Improved survival among HIV-infected individuals following initiation of antiretroviral therapy

被引:690
作者
Hogg, RS
Heath, KV
Yip, B
Craib, KJP
O'Shaughnessy, MV
Schechter, MT
Montaner, JSG
机构
[1] Univ British Columbia, St Pauls Hosp, AIDS Res Programme, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V6Z 1Y6, Canada
[2] Univ British Columbia, Dept Hlth Care & Epidemiol, Fac Med, Vancouver, BC V6Z 1Y6, Canada
[3] Univ British Columbia, Dept Pathol, Fac Med, Vancouver, BC V6Z 1Y6, Canada
[4] Univ British Columbia, Dept Med, Fac Med, Vancouver, BC V6Z 1Y6, Canada
[5] Canadian HIV Trials Network, Vancouver, BC, Canada
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1998年 / 279卷 / 06期
关键词
D O I
10.1001/jama.279.6.450
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context.-Clinical trials have established the efficacy of antiretroviral therapy with double-and triple-drug regimens for individuals infected with the human immunodeficiency virus (HIV), but the effectiveness of these regimens in the population of patients not enrolled in clinical trials is unknown. Objective.-To characterize survival following the initiation of antiretroviral therapy among HIV-infected individuals in the province of British Columbia. Design.-Prospective, population-based Cohort study of patients with antiretroviral therapy available free of charge (median follow-up, 21 months). Setting.-Province of British Columbia, Canada. Patients.-All HIV-positive men and women 18 years of age or older in the province who were first prescribed any antiretroviral therapy between October 1992 and June 1996 and whose CD4(+) cell counts were less than 0.350x10(9)/L. Main Outcome Measures.-Rates of progression from initiation of antiretroviral therapy to death or a primary acquired immunodeficiency syndrome (AIDS) diagnosis for subjects who initially received zidovudine-, didanosine-, or zalcitabine-based therapy (ERA-I) and for those who initially received therapy regimens including lamivudine or stavudine (ERA-II). Results.-A total of 1178 patients (951 ERA-I, 227 ERA-II) were eligible, A total of 390 patients died (367 ERA-I, 23 ERA-II), yielding a crude mortality rate of 33.1%, ERA-I group subjects were almost twice as likely to die as ERA-II group subjects, with a mortality risk ratio of 1.86 (95% confidence interval [CI], 1.21-2.86, P=.005). After adjusting for Pneumocystis carinii and Mycobacterium avium prophylaxis use, AIDS diagnosis, CD4(+) cell count, sex, and age, ERA-I participants were 1.93 times (95% CI, 1.25-2.97; P=.003) more likely to die than ERA-II participants, Among patients without AIDS when treatment was started, ERA-I participants were 2.50 times (95% CI, 1.59-3.93; P<.001) more likely to progress to AIDS or death than ERA-II participants. Conclusion.-The HIV-infected individuals who received initial therapy with regimens including stavudine or lamivudine had significantly fewer mortality and longer AIDS-free survival than those who received initial therapy with regimens limited to zidovudine, didanosine, and zalcitabine.
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收藏
页码:450 / 454
页数:5
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