Impact of Intermittent Presumptive Treatment for Malaria in Pregnancy on Hospital Birth Outcomes on the Kenyan Coast

Author:

Kamau Alice1ORCID,Musau Moses1,Mwakio Stella2,Amadi David2,Nyaguara Amek2,Bejon Philip23,Seale Anna C2456,Berkley James A17,Snow Robert W13

Affiliation:

1. Public Health Research, Kenya Medical Research Institute–Wellcome Trust Research Programme , Nairobi , Kenya

2. Epidemiology and Demography, Kenya Medical Research Institute–Wellcome Trust Research Programme , Kilifi , Kenya

3. Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford , Oxford , United Kingdom

4. Epidemiology and Population Health, London School of Hygiene & Tropical Medicine , London , United Kingdom

5. College of Health and Medical Sciences, Haramaya University , Harar , Ethiopia

6. Warwick Medical School, University of Warwick , Coventry , United Kingdom

7. Centre for Clinical Vaccinology and Tropical Medicine, Churchill Hospital, University of Oxford , Oxford , United Kingdom

Abstract

Abstract Background Intermittent preventive treatment (IPTp) for pregnant women with sulfadoxine–pyrimethamine (SP) is widely implemented for the prevention of malaria in pregnancy and adverse birth outcomes. The efficacy of SP is declining, and there are concerns that IPTp may have reduced impact in areas of high resistance. We sought to determine the protection afforded by SP as part of IPTp against adverse birth outcomes in an area with high levels of SP resistance on the Kenyan coast. Methods A secondary analysis of surveillance data on deliveries at the Kilifi County Hospital between 2015 and 2021 was undertaken in an area of low malaria transmission and high parasite mutations associated with SP resistance. A multivariable logistic regression model was developed to estimate the effect of SP doses on the risk of low birthweight (LBW) deliveries and stillbirths. Results Among 27 786 deliveries, 3 or more doses of IPTp-SP were associated with a 27% reduction in the risk of LBW (adjusted odds ratio [aOR], 0.73; 95% confidence interval [CI], .64–.83; P < .001) compared with no dose. A dose-response association was observed with increasing doses of SP from the second trimester linked to increasing protection against LBW deliveries. Three or more doses of IPTp-SP were also associated with a 21% reduction in stillbirth deliveries (aOR, 0.79; 95% CI, .65–.97; P = .044) compared with women who did not take any dose of IPTp-SP. Conclusions The continued significant association of SP on LBW deliveries suggests that the intervention may have a non-malaria impact on pregnancy outcomes.

Funder

Wellcome Trust

DFID

Global Health

Bill and Melinda Gates Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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