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全国扩大获得抗逆转录病毒治疗机会方案的长期结局:智利艾滋病队列。

Long-term outcomes of a national expanded access program to antiretroviral therapy: the Chilean AIDS cohort.

机构信息

University of Chile School of Medicine, Santiago, Chile.

出版信息

J Acquir Immune Defic Syndr. 2010 Nov;55(3):368-74. doi: 10.1097/QAI.0b013e3181eb4fb9.

Abstract

OBJECTIVE

To evaluate impact of the program after up to 6 years of follow-up in survival, virologic, and immunologic response.

METHODS

Prospective follow-up of patients initiating first highly active antiretroviral therapy from 2001 to 2007. Chile began in 2001 an expanded access program to antiretroviral therapy. The Chilean AIDS Cohort has enrolled >85% of patients from this program in the public health system.

STATISTICAL ANALYSIS

χ², Fisher tests, survival, univariate and multivariate analysis.

RESULTS

Five thousand one hundred fifteen adults (16% women); median follow-up: 3.64 years (18,159 patient-years). At baseline: median age, 35.8 years; 45.6% had clinical AIDS; median CD4 cell count, 102 cells per cubic millimeter. Global mortality, 9.0%; loss to follow-up, 6.8%. Probability of survival at 1 and 5 years were 0.95 and 0.89, respectively. First regimen was maintained in 72% of those alive and in control at 1 year and 48% at end of study. Main reason for therapy change/discontinuation was drug toxicity (44.9%). At last visit, 74% of active patients had viral suppression, and median CD4 cell count had reached 301 cells per cubic millimeter.

CONCLUSIONS

In this middle-income country, wide access highly active antiretroviral therapy has been successfully implemented and evaluated. Despite advanced disease at initiation, survival, clinical, virologic, and immunologic outcomes have been comparable with that of industrialized countries.

摘要

目的

在最长 6 年的随访中评估该方案对生存率、病毒学和免疫学应答的影响。

方法

对 2001 年至 2007 年期间首次接受高效抗逆转录病毒治疗的患者进行前瞻性随访。智利于 2001 年启动了一项扩大获得抗逆转录病毒治疗的方案。智利艾滋病队列已将该方案中超过 85%的患者纳入公共卫生系统。

统计分析

χ²、Fisher 检验、生存分析、单变量和多变量分析。

结果

5115 名成年人(16%为女性);中位随访时间:3.64 年(18159 人年)。基线时:中位年龄 35.8 岁;45.6%有临床艾滋病;中位 CD4 细胞计数 102 个/立方毫米。总死亡率为 9.0%;失访率为 6.8%。1 年和 5 年的生存率分别为 0.95 和 0.89。在存活且 1 年时处于对照组的患者中,有 72%的患者保留了最初的治疗方案,在研究结束时保留了 48%。治疗方案改变/终止的主要原因是药物毒性(44.9%)。在最后一次就诊时,74%的活跃患者病毒得到抑制,中位 CD4 细胞计数达到 301 个/立方毫米。

结论

在这个中等收入国家,广泛获得高效抗逆转录病毒治疗已成功实施并得到评估。尽管起始时疾病已处于晚期,但生存率、临床、病毒学和免疫学结局与工业化国家相当。

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