Artesunate plus mefloquine versus mefloquine for treating uncomplicated malaria (Review)

dc.contributor.author Bukirwa, H.
dc.contributor.author Orton, L.C
dc.date.accessioned 2012-02-16T10:04:15Z
dc.date.available 2012-02-16T10:04:15Z
dc.date.issued 2010
dc.description.abstract Background Multiple-drug-resistant malaria is widespread, and in South-East Asia resistance is high against nearly all single therapy antimalarial drugs. Here, and in other areas with low malaria transmission, the combination of artesunate and mefloquine may provide an effective alternative. Objectives To compare artesunate plus mefloquine with mefloquine alone for treating uncomplicated Plasmodium falciparum malaria. Search strategy We searched the Cochrane Infectious Diseases Group Specialized Register (May 2005), CENTRAL (The Cochrane Library Issue 2, 2005), MEDLINE (1966 toMay 2005), EMBASE (1988 toMay 2005), LILACS (May 2005), BIOSIS (1985 to June 2005), conference proceedings, and reference lists. We also contacted researchers, organizations, and pharmaceutical companies. Selection criteria Randomized and quasi-randomized controlled trials comparing artesunate plus mefloquine with mefloquine alone for treating uncomplicated malaria. Data collection and analysis Two authors independently applied the inclusion criteria, extracted data, and assessed methodological quality. The primary outcome was treatment failure by day 28, defined as evidence of parasitaemia with or without clinical failure between days zero (start of treatment) and 28. For dichotomous data we calculated risk ratios (RR) and 95% confidence intervals (CI). Main results Eight trials involving 1996 participants met the inclusion criteria. All were conducted in areas with low malaria transmission, seven in South-East Asia and one in the Peruvian Amazon. The doses and dosing regimens of artesunate and mefloquine varied across trials. The trials using a total dose of 25 mg/kg mefloquine and 10 mg artesunate reported fewer treatment failures with the combination at all time points: day 28 (RR 0.17, 95% CI 0.06 to 0.47; 824 participants, 4 trials), day 42 (RR 0.23, 95% CI 0.14 to 0.39; 298 participants, 1 trial), and day 63 (RR 0.26, 95% CI 0.09 to 0.77; 501 participants, 2 trials). The results for parasitaemia showed a similar trend. Trials using a lower dose of artesunate tended to favour the artesunate plus mefloquine combination. Overall, adverse events were similar across treatment arms. Authors’ conclusions Artesunate plus mefloquine performs better than mefloquine alone for treating uncomplicated falciparum malaria in areas with low malaria transmission. A total dose of 25 mg/kg mefloquine and at least 10 mg artesunate leads to higher cure rates. Better reporting of methods and standardisation of outcomes would help the interpretation of future trials. 2008: As monotherapy is no longer recommended by theWorld Health Organization for malaria treatment, the authors do not intend to update this review. en_US
dc.identifier.citation Bukirwa, H., Orton, L.C. (2010). Artesunate plus mefloquine versus mefloquine for treating uncomplicated malaria (Review). CochraneDatabase of Systematic Reviews, 1 en_US
dc.identifier.issn 1469-493X
dc.identifier.uri DOI: 10.1002/14651858.CD004531.pub2.
dc.identifier.uri http://hdl.handle.net/10570/435
dc.language.iso en en_US
dc.publisher Cochrane Collaboration en_US
dc.subject Multiple-drug-resistant malaria en_US
dc.subject Plasmodium falciparum en_US
dc.subject Combination of mefloquine en_US
dc.subject Antimalarial therapy en_US
dc.subject South-East Asia en_US
dc.subject Combination of artesunate en_US
dc.subject Malaria en_US
dc.title Artesunate plus mefloquine versus mefloquine for treating uncomplicated malaria (Review) en_US
dc.type Journal article, peer reviewed en_US
Files
Original bundle
Now showing 1 - 1 of 1
Thumbnail Image
Name:
bukirwa-orton-chs-res.pdf
Size:
368.24 KB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: