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

Autor: I. J. Ansotegui, Bruce L. Zuraw, Stephen Betschel, Marcus Maurer, Alexander Nast, Paul Potter, Marc A. Riedl, Inmaculada Martinez-Saguer, Mario Sánchez-Borges, Henriette Farkas, Ruby Pawankar, Emel Aygören-Pürsün, Bruce Ritchie, Constance H. Katelaris, Hilary Longhurst, Lanny J. Rosenwasser, W. R. Lumry, Timothy J. Craig, R. Lockey, Markus Magerl, Yuxiang Zhi, Michihiro Hide, Dumitru Moldovan, Tom Bowen, Konrad Bork, H. Balle Boysen, Anete Sevciovic Grumach
Přispěvatelé: Department of Medicine, Faculty of Health Sciences, Apollo - University of Cambridge Repository
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Male
Aftercare
32 Biomedical and Clinical Sciences
Lanadelumab
C1-inhibitor
Disease
Guideline
Recommendations
0302 clinical medicine
Pregnancy
Diagnosis
Immunology and Allergy
030212 general & internal medicine
Precision Medicine
Child
Hereditary angioedema
Consensus conference
Self-administration
Management
GRADE
Female
Complement C1 Inhibitor Protein
Quality of life
Adult
Pulmonary and Respiratory Medicine
medicine.medical_specialty
What treatment
Consensus
Adolescent
Health Planning Guidelines
Immunology
MEDLINE
Dysfunctional family
7.3 Management and decision making
Young Adult
03 medical and health sciences
Rare Diseases
Quality of life (healthcare)
Clinical Research
Terminology as Topic
Individualized therapy
medicine
Humans
Lactation
Final version
Prophylaxis
business.industry
Prevention
Angioedemas
Hereditary

Precision medicine
medicine.disease
3211 Oncology and Carcinogenesis
030228 respiratory system
Family medicine
Therapy
business
7 Management of diseases and conditions
Zdroj: World Allergy Organization Journal
DOI: 10.17863/cam.21827
Popis: 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.
Databáze: OpenAIRE