Literature DB >> 12479545

Artesunate and mefloquine given simultaneously for three days via a prepacked blister is equally effective and tolerated as a standard sequential treatment of uncomplicated acute Plasmodium falciparum malaria: randomized, double-blind study in Thailand.

S Krudsood1, S Looareesuwan, U Silachamroon, K Chalermrut, D Pittrow, N Cambon, E A Mueller.   

Abstract

The combination of artesunate and mefloquine is currently one of the most effective treatments against multidrug-resistant Plasmodium falciparum malaria. To improve patient compliance to such a combination, the two agents have been combined in a prepacked single blister. Patients were instructed to simultaneously co-administer the drugs once a day for three days. In the present randomized, double-blind, parallel group, comparative, single center study in Thailand, this concept was investigated in 204 adults and children with acute, uncomplicated P. falciparum malaria. Patients were randomized into two treatment groups and received once a day over a three-day period the following: Group A received artesunate, 4-5 mg/kg/day, and mefloquine, total dose = 25 mg/kg, approximately 8.5 mg/kg/day, simultaneously. Group B received artesunate, 4-5 mg/kg/day, and mefloquine, total dose = 25 mg/kg, sequentially (i.e., no mefloquine dose on the first day, 15 mg/kg on the second day, and 10 mg/kg on the third day). Both treatment groups showed no relevant differences in baseline demographic and clinical characteristics. Intent-to-treat analysis revealed a cure rate at day 28 (primary endpoint) of 100% in group A and 99% in group B (difference not significant). The secondary endpoints of mean time to fever clearance (group A = 34 hours, group B = 31 hours) and mean time to parasite clearance (group A = 44 hours group B = 48 hours) were similar between groups (both differences not significant). Tolerability was good in both treatment groups, with no difference in the overall incidence of adverse events. There was a low incidence of nausea/vomiting (4.9% in both groups) and central nervous system side effects (4.9% in group A versus 8.8% in group B). These were comparable between groups and generally of a mild nature. The three-day combination of artesunate and mefloquine (Artequin, Mepha, Ltd., Aesch, Switzerland) with the introduction of mefloquine on day 1 offers a practical dosing regimen that is highly effective and well tolerated in patients of different ages with uncomplicated P. falciparum malaria. It is likely that the prepacked blister approach translates clinically into a better patient compliance, thereby contributing to limit the development of drug resistance.

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Year:  2002        PMID: 12479545     DOI: 10.4269/ajtmh.2002.67.465

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  7 in total

1.  Efficacy and safety of a new pediatric artesunate-mefloquine drug formulation for the treatment of uncomplicated falciparum malaria in Gabon.

Authors:  Marielle K Bouyou-Akotet; Michael Ramharter; Edgard Brice Ngoungou; Modeste Mabika Mamfoumbi; Mireille Pemba Mihindou; Michel A Missinou; Florian Kurth; Sabine Bélard; Selidji T Agnandji; Saadou Issifou; János L Heidecker; Sonja Trapp; Peter G Kremsner; Maryvonne Kombila
Journal:  Wien Klin Wochenschr       Date:  2010-03       Impact factor: 1.704

Review 2.  Unit-dose packaged drugs for treating malaria.

Authors:  L Orton; G Barnish
Journal:  Cochrane Database Syst Rev       Date:  2005-04-18

Review 3.  Interventions for enhancing medication adherence.

Authors:  Robby Nieuwlaat; Nancy Wilczynski; Tamara Navarro; Nicholas Hobson; Rebecca Jeffery; Arun Keepanasseril; Thomas Agoritsas; Niraj Mistry; Alfonso Iorio; Susan Jack; Bhairavi Sivaramalingam; Emma Iserman; Reem A Mustafa; Dawn Jedraszewski; Chris Cotoi; R Brian Haynes
Journal:  Cochrane Database Syst Rev       Date:  2014-11-20

4.  Tolerability and efficacy of a pediatric granule formulation of artesunate-mefloquine in young children from Cameroon with uncomplicated falciparum malaria.

Authors:  Félix Tietche; David Chelo; Njiki Kinkela Mina Ntoto; Florence Minjiwa Djoukoue; Christoph Hatz; Sarabel Frey; Adrian Frentzel; Sonja Trapp; Roland Zielonka; Edgar A Mueller
Journal:  Am J Trop Med Hyg       Date:  2010-06       Impact factor: 2.345

5.  An open-label, randomised study of dihydroartemisinin-piperaquine versus artesunate-mefloquine for falciparum malaria in Asia.

Authors:  Neena Valecha; Aung Pyae Phyo; Mayfong Mayxay; Paul N Newton; Srivicha Krudsood; Sommay Keomany; Maniphone Khanthavong; Tiengkham Pongvongsa; Ronnatrai Ruangveerayuth; Chirapong Uthaisil; David Ubben; Stephan Duparc; Antonella Bacchieri; Marco Corsi; Bappanad H K Rao; Prabash C Bhattacharya; Nagesh Dubhashi; Susanta K Ghosh; Vas Dev; Ashwani Kumar; Sasithon Pukrittayakamee; Sasithon Pukittayakamee
Journal:  PLoS One       Date:  2010-07-30       Impact factor: 3.240

6.  A study protocol for a randomised open-label clinical trial of artesunate-mefloquine versus chloroquine in patients with non-severe Plasmodium knowlesi malaria in Sabah, Malaysia (ACT KNOW trial).

Authors:  M J Grigg; T William; P Dhanaraj; J Menon; B E Barber; L von Seidlein; G Rajahram; R N Price; N M Anstey; T W Yeo
Journal:  BMJ Open       Date:  2014-08-19       Impact factor: 2.692

7.  Efficacy, safety and tolerability of artesunate-mefloquine in the treatment of uncomplicated Plasmodium falciparum malaria in four geographic zones of Nigeria.

Authors:  Philip U Agomo; Martin M Meremikwu; Ismaila M Watila; Innocent J Omalu; Friday A Odey; Stephen Oguche; Valentine I Ezeiru; Olugbenga O Aina
Journal:  Malar J       Date:  2008-09-09       Impact factor: 2.979

  7 in total

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