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阿苯达唑和乙胺嗪治疗人体弓蛔虫病疗效的回顾性研究

A Retrospective Study of the Efficacy of Albendazole and Diethylcarbamazine for the Treatment of Human Toxocariasis.

作者信息

Magnaval Jean-François, Fillaux Judith, Berry Antoine

机构信息

Service de Parasitologie Médicale, Faculté de Médecine, Université de Toulouse III, 37 allées Jules-Guesde, 31000 Toulouse, France.

Service de Parasitologie-Mycologie, Hôpital Purpan, Centre Hospitalier Universitaire de Toulouse, 330 avenue de Grande-Bretagne, 31059 Toulouse, France.

出版信息

Pathogens. 2022 Jul 20;11(7):813. doi: 10.3390/pathogens11070813.

Abstract

In the Department of Parasitology and Mycology of Toulouse University Hospitals, patients presenting with common/covert toxocariasis were treated either with albendazole (39 cases) or with diethylcarbamazine (32 cases). Albendazole (ABZ) was given at 10 mg/kg b/w daily for 14 days, and diethylcarbamazine (DEC) was given at 4 mg/kg b/w daily for 21 days. In both groups, follow-up consultations occurred approximately 48 days after the end of the anthelmintic therapy. ABZ and DEC displayed a similar efficacy on the kinetics of the clinical picture (-64.5% of reduction vs. -72.7%, respectively) and on the levels of blood eosinophilia, serum eosinophil cationic protein and serum total IgE. However, the effect of the medication on the laboratory parameters was moderate. The rate of adverse reactions was similar in both groups (38% for ABZ vs. 31% for DEC), but DEC-treated patients complained of more intense and long-lasting side effects. The DEC group had more major adverse reactions, resulting in the termination of the anthelmintic treatment. The results from this retrospective study bring further arguments for considering ABZ, given at 10 mg/kg daily for 2 weeks, as the drug of choice in the treatment of human toxocariasis.

摘要

在图卢兹大学医院的寄生虫学和真菌学系,对患有常见/隐性弓蛔虫病的患者分别采用阿苯达唑(39例)或乙胺嗪(32例)进行治疗。阿苯达唑(ABZ)按每日10 mg/kg体重给药,持续14天;乙胺嗪(DEC)按每日4 mg/kg体重给药,持续21天。两组均在驱虫治疗结束后约48天进行随访咨询。ABZ和DEC在临床症状的变化动力学方面显示出相似的疗效(分别降低64.5%和72.7%),在血液嗜酸性粒细胞水平、血清嗜酸性粒细胞阳离子蛋白和血清总IgE方面也是如此。然而,药物对实验室参数的影响中等。两组的不良反应发生率相似(ABZ组为38%,DEC组为31%),但接受DEC治疗的患者抱怨副作用更强烈且持续时间更长。DEC组有更多严重不良反应,导致驱虫治疗终止。这项回顾性研究的结果为将每日10 mg/kg体重给药2周的ABZ作为治疗人类弓蛔虫病的首选药物提供了进一步的依据。

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