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CD4+ 细胞计数检测比 HIV 疾病临床分期更能有效识别资源有限环境下适合接受抗逆转录病毒治疗的孕妇和产后妇女。

CD4+ cell count testing more effective than HIV disease clinical staging in identifying pregnant and postpartum women eligible for antiretroviral therapy in resource-limited settings.

机构信息

International Center for AIDS Care and Treatment Programs, Mailman School of Public Health, Columbia University, New York, NY 10032, USA.

出版信息

J Acquir Immune Defic Syndr. 2010 Nov;55(3):404-10. doi: 10.1097/QAI.0b013e3181e73f4b.

Abstract

OBJECTIVE

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.

METHODS

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.

RESULTS

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%.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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%。

结论

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。

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