US HAEA Medical Advisory Board 2020 Guidelines for the Management of Hereditary Angioedema.
Bradykinin
C1 inhibitor
Hereditary angioedema
Management
On-demand treatment
Prophylactic treatment
Journal
The journal of allergy and clinical immunology. In practice
ISSN: 2213-2201
Titre abrégé: J Allergy Clin Immunol Pract
Pays: United States
ID NLM: 101597220
Informations de publication
Date de publication:
01 2021
01 2021
Historique:
received:
16
12
2019
revised:
28
08
2020
accepted:
29
08
2020
pubmed:
9
9
2020
medline:
22
5
2021
entrez:
8
9
2020
Statut:
ppublish
Résumé
Scientific and clinical progress together with the development of effective novel therapeutic options has engendered multiple important changes in the diagnosis and management of hereditary angioedema (HAE). We now update and extend the 2013 United States Hereditary Angioedema Association Medical Advisory Board guidelines for the treatment and management of HAE. The guidelines are based on a comprehensive literature review with recommendations indicating both the strength of our recommendation and the quality of the underlying evidence. Guidelines are provided regarding the classification, diagnosis, on-demand treatment, prophylactic treatment, special considerations for women and children, development of a comprehensive management and monitoring plan, and assessment of burden of illness for both HAE due to C1 inhibitor deficiency and HAE with normal C1 inhibitor. Advances in HAE treatment now allow the development of management plans that can help many patients with HAE lead a normal life. Achieving this goal requires that physicians be familiar with the diagnostic and therapeutic transformations that have occurred in recent years.
Identifiants
pubmed: 32898710
pii: S2213-2198(20)30878-3
doi: 10.1016/j.jaip.2020.08.046
pii:
doi:
Substances chimiques
Complement C1 Inhibitor Protein
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
132-150.e3Informations de copyright
Published by Elsevier Inc.