遗传性血管性水肿的疾病负担:魁北克法裔加拿大人调查的启示

IF 3.5 3区 医学 Q2 IMMUNOLOGY Journal of Immunology Research Pub Date : 2024-03-07 DOI:10.1155/2024/3028617
Jean-Nicolas Boursiquot, Hugo Chapdelaine, Charles St-Pierre, Jacques Hébert
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引用次数: 0

摘要

背景。有关加拿大人遗传性血管性水肿(HAE)的临床概况和疾病负担的数据十分有限。目的。本研究旨在评估患有 HAE I 型、II 型和 C1 抑制剂(nC1-INH)水平正常的加拿大人的 HAE 疾病特征和疾病负担。材料与方法。HAE 患者组织 Angio-oédeme héréditaire du Québec 于 2019 年 5 月至 2020 年 2 月在加拿大魁北克省开展并传播了一项包含 46 个项目的患者调查,以评估临床特征和疾病负担。调查获得了研究审查委员会的伦理批准。调查结果显示在 35 名受访者中,最常见的是 HAE I 型(46%),其次是 nC1-INH(43%)。女性受访者首次出现症状时的年龄明显小于男性()。在确诊之前,69% 的参与者接受了不必要的治疗和手术,从首次出现症状到确诊之间的时间延迟了 10 年。在开始目前的治疗之前,42% 的参与者每周都会发作一次 HAE。大多数参与者认为发作部位在腹部(89%),其次是喉部(66%)、足部(66%)、手部(63%)和面部(63%)。大多数发作为重度或中度,但几乎有一半的患者在最后一次去急诊科(ED)就诊时等待了>1小时才得到治疗。HAE与健康相关的生活质量下降有关,导致个人和职业生活功能严重受损。与HAE I/II型相比,HAE nC1-INH型患者更常使用氨甲环酸进行长期预防性治疗,但病情控制较差,导致发作次数和急诊就诊次数增加。结论HAE在这一患者群体中表现为频繁的中重度发作和较高的疾病负担;HAE亚型可能会对护理要求产生不同的影响。治疗医生迫切需要加强对 HAE 的认识和教育。
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The Disease Burden of Hereditary Angioedema: Insights from a Survey in French-Canadians from Quebec
Background. Limited data are available on the clinical profile and disease burden of hereditary angioedema (HAE) in Canadians. Objective. This study aimed to assess HAE disease characteristics and the burden of disease in Canadians with HAE types I, II, and normal levels of C1 inhibitor (nC1-INH). Materials and Methods. A 46-item patient survey evaluating clinical characteristics and burden of disease was developed and disseminated by the HAE patient organization Angio-oédeme héréditaire du Québec in Quebec, Canada, from May 2019 to February 2020. The survey received Research Review Board ethics approval. Results. In the 35 respondents, HAE type I was the most common (46%), followed by nC1-INH (43%). Female participants were significantly younger at first symptom presentation than males (). Prior to diagnosis, 69% of participants underwent unnecessary treatments and procedures, with a 10-year delay between first symptoms and diagnosis. Before starting the current treatment, 42% of participants experienced weekly HAE attacks. Most participants identified experiencing attacks in the abdomen (89%), followed by the larynx (66%), feet (66%), hands (63%), and face (63%). Most attacks were severe or moderate, yet almost half of patients waited >1 hr before getting medical attention at their last emergency department (ED) visit. HAE was associated with decreased health-related quality of life, leading to significant functional impairment in personal and professional life. As compared to HAE type I/II, patients with HAE nC1-INH were treated more often with tranexamic acid for long-term prophylaxis, and their condition was less controlled, resulting in more attacks and ED visits. Conclusion. HAE manifests in this patient population as frequent moderate-to-severe attacks and a high disease burden; the HAE subtype may differentially affect care requirements. There is an urgent need for increased awareness and education on HAE among treating physicians.
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来源期刊
CiteScore
6.90
自引率
2.40%
发文量
423
审稿时长
15 weeks
期刊介绍: Journal of Immunology Research is a peer-reviewed, Open Access journal that provides a platform for scientists and clinicians working in different areas of immunology and therapy. The journal publishes research articles, review articles, as well as clinical studies related to classical immunology, molecular immunology, clinical immunology, cancer immunology, transplantation immunology, immune pathology, immunodeficiency, autoimmune diseases, immune disorders, and immunotherapy.
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