遗传性血管性水肿的未满足需求:一项国际医师调查。

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Thomas Buttgereit, Felix Aulenbacher, Adil Adatia, Carolina Vera Ayala, Maryam Ali Al-Nesf, Sabine Altrichter, Mohamed Abuzakouk, Mona Al-Ahmad, Ramzy Mohammed Ali, Alejandro Berardi, Isabelle Boccon-Gibod, Laurence Bouillet, Luisa Brussino, Marko Barešić, Paula J Busse, Stephen D Betschel, Herberto Chong-Neto, Oscar Calderón Llosa, Timothy J Craig, Anthony D Dorr, Sérgio Duarte Dortas Junior, Daria Fomina, Henriette Farkas, Jie Shen Fok, Anete S Grumach, Jens Greve, Mar Guilarte, Margarida Gonçalo, Vesna Grivcheva-Panovska, Michihiro Hide, Roman Hakl, Ankur Jindal, Constance H Katelaris, Shailajah Kamaleswaran, Tamar Kinaciyan, Elena Latysheva, José Ignacio Larco Sousa, Ramón Lleonart Bellfill, Hassan Mobayed, Martin Metz, Iman Nasr, Natasa T Mitrevska, Stefania Nicola, Claudio Alberto Salvador Parisi, Grzegorz Porebski, Jonny Peter, Mariana Paes Leme Ferriani, Nelson Rosario Filho, Bülent Enis Şekerel, Faradiba Sarquis Serpa, Marcin Stobiecki, Susanne Trainotti, Anna Valerieva, Chamard Wongsa, Jane C Y Wong, Esra Yucel, Yinglei Li, Chiara Nenci, Marcus Maurer, Markus Magerl, Philip H Li
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引用次数: 0

摘要

背景:遗传性血管性水肿(HAE)是一种罕见且可能危及生命的遗传性疾病,其特征是血管性水肿发作不可预测。MENTALIST(遗传性血管性水肿未满足需求——全球医生视角)是继世界过敏组织(WAO)/欧洲过敏与临床免疫学学会(EAACI) HAE指南最新更新后,首次发现HAE未满足需求并确定最佳管理障碍的国际调查。方法:这项基于网络的调查包括24个关于HAE管理和未满足需求的问题。来自血管水肿参考和卓越网络中心的hae专家医生根据他们自己的观点和患者的观点对未满足的需求进行排名,使用10分李克特量表,范围从0(没有挑战/未满足的需求)到10(巨大挑战/未满足的需求)。结果:来自32个国家的64名应答者中,大多数(91%)在HAE管理方面有50年的经验。总体而言,48%的受访者(n = 31/64)报告了以下结论:MENTALIST研究结果强调需要消除实现HAE治疗目标的障碍,并呼吁采取行动改善治疗可及性,为医生和患者提供更多教育,与患者组织和行业利益相关者进行关键合作,最终优化HAE治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unmet needs in hereditary angioedema: an international survey of physicians.

Background: Hereditary angioedema (HAE) is a rare and potentially life-threatening genetic disorder characterized by unpredictable attacks of angioedema. MENTALIST (UnMEt Needs in herediTAry angioedema-a gLobal physIcian perSpecTive) is the first international survey uncovering unmet needs and identifying barriers to optimal management in HAE following the latest update of the World Allergy Organization (WAO)/European Academy of Allergy and Clinical Immunology (EAACI) HAE guidelines.

Methods: This web-based survey comprised 24 questions on HAE management and unmet needs. HAE-expert physicians from the Angioedema Centers of Reference and Excellence network ranked unmet needs according to their own perspectives and their patients' perspectives, using a 10-point Likert scale ranging from 0 (not a challenge/unmet need at all) to 10 (huge challenge/unmet need).

Results: Of 64 respondents from 32 countries, most (91%) had > 5 years of experience in managing HAE. Overall, 48% of respondents (n = 31/64) reported that < 50% of their patients had achieved the WAO/EAACI HAE treatment goals of total disease control and "normalization" of life at the time of the survey. Implementation of consensus recommendations was found to be inconsistent across regions. Gaps in non-HAE-expert physician knowledge, treatment costs, and reimbursement for long-term prophylaxis were the highest-priority challenges according to the respondents. Burden of disease remains a challenge among patients, as reported by their physicians.

Conclusions: The MENTALIST findings highlight a need for removal of barriers to HAE treatment goals and propose a call to action to improve access to treatments, for greater provision of education for physicians and patients, critical collaboration with patient organizations and industry stakeholders and ultimately to optimize HAE care.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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