Maternal anaemia and duration of zidovudine in antiretroviral regimens for preventing mother-to-child transmission: a randomized trial in three African countries

被引:13
作者
Sartorius, Benn K. D. [1 ,2 ]
Chersich, Matthew F. [1 ,3 ]
Mwaura, Mary [4 ]
Meda, Nicolas [5 ]
Temmerman, Marleen [3 ]
Newell, Marie Louise [6 ]
Farley, Timothy M. M. [7 ]
Luchters, Stanley [1 ,3 ,8 ]
机构
[1] Univ Witwatersrand, Fac Hlth Sci, Sch Publ Hlth, Johannesburg, South Africa
[2] Univ KwaZulu Natal, Sch Nursing & Publ Hlth, Discipline Publ Hlth Med, Mtubatuba, South Africa
[3] Univ Ghent, Dept Obstet & Gynaecol, Int Ctr Reprod Hlth, B-9000 Ghent, Belgium
[4] Int Ctr Reprod Hlth, Mombasa, Kenya
[5] Ctr Muraz, Bobo Dioulasso, Burkina Faso
[6] Univ KwaZulu Natal, Africa Ctr Hlth & Populat Studies, Mtubatuba, Kwazulu Natal, South Africa
[7] Sigma3 Serv SARL, Nyon, Switzerland
[8] Burnet Inst, Ctr Int Hlth, Melbourne, Vic 3004, Australia
关键词
Zidovudine; Pregnancy; HIV; Sub-Saharan Africa; Anaemia; Drug toxicity; HUMAN-IMMUNODEFICIENCY-VIRUS; HIV-INFECTED WOMEN; ORAL ZIDOVUDINE; PREGNANT-WOMEN; BURKINA-FASO; COTE-DIVOIRE; DOUBLE-BLIND; LARGE COHORT; 1ST YEAR; PREVALENCE;
D O I
10.1186/1471-2334-13-522
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Although substantiated by little evidence, concerns about zidovudine-related anaemia in pregnancy have influenced antiretroviral (ARV) regimen choice for preventing mother-to-child transmission of HIV-1, especially in settings where anaemia is common. Methods: Eligible HIV-infected pregnant women in Burkina Faso, Kenya and South Africa were followed from 28 weeks of pregnancy until 12-24 months after delivery (n = 1070). Women with a CD4 count of 200 500cells/mm(3) and gestational age 28-36 weeks were randomly assigned to zidovudine-containing triple-ARV prophylaxis continued during breastfeeding up to 6-months, or to zidovudine during pregnancy plus single-dose nevirapine (sd-NVP) at labour. Additionally, two cohorts were established, women with CD4 counts: <200 cells/mm(3) initiated antiretroviral therapy, and >500 cells/mm(3) received zidovudine during pregnancy plus sd-NVP at labour. Mild (haemoglobin 8.0-10.9 g/dl) and severe anaemia (haemoglobin < 8.0 g/dl) occurrence were assessed across study arms, using Kaplan-Meier and multivariable Cox proportional hazards models. Results: At enrolment (corresponded to amedian 32 weeks gestation), median haemoglobin was 10.3 g/dl (IQR = 9.2-11.1). Severe anaemia occurred subsequently in 194 (18.1%) women, mostly in those with low baseline haemoglobin, lowest socio-economic category, advanced HIV disease, prolonged breastfeeding (>= 6 months) and shorter ARV exposure. Severe anaemia incidence was similar in the randomized arms (equivalence P-value = 0.32). After 1-2months of ARV's, severe anaemia was significantly reduced in all groups, though remained highest in the low CD4 cohort. Conclusions: Severe anaemia occurs at a similar rate in women receiving longer triple zidovudine-containing regimens or shorter prophylaxis. Pregnant women with pre-existing anaemia and advanced HIV disease require close monitoring.
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页数:14
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