Publication: Pharmacokinetics of intramuscular artemether in patients with severe falciparum malaria with or without acute renal failure
Issued Date
1998-06-23
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ISSN
03065251
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2-s2.0-0031812372
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Mahidol University
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SCOPUS
Bibliographic Citation
British Journal of Clinical Pharmacology. Vol.45, No.6 (1998), 597-600
Suggested Citation
J. Karbwang, K. Na-Bangchang, T. Tin, K. Sukontason, W. Rimchala, T. Harinasuta Pharmacokinetics of intramuscular artemether in patients with severe falciparum malaria with or without acute renal failure. British Journal of Clinical Pharmacology. Vol.45, No.6 (1998), 597-600. doi:10.1046/j.1365-2125.1998.00723.x Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/18515
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Title
Pharmacokinetics of intramuscular artemether in patients with severe falciparum malaria with or without acute renal failure
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Abstract
Aims The pharmacokinetics of intramuscular artemether and its major plasma metabolite-dihydroartemisinin, were investigated in patients with severe manifestations of falciparum malaria. Methods Six severe falciparum malaria patients with acute renal failure (ARF) and 11 without ARF were recruited into the study. They were treated with intramuscular artemether at a loading dose of 160 mg, followed by daily doses of 80 mg for another 6 days (total dose 640 mg). Results Patients with and without ARF showed a good initial response to treatment; the parasite and fever clearance times were 66(30-164) and 76(36-140) h [median(range)], respectively. None had reappearance of parasitaemia in their peripheral blood smear within 7 days of initiation of treatment. In comatose patients, the time to recovery of consciousness was 51.6(22-144) h. Artemether was detected in plasma as early as 1 h after a 160 mg dose, and declined to undetectable levels within 24 h in most cases. Patients with ARF had significantly higher C(max) [2.38(1.89- 3.95) vs 1.56(1.05-3.38)ng ml-1 mg-1 dose], AUC [35.4(22-52.9) vs 25.2(13.4-52.9) ng ml-1 hmg-1 dose], and lower V(z)/F [5.45(3.2-6.9) vs 8.6(4.2-12.3) l kg-1] and CL/F [7.4(5.4-13.8) vs 19.1(8.5-25.1)ml min-1 kg-1) when compared with those without ARF. In addition, t(2),z was significantly longer in ARF patients [7.0(5.5-10.0) us 5.7(4.2-6.6) hi. The pharmacokinetics of dihydroartemisinin in the two groups of patients were comparable. Conclusions ARF significantly modified the pharmacokinetics of intramuscular artemether. The changes could be attributed to either improved absorption/bioavailability, a reduction of systemic clearance, or a change in plasma protein binding of the drug.