypertriglycemia
>   or hypercholesterolemia were not found to be predisposing factors, as is
>   described in the literature. In the present study, more case patients
presented
>   with high total cholesterol levels than did control subjects, and the number
of
>   case patients with hypertriglyceridemia was 5-fold greater than the number
of
>   control subjects with hypertriglyceridemia…….? see author 'Discussion
Below'
>
>   Clinical Infectious Diseases April 2005;40:1188-1193
>
>   Sylvie Lawson-Ayayi,1,2 Fabrice Bonnet,1,2 Elise Bernardin,1 Jean-Marie
>   Ragnaud,2 Denis Lacoste,2 Denis Malvy,2 Marie-Josée Blaizeau,2 Ghada M
>   iremont-Salamé,3 Michel Dupon,2 Patrick Mercié,1,2 and François Dabis,1,2
for
the Groupe
>   d'Epidémiologie Clinique du SIDA en Aquitaine (GECSA)a
>
>   1Institut National de la Santé et de la Recherche Médicale Unité 593,
>   Institut de Santé Publique, d'Epidémiologie et de Développement, and
2Centre
>   d'Information et de Soins de l'Immunodéficience Humaine, and 3Centre
Régional
de
>   Pharmacovigilance, Département de Pharmacologie, Equipe d'Accueil 3676,
Centre
>   Hospitalo-Universitaire de Bordeaux, Bordeaux, France
>
>   Using a case-control study design, we studied the factors associated with
>   HIV-related avascular necrosis (AN). During a 6-year period, 12 symptomatic
AN
>   cases were validated, and each case was individually matched with 3 control
>   cases. A conditional logistic regression model showed that current alcohol
>   consumption and a history of steroid use were the only factors associated
with the
>   occurrence of AN.
>
>   Since HAART was introduced and its use has become widespread in
>   industrialized countries, rates of mortality and severe morbidity related to
HIV infection
>   have been drastically reduced. Although survival rates and quality of life
>   have improved among HIV-infected individuals, adverse consequences of
long-term
>   exposure to antiretroviral regimens have emerged [1-4]. Particularly,
metabolic
>   complications have been diagnosed in HIV-infected patients who are treated
>   with HAART, and they have been associated with the receipt of protease
>   inhibitors (PIs) and nonnucleoside reverse-transcriptase inhibitors (NNRTIs)
[5-8].
>   More recently, cases of avascular necrosis (AN), also referred to as
>   osteonecrosis, have been reported [9-20], but few studies have reported an
increased
>   incidence of this severe bone disorder [3, 4]. The incidence of asymptomatic
AN
>   among HIV-infected patients was estimated to be 4.4%, through systematic
>   screening with MRI [21]. The annual incidence of AN, whether symptomatic or
not, in
>   the general population has been estimated to be between 0.010% and 0.135%
[15,
>   22-24]. Thus, the incidence of AN among HIV-infected adults has been found
to
>   be 〜45 times greater than the incidence in the general population [15],
which
>   suggests that its occurrence is a consequence of or a complication of either
>   HIV infection or receipt of HAART [25].
>
>   Several risk factors and conditions, such as hyperlipidemia, alcohol abuse,
>   steroid use, pancreatitis, and underlying vascular diseases, have been
>   postulated to be associated with AN [14, 26]. Case reports also have
suggested that
>   HIV infection and antiretroviral therapy, particularly HAART regimens, could
>   also be risk factors for AN, independent of underlying comorbidities [17];
>   however, to our knowledge, no systematic study has been conducted thus far.
We
>   studied the main known and hypothesized risk factors for symptomatic cases
of AN
>   that were identified in a large cohort of HIV-infected patients.
>
>   Results.      Through December 2002, a total of 12 symptomatic AN cases were
>   identified and validated. Eleven of the 12 cases were in men. The median age
>   of the case patients was 38.3 years (interquartile range [IQR], 36.2-45.2),
and
>   9 case patients had received a diagnosis of AIDS. The median time since
>   diagnosis of HIV infection was 10.4 years (IQR, 8.6-12.9). All case patients
had
>   been exposed to HAART (consisting of at least 3 antiretroviral drugs,
including
>   a PI or an NNRTI) before the occurrence of AN. Criteria used for matching
had
>   comparable values in the case and control groups at baseline: median ages
were
>   38.3 years and 38.4 years, respectively (P = .83); median CD4+ cell counts
at
>   the time of diagnosis of HIV infection were 266.5 cells/mL and 272.0
>   cells/mL, respectively (P = .66); and median durations of HIV infection
since the time
>   of diagnosis were 123.0 months and 125.1 months, respectively (P = 94).
>
>   In univariate analyses, case patients were more likely than control subjects
>   to be men who reported sex with men, to have fat accumulation, and to engage
>   in regular or heavy alcohol use, according to physicians' reports. Neither
>   receipt of a specific antiretroviral drug nor the duration of HAART was
associated
>   with AN. However, history of intravenous or oral course of steroid treatment
>   was associated with AN occurrence at a borderline level of statistical
>   significance.
>
>   In the multivariate analyses, the only adjusted matched OR (aOR) >1 was for
>   alcohol consumption (P = .02). Statistical association appeared to be of
>   borderline significance in the reduced model with regard to fat accumulation
(P =
>   .07) and receipt of efavirenz, ritonavir, or nelfinavir (P = .08, P = .05,
and P
>   = .09, respectively).
>
>   When all factors identified by the 2 initial multivariate analyses were
>   combined in the final model, the risk of the occurrence of AN remained
>   significantly associated with alcohol consumption (aOR, 20.48; 95% CI,
1.83-229.72; P
=
>   .01) and history of steroid use (aOR, 16.96; 95% CI, 1.20-239.12; P = .04),
>   whereas fat accumulation failed to be associated with the occurrence of AN
(aOR,
>   22.67; 95% CI, 0.69-745.95; P = .08).
>
>   Author Discussion
>   This comparative analysis investigating a wide range of factors revealed
that
>   current alcohol use and a history of steroid use were strongly associated
>   with the occurrence of AN. The findings of the present study also provided a
>   presumption of an association of AN with fat accumulation. The association
of the
>   occurrence of AN with receipt of HAART or the individual components of HAART
>   was not confirmed. Despite the fact that a trend for association with AN was
>   detected for receipt of individual drugs, receipt of PIs or NNRTIs , when
>   considered as cumulative exposure before the diagnosis of AN, could not be
>   identified as having an association with the occurrence of AN. Nevertheless,
the role
>   of antiretroviral therapy, if any, is probably limited, compared with the
roles
>   of steroid use and alcohol use.
>
>   Hypertriglycemia or hypercholesterolemia were not found to be predisposing
>   factors, as is described in the literature [23, 28]. In the present study,
more
>   case patients presented with high total cholesterol levels than did control
>   subjects, and the number of case patients with hypertriglyceridemia was
5-fold
>   greater than the number of control subjects with hypertriglyceridemia (data
not
>   shown). The potential link between hyperlipidemia and AN supports the
>   hypothesis that the use of PIs is implicated, through an increase of serum
lipid
>   levels, in the occurrence of AN [29]. Scribner et al. [22] have suggested
that
>   moderate hypertriglyceridemia is an independent risk factor for the
occurrence of
>   AN but that severe hypertriglyceridemia is more likely to be associated with
>   AN by means of PI therapy.
>
>   Previous studies have concluded that HIV infection alone may be a risk
factor
>   for AN [28, 30]. Although it has been speculated that receipt of HAART is
>   associated with the occurrence of AN [10], no association between this bone
>   disorder and the receipt or duration of antiretroviral therapy has been
observed in
>   the present comparative study. This is possibly because antiretroviral
>   therapy is widely used in hospital-based cohorts with unlimited access to
care, as
>   is the case in France. The lack of an association between the receipt of PIs
>   and the occurrence of AN has been observed in other studies, as well [16,
21,
>   24, 31].
>
>   Steroid use and alcohol abuse are the most common risk factors associated
>   with AN [26]. Indeed, in the present study, a history of steroid use was
>   independently associated with a high risk of AN, and the association did
persist when
>   the analysis was adjusted for other variables. This result confirmed
findings
>   of previous case-control studies that reported an association between
steroid
>   use and the occurrence of AN but could not control for as many factors as we
>   did in the present analysis [22, 31]. Miller et al. [21] indicated that even
>   short courses of steroid treatment increased this risk substantially. In the
>   present study, "alcohol use" was defined as the consumption of any
combination of
>   different types of alcohol (wine, beer, and cocktails). Because French
>   consumers usually record a more regular intake of alcoholic beverages than
do
>   consumers elsewhere in the world, we considered regular or heavy drinkers to
be the
>   "high-exposure" category. The estimation of this risk factor by physicians
>   from patients' self-reported behavior could have introduced a bias that is a
>   common limitation of studies on alcohol intake. We could not investigate
>   hereditary vascular diseases-in particular, the presence of antiphospholipid
>   antibodies, which may contribute to the occurrence of AN, given its high
prevalence
>   among HIV-infected patients [32].
>
>   To our knowledge, the present analysis is the first to investigate the
>   contribution of antiretroviral therapy to the occurrence of AN in detail and
by use
>   of a powerful comparative design, and the first to finally rule out its
role.
>   HIV-infected patients with asymptomatic cases of AN were not included in the
>   present study, because of the system we used to find cases. Thus, we
evaluated
>   only symptomatic cases of AN, and our findings should not be extrapolated to
>   all cases of AN. Because the limited number of cases may have affected the
>   outcome of the present study, large, collaborative epidemiological studies
are
>   still needed to confirm our results and to fully evaluate the role of
>   antiretroviral therapy in AN, symptomatic or not. Finally, the mechanisms
that lead to
AN
>   in HIV-infected patients must also be determined. In the interim, the first
>   line of prevention of this bone disorder in HIV-infected patients should be
the
>   cessation of alcohol consumption and the limitation of steroid prescription.
>
>   Patients and methods.      We performed a case-control study nested within
>   the Aquitaine Cohort [27]. The Aquitaine Cohort comprises patients enrolled
>   through a hospital-based surveillance system of HIV infection in
southwestern
>   France. Beginning in 1987, adult inpatients and outpatients were enrolled
>   prospectively in the present case-control study if they were referred by
participating
>   hospital wards, had confirmed HIV-1 infection and at least 1 follow-up visit
>   after enrollment or a documented date of death after initial reporting, and
>   provided informed consent. Follow-up is based on clinical practice; a
>   standardized reporting form for epidemiological, clinical, biological, and
therapeutic
>   data is completed by physicians at the time of each hospital contact, which
>   generally occur every 3 or 6 months or in the case of any intercurrent
event.
>
>   All symptomatic cases of AN that were reported through December 2002 through
>   either the cohort monitoring system or the pharmaco-epidemiology information
>   system maintained by the Bordeaux University Hospital were systematically
>   investigated. These 2 reporting systems allowed us to identify AN cases that
had
>   been diagnosed by physicians since the first AN case notification in 1997.
>   Symptomatic AN cases were detected on the basis of clinical symptoms and
confirmed
>   by radiological or scintigraphical imaging. For each patient with a
confirmed
>   case, we randomly selected 3 control subjects from the Aquitaine Cohort
>   database who showed no clinical evidence of AN and who could be matched on
the
basis
>   of age (±3 years), time since the diagnosis of HIV infection (±2 years),
CD4+
>   cell count at the time of diagnosis of HIV infection (i.e., <200 cells/mL,
>   200-349 cells/mL, 350-499 cells/mL, or &ges;500 cells/mL), and duration of
>   follow-up after the diagnosis of HIV infection. Information on demographic
>   characteristics, clinical data, biological values, and antiretroviral
therapy use were
>   retrieved from the database for case patients and control subjects and were
>   systematically verified using clinical records for the purpose of the
present
>   study.
>
>   Association of the occurrence of AN with a given variable was estimated by
>   the matched odds ratio (OR). A conditional logistic regression model was
used to
>   analyze the simultaneous effects of several independent factors. A variable
>   was included in the multivariate model if it was associated with the
occurrence
>   of AN at a statistical significance of P < .25 in univariate analysis.
>   Because of the small number of observations relative to the number of
variables, 2
>   models were first developed: one model with demographic, clinical, and
>   biological variables, and the other with variables relating to
antiretroviral therapy.
>   In each model, a backward stepwise procedure was applied to remove variables
>   that were not significantly associated with the occurrence of AN. A forward
>   selection was then applied for the robustness of the analysis. The variables
>   that were retained in the 2 separate models were included in a final model.
>   Models were fitted using STATA software, version 5.0 (Stata).
>
>   REFERENCES
>   1.      Herman JS, Easterbrook PJ. The metabolic toxicities of
antiretroviral
>   therapy. Int J STD AIDS 2001; 12:555-62. First citation in article | PubMed
>   2.      Powderly WG. Long-term exposure to lifelong therapies. J Acquir
>   Immune Defic Syndr 2002; 29(Suppl 1):S28-40. First citation in article |
PubMed
>   3.      Gutierrez F, Padilla S, Ortega E, et al. Avascular necrosis of the
>   bone in HIV-infected patients: incidence and associated factors. AIDS 2002;
>   16:481-3. First citation in article | PubMed
>   4.      Keruly JC, Moore RD. Incidence and risk factors for avascular
>   necrosis (AVN) in HIV-infected persons [abstract H-2]. In: Program and
abstracts of
>   the 10th Conference on Retrovirus and Opportunistic Infections (Boston).
2003.
>   First citation in article
>   5.      Fellay J, Boubaker K, Ledergerber B, et al. Prevalence of adverse
>   events associated with potent antiretroviral treatment: Swiss HIV Cohort
Study.
>   Lancet 2001; 358:1322-7. First citation in article | PubMed
>   6.      Bonfanti P, Ricci E, Landonio S, et al. Predictors of protease
>   inhibitor-associated adverse events. Biomed Pharmacother 2001; 55:321-3.
First
>   citation in article | PubMed
>   7.      Bonnet F, Lawson-Ayayi S, Thiébaut R, et al. A cohort study of
>   nevirapine tolerance in clinical practice: French Aquitaine Cohort,
1997-1999. Clin
>   Infect Dis 2002; 35:1231-7. First citation in article | Full Text | PubMed
>   8.      Montessori V, Press N, Harris M, Akagi L, Montaner JS. Adverse
>   effects of antiretrovial therapy for HIV infection. CMAJ 2004; 170:229-38.
First
>   citation in article | PubMed
>   9.      Olive A, Queralt C, Sirera G, Centelles M, Force L. Osteonecrosis
and
>   HIV infection: four more cases. J Rheumatol 1998; 25:1243-4. First citation
>   in article | PubMed
>   10.      Meyer D, Behrens G, Schmidt RE, Stoll M. Osteonecrosis of the
>   femoral head in patients receiving HIV protease inhibitors. AIDS 1999;
13:1147-8.
>   First citation in article | PubMed
>   11.      Johns DG, Gill MJ. Avascular necrosis in HIV infection. AIDS 1999;
>   13:1997. First citation in article | PubMed
>   12.      Blangy H, Loeuille D, Chary-Valckenaere I, Christian B, May T,
>   Gillet P. Osteonecrosis of the femoral head in HIV-1 patients: four
additional
>   cases. AIDS 2000; 14:2214-5. First citation in article | PubMed
>   13.      Roudière L, Viard JP. Ostenecrosis of the hip, lipodystrophy and
>   antiretroviral treatment. AIDS 2000; 14:2056. First citation in article |
PubMed
>   14.      Wolfe CJ, Taylor-Butler KL. Avascular necrosis: a case history and
>   literature review. Arch Fam Med 2000; 9:291-4. First citation in article |
>   PubMed
>   15.      Brown P, Crane L. Avascular necrosis of bone in patients with human
>   immunodeficiency virus infection: report of 6 cases and review of the
>   literature. Clin Infect Dis 2001; 32:1221-6. First citation in article |
Full Text |
>   PubMed
>   16.      Gaughan DM, Mofenson LM, Hughes MD, Seage GR, Ciupak GL, Oleske JM.
>   The Pediatric AIDS Clinical Trials Group. Osteonecrosis of the hip
>   (Legg-Calvé-Perthes disease) in human immunodeficiency virus-infected
children.
>   Pediatrics 2002; 109:E74. First citation in article | PubMed
>   17.      Bongiovanni M, Chiesa E, Riva A, D'Arminio Monforte A, Bini T.
>   Avascular necrosis of the femoral head in a HIV-1 infected patient receiving
>   lopinavir/ritonavir. Int J Antimicrob Agents 2003; 22:630-1. First citation
in
>   article | PubMed
>   18.      Valencia ME, Barreiro P, Soriano V, Blanco F, Moreno V, Lahoz JG.
>   Avascular necrosis in HIV-infected patients receiving antiretroviral
treatment:
>   study of 7 cases. HIV Clin Trials 2003; 4:132-6. First citation in article |
>   PubMed
>   19.      Gasiorowski J, Knysz B, Sokolska V, Gladysz A. Avascular necrosis
of
>   femoral heads in a man with HIV infection. Lancet Infect Dis 2003; 3:708.
>   First citation in article | PubMed
>   20.      Calza L, Manfredi R, Chiodo F. Osteonecrosis in HIV-infected
>   patients and its correlation with highly active antiretroviral therapy
(HAART) [in
>   French]. Presse Med 2003; 32:595-8. First citation in article | PubMed
>   21.      Miller KD, Masur H, Jones EC, et al. High prevalence of
>   osteonecrosis of the femoral head in HIV-infected adults. Ann Intern Med
2002; 137:
17-25.
>   First citation in article | PubMed
>   22.      Scribner A, Troia-Cancio PV, Cox BA, et al. Osteonecrosis in HIV: a
>   case-control study. J Acquir Immune Defic Syndr 2000; 25:19-25. First
citation
>   in article | PubMed
>   23.      Allison GT, Bostrom MP, Glesby MJ. Osteonecrosis in HIV disease:
>   epidemiology, etiologies, and clinical management. AIDS 2003; 17:1-9. First
>   citation in article | PubMed
>   24.      Keruly JC, Chaisson RE, Moore RD. Increasing incidence of avascular
>   necrosis of the hip in HIV-infected patients. J Acquir Immune Defic Syndr
>   2001; 28:101-2. First citation in article | PubMed
>   25.      Monier P, McKown K, Bronze MS. Osteonecrosis complicating highly
>   active antiretroviral therapy in patients infected with human
immunodeficiency
>   virus. Clin Infect Dis 2000; 31:1488-92. First citation in article | Full
Text |
>   PubMed
>   26.      Blacksin MF, Kloser PC, Simon J. Avascular necrosis of bone in
human
>   immunodeficiency virus infected patients. Clin Imaging 1999; 23:314-8. First
>   citation in article | PubMed
>   27.      Marimoutou C, Chêne G, Dabis F, Lacoste D, Salamon R. Human
>   immunodeficiency virus infection and AIDS in Aquitaine: 10 years' experience
of a
>   hospital information system, 1985-1995. Le Groupe d'Epidemiologie Clinique
du SIDA
>   en Aquitaine (GECSA) [in French]. Presse Med 1997; 26:703-10. First citation
>   in article | PubMed
>   28.      Ries MD, Barcohana B, Davidson A, Jergesen HE, Paiement GD.
>   Association between human immunodeficiency virus and osteonecrosis of the
femoral
>   head. J Arthroplasty 2002; 17:135-9. First citation in article | PubMed
>   29.      Bonfanti P, Grabbuti A, Carradori S, et al. Osteonecrosis in
>   protease inhibitor-treated patients. Orthopedics 2001; 24:271-2. First
citation in
>   article | PubMed
>   30.      Skiest DJ. Osteonecrosis in human imunodeficiency virus-infected
>   patients may not be related to immune reconstitution. Clin Infect Dis 2001;
>   33:268-9. First citation in article | Full Text | PubMed
>   31.      Glesby MJ, Hoover DR, Vaamonde CM. Osteonecrosis in patients
>   infected with human immunodeficiency virus: a case-control study. J Infect
Dis 2001;
>   184:519-23. First citation in article | Full Text | PubMed
>   32.      Bonnet F, Pineau JJ, Taupin JL, et al. Prevalence of
>   cryoglobulinemia and serological markers of autoimmunity in human
immunodeficiency virus
>   infected individuals: a cross-sectional study of 97 patients. J Rheumatol
2003;
>   30:2005-10. First citation in article | PubMed
>
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 2
>      Date: Thu, 31 Mar 2005 14:52:57 -0800 (PST)
>      From: Mike DC <mikedcguy@y...<mailto:mikedcguy@y...>>
>   Subject: Re: More on abacavir-induced neuropsychiatric reactions
>
>
>   This is all VERY INTERESTING.  I tried Sustiva and
>   couldn't stand it.  My doctor then tried Abacavir, and
>   I told him I still felt "messed up," so we stopped
>   that as well.  This was all a few years ago.
>   At the time, my doctor told me that Abacavir wasn't
>   known to have such side effects.  I felt very
>   disoriented on the stuff.  Thanks Nelson for posting
>   all of this on Abacavir - it feels like a mystery has
>   been solved (and I feel slightly vindicated).  These
>   meds really can have a range of side effects for
>   diffent people. OH well ...
>
>
>   --- PoWeRTX@a...<mailto:PoWeRTX@a...> wrote:
>
>   > This happened  to me also. I know several  people
>   > that have had the same
>   > problem on Ziagen. Doctors and patients do not  know
>   > about this.
>   > More on abacavir-induced neuropsychiatric reactions.
>   >
>   > Foster R, Taylor C, Everall IP.
>   > AIDS. 2004 Dec 3;18(18):2449.
>   > It is increasingly recognized that  antiretroviral
>   > medications may induce
>   > severe, but transient, changes in mental  state.
>   > These are uncommon and
>   > idiosyncratic, with the literature containing only
>   > two published reports suggesting
>   > that abacavir (Ziagen), a nucleoside reverse
>   > transcriptase inhibitor, may
>   > induce a range of neuropsychiatric disorders in
>   > seropositive individuals. These
>   > include depression, suicidal thoughts, auditory
>   > hallucinations [_1_
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e<http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/
ovidweb.cgi?QS2=434f4e1a73d37e>
>   >
>
8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8
d6761
>   >
>
84e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af53
4fa8b6
