期刊
TRANSFUSION AND APHERESIS SCIENCE
卷 29, 期 3, 页码 205-214出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.transci.2003.08.009
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C1 esterase inhibitor (CI-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)/Societe d'angioedeme hereditaire 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 CI-INH deficiency in Canada for discussion at our International Conference on Hereditary Angioedema to be held in Toronto, Canada, October 24th to 26th, 2003. (C) 2003 Elsevier Ltd. All rights reserved.
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