Therapeutic efficacy of sulphadoxine-pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in Burkina Faso

<p>Abstract</p> <p>Background</p> <p>A reduction in the therapeutic efficacy of chloroquine (CQ) and sulphadoxine-pyrimethamine (SP) has recently been observed in Burkina Faso. As these two drugs are used in pregnancy, their efficacy in pregnant women was studied to dir...

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Main Authors: Koné Bibiane, Traoré Salifou, Nezien Désiré, Coulibaly Sheick, Magnussen Pascal
Format: Article
Language:English
Published: BMC 2006-06-01
Series:Malaria Journal
Online Access:http://www.malariajournal.com/content/5/1/49
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author Koné Bibiane
Traoré Salifou
Nezien Désiré
Coulibaly Sheick
Magnussen Pascal
author_facet Koné Bibiane
Traoré Salifou
Nezien Désiré
Coulibaly Sheick
Magnussen Pascal
author_sort Koné Bibiane
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>A reduction in the therapeutic efficacy of chloroquine (CQ) and sulphadoxine-pyrimethamine (SP) has recently been observed in Burkina Faso. As these two drugs are used in pregnancy, their efficacy in pregnant women was studied to directly assess the level of drug resistance in this specific population, rather than to extrapolate results of studies conducted in children < 5 years of age.</p> <p>Methods</p> <p>During the malaria transmission season of 2003 in Ouagadougou, the clinical efficacy of SP and CQ, using the WHO 28-day protocol, was assessed in primigravidae and secundigravidae presenting with uncomplicated malaria.</p> <p>Results</p> <p>PCR-corrected results by day 28 showed that among 62 women treated with SP, eight (12.9%) experienced late parasitological failure, but no clinical failures. Among 60 women treated with CQ, the overall failure rate was 46.7% including 1.7% early treatment failures, 5% late clinical failures and 40% late parasitological failures. SP induced a haemoglobin gain of 0.3 g/dL by day 14 and 0.9 g/dL by day 28. Treatment responses were independent of gravidity, gestational age and prior antenatal care visits.</p> <p>Conclusion</p> <p>While CQ should no longer be used, the efficacy of SP is still compatible with use for intermittent preventive treatment (IPT) in pregnancy. However, given the possible spread of resistance, the drug should be restricted in its use.</p>
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spelling doaj.art-8b67eb2f03864785a7011f8f952fe4a32022-12-22T01:19:37ZengBMCMalaria Journal1475-28752006-06-01514910.1186/1475-2875-5-49Therapeutic efficacy of sulphadoxine-pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in Burkina FasoKoné BibianeTraoré SalifouNezien DésiréCoulibaly SheickMagnussen Pascal<p>Abstract</p> <p>Background</p> <p>A reduction in the therapeutic efficacy of chloroquine (CQ) and sulphadoxine-pyrimethamine (SP) has recently been observed in Burkina Faso. As these two drugs are used in pregnancy, their efficacy in pregnant women was studied to directly assess the level of drug resistance in this specific population, rather than to extrapolate results of studies conducted in children < 5 years of age.</p> <p>Methods</p> <p>During the malaria transmission season of 2003 in Ouagadougou, the clinical efficacy of SP and CQ, using the WHO 28-day protocol, was assessed in primigravidae and secundigravidae presenting with uncomplicated malaria.</p> <p>Results</p> <p>PCR-corrected results by day 28 showed that among 62 women treated with SP, eight (12.9%) experienced late parasitological failure, but no clinical failures. Among 60 women treated with CQ, the overall failure rate was 46.7% including 1.7% early treatment failures, 5% late clinical failures and 40% late parasitological failures. SP induced a haemoglobin gain of 0.3 g/dL by day 14 and 0.9 g/dL by day 28. Treatment responses were independent of gravidity, gestational age and prior antenatal care visits.</p> <p>Conclusion</p> <p>While CQ should no longer be used, the efficacy of SP is still compatible with use for intermittent preventive treatment (IPT) in pregnancy. However, given the possible spread of resistance, the drug should be restricted in its use.</p>http://www.malariajournal.com/content/5/1/49
spellingShingle Koné Bibiane
Traoré Salifou
Nezien Désiré
Coulibaly Sheick
Magnussen Pascal
Therapeutic efficacy of sulphadoxine-pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in Burkina Faso
Malaria Journal
title Therapeutic efficacy of sulphadoxine-pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in Burkina Faso
title_full Therapeutic efficacy of sulphadoxine-pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in Burkina Faso
title_fullStr Therapeutic efficacy of sulphadoxine-pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in Burkina Faso
title_full_unstemmed Therapeutic efficacy of sulphadoxine-pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in Burkina Faso
title_short Therapeutic efficacy of sulphadoxine-pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in Burkina Faso
title_sort therapeutic efficacy of sulphadoxine pyrimethamine and chloroquine for the treatment of uncomplicated malaria in pregnancy in burkina faso
url http://www.malariajournal.com/content/5/1/49
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