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用氨甲环酸治疗非遗传性血管性水肿。一项为期6个月的安慰剂对照试验,4年后进行随访。

Non-hereditary angioedema treated with tranexamic acid. A 6-month placebo controlled trial with follow-up 4 years later.

作者信息

Munch E P, Weeke B

出版信息

Allergy. 1985 Feb;40(2):92-7. doi: 10.1111/j.1398-9995.1985.tb02666.x.

Abstract

Ten patients with frequent attacks of non-hereditary angioedema were treated with tranexamic acid or placebo in a double blind manner, each period lasting 3 months. During the tranexamic acid period nine patients became symptom-free, or substantially improved, while one was unaffected (P less than 0.05). In four patients itching was a major accompanying complaint which was relieved in three. Diarrhoea and abdominal discomfort were more pronounced during tranexamic acid treatment (P less than 0.05), but only necessitated dose reduction in one patient. Four years later contact was obtained with eight of the nine responders and six were still taking tranexamic acid regularly, while in two patients the attacks were so infrequent that the drug was not taken regularly.

摘要

10例非遗传性血管性水肿频繁发作的患者,采用氨甲环酸或安慰剂进行双盲治疗,每个疗程持续3个月。在氨甲环酸治疗期间,9例患者症状消失或显著改善,1例无变化(P<0.05)。4例患者主要伴随瘙痒症状,其中3例症状缓解。氨甲环酸治疗期间腹泻和腹部不适更为明显(P<0.05),但仅1例患者需要减少剂量。4年后,9例有反应的患者中有8例取得联系,6例仍在规律服用氨甲环酸,2例发作频率很低,未规律服药。

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1
WAO Guideline for the Management of Hereditary Angioedema.WAO 遗传性血管性水肿管理指南。
World Allergy Organ J. 2012 Dec;5(12):182-99. doi: 10.1097/WOX.0b013e318279affa.

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