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[在治疗突眼性甲状腺肿中可归因于卡比马唑的意外情况]

[Accidents attributable to carbimazole in the treatment of Basedow's disease].

作者信息

Le Guerrier A M, Lorcy Y, Allannic H

出版信息

Ann Endocrinol (Paris). 1984;45(6):381-5.

PMID:6549531
Abstract

A series of 365 patients (330 women, 35 men) followed up for 9 years during treatment with 20 to 70 mg/day of carbimazole for an average duration of 18 months (range: 2 months to 6 years) was analyzed to evaluate frequency and type of accidents imputable to this synthetic antithyroid agent. Etiopathogenicity of these incidents is reviewed based on reports in the published literature. The product was extremely well tolerated by 349 patients. Minor side effects (hematologic in 0,8%, cutaneous in 1,4% and digestive in 1,6% of cases) were reported in 14 cases (3,8% of cases) and interruption of carbimazole treatment was necessary in 7 of these patients. Major accidents of favorable outcome (Lyell's syndrome, agranulocytosis) were observed in 2 patients (0,6% of cases). Two hypotheses can be evoked to explain their origin: a toxic cause mainly for the hematologic complication or an immuno-allergic mechanism suggested by the rapid onset of complications after beginning treatment. Carbimazole should not, therefore, be considered as a product lacking risks and the accidents observed strongly suggest the need for biological and particularly strict clinical surveillance of patients treated, the appearance of any sign of infection necessitating immediate full and differential blood counts and discontinuation of all therapy.

摘要

对365例患者(330例女性,35例男性)进行了为期9年的随访分析,这些患者在接受20至70毫克/天的卡比马唑治疗期间,平均疗程为18个月(范围:2个月至6年),以评估这种合成抗甲状腺药物所致不良反应的频率和类型。基于已发表文献中的报告,对这些事件的病因进行了综述。349例患者对该产品耐受性极佳。14例患者(占病例的3.8%)报告了轻微副作用(血液学副作用占0.8%,皮肤副作用占1.4%,消化系统副作用占1.6%),其中7例患者需要中断卡比马唑治疗。观察到2例患者(占病例的0.6%)出现了转归良好的严重不良反应(中毒性表皮坏死松解症、粒细胞缺乏症)。可以提出两种假设来解释其病因:血液学并发症主要由毒性原因引起,或者治疗开始后并发症迅速出现提示存在免疫过敏机制。因此,不应认为卡比马唑是一种无风险的产品,所观察到的不良反应强烈提示需要对接受治疗的患者进行生物学监测,尤其是严格的临床监测,出现任何感染迹象都需要立即进行全面和分类血常规检查,并停止所有治疗。

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