>   > #17) ]  and frank psychosis [_2_
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d154<http://
gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d154>
>   >
>
97b83b9e5baab68f6262d35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8
092db
>   > 6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#18) ].
>   >  Of note is the fact
>   > that the subjects in these cases were all female
>   > with CD4  cell counts below 500
>   > cells/µl. Here we report, for the first time, a
>   > case of a  possible
>   > abacavir-induced neuropsychiatric reaction in a
>   > seropositive Caucasian  man with a
>   > higher CD4 cell count.
>   > The patient was a 44-year-old gay man who was
>   > diagnosed HIV positive in
>   > 1993. He was referred to psychiatric services in
>   > 2000  after the psychologist whom
>   > he had been seeing became concerned about the
>   > patient's ongoing depressive
>   > symptoms. He had previously been treated with
>   > various antidepressants and
>   > triple therapies for HIV, and was currently
>   > receiving citalopram 30 mg a day in
>   > addition to tenofovir 245 mg per day,  nevirapine
>   > 200 mg twice a day and
>   > abacavir 300 mg twice a day. He had previously  been
>   > taking didanosine, but this was
>   > changed to abacavir because of  lipodystrophy.
>   > Approximately one week after commencing  abacavir,
>   > the patient started to
>   > complain of feeling tired and ‘stoned'. He also
>   > complained of headaches, which
>   > were described as ‘constant and throbbing’ and
>   > ‘located in the middle of my
>   > brain'. He reported the onset of bad dreams, which
>   > he referred to as ‘night
>   > terrors'. These were described as vivid and
>   > terrifying,  but the actual content
>   > could not be recalled. He denied any associated
>   > physical  symptoms such as
>   > night sweats or any recent physical illness. His CD4
>   > cell count  at this time was
>   > 557 cells/µl and his viral load was less than 50
>   > copies/ml. Of  note is the
>   > fact that despite his dreams he now felt that his
>   > previously low  mood had
>   > improved to the extent that he was expressing the
>   > desire to cease  taking
>   > citalopram.
>   > Two weeks after reporting the above problems,  the
>   > patient was reviewed by
>   > the HIV physician who changed the abacavir back to
>   > didanosine. Within 24 h of
>   > this the patient reported that his headaches and bad
>   >  dreams had stopped, and
>   > that he was feeling less fatigued. At one month
>   > follow-up he remained free of
>   > these symptoms, and his mood remained settled. The
>   > citalopram was eventually
>   > reduced gradually and finally stopped.
>   > This case suggests that abacavir may, in rare
>   > cases, induce unpleasant but
>   > non-specific neuropsychiatric side-effects, which
>   > can resolve rapidly upon
>   > stopping this medication. Although it has been
>   > suggested that abacavir may be
>   > associated with new-onset depression [_1_
>   > (http://gateway.ut.ovid.com.ezproxyhost.library<http://
gateway.ut.ovid.com.ezproxyhost.library/>.
>   >
>   tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d
35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da
>   >
>   8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#17)
>   > ],  this was not
>   > apparent in the current case. In that earlier
>   > publication [_1_
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3<http://
gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3>
>   >
>
ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d676184
e80885
>   >
>
5bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#17
)
>   > ],
>   >  depression and night sweats were reported in one
>   > patient, with depression,
>   > suicidal ideation, headache, auditory hallucinations
>   > and anorexia in the
>   > second.  The patients in those cases were both HIV
>   > positive Caucasian women.
>   > Similarly, a  more recent publication described a
>   > case of putative abacavir-induced
>   > psychosis  occurring in an African woman [_2_
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b5<http://
gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b5>
>   >
>
3d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d676184e808855bd7f41
5e7acd
>   >
>   48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#18)
>   > ]  who became
>   > symptom-free after the cessation and substitution of
>   > this  medication.
>   > The current report suggests that men can also  be
>   > adversely affected by
>   > abacavir-associated neuropsychiatric problems, even
>   > at  a higher CD4 cell count
>   > accompanied by a low viral load. Furthermore,
>   > symptoms  may rapidly resolve upon
>   > discontinuation of abacavir and the substitution of
>   > a  suitable alternative
>   > antiretroviral agent. It is possible that headache
>   > and mood  alterations may be
>   > early indicators of neuropsychiatric sequelae
>   > associated with  abacavir. These
>   > should be investigated and monitored closely to
>   > exclude possible  organic
>   > factors. Management should be carried out in
>   > collaboration with both HIV
>   > physicians and specialist psychiatrists.
>   > References
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d
3<http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d
3>
>   >
>
5fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d
164cd5
>   > 11242a35a0302af534fa8b6#toc)
>   > 1. Colebunders R, Hilbrands R, De Roo A, Pelgrom J.
>   > Neuropsychiatric reaction
>   > induced by abacavir.  Am J Med 2002; 113:616.
>   > _ExternalResolverBasic_
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
Link+Set+Ref=0<http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/
ovidweb.cgi?Link+Set+Ref=0>
>   >
>   0002030-200412030
-00021|00000439_2002_113_616_colebunders_neuropsychiatric_|00
>   >
>   002030-200412030-00021#xpointer(id(R1-21))|1103920|http://acs.ovid.com/acs/
.f6
>   >
>
489bf4937db0b6e5a4e52b4a0f690866ea468998ca8e6ac6e6d949d499ba8ceb07ec98d25
42738
>   >
>
eb60d9d5afd443af26842fbd2b397e36e9ea7cf26a19744cf8bf2cf6fefeecf6eb.gif|ovftdb|
>   >
>   00000439-200211000
-00018&P=17&S=IDNJHKJKBAMCKK00D&WebLinkReturn=Full+Text=L|S.
>   > sh.15.16|0|00002030-200412030-00021)
>   > _Bibliographic  Links_
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
Link+Set+Ref=00002030<http://gateway.ut.ovid.com.ezproxyhost.library.tmcedu/gw2/
ovidweb.cgi?Link+Set+Ref=00002030>-
>   >
>   200412030
-00021|00000439_2002_113_616_colebunders_neuropsychiatric_|00002030-2
>   >
>  
00412030-00021#xpointer(id(R1-21))|60|http://acs.ovid.com/acs/.6f8cf7c31ada011
>   >
>
97afb0a1ba3d293b287b71168019f9ea6ec0cdc7f51235e3420b469cc1e8a8406f3c6be4f1
4376
>   >
>   dfd09416d1f878f23bb78.gif|ovftdb|00000439-200211000
-00018&P=17&S=IDNJHKJKBAMCK
>   >
>   K00D&WebLinkReturn=Full+Text=L|S.sh.15.16|0|00002030-200412030-00021)
>   >
>   > _[Context  Link]_
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d
3<http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d
3>
>   >
>
5fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d
164cd5
>   > 11242a35a0302af534fa8b6#10)
>   > 2. Foster R, Olajide D, Everall IP. Antiretroviral
>   > therapy-induced psychosis:
>   > case report and brief  review of the literature. HIV
>   > Med  2003; 4:139"144.
>   > _[Context  Link]_
>   >
>   (http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f62<ht
tp://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?
QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f62>
>   >
>
62d35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2
cb6d16
>   > 4cd511242a35a0302af534fa8b6#10) Accession Number:
>   > 00002030-200412030-00021
>   >
>   > In  health,
>   >
>   > Nelson Vergel
>   > Director
>   > Program for Wellness Restoration,  PoWeR
>   > A 501 (c) 3 non profit national  organization
>   > powerusa.org
>   > salvagetherapies.org
>   > faciawasting.org
>   >
>   >
>   > Disclaimer
>   >
>   > This  information (and any accompanying printed
>   > material) is not intended to
>   > replace  the attention or advice of a physician or
>   > other health care
>   > professional. Anyone  who wishes to embark on any
>   > dietary, drug, exercise, or other
>   > lifestyle change  intended to prevent or treat a
>   > specific disease or condition
>   > should first  consult with and seek clearance from a
>   > qualified health care
>   > professional.
>   >
>
>
>   __________________________________________________
>   Do You Yahoo!?
>   Tired of spam?  Yahoo! Mail has the best spam protection around
>   http://mail.yahoo.com<http://mail.yahoo.com/>
>
>
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 3
>      Date: Thu, 31 Mar 2005 19:28:51 EST
>      From: Sotoway@a...<mailto:Sotoway@a...>
>   Subject: Sculptra and Dr. Frechette
>
>   Hi All;
>
>   I had my second treatment with the great Doctor my face appears completely
>   restored.  It was a bit uncomfortable, but worth the discomfort.  I 
strongly
>   recommend him.  He is patient and shows great deal of  expertise.  I believe
>   that the massage and cold ice treatment play a big  role in the prevention
of
>   bumps under the skin that a lot of you have been  complaining about.  If
anyone
>   can wants to see him he has an office in New  york as well as San Francisco.
>
>
>   Nancy
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 4
>      Date: Thu, 31 Mar 2005 21:15:18 EST
>      From: Fit4fundc@a...<mailto:Fit4fundc@a...>
>   Subject: Re: cheekbone implants
>
>   Cheek implants have their advantages too.   The implants can be trimmed.
They
>   come in different sizes and shapes.   If you don't like the really wide ones
>   but you like the fact that it is very thick, the surgeon can trim it so it
>   isn't so wide.   My surgeon inserted the largest pair and they were still a
>   little to wide for me.    They gave me too much of a cheek and too wide up
near my
>   eye socket and to the side of my face.   I had a few infections and one had
to
>   be removed twice.   If I had it to do all over, I would opt for only the
>   fillers like BioAlcamid.
>
>   Cheek implants can change the look of your face to something you never
looked
>   like.   Personally, I like long hard faces on men.   My cheeks implants made
>   me more rounded, not what I really wanted.   However, they did fill up the
>   thumb prints in my face.
>
>   It's a hard choice sometimes.
>
>
>   Lester in DC
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 5
>      Date: Thu, 31 Mar 2005 21:50:21 EST
>      From: PoWeRTX@a...<mailto:PoWeRTX@a...>
>   Subject: Two good suggestions from a member
>
>
>       *   Rather than copy a whole article  onto this yahoo group if you could
>   give the name of the article (and topic if  not evident in the name), what
you
>   found interesting and the URL where to  find the complete article along with
>   the source information.
>       *   When replying to a message delete everything  below the first line
of
>   the message you are replying to, as it shows up  numerous times for the
>   person who has subscribed to this group to receive the  emails in digest
form.  If
>   you leave the sender, subject and first line  of the message almost anyone
>   would understand what message you are responding  to.
>
>
>   In  health,
>
>   Nelson Vergel
>   Director
>   Program for Wellness Restoration,  PoWeR
>   A 501 (c) 3 non profit national  organization
>   powerusa.org
>   salvagetherapies.org
>   faciawasting.org
>
>
>   Disclaimer
>
>   This  information (and any accompanying printed material) is not intended to
>   replace  the attention or advice of a physician or other health care
>   professional. Anyone  who wishes to embark on any dietary, drug, exercise,
or other
>   lifestyle change  intended to prevent or treat a specific disease or
condition
>   should first  consult with and seek clearance from a qualified health care
>   professional.
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 6
>      Date: Thu, 31 Mar 2005 23:30:51 EST
>      From: beefymusclebud@a...<mailto:beefymusclebud@a...>
>   Subject: Abdominal Adiposity the Best Predictor of Type 2 Diabetes in Men
>
>
>   Abdominal Adiposity the Best Predictor of Type 2 Diabetes in  Men
>
>
>   NEW YORK Mar 31 - Both overall obesity, denoted by higher BMI, and abdominal
>   obesity, reflected by higher waist circumference strongly and independently
>   predict risk of type 2 diabetes in men, but abdominal obesity appears to be
>   the  better predictor, new research shows.
>   "Both BMI and waist circumference are useful for assessing health risk and
>   should be measured in clinical settings and epidemiologic research whenever
>   possible," the investigators say. But abdominal fat measured by waist
>   circumference "can indicate a strong risk for diabetes whether or not a man
is
>   considered overweight or obese according to his BMI," lead author Dr. Youfa
Wang
>   added in a statement.
>   In the study, investigators compared the predictive power of BMI, waist
>   circumference (WC) and waist-to-hip ratio (WHR) for the development of type
2
>   diabetes in 27,270 men participating in the Health Professionals Follow-up
>   Study.
>   During 13 years of follow up, a total of 884 men developed type 2 diabetes,
>   Dr. Wang, from Johns Hopkins Bloomberg School of Public Health in Baltimore,
>   and  colleagues report in the March issue of the American Journal of
Clinical
>   Nutrition.
>   According to the team, the age-adjusted relative risks across quintiles of
>   WC, starting at a WC of 73.7 to 86.4 cm (29 to 34 inches) and going up to
101.6
>    to 157.5 cm, were 1.0, 2.0, 2.7, 5.0, and 12.0, respectively, they report.
>   For WHR, relative risks across increasing quintiles were 1.0, 2.1, 2.7, 3.6,
>   and 6.9 and for BMI they were 1.0, 1.1, 1.8, 2.9, and 7.9, respectively.
>   "Our findings support the contention that the measurement of WC should be
>   used in clinical practice instead of WHR," the investigators write.
>   The study findings also suggest that the currently recommended cutoff for
>   high waist circumference of 102 cm (40 inches) for men may need to be
lowered to
>    95 cm. "Many of the men who developed type 2 diabetes had measurements
lower
>    than the cutoff, Dr. Wang explained, "and the risk associated with the
waist
>    circumference increased at a much lower level."
>   Am J Clin Nutr 2005;81:555-563.
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 7
>      Date: Thu, 31 Mar 2005 23:33:25 EST
>      From: beefymusclebud@a...<mailto:beefymusclebud@a...>
>   Subject: One stop patient assistence, this is important
>
>   Some Free Medicine Programs Too Complex: Survey
>
>   Mar 30 - Drug company programs that offer free medicines to the poor are 
too
>   time-consuming and complex for some health clinics that serve mostly
>   low-income patients, according to a survey released on Tuesday.
>   Of 214 clinics in five states that were surveyed in 2002, forty-eight said
>   they did not participate in patient assistance programs that provide free
>   medicines to people who cannot afford them.
>   More than two thirds of the clinics that did not take part said the programs
>   were cumbersome and took too much time. Some companies required tax returns
>   and  made other unrealistic demands for income documentation, the survey
said.
>   The Pharmaceutical Research and Manufacturers of America, an industry group,
>   has encouraged companies to simplify application forms, spokesman Ken
Johnson
>    said.
>   "Can we do a better job? Yes, and we will," he said.
>   Early next month, the industry will unveil a new program that will provide
>   one-stop access to 275 existing patient assistance programs, Johnson  said.
>   "We are going to make it easier and quicker to obtain information," he said,
>   adding that millions of people already get free or discounted drugs from
>   manufacturers each year.
>   The health-clinic survey found the drug donation programs consumed an
average
>    of 12 hours of pharmacist time, and 99 hours of other staff time, per
month.
>   While clinic staff believed the donated drugs filled an important need, they
>   "don't understand why complicated and changing programs must take so much
>   time  away from patient care," said Kathryn Duke, the study's lead author
and
>   director  for the Medicine for People in Need program of the nonprofit
Public
>   Health  Institute.
>   The study, funded by the philanthropic California Health Care Foundation,
>   will be published in the April 1st edition of the American Journal of
>   Health-System Pharmacy.
>   Charitable programs from GlaxoSmithKline Plc, Novartis AG and
Schering-Plough
>    Corp. were identified as least likely to be used, while others offered by
>   Pfizer  Inc., Bristol-Myers Squibb Co. and Merck & Co. Inc. were used most
>   frequently.
>   GlaxoSmithKline spokeswoman Patricia Seif said the company donated medicines
>   worth $372 million last year to U.S. patients. "We try to make it easy" to
>   participate, she said, adding that many patients get the requested drugs the
>   same  day.
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 8
>      Date: Fri, 1 Apr 2005 16:04:34 EST
>      From: PoWeRTX@a...<mailto:PoWeRTX@a...>
>   Subject: Assessing the Relationship Between Fatigue and Mitochondrial
Toxicity in
Patient
>
>
>   Both HIV infection and antiretroviral nucleoside analogues (nucleoside
>   reverse transcriptase inhibitors or NRTIs) are known to affect mitochondrial
DNA
>   content and mitochondrial function. A number of important clinical syndromes
>   observed in HIV-infected persons relate to mitochondrial dysfunction
including
>   lactic acidosis, myopathy, cardiomyopathy, pancreatitis, peripheral
>   neuropathy,  and possibly lipodystrophy. Fatigue, one of the most prevalent
complaints
>   among  persons with HIV infection, may also be the result of mitochondrial
>   toxicity,  though this has not been clearly established.
>   _http://clinicaltrials.gov/ct/show/NCT00106795?order=201_
>  
(http://clinicaltrials.gov/ct/show/NCT00106795?order=201<http://clinicaltrials.g\
ov/
ct/show/NCT00106795?order=201>)
>
>   In  health,
>
>   Nelson Vergel
>   Director
>   Program for Wellness Restoration,  PoWeR
>   A 501 (c) 3 non profit national  organization
>   powerusa.org
>   salvagetherapies.org
>   faciawasting.org
>
>
>   Disclaimer
>
>   This  information (and any accompanying printed material) is not intended to
>   replace  the attention or advice of a physician or other health care
>   professional. Anyone  who wishes to embark on any dietary, drug, exercise,
or other
>   lifestyle change  intended to prevent or treat a specific disease or
condition
>   should first  consult with and seek clearance from a qualified health care
>   professional.
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 9
>      Date: Fri, 1 Apr 2005 16:06:48 EST
>      From: PoWeRTX@a...<mailto:PoWeRTX@a...>
>   Subject: MRI to assess facial wasting and AVN
>
>
>
>   This study will examine risk factors for facial wasting and avascular
>   necrosis (AVN, a type of damage to the hip and other bones) in HIV-infected
>   patients. The prevalence and natural history of AVN are also being
evaluated.  This
>   study will use magnetic resonance imaging (MRI) to identify and monitor 
these
>   conditions in patients with and without diagnosed AVN and to identify risk
>   factors.
>   _http://clinicaltrials.gov/ct/show/NCT00001762?order=202_
>  
(http://clinicaltrials.gov/ct/show/NCT00001762?order=202<http://clinicaltrials.g\
ov/
ct/show/NCT00001762?order=202>)
>   In  health,
>
>   Nelson Vergel
>   Director
>   Program for Wellness Restoration,  PoWeR
>   A 501 (c) 3 non profit national  organization
>   powerusa.org
>   salvagetherapies.org
>   faciawasting.org
>
>
>   Disclaimer
>
>   This  information (and any accompanying printed material) is not intended to
>   replace  the attention or advice of a physician or other health care
>   professional. Anyone  who wishes to embark on any dietary, drug, exercise,
or other
>   lifestyle change  intended to prevent or treat a specific disease or
condition
>   should first  consult with and seek clearance from a qualified health care
>   professional.
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>   Message: 10
>      Date: Thu, 31 Mar 2005 21:45:31 EST
>      From: PoWeRTX@a...<mailto:PoWeRTX@a...>
>   Subject: HIV Transplant study website
>
>
>   _http://spitfire.emmes.com/study/htr/_
(http://spitfire.emmes.com/study/htr/<http:/
/spitfire.emmes.com/study/htr/>)
>
>
>   In  health,
>
>   Nelson Vergel
>   Director
>   Program for Wellness Restoration,  PoWeR
>   A 501 (c) 3 non profit national  organization
>   powerusa.org
>   salvagetherapies.org
>   faciawasting.org
>
>
>   Disclaimer
>
>   This  information (and any accompanying printed material) is not intended to
>   replace  the attention or advice of a physician or other health care
>   professional. Anyone  who wishes to embark on any dietary, drug, exercise,
or other
>   lifestyle change  intended to prevent or treat a specific disease or
condition
>   should first  consult with and seek clearance from a qualified health care
>   professional.
>
>
>   [This message contained attachments]
>
>
>
>   ________________________________________________________________________
>   ________________________________________________________________________
>
>
>   Welcome to our PozHealth group!
>   If you received this email from someone who forwarded it to you and would
like to join
this group, send a blank email to PozHealth-subscribe@yahoogroups.com<mailto:
PozHealth-subscribe@yahoogroups.com> and you will get an email with instructions
to
follow. You can chose to receive single emails or a daily digest (collection of
emails). You
can post pictures, images, attach files and search by keyword old postings in
the group.
>
>   For those of you who are members already and want to switch from single
emails to
digest or vice versa, visit www.yahoogroups.com<http://www.yahoogroups.com/>,
click
on PozHealth, then on "edit my membership" and go down to your selection. The
list
administrator does not process any requests, so this is a do-it-yourself easy
process ! :)
>   Thanks for joining. You will learn and share a lot in this group!
>
>   NOTE: I moderate, approve or disapprove emails before they are posted.
Please follow
the guidelines shown in the homepage. I will not allow rudeness, sexually 
explicit
material, attacks, and anyone who does not follow the rules. If you are not OK
with this,
please do not join the group.
>
>   Forward this email to anyone who may benefit from this information! Thanks!
>   In Health,
>
>   Nelson Vergel (PoWeRTX@a...<mailto:PoWeRTX@a...>)
>   List Founder and Moderator
>
>   ------------------------------------------------------------------------
>   Yahoo! Groups Links
>
>
>
>
>   ------------------------------------------------------------------------

