Bowen Tom, Hebert Jacques, Ritchie Bruce, Burnham Jeanne, MacSween Mike, Warrington Richard, Yang William, Issekutz Andrew, Karitsiotis Nick, McCombie Nancy, Giulivi Tony
The Canadian Hereditary, Angioedema Society (CHAES)/ Société d'angioédème héréditaire du Canada, Canada.
Transfus Apher Sci. 2003 Dec;29(3):205-14. doi: 10.1016/j.transci.2003.08.009.
C1 esterase inhibitor (C1-INH) deficiency is a rare disorder that lacks consensus for diagnosis therapy and management. Recognizing that Canada is behind the European approach to this disorder, we have formed the Canadian Hereditary Angioedema Society (CHAES)/Société d'angioédème héréditaire du Canada (SAHC) to foster knowledge of this disorder in Canada and to advance care of patients with this disorder in Canada. We here present a review of treatment of this disorder in Canada including prevention of angioedema events and use of replacement therapy and present an algorithm for diagnosis therapy and management of C1-INH deficiency in Canada for discussion at our International Conference on Hereditary Angioedema to be held in Toronto, Canada, October 24th to 26th, 2003.
C1酯酶抑制剂(C1-INH)缺乏症是一种罕见疾病,在诊断、治疗和管理方面缺乏共识。认识到加拿大在处理该疾病的方法上落后于欧洲,我们成立了加拿大遗传性血管性水肿协会(CHAES)/加拿大遗传性血管性水肿协会(SAHC),以促进加拿大对该疾病的了解,并推动加拿大对该疾病患者的护理。我们在此介绍加拿大对该疾病的治疗综述,包括血管性水肿事件的预防和替代疗法的使用,并提出加拿大C1-INH缺乏症的诊断、治疗和管理算法,以供在2003年10月24日至26日于加拿大多伦多举行的遗传性血管性水肿国际会议上进行讨论。