HAE Management Recommendations
US HAEA Medical Advisory Board Recommendations for the Management of Hereditary Angioedema Due to C1 Inhibitor Deficiency

The treatment of Hereditary Angioedema (HAE) has undergone dramatic changes as newer medicines have become available in recent years. Optimal care of these patients requires a comprehensive management plan.

To develop state-of-the-art recommendations for the treatment and management of HAE due to C1 inhibitor (C1INH) deficiency in the United States.

Members of the US Hereditary Angioedema Association Medical Advisory Board began by reviewing the literature concerning treatment of HAE. Preliminary recommendations were developed based on the literature review, discussions in a face-to-face meeting, and refinements in a series of drafts. Final recommendations reflect the unanimous consensus of the medical advisory board and the US Hereditary Angioedema Association leadership.

Recommendations are provided regarding a comprehensive care plan for HAE, including the following: development of an overall management plan, treatment of angioedema attacks, prophylactic treatment, and patient monitoring.

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This information originally appeared as an article in The Journal of Allergy and Clinical Immunology In Practice

HAE Primer
We're pleased to announce that the HAEA joined forces with the prestigious medical journal Allergy and Asthma Proceedings and HAE physician-experts to develop a special supplemental edition on HAE diagnosis and management. The published supplement contains 14 peer reviewed articles on a range of vitally important HAE topics.

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