#11444 From: JuLev@...
Date: Sun Apr 3, 2005 9:02 pm
Subject: HIV Prevention & Methamphetamine
JuLev@...
Send Email Send Email
 
NATAP - www.natap.org

AIDS Fighters Face a Resistant Form of Apathy

NY Times, Sunday April 3, 2005
By ANDREW JACOBS

Where have all the condoms gone?

Don't try looking at the Monster, the Hangar, Starlight or Barracuda. On a recent evening, these and more than a dozen other Manhattan gay bars were well stocked with free going-out guides, but not a scrap of literature about H.I.V. prevention or the perils of crystal meth. As for condoms, the frontline defense against sexually transmitted diseases, only one establishment stocked them - behind the bar.

As part of his graduate course work at New York University, Michael Marino set out last winter to compare the AIDS prevention efforts of New York and London. He was troubled by what he found. At most New York bars, and even at some bedrock gay and AIDS service institutions, educational pamphlets and free condoms were hard to find, if not impossible. In London, Mr. Marino found them easily.

"No wonder things are getting so out of control here," he said.

Condoms, which still can be found in vending machines at a handful of places, were once given away by the bucketful. While no one believes free condoms will completely halt the spread of H.I.V., their disappearance from bars, the equivalent of a town hall for some gay men, is a telling indicator of how much steam has been lost in the fight against AIDS.

Although the city health department's recent warning about a rare, possibly more virulent strain of H.I.V. has caused a stir among gay men, many AIDS activists hold out little hope the news will prompt substantial or lasting changes in behavior. They point to the continued popularity of methamphetamine, which has contributed to a rise in condomless intercourse, known as barebacking, and the widespread apathy in which H.I.V. is seen as a nuisance, not a potential killer.

Compounding this laissez-faire attitude, they complain, are drug company advertisements that gloss over the disease's effects by portraying patients as the picture of perfect health.

Locally, at least, the statistics paint a mixed picture. The number of new H.I.V. infections among men who have sex with men declined slightly from 2001 to 2003, according to the most recent figures available, although in much of the country that number has been rising. But AIDS service providers, pointing to a recent spike in syphilis cases and the rise of methamphetamine abuse among gay men, fear it is only a matter of time before New York faces a new surge in infections.

The challenge is far more complicated than handing bar patrons informational brochures and telling them to be good, prevention specialists say.

"Just because folks are well informed doesn't mean they'll necessarily make the wisest choices in terms of their health," said Dr. Ronald O. Valdiserri, who oversees AIDS prevention at the Centers for Disease Control and Prevention. "This is true of all humanity, not just gay men."

The reality that gay men continue to have unprotected sex has been vexing health experts for 20 years, although the struggle became even more daunting in the mid-1990's, when a new class of medications sharply reduced death rates and fed the misconception that AIDS is only about as troublesome as the flu.

And then there are those who disdain condoms. With the specter of imminent death gone, the idea of using condoms has become an annoyance for many. "Let's face it, sex with a condom is not as good," said Dr. Robert L. Klitzman, a psychiatrist and professor at Columbia University. "Sex is supposed to be an incredibly intimate moment, and it's not as intimate when there's a piece of plastic between you and your partner."

There is a growing sense that the traditional sloganeering about condoms and club drugs is about as effective as birth-control campaigns that rely on abstinence. The only hope for changing behavior, public health experts and psychologists say, is to recognize and address the underlying factors that propel men into risky situations. Loneliness, alienation and self-hatred, they say, are the real culprits that need to be addressed.

But others, describing such talk as nave, say it makes more sense to stress personal responsibility. Demonize crystal meth, stigmatize unprotected sex and remind people that living with H.I.V. can be grueling, or worse. An important first step, they say, would be to stop running pharmaceutical ads that portray people with AIDS as carefree and virile.

Other ideas include following the lead of the San Francisco health department, which is seeking strict limitations on the availability of erectile dysfunction drugs that counteract the impotence induced by crystal meth and encourage the spread of sexually transmitted diseases.

Many AIDS activists in New York, describing current public service campaigns as toothless and ineffective, say bus ads and billboards should remind people that AIDS is a devastating and entirely avoidable illness.

Many prevention advocates agree that only a creative, ever-changing arsenal of tactics can reduce the number of new H.I.V. infections. They point out that it has taken years and millions of dollars to change public attitudes about tobacco and seat belts, and even now reasonable people lapse into old ways.

"Everyone knows smoking is bad for you, but we still print those health warnings on cigarette packs," said Kwame M. Banks, a consultant specializing in prevention work. "People need to hear these messages 100 times a day. That's the way these things work."

Still, when it comes to H.I.V. and AIDS, some wonder whether it is time for a new strategy. Perry Halkitis, a psychologist at New York University who studies the relationship between drug use and sex, believes that many gay men who engage in risky behavior are grappling with profound mental health issues.

"People are not taking risks because they're stupid, or because they wake up one day and say, 'I'm going to take a risk today,' " Dr. Halkitis said. "They do it because the sexual risk fulfills a need, or somehow makes them feel better about themselves."

He and others say any successful fight against H.I.V. must deal with depression, substance abuse and low self-esteem, problems that studies have shown affect gay men at disproportionately higher rates.

"Many people might argue that as a community, we suffer from post-traumatic stress disorder because we're so ostracized by society," Dr. Halkitis said. "Being rejected by family, by our churches, and these days by our government most certainly has an impact."

That emotional fragility has been compounded by the trauma of the 1980's and early 90's, when sickness and death permeated the lives of so many. Peter Staley, a veteran AIDS activist, said it was no coincidence that some of the first people in New York to pick up crystal meth habits have been men 35 to 45 years old.

"We are the long-term survivors who watched friends die, who never thought we'd live to have a midlife crisis," said Mr. Staley, who is H.I.V.-positive and himself a recovering meth addict. "Then the new medications came along, and suddenly everyone returned to their old lives and people moved on to other issues, like gays in the military and gay marriage. Where was the communal processing of the emotional hell we had just gone through? I think as a result we're a deeply scarred group."

While such scars can lead to substance abuse, psychologists say the internalized homophobia and deep-seated feelings of low self-worth are just as powerful. That is where the allure of crystal meth kicks in. Those who have used the drug say it tends to blot out feelings of vulnerability, boosts self-confidence and imbues them with a false sense of connection to strangers.

Then there are the "bug chasers," H.I.V.-negative men who actively seek infection. Although such men are thought to be few in number, mental health experts say the phenomenon reflects the intense alienation that many gay men feel. Louis Pansulla, a psychoanalyst who runs gay therapy groups in New York, said younger men, in the generation that missed the darkest days of the AIDS crisis, believe that infection will win them membership into a clique, albeit one coping with a dreaded disease.

"It's almost a longing to belong, even though it's a completely unconscious thing," he said.

Michelangelo Signorile, the host of a gay-themed talk show on Sirius Satellite Radio, takes a less nuanced view: "If everyone in your group is beautiful, taking steroids, barebacking and H.I.V. positive, having the virus doesn't seem like such a bad thing."

It is for that reason that Michael Weinstein, president of the AIDS Healthcare Foundation, believes the disease is due for an image makeover. He cites a hard-to-miss ad in last month's Out magazine that is embedded with a tiny audio chip and features two robust men on a beach. Opening the magazine sets off the trill of a ringing phone and a man's voice essentially saying he is having too much fun to worry about his chronic illness. Mr. Weinstein has asked the ad's sponsor, Bristol-Myers Squibb, to stop using the ad for the drug, Reyataz. A spokeswoman said the company was re-examining its advertising campaigns.

"People are in such denial about how serious H.I.V. is," Mr. Weinstein said. "Unfortunately, the best prevention is seeing people die."

Of course, frontline prevention workers hope to avoid a new wave of deaths. At Gay Men's Health Crisis, prevention workers are planning a series of events that seek to promote "connectedness and community."

Others are creating antidrug messages that masquerade as packets of meth that can be dropped on dance floors. A series of subway ads unveiled by the state for the first time shifts responsibility to those who are already infected.

And then there are people like Daniel Carlson, a former marketing executive who became so disgusted by the number of men soliciting unprotected sex online that he and a friend started a group to combat the prevailing ethos about sex and drugs. In the past two years, the group, H.I.V. Forum, has organized a half-dozen town hall meetings on crystal meth and unprotected sex that have drawn packed houses.

"I know it sounds touchy-feely, but if we could just emphasize a little bit more community and brotherhood," Mr. Carlson said. "We have to decide whether we're going to be selfish or whether we're going to care about one another."

Gays Mobilize Against Meth Addiction

By DAVID CRARY
The Associated Press

NEW YORK (AP) - It's a Friday evening, traditional kickoff time for the party scene in New York's gay community, but the 75 men packed into a small room at a gay health center aren't in a partying mood. Through a humbling 12-step program modeled after Alcoholics Anonymous, they are battling to kick their addiction to methamphetamine, and in doing so escape an epidemic that is roiling urban gay communities nationwide with disease, despair, embarrassment and anger.

Meth is an equal-opportunity menace - many thousands of men and women, gay and straight, have fallen prey to it in rural villages, placid suburbs and city slums. But gay leaders in New York, California and elsewhere bluntly acknowledge that their communities have distinctive problems with the drug, and an unavoidable responsibility to combat it.

``Years from now we'll look back, as gay men, and be pretty despondent that we popularized and glamorized this drug,'' said Dan Carlson, an ex-addict who has become one of New York's leading anti-meth campaigners.

``I'm not anti-partying or anti-sex,'' he said. ``But how can we fight for our rights as a sexual minority if we don't establish what's right and wrong in our community, and look out for each other.''

Crystal meth - which can be snorted, smoked or injected - has been a popular gay party drug on the West Coast for more than a decade, and in New York since the late 1990s. In many cities, however, gay activists and health officials were not quick to confront the fact that the drug, by curbing inhibitions and boosting energy, encourages unsafe multi-partner sex and thus increases the risk of HIV transmission.

In New York, alarm over meth intensified in February, when health officials reported a rare strain of highly resistant, rapidly progressing HIV in a gay man who regularly engaged in meth-fueled sex parties. But the tide began turning against the drug a year earlier, when gay activists held the first of several forums on the epidemic and an ex-addict named Peter Staley circulated posters with an eye-catching message: ``Buy Crystal. Get HIV Free.''

Staley, a bond trader-turned-AIDS activist, is guardedly optimistic that the forums and ad campaigns are helping stigmatize the drug.

``A year and a half ago, this was a whispered-about epidemic,'' he said. ``If it came up, it was someone bragging about their wild weekend on meth, and no one had the courage to say, 'What the hell are you laughing about?'

``That's completely changed,'' Staley said. ``When gay men ask a friend about it now, they're as likely to hear, 'That stuff destroys lives,' as they are to hear, 'Oh, you should try this; it's amazing.'''

One indicator that the anti-meth message is spreading is a surge of addicts seeking help at Crystal Meth Anonymous and other recovery programs.

Meth Anonymous started in New York six years ago with one weekly meeting, attended by a half-dozen men. It now offers 24 meetings a week, attended by anywhere from a dozen to more than 100 people.

Some of the men at the recent Friday meeting, clearly on edge, were just beginning their attempt to quit; others had been off meth for two years, yet still embraced the intensive group support in trying to stay sober.

The evening's speaker, a former flight attendant celebrating one year off meth, riveted the audience with a wrenching account of his unhappy youth, his descent into prolonged addiction, his years as a hustler getting paid for sex even as he contracted HIV and other diseases. ``Darkness'' was how he described his life at the nadir.

The spiritual, abstinence-only philosophy of Meth Anonymous works for some men, but repels others. Some counselors espouse an alternative known as ``harm reduction,'' cautioning users about meth's risks while encouraging addicts who can't quit to avoid overdoses, take care of their health and - to the extent possible - engage in safe sex even while high.

Jean Malpas, a gay psychotherapist in New York, has been handling meth-related cases for four years. He won't condemn harm reduction, but says he has yet to encounter anyone who can use meth recreationally without developing an addiction.

``At some point, when Friday night comes along, they don't know what else to do,'' he said.

Increased publicity about the gay meth epidemic comes at an awkward time for the national gay-rights movement as it pushes for same-sex marriage rights.

``There is anger at the opportunity this phenomenon is giving the rest of the world to associate the gay identity with promiscuous sex, with out-of-control behavior,'' Malpas said. ``We don't need additional opportunities to be perceived negatively.''

Kathleen Watt, who runs the Van Ness addiction-recovery center in Los Angeles, believes some major gay advocacy groups have tried to play down the epidemic.

``They're afraid people are going to say, 'Why should we put money into HIV treatment when these guys are knowingly going out and having sex and infecting other people?''' she said.

Matt Foreman, executive director of the National Gay and Lesbian Task Force, said some accounts of the gay meth problem had been ``salacious'' and ``overjudgmental'' - highlighting the role of promiscuous sex while underplaying the destructive addictiveness of meth for any user, gay or straight. He praised gay activists for taking the lead in fighting the epidemic.

Foreman and other gay-rights leaders also note that even in the hardest-hit communities, most gay men don't use meth. Estimates have ranged from 10 percent or 20 percent of all gay men, and as high as 40 percent in San Francisco - by any measure a problem that can't be wished away.

Perry Halkitis, a New York University psychologist specializing in the study of HIV/AIDS and drugs, says the root cause of meth addiction for many gays is not sex or partying, but deeper problems of isolation and low self-esteem, particularly if they are HIV positive.

``Users are often experiencing mental health problems,'' he said. ``You have this really vicious cycle - HIV, meth, depression.''

Experts say many men in this category are experiencing ``safe-sex fatigue'' - they are tired of using condoms, believe medication can contain their HIV, and are emboldened by meth to forget their difficulties and engage in unprotected sex. ``Meth was the drug that would turn your head off and allow you to have the sex you thought you were missing out on,'' Kathleen Watt said.

At the Callen-Lorde health center, which serves New York's gay community, the staff wrestles constantly with cases involving meth and unsafe sex.

``Safer sex is not everybody's idea of a good time,'' said Callen-Lorde's executive director, Jay Laudato. ``When you're high, you decide not to make the healthy choice - you think, 'Why should I?'''

The resulting addictions are often disastrous, Laudato said - men lose their jobs, their friends and, because of one alarming side effect, even their teeth.

The current prevention campaigning tries to promote the concept of healthy, meth-free sex. Peter Staley's latest ads, for example, feature posters of buff male models, accompanied by the slogan, ``Crystal Free and Sexy.''

New York City's health department contributed $300,000 last year to support the activists' education campaigns. More money is coming this year.

``When gay men saw their peers' lives destroyed, it was like another HIV/AIDS plague,'' said Brett Larson, director of the city's office of lesbian and gay health. ``This was something they weren't going to tolerate. The community has done an incredible job getting the word out.''

One of the celebrities who enlisted in the campaign is John Cameron Mitchell, director and star of the hit film ``Hedwig and the Angry Inch.''

``I've seen a lot of friends wasting away - they start to look like a ghost and can't even see it,'' he said. ``What we need are intelligent scare tactics, to convince people the drug is uncool.''

Such messages may not sway hard-core users, Mitchell said, but should be targeted at gays who might be tempted to sample meth, particularly newcomers to big cities.

``You have a lot of young gay men coming into the city - they were the nerds in high school, the wallflower, the ugly kid,'' he said. ``They feel the city is the place to be sexy, to be a star, and they get a false burst of confidence with a drug like this.''

Internet gay sex sites are a particular concern to anti-meth activists. Staley said at least one major site has been cooperative, displaying health messages amid the dating profiles. Other sites have been slow to help, and personal ads hinting at sex-and-meth parties still appear, though less often than a year ago, he said.

In California, West Hollywood Mayor John Duran has been discussing anti-meth strategies with players in the gay sex industry including pornographic filmmakers and sex club operators.

``We didn't come through the AIDS epidemic, and the battles over gays in the military and gay marriage, to end up here, a community filled with drug addicts,'' said Duran, who is gay and HIV-positive. ``We've fought too long and too hard to let this drug take us down.''

On the Net:

Crystal Meth Anonymous: http://www.crystalmeth.org/index.php

#11443 From: beefymusclebud@...
Date: Sun Apr 3, 2005 7:08 pm
Subject: AVN and sterods
beefymusclebud
Offline Offline
Send Email Send Email
 
I agree that the issue of what sort of steroids is being discussed must be made clear, but I think it's not maliciousness that the guy (I'm not sure who) who sent the article had in mind when it got posted.
 
Sometimes, those of us who post information on this list get a little tired and don't thoroughly read the entire content of every articles we post....often I want to just get it up on the list to do the job of getting information out...so I'm sure that was the case of the article about steroids and AVN. 
 
I know in my case when I read 20 or 30 papers a day on medical issues and 5 times that on political issues for my blog, I'm bound to make a mistake and post something here with out clarification. I hope people would forgive me rather then handing me back my head.

#11442 From: PoWeRTX@...
Date: Mon Apr 4, 2005 9:42 am
Subject: Fwd: LIVING WILL, HEALTH CARE SURROGATE & HEALTHCARE DIRECTIVE FORMS
nelsonvergel
Offline Offline
Send Email Send Email
 
 
WILL BE GLAD TO PROVIDE YOU WITH THE FOLLOWING PACKAGE:
 
LIVING WILL FORM
HEALTH CARE DESIGNATED SURROGATE FORM
HEALTHCARE ADVANCE DIRECTIVE FORM
UNIFORM DONOR FORM
 
RED HISPANA IS REQUESTING A $10 TAX DEDUCTIBLE DONATION FOR EACH PACKAGE ORDERED
 
HAVE IT NOTORIZED AND COPIES GIVEN TO YOUR HEALTHCARE PROVIDERS AND YOUR APPOINTEES
 
RED HISPANA IS A 501 (C) 3 NON PROFIT AGENCY
 
MAIL CHECK PAYABLE TO "RED HISPANA FL" WITH YOUR ADDRESS INFO TO:
 
RED HISPANA FLORIDA
6565 TAFT STREET
SUITE 401
HOLLYWOOD, FLORIDA 33024
 
PLEASE ALLOW 5 - 7  DAYS FOR DELIVERY
 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.
RED HISPANA FLORIDA
 
WILL BE GLAD TO PROVIDE YOU WITH THE FOLLOWING PACKAGE:
 
LIVING WILL FORM
HEALTH CARE DESIGNATED SURROGATE FORM
HEALTHCARE ADVANCE DIRECTIVE FORM
UNIFORM DONOR FORM
 
RED HISPANA IS REQUESTING A $10 TAX DEDUCTIBLE DONATION FOR EACH PACKAGE ORDERED
 
HAVE IT NOTORIZED AND COPIES GIVEN TO YOUR HEALTHCARE PROVIDERS AND YOUR APPOINTEES
 
RED HISPANA IS A 501 (C) 3 NON PROFIT AGENCY
 
MAIL CHECK PAYABLE TO "RED HISPANA FL" WITH YOUR ADDRESS INFO TO:
 
RED HISPANA FLORIDA
6565 TAFT STREET
SUITE 401
HOLLYWOOD, FLORIDA 33024
 
PLEASE ALLOW 5 - 7  DAYS FOR DELIVERY

#11441 From: Steve <simonadyjf@...>
Date: Mon Apr 4, 2005 1:32 pm
Subject: Re: Two good suggestions from a member
simonadyjf
Offline Offline
Send Email Send Email
 
I disagree with the second point below.  If someone is responding to a posting, I don't want to have to go look for the original comment.  It makes it easy to maintain the continuity if the original is attached to the comment..
 
As for the first point, sometimes the articles are from sites you have to register for, and that can be a pain if you only want to look at that particular article.   So, I hope members keep that in mind when they are making their posts.
 
Thanks, Steve

PoWeRTX@... wrote:
  • Rather than copy a whole article onto this yahoo group if you could give the name of the article (and topic if not evident in the name), what you found interesting and the URL where to find the complete article along with the source information.
  • When replying to a message delete everything below the first line of the message you are replying to, as it shows up numerous times for the person who has subscribed to this group to receive the emails in digest form.  If you leave the sender, subject and first line of the message almost anyone would understand what message you are responding to.
 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.


Welcome to our PozHealth group!
If you received this email from someone who forwarded it to you and would like to join this group, send a blank email to PozHealth-subscribe@yahoogroups.com and you will get an email with instructions to follow. You can chose to receive single emails or a daily digest (collection of emails). You can post pictures, images, attach files and search by keyword old postings in the group.

For those of you who are members already and want to switch from single emails to digest or vice versa, visit www.yahoogroups.com, click on PozHealth, then on "edit my membership" and go down to your selection. The list administrator does not process any requests, so this is a do-it-yourself easy process ! :)
Thanks for joining. You will learn and share a lot in this group!

NOTE: I moderate, approve or disapprove emails before they are posted. Please follow the guidelines shown in the homepage. I will not allow rudeness, sexually  explicit material, attacks, and anyone who does not follow the rules. If you are not OK with this, please do not join the group.

Forward this email to anyone who may benefit from this information! Thanks!
In Health,

Nelson Vergel (PoWeRTX@...)
List Founder and Moderator


__________________________________________________
Do You Yahoo!?
Tired of spam? Yahoo! Mail has the best spam protection around
http://mail.yahoo.com


#11440 From: GetWell@...
Date: Sun Apr 3, 2005 4:36 pm
Subject: Management of Hypertension in HIV-Infected Patients
getwell1
Offline Offline
Send Email Send Email
 
 
 
Management of Hypertension in HIV-Infected Patients

Laura P. Svetkey, MD
Professor of Medicine, Division of Nephrology
Director, Duke Hypertension Center
Duke University Medical Center
Durham, North Carolina

William L. Fan, MD
Duke University Medical Center
Durham, North Carolina


Introduction

The advent of highly active antiretroviral therapy (HAART) in the treatment of HIV disease has revolutionized the care of HIV-infected patients. Encouraging outcomes such as increasing CD4+ cell counts and decreasing incidences of opportunistic infections are more common today than before the introduction of HAART. With the reductions in HIV-related morbidity and mortality brought on by HAART, patients with HIV are living longer, and their clinicians are having to focus on diseases and conditions that typically affect the middle-aged, non-HIV-infected population, such as hypertension, hyperlipidemia, diabetes mellitus, and visceral fat accumulation, all considered risk factors for cardiovascular disease (CVD).

