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葡糖胺锑钠治疗动物源性皮肤利什曼病的疗效。

Glucantime efficacy in the treatment of zoonotic cutaneous leishmaniasis.

作者信息

Pourmohammadi B, Motazedian M H, Handjani F, Hatam G H R, Habibi S, Sarkari B

机构信息

Department of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Southeast Asian J Trop Med Public Health. 2011 May;42(3):502-8.

Abstract

Pentavalent antimony (SbV) compounds are still considered the first line of treatment for all forms of leishmaniasis. There have been reports of drug resistance and unresponsiveness to treatment with these drugs. We investigated the clinical response to treatment of cutaneous leishmaniasis with glucantime, the drug of choice for all forms of leishmaniasis in Iran. All individuals suspected of cutaneous leishmaniasis from October 2007 to March 2008 were included in the study if met specific criteria. After laboratory diagnosis and parasite identification by PCR, 43 patients agreed to participate and complete the protocol for treatment. Meglumine antimoniate (glucantime) was given at a dose of 20 mg/kg/day for 20 days (two 10-day periods) according to a World Health Organization (WHO) recommended protocol. Response to treatment was evaluated 6 weeks after initiation of treatment. Fifteen patients (34.9%) were clinically unresponsive to glucantime treatment while the remaining 28 patients (65.1%) responded to treatment. There were no statistically significant differences by occupation, gender, chronicity of the disease before starting treatment, number of lesions, or age between the glucantime sensitive and resistant patients. Our study showed a significant level of unresponsiveness to glucantime among patients with cutaneous leishmaniasis caused by Leishmania major in Iran. These findings highlight the need for new treatment regimens.

摘要

五价锑(SbV)化合物仍被视为治疗所有类型利什曼病的一线药物。已有关于这些药物耐药性和治疗无反应性的报道。我们调查了使用葡糖胺锑(伊朗治疗所有类型利什曼病的首选药物)治疗皮肤利什曼病的临床反应。2007年10月至2008年3月期间,所有疑似皮肤利什曼病且符合特定标准的个体均纳入本研究。经实验室诊断并用聚合酶链反应(PCR)鉴定寄生虫后,43名患者同意参与并完成治疗方案。根据世界卫生组织(WHO)推荐的方案,按20mg/kg/天的剂量给予葡甲胺锑(葡糖胺锑),共20天(两个10天疗程)。治疗开始6周后评估治疗反应。15名患者(34.9%)对葡糖胺锑治疗无临床反应,其余28名患者(65.1%)对治疗有反应。在职业、性别、开始治疗前疾病的慢性程度、皮损数量或年龄方面,对葡糖胺锑敏感和耐药的患者之间无统计学显著差异。我们的研究表明,在伊朗,由硕大利什曼原虫引起的皮肤利什曼病患者中,对葡糖胺锑无反应的比例很高。这些发现凸显了对新治疗方案的需求。

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