Burke Rachael M, Rickman Hannah M, Singh Vindi, Corbett Elizabeth L, Ayles Helen, Jahn Andreas, Hosseinipour Mina C, Wilkinson Robert J, MacPherson Peter
Malawi-Liverpool-Wellcome Clinical Research Programme, Blantyre, Malawi.
Clinical Research Department, Faculty of Infectious and Tropical Disease, London School of Hygiene and Tropical Medicine, London, UK.
J Int AIDS Soc. 2021 Jul;24(7):e25772. doi: 10.1002/jia2.25772.
HIV and tuberculosis are frequently diagnosed concurrently. In March 2021, World Health Organization recommended that antiretroviral therapy (ART) should be started within two weeks of tuberculosis treatment start, at any CD4 count. We assessed whether earlier ART improved outcomes in people with newly diagnosed HIV and tuberculosis.
We did a systematic review by searching nine databases for trials that compared earlier ART to later ART initiation in people with HIV and tuberculosis. We included studies published from database inception to 12 March 2021. We compared ART within four weeks versus ART more than four weeks after TB treatment, and ART within two weeks versus ART between two and eight weeks, and stratified analysis by CD4 count. The main outcome was death; secondary outcomes included IRIS and AIDS-defining events. We pooled effect estimates using random effects meta-analysis.
We screened 2468 abstracts, and identified nine trials. Among people with all CD4 counts, there was no difference in mortality by earlier ART (≤4 week) versus later ART (>4 week) (risk difference [RD] 0%, 95% confidence interval [CI] -2% to +1%). Among people with CD4 count ≤50 cells/mm , earlier ART (≤4 weeks) reduced risk of death (RD -6%, -10% to -1%). Among people with all CD4 counts earlier ART (≤4 weeks) increased the risk of IRIS (RD +6%, 95% CI +2% to +10%) and reduced the incidence of AIDS-defining events (RD -2%, 95% CI -4% to 0%). Results were similar when trials were restricted to the four trials which permitted comparison of ART within two weeks to ART between two and eight weeks. Trials were conducted between 2004 and 2014, before recommendations to treat HIV at any CD4 count or to rapidly start ART in people without TB. No trials included children or pregnant women. No trials included integrase inhibitors in ART regimens.
Earlier ART did not alter risk of death overall among people living with HIV who had TB disease. For logistical and patient preference reasons, earlier ART initiation for everyone with TB and HIV may be preferred to later ART.
HIV和结核病常同时被诊断出来。2021年3月,世界卫生组织建议,无论CD4细胞计数多少,抗逆转录病毒疗法(ART)应在开始治疗结核病的两周内启动。我们评估了早期ART是否能改善新诊断出的HIV和结核病患者的治疗效果。
我们通过检索九个数据库进行系统评价,以寻找比较HIV和结核病患者早期ART与晚期ART启动的试验。我们纳入了从数据库建立到2021年3月12日发表的研究。我们比较了结核病治疗后四周内的ART与四周后的ART,以及两周内的ART与两周至八周之间的ART,并按CD4细胞计数进行分层分析。主要结局是死亡;次要结局包括免疫重建炎症综合征(IRIS)和艾滋病界定事件。我们使用随机效应荟萃分析汇总效应估计值。
我们筛选了2468篇摘要,确定了9项试验。在所有CD4细胞计数的患者中,早期ART(≤4周)与晚期ART(>4周)相比,死亡率没有差异(风险差[RD] 0%,95%置信区间[CI] -2%至+1%)。在CD4细胞计数≤50个/mm³的患者中,早期ART(≤4周)降低了死亡风险(RD -6%,-10%至-1%)。在所有CD4细胞计数的患者中,早期ART(≤4周)增加了IRIS的风险(RD +6%,95% CI +2%至+10%),并降低了艾滋病界定事件的发生率(RD -2%,95% CI -4%至0%)。当试验仅限于四项允许比较两周内的ART与两周至八周之间的ART的试验时,结果相似。试验在2004年至2014年期间进行,当时还没有在任何CD4细胞计数时治疗HIV或在无结核病患者中迅速启动ART的建议。没有试验纳入儿童或孕妇。没有试验在ART方案中纳入整合酶抑制剂。
早期ART并没有改变患有结核病的HIV感染者的总体死亡风险。出于后勤和患者偏好的原因,对于所有结核病合并HIV患者,早期启动ART可能比晚期ART更可取。