Burden of Hypertension and Other CVD Risk Factors

In the general population, 50 million Americans (1 in 4 adults) are estimated to have hypertension.[1] Hypertension is the most common primary diagnosis in the United States, accounting for 35 million office visits each year, and is the most common risk factor for both cardiovascular and renal disease.[2]

The prevalence of hypertension in the HIV-infected population remains unclear. Estimates suggest that the prevalence of hypertension in the HIV-infected population before the introduction of HAART was similar to that of the general population (between 20% and 25%).[3] The Data Collection on Adverse Events of Anti-HIV Drugs (DAD) study evaluated baseline data from 17,852 subjects in the HAART era and observed that more than 8% of the study population had hypertension.[4] Other results from this cross-sectional, multicenter study revealed that traditional cardiovascular risk factors, such as tobacco use, dyslipidemia, and family history of coronary heart disease, are prevalent among patients on HAART. The presence of these powerful cardiac risk factors further emphasizes the importance of treating hypertension in HIV-infected patients. Clinicians who assume responsibility for the primary care of their HIV-infected patients must now address issues related to the reduction of cardiac risk factors, in addition to managing the patient's HIV disease.

The relationship between HAART and blood pressure has not been carefully studied, and existing data do not consistently demonstrate that HAART routinely raises blood pressure. Nonetheless, clinicians must recognize the growing consensus that the very drugs used to treat HIV may exacerbate cardiac risk factors such as hyperlipidemia, insulin resistance, and increased visceral fat.

Why Treat Hypertension?

As mentioned, hypertension is the most prevalent risk factor for cardiovascular and renal disease in the general population and accounts for approximately 35% of atherosclerotic disease.[5] The magnitude of CVD risk that is attributed to hypertension is comparable to the risk from a low-density lipoprotein (LDL) cholesterol reading of > 160 mg/dL.[6] In addition, hypertension increases the risk of peripheral vascular disease and congestive heart failure by more than 2-fold and the risk of end-stage renal disease by more than 4-fold.[7-9]

Fortunately, treatment of hypertension can reduce its associated risks. Antihypertensive therapy reduces the risk of stroke by approximately 35%, congestive heart failure by 42%, and coronary heart disease by 28%.[10-13] Since renal diseases such as HIV-associated neuropathy (HIVAN) are prevalent in the HIV-infected population, it is important to note that adequate control of high blood pressure can delay progression of kidney dysfunction. Therefore, an important key to reducing the burden of hypertension-related CVD and chronic kidney disease is to increase the proportion of HIV-infected patients who achieve adequate control of their blood pressure—an important goal for HIV-infected patients, who are now living much longer than ever before.

Classification of Hypertension

The 2003 Joint National Committee on Prevention, Detection, Evaluation, and the Treatment of High Blood Pressure (JNC 7) guidelines classify blood pressure by stage and provide recommendations for treatment and follow-up.[14] The JNC 7 classification system consists of 3 main blood pressure categories: normal, prehypertension, and hypertension, which are shown in Table 1. In general, normal blood pressure for adults consists of a systolic blood pressure (SBP) reading of < 120 mm Hg and a diastolic blood pressure (DBP) reading of < 80 mm Hg, or 120/80 mm Hg.

Table 1. JNC 7 Blood Pressure Classification for Adults[14]

Classification Systolic and Diastolic Blood Pressure
Normal SBP < 120 and DBP < 80 mm Hg
Prehypertension SBP 120-139 or DBP 80-89 mm Hg
Stage 1 hypertension SBP 140-159 or DBP 90-99 mm Hg
Stage 2 hypertension SBP ≥ 160 or DBP ≥ 100 mm Hg

DBP, diastolic blood pressure; SBP, systolic blood pressure

Prehypertension is a new category derived from the previous guidelines, that includes patients with ranges of SBP from 120 to 139 mm Hg and/or of DBP from 80 to 89 mm Hg. Note that prehypertension is not a disease category; rather, it is a guideline for identifying individuals at high risk of developing hypertension to alert both patients and clinicians of this risk so that they can consider appropriate interventions for preventing or delaying development of the disease. Careful attention to patients in the prehypertension category is important because several studies indicate that mortality rates for myocardial infarctions (MIs), strokes, and other vascular diseases increase progressively with a rise in blood pressure and can begin at levels as low as 115/75 mm Hg.[15]

As shown in Table 1, hypertension is subdivided into 2 stages: stage 1 includes SBP ranges between 140 and 159 mm Hg or DBP ranges between 90 and 99 mm Hg, and stage 2 hypertension consists of SBP > 160 or DBP > 100 mm Hg.[14]

Management of Hypertension

The medical literature gives no indication that HIV-infected patients with hypertension or prehypertension should be managed in a way other than that recommended in the JNC 7 guidelines. For patients with stage 1 or 2 uncomplicated hypertension, the target blood pressure level is < 140/90 mm Hg. In HIV-positive patients with comorbidities such as diabetes or chronic kidney disease, a target blood pressure level of < 130/80 mm Hg is recommended.[14]

Lifestyle modification, an indispensable part of hypertension management that is recommended for all hypertensive patients, is the only intervention recommended for prehypertension. As shown in Table 2, appropriate lifestyle modification includes adoption of the Dietary Approaches to Stop Hypertension (DASH) eating plan,[16] which includes a diet rich in fruits, vegetables, and low-fat dairy products with a reduced content of dietary cholesterol and saturated and total fat. DASH also contains abundant levels of potassium and calcium. Lifestyle modification intervention also urges patients to engage in regular aerobic activity and to limit alcohol intake to no more than 2 drinks per day for men and 1 drink per day for women.

Table 2. Management of Hypertension: Lifestyle Modifications*

Modification Recommendation Estimated SBP Reduction (mm Hg)†
Reduce weight Maintain normal body weight (BMI, 18.5-24.9 kg/m2) 5-20 per 10-kg weight loss
Adopt DASH eating plan Consume a diet rich in fruits, vegetables, and low-fat dairy products with reduced saturated and total fat 8-14
Reduce dietary sodium intake Reduce intake to ≤ 100 mEq/L (2.4 g sodium or 6 g NaCl) 2-8
Increase physical activity Engage in regular aerobic physical activity (≥30 min/day, most days) 4-9
Limit alcohol consumption Limit consumption to ≤ 2 drinks/day (1 oz or 30 mL ethanol) for most men or ≤ 1 drink/day for women and lighter-weight people 2-4

BMI, body mass index; DASH, Dietary Approaches to Stop Hypertension; SBP, systolic blood pressure.
* Smoking cessation decreases overall cardiovascular risk.
†Effects are dose and time dependent and may be higher in some individuals.

If a patient continues to be hypertensive after a trial of lifestyle modification, a thiazide diuretic is the preferred agent for initial treatment. The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT), which involved more than 40,000 hypertensive individuals, found no differences in primary coronary heart disease (CHD) outcome or mortality between thiazide-type diuretics, the angiotensin-converting enzyme inhibitor (ACEI) lisinopril, or the calcium channel blocker (CCB) amlodipine.[13] Although thiazides are typically recommended for the treatment of hypertension because of their low cost, ACEIs, angiotensin II receptor blockers (ARBs), beta-blockers (BBs), CCBs, or a combination may be considered. ALLHAT also showed that effective treatment of two-thirds of patients requires 2 or more antihypertensive drugs. As shown in Figure 1, recommended treatment for patients with stage 2 hypertension includes a 2-drug regimen consisting of a thiazide and 1 other antihypertensive agent.[14] For patients with stage 1 hypertension thiazide-type diuretics are typically used, though some physicians may consider one of the other antihypertensive agents or a combination. Compelling indications for individual drug classes are listed in Table 3.

Figure 1. Recommendations for the treatment of hypertension

Figure 1

Table 3. Compelling Indications for Specific Drug Classes

Indication Recommended Drugs
Heart failure Diuretic, BB, ACEI, ARB, aldosterone antagonist
Post-myocardial infarction BB, ACEI, aldosterone antagonist
High coronary disease risk Diuretic, BB, ACEI, CCB
Diabetes mellitus Diuretic, BB, ACEI, ARB, CCB
Chronic kidney disease ACEI, ARB
Recurrent-stroke prevention Diuretic, ACEI

ACEI, angiotensin-converting enzyme inhibitor; ARB, angiotensin II receptor blocker; BB, beta-blocker; CCB, calcium channel blocker

Clinicians should consider individual patients' comorbid conditions when selecting classes of antihypertensive drugs for treatment. HIVAN is a notable comorbid condition for this patient population. Because HIVAN is characterized by proteinuria, clinicians are urged to use urinalysis to screen high-risk patients for proteinuria. Patients with evidence of kidney disease should have a blood pressure goal of < 130/80 mm Hg. Given the efficacy of ACEIs, clinicians may consider using one as a first-line agent when a patient's plasma creatinine is less than 2 mg/dL or there is no evidence of hyperkalemia.

HAART and Hypertension Medications

Currently, no contraindications exist regarding the use of any class of antihypertensive agents in the treatment of HIV-infected patients receiving HAART. However, the clinician must be aware of some pitfalls when treating hypertension in these patients.

Since several antihypertensive medications are on the market, CCBs should be avoided because they have been reported to interact with protease inhibitors (PIs). For example, the potential increase in serum concentrations of a CCB during concomitant use of ritonavir or atazanavir could lead to hypotension and bradycardia.[17] On the other hand, when serum concentrations of a CCB are decreased by a drug such as nevirapine, the clinician may be unable to effectively control the patient's blood pressure or heart rate,[18] both of which must be carefully monitored if this antihypertensive drug class is used.

Beta-blocker serum levels have also been known to be altered in patients receiving PIs. For example, atenolol levels are increased in patients taking atazanavir, and the beta-blocker effects of metoprolol may be enhanced in those receiving ritonavir.[17,19]

Nephrolithiasis is a well-established complication of indinavir therapy. Since volume depletion is a known risk factor for the development of kidney stones, diuretics should be used with extreme caution in patients receiving indinavir. To avoid volume depletion, clinicians should recommend that such patients drink at least 48 oz of water each day.[20]

Conclusion

The great strides made in developing effective antiretroviral therapy have substantially reduced the burden of HIV disease; consequently, HIV-infected patients are living longer. Clinicians who treat HIV-infected patients now have additional responsibilities for long-term primary care, including the management of cardiovascular disease risk factors. Proper management of hypertension has become an important component in the care of some HIV-infected patients. Fortunately, well-researched antihypertensive lifestyle interventions and pharmacologic therapies have been developed to help the clinician deal with this emerging issue in the HIV-infected population.

References

1. Burt VL, Whelton P, Roccella E, et al. Prevalence of hypertension in the US adult population. Results from the Third National Health and Nutrition Examination Survey, 1988-1991. Hypertension. 1995;25:305-313.

2. Hypertension Working Group. Working Group Report on Primary Prevention of Hypertension. National High Blood Pressure Education Program. National Heart, Lung, and Blood Institute document. 2000; Bethesda, Maryland: National Institutes of Health.

3. Aoun S, Ramos E. Hypertension in the HIV-infected patient. Curr Hypertens Rep. 2000;2:478-481.

4. Friis-Moller N, Weber R, Reiss P, et al. Cardiovascular disease risk factors in HIV patients--association with antiretroviral therapy: results from the DAD study. AIDS. 2003;17:1179-1193.

5. Kannel WB. Blood pressure as a cardiovascular risk factor: prevention and treatment. JAMA. 1996;275:1571-1576.

6. Wilson PW, C'Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB. Prediction of coronary heart disease using risk factor categories. Circulation. 1998;97:1837-1847.

7. Levy D, Larson MG, Vasan RS, Kamek WB, Ho KK, et al. The progression from hypertension to congestive heart failure. JAMA. 1996;275:1557-1562.

8. Klag MJ, Whelton PK, Randall BL, et al. Blood pressure and end-stage renal disease in men. N Engl J Med. 1996;334:13-18.

9. Smith SR, Svetkey LP, Dennis VW. Racial differences in the incidence and progression of renal diseases. Kidney Int. 1991;40:815-822.

10. Psaty BM, Smith NL, Siscovick DS, et al. Health outcomes associated with antihypertensive therapies used as first-line agents. A systematic review and meta-analysis. JAMA. 1997;277:739-745.

11. SHEP Cooperative Research Group. Prevention of stroke by antihypertensive drug treatment in older persons with isolated systolic hypertension: final results of the Systolic Hypertension in the Elderly Program (SHEP). JAMA. 1991;265:3255-3264.

12. Gueyffier F, Froment A, Gouton M. New meta-analysis of treatment trials of hypertension: improving the estimate of therapeutic benefit. J Hum Hypertens. 1996;10:1-8.

13. Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA. 2002;288:2981-2997.

14. Chobanian AV, Bakris GL, Black HR, et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension. 2003;42:1206-1252.

15. Lewington S, Clark R, Qizilbash N, Peto R, Collins R. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet. 2002;360:1903-1913.

16. Appel LJ, Moore TJ, Obarzanek E, et al. A clinical trial of the effects of dietary patterns on blood pressure. DASH Collaborative Research Group. N Engl J Med. 1997;336:1117-1124.

17. Reyataz [package insert]. Princeton, New Jersey: Bristol-Myers Squibb Company; 2004.

18. Viramune [package insert]. Ridgefield, Connecticut: Boehringer Ingelheim; 2004.

19. Norvir [package insert]. North Chicago, Illinois: Abbott Laboratories; 2003.

20. Crixivan [package insert]. Whitehouse Station, New Jersey: Merck & Co., Inc.; 2004.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

#11439 From: "Rachel Pobi" <LvrOfNatur@...>
Date: Sun Apr 3, 2005 3:40 pm
Subject: re: UPDATE ON THE INVESTIGATION OF A RARE STRAIN OF HIV IN A NEW YORK CITY RESIDENT
rachelsmename
Offline Offline
Send Email Send Email
 
Hi everyone,
    I just want to be clear on what they mean by strain for my presentations.  When they say strain are they talking about it being multi-resistent to drugs? Is strain synonamous with the number of mutations? Would it still be considered HIV-1 or would it have a different number?
I appreciate any help on this because I know that students will ask. I want to give them good information.
 
Thanks,
Rachel
 
 

#11438 From: JuLev@...
Date: Sun Apr 3, 2005 7:34 am
Subject: This Week in HBV Coverage- NATAP
JuLev@...
Send Email Send Email
 
NATAP Website: recent coverage in hepatitis B
http://www.natap.org/hbv.htm

Sensitive HCV RNA Test: use at week 24 - (03/31/05)

Impact of hepatitis C on health related quality of life: A systematic review and quantitative assessment - (03/31/05)

Statins and hepatotoxicity: Focus on patients with fatty liver - (03/31/05)

Mitochondrial DNA depletion in liver tissue of patients infected with hepatitis C virus: contributing effect of HIV infection? - (03/31/05)

Sex and Hepatitis C Transmission - (03/31/05)

Insulin Resistance Impairs Response to IFN/RBV - (03/31/05)

Roche Announces New Study to Evaluate Pegasys and Copegus to Treat Hepatitis C in Liver Transplant Patients - (03/22/05)

Pegasys + Methadone PK - (03/21/05)

Second Forum on Liver Transplantation: Liver transplantation for hepatitis C: how to control the virus? - (03/18/05)

Should we treat patients with chronic hepatitis C on the waiting list? - (03/18/05)

Diabetes Increases Risk of Liver Cancer - (03/15/05)

CROI:
12th CROI HCV Report - (03/08/04)

First European recommendations for the treatment of patients co-infected with HIV and Hepatitis B and C viruses - (03/07/05)

CROI:
Accelerated Liver Disease Progression in HCV/HIV Coinfection - (03/07/04)

FDA Approves Pegasys and Copegus as Only Hepatitis C Treatment for HIV Patients - (03/02/05)

HCV, HIV & Non-Hodgins Lymphoma - (03/02/05)

CROI:
Sexual HCV Transmission Reported Among MSM - (03/02/05)

CROI:
AZT Causes Anemia During Ribavirin/Interferon Therapy; EPO Improves Anemia - (03/01/05)

CROI:
24 Week RESIST Study Analysis: the efficacy of tipranavir/ritonavir is superior to lopinavir/r, and the TPV/r treatment response is enhanced by inclusion of genotypically active antiretrovirals in the optimized background regimen (OBR) - (03/01/05)

How Hepatitis C Short-Circuits the Immune System - (02/22/05)

Coinfected Patients Can Respond Better Than previously Observed - (02/22/05)

Medicaid Utilization of IFN/RBV for HCV Therapy - (02/22/05)

CD8/CTLs Predict Response to IFN/RBV Therapy - (02/22/05)

Infection with concurrent multiple hepatitis C virus genotypes is associated with faster HIV disease progression - (02/18/05)

The Spectrum of Chronic Hepatitis C Virus Infection in the Virginia Correctional System: Development of a Strategy for the Evaluation and Treatment of Inmates with HCV - (02/18/05)

#11437 From: JuLev@...
Date: Sun Apr 3, 2005 7:31 am
Subject: This Week in HCV Coverage- NATAP
JuLev@...
Send Email Send Email
 
NATAP Website: recent coverage in Hepatitis C
http://www.natap.org/hcv.htm

Sensitive HCV RNA Test: use at week 24 - (03/31/05)

Impact of hepatitis C on health related quality of life: A systematic review and quantitative assessment - (03/31/05)

Statins and hepatotoxicity: Focus on patients with fatty liver - (03/31/05)

Mitochondrial DNA depletion in liver tissue of patients infected with hepatitis C virus: contributing effect of HIV infection? - (03/31/05)

Sex and Hepatitis C Transmission - (03/31/05)

Insulin Resistance Impairs Response to IFN/RBV - (03/31/05)

Roche Announces New Study to Evaluate Pegasys and Copegus to Treat Hepatitis C in Liver Transplant Patients - (03/22/05)

Pegasys + Methadone PK - (03/21/05)

Second Forum on Liver Transplantation: Liver transplantation for hepatitis C: how to control the virus? - (03/18/05)

Should we treat patients with chronic hepatitis C on the waiting list? - (03/18/05)

Diabetes Increases Risk of Liver Cancer - (03/15/05)

CROI:
12th CROI HCV Report - (03/08/04)

First European recommendations for the treatment of patients co-infected with HIV and Hepatitis B and C viruses - (03/07/05)

CROI:
Accelerated Liver Disease Progression in HCV/HIV Coinfection - (03/07/04)

FDA Approves Pegasys and Copegus as Only Hepatitis C Treatment for HIV Patients - (03/02/05)

HCV, HIV & Non-Hodgins Lymphoma - (03/02/05)

CROI:
Sexual HCV Transmission Reported Among MSM - (03/02/05)

CROI:
AZT Causes Anemia During Ribavirin/Interferon Therapy; EPO Improves Anemia - (03/01/05)

CROI:
24 Week RESIST Study Analysis: the efficacy of tipranavir/ritonavir is superior to lopinavir/r, and the TPV/r treatment response is enhanced by inclusion of genotypically active antiretrovirals in the optimized background regimen (OBR) - (03/01/05)

How Hepatitis C Short-Circuits the Immune System - (02/22/05)

Coinfected Patients Can Respond Better Than previously Observed - (02/22/05)

Medicaid Utilization of IFN/RBV for HCV Therapy - (02/22/05)

CD8/CTLs Predict Response to IFN/RBV Therapy - (02/22/05)

Infection with concurrent multiple hepatitis C virus genotypes is associated with faster HIV disease progression - (02/18/05)

The Spectrum of Chronic Hepatitis C Virus Infection in the Virginia Correctional System: Development of a Strategy for the Evaluation and Treatment of Inmates with HCV - (02/18/05)

#11436 From: JuLev@...
Date: Sun Apr 3, 2005 7:27 am
Subject: This Week in HIV Coverage- NATAP
JuLev@...
Send Email Send Email
 
NATAP Website: recent highlights in HIV & 12th CROI

HIV
http://www.natap.org/hiv.htm

25% of Women in WIHS Stop HAART for at least 6 Months - (04/01/05)
 
Sustiva & Pregnancy: Change in Label from Pregnancy Category C to D - (04/01/05)
 
Single HIV Genotypic Resistance Test Can Underestimate Degree of Drug Resistance - (04/01/05)
 
"Women At Risk: The Health of Women in New York City" Report Released - (04/01/05)
 
UPDATE ON THE INVESTIGATION OF A RARE STRAIN OF HIV IN A NEW YORK CITY RESIDENT - (04/01/05)
 
Statins and hepatotoxicity: Focus on patients with fatty liver - (03/31/05)
 
Mitochondrial DNA depletion in liver tissue of patients infected with hepatitis C virus: contributing effect of HIV infection? - (03/31/05)
 
Gilead and Japan Tobacco Sign Licensing Agreement for Novel HIV Integrase Inhibitor - (03/22/05)
 
High Rates of ART Resistance Reported in Naives - (03/22/05)
 
Treatment of Facial Lipoatrophy With Intradermal Injections of Polylactic Acid in HIV-Infected Patients - (03/21/05)
 
R5 to X4 Switch of the Predominant HIV-1 Population in Cellular Reservoirs During Effective Highly Active Antiretroviral Therapy - (03/21/05)
 
Alendronate, Vitamin D, and Calcium for the Treatment of Osteopenia/Osteoporosis Associated With HIV Infection - (03/21/05)
 
NYC Case: Infection with multidrug resistant, dual-tropic HIV-1 and rapid progression to AIDS: a case report - (03/21/05)
 
CROI:
Key clinical studies in initial and switch therapy - Dr Graeme Moyle MD, MBBS (03/17/04)
 
CROI:
Resistance part II (ddI and tipranavir resistance news) - Report Written by Nancy Shulman (03/17/04)


12th Conference on Retroviruses and Opportunistic Infections (CROI)
Feb 22-25, 2005
Boston, MA
http://www.natap.org/2005/CROI/croi.htm

     •    
Key clinical studies in initial and switch therapy - Dr Graeme Moyle MD, MBBS (03/17/04)
 
