Department of Internal Neurology, Tianjin Huanhu Hospital, Tianjin, China.
Eur Rev Med Pharmacol Sci. 2018 Mar;22(5):1478-1484. doi: 10.26355/eurrev_201803_14496.
Orolingual angioedema (OA) is a rare clinical complication with a potentially fatal risk that occurs after the intravenous application of alteplase (rt-PA) in patients with acute ischemic stroke. The purpose of this work is to investigate the related factors of OA in patients with acute ischemic stroke after the administration of intravenous thrombolytic therapy, to improve the predictive ability of OA during intravenous thrombolytic therapy, and to reduce the prevalence of complications.
We recruited 1223 cases of patients with acute ischemic stroke that were treated in the Department of Neurology No. 4 of the Tianjin Huanhu Hospital from June 2014 to April 2015. The clinical manifestations of rt-PA related OA were recorded, the clinical prevalence was counted, related factors of OA after intravenous thrombolytic therapy were analyzed, and the risk assessment of rt-PA related OA was conducted.
14 cases of patients developed OA, with a prevalence rate of 1.14%. Among them, 5 had a history of urticaria, 4 of drug allergy, and 3 of food allergy. Among the 14 cases of patients, 10 developed OA in the process of intravenous thrombolysis and 4 after intravenous thrombolysis, 12 showed lip edema, 9 showed extensive swelling of tongue, 3 showed swelling of lateral tongue, 3 were complicated by respiratory distress, 10 showed infarction in the middle cerebral artery territory, and 6 had previously been given oral ACEI drugs.
Orolingual angioedema is a rare complication that occurs after rt-PA intravenous thrombolytic therapy; when serious, it may endanger a patient's life. If patients take an oral hypotension such as ACEI drugs before the onset of OA, they have a history of allergies, or the lesion is an infraction in the dominated area of the middle cerebral artery, the risk of OA after rt-PA intravenous thrombolytic therapy will be increased. The prevalence of OA should be monitored during the rt-PA intravenous thrombolytic therapy process; timely detection and early intervention should be conducted, which can avoid serious adverse consequences.
血管性水肿是一种罕见的临床并发症,具有潜在的致命风险,在急性缺血性脑卒中患者中静脉应用阿替普酶(rt-PA)后会发生。本研究旨在探讨急性缺血性脑卒中患者静脉溶栓治疗后发生血管性水肿的相关因素,提高 rt-PA 相关血管性水肿的预测能力,降低并发症的发生率。
本研究纳入了 2014 年 6 月至 2015 年 4 月在天津市环湖医院神经内科 4 病区治疗的 1223 例急性缺血性脑卒中患者。记录 rt-PA 相关血管性水肿的临床表现,统计临床发病率,分析静脉溶栓治疗后发生血管性水肿的相关因素,并进行 rt-PA 相关血管性水肿风险评估。
14 例患者发生血管性水肿,发病率为 1.14%。其中,5 例有荨麻疹病史,4 例有药物过敏史,3 例有食物过敏史。14 例患者中,10 例在静脉溶栓过程中发生血管性水肿,4 例在静脉溶栓后发生血管性水肿,12 例表现为唇部水肿,9 例表现为舌广泛肿胀,3 例表现为侧舌肿胀,3 例伴有呼吸困难,10 例表现为大脑中动脉分布区梗死,6 例患者在发病前曾服用口服 ACEI 类药物。
血管性水肿是 rt-PA 静脉溶栓治疗后罕见的并发症,严重时可能危及患者生命。如果患者在发生血管性水肿前服用 ACEI 类等口服降压药、有过敏史或病变为大脑中动脉优势区梗死,rt-PA 静脉溶栓治疗后发生血管性水肿的风险会增加。在 rt-PA 静脉溶栓治疗过程中应监测血管性水肿的发病率;及时发现并早期干预,可以避免严重的不良后果。