Risk of Adverse Birth Outcomes in Two Cohorts of Pregnant Women With HIV in Zambia. Issue 3 (21st January 2022)

• Record Type: Journal Article
• Authors: Price, Joan T.; Sebastião, Yuri V.; Vwalika, Bellington; Cole, Stephen R.; Mbewe, Felistas M.; Phiri, Winifreda M.; Freeman, Bethany L.; Kasaro, Margaret P.; Peterson, Marc; Rouse, Dwight J.; Stringer, Elizabeth M.; Stringer, Jeffrey S. A.
• Is Part Of: Epidemiology. Volume 33:Issue 3(2022)
• Page Start: 422
• Page End: 430
• Publication Date: 2022-01-21
• Subjects: HIV -- Preterm birth -- Stillbirth -- Pregnancy -- Zambia -- Marginal structural models -- Inverse probability weighting; Epidemiology -- Periodicals; Epidemiology -- Environmental aspects -- Periodicals; Epidemiology -- Periodicals; 614.405
• DOI: 10.1097/EDE.0000000000001465
• Languages: English
• ISSNs: 1044-3983

Abstract

Abstract : Background: A trial of progesterone to prevent preterm birth among HIV-infected Zambian women [Improving Pregnancy Outcomes with Progesterone (IPOP)] found no treatment effect, but the risk of the primary outcome was among the lowest ever documented in women with HIV. In this secondary analysis, we compare the risks of preterm birth (<37 weeks), stillbirth, and a composite primary outcome comprising the two in IPOP versus an observational pregnancy cohort [Zambian Preterm Birth Prevention Study (ZAPPS)] in Zambia, to evaluate reasons for the low risk in IPOP. Methods: Both studies enrolled women before 24 gestational weeks, during August 2015–September 2017 (ZAPPS) and February 2018–January 2020 (IPOP). We used linear probability and log-binomial regression to estimate risk differences and risk ratios (RR), before and after restriction and standardization with inverse probability weights. Results: The unadjusted risk of composite outcome was 18% in ZAPPS (N = 1450) and 9% in IPOP (N = 791) (RR = 2.0; 95% CI = 1.6, 2.6). After restricting and standardizing the ZAPPS cohort to the distribution of IPOP baseline characteristics, the risk remained higher in ZAPPS (RR = 1.6; 95% CI = 1.0, 2.4). The lower risk of preterm/stillbirth in IPOP was only partially explained by measured risk factors. Conclusions: Possible benefits in IPOP of additional monetary reimbursement, more frequent visits, and group-based care warrant further investigation.