     •    
Resistance part II (ddI and tipranavir resistance news) - Report Written by Nancy Shulman (03/17/04)
 
     •    
Nevirapine MTCT--Drug resistance at the 12th CROI - Report Written by Nancy Shulman (03/17/04)
 
     •    
Switch to Tenofovir Improved Lipids, Fat Loss - (03/15/04)
 
     •    
FDA Reports Higher Abacavir Hypersensitivity, 8% vs 5% - (03/15/04)
 
     •    
New Antiretrovirals at 12th CROI - Reported for NATAP by Mike Youle, MD - (03/10/04)
 
     •    
Prevention of mother-to-child transmission and nevirapine resistance - Reported for NATAP by David Margolis, MD - (03/09/04)
 
     •    
Innate Immunity: natural cellular mechanisms that battle HIV - Reported for NATAP by David Margolis, MD - (03/09/04)
 
     •    
Predicting Response to DDI - Reported for NATAP by David Margolis, MD - (03/09/04)
 
     •    
Choosing When to Use Tipranavir - Reported for NATAP by David Margolis, MD - (03/09/04)
 
     •    
HIV latency and persistent, low-level viremia - Reported for NATAP by David Margolis, MD - (03/09/04)
 
     •    
Leading Causes of Death in HIV....liver disease, AIDS, heart disease, malignancies - Reported for NATAP by David Margolis, MD - (03/09/04)
 
     •    
12th CROI HCV Report - (03/08/04)
 
     •    
CLINICAL PHARMACOLOGY AT THE 12th CROI- John G. Gerber, M.D. (03/08/04)
 
     •    
"Entecavir in HIV/HBV Co-Infected Patients: Safety and Efficacy in a Phase II Study (ETV-038)" - (03/08/04)
 
     •    
Liver Transplants in Hepatitis/HIV Coinfection at 12th CROI - (03/08/04)
 
     •    
Accelerated Liver Disease Progression in HCV/HIV Coinfection - (03/07/04)
 
     •    
Effect of Aging on Epidemiologic and Clinical Features in HIV-infected Individuals with Neurological Disorders - (03/07/04)
 
     •    
Impact of HAART on NeuroAIDS - (03/07/04)
 
     •    
Kaletra Independently Reduces HIV Replication in Cerebrospinal Fluid - (03/07/04)
 
     •    
DAPD + Fuzeon Pilot Study: ACTG 5118 - (03/07/04)
 
     •    
Advancing towards the therapeutic use of chemokine receptor blockade (CCR5-Entry Inhibitors) - Reported for NATAP by David Margolis, MD - (03/07/04)
 
     •    
Improved Lipids After Switch to Reyataz - (03/04/04)
 
     •    
Switch to ATV/r Improves Lipids - (03/04/04)
 
     •    
Tenofovir for HBV/HIV Coinfection - (03/03/04)
 
     •    
"Beyond Serum Creatinine: Identification of Renal Insufficiency Using GFR: Implications for Clinical Research and Care" - (03/03/04)
 
     •    
Reyataz/r: 96 week Study 045 results - (03/03/04)
 
     •    
Improving the Clinical Assessment of Renal Function in HIV - (03/02/04)
 
     •    
Decline in Renal Function Associated with Tenofovir DF (TDF) Compared to Nucleoside Reverse Transcriptase Inhibitor (NRTI) Treatment - (03/02/04)
 
     •    
Switch for Lipoatrophy to Abacavir or LPV/r+NVP - (03/02/04)
 
     •    
Switching to Tenofovir or Lower d4T Dose Improves Lipids/Limb & Total Fat - (03/02/04)
 
     •    
Triple NRTI Regimen: Combivir+Tenofovir - (03/02/04)
 
     •    
Sexual HCV Transmission Reported Among MSM - (03/02/04)
 
     •    
AZT Causes Anemia During Ribavirin/Interferon Therapy; EPO Improves Anemia - (03/01/04)
 
     •    
HIV Prevalence Among Blacks Increases in Federal Govt Survey - (03/01/04)
 
     •    
Two New Viruses Reported Belonging to AIDS Family - (03/01/04)
 
     •    
TMC278, new NNRTI, 7-day study results - (03/01/04)
 
     •    
PA-457, new HIV drug, maturation inhibitor - (03/01/04)
 
     •    
RAVE Study: switch to tenofovir or abacavir from AZT or d4T - (03/01/04)
 
     •    
Merck Integrase Inhibitor: -1.8 log reduction in 10-day study - (03/01/04)
 
     •    
TMC114/r in 3-Class Experienced Patients: 24-week interim analysis - (03/01/04)
 
     •    
24 Week RESIST Study Analysis: the efficacy of tipranavir/ritonavir is superior to lopinavir/r, and the TPV/r treatment response is enhanced by inclusion of genotypically active antiretrovirals in the optimized background regimen (OBR) - (03/01/04)
 
     •    
Switching to Thymidine Analogue Sparing or Nuke Sparing Regimen improves Lipoatrophy: 24 week results of a prospective randomized clinical trial, AACTG 5110 - (02/25/04)
 
     •    
Switching off AZT or d4T to Tenofovir or Abacavir Improves Limb Fat After 48 weeks - (02/25/04)
 
     •    
IMPACT OF BASELINE GENOTYPIC RESISTANCE ON RESPONSE TO TIPRANAVIR/r in RESIST STUDIES - (02/25/04)
 
     •    
24 Week RESIST Study Analysis: the efficacy of tipranavir/ritonavir - (02/25/04)
 


 


#11435 From: "t a" <tarantxx@...>
Date: Sat Apr 2, 2005 10:23 pm
Subject: Re: Sculpra and Dr. Frechette
tainas59
Offline Offline
Send Email Send Email
 

I had my face treated in November of 2001 by Dr. Frechette.  He massaged my face and so did I as he had told me to do.  Suddenly, in February of 2003, my face swell up.  If someone would have seen me for the first time, they probably would not have noticed it but people who knew me, saw the difference.  I went back to Dr. Frechette who gave me some injections of cortison and that took care of the swelling. He or I had no idea why I had this late reaction such a long time after the treatments (I had 2)  but could not think of anything else that could have caused it.  Scultra or Newfill as it was called then lasted well over 2 years.  If I were willing to spend money again, I would still use sculptra, even after the "allergic" reaction I had.  My opinion is that the lumping has less to do with the doctor and more with the individual patient's tolerance.
Brigitte
 
----- Original Message -----
Sent: Saturday, April 02, 2005 12:32 PM
Subject: [PozHealth] Digest Number 974


------------------------ Yahoo! Groups Sponsor --------------------~-->
Help save the life of a child.  Support St. Jude Children's Research Hospital's
'Thanks & Giving.'
http://us.click.yahoo.com/0iazvD/5WnJAA/xGEGAA/WzSolB/TM
--------------------------------------------------------------------~->

There are 10 messages in this issue.

Topics in this digest:

      1. Avascular Necrosis Risk Factors-steroids, alcohol
           From: JuLev@...
      2. Re: More on abacavir-induced neuropsychiatric reactions
           From: Mike DC <mikedcguy@...>
      3. Sculptra and Dr. Frechette
           From: Sotoway@...
      4. Re: cheekbone implants
           From: Fit4fundc@...
      5. Two good suggestions from a member
           From: PoWeRTX@...
      6. Abdominal Adiposity the Best Predictor of Type 2 Diabetes in Men
           From: beefymusclebud@...
      7. One stop patient assistence, this is important
           From: beefymusclebud@...
      8. Assessing the Relationship Between Fatigue and Mitochondrial Toxicity in Patient
           From: PoWeRTX@...
      9. MRI to assess facial wasting and AVN
           From: PoWeRTX@...
     10. HIV Transplant study website
           From: PoWeRTX@...


________________________________________________________________________
________________________________________________________________________

Message: 1        
   Date: Thu, 31 Mar 2005 17:00:37 EST
   From: JuLev@...
Subject: Avascular Necrosis Risk Factors-steroids, alcohol

NATAP - www.natap.org

Avascular Necrosis in HIV-Infected Patients:
A Case-Control Study from the Aquitaine Cohort, 1997-2002, France

“…… This comparative analysis (CID 4/2005) investigating a wide range of
factors revealed that current alcohol use and a history of steroid use were
strongly associated with the occurrence of AN….history of steroid use was
independently associated with a high risk of AN…...even short courses of steroid
treatment increased this risk substantially….the first line of prevention of this
bone disorder in HIV-infected patients should be the cessation of alcohol
consumption and the limitation of steroid prescription….Although it has been
speculated that receipt of HAART is associated with the occurrence of AN, no
association between this bone disorder and the receipt or duration of antiretroviral
therapy has been observed in the present comparative study…….Hypertriglycemia
or hypercholesterolemia were not found to be predisposing factors, as is
described in the literature. In the present study, more case patients presented
with high total cholesterol levels than did control subjects, and the number of
case patients with hypertriglyceridemia was 5-fold greater than the number of
control subjects with hypertriglyceridemia…….” see author 'Discussion Below'

Clinical Infectious Diseases April 2005;40:1188-1193

Sylvie Lawson-Ayayi,1,2 Fabrice Bonnet,1,2 Elise Bernardin,1 Jean-Marie
Ragnaud,2 Denis Lacoste,2 Denis Malvy,2 Marie-Josée Blaizeau,2 Ghada M
iremont-Salamé,3 Michel Dupon,2 Patrick Mercié,1,2 and François Dabis,1,2 for the Groupe
d'Epidémiologie Clinique du SIDA en Aquitaine (GECSA)a

1Institut National de la Santé et de la Recherche Médicale Unité 593,
Institut de Santé Publique, d'Epidémiologie et de Développement, and 2Centre
d'Information et de Soins de l'Immunodéficience Humaine, and 3Centre Régional de
Pharmacovigilance, Département de Pharmacologie, Equipe d'Accueil 3676, Centre
Hospitalo-Universitaire de Bordeaux, Bordeaux, France

Using a case-control study design, we studied the factors associated with
HIV-related avascular necrosis (AN). During a 6-year period, 12 symptomatic AN
cases were validated, and each case was individually matched with 3 control
cases. A conditional logistic regression model showed that current alcohol
consumption and a history of steroid use were the only factors associated with the
occurrence of AN.

Since HAART was introduced and its use has become widespread in
industrialized countries, rates of mortality and severe morbidity related to HIV infection
have been drastically reduced. Although survival rates and quality of life
have improved among HIV-infected individuals, adverse consequences of long-term
exposure to antiretroviral regimens have emerged [1-4]. Particularly, metabolic
complications have been diagnosed in HIV-infected patients who are treated
with HAART, and they have been associated with the receipt of protease
inhibitors (PIs) and nonnucleoside reverse-transcriptase inhibitors (NNRTIs) [5-8].
More recently, cases of avascular necrosis (AN), also referred to as
osteonecrosis, have been reported [9-20], but few studies have reported an increased
incidence of this severe bone disorder [3, 4]. The incidence of asymptomatic AN
among HIV-infected patients was estimated to be 4.4%, through systematic
screening with MRI [21]. The annual incidence of AN, whether symptomatic or not, in
the general population has been estimated to be between 0.010% and 0.135% [15,
22-24]. Thus, the incidence of AN among HIV-infected adults has been found to
be 〜45 times greater than the incidence in the general population [15], which
suggests that its occurrence is a consequence of or a complication of either
HIV infection or receipt of HAART [25].

Several risk factors and conditions, such as hyperlipidemia, alcohol abuse,
steroid use, pancreatitis, and underlying vascular diseases, have been
postulated to be associated with AN [14, 26]. Case reports also have suggested that
HIV infection and antiretroviral therapy, particularly HAART regimens, could
also be risk factors for AN, independent of underlying comorbidities [17];
however, to our knowledge, no systematic study has been conducted thus far. We
studied the main known and hypothesized risk factors for symptomatic cases of AN
that were identified in a large cohort of HIV-infected patients.

Results.      Through December 2002, a total of 12 symptomatic AN cases were
identified and validated. Eleven of the 12 cases were in men. The median age
of the case patients was 38.3 years (interquartile range [IQR], 36.2-45.2), and
9 case patients had received a diagnosis of AIDS. The median time since
diagnosis of HIV infection was 10.4 years (IQR, 8.6-12.9). All case patients had
been exposed to HAART (consisting of at least 3 antiretroviral drugs, including
a PI or an NNRTI) before the occurrence of AN. Criteria used for matching had
comparable values in the case and control groups at baseline: median ages were
38.3 years and 38.4 years, respectively (P = .83); median CD4+ cell counts at
the time of diagnosis of HIV infection were 266.5 cells/mL and 272.0
cells/mL, respectively (P = .66); and median durations of HIV infection since the time
of diagnosis were 123.0 months and 125.1 months, respectively (P = .94).

In univariate analyses, case patients were more likely than control subjects
to be men who reported sex with men, to have fat accumulation, and to engage
in regular or heavy alcohol use, according to physicians' reports. Neither
receipt of a specific antiretroviral drug nor the duration of HAART was associated
with AN. However, history of intravenous or oral course of steroid treatment
was associated with AN occurrence at a borderline level of statistical
significance.

In the multivariate analyses, the only adjusted matched OR (aOR) >1 was for
alcohol consumption (P = .02). Statistical association appeared to be of
borderline significance in the reduced model with regard to fat accumulation (P =
.07) and receipt of efavirenz, ritonavir, or nelfinavir (P = .08, P = .05, and P
= .09, respectively).

When all factors identified by the 2 initial multivariate analyses were
combined in the final model, the risk of the occurrence of AN remained
significantly associated with alcohol consumption (aOR, 20.48; 95% CI, 1.83-229.72; P =
.01) and history of steroid use (aOR, 16.96; 95% CI, 1.20-239.12; P = .04),
whereas fat accumulation failed to be associated with the occurrence of AN (aOR,
22.67; 95% CI, 0.69-745.95; P = .08).

Author Discussion
This comparative analysis investigating a wide range of factors revealed that
current alcohol use and a history of steroid use were strongly associated
with the occurrence of AN. The findings of the present study also provided a
presumption of an association of AN with fat accumulation. The association of the
occurrence of AN with receipt of HAART or the individual components of HAART
was not confirmed. Despite the fact that a trend for association with AN was
detected for receipt of individual drugs, receipt of PIs or NNRTIs , when
considered as cumulative exposure before the diagnosis of AN, could not be
identified as having an association with the occurrence of AN. Nevertheless, the role
of antiretroviral therapy, if any, is probably limited, compared with the roles
of steroid use and alcohol use.

Hypertriglycemia or hypercholesterolemia were not found to be predisposing
factors, as is described in the literature [23, 28]. In the present study, more
case patients presented with high total cholesterol levels than did control
subjects, and the number of case patients with hypertriglyceridemia was 5-fold
greater than the number of control subjects with hypertriglyceridemia (data not
shown). The potential link between hyperlipidemia and AN supports the
hypothesis that the use of PIs is implicated, through an increase of serum lipid
levels, in the occurrence of AN [29]. Scribner et al. [22] have suggested that
moderate hypertriglyceridemia is an independent risk factor for the occurrence of
AN but that severe hypertriglyceridemia is more likely to be associated with
AN by means of PI therapy.

Previous studies have concluded that HIV infection alone may be a risk factor
for AN [28, 30]. Although it has been speculated that receipt of HAART is
associated with the occurrence of AN [10], no association between this bone
disorder and the receipt or duration of antiretroviral therapy has been observed in
the present comparative study. This is possibly because antiretroviral
therapy is widely used in hospital-based cohorts with unlimited access to care, as
is the case in France. The lack of an association between the receipt of PIs
and the occurrence of AN has been observed in other studies, as well [16, 21,
24, 31].

Steroid use and alcohol abuse are the most common risk factors associated
with AN [26]. Indeed, in the present study, a history of steroid use was
independently associated with a high risk of AN, and the association did persist when
the analysis was adjusted for other variables. This result confirmed findings
of previous case-control studies that reported an association between steroid
use and the occurrence of AN but could not control for as many factors as we
did in the present analysis [22, 31]. Miller et al. [21] indicated that even
short courses of steroid treatment increased this risk substantially. In the
present study, "alcohol use" was defined as the consumption of any combination of
different types of alcohol (wine, beer, and cocktails). Because French
consumers usually record a more regular intake of alcoholic beverages than do
consumers elsewhere in the world, we considered regular or heavy drinkers to be the
"high-exposure" category. The estimation of this risk factor by physicians
from patients' self-reported behavior could have introduced a bias that is a
common limitation of studies on alcohol intake. We could not investigate
hereditary vascular diseases-in particular, the presence of antiphospholipid
antibodies, which may contribute to the occurrence of AN, given its high prevalence
among HIV-infected patients [32].

To our knowledge, the present analysis is the first to investigate the
contribution of antiretroviral therapy to the occurrence of AN in detail and by use
of a powerful comparative design, and the first to finally rule out its role.
HIV-infected patients with asymptomatic cases of AN were not included in the
present study, because of the system we used to find cases. Thus, we evaluated
only symptomatic cases of AN, and our findings should not be extrapolated to
all cases of AN. Because the limited number of cases may have affected the
outcome of the present study, large, collaborative epidemiological studies are
still needed to confirm our results and to fully evaluate the role of
antiretroviral therapy in AN, symptomatic or not. Finally, the mechanisms that lead to AN
in HIV-infected patients must also be determined. In the interim, the first
line of prevention of this bone disorder in HIV-infected patients should be the
cessation of alcohol consumption and the limitation of steroid prescription.

Patients and methods.      We performed a case-control study nested within
the Aquitaine Cohort [27]. The Aquitaine Cohort comprises patients enrolled
through a hospital-based surveillance system of HIV infection in southwestern
France. Beginning in 1987, adult inpatients and outpatients were enrolled
prospectively in the present case-control study if they were referred by participating
hospital wards, had confirmed HIV-1 infection and at least 1 follow-up visit
after enrollment or a documented date of death after initial reporting, and
provided informed consent. Follow-up is based on clinical practice; a
standardized reporting form for epidemiological, clinical, biological, and therapeutic
data is completed by physicians at the time of each hospital contact, which
generally occur every 3 or 6 months or in the case of any intercurrent event.

All symptomatic cases of AN that were reported through December 2002 through
either the cohort monitoring system or the pharmaco-epidemiology information
system maintained by the Bordeaux University Hospital were systematically
investigated. These 2 reporting systems allowed us to identify AN cases that had
been diagnosed by physicians since the first AN case notification in 1997.
Symptomatic AN cases were detected on the basis of clinical symptoms and confirmed
by radiological or scintigraphical imaging. For each patient with a confirmed
case, we randomly selected 3 control subjects from the Aquitaine Cohort
database who showed no clinical evidence of AN and who could be matched on the basis
of age (±3 years), time since the diagnosis of HIV infection (±2 years), CD4+
cell count at the time of diagnosis of HIV infection (i.e., <200 cells/mL,
200-349 cells/mL, 350-499 cells/mL, or &ges;500 cells/mL), and duration of
follow-up after the diagnosis of HIV infection. Information on demographic
characteristics, clinical data, biological values, and antiretroviral therapy use were
retrieved from the database for case patients and control subjects and were
systematically verified using clinical records for the purpose of the present
study.

Association of the occurrence of AN with a given variable was estimated by
the matched odds ratio (OR). A conditional logistic regression model was used to
analyze the simultaneous effects of several independent factors. A variable
was included in the multivariate model if it was associated with the occurrence
of AN at a statistical significance of P < .25 in univariate analysis.
Because of the small number of observations relative to the number of variables, 2
models were first developed: one model with demographic, clinical, and
biological variables, and the other with variables relating to antiretroviral therapy.
In each model, a backward stepwise procedure was applied to remove variables
that were not significantly associated with the occurrence of AN. A forward
selection was then applied for the robustness of the analysis. The variables
that were retained in the 2 separate models were included in a final model.
Models were fitted using STATA software, version 5.0 (Stata).

