Gupta Ravindra K, Van Vugt Michele, Paiphun Lucy, Slight Thra, Looareesuwan Sornchai, White Nicholas J, Nosten François
Department of Infection, St. Thomas' Hospital, London, United Kingdom.
Am J Trop Med Hyg. 2005 Aug;73(2):267-8.
Combinations are set to become the mainstay in treatment and prophylaxis of malaria due to Plasmodium falciparum. Various antimalarials have been implicated in cardiotoxicity via prolongation of the QTc interval. Atovaquone-proguanil is an effective and increasingly popular antimalarial choice when used alone or with artesunate in areas of drug resistance. We report the results of an investigation carried out on the Thai-Burmese border in 42 patients randomized to receive either atovaquone-proguanil or atovaquone-proguanil-artesunate for three days. Electrocardiographic recordings were made at baseline and one hour after each dose. There was no statistically significant change in QTc interval between baseline and any subsequent readings in either treatment group or the cohort as a whole. We conclude that atovaquone-proguanil shows no evidence of cardiotoxicity either alone or when combined with artesunate.
由于恶性疟原虫,联合用药将成为疟疾治疗和预防的主要手段。各种抗疟药都曾因QTc间期延长而导致心脏毒性。阿托伐醌-氯胍单独使用或与青蒿琥酯联合用于耐药地区时,是一种有效且越来越受欢迎的抗疟选择。我们报告了在泰缅边境对42例患者进行的一项调查结果,这些患者被随机分为两组,分别接受阿托伐醌-氯胍或阿托伐醌-氯胍-青蒿琥酯治疗三天。在基线以及每次给药后一小时进行心电图记录。在任何一个治疗组或整个队列中,基线与任何后续读数之间的QTc间期均无统计学显著变化。我们得出结论,阿托伐醌-氯胍单独使用或与青蒿琥酯联合使用时,均未显示出心脏毒性的证据。