Price R, Simpson J A, Teja-Isavatharm P, Than M M, Luxemburger C, Heppner D G, Chongsuphajaisiddhi T, Nosten F, White N J
Shoklo Malaria Research Unit, Mae Sod, Tak Province, Bangkok, Thailand.
Antimicrob Agents Chemother. 1999 Feb;43(2):341-6. doi: 10.1128/AAC.43.2.341.
Combining artemisinin or a derivative with mefloquine increases cure rates in falciparum malaria patients, reduces transmission, and may slow the development of resistance. The combination of artesunate, given for 3 days, and mefloquine is now the treatment of choice for uncomplicated multidrug-resistant falciparum malaria acquired on the western or eastern borders of Thailand. To optimize mefloquine administration in this combination, a prospective study of mefloquine pharmacokinetics was conducted with 120 children (4 to 15 years old) with acute uncomplicated falciparum malaria, who were divided into four age- and sex-matched groups. The patients all received artesunate (4 mg/kg of body weight/day orally for 3 days and mefloquine as either (i) a single dose (25 mg/kg) on day 2 with food, (ii) a split dose (15 mg/kg on day 2 and 10 mg/kg on day 3) with food, (iii) a single dose (25 mg/kg) on day 0 without food, or (iv) a single dose (25 mg/kg) on day 2 without food. Delaying administration of mefloquine until day 2 was associated with a mean (95% confidence interval) increase in estimated oral bioavailability of 72% (36 to 109%). On day 2 coadministration with food did not increase mefloquine absorption significantly, and there were no significant differences between patients receiving split- and single-dose administration. In combination with artesunate, mefloquine administration should be delayed until the second or third day after presentation.
将青蒿素或其衍生物与甲氟喹联合使用可提高恶性疟患者的治愈率,减少传播,并可能减缓耐药性的发展。青蒿琥酯连用3天与甲氟喹的联合用药,现已成为泰国西部或东部边境获得性单纯性耐多药恶性疟的首选治疗方法。为了优化该联合用药中甲氟喹的给药方式,对120名(4至15岁)急性单纯性恶性疟儿童进行了甲氟喹药代动力学的前瞻性研究,这些儿童被分为四个年龄和性别匹配的组。所有患者均接受青蒿琥酯(口服4mg/kg体重/天,连用3天),甲氟喹给药方式如下:(i)第2天单剂量(25mg/kg)与食物同服;(ii)分剂量(第2天15mg/kg,第3天10mg/kg)与食物同服;(iii)第0天单剂量(25mg/kg)空腹服用;或(iv)第2天单剂量(25mg/kg)空腹服用。将甲氟喹给药推迟至第2天,估计口服生物利用度平均(95%置信区间)增加72%(36%至109%)。第2天与食物同服并未显著增加甲氟喹的吸收,接受分剂量和单剂量给药的患者之间也无显著差异。与青蒿琥酯联合使用时,甲氟喹的给药应推迟至就诊后的第二天或第三天。