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阿泰康与青蒿琥酯-甲氟喹治疗泰国急性无并发症恶性疟的开放随机临床试验。

An open randomized clinical trial of Artecom vs artesunate-mefloquine in the treatment of acute uncomplicated falciparum malaria in Thailand.

作者信息

Wilairatana P, Krudsood S, Chalermrut K, Pengruksa C, Srivilairit S, Silachamroon U, Treeprasertsuk S, Looareesuwan S

机构信息

Hospital for Tropical Diseases, Faculty of Tropical Medicine, Mahidol University, Rajthevi, Bangkok, Thailand.

出版信息

Southeast Asian J Trop Med Public Health. 2002 Sep;33(3):519-24.

Abstract

The efficacy and safety of Artecom were assessed in an open randomized trial in adults presenting with acute, uncomplicated Plasmodium falciparum malaria in Thailand. Three hundred and fifty-two patients were randomly enroled at the ratio of 2:1 into group A:B and received Artecom (group A) and the standard combination of artesunate and mefloquine (group B) respectively. All patients had rapid initial clinical and parasitological responses. There were no significant differences in fever clearance time and parasite clearance time between the two groups. The 28-day cure rates were high as 97% in both groups. Artecom was effective and well-tolerated as artesunate-mefloquine, the current treatment in this area of multidrug-resistant P. falciparum malaria.

摘要

在泰国针对患有急性、非复杂性恶性疟原虫疟疾的成年人开展的一项开放性随机试验中,对Artecom的疗效和安全性进行了评估。352名患者按2:1的比例随机分为A组和B组,分别接受Artecom(A组)和青蒿琥酯与甲氟喹的标准联合用药(B组)。所有患者最初均有快速的临床和寄生虫学反应。两组之间的退热时间和寄生虫清除时间无显著差异。两组的28天治愈率均高达97%。Artecom与青蒿琥酯-甲氟喹(该地区目前用于治疗多重耐药恶性疟原虫疟疾的药物)一样有效且耐受性良好。

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