School of Medicine, Johns Hopkins University, Baltimore, Maryland, United States of America.
PLoS One. 2011;6(12):e28691. doi: 10.1371/journal.pone.0028691. Epub 2011 Dec 29.
We systematically reviewed observational studies of early mortality post-antiretroviral therapy (ART) initiation in low- and middle-income countries (LMIC) in Asia, Africa, and Central and South America, as defined by the World Bank, to summarize what is known.
Studies published in English between January 1996 and December 2010 were searched in Medline and EMBASE. Three independent reviewers examined studies of mortality within one year post-ART. An article was included if the study was conducted in a LMIC, participants were initiating ART in a non-clinical trial setting and were ≥15 years. Fifty studies were included; 38 (76%) from sub-Saharan Africa (SSA), 5 (10%) from Asia, 2 (4%) from the Americas, and 5 (10%) were multi-regional. Median follow-up time and pre-ART CD4 cell count ranged from 3-55 months and 11-192 cells/mm(3), respectively. Loss-to-follow-up, reported in 40 (80%) studies, ranged from 0.3%-27%. Overall, SSA had the highest pooled 12-month mortality probability of 0.17 (95% CI 0.11-0.24) versus 0.11 (95% CI 0.10-0.13) for Asia, and 0.07 (95% CI 0.007-0.20) for the Americas. Of 14 (28%) studies reporting cause-specific mortality, tuberculosis (TB) (5%-44%), wasting (5%-53%), advanced HIV (20%-37%), and chronic diarrhea (10%-25%) were most common. Independent factors associated with early mortality in 30 (60%) studies included: low baseline CD4 cell count, male sex, advanced World Health Organization clinical stage, low body mass index, anemia, age greater than 40 years, and pre-ART quantitative HIV RNA.
Significant heterogeneity in outcomes and in methods of reporting outcomes exist among published studies evaluating mortality in the first year after ART initiation in LMIC. Early mortality rates are highest in SSA, and opportunistic illnesses such as TB and wasting syndrome are the most common reported causes of death. Strategies addressing modifiable risk factors associated with early death are urgently needed.
我们系统性地回顾了在世界银行定义的亚洲、非洲、中美洲和南美洲的低收入和中等收入国家(LMIC)中,抗逆转录病毒治疗(ART)启动后早期死亡率的观察性研究,以总结目前的认识。
在 Medline 和 EMBASE 中搜索了 1996 年 1 月至 2010 年 12 月间发表的英文研究。如果研究在 LMIC 进行,参与者在非临床试验环境中开始接受 ART,且年龄大于等于 15 岁,则将该研究纳入。共纳入 50 项研究;38 项(76%)来自撒哈拉以南非洲(SSA),5 项(10%)来自亚洲,2 项(4%)来自美洲,5 项(10%)来自多个地区。中位随访时间和 ART 前 CD4 细胞计数分别为 3-55 个月和 11-192 个细胞/mm3。在 40 项(80%)研究中报告了失访情况,范围为 0.3%-27%。总的来说,SSA 的 12 个月死亡率最高,为 0.17(95%CI 0.11-0.24),而亚洲为 0.11(95%CI 0.10-0.13),美洲为 0.07(95%CI 0.007-0.20)。在报告特定原因死亡率的 14 项(28%)研究中,最常见的死因包括结核(TB)(5%-44%)、消瘦(5%-53%)、晚期 HIV(20%-37%)和慢性腹泻(10%-25%)。在 30 项(60%)研究中,与早期死亡率相关的独立因素包括:基线 CD4 细胞计数低、男性、晚期世界卫生组织临床分期、低体重指数、贫血、年龄大于 40 岁和 ART 前定量 HIV RNA。
在评估 LMIC 中 ART 启动后第一年死亡率的已发表研究中,结果存在显著的异质性,且报告结果的方法也存在显著异质性。在 SSA,早期死亡率最高,TB 和消瘦综合征等机会性疾病是最常见的死亡原因。迫切需要制定针对与早期死亡相关的可改变风险因素的策略。