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.

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

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 12 07 2021
revised: 16 09 2021
accepted: 30 09 2021
entrez: 8 11 2021
pubmed: 9 11 2021
medline: 9 11 2021
Statut: epublish

Résumé

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 (ISTp-ACT) compared to IPTp-SP, and understand the importance of subpatent infections. 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 Five trials conducted between 2007 and 2014 contributed (10,821 pregnancies), two from high SP-resistance areas where 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. Centers for Disease Control and Prevention and Worldwide Antimalarial Resistance Network.

Sections du résumé

BACKGROUND 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 (ISTp-ACT) compared to IPTp-SP, and understand the importance of subpatent infections.
METHODS 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
FINDINGS RESULTS
Five trials conducted between 2007 and 2014 contributed (10,821 pregnancies), two from high SP-resistance areas where
INTERPRETATION CONCLUSIONS
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.
FUNDING BACKGROUND
Centers for Disease Control and Prevention and Worldwide Antimalarial Resistance Network.

Identifiants

pubmed: 34746720
doi: 10.1016/j.eclinm.2021.101160
pii: S2589-5370(21)00440-5
pmc: PMC8556518
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101160

Subventions

Organisme : Medical Research Council
ID : MC_PC_MR/P006914/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R010161/1
Pays : United Kingdom

Déclaration de conflit d'intérêts

All authors declare no competing interests.

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Auteurs

Julie R Gutman (JR)

Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Carole Khairallah (C)

Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Kasia Stepniewska (K)

WorldWide Antimalarial Resistance Network (WWARN), Oxford, UK.
Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Infectious Diseases Data Observatory (IDDO), Oxford, UK.

Harry Tagbor (H)

University of Health and Allied Science, Ho, Ghana.

Mwayiwawo Madanitsa (M)

College of Medicine, University of Malawi, Blantyre, Malawi.

Matthew Cairns (M)

London School of Hygiene and Tropical Medicine, UK.

Anne Joan L'lanziva (AJ)

Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.

Linda Kalilani (L)

College of Medicine, University of Malawi, Blantyre, Malawi.

Kephas Otieno (K)

Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.

Victor Mwapasa (V)

College of Medicine, University of Malawi, Blantyre, Malawi.

Steve Meshnick (S)

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, USA.

Simon Kariuki (S)

Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.

Daniel Chandramohan (D)

London School of Hygiene and Tropical Medicine, UK.

Meghna Desai (M)

Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Steve M Taylor (SM)

Division of Infectious Diseases and Duke Global Health Institute, Duke University Medical Center, Durham, NC, USA.

Brian Greenwood (B)

London School of Hygiene and Tropical Medicine, UK.

Feiko O Ter Kuile (FO)

Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Kenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.

Classifications MeSH