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Intermittent screening and treatment with artemisinin-combination therapy versus intermittent preventive treatment with sulphadoxine-pyrimethamine for malaria in pregnancy: a systematic review and individual participant data meta-analysis of randomised clinical trials

期刊

ECLINICALMEDICINE
卷 41, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.eclinm.2021.101160

关键词

Malaria; pregnancy; intermittent preventive treatment; intermittent screening; sulphadoxine-pyrimethamine; artemisinin combination therapy

资金

  1. Worldwide Antimalarial Resistance Network (WWARN) - Bill & Melinda Gates Foundation [OPP1181807]
  2. US Centers for Disease Control and Prevention (CDC)
  3. Liverpool School of Tropical Medicine (LSTM)
  4. Bill and Melinda Gates Foundation [OPP1181807] Funding Source: Bill and Melinda Gates Foundation

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The study found that ISTp-ACT was not superior to IPTp-SP in the prevention of malaria during pregnancy, and may result in more subpatent infections. Subpatent infections were associated with increased risk of low birthweight and preterm delivery.
Background: In sub-Saharan Africa, the efficacy of intermittent preventive therapy in pregnancy with sulphadoxine-pyrimethamine (IPTp-SP) for malaria in pregnancy is threatened by parasite resistance. We conducted an individual-participant data (IPD) meta-analysis to assess the efficacy of intermittent screening with malaria rapid diagnostic tests (RDTs) and treatment of RDT-positive women with artemisinin-based combination therapy (ISTpACT) compared to IPTp-SP, and understand the importance of subpatent infections. Methods: We searched MEDLINE and the Malaria-in-Pregnancy Library on May 6, 2021 for trials comparing ISTp-ACT and IPTp-SP. Generalised linear regression was used to compare adverse pregnancy outcomes (composite of small-for-gestational-age, low birthweight (LBW), or preterm delivery) and peripheral or placental Plasmodium falciparum at delivery. The effects of subpatent (PCR-positive, RDT/microscopy-negative) infections were assessed in both arms pooled using multi-variable fixed-effect models adjusting for the number of patent infections. Findings: Five trials conducted between 2007 and 2014 contributed (10,821 pregnancies), two from high SP-resistance areas where dhfr/dhps quintuple mutant parasites are saturated, but sextuple mutants are still rare (Kenya and Malawi), and three from low-resistance areas (West-Africa). Four trials contributed IPD data (N=10,362). At delivery, the prevalence of any malaria infection (relative risk [RR]=1.08, 95% CI 1.00-1.16, I-2=67.0 %) and patent infection (RR=1.02, 0.61-1.16, I-2=0.0%) were similar. Subpatent infections were more common in ISTp recipients (RR=1.31, 1.05-1.62, I-2=0.0%). There was no difference in adverse pregnancy outcome (RR=1.00, 0.96-1.05; studies=4, N=9,191, I-2=54.5%). Subpatent infections were associated with LBW (adjusted RR=1.13, 1.07-1.19), lower mean birthweight (adjusted mean difference=32g, 15-49), and preterm delivery (aRR=1.35, 1.15-1.57). Interpretation: ISTp-ACT was not superior to IPTp-SP and may result in more subpatent infections than the existing IPTp-SP policy. Subpatent infections were associated with increased LBW and preterm delivery. More sensitive diagnostic tests are needed to detect and treat low-grade infections. Published by Elsevier Ltd.

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