Riha Heidi M, Summers Bryant B, Rivera Jessica V, Van Berkel Megan A
Department of Pharmacy, Erlanger Health System, Chattanooga, Tennessee.
Department of Pharmacy, Henry Ford Hospital, Detroit, Michigan.
J Emerg Med. 2017 Nov;53(5):662-679. doi: 10.1016/j.jemermed.2017.05.037. Epub 2017 Sep 20.
Angiotensin-converting enzyme inhibitor (ACEI)-induced angioedema can occur at any point during therapy and, when severe, can require mechanical ventilation. Standard agents for anaphylactic reactions have limited efficacy for bradykinin-mediated angioedema and, therefore, agents approved for hereditary angioedema are increasingly prescribed for these patients.
This systematic review critically evaluates evidence describing the off-label use of fresh frozen plasma (FFP), prothrombin complex concentrate (PCC), complement 1 esterase inhibitor (C1-INH), icatibant, and ecallantide for treatment of ACEI-induced angioedema.
A PubMed search was conducted and articles were cross-referenced for additional citations. All full-text clinical trials, case series, and case reports published in the English language describing pharmacologic treatment of ACEI-induced angioedema were included. Thirty-seven publications detailing FFP, PCC, and regimens approved for hereditary angioedema, including icatibant, ecallantide, and C1-INH, are reviewed extensively.
While findings of decreased time to symptom resolution or a cessation in symptom progression have been reported with each of these therapies, additional data showing clinically relevant implications, such as reduced intensive care unit length of stay or avoidance of mechanical ventilation, are warranted, especially when taking cost into consideration. FFP has limited evidence demonstrating a benefit for treatment of ACEI-induced angioedema without consistent dosing strategies. However, given its wide availability and low potential for adverse reactions, FFP therapy may be reasonable. Of the novel agents traditionally used for hereditary angioedema, icatibant has the highest level of evidence and has been reported to be successful in limiting the progression of angioedema.
血管紧张素转换酶抑制剂(ACEI)诱发的血管性水肿可在治疗过程中的任何时间发生,严重时可能需要机械通气。用于过敏反应的标准药物对缓激肽介导的血管性水肿疗效有限,因此,越来越多地为这些患者开具获批用于遗传性血管性水肿的药物。
本系统综述严格评估了描述新鲜冷冻血浆(FFP)、凝血酶原复合物浓缩物(PCC)、补体1酯酶抑制剂(C1-INH)、依卡替班和艾卡拉肽用于治疗ACEI诱发的血管性水肿的非适应证使用证据。
进行了PubMed检索,并交叉引用文章以获取更多参考文献。纳入了所有以英文发表的描述ACEI诱发的血管性水肿药物治疗的全文临床试验、病例系列和病例报告。广泛综述了37篇详细介绍FFP、PCC以及获批用于遗传性血管性水肿的治疗方案(包括依卡替班、艾卡拉肽和C1-INH)的出版物。
虽然已报道这些疗法中的每一种都能缩短症状缓解时间或停止症状进展,但仍需要更多数据来显示其临床相关意义,如缩短重症监护病房住院时间或避免机械通气,尤其是在考虑成本时。FFP治疗ACEI诱发的血管性水肿的获益证据有限,且给药策略不一致。然而,鉴于其广泛可得且不良反应可能性低,FFP治疗可能是合理的。在传统用于遗传性血管性水肿的新型药物中,依卡替班的证据水平最高,据报道可成功限制血管性水肿的进展。