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单剂量强力霉素联合乙胺嗪治疗班氏丝虫病。

A single dose of doxycycline in combination with diethylcarbamazine for treatment of bancroftian filariasis.

作者信息

Sanprasert Vivornpun, Sujariyakul Anupong, Nuchprayoon Surang

机构信息

Lymphatic Filariasis Research Unit, Department of Parasitology, Chulalongkorn University, Bangkok, Thailand.

出版信息

Southeast Asian J Trop Med Public Health. 2010 Jul;41(4):800-12.

Abstract

Standard treatment of lymphatic filariasis with diethylcarbamazine (DEC) is associated with systemic adverse reactions, thought to be due to the release of microfilariae material and Wolbachia endosymbiotic bacteria into the blood. Combination treatments with doxycycline for 3-8 weeks are more effective than standard treatment. However, long-term use of antibiotics may contribute to drug resistance and are not practical for use in remote areas. We assessed whether a single dose of doxycycline combined with the standard DEC regimen would reduce the incidence and severity of adverse reactions and increase the efficacy of standard treatment. Forty-four subjects from Tak Province were recruited into the randomized double-blind clinical trial study: 25 received DEC (300 mg) combined with a placebo, and 19 received DEC (300 mg) combined with doxycycline (200 mg). The incidences of adverse reactions to standard treatment were lower in the doxycycline group (45.5%) than in the placebo group (58.8%). Severe reactions occurred only in the placebo group (3 of 25 subjects). The severity of adverse reactions was significantly lower in the doxycycline group (mean score 0.45) than in the placebo group (mean score 1.17). The levels of IL-6 and Wolbachia DNA in the plasma were significantly lower in the doxycycline group. The filarial antigen levels were significantly lower in the doxycycline group at months 6 after treatment.

摘要

用乙胺嗪(DEC)对淋巴丝虫病进行标准治疗会引发全身不良反应,据认为这是由于微丝蚴物质和沃尔巴克氏体共生菌释放到血液中所致。用强力霉素进行3 - 8周的联合治疗比标准治疗更有效。然而,长期使用抗生素可能会导致耐药性,并且在偏远地区使用并不实际。我们评估了单剂量强力霉素与标准DEC疗法联合使用是否会降低不良反应的发生率和严重程度,并提高标准治疗的疗效。来自Tak省的44名受试者被纳入随机双盲临床试验研究:25人接受DEC(300毫克)加安慰剂,19人接受DEC(300毫克)加强力霉素(200毫克)。强力霉素组对标准治疗的不良反应发生率(45.5%)低于安慰剂组(58.8%)。严重反应仅发生在安慰剂组(25名受试者中有3人)。强力霉素组不良反应的严重程度(平均评分0.45)明显低于安慰剂组(平均评分1.17)。强力霉素组血浆中白细胞介素-6和沃尔巴克氏体DNA水平明显较低。治疗后6个月,强力霉素组的丝虫抗原水平明显较低。

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