Idiopathic non-mast cell angioedema: Treatment insights from global experts.

IF 2.6 3区 医学 Q2 ALLERGY
Sandra C Christiansen, Bruce L Zuraw
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引用次数: 0

Abstract

Background: Idiopathic non-mast cell angioedema (INMA) is a rare disease typified by recurrent attacks of cutaneous and subcutaneous swelling. Every attack carries the potential for severe morbidity and, in the case of laryngeal involvement, mortality. Whereas therapies approved for hereditary angioedema (HAE) have been used in the care of patients with INMA, little is known with regard to their efficacy for the treatment of this disease. Objective: The objective was to gather evidence from global experts, ranking their assessment of on-demand therapy (ODT) and long-term prophylactic (LTP) treatment efficacy for INMA. Methods: A survey was developed and distributed to international experts invited to attend a 2023 symposium. INMA was diagnosed by standardized criteria. Linkert scales were used to rate the efficacy for ODT and LTP therapy. Enrollment was closed after 1 month and the data were analyzed. Results: Surveys were distributed to 31 experts from 16 countries with a 77% response rate (n = 24) reporting on 300 patients with INMA. Efficacy rankings of ODT were the following: icatibant (14 experts with 93 treated patients), 46.2% high and 38.7% moderate; and plasma-derived C1 inhibitor (C1INH) (13 experts with 31 treated patients), 32.3% moderate and 45.2% mild. Efficacy rankings of LTP were the following: antifibrinolytics (11 experts with 52 treated patients), 23.1% high and 38.5% moderate; lanadelumab (5 experts with 19 treated patients), 21% high and 79% moderate; and subcutaneous C1INH (3 experts with 19 treated patients), 21.1% moderate and 79.0% mild. LTP efficacy was also recorded for berotralstat and progestin. Conclusion: Icatibant (ODT) and either antifibrinolytics or lanadelumab (LTP) were ranked as the most efficacious treatments for the patients with INMA (among medications with at least five treated patients) by the expert physicians. Progestins, berotralstat, and plasma derived C1INH each demonstrated a favorable prophylactic effect; however, broader experience will be required to formulate overall recommendations.

特发性非肥大细胞血管性水肿:全球专家的治疗见解。
背景:特发性非肥大细胞血管性水肿(INMA)是一种罕见的疾病,以反复发作的皮肤和皮下肿胀为特征。每次发作都有可能导致严重的发病率,在喉部受累的情况下,可能导致死亡。尽管已批准用于遗传性血管性水肿(HAE)的治疗方法已用于INMA患者的护理,但对其治疗该病的疗效知之甚少。目的:目的是收集来自全球专家的证据,对他们对INMA的按需治疗(ODT)和长期预防(LTP)治疗效果的评估进行排名。方法:对受邀参加2023年研讨会的国际专家进行问卷调查。通过标准化标准诊断INMA。采用Linkert量表评价ODT和LTP治疗的疗效。1个月后停止入组,并对数据进行分析。结果:来自16个国家的31位专家对300例INMA患者进行了问卷调查,应答率为77% (n = 24)。ODT疗效排名:伊卡止咳(14名专家93例),高46.2%,中38.7%;血浆源性C1抑制剂(C1INH)(13位专家,31例治疗患者),中度32.3%,轻度45.2%。LTP疗效排名如下:抗纤溶药物(11名专家,52例患者),高效23.1%,中效38.5%;Lanadelumab(5名专家,19名接受治疗的患者),21%高,79%中;皮下C1INH(专家3人,治疗患者19例),中度21.1%,轻度79.0%。贝曲司他和黄体酮的LTP疗效也被记录。结论:依卡替班特(ODT)和抗纤溶药物或lanadelumab (LTP)被专家医师评为治疗INMA患者最有效的治疗方法(至少有5例患者接受治疗的药物)。黄体酮、贝曲司他和血浆源性C1INH均显示出良好的预防作用;但是,需要更广泛的经验来拟订通盘建议。
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来源期刊
CiteScore
5.70
自引率
35.70%
发文量
106
审稿时长
6-12 weeks
期刊介绍: Allergy & Asthma Proceedings is a peer reviewed publication dedicated to distributing timely scientific research regarding advancements in the knowledge and practice of allergy, asthma and immunology. Its primary readership consists of allergists and pulmonologists. The goal of the Proceedings is to publish articles with a predominantly clinical focus which directly impact quality of care for patients with allergic disease and asthma. Featured topics include asthma, rhinitis, sinusitis, food allergies, allergic skin diseases, diagnostic techniques, allergens, and treatment modalities. Published material includes peer-reviewed original research, clinical trials and review articles.
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