International Center for AIDS Care and Treatment Programs, Mailman School of Public Health, Columbia University, New York, NY 10032, USA.
J Acquir Immune Defic Syndr. 2010 Nov;55(3):404-10. doi: 10.1097/QAI.0b013e3181e73f4b.
Identifying antiretroviral therapy (ART) eligible HIV-infected (HIV+) pregnant women and rapidly initiating treatment preserves maternal health and prevents mother-to-child transmission. However, there have been few investigations of the performance of ART eligibility criteria in pregnant and postpartum women in resource-limited settings.
Pregnant and recently postpartum HIV+ women received CD4+ cell count and World Health Organization (WHO) clinical staging at enrollment into the mother-to-child transmission Plus Initiative. We compared immunologic and clinical criteria based on 2009 WHO ART treatment guidelines (WHO stage 3/4 or CD4+ cell count ≤350 cells/mm³) in identifying ART eligible women.
Among 6036 women (62% antepartum, 38% postpartum), 2915 (48%) were ART eligible. Only 23% had WHO stage 3 or 4 disease, whereas 94% met CD4+ cell count criterion. Among 5356 women with WHO stage 1 or 2 disease, 2235 (42%) had CD4+ ≤350 cells per cubic millimeter. Change of CD4+ cell count ART eligibility threshold from ≤200 to ≤350 cells per cubic millimeter increased the proportion of ART eligible women from 21% to 45%.
Use of CD4+ cell count criterion is superior to clinical staging in identifying pregnant and postpartum HIV+ women eligible for ART. Improving access to CD4+ testing is essential to identify and treat eligible women, optimizing maternal and child health outcomes.
识别适合接受抗逆转录病毒疗法(ART)的 HIV 感染(HIV +)孕妇,并迅速启动治疗,可维护母婴健康并预防母婴传播。然而,在资源有限的环境中,针对适合接受 ART 的孕妇和产后妇女的 ART 资格标准的表现,仅有少量研究进行了调查。
母婴传播 Plus 倡议在招募 HIV +孕妇和产后不久的妇女时,为她们提供 CD4+细胞计数和世界卫生组织(WHO)临床分期。我们比较了基于 2009 年 WHO ART 治疗指南(WHO 分期 3/4 或 CD4+细胞计数≤350 个细胞/立方毫米)的免疫和临床标准,以确定适合接受 ART 的妇女。
在 6036 名妇女(62%为产前,38%为产后)中,有 2915 名(48%)符合 ART 资格。仅有 23%患有 WHO 分期 3 或 4 期疾病,而 94%符合 CD4+细胞计数标准。在 5356 名患有 WHO 分期 1 或 2 期疾病的妇女中,有 2235 名(42%)的 CD4+细胞计数≤350 个细胞/立方毫米。将 CD4+细胞计数 ART 资格标准的阈值从≤200 个细胞/立方毫米更改为≤350 个细胞/立方毫米,使符合 ART 资格的妇女比例从 21%增加到 45%。
使用 CD4+细胞计数标准比临床分期更能识别适合接受 ART 的孕妇和产后 HIV +妇女。改善 CD4+检测的获取对于识别和治疗符合条件的妇女至关重要,这有助于优化母婴健康结局。