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AIDS. 2013 Nov 13;27(17):2809-15. doi: 10.1097/01.aids.0000432540.59786.6d.
2
Relationship between mortality and feeding modality among children born to HIV-infected mothers in a research setting: the Kesho Bora study.研究环境中 HIV 感染母亲所生儿童的死亡率与喂养方式之间的关系:Kesho Bora 研究。
AIDS. 2013 Jun 19;27(10):1621-30. doi: 10.1097/QAD.0b013e32835d5226.
3
Infant feeding modes and determinants among HIV-1-infected African Women in the Kesho Bora Study.凯索博拉研究中感染 HIV-1 的非洲妇女的婴儿喂养模式和决定因素。
J Acquir Immune Defic Syndr. 2013 Jan 1;62(1):109-18. doi: 10.1097/QAI.0b013e318277005e.
4
Effects of cessation of breastfeeding in HIV-1-exposed, uninfected children in Malawi.马拉维艾滋病毒 1 型暴露但未感染儿童停止母乳喂养的效果。
Clin Infect Dis. 2011 Aug;53(4):388-95. doi: 10.1093/cid/cir413.
5
High rates of all-cause and gastroenteritis-related hospitalization morbidity and mortality among HIV-exposed Indian infants.在印度,HIV 暴露婴儿的全因和与胃肠炎相关的住院发病率和死亡率都很高。
BMC Infect Dis. 2011 Jul 15;11:193. doi: 10.1186/1471-2334-11-193.
6
Breastfeeding in HIV exposed infants significantly improves child health: a prospective study.HIV 暴露婴儿母乳喂养显著改善儿童健康:一项前瞻性研究。
Matern Child Health J. 2012 Apr;16(3):632-40. doi: 10.1007/s10995-011-0795-8.
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Relationship of exclusive breast-feeding to infections and growth of Tanzanian children born to HIV-infected women.坦桑尼亚感染 HIV 妇女所生儿童纯母乳喂养与感染和生长的关系。
Public Health Nutr. 2011 Jul;14(7):1251-8. doi: 10.1017/S136898001000306X. Epub 2011 Feb 16.
8
Triple antiretroviral compared with zidovudine and single-dose nevirapine prophylaxis during pregnancy and breastfeeding for prevention of mother-to-child transmission of HIV-1 (Kesho Bora study): a randomised controlled trial.三重抗逆转录病毒治疗与齐多夫定和单剂量奈韦拉平预防方案在妊娠期和哺乳期用于预防 HIV-1 母婴传播的比较(肯尼亚母婴传播预防研究):一项随机对照试验。
Lancet Infect Dis. 2011 Mar;11(3):171-80. doi: 10.1016/S1473-3099(10)70288-7. Epub 2011 Jan 13.
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Morbidity among human immunodeficiency virus-exposed but uninfected, human immunodeficiency virus-infected, and human immunodeficiency virus-unexposed infants in Zimbabwe before availability of highly active antiretroviral therapy.在高效抗逆转录病毒疗法问世之前,津巴布韦的人类免疫缺陷病毒暴露但未感染、人类免疫缺陷病毒感染和未暴露于人类免疫缺陷病毒的婴儿的发病率。
Pediatr Infect Dis J. 2011 Jan;30(1):45-51. doi: 10.1097/INF.0b013e3181ecbf7e.
10
Safety and effectiveness of antiretroviral drugs during pregnancy, delivery and breastfeeding for prevention of mother-to-child transmission of HIV-1: the Kesho Bora Multicentre Collaborative Study rationale, design, and implementation challenges.抗逆转录病毒药物在妊娠、分娩和哺乳期用于预防 HIV-1 母婴传播的安全性和有效性:肯尼亚 Kesho Bora 多中心合作研究的原理、设计和实施挑战。
Contemp Clin Trials. 2011 Jan;32(1):74-85. doi: 10.1016/j.cct.2010.09.008. Epub 2010 Sep 17.

非洲暴露于艾滋病病毒但未感染的婴儿出生后前6个月喂养方式与发病率的关系:科肖博拉研究

Morbidity in relation to feeding mode in African HIV-exposed, uninfected infants during the first 6 mo of life: the Kesho Bora study.

作者信息

Bork Kirsten A, Cournil Amandine, Read Jennifer S, Newell Marie-Louise, Cames Cécile, Meda Nicolas, Luchters Stanley, Mbatia Grace, Naidu Kevindra, Gaillard Philippe, de Vincenzi Isabelle

机构信息

From the Institut de Recherche pour le Développement (IRD), UMI233 IRD/Université de Montpellier 1, Montpellier, France (KAB, AC, and CC); the Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD (JSR); the Africa Centre for Health and Population Studies, University of KwaZulu-Natal, Somkhele, South Africa (M-LN); the Centre Muraz, Bobo-Dioulasso, Burkina Faso (NM); the International Centre for Reproductive Health, Mombasa, Kenya (SL); the Kenyatta National Hospital and University of Nairobi, Nairobi, Kenya (GM); the University of KwaZulu-Natal, Durban, South African Republic (KN); and the WHO, Reproductive Health and Research, Geneva, Switzerland (PG and IdV).

