The international WAO/EAACI guideline for the management of hereditary angioedema – the 2017 revision and update | World Allergy Organization Journal | Full Text

The international WAO/EAACI guideline for the management of hereditary angioedema – the 2017 revision and update | World Allergy Organization Journal | Full Text

World Allergy Organization Journal



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The international WAO/EAACI guideline for the management of hereditary angioedema – the 2017 revision and update

• Marcus Maurer†Email author,
• Markus Magerl†,
• Ignacio Ansotegui,
• Emel Aygören-Pürsün,
• Stephen Betschel,
• Konrad Bork,
• Tom Bowen,
• Henrik Balle Boysen,
• Henriette Farkas,
• Anete S. Grumach,
• Michihiro Hide,
• Constance Katelaris,
• Richard Lockey,
• Hilary Longhurst,
• William R. Lumry,
• Inmaculada Martinez-Saguer,
• Dumitru Moldovan,
• Alexander Nast,
• Ruby Pawankar,
• Paul Potter,
• Marc Riedl,
• Bruce Ritchie,
• Lanny Rosenwasser,
• Mario Sánchez-Borges,
• Yuxiang Zhi,
• Bruce Zuraw and
• Timothy Craig

†Contributed equally

World Allergy Organization Journal201811:5

https://doi.org/10.1186/s40413-017-0180-1

©  The Author(s). 2018

• Received: 3 December 2017
• Accepted: 6 December 2017
• Published: 27 February 2018

Abstract

Hereditary Angioedema (HAE) is a rare and disabling disease. Early diagnosis and appropriate therapy are essential. This update and revision of the global guideline for HAE provides up-to-date consensus recommendations for the management of HAE. In the development of this update and revision of the guideline, an international expert panel reviewed the existing evidence and developed 20 recommendations that were discussed, finalized and consented during the guideline consensus conference in June 2016 in Vienna. The final version of this update and revision of the guideline incorporates the contributions of a board of expert reviewers and the endorsing societies. The goal of this guideline update and revision is to provide clinicians and their patients with guidance that will assist them in making rational decisions in the management of HAE with deficient C1-inhibitor (type 1) and HAE with dysfunctional C1-inhibitor (type 2). The key clinical questions covered by these recommendations are: 1) How should HAE-1/2 be defined and classified?, 2) How should HAE-1/2 be diagnosed?, 3) Should HAE-1/2 patients receive prophylactic and/or on-demand treatment and what treatment options should be used?, 4) Should HAE-1/2 management be different for special HAE-1/2 patient groups such as pregnant/lactating women or children?, and 5) Should HAE-1/2 management incorporate self-administration of therapies and patient support measures?

This article is co-published with permission in Allergy and the World Allergy Organization Journal.

Keywords

• Hereditary angioedema
• C1-inhibitor
• Diagnosis
• Therapy
• Management
• Individualized therapy
• GRADE
• Guideline
• Prophylaxis
• Quality of life
• Recommendations
• Self-administration