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切换至艾卡替班特治疗高疾病活动度遗传性血管性水肿患者:病例报告。

Switch to icatibant in a patient affected by hereditary angioedema with high disease activity: a case report.

出版信息

Int J Immunopathol Pharmacol. 2012 Jan-Mar;25(1):269-73. doi: 10.1177/039463201202500130.

Abstract

Icatibant, an antagonist of the bradykinin B2 receptor, was approved for the treatment of acute attacks of hereditary angioedema in the EU in 2008. This paper presents the case of a 65-year-old woman affected by frequent acute attacks of hereditary angioedema who benefitted from a change of therapy to icatibant, following years of treatment with C1-inhibitor.

摘要

伊卡替班,缓激肽 B2 受体拮抗剂,于 2008 年在欧盟被批准用于治疗遗传性血管性水肿的急性发作。本文报告了一例 65 岁女性患者,她常患有遗传性血管性水肿的急性发作,在使用 C1 抑制剂治疗多年后,改用伊卡替班治疗后获益。

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