出版信息

Am J Clin Nutr. 2014 Dec;100(6):1559-68. doi: 10.3945/ajcn.113.082149. Epub 2014 Oct 22.

DOI:10.3945/ajcn.113.082149
PMID:25411291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4232020/
Abstract

BACKGROUND

Refraining from breastfeeding to prevent HIV transmission has been associated with increased morbidity and mortality in HIV-exposed African infants.

OBJECTIVE

The objective was to assess risks of common and serious infectious morbidity by feeding mode in HIV-exposed, uninfected infants ≤6 mo of age with special attention to the issue of reverse causality.

DESIGN

HIV-infected pregnant women from 5 sites in Burkina Faso, Kenya, and South Africa were enrolled in the prevention of mother-to-child transmission Kesho Bora trial and counseled to either breastfeed exclusively and cease by 6 mo postpartum or formula feed exclusively. Maternal-reported morbidity (fever, diarrhea, and vomiting) and serious infectious events (SIEs) (gastroenteritis and lower respiratory tract infections) were investigated for 751 infants for 2 age periods (0-2.9 and 3-6 mo) by using generalized linear mixed models with breastfeeding as a time-dependent variable and adjustment for study site, maternal education, economic level, and cotrimoxazole prophylaxis.

RESULTS

Reported morbidity was not significantly higher in nonbreastfed compared with breastfed infants [OR: 1.31 (95% CI: 0.97, 1.75) and 1.21 (0.90, 1.62) at 0-2.9 and 3-6 mo of age, respectively]. Between 0 and 2.9 mo of age, never-breastfed infants had increased risks of morbidity compared with those of infants who were exclusively breastfed (OR: 1.49; 95% CI: 1.01, 2.2; P = 0.042). The adjusted excess risk of SIEs in nonbreastfed infants was large between 0 and 2.9 mo (OR: 6.0; 95% CI: 2.2, 16.4; P = 0.001). Between 3 and 6 mo, the OR for SIEs was sensitive to the timing of breastfeeding status, i.e., 4.3 (95% CI: 1.2, 15.3; P = 0.02) when defined at end of monthly intervals and 2.0 (95% CI: 0.8, 5.0; P = 0.13) when defined at the beginning of intervals. Of 52 SIEs, 3 mothers reported changes in feeding mode during the SIE although none of the mothers ceased breastfeeding completely.

CONCLUSIONS

Not breastfeeding was associated with increased risk of serious infections especially between 0 and 2.9 mo of age. The randomized controlled trial component of the Kesho Bora study was registered at Current Controlled Trials (www.controlled-trials.com) as ISRCTN71468401.

摘要

背景

为预防艾滋病毒传播而避免母乳喂养与非洲艾滋病毒暴露婴儿的发病率和死亡率上升有关。

目的

评估6个月及以下艾滋病毒暴露且未感染婴儿因喂养方式导致的常见和严重感染性疾病发病风险,特别关注反向因果关系问题。

设计

来自布基纳法索、肯尼亚和南非5个地点的感染艾滋病毒的孕妇参加了预防母婴传播的“凯索博拉”试验,并接受咨询,建议她们要么纯母乳喂养并在产后6个月停止,要么完全用配方奶喂养。通过使用广义线性混合模型,将母乳喂养作为时间依赖变量,并对研究地点、母亲教育程度、经济水平和复方新诺明预防措施进行调整,对751名婴儿在2个年龄阶段(0 - 2.9个月和3 - 6个月)的母亲报告的发病率(发热、腹泻和呕吐)和严重感染事件(SIEs,即胃肠炎和下呼吸道感染)进行了调查。

结果

与母乳喂养的婴儿相比,非母乳喂养婴儿报告的发病率没有显著更高[分别在0 - 2.9个月和3 - 6个月龄时,比值比(OR):1.31(95%置信区间:0.97,1.75)和1.21(0.90,1.62)]。在0至2.9个月龄之间,从未母乳喂养的婴儿与纯母乳喂养的婴儿相比,发病风险增加(OR:1.49;95%置信区间:1.01,2.2;P = 0.042)。在0至2.9个月之间,非母乳喂养婴儿SIEs的调整后超额风险很大(OR:6.0;95%置信区间:2.2,16.4;P = 0.001)。在3至6个月之间,SIEs的OR对母乳喂养状态的定义时间敏感,即在每月间隔结束时定义为4.3(95%置信区间:1.2,15.3;P = 0.02),在间隔开始时定义为2.0(95%置信区间:0.8,5.0;P = 0.13)。在52例SIEs中,3名母亲报告在SIE期间喂养方式有变化,尽管没有母亲完全停止母乳喂养。

结论

不进行母乳喂养与严重感染风险增加有关,尤其是在0至2.9个月龄之间。凯索博拉研究的随机对照试验部分已在“当前对照试验”(www.controlled-trials.com)注册,注册号为ISRCTN71468401。