Efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant Plasmodium falciparum malaria in Thailand

A combination of atovaquone-proguanil (Malarone®; GlaxoSmithKline, Research Triangle Park, NC) was previously shown to be highly effective in the treatment of uncomplicated Plasmodium falciparum malaria. However, there are only limited recent efficacy data, particularly from regions of multidrug res...

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Main Authors: Srivicha Krudsood, Samir N. Patel, Nopaddon Tangpukdee, Wipa Thanachartwet, Wattana Leowattana, Karnchana Pornpininworakij, Andrea K. Boggild, Sornchai Looareesuwan, Kevin C. Kain
Other Authors: Toronto General Hospital
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/24565
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spelling th-mahidol.245652018-08-24T09:07:50Z Efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant Plasmodium falciparum malaria in Thailand Srivicha Krudsood Samir N. Patel Nopaddon Tangpukdee Wipa Thanachartwet Wattana Leowattana Karnchana Pornpininworakij Andrea K. Boggild Sornchai Looareesuwan Kevin C. Kain Toronto General Hospital Mahidol University Immunology and Microbiology Medicine A combination of atovaquone-proguanil (Malarone®; GlaxoSmithKline, Research Triangle Park, NC) was previously shown to be highly effective in the treatment of uncomplicated Plasmodium falciparum malaria. However, there are only limited recent efficacy data, particularly from regions of multidrug resistance. In this study, we examined the efficacy of atovaquone-proguanil for the treatment of uncomplicated P. falciparum malaria on the Thailand-Myanmar border. Patients were given directly observed atovaquone-proguanil (1,000 mg/400 mg) once a day for three days and followed-up for four weeks in a non-transmission area. Of 140 eligible patients enrolled in this open-label study, 97.8% (95% confidence interval = 95.4-100%) responded to therapy and remained clear of parasitemia at follow-up. Mean parasite clearance time was 41.9 hours and mean fever clearance time was 37.1 hours. On the basis of genotyping, three cases of treatment failure were identified (1 RIII and 2 RI). These data indicate that atovaquone-proguanil remains highly efficacious for the treatment of multidrug-resistant P. falciparum malaria in Thailand. Copyright © 2007 by The American Society of Tropical Medicine and Hygiene. 2018-08-24T01:53:52Z 2018-08-24T01:53:52Z 2007-04-01 Article American Journal of Tropical Medicine and Hygiene. Vol.76, No.4 (2007), 655-658 00029637 2-s2.0-34249698953 https://repository.li.mahidol.ac.th/handle/123456789/24565 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34249698953&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Immunology and Microbiology
Medicine
spellingShingle Immunology and Microbiology
Medicine
Srivicha Krudsood
Samir N. Patel
Nopaddon Tangpukdee
Wipa Thanachartwet
Wattana Leowattana
Karnchana Pornpininworakij
Andrea K. Boggild
Sornchai Looareesuwan
Kevin C. Kain
Efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant Plasmodium falciparum malaria in Thailand
description A combination of atovaquone-proguanil (Malarone®; GlaxoSmithKline, Research Triangle Park, NC) was previously shown to be highly effective in the treatment of uncomplicated Plasmodium falciparum malaria. However, there are only limited recent efficacy data, particularly from regions of multidrug resistance. In this study, we examined the efficacy of atovaquone-proguanil for the treatment of uncomplicated P. falciparum malaria on the Thailand-Myanmar border. Patients were given directly observed atovaquone-proguanil (1,000 mg/400 mg) once a day for three days and followed-up for four weeks in a non-transmission area. Of 140 eligible patients enrolled in this open-label study, 97.8% (95% confidence interval = 95.4-100%) responded to therapy and remained clear of parasitemia at follow-up. Mean parasite clearance time was 41.9 hours and mean fever clearance time was 37.1 hours. On the basis of genotyping, three cases of treatment failure were identified (1 RIII and 2 RI). These data indicate that atovaquone-proguanil remains highly efficacious for the treatment of multidrug-resistant P. falciparum malaria in Thailand. Copyright © 2007 by The American Society of Tropical Medicine and Hygiene.
author2 Toronto General Hospital
author_facet Toronto General Hospital
Srivicha Krudsood
Samir N. Patel
Nopaddon Tangpukdee
Wipa Thanachartwet
Wattana Leowattana
Karnchana Pornpininworakij
Andrea K. Boggild
Sornchai Looareesuwan
Kevin C. Kain
format Article
author Srivicha Krudsood
Samir N. Patel
Nopaddon Tangpukdee
Wipa Thanachartwet
Wattana Leowattana
Karnchana Pornpininworakij
Andrea K. Boggild
Sornchai Looareesuwan
Kevin C. Kain
author_sort Srivicha Krudsood
title Efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant Plasmodium falciparum malaria in Thailand
title_short Efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant Plasmodium falciparum malaria in Thailand
title_full Efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant Plasmodium falciparum malaria in Thailand
title_fullStr Efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant Plasmodium falciparum malaria in Thailand
title_full_unstemmed Efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant Plasmodium falciparum malaria in Thailand
title_sort efficacy of atovaquone-proguanil for treatment of acute multidrug-resistant plasmodium falciparum malaria in thailand
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/24565
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