REFERENCES
1.      Herman JS, Easterbrook PJ. The metabolic toxicities of antiretroviral
therapy. Int J STD AIDS 2001; 12:555-62. First citation in article | PubMed
2.      Powderly WG. Long-term exposure to lifelong therapies. J Acquir
Immune Defic Syndr 2002; 29(Suppl 1):S28-40. First citation in article | PubMed
3.      Gutierrez F, Padilla S, Ortega E, et al. Avascular necrosis of the
bone in HIV-infected patients: incidence and associated factors. AIDS 2002;
16:481-3. First citation in article | PubMed
4.      Keruly JC, Moore RD. Incidence and risk factors for avascular
necrosis (AVN) in HIV-infected persons [abstract H-2]. In: Program and abstracts of
the 10th Conference on Retrovirus and Opportunistic Infections (Boston). 2003.
First citation in article
5.      Fellay J, Boubaker K, Ledergerber B, et al. Prevalence of adverse
events associated with potent antiretroviral treatment: Swiss HIV Cohort Study.
Lancet 2001; 358:1322-7. First citation in article | PubMed
6.      Bonfanti P, Ricci E, Landonio S, et al. Predictors of protease
inhibitor-associated adverse events. Biomed Pharmacother 2001; 55:321-3. First
citation in article | PubMed
7.      Bonnet F, Lawson-Ayayi S, Thiébaut R, et al. A cohort study of
nevirapine tolerance in clinical practice: French Aquitaine Cohort, 1997-1999. Clin
Infect Dis 2002; 35:1231-7. First citation in article | Full Text | PubMed
8.      Montessori V, Press N, Harris M, Akagi L, Montaner JS. Adverse
effects of antiretrovial therapy for HIV infection. CMAJ 2004; 170:229-38. First
citation in article | PubMed
9.      Olive A, Queralt C, Sirera G, Centelles M, Force L. Osteonecrosis and
HIV infection: four more cases. J Rheumatol 1998; 25:1243-4. First citation
in article | PubMed
10.      Meyer D, Behrens G, Schmidt RE, Stoll M. Osteonecrosis of the
femoral head in patients receiving HIV protease inhibitors. AIDS 1999; 13:1147-8.
First citation in article | PubMed
11.      Johns DG, Gill MJ. Avascular necrosis in HIV infection. AIDS 1999;
13:1997. First citation in article | PubMed
12.      Blangy H, Loeuille D, Chary-Valckenaere I, Christian B, May T,
Gillet P. Osteonecrosis of the femoral head in HIV-1 patients: four additional
cases. AIDS 2000; 14:2214-5. First citation in article | PubMed
13.      Roudière L, Viard JP. Ostenecrosis of the hip, lipodystrophy and
antiretroviral treatment. AIDS 2000; 14:2056. First citation in article | PubMed
14.      Wolfe CJ, Taylor-Butler KL. Avascular necrosis: a case history and
literature review. Arch Fam Med 2000; 9:291-4. First citation in article |
PubMed
15.      Brown P, Crane L. Avascular necrosis of bone in patients with human
immunodeficiency virus infection: report of 6 cases and review of the
literature. Clin Infect Dis 2001; 32:1221-6. First citation in article | Full Text |
PubMed
16.      Gaughan DM, Mofenson LM, Hughes MD, Seage GR, Ciupak GL, Oleske JM.
The Pediatric AIDS Clinical Trials Group. Osteonecrosis of the hip
(Legg-Calvé-Perthes disease) in human immunodeficiency virus-infected children.
Pediatrics 2002; 109:E74. First citation in article | PubMed
17.      Bongiovanni M, Chiesa E, Riva A, D'Arminio Monforte A, Bini T.
Avascular necrosis of the femoral head in a HIV-1 infected patient receiving
lopinavir/ritonavir. Int J Antimicrob Agents 2003; 22:630-1. First citation in
article | PubMed
18.      Valencia ME, Barreiro P, Soriano V, Blanco F, Moreno V, Lahoz JG.
Avascular necrosis in HIV-infected patients receiving antiretroviral treatment:
study of 7 cases. HIV Clin Trials 2003; 4:132-6. First citation in article |
PubMed
19.      Gasiorowski J, Knysz B, Sokolska V, Gladysz A. Avascular necrosis of
femoral heads in a man with HIV infection. Lancet Infect Dis 2003; 3:708.
First citation in article | PubMed
20.      Calza L, Manfredi R, Chiodo F. Osteonecrosis in HIV-infected
patients and its correlation with highly active antiretroviral therapy (HAART) [in
French]. Presse Med 2003; 32:595-8. First citation in article | PubMed
21.      Miller KD, Masur H, Jones EC, et al. High prevalence of
osteonecrosis of the femoral head in HIV-infected adults. Ann Intern Med 2002; 137:17-25.
First citation in article | PubMed
22.      Scribner A, Troia-Cancio PV, Cox BA, et al. Osteonecrosis in HIV: a
case-control study. J Acquir Immune Defic Syndr 2000; 25:19-25. First citation
in article | PubMed
23.      Allison GT, Bostrom MP, Glesby MJ. Osteonecrosis in HIV disease:
epidemiology, etiologies, and clinical management. AIDS 2003; 17:1-9. First
citation in article | PubMed
24.      Keruly JC, Chaisson RE, Moore RD. Increasing incidence of avascular
necrosis of the hip in HIV-infected patients. J Acquir Immune Defic Syndr
2001; 28:101-2. First citation in article | PubMed
25.      Monier P, McKown K, Bronze MS. Osteonecrosis complicating highly
active antiretroviral therapy in patients infected with human immunodeficiency
virus. Clin Infect Dis 2000; 31:1488-92. First citation in article | Full Text |
PubMed
26.      Blacksin MF, Kloser PC, Simon J. Avascular necrosis of bone in human
immunodeficiency virus infected patients. Clin Imaging 1999; 23:314-8. First
citation in article | PubMed
27.      Marimoutou C, Chêne G, Dabis F, Lacoste D, Salamon R. Human
immunodeficiency virus infection and AIDS in Aquitaine: 10 years' experience of a
hospital information system, 1985-1995. Le Groupe d'Epidemiologie Clinique du SIDA
en Aquitaine (GECSA) [in French]. Presse Med 1997; 26:703-10. First citation
in article | PubMed
28.      Ries MD, Barcohana B, Davidson A, Jergesen HE, Paiement GD.
Association between human immunodeficiency virus and osteonecrosis of the femoral
head. J Arthroplasty 2002; 17:135-9. First citation in article | PubMed
29.      Bonfanti P, Grabbuti A, Carradori S, et al. Osteonecrosis in
protease inhibitor-treated patients. Orthopedics 2001; 24:271-2. First citation in
article | PubMed
30.      Skiest DJ. Osteonecrosis in human imunodeficiency virus-infected
patients may not be related to immune reconstitution. Clin Infect Dis 2001;
33:268-9. First citation in article | Full Text | PubMed
31.      Glesby MJ, Hoover DR, Vaamonde CM. Osteonecrosis in patients
infected with human immunodeficiency virus: a case-control study. J Infect Dis 2001;
184:519-23. First citation in article | Full Text | PubMed
32.      Bonnet F, Pineau JJ, Taupin JL, et al. Prevalence of
cryoglobulinemia and serological markers of autoimmunity in human immunodeficiency virus
infected individuals: a cross-sectional study of 97 patients. J Rheumatol 2003;
30:2005-10. First citation in article | PubMed



[This message contained attachments]



________________________________________________________________________
________________________________________________________________________

Message: 2        
   Date: Thu, 31 Mar 2005 14:52:57 -0800 (PST)
   From: Mike DC <mikedcguy@...>
Subject: Re: More on abacavir-induced neuropsychiatric reactions


This is all VERY INTERESTING.  I tried Sustiva and
couldn't stand it.  My doctor then tried Abacavir, and
I told him I still felt "messed up," so we stopped
that as well.  This was all a few years ago. 
At the time, my doctor told me that Abacavir wasn't
known to have such side effects.  I felt very
disoriented on the stuff.  Thanks Nelson for posting
all of this on Abacavir - it feels like a mystery has
been solved (and I feel slightly vindicated).  These
meds really can have a range of side effects for
diffent people. OH well ...


--- PoWeRTX@... wrote:

> This happened  to me also. I know several  people
> that have had the same
> problem on Ziagen. Doctors and patients do not  know
> about this. 
> More on abacavir-induced neuropsychiatric reactions.
>
> Foster R, Taylor C, Everall IP.
> AIDS. 2004 Dec 3;18(18):2449.
> It is increasingly recognized that  antiretroviral
> medications may induce
> severe, but transient, changes in mental  state.
> These are uncommon and
> idiosyncratic, with the literature containing only
> two published reports suggesting
> that abacavir (Ziagen), a nucleoside reverse
> transcriptase inhibitor, may
> induce a range of neuropsychiatric disorders in
> seropositive individuals. These
> include depression, suicidal thoughts, auditory
> hallucinations [_1_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e
>
8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d6761
>
84e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6
> #17) ]  and frank psychosis [_2_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d154
>
97b83b9e5baab68f6262d35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db
> 6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#18) ].
>  Of note is the fact
> that the subjects in these cases were all female
> with CD4  cell counts below 500
> cells/µl. Here we report, for the first time, a
> case of a  possible
> abacavir-induced neuropsychiatric reaction in a
> seropositive Caucasian  man with a
> higher CD4 cell count.
> The patient was a 44-year-old gay man who was
> diagnosed HIV positive in
> 1993. He was referred to psychiatric services in
> 2000  after the psychologist whom
> he had been seeing became concerned about the
> patient's ongoing depressive
> symptoms. He had previously been treated with
> various antidepressants and
> triple therapies for HIV, and was currently
> receiving citalopram 30 mg a day in
> addition to tenofovir 245 mg per day,  nevirapine
> 200 mg twice a day and
> abacavir 300 mg twice a day. He had previously  been
> taking didanosine, but this was
> changed to abacavir because of  lipodystrophy.
> Approximately one week after commencing  abacavir,
> the patient started to
> complain of feeling tired and ‘stoned'. He also
> complained of headaches, which
> were described as ‘constant and throbbing’ and
> ‘located in the middle of my
> brain'. He reported the onset of bad dreams, which
> he referred to as ‘night
> terrors'. These were described as vivid and
> terrifying,  but the actual content
> could not be recalled. He denied any associated
> physical  symptoms such as
> night sweats or any recent physical illness. His CD4
> cell count  at this time was
> 557 cells/µl and his viral load was less than 50
> copies/ml. Of  note is the
> fact that despite his dreams he now felt that his
> previously low  mood had
> improved to the extent that he was expressing the
> desire to cease  taking
> citalopram.
> Two weeks after reporting the above problems,  the
> patient was reviewed by
> the HIV physician who changed the abacavir back to
> didanosine. Within 24 h of
> this the patient reported that his headaches and bad
>  dreams had stopped, and
> that he was feeling less fatigued. At one month
> follow-up he remained free of
> these symptoms, and his mood remained settled. The
> citalopram was eventually
> reduced gradually and finally stopped.
> This case suggests that abacavir may, in rare
> cases, induce unpleasant but
> non-specific neuropsychiatric side-effects, which
> can resolve rapidly upon
> stopping this medication. Although it has been
> suggested that abacavir may be
> associated with new-onset depression [_1_
> (http://gateway.utovid.com.ezproxyhost.library.
>
tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da
>
8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#17)
> ],  this was not
> apparent in the current case. In that earlier
> publication [_1_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e8c8a96d3
>
ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d676184e80885
>
5bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#17)
> ],
>  depression and night sweats were reported in one
> patient, with depression, 
> suicidal ideation, headache, auditory hallucinations
> and anorexia in the
> second.  The patients in those cases were both HIV
> positive Caucasian women.
> Similarly, a  more recent publication described a
> case of putative abacavir-induced
> psychosis  occurring in an African woman [_2_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b5
>
3d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d676184e808855bd7f415e7acd
>
48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#18)
> ]  who became
> symptom-free after the cessation and substitution of
> this  medication.
> The current report suggests that men can also  be
> adversely affected by
> abacavir-associated neuropsychiatric problems, even
> at  a higher CD4 cell count
> accompanied by a low viral load. Furthermore,
> symptoms  may rapidly resolve upon
> discontinuation of abacavir and the substitution of
> a  suitable alternative
> antiretroviral agent. It is possible that headache
> and mood  alterations may be
> early indicators of neuropsychiatric sequelae
> associated with  abacavir. These
> should be investigated and monitored closely to
> exclude possible  organic
> factors. Management should be carried out in
> collaboration with both HIV 
> physicians and specialist psychiatrists.
> References
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d3
>
5fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd5
> 11242a35a0302af534fa8b6#toc)
> 1. Colebunders R, Hilbrands R, De Roo A, Pelgrom J.
> Neuropsychiatric reaction
> induced by abacavir.  Am J Med 2002; 113:616.
> _ExternalResolverBasic_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?Link+Set+Ref=0
>
0002030-200412030-00021|00000439_2002_113_616_colebunders_neuropsychiatric_|00
>
002030-200412030-00021#xpointer(id(R1-21))|1103920|http://acs.ovid.com/acs/f6
>
489bf4937db0b6e5a4e52b4a0f690866ea468998ca8e6ac6e6d949d499ba8ceb07ec98d2542738
>
eb60d9d5afd443af26842fbd2b397e36e9ea7cf26a19744cf8bf2cf6fefeecf6eb.gif|ovftdb|
>
00000439-200211000-00018&P=17&S=IDNJHKJKBAMCKK00D&WebLinkReturn=Full+Text=L|S
> sh.15.16|0|00002030-200412030-00021) 
> _Bibliographic  Links_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?Link+Set+Ref=00002030-
>
200412030-00021|00000439_2002_113_616_colebunders_neuropsychiatric_|00002030-2
>
00412030-00021#xpointer(id(R1-21))|60|http://acs.ovid.com/acs/.6f8cf7c31ada011
>
97afb0a1ba3d293b287b71168019f9ea6ec0cdc7f51235e3420b469cc1e8a8406f3c6be4f14376
>
dfd09416d1f878f23bb78.gif|ovftdb|00000439-200211000-00018&P=17&S=IDNJHKJKBAMCK
>
K00D&WebLinkReturn=Full+Text=L|S.sh.15.16|0|00002030-200412030-00021)

> _[Context  Link]_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d3
>
5fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd5
> 11242a35a0302af534fa8b6#10) 
> 2. Foster R, Olajide D, Everall IP. Antiretroviral
> therapy-induced psychosis:
> case report and brief  review of the literature. HIV
> Med  2003; 4:139–144.
> _[Context  Link]_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f62
>
62d35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d16
> 4cd511242a35a0302af534fa8b6#10) Accession Number:
> 00002030-200412030-00021

> In  health,
>
> Nelson Vergel
> Director
> Program for Wellness Restoration,  PoWeR
> A 501 (c) 3 non profit national  organization
> powerusa.org
> salvagetherapies.org
> faciawasting.org
>
>
> Disclaimer
>
> This  information (and any accompanying printed
> material) is not intended to
> replace  the attention or advice of a physician or
> other health care
> professional. Anyone  who wishes to embark on any
> dietary, drug, exercise, or other
> lifestyle change  intended to prevent or treat a
> specific disease or condition
> should first  consult with and seek clearance from a
> qualified health care 
> professional.
>


__________________________________________________
Do You Yahoo!?
Tired of spam?  Yahoo! Mail has the best spam protection around
http://mail.yahoo.com





________________________________________________________________________
________________________________________________________________________

Message: 3        
   Date: Thu, 31 Mar 2005 19:28:51 EST
   From: Sotoway@...
Subject: Sculptra and Dr. Frechette

Hi All;
 
I had my second treatment with the great Doctor my face appears completely 
restored.  It was a bit uncomfortable, but worth the discomfort.  I  strongly
recommend him.  He is patient and shows great deal of  expertise.  I believe
that the massage and cold ice treatment play a big  role in the prevention of
bumps under the skin that a lot of you have been  complaining about.  If anyone
can wants to see him he has an office in New  york as well as San Francisco.  
 
 
Nancy


[This message contained attachments]



________________________________________________________________________
________________________________________________________________________

Message: 4        
   Date: Thu, 31 Mar 2005 21:15:18 EST
   From: Fit4fundc@...
Subject: Re: cheekbone implants

Cheek implants have their advantages too.   The implants can be trimmed. They
come in different sizes and shapes.   If you don't like the really wide ones
but you like the fact that it is very thick, the surgeon can trim it so it
isn't so wide.   My surgeon inserted the largest pair and they were still a
little to wide for me.    They gave me too much of a cheek and too wide up near my
eye socket and to the side of my face.   I had a few infections and one had to
be removed twice.   If I had it to do all over, I would opt for only the
fillers like BioAlcamid.  

Cheek implants can change the look of your face to something you never looked
like.   Personally, I like long hard faces on men.   My cheeks implants made
me more rounded, not what I really wanted.   However, they did fill up the
thumb prints in my face.

It's a hard choice sometimes.


Lester in DC


[This message contained attachments]



________________________________________________________________________
________________________________________________________________________

Message: 5        
   Date: Thu, 31 Mar 2005 21:50:21 EST
   From: PoWeRTX@...
Subject: Two good suggestions from a member

 
    *   Rather than copy a whole article  onto this yahoo group if you could
give the name of the article (and topic if  not evident in the name), what you
found interesting and the URL where to  find the complete article along with
the source information. 
    *   When replying to a message delete everything  below the first line of
the message you are replying to, as it shows up  numerous times for the
person who has subscribed to this group to receive the  emails in digest form.  If
you leave the sender, subject and first line  of the message almost anyone
would understand what message you are responding  to.

 
In  health,

Nelson Vergel
Director
Program for Wellness Restoration,  PoWeR
A 501 (c) 3 non profit national  organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This  information (and any accompanying printed material) is not intended to
replace  the attention or advice of a physician or other health care
professional. Anyone  who wishes to embark on any dietary, drug, exercise, or other
lifestyle change  intended to prevent or treat a specific disease or condition
should first  consult with and seek clearance from a qualified health care 
professional.


[This message contained attachments]



________________________________________________________________________
________________________________________________________________________

Message: 6        
   Date: Thu, 31 Mar 2005 23:30:51 EST
   From: beefymusclebud@...
Subject: Abdominal Adiposity the Best Predictor of Type 2 Diabetes in Men

 
Abdominal Adiposity the Best Predictor of Type 2 Diabetes in  Men


NEW YORK Mar 31 - Both overall obesity, denoted by higher BMI, and abdominal 
obesity, reflected by higher waist circumference strongly and independently 
predict risk of type 2 diabetes in men, but abdominal obesity appears to be
the  better predictor, new research shows.
"Both BMI and waist circumference are useful for assessing health risk and 
should be measured in clinical settings and epidemiologic research whenever 
possible," the investigators say. But abdominal fat measured by waist 
circumference "can indicate a strong risk for diabetes whether or not a man is 
considered overweight or obese according to his BMI," lead author Dr. Youfa Wang 
added in a statement.
In the study, investigators compared the predictive power of BMI, waist 
circumference (WC) and waist-to-hip ratio (WHR) for the development of type 2 
diabetes in 27,270 men participating in the Health Professionals Follow-up 
Study.
During 13 years of follow up, a total of 884 men developed type 2 diabetes, 
Dr. Wang, from Johns Hopkins Bloomberg School of Public Health in Baltimore,
and  colleagues report in the March issue of the American Journal of Clinical 
Nutrition.
According to the team, the age-adjusted relative risks across quintiles of 
WC, starting at a WC of 73.7 to 86.4 cm (29 to 34 inches) and going up to 101.6
 to 157.5 cm, were 1.0, 2.0, 2.7, 5.0, and 12.0, respectively, they report.
For WHR, relative risks across increasing quintiles were 1.0, 2.1, 2.7, 3.6, 
and 6.9 and for BMI they were 1.0, 1.1, 1.8, 2.9, and 7.9, respectively.
"Our findings support the contention that the measurement of WC should be 
used in clinical practice instead of WHR," the investigators write.
The study findings also suggest that the currently recommended cutoff for 
high waist circumference of 102 cm (40 inches) for men may need to be lowered to
 95 cm. "Many of the men who developed type 2 diabetes had measurements lower
 than the cutoff, Dr. Wang explained, "and the risk associated with the waist
 circumference increased at a much lower level."
Am J Clin Nutr 2005;81:555-563.


[This message contained attachments]



________________________________________________________________________
________________________________________________________________________

Message: 7        
   Date: Thu, 31 Mar 2005 23:33:25 EST
   From: beefymusclebud@...
Subject: One stop patient assistence, this is important

Some Free Medicine Programs Too Complex: Survey
 
Mar 30 - Drug company programs that offer free medicines to the poor are  too
time-consuming and complex for some health clinics that serve mostly 
low-income patients, according to a survey released on Tuesday.
Of 214 clinics in five states that were surveyed in 2002, forty-eight said 
they did not participate in patient assistance programs that provide free 
medicines to people who cannot afford them.
More than two thirds of the clinics that did not take part said the programs 
were cumbersome and took too much time. Some companies required tax returns
and  made other unrealistic demands for income documentation, the survey said.
The Pharmaceutical Research and Manufacturers of America, an industry group, 
has encouraged companies to simplify application forms, spokesman Ken Johnson
 said.
"Can we do a better job? Yes, and we will," he said.
Early next month, the industry will unveil a new program that will provide 
one-stop access to 275 existing patient assistance programs, Johnson  said.
"We are going to make it easier and quicker to obtain information," he said, 
adding that millions of people already get free or discounted drugs from 
manufacturers each year.
The health-clinic survey found the drug donation programs consumed an average
 of 12 hours of pharmacist time, and 99 hours of other staff time, per month.
While clinic staff believed the donated drugs filled an important need, they 
"don't understand why complicated and changing programs must take so much
time  away from patient care," said Kathryn Duke, the study's lead author and
director  for the Medicine for People in Need program of the nonprofit Public
Health  Institute.
The study, funded by the philanthropic California Health Care Foundation, 
will be published in the April 1st edition of the American Journal of 
Health-System Pharmacy.
Charitable programs from GlaxoSmithKline Plc, Novartis AG and Schering-Plough
 Corp. were identified as least likely to be used, while others offered by
Pfizer  Inc., Bristol-Myers Squibb Co. and Merck & Co. Inc. were used most 
frequently.
GlaxoSmithKline spokeswoman Patricia Seif said the company donated medicines 
worth $372 million last year to U.S. patients. "We try to make it easy" to 
participate, she said, adding that many patients get the requested drugs the 
same  day.


[This message contained attachments]



________________________________________________________________________
________________________________________________________________________

Message: 8        
   Date: Fri, 1 Apr 2005 16:04:34 EST
   From: PoWeRTX@...
Subject: Assessing the Relationship Between Fatigue and Mitochondrial Toxicity in Patient

 
Both HIV infection and antiretroviral nucleoside analogues (nucleoside 
reverse transcriptase inhibitors or NRTIs) are known to affect mitochondrial DNA 
content and mitochondrial function. A number of important clinical syndromes 
observed in HIV-infected persons relate to mitochondrial dysfunction including 
lactic acidosis, myopathy, cardiomyopathy, pancreatitis, peripheral
neuropathy,  and possibly lipodystrophy. Fatigue, one of the most prevalent complaints
among  persons with HIV infection, may also be the result of mitochondrial
toxicity,  though this has not been clearly established.
_http://clinicaltrials.gov/ct/show/NCT00106795?order=201_
(http://clinicaltrials.gov/ct/show/NCT00106795?order=201)
 
In  health,

Nelson Vergel
Director
Program for Wellness Restoration,  PoWeR
A 501 (c) 3 non profit national  organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This  information (and any accompanying printed material) is not intended to
replace  the attention or advice of a physician or other health care
professional. Anyone  who wishes to embark on any dietary, drug, exercise, or other
lifestyle change  intended to prevent or treat a specific disease or condition
should first  consult with and seek clearance from a qualified health care 
professional.


