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Impact on pregnancy outcomes of intermittent preventive treatment with sulfadoxine-pyrimethamine in urban and peri-urban Papua New Guinea: a retrospective cohort study.
Cellich, Philip; Unger, Holger W; Rogerson, Stephen J; Mola, Glen D L.
Affiliation
  • Cellich P; Division of Obstetrics and Gynaecology, School of Medicine and Health Sciences, Port Moresby General Hospital, University of Papua New Guinea, Port Moresby, Papua New Guinea. philip.cellich@health.nsw.gov.au.
  • Unger HW; Department of Obstetrics and Gynaecology, Canterbury Hospital, 575 Canterbury Road, Campsie 2194, NSW, Australia. philip.cellich@health.nsw.gov.au.
  • Rogerson SJ; Menzies School of Health Research, Charles Darwin University, PO Box 41096, Casuarina 0810, NT, Australia. holger.unger@menzies.edu.au.
  • Mola GDL; Department of Obstetrics and Gynaecology, Royal Darwin Hospital, Darwin, NT, Australia. holger.unger@menzies.edu.au.
Malar J ; 23(1): 201, 2024 Jul 05.
Article in En | MEDLINE | ID: mdl-38970076
ABSTRACT

BACKGROUND:

Intermittent preventive treatment in pregnancy with sulfadoxine-pyrimethamine (IPTp-SP) reduces malaria-attributable adverse pregnancy outcomes and may also prevent low birth weight (< 2,500 g) through mechanisms independent of malaria. Malaria transmission in Papua New Guinea (PNG) is highly heterogeneous. The impact of IPTp-SP on adverse birth outcomes in settings with little or no malaria transmission, such as PNG's capital city Port Moresby, is unknown.

METHODS:

A retrospective cohort study was conducted amongst HIV-negative women with a singleton pregnancy who delivered at Port Moresby General Hospital between 18 July and 21 August 2022. The impact of IPTp-SP doses on adverse birth outcomes and anaemia was assessed using logistic and linear regression models, as appropriate.

RESULTS:

Of 1,140 eligible women amongst 1,228 consecutive births, 1,110 had a live birth with a documented birth weight. A total of 156 women (13.7%) did not receive any IPTp-SP, 347 women (30.4%) received one, 333 (29.2%) received two, and 304 (26.7%) received the recommended ≥ 3 doses of IPTp-SP. A total of 65 of 1,110 liveborn babies (5.9%) had low birth weight and there were 34 perinatal deaths (3.0%). Anaemia (haemoglobin < 100 g/L) was observed in 30.6% (243/793) of women, and 14 (1.2%) had clinical malaria in pregnancy. Compared to women receiving 0-1 dose of IPTp-SP, women receiving ≥ 2 doses had lower odds of LBW (adjusted odds ratio [aOR] 0.50; 95% confidence interval [CI] 0.26, 0.96), preterm birth (aOR 0.58; 95% CI 0.32, 1.04), perinatal death (aOR 0.49; 95% CI 0.18, 1.38), LBW/perinatal death (aOR 0.55; 95% CI 0.27, 1.12), and anaemia (OR 0.50; 95% CI 0.36, 0.69). Women who received 2 doses versus 0-1 had 45% lower odds of LBW (aOR 0.55, 95% CI 0.27, 1.10), and a 16% further (total 61%) reduction with ≥ 3 doses (aOR 0.39, 95% CI 0.14, 1.05). Birth weights for women who received 2 or ≥ 3 doses versus 0-1 were 81 g (95% CI -3, 166) higher, and 151 g (58, 246) higher, respectively.

CONCLUSIONS:

Provision of IPTp-SP in a low malaria-transmission setting in PNG appears to translate into substantial health benefits, in a dose-response manner, supporting the strengthening IPTp-SP uptake across all transmission settings in PNG.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrimethamine / Sulfadoxine / Pregnancy Outcome / Drug Combinations / Malaria / Antimalarials Limits: Adolescent / Adult / Female / Humans / Newborn / Pregnancy Language: En Journal: Malar J Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrimethamine / Sulfadoxine / Pregnancy Outcome / Drug Combinations / Malaria / Antimalarials Limits: Adolescent / Adult / Female / Humans / Newborn / Pregnancy Language: En Journal: Malar J Year: 2024 Document type: Article