US HAEA Medical Advisory Board 2020 Guidelines for the Management of Hereditary Angioedema.


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
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.e3

Informations de copyright

Published by Elsevier Inc.

Auteurs

Paula J Busse (PJ)

Division of Rheumatology, Allergy, and Immunology, Department of Medicine, Mount Sinai School of Medicine, New York, NY.

Sandra C Christiansen (SC)

Division of Rheumatology, Allergy, and Immunology, Department of Medicine, University of California San Diego, La Jolla, Calif.

Marc A Riedl (MA)

Division of Rheumatology, Allergy, and Immunology, Department of Medicine, University of California San Diego, La Jolla, Calif.

Aleena Banerji (A)

Division of Rheumatology, Allergy and Immunology, Department of Medicine, Harvard Medical School, Boston, Mass.

Jonathan A Bernstein (JA)

Division of Immunology, Rheumatology, and Allergy, Department of Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.

Anthony J Castaldo (AJ)

US Hereditary Angioedema Association, Fairfax City, Va.

Timothy Craig (T)

Division of Allergy, Asthma, and Immunology, Department of Medicine, Pediatrics, and Graduate Studies, Pennsylvania State University, Hershey, Pa.

Mark Davis-Lorton (M)

Division of Rheumatology, Allergy and Clinical Immunology, Department of Medicine, NYU Winthrop Hospital, Mineola, NY.

Michael M Frank (MM)

Department of Pediatrics, Duke University Medical Center, Durham, NC.

H Henry Li (HH)

Medicine Service, Institute for Asthma and Allergy, Chevy Chase, Md.

William R Lumry (WR)

Allergy and Asthma Research Associates Research Center, Dallas, Tex.

Bruce L Zuraw (BL)

Division of Rheumatology, Allergy, and Immunology, Department of Medicine, University of California San Diego, La Jolla, Calif; San Diego Veterans Administration Healthcare, San Diego, Calif. Electronic address: bzuraw@ucsd.edu.

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