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Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema
Tom Bowen1, Marco Cicardi, Henriette Farkas
1Department of Medicine and Paeditrics, University of Calgary, Calgary, Alberta T2N 2T8, Canada. tbowen@pol.net
Insights
C1 inhibitor deficiency (hereditary angioedema [HAE]) diagnosis and management lacked consensus. A 2003 Canadian conference convened experts to create a consensus algorithm for HAE care, acknowledging limited evidence but emphasizing collaborative agreement.
Area of Science:
- Immunology
- Rare Diseases
- Clinical Consensus
Background:
- Hereditary angioedema (HAE) is a rare genetic disorder characterized by C1 inhibitor deficiency, leading to recurrent swelling attacks.
- A significant lack of consensus exists regarding the diagnosis, therapy, and management of HAE, particularly in Canada.
- Previous European initiatives, including workshops and a registry, aimed to advance HAE knowledge.
Framework:
- A Canadian International Consensus Conference was held in Toronto in October 2003, bringing together European and North American experts.
- The conference aimed to foster consensus on HAE diagnosis, therapy, and management among major treatment centers.
- A consensus algorithm approach was discussed and developed based on available information.
Implementation:
- The consensus algorithm was developed through presentations and discussions involving investigators from Europe and North America.
- The algorithm represents a collaborative effort by patient-care providers, patient group representatives, and individual patients.
- The document acknowledges a paucity of high-level evidence, such as double-blind placebo-controlled trials, supporting the algorithm.
Implications:
- The developed algorithm provides a recommended approach for HAE diagnosis, therapy, and management as of 2003.
- The algorithm is considered a 'living document' requiring validation and future review at international HAE meetings.
- This consensus approach, while requiring further evidence, strengthens HAE care through collaborative agreement among stakeholders.
Abstract:
C1 inhibitor deficiency (hereditary angioedema [HAE]) is a rare disorder for which there is a lack of consensus concerning diagnosis, therapy, and management, particularly in Canada. European initiatives have driven the approach to managing HAE with 3 C1-INH Deficiency Workshops held every 2 years in Hungary starting in 1999, with the third Workshop having recently been held in May 2003. The European Contact Board has established a European HAE Registry that will hopefully advance our knowledge of this disorder. The Canadian Hereditary Angioedema Society/Société d'Angioédème Héréditaire du Canada organized a Canadian International Consensus Conference held in Toronto, Ontario, Canada, on October 24 to 26, 2003, to foster consensus between major European and North American HAE treatment centers. Papers were presented by investigators from Europe and North America, and this consensus algorithm approach was discussed. There is a paucity of double-blind placebo-controlled trials in the treatment of HAE, making levels of evidence to support the algorithm less than optimal. Enclosed is the consensus algorithm approach recommended for the diagnosis, therapy, and management of HAE and agreed to by the authors of this article. This document is only a consensus algorithm approach and requires validation. As such, participants agreed to make this a living 2003 algorithm (ie, a work in progress) and agreed to review its content at future international HAE meetings. The consensus, however, has strength in that it was arrived at by the meeting of patient-care providers along with patient group representatives and individual patients reviewing information available to date and reaching agreement on how to approach the diagnosis, therapy, and management of HAE circa 2003. Hopefully evidence to support approaches to the management of HAE will approach the level of meta-analysis of randomized controlled trials in the near future.
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