A Non-Inferiority, Individually Randomized Trial of Intermittent Screening and Treatment versus Intermittent Preventive Treatment in the Control of Malaria in Pregnancy

dc.contributor.author
Tagbor, Harry
dc.contributor.author
Cairns, Matthew
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Bojang, Kalifa
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Coulibaly, Sheikh
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Kayentao, Kassoum
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Williams, John
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Abubakar, Ismaela
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Akor, Francis
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Mohammed, Khalifa
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Bationo, Richard
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Dabira, Edgar
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Soulama, Alamissa
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Djimdé, Moussa
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Guirou, Etienne
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Awine, Timothy
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Quaye, Stephen L.
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Njie, Fanta
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Ordi i Majà, Jaume
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Doumbo, Ogobara
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Hodgson, Abraham
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Oduro, Abraham
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Meshnick, Steven R.
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Taylor, Steve
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Magnussen, Pascal
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Ter Kuile, Feiko O.
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Woukeu, Arouna
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Milligan, Paul
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Chandramohan, Daniel
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Greenwood, Brian
dc.date.issued
2016-02-04T13:36:38Z
dc.date.issued
2016-02-04T13:36:38Z
dc.date.issued
2015-08-10
dc.date.issued
2016-02-02T15:35:25Z
dc.identifier
1932-6203
dc.identifier
https://hdl.handle.net/2445/69255
dc.identifier
26258474
dc.description.abstract
BACKGROUND: The efficacy of intermittent preventive treatment for malaria with sulfadoxine-pyrimethamine (IPTp-SP) in pregnancy is threatened in parts of Africa by the emergence and spread of resistance to SP. Intermittent screening with a rapid diagnostic test (RDT) and treatment of positive women (ISTp) is an alternative approach. METHODS AND FINDINGS: An open, individually randomized, non-inferiority trial of IPTp-SP versus ISTp was conducted in 5,354 primi- or secundigravidae in four West African countries with a low prevalence of resistance to SP (The Gambia, Mali, Burkina Faso and Ghana). Women in the IPTp-SP group received SP on two or three occasions whilst women in the ISTp group were screened two or three times with a RDT and treated if positive for malaria with artemether-lumefantrine (AL). ISTp-AL was non-inferior to IPTp-SP in preventing low birth weight (LBW), anemia and placental malaria, the primary trial endpoints. The prevalence of LBW was 15.1% and 15.6% in the IPTp-SP and ISTp-AL groups respectively (OR = 1.03 [95% CI: 0.88, 1.22]). The mean hemoglobin concentration at the last clinic attendance before delivery was 10.97g/dL and 10.94g/dL in the IPTp-SP and ISTp-AL groups respectively (mean difference: -0.03 g/dL [95% CI: -0.13, +0.06]). Active malaria infection of the placenta was found in 24.5% and in 24.2% of women in the IPTp-SP and ISTp-AL groups respectively (OR = 0.95 [95% CI 0.81, 1.12]). More women in the ISTp-AL than in the IPTp-SP group presented with malaria parasitemia between routine antenatal clinics (310 vs 182 episodes, rate difference: 49.4 per 1,000 pregnancies [95% CI 30.5, 68.3], but the number of hospital admissions for malaria was similar in the two groups. CONCLUSIONS: Despite low levels of resistance to SP in the study areas, ISTp-AL performed as well as IPTp-SP. In the absence of an effective alternative medication to SP for IPTp, ISTp-AL is a potential alternative to IPTp in areas where SP resistance is high. It may also have a role in areas where malaria transmission is low and for the prevention of malaria in HIV positive women receiving cotrimoxazole prophylaxis in whom SP is contraindicated. TRIAL REGISTRATION: ClinicalTrials.gov NCT01084213 Pan African Clinical trials Registry PACT201202000272122.
dc.format
17 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Public Library of Science (PLoS)
dc.relation
Reproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0132247
dc.relation
PLoS One, 2015, vol. 10, num. 8, p. e0132247
dc.relation
http://dx.doi.org/10.1371/journal.pone.0132247
dc.rights
cc by (c) Tagbor et al., 2015
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Fonaments Clínics)
dc.subject
Assaigs clínics de medicaments
dc.subject
Malària
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Complicacions en l'embaràs
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Medicina preventiva
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Drug testing
dc.subject
Malaria
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Complications of pregnancy
dc.subject
Preventive medicine
dc.title
A Non-Inferiority, Individually Randomized Trial of Intermittent Screening and Treatment versus Intermittent Preventive Treatment in the Control of Malaria in Pregnancy
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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