Betschel Stephen, Badiou Jacquie, Binkley Karen, Borici-Mazi Rozita, Hébert Jacques, Kanani Amin, Keith Paul, Lacuesta Gina, Waserman Susan, Yang Bill, Aygören-Pürsün Emel, Bernstein Jonathan, Bork Konrad, Caballero Teresa, Cicardi Marco, Craig Timothy, Farkas Henriette, Grumach Anete, Katelaris Connie, Longhurst Hilary, Riedl Marc, Zuraw Bruce, Berger Magdelena, Boursiquot Jean-Nicolas, Boysen Henrik, Castaldo Anthony, Chapdelaine Hugo, Connors Lori, Fu Lisa, Goodyear Dawn, Haynes Alison, Kamra Palinder, Kim Harold, Lang-Robertson Kelly, Leith Eric, McCusker Christine, Moote Bill, O'Keefe Andrew, Othman Ibraheem, Poon Man-Chiu, Ritchie Bruce, St-Pierre Charles, Stark Donald, Tsai Ellie
1University of Toronto, Toronto, ON Canada.
HAE Canada, Notre Dame des Lourdes, MB Canada.
Allergy Asthma Clin Immunol. 2019 Nov 25;15:72. doi: 10.1186/s13223-019-0376-8. eCollection 2019.
This is an update to the 2014 Canadian Hereditary Angioedema Guideline with an expanded scope to include the management of hereditary angioedema (HAE) patients worldwide. It is a collaboration of Canadian and international HAE experts and patient groups led by the Canadian Hereditary Angioedema Network. The objective of this guideline is to provide evidence-based recommendations, using the GRADE system, for the management of patients with HAE. This includes the treatment of attacks, short-term prophylaxis, long-term prophylaxis, and recommendations for self-administration, individualized therapy, quality of life, and comprehensive care. New to the 2019 version of this guideline are sections covering the diagnosis and recommended therapies for acute treatment in HAE patients with normal C1-INH, as well as sections on pregnant and paediatric patients, patient associations and an HAE registry. Hereditary angioedema results in random and often unpredictable attacks of painful swelling typically affecting the extremities, bowel mucosa, genitals, face and upper airway. Attacks are associated with significant functional impairment, decreased health-related quality of life, and mortality in the case of laryngeal attacks. Caring for patients with HAE can be challenging due to the complexity of this disease. The care of patients with HAE in Canada, as in many countries, continues to be neither optimal nor uniform. It lags behind some other countries where there are more organized models for HAE management, and greater availability of additional licensed therapeutic options. It is anticipated that providing this guideline to caregivers, policy makers, patients, and advocates will not only optimize the management of HAE, but also promote the importance of individualized care. The primary target users of this guideline are healthcare providers who are managing patients with HAE. Other healthcare providers who may use this guideline are emergency and intensive care physicians, primary care physicians, gastroenterologists, dentists, otolaryngologists, paediatricians, and gynaecologists who will encounter patients with HAE and need to be aware of this condition. Hospital administrators, insurers and policy makers may also find this guideline helpful.
这是对2014年《加拿大遗传性血管性水肿指南》的更新,范围有所扩大,涵盖全球遗传性血管性水肿(HAE)患者的管理。它是由加拿大遗传性血管性水肿网络牵头,加拿大和国际HAE专家及患者团体合作完成的。本指南的目的是使用GRADE系统,为HAE患者的管理提供基于证据的建议。这包括发作的治疗、短期预防、长期预防,以及自我给药、个体化治疗、生活质量和综合护理的建议。2019年版本指南新增了关于C1-INH正常的HAE患者急性治疗的诊断和推荐疗法的章节,以及关于孕妇和儿科患者、患者协会和HAE登记处的章节。遗传性血管性水肿会导致随机且通常不可预测的疼痛性肿胀发作,通常影响四肢、肠道黏膜、生殖器、面部和上呼吸道。发作会导致严重的功能障碍、健康相关生活质量下降,喉部发作时还会导致死亡。由于这种疾病的复杂性,护理HAE患者可能具有挑战性。在加拿大,如同在许多国家一样,对HAE患者的护理既不理想也不统一。它落后于其他一些国家,在这些国家有更有组织的HAE管理模式,并且有更多额外的获批治疗选择可供使用。预计向护理人员、政策制定者、患者和倡导者提供本指南不仅将优化HAE的管理,还将促进个体化护理的重要性。本指南的主要目标用户是管理HAE患者的医疗保健提供者。其他可能使用本指南的医疗保健提供者包括急诊科和重症监护医生、初级保健医生、胃肠病学家、牙医、耳鼻喉科医生、儿科医生和妇科医生,他们会遇到HAE患者,需要了解这种疾病。医院管理人员、保险公司和政策制定者也可能会发现本指南很有帮助。