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甲氟喹-多西环素及青蒿琥酯-多西环素治疗急性非复杂性恶性疟的随机试验

Randomized trial of mefloquine-doxycycline, and artesunate-doxycycline for treatment of acute uncomplicated falciparum malaria.

作者信息

Looareesuwan S, Viravan C, Vanijanonta S, Wilairatana P, Charoenlarp P, Canfield C J, Kyle D E

机构信息

Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

出版信息

Am J Trop Med Hyg. 1994 Jun;50(6):784-9. doi: 10.4269/ajtmh.1994.50.784.

Abstract

One hundred nine adult patients with acute uncomplicated falciparum malaria were randomly selected to receive combinations of either doxycycline plus mefloquine or doxycycline plus artesunate. Fifty-four patients received mefloquine (1,250 mg divided between two doses of 750 and 500 mg six hours apart) with doxycycline and 55 patients received artesunate (300 mg total for 2.5 days; 100 mg followed by 50 mg every 12 hr for 2.5 days) with doxycycline. Doxycycline was administered in doses of 200 mg once a day for seven days. All patients were admitted to the hospital for 28 days to exclude reinfection. Ninety-seven patients completed the study; 12 patients left prior to completion of follow-up for reasons unrelated to their treatment. Cure rates for the two groups were 96% (46 of 48) for mefloquine plus doxycycline and 80% (39 of 49) for artesunate plus doxycycline. Mean fever and parasite clearance times were significantly shorter in the group that received artesunate plus doxycycline (38.7 and 41.3 hr) than mefloquine plus doxycycline (64.3 and 69.0 hr), respectively. In vitro drug sensitivity testing of selected isolates obtained prior to treatment indicated that eight of nine admission isolates were resistant to mefloquine; all isolates were susceptible to artesunate. Recrudescent isolates failed to show a pattern of decreased sensitivity to the drugs to which the parasites had been exposed during treatment; the studies showed decreased sensitivity to doxycycline in only two of eight isolates tested.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

109例急性非复杂性恶性疟成年患者被随机选取,接受强力霉素联合甲氟喹或强力霉素联合青蒿琥酯的治疗方案。54例患者接受甲氟喹(1250mg分两剂,间隔6小时,分别为750mg和500mg)加强力霉素治疗,55例患者接受青蒿琥酯(2.5天共300mg;首剂100mg,随后每12小时50mg,共2.5天)加强力霉素治疗。强力霉素剂量为每日200mg,连用7天。所有患者入院28天以排除再感染。97例患者完成研究;12例患者在随访结束前因与治疗无关的原因离开。甲氟喹加强力霉素组和青蒿琥酯加强力霉素组的治愈率分别为96%(48例中的46例)和80%(49例中的39例)。接受青蒿琥酯加强力霉素组的平均退热时间和寄生虫清除时间(分别为38.7小时和41.3小时)明显短于甲氟喹加强力霉素组(分别为64.3小时和69.0小时)。治疗前对所选分离株进行的体外药敏试验表明,9株入院分离株中有8株对甲氟喹耐药;所有分离株对青蒿琥酯敏感。复发分离株未表现出对治疗期间寄生虫所接触药物敏感性降低的模式;研究显示,在8株受试分离株中只有2株对强力霉素敏感性降低。(摘要截短于250字)

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