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在埃塞俄比亚、印度和乌干达,对婴儿延长奈韦拉平用药至6周龄以预防通过母乳喂养传播艾滋病毒:三项随机对照试验的分析

Extended-dose nevirapine to 6 weeks of age for infants to prevent HIV transmission via breastfeeding in Ethiopia, India, and Uganda: an analysis of three randomised controlled trials.

作者信息

Bedri Abubaker, Gudetta Berhanu, Isehak Abdulhamid, Kumbi Solomon, Lulseged Sileshi, Mengistu Yohannes, Bhore Arvind V, Bhosale Ramesh, Varadhrajan Venkat, Gupte Nikhil, Sastry Jayagowri, Suryavanshi Nishi, Tripathy Srikanth, Mmiro Francis, Mubiru Michael, Onyango Carolyne, Taylor Adrian, Musoke Philippa, Nakabiito Clemensia, Abashawl Aida, Adamu Rahel, Antelman Gretchen, Bollinger Robert C, Bright Patricia, Chaudhary Mohammad A, Coberly Jacqueline, Guay Laura, Fowler Mary Glenn, Gupta Amita, Hassen Elham, Jackson J Brooks, Moulton Lawrence H, Nayak Uma, Omer Saad B, Propper Lidia, Ram Malathi, Rexroad Vivian, Ruff Andrea J, Shankar Anita, Zwerski Sheryl

出版信息

Lancet. 2008 Jul 26;372(9635):300-13. doi: 10.1016/S0140-6736(08)61114-9.

Abstract

BACKGROUND

UNICEF/WHO recommends that infants born to HIV-infected mothers who do not have access to acceptable, feasible, affordable, sustainable, and safe replacement feeding should be exclusively breastfed for at least 6 months. The aim of three trials in Ethiopia, India, and Uganda was to assess whether daily nevirapine given to breastfed infants through 6 weeks of age can decrease HIV transmission via breastfeeding.

METHODS

HIV-infected women breastfeeding their infants were eligible for participation. Participants were randomly assigned to receive either single-dose nevirapine (nevirapine 200 mg to women in labour and nevirapine 2 mg/kg to newborns after birth) or 6 week extended-dose nevirapine (nevirapine 200 mg to women in labour and nevirapine 2 mg/kg to newborn babies after birth plus nevirapine 5 mg daily from days 8-42 for the infant). The randomisation sequences were generated by computer at a central data coordinating centre. The primary endpoint was HIV infection at 6 months of age in infants who were HIV PCR negative at birth. Analyses were by modified intention to treat, excluding infants with missing specimens and those with indeterminate or confirmed HIV infection at birth. These studies are registered with ClinicalTrials.gov, numbers NCT00074399, NCT00061321, and NCT00639938.

FINDINGS

2024 liveborn infants randomised in the study had at least one specimen tested before 6 months of age (1047 infants in the single-dose group and 977 infants in the extended-dose group). The modified intention-to-treat population included 986 infants in the single-dose group and 901 in the extended-dose group. At 6 months, 87 children in the single-dose group and 62 in the extended-dose group were infected with HIV (relative risk 0.80, 95% CI 0.58-1.10; p=0.16). At 6 weeks of age, 54 children in the single-dose group and 25 in the extended-dose group were HIV positive (0.54, 0.34-0.85; p=0.009). 393 infants in the single-dose group and 346 in the extended-dose group experienced grade 3 or 4 serious adverse events during the study (p=0.54).

INTERPRETATION

Although a 6-week regimen of daily nevirapine might be associated with a reduction in the risk of HIV transmission at 6 weeks of age, the lack of a significant reduction in the primary endpoint-risk of HIV transmission at 6 months-suggests that a longer course of daily infant nevirapine to prevent HIV transmission via breast milk might be more effective where access to affordable and safe replacement feeding is not yet available and where the risks of replacement feeding are high.

FUNDING

US National Institutes of Health; US National Institute of Allergy and Infectious Diseases; Fogarty International Center.

摘要

背景

联合国儿童基金会/世界卫生组织建议,对于无法获得可接受、可行、可负担、可持续且安全的替代喂养方式的感染艾滋病毒母亲所生婴儿,应进行纯母乳喂养至少6个月。在埃塞俄比亚、印度和乌干达进行的三项试验旨在评估,给6周龄以内的母乳喂养婴儿每日服用奈韦拉平是否能降低通过母乳喂养传播艾滋病毒的风险。

方法

感染艾滋病毒且正在母乳喂养婴儿的妇女有资格参与。参与者被随机分配接受单剂量奈韦拉平(临分娩时给母亲服用200毫克奈韦拉平,出生后给新生儿服用2毫克/千克奈韦拉平)或6周延长剂量奈韦拉平(临分娩时给母亲服用200毫克奈韦拉平,出生后给新生儿服用2毫克/千克奈韦拉平,外加婴儿从第8天至42天每天服用5毫克奈韦拉平)。随机分组序列由中央数据协调中心通过计算机生成。主要终点是出生时艾滋病毒聚合酶链反应检测呈阴性的婴儿在6个月龄时的艾滋病毒感染情况。分析采用改良意向性分析,排除标本缺失的婴儿以及出生时艾滋病毒感染情况不确定或已确诊的婴儿。这些研究已在ClinicalTrials.gov注册,编号分别为NCT00074399、NCT00061321和NCT00639938。

结果

该研究中随机分组的2024名活产婴儿在6个月龄前至少有一份标本接受检测(单剂量组1047名婴儿,延长剂量组977名婴儿)。改良意向性分析人群包括单剂量组986名婴儿和延长剂量组901名婴儿。6个月时,单剂量组87名儿童和延长剂量组62名儿童感染艾滋病毒(相对风险0.80,95%置信区间0.58 - 1.10;p = 0.16)。6周龄时,单剂量组54名儿童和延长剂量组25名儿童艾滋病毒呈阳性(0.54,0.34 - 0.85;p = 0.009)。单剂量组393名婴儿和延长剂量组346名婴儿在研究期间发生3级或4级严重不良事件(p = 0.54)。

解读

尽管每日服用奈韦拉平6周的方案可能与6周龄时艾滋病毒传播风险降低有关,但在6个月这一主要终点——艾滋病毒传播风险未显著降低,这表明在无法获得可负担且安全的替代喂养方式以及替代喂养风险较高的情况下,给婴儿每日服用更长疗程的奈韦拉平以预防通过母乳传播艾滋病毒可能更有效。

资助

美国国立卫生研究院;美国国立过敏与传染病研究所;福格蒂国际中心。

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