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The International/Canadian Hereditary Angioedema Guideline.
Stephen Betschel1, Jacquie Badiou2, Karen Binkley1
11University of Toronto, Toronto, ON Canada.
This updated guideline offers evidence-based recommendations for managing hereditary angioedema (HAE) globally. It emphasizes individualized care, treatment of attacks, prophylaxis, and comprehensive management strategies for HAE patients worldwide.
Area of Science:
- Medical Guidelines
- Rare Diseases
- Immunology
Background:
- Hereditary angioedema (HAE) causes unpredictable swelling attacks, impacting quality of life and potentially causing mortality.
- Optimal and uniform care for HAE patients is lacking globally, necessitating updated management strategies.
- Existing HAE care models and therapeutic options vary significantly across countries.
Purpose of the Study:
- To provide updated, evidence-based recommendations for the global management of hereditary angioedema (HAE).
- To address acute treatment, prophylaxis, and comprehensive care for HAE patients, including special populations.
- To promote individualized therapy and improve the quality of life for individuals with HAE.
Main Methods:
- Utilized the GRADE system for evidence-based recommendation development.
- Incorporated input from Canadian and international HAE experts and patient groups.
- Expanded scope to include worldwide HAE patient management, diagnosis, and therapies.
Main Results:
- Presents recommendations for HAE attack treatment, short-term and long-term prophylaxis.
- Includes new guidance on diagnosing and treating HAE with normal C1-INH.
- Addresses management in pregnant and pediatric patients, patient associations, and HAE registries.
Conclusions:
- The guideline aims to optimize HAE management and promote individualized care globally.
- It serves as a vital resource for healthcare providers, policymakers, and patient advocates.
- Implementation is expected to improve patient outcomes and quality of life for those with HAE.
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