Faisant Charles, Armengol Guillaume, Bouillet Laurence, Boccon-Gibod Isabelle, Villier Céline, Lévesque Hervé, Cottin Judith, Massy Nathalie, Benhamou Ygal
Internal Medicine Department, Grenoble University Hospital, Grenoble, France.
Grenoble Alps University, Grenoble, France.
J Clin Immunol. 2016 Jan;36(1):95-102. doi: 10.1007/s10875-015-0228-3. Epub 2015 Dec 28.
Bradykinin-mediated angioedema (AE) is a rare side effect of some medications, including angiotensin converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARB). In France, side-effects to treatments are reported to the national pharmacovigilance database.
The national MedDRA database was searched using the term "angioedema". Patients were included if they met the clinical criteria corresponding to bradykinin-mediated AE, if their C1-inhibitor levels were normal, and if they were treated with an ACEi or an ARB.
7998 cases of AE were reported between 1994 and 2013. Among these, 112 met the criteria for bradykinin-mediated AE with normal C1-inhibitor levels. On the 112 drug-AE, patients were treated with an ARB in 21% of cases (24 patients), or an ACEi in 77% of cases (88 patients), in combination with another treatment in 17 cases (mTORi for 3 patients, iDPP-4 for 1 patient, hormonal treatment for 7 patients). ENT involvement was reported in 90% of cases (tongue: 48.2%, larynx: 23.2%). The median duration of treatment before the first attack was 720 days, and the mean duration of attacks was 36.6 h. Forty-one percent (19/46) of patients relapsed after discontinuing treatment.
Angioedema triggered by medication blocking the renin/angiotensin system is rare but potentially severe, with a high risk of recurrence despite cessation of the causative drug.
缓激肽介导的血管性水肿(AE)是某些药物(包括血管紧张素转换酶抑制剂(ACEi)和血管紧张素受体阻滞剂(ARB))的一种罕见副作用。在法国,治疗的副作用会上报至国家药物警戒数据库。
使用术语“血管性水肿”搜索国家MedDRA数据库。若患者符合缓激肽介导的AE的临床标准、C1抑制剂水平正常且接受了ACEi或ARB治疗,则纳入研究。
1994年至2013年间共报告了7998例AE病例。其中,112例符合缓激肽介导的AE且C1抑制剂水平正常的标准。在这112例药物性AE中,21%的病例(24例患者)接受了ARB治疗,77%的病例(88例患者)接受了ACEi治疗,17例患者同时接受了其他治疗(3例患者接受了mTORi治疗,1例患者接受了iDPP-4治疗,7例患者接受了激素治疗)。90%的病例报告有耳鼻喉受累(舌头:48.2%,喉部:23.2%)。首次发作前的中位治疗持续时间为720天,发作的平均持续时间为36.6小时。41%(19/46)的患者在停药后复发。
由阻断肾素/血管紧张素系统的药物引发的血管性水肿虽罕见但可能很严重,尽管停用了致病药物,但复发风险仍很高。