ACE-inhibitor–related angioedema

N. Chan, A. Soliman
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引用次数: 1

Abstract

Otolaryngologists are called upon frequently to care for patients with potentially life-threatening angioedema. This condition usually is associated with angiotensin-converting enzyme (ACE) inhibitors. ACE inhibitors are among the most commonly prescribed medications worldwide because they are indicated in the management of hypertension, congestive heart failure, myocardial infarction, diabetic nephropathy, and chronic kidney disease.1,2 Angioedema is a potentially life-threatening adverse effect of ACE inhibitors, with a reported incidence of 0.1 to 6%.2-8 ACE-inhibitor-related angioedema is asymmetric, nonpitting, non tender edema that can appear anywhere in the body but commonly affects the head and neck area.' Otolaryngologists should be familiar with this drug class and its potential complications. ACE-inhibitor-related angioedema is not a true allergy but is considered an adverse class effect secondary to the mechanism of action. 2,4,s-1O The proposed pathophysiologic mechanism is the accumulation of bradykinin secondary to the inhibition of ACE.2,4,S However, this cannot explain how ACE-inhibitor-related angioedema can occur anytime from hours to deft ient h dth di ti 3411-13 cades a er a patient as starte e me lca IOn. ' , About a quarter of patients with ACE-inhibitor-related angioedema present within 1 week of starting the medication." On the other end of the spectrum, approximately half present after having been on the medication for at least a year," This may be explained by the fact that in the setting of ACE inhibition, aminopeptidase P (APP) and dipeptidyl peptidase 4 (DPP4) become responsible for breaking down the vasoactive peptides bradykinin and substance P, respectively." Factors adversely affecting these enzymes may trigger angioedema. 14 Female gender, African-American descent, and tobacco use are risk factors for the development of ACEinhibitor-related angioedema.3.4.6,7,14 Certain atopic diseases, such as seasonal allergies and asthma, may also be risk factors.Y'":" On the other hand, diabetes mellitus is possibly associated with a decreased risk because diabetic patients appear to have increased DPP4 activity to aid in the breakdown of substance p' ,14,IS Currently, no laboratory test exists to confirm the
ACE-inhibitor-related血管性水肿
耳鼻喉科医生经常被要求照顾可能危及生命的血管性水肿患者。这种情况通常与血管紧张素转换酶(ACE)抑制剂有关。ACE抑制剂是世界范围内最常用的处方药之一,因为它们适用于高血压、充血性心力衰竭、心肌梗死、糖尿病肾病和慢性肾病的治疗。血管性水肿是ACE抑制剂潜在的危及生命的不良反应,据报道发生率为0.1 - 6%。2-8 ace抑制剂相关性血管性水肿是一种不对称、无凹陷、无压痛性水肿,可出现在身体的任何部位,但通常影响头部和颈部。耳鼻喉科医生应该熟悉这类药物及其潜在的并发症。ace抑制剂相关性血管性水肿不是真正的过敏,但被认为是次于作用机制的不良反应。2,4,S - 10提出的病理生理机制是迟缓激肽的积累继发于ace的抑制。2,4,S然而,这并不能解释为什么ace抑制剂相关的血管性水肿可以在患者开始服用ace后的几小时至几分钟内的任何时间发生。约四分之一的ace抑制剂相关性血管性水肿患者在开始用药一周内出现。另一方面,大约一半的患者在服用药物至少一年后出现,“这可能是由于在ACE抑制的情况下,氨基肽酶P (APP)和二肽基肽酶4 (DPP4)分别负责分解血管活性肽缓动肽和P物质。”影响这些酶的不利因素可能引发血管性水肿。女性、非裔美国人后裔和吸烟是发生乙酰胆碱抑制剂相关血管性水肿的危险因素。某些特应性疾病,如季节性过敏和哮喘,也可能是危险因素。另一方面,糖尿病可能与风险降低有关,因为糖尿病患者似乎有增加的DPP4活性,以帮助物质p的分解,目前还没有实验室测试来证实这一点
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