[This message contained attachments]



________________________________________________________________________
________________________________________________________________________

Message: 9        
   Date: Fri, 1 Apr 2005 16:06:48 EST
   From: PoWeRTX@...
Subject: MRI to assess facial wasting and AVN


 
This study will examine risk factors for facial wasting and avascular 
necrosis (AVN, a type of damage to the hip and other bones) in HIV-infected 
patients. The prevalence and natural history of AVN are also being evaluated.  This
study will use magnetic resonance imaging (MRI) to identify and monitor  these
conditions in patients with and without diagnosed AVN and to identify risk 
factors. 
_http://clinicaltrials.gov/ct/show/NCT00001762?order=202_
(http://clinicaltrials.gov/ct/show/NCT00001762?order=202)
In  health,

Nelson Vergel
Director
Program for Wellness Restoration,  PoWeR
A 501 (c) 3 non profit national  organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This  information (and any accompanying printed material) is not intended to
replace  the attention or advice of a physician or other health care
professional. Anyone  who wishes to embark on any dietary, drug, exercise, or other
lifestyle change  intended to prevent or treat a specific disease or condition
should first  consult with and seek clearance from a qualified health care 
professional.


[This message contained attachments]



________________________________________________________________________
________________________________________________________________________

Message: 10       
   Date: Thu, 31 Mar 2005 21:45:31 EST
   From: PoWeRTX@...
Subject: HIV Transplant study website


_http://spitfire.emmes.com/study/htr/_ (http://spitfire.emmes.com/study/htr/)


In  health,

Nelson Vergel
Director
Program for Wellness Restoration,  PoWeR
A 501 (c) 3 non profit national  organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This  information (and any accompanying printed material) is not intended to
replace  the attention or advice of a physician or other health care
professional. Anyone  who wishes to embark on any dietary, drug, exercise, or other
lifestyle change  intended to prevent or treat a specific disease or condition
should first  consult with and seek clearance from a qualified health care 
professional.


[This message contained attachments]



________________________________________________________________________
________________________________________________________________________


Welcome to our PozHealth group!
If you received this email from someone who forwarded it to you and would like to join this group, send a blank email to PozHealth-subscribe@yahoogroups.com and you will get an email with instructions to follow. You can chose to receive single emails or a daily digest (collection of emails). You can post pictures, images, attach files and search by keyword old postings in the group.

For those of you who are members already and want to switch from single emails to digest or vice versa, visit www.yahoogroups.com, click on PozHealth, then on "edit my membership" and go down to your selection. The list administrator does not process any requests, so this is a do-it-yourself easy process ! :)
Thanks for joining. You will learn and share a lot in this group!

NOTE: I moderate, approve or disapprove emails before they are posted. Please follow the guidelines shown in the homepage. I will not allow rudeness, sexually  explicit material, attacks, and anyone who does not follow the rules. If you are not OK with this, please do not join the group.

Forward this email to anyone who may benefit from this information! Thanks!
In Health,

Nelson Vergel (PoWeRTX@...)
List Founder and Moderator

------------------------------------------------------------------------
Yahoo! Groups Links

<*> To visit your group on the web, go to:
    http://groups.yahoo.com/group/PozHealth/

<*> To unsubscribe from this group, send an email to:
    PozHealth-unsubscribe@yahoogroups.com

<*> Your use of Yahoo! Groups is subject to:
    http://docs.yahoo.com/info/terms/
 
------------------------------------------------------------------------





#11434 From: John Barrow <pozbod@...>
Date: Sat Apr 2, 2005 9:25 pm
Subject: history of steroid
johnftl59
Offline Offline
Send Email Send Email
 
It would be useful to contact the authors.  In general, anabolic
steroid use is much less in HIV patient in France, as the government is
much tighter in controlling use of these agents.

I believe they are talking about cortico steroids, but this needs to be
clarified.  The authors and journal editors should be strongly
reprimanded for their carelessness.

JB
On Apr 2, 2005, at 1:32 PM, PozHealth@yahoogroups.com wrote:

> This comparative analysis investigating a wide range of factors
> revealed that
> current alcohol use and a history of steroid use were strongly
> associated
> with the occurrence of AN.

#11433 From: John Barrow <pozbod@...>
Date: Sat Apr 2, 2005 8:42 pm
Subject: in the present study, a history of steroid
johnftl59
Offline Offline
Send Email Send Email
 
Whoever persists in writing "steroid" use, in a medical article is a
fucking moron.  What drugs are we talking about?  Corticosteroids for
inflammation and asthma?  Anabolic steroids for muscle building?  Isn't
this supposed to be a medical journal?

I am sick and tired of people who should know better using imprecise,
contradictory, and confusing terminology.    This is a question of
great community interest, and to use such idiotic verbage borders on
criminal.

My understanding remains that cortico-steroids are the problem. This
citation does a great job of muddying the waters, and it is uncalled
for.

JB
On Apr 2, 2005, at 1:32 PM, PozHealth@yahoogroups.com wrote:

> Steroid use and alcohol abuse are the most common risk factors
> associated
> with AN [26]. Indeed, in the present study, a history of steroid use
> was
> independently associated with a high risk of AN, and the association
> did persist when
> the analysis was adjusted for other variables.

#11432 From: rippedtothemax@...
Date: Sat Apr 2, 2005 1:02 pm
Subject: (no subject)
rippedtothemax@...
Send Email Send Email
 
Yesterday I finally got a call from the Patient Assistance Program at Dermik Labs concerning the application I (actually my Dr., Peter Englehard in South Beach) submitted on Dec 25th.  It took twelve weeks for them to finally get to me!  I'm in the $40k - $80K income range that qualifies me for the product at a reduced rate based on some sort of sliding scale - the details of which they won't divulge - but the bottom line is that they will sell me each kit, which consists of 2 vials of the injectable, for $400. The qualification I receive for the program is good for the next 18 months during which time they will sell me up to 6 kits of the product.  You pay them over the phone with a CC# and they send the Sculptra to your Dr.which takes about 3 - 5 days.  Dr. Englehard now has reduced his fee to $350 per treatment ($175 if you only need one vile) which brings the cost of each treatment to $750 - plus the airfare to Miami ($200aprox from Boston) so it comes to around $1000 per treatment which is about half the price of a treatment without the Patient Access program.  I have about 3 - 3.5 degree of lipoatrophy on the measurement scale they use so I'll probably need 3-4 treatments, provided my face responds well and builds up the necessary collagen between treatment injections.
 
As I said before I have a consultation scheduled in Toronto with Dr. Beniger on April 11th and after that I'll have more information on the Bio-Alcamid approach and cost etc. If you want to check out some information on Bio-Alcamid go to  http://www.faceforward.ca/
 
 
Once I meet with the Toronto Dr I'm going to have to decide on one of these two approaches for myself.  I'm sort of leaning toward Sculptra because it's done in a few stages and the effects won't be that noticeable to my friends and co-workers - those that don't know about my HIV+ situation that is.  Also I've seen a study done on Sculptra and there seems to have been no ill side effects in any of the patients in the study.  I'm going to ask the Toronto Dr if there are studies available on Bio-Alcamid that I can read to see if the same is true of that.

#11431 From: JM Friedman <jfrdmn@...>
Date: Sat Apr 2, 2005 4:26 pm
Subject: cheek/malar implants
jfrdmn@...
Send Email Send Email
 
Lester, do you still have the implants in place?  Is there any way to predict who will be liable to infections from them?  Are such infections common?--thanks--Hugo
 
PS  I myself certainly would prefer not to change the former look of my face if I could get it back, but some small change would be acceptable, after all, everything in the face does change anyway over time.  By the way, cheekbones are not typically very sexually dimorphic, absolutely and also relatively as compared with other parts of the face.  Male models in magazines may have very angular cheekbones, but most men don't. 

#11430 From: PoWeRTX@...
Date: Thu Mar 31, 2005 9:45 pm
Subject: HIV Transplant study website
nelsonvergel
Offline Offline
Send Email Send Email
 
 

 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.

#11429 From: PoWeRTX@...
Date: Fri Apr 1, 2005 4:06 pm
Subject: MRI to assess facial wasting and AVN
nelsonvergel
Offline Offline
Send Email Send Email
 
 

This study will examine risk factors for facial wasting and avascular necrosis (AVN, a type of damage to the hip and other bones) in HIV-infected patients. The prevalence and natural history of AVN are also being evaluated. This study will use magnetic resonance imaging (MRI) to identify and monitor these conditions in patients with and without diagnosed AVN and to identify risk factors.

http://clinicaltrials.gov/ct/show/NCT00001762?order=202

In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.

#11428 From: PoWeRTX@...
Date: Fri Apr 1, 2005 4:04 pm
Subject: Assessing the Relationship Between Fatigue and Mitochondrial Toxicity in Patient
nelsonvergel
Offline Offline
Send Email Send Email
 

Both HIV infection and antiretroviral nucleoside analogues (nucleoside reverse transcriptase inhibitors or NRTIs) are known to affect mitochondrial DNA content and mitochondrial function. A number of important clinical syndromes observed in HIV-infected persons relate to mitochondrial dysfunction including lactic acidosis, myopathy, cardiomyopathy, pancreatitis, peripheral neuropathy, and possibly lipodystrophy. Fatigue, one of the most prevalent complaints among persons with HIV infection, may also be the result of mitochondrial toxicity, though this has not been clearly established.

 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.

#11427 From: beefymusclebud@...
Date: Thu Mar 31, 2005 11:33 pm
Subject: One stop patient assistence, this is important
beefymusclebud
Offline Offline
Send Email Send Email
 
Some Free Medicine Programs Too Complex: Survey 
 
Mar 30 - Drug company programs that offer free medicines to the poor are too time-consuming and complex for some health clinics that serve mostly low-income patients, according to a survey released on Tuesday.

Of 214 clinics in five states that were surveyed in 2002, forty-eight said they did not participate in patient assistance programs that provide free medicines to people who cannot afford them.

More than two thirds of the clinics that did not take part said the programs were cumbersome and took too much time. Some companies required tax returns and made other unrealistic demands for income documentation, the survey said.

The Pharmaceutical Research and Manufacturers of America, an industry group, has encouraged companies to simplify application forms, spokesman Ken Johnson said.

"Can we do a better job? Yes, and we will," he said.

Early next month, the industry will unveil a new program that will provide one-stop access to 275 existing patient assistance programs, Johnson said.

"We are going to make it easier and quicker to obtain information," he said, adding that millions of people already get free or discounted drugs from manufacturers each year.

The health-clinic survey found the drug donation programs consumed an average of 12 hours of pharmacist time, and 99 hours of other staff time, per month.

While clinic staff believed the donated drugs filled an important need, they "don't understand why complicated and changing programs must take so much time away from patient care," said Kathryn Duke, the study's lead author and director for the Medicine for People in Need program of the nonprofit Public Health Institute.

The study, funded by the philanthropic California Health Care Foundation, will be published in the April 1st edition of the American Journal of Health-System Pharmacy.

Charitable programs from GlaxoSmithKline Plc, Novartis AG and Schering-Plough Corp. were identified as least likely to be used, while others offered by Pfizer Inc., Bristol-Myers Squibb Co. and Merck & Co. Inc. were used most frequently.

GlaxoSmithKline spokeswoman Patricia Seif said the company donated medicines worth $372 million last year to U.S. patients. "We try to make it easy" to participate, she said, adding that many patients get the requested drugs the same day.


#11426 From: beefymusclebud@...
Date: Thu Mar 31, 2005 11:30 pm
Subject: Abdominal Adiposity the Best Predictor of Type 2 Diabetes in Men
beefymusclebud
Offline Offline
Send Email Send Email
 
Abdominal Adiposity the Best Predictor of Type 2 Diabetes in Men


NEW YORK Mar 31 - Both overall obesity, denoted by higher BMI, and abdominal obesity, reflected by higher waist circumference strongly and independently predict risk of type 2 diabetes in men, but abdominal obesity appears to be the better predictor, new research shows.

"Both BMI and waist circumference are useful for assessing health risk and should be measured in clinical settings and epidemiologic research whenever possible," the investigators say. But abdominal fat measured by waist circumference "can indicate a strong risk for diabetes whether or not a man is considered overweight or obese according to his BMI," lead author Dr. Youfa Wang added in a statement.

In the study, investigators compared the predictive power of BMI, waist circumference (WC) and waist-to-hip ratio (WHR) for the development of type 2 diabetes in 27,270 men participating in the Health Professionals Follow-up Study.

During 13 years of follow up, a total of 884 men developed type 2 diabetes, Dr. Wang, from Johns Hopkins Bloomberg School of Public Health in Baltimore, and colleagues report in the March issue of the American Journal of Clinical Nutrition.

According to the team, the age-adjusted relative risks across quintiles of WC, starting at a WC of 73.7 to 86.4 cm (29 to 34 inches) and going up to 101.6 to 157.5 cm, were 1.0, 2.0, 2.7, 5.0, and 12.0, respectively, they report.

For WHR, relative risks across increasing quintiles were 1.0, 2.1, 2.7, 3.6, and 6.9 and for BMI they were 1.0, 1.1, 1.8, 2.9, and 7.9, respectively.

"Our findings support the contention that the measurement of WC should be used in clinical practice instead of WHR," the investigators write.

The study findings also suggest that the currently recommended cutoff for high waist circumference of 102 cm (40 inches) for men may need to be lowered to 95 cm. "Many of the men who developed type 2 diabetes had measurements lower than the cutoff, Dr. Wang explained, "and the risk associated with the waist circumference increased at a much lower level."

Am J Clin Nutr 2005;81:555-563.


#11425 From: PoWeRTX@...
Date: Thu Mar 31, 2005 9:50 pm
Subject: Two good suggestions from a member
nelsonvergel
Offline Offline
Send Email Send Email
 
  • Rather than copy a whole article onto this yahoo group if you could give the name of the article (and topic if not evident in the name), what you found interesting and the URL where to find the complete article along with the source information.
  • When replying to a message delete everything below the first line of the message you are replying to, as it shows up numerous times for the person who has subscribed to this group to receive the emails in digest form.  If you leave the sender, subject and first line of the message almost anyone would understand what message you are responding to.
 
In health,

Nelson Vergel
Director
Program for Wellness Restoration, PoWeR
A 501 (c) 3 non profit national organization
powerusa.org
salvagetherapies.org
faciawasting.org


Disclaimer

This information (and any accompanying printed material) is not intended to replace the attention or advice of a physician or other health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a qualified health care professional.

#11424 From: Fit4fundc@...
Date: Thu Mar 31, 2005 9:15 pm
Subject: Re: cheekbone implants
Fit4fundc@...
Send Email Send Email
 
Cheek implants have their advantages too.  The implants can be trimmed. They come in different sizes and shapes.  If you don't like the really wide ones but you like the fact that it is very thick, the surgeon can trim it so it isn't so wide.  My surgeon inserted the largest pair and they were still a little to wide for me.   They gave me too much of a cheek and too wide up near my eye socket and to the side of my face.  I had a few infections and one had to be removed twice.  If I had it to do all over, I would opt for only the fillers like BioAlcamid. 

Cheek implants can change the look of your face to something you never looked like.  Personally, I like long hard faces on men.  My cheeks implants made me more rounded, not what I really wanted.  However, they did fill up the thumb prints in my face.

It's a hard choice sometimes.


Lester in DC

#11423 From: Sotoway@...
Date: Thu Mar 31, 2005 7:28 pm
Subject: Sculptra and Dr. Frechette
Sotoway@...
Send Email Send Email
 
Hi All;
 
I had my second treatment with the great Doctor my face appears completely restored.  It was a bit uncomfortable, but worth the discomfort.  I strongly recommend him.  He is patient and shows great deal of expertise.  I believe that the massage and cold ice treatment play a big role in the prevention of bumps under the skin that a lot of you have been complaining about.  If anyone can wants to see him he has an office in New york as well as San Francisco.  
 
 
Nancy

#11422 From: Mike DC <mikedcguy@...>
Date: Thu Mar 31, 2005 10:52 pm
Subject: Re: More on abacavir-induced neuropsychiatric reactions
mikedcguy
Offline Offline
Send Email Send Email
 
This is all VERY INTERESTING.  I tried Sustiva and
couldn't stand it.  My doctor then tried Abacavir, and
I told him I still felt "messed up," so we stopped
that as well.  This was all a few years ago.
At the time, my doctor told me that Abacavir wasn't
known to have such side effects.  I felt very
disoriented on the stuff.  Thanks Nelson for posting
all of this on Abacavir - it feels like a mystery has
been solved (and I feel slightly vindicated).  These
meds really can have a range of side effects for
diffent people. OH well ...


--- PoWeRTX@... wrote:

> This happened  to me also. I know several  people
> that have had the same
> problem on Ziagen. Doctors and patients do not  know
> about this.
> More on abacavir-induced neuropsychiatric reactions.
>
> Foster R, Taylor C, Everall IP.
> AIDS. 2004 Dec 3;18(18):2449.
> It is increasingly recognized that  antiretroviral
> medications may induce
> severe, but transient, changes in mental  state.
> These are uncommon and
> idiosyncratic, with the literature containing only
> two published reports suggesting
> that abacavir (Ziagen), a nucleoside reverse
> transcriptase inhibitor, may
> induce a range of neuropsychiatric disorders in
> seropositive individuals. These
> include depression, suicidal thoughts, auditory
> hallucinations [_1_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f\
4e1a73d37e
>
8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d6761
>
84e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6
> #17) ]  and frank psychosis [_2_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f\
4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d154
>
97b83b9e5baab68f6262d35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db
> 6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#18) ].
>  Of note is the fact
> that the subjects in these cases were all female
> with CD4  cell counts below 500
> cells/µl. Here we report, for the first time, a
> case of a  possible
> abacavir-induced neuropsychiatric reaction in a
> seropositive Caucasian  man with a
> higher CD4 cell count.
> The patient was a 44-year-old gay man who was
> diagnosed HIV positive in
> 1993. He was referred to psychiatric services in
> 2000  after the psychologist whom
> he had been seeing became concerned about the
> patient's ongoing depressive
> symptoms. He had previously been treated with
> various antidepressants and
> triple therapies for HIV, and was currently
> receiving citalopram 30 mg a day in
> addition to tenofovir 245 mg per day,  nevirapine
> 200 mg twice a day and
> abacavir 300 mg twice a day. He had previously  been
> taking didanosine, but this was
> changed to abacavir because of  lipodystrophy.
> Approximately one week after commencing  abacavir,
> the patient started to
> complain of feeling tired and ‘stoned'. He also
> complained of headaches, which
> were described as ‘constant and throbbing’ and
> ‘located in the middle of my
> brain'. He reported the onset of bad dreams, which
> he referred to as ‘night
> terrors'. These were described as vivid and
> terrifying,  but the actual content
> could not be recalled. He denied any associated
> physical  symptoms such as
> night sweats or any recent physical illness. His CD4
> cell count  at this time was
> 557 cells/µl and his viral load was less than 50
> copies/ml. Of  note is the
> fact that despite his dreams he now felt that his
> previously low  mood had
> improved to the extent that he was expressing the
> desire to cease  taking
> citalopram.
> Two weeks after reporting the above problems,  the
> patient was reviewed by
> the HIV physician who changed the abacavir back to
> didanosine. Within 24 h of
> this the patient reported that his headaches and bad
>  dreams had stopped, and
> that he was feeling less fatigued. At one month
> follow-up he remained free of
> these symptoms, and his mood remained settled. The
> citalopram was eventually
> reduced gradually and finally stopped.
> This case suggests that abacavir may, in rare
> cases, induce unpleasant but
> non-specific neuropsychiatric side-effects, which
> can resolve rapidly upon
> stopping this medication. Although it has been
> suggested that abacavir may be
> associated with new-onset depression [_1_
> (http://gateway.ut.ovid.com.ezproxyhost.library.
>
tmc.edu/gw2/ovidweb.cgi?QS2=434f4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83\
b9e5baab68f6262d35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da
>
8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#17)
> ],  this was not
> apparent in the current case. In that earlier
> publication [_1_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f\
4e1a73d37e8c8a96d3
>
ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d676184e80885
>
5bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#17)
> ],
>  depression and night sweats were reported in one
> patient, with depression,
> suicidal ideation, headache, auditory hallucinations
> and anorexia in the
> second.  The patients in those cases were both HIV
> positive Caucasian women.
> Similarly, a  more recent publication described a
> case of putative abacavir-induced
> psychosis  occurring in an African woman [_2_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f\
4e1a73d37e8c8a96d3ba1aa0ba0d5b5
>
3d5e5632d15497b83b9e5baab68f6262d35fcac6cd23743905e8d676184e808855bd7f415e7acd
>
48b9da8092db6e57b008cbb2cb6d164cd511242a35a0302af534fa8b6#18)
> ]  who became
> symptom-free after the cessation and substitution of
> this  medication.
> The current report suggests that men can also  be
> adversely affected by
> abacavir-associated neuropsychiatric problems, even
> at  a higher CD4 cell count
> accompanied by a low viral load. Furthermore,
> symptoms  may rapidly resolve upon
> discontinuation of abacavir and the substitution of
> a  suitable alternative
> antiretroviral agent. It is possible that headache
> and mood  alterations may be
> early indicators of neuropsychiatric sequelae
> associated with  abacavir. These
> should be investigated and monitored closely to
> exclude possible  organic
> factors. Management should be carried out in
> collaboration with both HIV
> physicians and specialist psychiatrists.
> References
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f\
4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d3
>
5fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd5
> 11242a35a0302af534fa8b6#toc)
> 1. Colebunders R, Hilbrands R, De Roo A, Pelgrom J.
> Neuropsychiatric reaction
> induced by abacavir.  Am J Med 2002; 113:616.
> _ExternalResolverBasic_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?Link+Set\
+Ref=0
>
0002030-200412030-00021|00000439_2002_113_616_colebunders_neuropsychiatric_|00
>
002030-200412030-00021#xpointer(id(R1-21))|1103920|http://acs.ovid.com/acs/.f6
>
489bf4937db0b6e5a4e52b4a0f690866ea468998ca8e6ac6e6d949d499ba8ceb07ec98d2542738
>
eb60d9d5afd443af26842fbd2b397e36e9ea7cf26a19744cf8bf2cf6fefeecf6eb.gif|ovftdb|
>
00000439-200211000-00018&P=17&S=IDNJHKJKBAMCKK00D&WebLinkReturn=Full+Text=L|S.
> sh.15.16|0|00002030-200412030-00021)
> _Bibliographic  Links_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?Link+Set\
+Ref=00002030-
>
200412030-00021|00000439_2002_113_616_colebunders_neuropsychiatric_|00002030-2
>
00412030-00021#xpointer(id(R1-21))|60|http://acs.ovid.com/acs/.6f8cf7c31ada011
>
97afb0a1ba3d293b287b71168019f9ea6ec0cdc7f51235e3420b469cc1e8a8406f3c6be4f14376
>
dfd09416d1f878f23bb78.gif|ovftdb|00000439-200211000-00018&P=17&S=IDNJHKJKBAMCK
>
K00D&WebLinkReturn=Full+Text=L|S.sh.15.16|0|00002030-200412030-00021)
>
> _[Context  Link]_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f\
4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f6262d3
>
5fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d164cd5
> 11242a35a0302af534fa8b6#10)
> 2. Foster R, Olajide D, Everall IP. Antiretroviral
> therapy-induced psychosis:
> case report and brief  review of the literature. HIV
> Med  2003; 4:139–144.
> _[Context  Link]_
>
(http://gateway.ut.ovid.com.ezproxyhost.library.tmc.edu/gw2/ovidweb.cgi?QS2=434f\
4e1a73d37e8c8a96d3ba1aa0ba0d5b53d5e5632d15497b83b9e5baab68f62
>
62d35fcac6cd23743905e8d676184e808855bd7f415e7acd48b9da8092db6e57b008cbb2cb6d16
> 4cd511242a35a0302af534fa8b6#10) Accession Number:
> 00002030-200412030-00021
>
> In  health,
>
> Nelson Vergel
> Director
> Program for Wellness Restoration,  PoWeR
> A 501 (c) 3 non profit national  organization
> powerusa.org
> salvagetherapies.org
> faciawasting.org
>
>
> Disclaimer
>
> This  information (and any accompanying printed
> material) is not intended to
> replace  the attention or advice of a physician or
> other health care
> professional. Anyone  who wishes to embark on any
> dietary, drug, exercise, or other
> lifestyle change  intended to prevent or treat a
> specific disease or condition
> should first  consult with and seek clearance from a
> qualified health care
> professional.
>


