Antiretroviral therapy for HIV infection in 1996 - Recommendations of an international panel

被引:547
作者
Carpenter, CCJ
Fischl, MA
Hammer, SM
Hirsch, MS
Jacobsen, DM
Katzenstein, DA
Montaner, JSG
Richman, DD
Saag, MS
Schooley, RT
Thompson, MA
Vella, S
Yeni, PG
Volberding, PA
机构
[1] BROWN UNIV,SCH MED,PROVIDENCE,RI 02912
[2] UNIV MIAMI,SCH MED,MIAMI,FL
[3] HARVARD UNIV,SCH MED,BOSTON,MA
[4] STANFORD UNIV,MED CTR,STANFORD,CA 94305
[5] ST PAULS HOSP,VANCOUVER,BC V6Z 1Y6,CANADA
[6] UNIV CALIF SAN DIEGO,LA JOLLA,CA
[7] VET AFFAIRS MED CTR,SAN DIEGO,CA
[8] UNIV ALABAMA,BIRMINGHAM,AL
[9] UNIV COLORADO,SCH MED,DENVER,CO
[10] AIDS RES CONSORTIUM ATLANTA,ATLANTA,GA
[11] IST SUPER SANITA,I-00161 ROME,ITALY
[12] HOP BICHAT CLAUDE BERNARD,X BICHAT MED SCH,PARIS,FRANCE
[13] UNIV CALIF SAN FRANCISCO,SAN FRANCISCO,CA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1996年 / 276卷 / 02期
关键词
D O I
10.1001/jama.276.2.146
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective.-To provide clinical recommendations for antiretroviral therapy for human immunodeficiency virus (HIV) disease with currently (mid 1996) available drugs, When to start therapy, what to start with, when to change, and what to change to were addressed. Participants.-A 13-member panel representing international expertise in antiretroviral research and HIV patient care was selected by the International AIDS Society-USA. Evidence.-Available clinical and basic science data, including phase 3 controlled trials, clinical endpoint data, virologic and immunologic endpoint data, interim analyses, studies of HIV pathophysiology, and expert opinions of panel members were considered. Recommendations were limited to drugs available in mid 1996. Process.-For each question posed, 1 or more member(s) reviewed and presented available data. Recommendations were determined by group consensus (January 1996); revisions as warranted by new data were incorporated by group consensus (February-May 1996). Conclusions.-Recent data on HIV pathogenesis, methods to determine plasma HIV RNA, clinical trial data, and availability of new drugs point to the need for new approaches to treatment. Therapy is recommended based on CD4(+) cell count, plasma HIV RNA level, or clinical status, Preferred initial drug regimens include nucleoside combinations; at present protease inhibitors are probably best reserved for patients at higher progression risk. For treatment failure or drug intolerance, subsequent regimen considerations include reasons for changing therapy, available drug options, disease stage, underlying conditions, and concomitant medication(s). Therapy for primary (acute) infection, high-risk exposures to HIV, and maternal-to-fetal transmission are also addressed. Therapeutic approaches need to be updated as new data continue to emerge.
引用
收藏
页码:146 / 154
页数:9
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