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01.12.2012 | Research | Ausgabe 1/2012 Open Access

Malaria Journal 1/2012

Clindamycin plus quinine for treating uncomplicated falciparum malaria: a systematic review and meta-analysis

Zeitschrift:
Malaria Journal > Ausgabe 1/2012
Autoren:
Charles O Obonyo, Elizabeth A Juma
Wichtige Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1475-2875-11-2) contains supplementary material, which is available to authorized users.

Authors' contributions

COO developed the protocol, scanned the results of the literature search for potentially relevant trials, assessed potentially relevant trials for inclusion into the review, assessed the methodological quality of the included trials, independently extracted the data, entered the data into Review Manager, performed the statistical analysis, and drafted the manuscript. EAJ edited the protocol, assessed potentially relevant trials for inclusion into the review, assessed the methodological quality of the included trials and independently extracted the data. Both authors read and approved the final manuscript.

Abstract

Background

Artemisinin-based combinations are recommended for treatment of uncomplicated falciparum malaria, but are costly and in limited supply. Clindamycin plus quinine is an alternative non-artemisinin-based combination recommended by World Health Organization. The efficacy and safety of clindamycin plus quinine is not known. This systematic review aims to assess the efficacy of clindamycin plus quinine versus other anti-malarial drugs in the treatment of uncomplicated falciparum malaria.

Methods

All randomized controlled trials comparing clindamycin plus quinine with other anti-malarial drugs in treating uncomplicated malaria were included in this systematic review. Databases searched included: Cochrane Central Register of Controlled Trials, MEDLINE, EMBASE and LILACS. Two authors independently assessed study eligibility, extracted data and assessed methodological quality. The primary outcome measure was treatment failure by day 28. Dichotomous data was compared using risk ratio (RR), in a fixed effects model.

Results

Seven trials with 929 participants were included. Clindamycin plus quinine significantly reduced the risk of day 28 treatment failure compared with quinine (RR 0.14 [95% CI 0.07 to 0.29]), quinine plus sulphadoxine-pyrimethamine (RR 0.17 [95% CI 0.06 to 0.44]), amodiaquine (RR 0.11 [95% CI 0.04 to 0.27]), or chloroquine (RR 0.11 [95% CI 0.04 to 0.29]), but had similar efficacy compared with quinine plus tetracycline (RR 0.33 [95% CI 0.01 to 8.04]), quinine plus doxycycline (RR 1.00 [95% CI 0.21 to 4.66]), artesunate plus clindamycin (RR 0.57 [95% CI 0.26 to 1.24]), or chloroquine plus clindamycin (RR 0.38 [95% CI 0.13 to 1.10]). Adverse events were similar across treatment groups but were poorly reported.

Conclusion

The evidence on the efficacy of clindamycin plus quinine as an alternative treatment for uncomplicated malaria is inconclusive. Adequately powered trials are urgently required to compare this combination with artemisinin-based combinations.
Zusatzmaterial
Authors’ original file for figure 1
12936_2011_1965_MOESM1_ESM.pdf
Authors’ original file for figure 2
12936_2011_1965_MOESM2_ESM.pdf
Authors’ original file for figure 3
12936_2011_1965_MOESM3_ESM.pdf
Authors’ original file for figure 4
12936_2011_1965_MOESM4_ESM.pdf
Literatur
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