__________________________________________________
Do You Yahoo!?
Tired of spam?  Yahoo! Mail has the best spam protection around
http://mail.yahoo.com

#11421 From: JuLev@...
Date: Thu Mar 31, 2005 5:00 pm
Subject: Avascular Necrosis Risk Factors-steroids, alcohol
JuLev@...
Send Email Send Email
 
NATAP - www.natap.org

Avascular Necrosis in HIV-Infected Patients:
A Case-Control Study from the Aquitaine Cohort, 1997-2002, France

“…… This comparative analysis (CID 4/2005) investigating a wide range of factors revealed that current alcohol use and a history of steroid use were strongly associated with the occurrence of AN….history of steroid use was independently associated with a high risk of AN…...even short courses of steroid treatment increased this risk substantially….the first line of prevention of this bone disorder in HIV-infected patients should be the cessation of alcohol consumption and the limitation of steroid prescription….Although it has been speculated that receipt of HAART is associated with the occurrence of AN, no association between this bone disorder and the receipt or duration of antiretroviral therapy has been observed in the present comparative study…….Hypertriglycemia or hypercholesterolemia were not found to be predisposing factors, as is described in the literature. In the present study, more case patients presented with high total cholesterol levels than did control subjects, and the number of case patients with hypertriglyceridemia was 5-fold greater than the number of control subjects with hypertriglyceridemia…….” see author 'Discussion Below'

Clinical Infectious Diseases April 2005;40:1188-1193

Sylvie Lawson-Ayayi,1,2 Fabrice Bonnet,1,2 Elise Bernardin,1 Jean-Marie Ragnaud,2 Denis Lacoste,2 Denis Malvy,2 Marie-Josée Blaizeau,2 Ghada Miremont-Salamé,3 Michel Dupon,2 Patrick Mercié,1,2 and François Dabis,1,2 for the Groupe d'Epidémiologie Clinique du SIDA en Aquitaine (GECSA)a

1Institut National de la Santé et de la Recherche Médicale Unité 593, Institut de Santé Publique, d'Epidémiologie et de Développement, and 2Centre d'Information et de Soins de l'Immunodéficience Humaine, and 3Centre Régional de Pharmacovigilance, Département de Pharmacologie, Equipe d'Accueil 3676, Centre Hospitalo-Universitaire de Bordeaux, Bordeaux, France

Using a case-control study design, we studied the factors associated with HIV-related avascular necrosis (AN). During a 6-year period, 12 symptomatic AN cases were validated, and each case was individually matched with 3 control cases. A conditional logistic regression model showed that current alcohol consumption and a history of steroid use were the only factors associated with the occurrence of AN.

Since HAART was introduced and its use has become widespread in industrialized countries, rates of mortality and severe morbidity related to HIV infection have been drastically reduced. Although survival rates and quality of life have improved among HIV-infected individuals, adverse consequences of long-term exposure to antiretroviral regimens have emerged [1-4]. Particularly, metabolic complications have been diagnosed in HIV-infected patients who are treated with HAART, and they have been associated with the receipt of protease inhibitors (PIs) and nonnucleoside reverse-transcriptase inhibitors (NNRTIs) [5-8]. More recently, cases of avascular necrosis (AN), also referred to as osteonecrosis, have been reported [9-20], but few studies have reported an increased incidence of this severe bone disorder [3, 4]. The incidence of asymptomatic AN among HIV-infected patients was estimated to be 4.4%, through systematic screening with MRI [21]. The annual incidence of AN, whether symptomatic or not, in the general population has been estimated to be between 0.010% and 0.135% [15, 22-24]. Thus, the incidence of AN among HIV-infected adults has been found to be 45 times greater than the incidence in the general population [15], which suggests that its occurrence is a consequence of or a complication of either HIV infection or receipt of HAART [25].

Several risk factors and conditions, such as hyperlipidemia, alcohol abuse, steroid use, pancreatitis, and underlying vascular diseases, have been postulated to be associated with AN [14, 26]. Case reports also have suggested that HIV infection and antiretroviral therapy, particularly HAART regimens, could also be risk factors for AN, independent of underlying comorbidities [17]; however, to our knowledge, no systematic study has been conducted thus far. We studied the main known and hypothesized risk factors for symptomatic cases of AN that were identified in a large cohort of HIV-infected patients.

Results.     Through December 2002, a total of 12 symptomatic AN cases were identified and validated. Eleven of the 12 cases were in men. The median age of the case patients was 38.3 years (interquartile range [IQR], 36.2-45.2), and 9 case patients had received a diagnosis of AIDS. The median time since diagnosis of HIV infection was 10.4 years (IQR, 8.6-12.9). All case patients had been exposed to HAART (consisting of at least 3 antiretroviral drugs, including a PI or an NNRTI) before the occurrence of AN. Criteria used for matching had comparable values in the case and control groups at baseline: median ages were 38.3 years and 38.4 years, respectively (P = .83); median CD4+ cell counts at the time of diagnosis of HIV infection were 266.5 cells/mL and 272.0 cells/mL, respectively (P = .66); and median durations of HIV infection since the time of diagnosis were 123.0 months and 125.1 months, respectively (P = .94).

In univariate analyses, case patients were more likely than control subjects to be men who reported sex with men, to have fat accumulation, and to engage in regular or heavy alcohol use, according to physicians' reports. Neither receipt of a specific antiretroviral drug nor the duration of HAART was associated with AN. However,
history of intravenous or oral course of steroid treatment was associated with AN occurrence at a borderline level of statistical significance.

In the multivariate analyses, the only adjusted matched OR (aOR) >1 was for alcohol consumption (P = .02). Statistical association appeared to be of borderline significance in the reduced model with regard to fat accumulation (P = .07) and receipt of efavirenz, ritonavir, or nelfinavir (P = .08, P = .05, and P = .09, respectively).

When all factors identified by the 2 initial multivariate analyses were combined in the final model, the risk of the occurrence of AN remained significantly associated with
alcohol consumption (aOR, 20.48; 95% CI, 1.83-229.72; P = .01) and history of steroid use (aOR, 16.96; 95% CI, 1.20-239.12; P = .04), whereas fat accumulation failed to be associated with the occurrence of AN (aOR, 22.67; 95% CI, 0.69-745.95; P = .08).

Author Discussion
This comparative analysis investigating a wide range of factors revealed that current alcohol use and a history of steroid use were strongly associated with the occurrence of AN. The findings of the present study also provided a presumption of an association of AN with fat accumulation. The association of the occurrence of AN with receipt of HAART or the individual components of HAART was not confirmed. Despite the fact that a trend for association with AN was detected for receipt of individual drugs, receipt of PIs or NNRTIs , when considered as cumulative exposure before the diagnosis of AN, could not be identified as having an association with the occurrence of AN. Nevertheless, the role of antiretroviral therapy, if any, is probably limited, compared with the roles of steroid use and alcohol use.

Hypertriglycemia or hypercholesterolemia were not found to be predisposing factors, as is described in the literature [23, 28]. In the present study, more case patients presented with high total cholesterol levels than did control subjects, and the number of case patients with hypertriglyceridemia was 5-fold greater than the number of control subjects with hypertriglyceridemia (data not shown). The potential link between hyperlipidemia and AN supports the hypothesis that the use of PIs is implicated, through an increase of serum lipid levels, in the occurrence of AN [29]. Scribner et al. [22] have suggested that moderate hypertriglyceridemia is an independent risk factor for the occurrence of AN but that severe hypertriglyceridemia is more likely to be associated with AN by means of PI therapy.

Previous studies have concluded that HIV infection alone may be a risk factor for AN [28, 30]. Although it has been speculated that receipt of HAART is associated with the occurrence of AN [10], no association between this bone disorder and the receipt or duration of antiretroviral therapy has been observed in the present comparative study. This is possibly because antiretroviral therapy is widely used in hospital-based cohorts with unlimited access to care, as is the case in France. The lack of an association between the receipt of PIs and the occurrence of AN has been observed in other studies, as well [16, 21, 24, 31].

Steroid use and alcohol abuse are the most common risk factors associated with AN [26]. Indeed, in the present study, a history of steroid use was independently associated with a high risk of AN, and the association did persist when the analysis was adjusted for other variables. This result confirmed findings of previous case-control studies that reported an association between steroid use and the occurrence of AN but could not control for as many factors as we did in the present analysis [22, 31]. Miller et al. [21] indicated that even short courses of steroid treatment increased this risk substantially. In the present study, "alcohol use" was defined as the consumption of any combination of different types of alcohol (wine, beer, and cocktails). Because French consumers usually record a more regular intake of alcoholic beverages than do consumers elsewhere in the world, we considered regular or heavy drinkers to be the "high-exposure" category. The estimation of this risk factor by physicians from patients' self-reported behavior could have introduced a bias that is a common limitation of studies on alcohol intake. We could not investigate hereditary vascular diseases-in particular, the presence of antiphospholipid antibodies, which may contribute to the occurrence of AN, given its high prevalence among HIV-infected patients [32].

To our knowledge, the present analysis is the first to investigate the contribution of antiretroviral therapy to the occurrence of AN in detail and by use of a powerful comparative design, and the first to finally rule out its role. HIV-infected patients with asymptomatic cases of AN were not included in the present study, because of the system we used to find cases. Thus, we evaluated only symptomatic cases of AN, and our findings should not be extrapolated to all cases of AN. Because the limited number of cases may have affected the outcome of the present study, large, collaborative epidemiological studies are still needed to confirm our results and to fully evaluate the role of antiretroviral therapy in AN, symptomatic or not. Finally, the mechanisms that lead to AN in HIV-infected patients must also be determined. In the interim, the first line of prevention of this bone disorder in HIV-infected patients should be the cessation of alcohol consumption and the limitation of steroid prescription.

Patients and methods.     We performed a case-control study nested within the Aquitaine Cohort [27]. The Aquitaine Cohort comprises patients enrolled through a hospital-based surveillance system of HIV infection in southwestern France. Beginning in 1987, adult inpatients and outpatients were enrolled prospectively in the present case-control study if they were referred by participating hospital wards, had confirmed HIV-1 infection and at least 1 follow-up visit after enrollment or a documented date of death after initial reporting, and provided informed consent. Follow-up is based on clinical practice; a standardized reporting form for epidemiological, clinical, biological, and therapeutic data is completed by physicians at the time of each hospital contact, which generally occur every 3 or 6 months or in the case of any intercurrent event.

All symptomatic cases of AN that were reported through December 2002 through either the cohort monitoring system or the pharmaco-epidemiology information system maintained by the Bordeaux University Hospital were systematically investigated. These 2 reporting systems allowed us to identify AN cases that had been diagnosed by physicians since the first AN case notification in 1997. Symptomatic AN cases were detected on the basis of clinical symptoms and confirmed by radiological or scintigraphical imaging. For each patient with a confirmed case, we randomly selected 3 control subjects from the Aquitaine Cohort database who showed no clinical evidence of AN and who could be matched on the basis of age (±3 years), time since the diagnosis of HIV infection (±2 years), CD4+ cell count at the time of diagnosis of HIV infection (i.e., <200 cells/mL, 200-349 cells/mL, 350-499 cells/mL, or &ges;500 cells/mL), and duration of follow-up after the diagnosis of HIV infection. Information on demographic characteristics, clinical data, biological values, and antiretroviral therapy use were retrieved from the database for case patients and control subjects and were systematically verified using clinical records for the purpose of the present study.

Association of the occurrence of AN with a given variable was estimated by the matched odds ratio (OR). A conditional logistic regression model was used to analyze the simultaneous effects of several independent factors. A variable was included in the multivariate model if it was associated with the occurrence of AN at a statistical significance of P < .25 in univariate analysis. Because of the small number of observations relative to the number of variables, 2 models were first developed: one model with demographic, clinical, and biological variables, and the other with variables relating to antiretroviral therapy. In each model, a backward stepwise procedure was applied to remove variables that were not significantly associated with the occurrence of AN. A forward selection was then applied for the robustness of the analysis. The variables that were retained in the 2 separate models were included in a final model. Models were fitted using STATA software, version 5.0 (Stata).

REFERENCES
1.      Herman JS, Easterbrook PJ. The metabolic toxicities of antiretroviral therapy. Int J STD AIDS 2001; 12:555-62. First citation in article | PubMed
2.      Powderly WG. Long-term exposure to lifelong therapies. J Acquir Immune Defic Syndr 2002; 29(Suppl 1):S28-40. First citation in article | PubMed
3.      Gutierrez F, Padilla S, Ortega E, et al. Avascular necrosis of the bone in HIV-infected patients: incidence and associated factors. AIDS 2002; 16:481-3. First citation in article | PubMed
4.      Keruly JC, Moore RD. Incidence and risk factors for avascular necrosis (AVN) in HIV-infected persons [abstract H-2]. In: Program and abstracts of the 10th Conference on Retrovirus and Opportunistic Infections (Boston). 2003. First citation in article
5.      Fellay J, Boubaker K, Ledergerber B, et al. Prevalence of adverse events associated with potent antiretroviral treatment: Swiss HIV Cohort Study. Lancet 2001; 358:1322-7. First citation in article | PubMed
6.      Bonfanti P, Ricci E, Landonio S, et al. Predictors of protease inhibitor-associated adverse events. Biomed Pharmacother 2001; 55:321-3. First citation in article | PubMed
7.      Bonnet F, Lawson-Ayayi S, Thiébaut R, et al. A cohort study of nevirapine tolerance in clinical practice: French Aquitaine Cohort, 1997-1999. Clin Infect Dis 2002; 35:1231-7. First citation in article | Full Text | PubMed
8.      Montessori V, Press N, Harris M, Akagi L, Montaner JS. Adverse effects of antiretrovial therapy for HIV infection. CMAJ 2004; 170:229-38. First citation in article | PubMed
9.      Olive A, Queralt C, Sirera G, Centelles M, Force L. Osteonecrosis and HIV infection: four more cases. J Rheumatol 1998; 25:1243-4. First citation in article | PubMed
10.      Meyer D, Behrens G, Schmidt RE, Stoll M. Osteonecrosis of the femoral head in patients receiving HIV protease inhibitors. AIDS 1999; 13:1147-8. First citation in article | PubMed
11.      Johns DG, Gill MJ. Avascular necrosis in HIV infection. AIDS 1999; 13:1997. First citation in article | PubMed
12.      Blangy H, Loeuille D, Chary-Valckenaere I, Christian B, May T, Gillet P. Osteonecrosis of the femoral head in HIV-1 patients: four additional cases. AIDS 2000; 14:2214-5. First citation in article | PubMed
13.      Roudière L, Viard JP. Ostenecrosis of the hip, lipodystrophy and antiretroviral treatment. AIDS 2000; 14:2056. First citation in article | PubMed
14.      Wolfe CJ, Taylor-Butler KL. Avascular necrosis: a case history and literature review. Arch Fam Med 2000; 9:291-4. First citation in article | PubMed
15.      Brown P, Crane L. Avascular necrosis of bone in patients with human immunodeficiency virus infection: report of 6 cases and review of the literature. Clin Infect Dis 2001; 32:1221-6. First citation in article | Full Text | PubMed
16.      Gaughan DM, Mofenson LM, Hughes MD, Seage GR, Ciupak GL, Oleske JM. The Pediatric AIDS Clinical Trials Group. Osteonecrosis of the hip (Legg-Calvé-Perthes disease) in human immunodeficiency virus-infected children. Pediatrics 2002; 109:E74. First citation in article | PubMed
17.      Bongiovanni M, Chiesa E, Riva A, D'Arminio Monforte A, Bini T. Avascular necrosis of the femoral head in a HIV-1 infected patient receiving lopinavir/ritonavir. Int J Antimicrob Agents 2003; 22:630-1. First citation in article | PubMed
18.      Valencia ME, Barreiro P, Soriano V, Blanco F, Moreno V, Lahoz JG. Avascular necrosis in HIV-infected patients receiving antiretroviral treatment: study of 7 cases. HIV Clin Trials 2003; 4:132-6. First citation in article | PubMed
19.      Gasiorowski J, Knysz B, Sokolska V, Gladysz A. Avascular necrosis of femoral heads in a man with HIV infection. Lancet Infect Dis 2003; 3:708. First citation in article | PubMed
20.      Calza L, Manfredi R, Chiodo F. Osteonecrosis in HIV-infected patients and its correlation with highly active antiretroviral therapy (HAART) [in French]. Presse Med 2003; 32:595-8. First citation in article | PubMed
21.      Miller KD, Masur H, Jones EC, et al. High prevalence of osteonecrosis of the femoral head in HIV-infected adults. Ann Intern Med 2002; 137:17-25. First citation in article | PubMed
22.      Scribner A, Troia-Cancio PV, Cox BA, et al. Osteonecrosis in HIV: a case-control study. J Acquir Immune Defic Syndr 2000; 25:19-25. First citation in article | PubMed
23.      Allison GT, Bostrom MP, Glesby MJ. Osteonecrosis in HIV disease: epidemiology, etiologies, and clinical management. AIDS 2003; 17:1-9. First citation in article | PubMed
24.      Keruly JC, Chaisson RE, Moore RD. Increasing incidence of avascular necrosis of the hip in HIV-infected patients. J Acquir Immune Defic Syndr 2001; 28:101-2. First citation in article | PubMed
25.      Monier P, McKown K, Bronze MS. Osteonecrosis complicating highly active antiretroviral therapy in patients infected with human immunodeficiency virus. Clin Infect Dis 2000; 31:1488-92. First citation in article | Full Text | PubMed
26.      Blacksin MF, Kloser PC, Simon J. Avascular necrosis of bone in human immunodeficiency virus infected patients. Clin Imaging 1999; 23:314-8. First citation in article | PubMed
27.      Marimoutou C, Chêne G, Dabis F, Lacoste D, Salamon R. Human immunodeficiency virus infection and AIDS in Aquitaine: 10 years' experience of a hospital information system, 1985-1995. Le Groupe d'Epidemiologie Clinique du SIDA en Aquitaine (GECSA) [in French]. Presse Med 1997; 26:703-10. First citation in article | PubMed
28.      Ries MD, Barcohana B, Davidson A, Jergesen HE, Paiement GD. Association between human immunodeficiency virus and osteonecrosis of the femoral head. J Arthroplasty 2002; 17:135-9. First citation in article | PubMed
29.      Bonfanti P, Grabbuti A, Carradori S, et al. Osteonecrosis in protease inhibitor-treated patients. Orthopedics 2001; 24:271-2. First citation in article | PubMed
30.      Skiest DJ. Osteonecrosis in human imunodeficiency virus-infected patients may not be related to immune reconstitution. Clin Infect Dis 2001; 33:268-9. First citation in article | Full Text | PubMed
31.      Glesby MJ, Hoover DR, Vaamonde CM. Osteonecrosis in patients infected with human immunodeficiency virus: a case-control study. J Infect Dis 2001; 184:519-23. First citation in article | Full Text | PubMed
32.      Bonnet F, Pineau JJ, Taupin JL, et al. Prevalence of cryoglobulinemia and serological markers of autoimmunity in human immunodeficiency virus infected individuals: a cross-sectional study of 97 patients. J Rheumatol 2003; 30:2005-10. First citation in article | PubMed


Messages 11421 - 11450 of 31349   Newest  |  < Newer  |  Older >  |  Oldest
Advanced
Add to My Yahoo!      XML What's This?

Copyright 2009 Yahoo! Inc. All rights reserved.
Privacy Policy - Terms of Service - Guidelines - Help