Zadrozny Sabrina, Westreich Daniel, Hudgens Michael G, Chasela Charles, Jamieson Denise J, Martinson Francis, Zimba Chifundo, Tegha Gerald, Hoffman Irving, Miller William C, Pence Brian W, King Caroline C, Kourtis Athena P, Msungama Wezi, van der Horst Charles
Carolina Population Center, Universitiy of North Carolina, Chapel Hill.
Department of Epidemiology, University of North Carolina, Chapel Hill.
Paediatr Perinat Epidemiol. 2017 Mar;31(2):134-143. doi: 10.1111/ppe.12337. Epub 2017 Feb 16.
The relationship between mastitis and antiretroviral therapy among HIV-positive, breast-feeding women is unclear.
In the Breastfeeding, Antiretrovirals, and Nutrition (BAN) study, conducted in Lilongwe, Malawi, 2369 mother-infant pairs were randomized to a nutritional supplement group and to one of three treatment groups: maternal antiretroviral therapy (ART), infant nevirapine (NVP) or standard of care for 24 weeks of exclusive breast-feeding and 4 weeks of weaning. Among 1472 HIV-infected women who delivered live infants between 2004 and 2007, we estimated cumulative incidence functions and sub-distribution hazard ratios (HR) of mastitis or breast inflammation comparing women in maternal ART (n = 487) or infant nevirapine (n = 492) groups to the standard of care (n = 493). Nutritional supplement groups (743 took, 729 did not) were also compared.
Through 28-weeks post-partum, 102 of 1472 women experienced at least one occurrence of mastitis or breast inflammation. The 28-week risk was higher for maternal ART (risk difference (RD) 4.5, 95% confidence interval (CI) 0.9, 8.1) and infant NVP (RD 3.6, 95% CI 0.3, 6.9) compared to standard of care. The hazard of late-appearing mastitis or breast inflammation (from week 5-28) was also higher for maternal ART (HR 6.7, 95% CI 2.0, 22.6) and infant NVP (HR 5.1, 95% CI 1.5, 17. 5) compared to the standard of care.
Mastitis or breast inflammation while breast-feeding is a possible side effect for women taking prophylactic ART and women whose infants take NVP, warranting additional research in the context of postnatal HIV transmission.
在感染艾滋病毒且正在进行母乳喂养的女性中,乳腺炎与抗逆转录病毒疗法之间的关系尚不清楚。
在马拉维利隆圭开展的母乳喂养、抗逆转录病毒药物与营养(BAN)研究中,2369对母婴被随机分为营养补充剂组和三个治疗组之一:母亲抗逆转录病毒疗法(ART)组、婴儿奈韦拉平(NVP)组或纯母乳喂养24周及断奶4周的标准治疗组。在2004年至2007年间分娩活婴的1472名感染艾滋病毒的女性中,我们比较了母亲接受抗逆转录病毒疗法(n = 487)或婴儿接受奈韦拉平(n = 492)组与标准治疗组(n = 493)的女性,估计了乳腺炎或乳腺炎症的累积发病率函数和亚分布风险比(HR)。还比较了营养补充剂组(743人服用,729人未服用)。
至产后28周,1472名女性中有102人至少发生过一次乳腺炎或乳腺炎症。与标准治疗相比,母亲接受抗逆转录病毒疗法组(风险差(RD)4.5,95%置信区间(CI)0.9,8.1)和婴儿接受奈韦拉平组(RD 3.6,95%CI 0.3,6.9)的28周风险更高。与标准治疗相比,母亲接受抗逆转录病毒疗法组(HR 6.7,95%CI 2.0,22.6)和婴儿接受奈韦拉平组(HR 5.1,95%CI 1.5,17.5)出现晚期乳腺炎或乳腺炎症(第5至28周)的风险也更高。
母乳喂养期间的乳腺炎或乳腺炎症可能是接受预防性抗逆转录病毒疗法的女性以及婴儿接受奈韦拉平的女性的一种副作用,这需要在产后艾滋病毒传播背景下进行更多研究。