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dc.contributor.authorMaurer, Marcus
dc.contributor.authorMagerl, Markus
dc.contributor.authorAnsotegui, Ignacio
dc.contributor.authorAygören-Pürsün, Emel
dc.contributor.authorBetschel, Stephen
dc.contributor.authorBork, Konrad
dc.contributor.authorBowen, Tom
dc.contributor.authorBoysen, Henrik B
dc.contributor.authorFarkas, Henriette
dc.contributor.authorGrumach, Anete S.
dc.contributor.authorHide, Michihiro
dc.contributor.authorKatelaris, Constance
dc.contributor.authorLockey, Richard
dc.contributor.authorLonghurst, Hilary
dc.contributor.authorLumry, William R.
dc.contributor.authorMartinez-Saguer, Inmaculada
dc.contributor.authorMoldovan, Dumitru
dc.contributor.authorNast, Alexander
dc.contributor.authorPawankar, Ruby
dc.contributor.authorPotter, Paul
dc.contributor.authorRiedl, Marc
dc.contributor.authorRitchie, Bruce
dc.contributor.authorRosenwasser, Lanny
dc.contributor.authorSánchez-Borges, Mario
dc.contributor.authorZhi, Yuxiang
dc.contributor.authorZuraw, Bruce
dc.contributor.authorCraig, Timothy
dc.date.accessioned2018-04-09T11:33:27Z
dc.date.available2018-04-09T11:33:27Z
dc.date.issued2018-02-27
dc.identifier.citationWorld Allergy Organization Journal. 2018 Feb 27;11(1):5
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/274694
dc.description.abstractAbstract 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.
dc.titleThe international WAO/EAACI guideline for the management of hereditary angioedema – the 2017 revision and update
dc.typeJournal Article
dc.date.updated2018-04-09T11:33:25Z
dc.language.rfc3066en
dc.rights.holderThe Author(s).
dc.identifier.doi10.17863/CAM.21827
rioxxterms.versionofrecord10.1186/s40413-017-0180-1


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