Malaria Journal

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Chloroquine-resistant Plasmodium vivax malaria in Debre Zeit, Ethiopia

Hiwot Teka1,2*, Beyene Petros1, Lawrence Yamuah2, Gezahegn Tesfaye3, Ibrahim Elhassan6, Simon Muchohi4, Gilbert Kokwaro4,5, Abraham Aseffa2 and Howard Engers2

Author Affiliations

1 Department of Biology, Addis Ababa University, Addis Ababa, Ethiopia

2 Armauer Hansen Research Institute (AHRI), Addis Ababa, Ethiopia

3 Federal Ministry of Health, Malaria and Other Vector borne Diseases Prevention and Control, Addis Ababa, Ethiopia

4 Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme, Centre for Geographic Medicine Research (Coast), Kilifi, Kenya

5 Department of Pharmaceutics and Pharmacy Practice, School of Pharmacy, University of Nairobi, Nairobi, Kenya

6 Institute of endemic diseases, University of Khartoum, Sudan

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Malaria Journal 2008, 7:220 doi:10.1186/1475-2875-7-220

Published: 29 October 2008

Abstract

Background

Plasmodium vivax accounts for about 40% of all malaria infection in Ethiopia. Chloroquine (CQ) is the first line treatment for confirmed P. vivax malaria in the country. The first report of CQ treatment failure in P. vivax was from Debre Zeit, which suggested the presence of chloroquine resistance.

Methods

An in vivo drug efficacy study was conducted in Debre Zeit from June to August 2006. Eighty-seven patients with microscopically confirmed P. vivax malaria, aged between 8 months and 52 years, were recruited and treated under supervision with CQ (25 mg/kg over three days). Clinical and parasitological parameters were assessed during the 28 day follow-up period. CQ and desethylchloroquine (DCQ) blood and serum concentrations were determined with high performance liquid chromatography (HPLC) in patients who showed recurrent parasitaemia.

Results

Of the 87 patients recruited in the study, one was lost to follow-up and three were excluded due to P. falciparum infection during follow-up. A total of 83 (95%) of the study participants completed the follow-up. On enrolment, 39.8% had documented fever and 60.2% had a history of fever. The geometric mean parasite density of the patients was 7045 parasites/μl. Among these, four patients had recurrent parasitaemia on Day 28. The blood CQ plus DCQ concentrations of these four patients were all above the minimal effective concentration (> 100 ng/ml).

Conclusion

Chloroquine-resistant P. vivax parasites are emerging in Debre Zeit, Ethiopia. A multi-centre national survey is needed to better understand the extent of P. vivax resistance to CQ in Ethiopia.