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在泰国进行的一项随机、双盲、对照试验,比较蒿甲醚和本芴醇新口服复方制剂(CGP 56697)与甲氟喹治疗急性恶性疟的疗效。

A randomized, double-blind, comparative trial of a new oral combination of artemether and benflumetol (CGP 56697) with mefloquine in the treatment of acute Plasmodium falciparum malaria in Thailand.

作者信息

Looareesuwan S, Wilairatana P, Chokejindachai W, Chalermrut K, Wernsdorfer W, Gemperli B, Gathmann I, Royce C

机构信息

Department of Clinical Tropical Medicine and Hospital for Tropical Diseases, Faculty of Tropical Medicine, Mahidol University, Thailand.

出版信息

Am J Trop Med Hyg. 1999 Feb;60(2):238-43. doi: 10.4269/ajtmh.1999.60.238.

Abstract

CGP 56697, a new oral fixed combination of artemether and benflumetol, was tested in a double-blinded, randomized trial in 252 adult patients treated either with CGP 56697 (4 x 4 tablets each containing 20 mg of artemether and 120 mg of benflumetol, given at 0, 8, 24, and 48 hr), or with mefloquine (three tablets of 250 mg at initial diagnosis, followed by two tablets of 250 mg at 8 hr). Baseline data of the two groups were comparable. The 28-day cure rate with CGP 56697 was lower than with mefloquine (69.3% versus 82.4%; P = 0.002). However, CGP 56697 was more effective than mefloquine in parasite clearance time (43 hr versus 66 hr; P < 0.001) fever clearance time (32 hr versus 54 hr; P < 0.005), and gametocyte clearance time (152 hr versus 331 hr; P < 0.001). This study revealed that CGP 56697 is effective against multidrug-resistant Plasmodium falciparum malaria in Thailand, but higher doses will probably be needed to improve the cure rate.

摘要

CGP 56697是一种新的蒿甲醚和本芴醇口服复方制剂,在一项双盲随机试验中,对252例成年患者进行了测试,这些患者分别接受CGP 56697(4×4片,每片含20毫克蒿甲醚和120毫克本芴醇,在0、8、24和48小时给药)或甲氟喹(初诊时服用3片250毫克,8小时后再服用2片250毫克)治疗。两组的基线数据具有可比性。CGP 56697的28天治愈率低于甲氟喹(69.3%对82.4%;P = 0.002)。然而,CGP 56697在疟原虫清除时间(43小时对66小时;P < 0.001)、发热清除时间(32小时对54小时;P < 0.005)和配子体清除时间(152小时对331小时;P < 0.001)方面比甲氟喹更有效。这项研究表明,CGP 56697对泰国的多重耐药恶性疟有效,但可能需要更高剂量来提高治愈率。

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