Evidence map›Paper›PMID 41657027›Full record

Trial reportInternational journal of epidemiology2026

Impact of intermittent preventive treatment of malaria in pregnancy with sulfadoxine-pyrimethamine on sexually transmitted and reproductive tract infections: results from a randomized trial in Uganda.

Harriet Adrama, Erin J Dela Cruz, Nida Ozarslan, Abel Kakuru, Bakar Odongo, Stephanie L Gaw, Jade Benjamin-Chung, Jimmy Kizza, Miriam Aguti, John Ategeka and 8 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in International journal of epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Harriet AdramaInfectious Diseases Research Collaboration, Kampala, Uganda.
Erin J Dela CruzDepartment of Medicine, University of California San Francisco, San Francisco, CA, United States.
Nida OzarslanDepartment of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, CA, United States.
Abel KakuruInfectious Diseases Research Collaboration, Kampala, Uganda.
Bakar OdongoInfectious Diseases Research Collaboration, Kampala, Uganda.
Stephanie L GawDepartment of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, CA, United States.
Jade Benjamin-ChungDepartment of Epidemiology and Population Health, Stanford University, Palo Alto, CA, United States.ORCID 0000-0003-3631-3132
Jimmy KizzaInfectious Diseases Research Collaboration, Kampala, Uganda.
Miriam AgutiInfectious Diseases Research Collaboration, Kampala, Uganda.
John AtegekaInfectious Diseases Research Collaboration, Kampala, Uganda.
Peter OlwochInfectious Diseases Research Collaboration, Kampala, Uganda.ORCID 0000-0002-7396-3348
Miriam NakalembeDepartment of Medicine, College of Health Sciences, Makerere University, Kampala, Uganda.
Bishop OpiraInfectious Diseases Research Collaboration, Kampala, Uganda.
Tamara D ClarkDepartment of Medicine, University of California San Francisco, San Francisco, CA, United States.
Moses R KamyaInfectious Diseases Research Collaboration, Kampala, Uganda.
Philip J RosenthalDepartment of Medicine, University of California San Francisco, San Francisco, CA, United States.ORCID 0000-0002-7953-7622
Grant DorseyDepartment of Medicine, University of California San Francisco, San Francisco, CA, United States.ORCID 0000-0003-0740-0317
Michelle E RohInstitute for Global Health Sciences, University of California San Francisco, San Francisco, CA, United States.ORCID 0000-0002-6268-0801

Funding

BIOLOGY OF INFECTIOUS DISEASES TRAINING PROGRAMT32AI007641 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MATTHEW G DORSEY · 2000 to 2026
$6.9M
Optimal chemopreventive regimens to prevent malaria and improve birth outcomes in UgandaU01AI141308 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DORSEY, MATTHEW G, ROSENTHAL, PHILIP JON · 2020 to 2024
$6.0M
Examining the mechanisms and optimization of malaria chemoprevention strategies to improve birth outcomes in AfricaR00HD111572 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI ROH, MICHELLE · 2025 to 2025
$743k
Mentoring translational researchers in perinatal infectious diseasesK24AI188458 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Stephanie Lina Gaw · 2025 to 2026
$412k
Examining the mechanisms and optimization of malaria chemoprevention strategies to improve birth outcomes in AfricaK99HD111572 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROH, MICHELLE · 2023 to 2024
$246k
Eunice Kennedy Shriver National Institute of Child Health & Human Development K99/R00 HD111572National Institute of Allergy and Infectious Diseases K24AI188458National Institute of Allergy and Infectious Diseases T32AI007641National Institute of Allergy and Infectious Diseases U01AI141308NIAID NIH HHS K24 AI188458NIAID NIH HHS T32 AI007641NIAID NIH HHS U01 AI141308NICHD NIH HHS K99 HD111572NICHD NIH HHS R00 HD111572NIH HHS
6 · The paper itself

Abstract

backgroundIn sub-Saharan Africa, sexually transmitted and reproductive tract infections (STIs/RTIs) are important but underdiagnosed risk factors for adverse pregnancy outcomes. Sulfadoxine-pyrimethamine (SP), used for the intermittent preventive treatment of malaria in pregnancy (IPTp), may reduce the STI/RTI burden due to its antimicrobial activity. We assessed the impact of IPTp regimens on STI/RTI prevalence and evaluated associations between STIs/RTIs and adverse birth outcomes.

methodsWe conducted a secondary analysis of a randomized-controlled trial comparing monthly IPTp with SP, dihydroartemisinin-piperaquine (DP), or DP+SP among pregnant women in Uganda. Vaginal swabs collected at or near delivery were tested for Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, and Group B Streptococcus (GBS) by using GeneXpert; bacterial vaginosis was assessed by using Nugent scoring. Log-binomial regression was used to compare STI/RTI prevalence between IPTp arms; IPTp-DP served as the reference arm. Multivariable Poisson regression with robust standard errors was used to evaluate associations between infections and preterm delivery, term low birthweight (LBW), overall LBW, and small-for-gestational age.

resultsAmong the 2265 participants assessed, the IPTp-SP arm had an 80% [95% confidence interval (CI): 67%-88%] lower prevalence of C. trachomatis (2.5% vs 12.4%) and a 35% (95% CI: 1%-57%) lower prevalence of GBS (7.7% vs 11.7%) at delivery compared with the IPTp-DP arm. Chlamydia trachomatis was associated with increased preterm delivery [prevalence ratio (PR) = 1.86, 95% CI: 1.07-3.25] and GBS was associated with increased term LBW (PR = 2.08, 95% CI: 1.06-4.08).

conclusionMonthly IPTp-SP may reduce the risk of adverse birth outcomes through its activity against C. trachomatis and GBS, highlighting its potential non-malarial benefits.

Indexed as

AntimalarialsMalariaPregnancy Complications, InfectiousPregnancy Complications, ParasiticPyrimethamineReproductive Tract InfectionsSexually Transmitted DiseasesSulfadoxineAdolescentAdultArtemisininsChlamydia InfectionsChlamydia trachomatisDrug CombinationsFemaleGonorrheaAntimalarialsArtemisininsartenimolDrug Combinationsfanasil, pyrimethamine drug combinationpiperaquinePiperazinesPyrimethamineQuinolinesSulfadoxinebacterial vaginosisChlamydia trachomatisGroup B Streptococcusintermittent preventive treatment in pregnancyNeisseria gonorrhoeaereproductive tract infectionssexually transmitted infectionssulfadoxine–pyrimethamineTrichomonas vaginalis

Identifiers

PMID41657027
PMCPMC13104154

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.