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组胺H2受体阻滞剂引起的IgE介导的药物热。

IgE-mediated drug fever due to histamine H2-receptor blockers.

作者信息

Hiraide A, Yoshioka T, Ohshima S

机构信息

Department of Traumatology, Osaka University Medical School, Japan.

出版信息

Drug Saf. 1990 Nov-Dec;5(6):455-7. doi: 10.2165/00002018-199005060-00006.

Abstract

Drug-induced fever due to histamine H2-receptor blockers was experienced by a 55-year-old man. The patient became febrile 5 days after receiving cimetidine, and continued to be febrile until the drug was stopped. His maximum body temperature was above 40 degrees C. Challenge tests with cimetidine and ranitidine showed that the fever was caused by the H2-blocker. The patient's serum IgE concentration increased markedly to 2590 IU/ml 10 days after admission, and skin tests for cimetidine and ranitidine were positive. Lymphocyte stimulation tests were positive for both drugs (stimulation indices: 193% for cimetidine and 325% for ranitidine). Cimetidine-induced fever has generally been thought to be due to a direct effect on the thermoregulatory centre in the hypothalamus, on the basis of experimental studies of the injection of cimetidine to the cerebral ventricles. However, clinical evidence has not excluded an allergic involvement in this type of drug-induced fever. This patient's fever was proven to be due to administration of the H2-blocker, and the mechanism of action was IgE-mediated.

摘要

一名55岁男性出现了由组胺H2受体阻滞剂引起的药物性发热。该患者在接受西咪替丁治疗5天后发热,并持续发热直至停药。他的最高体温超过40摄氏度。用西咪替丁和雷尼替丁进行的激发试验表明,发热是由H2阻滞剂引起的。患者入院10天后血清IgE浓度显著升高至2590 IU/ml,西咪替丁和雷尼替丁的皮肤试验呈阳性。两种药物的淋巴细胞刺激试验均为阳性(刺激指数:西咪替丁为193%,雷尼替丁为325%)。基于向脑室注射西咪替丁的实验研究,西咪替丁引起的发热通常被认为是由于对下丘脑体温调节中枢的直接作用。然而,临床证据并未排除这种类型的药物性发热存在过敏因素。该患者的发热被证实是由于使用了H2阻滞剂,其作用机制是IgE介导的。

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