MMWR Recomm Rep. 1998 Jan 30;47(RR-2):1-30.
These recommendations update the 1994 guidelines developed by the Public Health Service for the use of zidovudine (ZDV) to reduce the risk for perinatal human immunodeficiency virus type 1 (HIV-1) transmission. This report provides health-care providers with information for discussion with HIV-1-infected pregnant women to enable such women to make an informed decision regarding the use of antiretroviral drugs during pregnancy. Various circumstances that commonly occur in clinical practice are presented as scenarios and the factors influencing treatment considerations are highlighted in this report. In February 1994, the results of Pediatric AIDS Clinical Trials Group (PACTG) Protocol 076 documented that ZDV chemoprophylaxis could reduce perinatal HIV-1 transmission by nearly 70%. Epidemiologic data have since confirmed the efficacy of ZDV for reduction of perinatal transmission and have extended this efficacy to children of women with advanced disease, low CD4+ T-lymphocyte counts, and prior ZDV therapy. Additionally, substantial advances have been made in the understanding of the pathogenesis of HIV-1 infection and in the treatment and monitoring of HIV-1 disease. These advances have resulted in changes in standard antiretroviral therapy for HIV-1-infected adults. More aggressive combination drug regimens that maximally suppress viral replication are now recommended. Although considerations associated with pregnancy may affect decisions regarding timing and choice of therapy, pregnancy is not a reason to defer standard therapy. The use of antiretroviral drugs in pregnancy requires unique considerations, including the potential need to alter dosing as a result of physiologic changes associated with pregnancy, the potential for adverse short- or long-term effects on the fetus and newborn, and the effectiveness for reducing the risk for perinatal transmission. Data to address many of these considerations are not yet available. Therefore, offering antiretroviral therapy to HIV-1-infected women during pregnancy, whether primarily to treat HIV-1 infection, to reduce perinatal transmission, or for both purposes, should be accompanied by a discussion of the known and unknown short- and long-term benefits and risks of such therapy for infected women and their infants. Standard antiretroviral therapy should be discussed with and offered to HIV-1-infected pregnant women. Additionally, to prevent perinatal transmission, ZDV chemoprophylaxis should be incorporated into the antiretroviral regimen.
这些建议更新了1994年公共卫生服务部制定的关于使用齐多夫定(ZDV)降低围产期1型人类免疫缺陷病毒(HIV-1)传播风险的指南。本报告为医疗保健提供者提供信息,以便与感染HIV-1的孕妇进行讨论,使这些妇女能够就是否在孕期使用抗逆转录病毒药物做出明智的决定。本报告以临床场景的形式呈现了临床实践中常见的各种情况,并突出了影响治疗决策的因素。1994年2月,儿童艾滋病临床试验组(PACTG)076号方案的结果表明,ZDV化学预防可使围产期HIV-1传播减少近70%。此后的流行病学数据证实了ZDV在降低围产期传播方面的疗效,并将这种疗效扩展到患有晚期疾病、CD4+T淋巴细胞计数低以及曾接受ZDV治疗的妇女所生的儿童。此外,在对HIV-1感染发病机制的理解以及HIV-1疾病的治疗和监测方面取得了重大进展。这些进展导致了针对感染HIV-1的成年人的标准抗逆转录病毒疗法的改变。现在推荐采用更积极的联合药物方案,以最大限度地抑制病毒复制。虽然与怀孕相关的因素可能会影响治疗时机和治疗选择的决定,但怀孕并不是推迟标准治疗的理由。在孕期使用抗逆转录病毒药物需要特别考虑,包括由于与怀孕相关的生理变化可能需要调整剂量、对胎儿和新生儿可能产生的短期或长期不良影响,以及降低围产期传播风险的有效性。解决其中许多问题的数据尚未获得。因此,在孕期为感染HIV-1的妇女提供抗逆转录病毒治疗时,无论主要目的是治疗HIV-1感染、降低围产期传播风险还是两者兼顾,都应与她们讨论这种治疗对感染妇女及其婴儿已知和未知的短期和长期益处及风险。应与感染HIV-1的孕妇讨论并提供标准抗逆转录病毒治疗。此外,为预防围产期传播,应将ZDV化学预防纳入抗逆转录病毒治疗方案。