Consensus on diagnosis and management of hereditary angioedema in Greece.

IF 2.6 Q2 ALLERGY
A E Germenis, E Kompoti, G N Konstantinou, M Makris, E Manousakis, N Mikos, J Paraskevopoulos, M Speletas, E Stefanaki, E Farmaki, F Psarros
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引用次数: 0

Abstract

Summary: HAE is a rare disease manifesting with recurrent attacks of disabling and potentially life-threatening angioedema for which early diagnosis and effective therapy are critical. Recent scientific progress and the development of novel therapeutic options has engendered multiple important changes in the diagnosis and management of the disease. In an attempt to encourage and facilitate the use of this progress for all patients, the Hellenic Society of Angioedema has undertaken the effort to develop consensus recommendations for the diagnosis, treatment and management of hereditary angioedema in special patients' groups. To this aim a panel of 11 experts was assembled and a modified Delphi method was used. After a comprehensive review of relevant literature from the last five years retrieved from Medline, the initial text of the recommendations was formulated and consensus was sought among the experts. The consensus included statements that were agreed by more than 80% of the experts. This article presents the 24 consensus recommendations that were finally formulated.

希腊遗传性血管性水肿的诊断和治疗共识。
摘要:HAE是一种罕见的疾病,表现为致残和潜在危及生命的血管性水肿的反复发作,早期诊断和有效治疗至关重要。最近的科学进步和新的治疗选择的发展已经在疾病的诊断和管理方面产生了多个重要的变化。为了鼓励和促进所有患者使用这一进展,希腊血管性水肿学会已经开始努力为特殊患者群体的遗传性血管性水肿的诊断、治疗和管理制定共识建议。为此目的,召集了一个由11名专家组成的小组,并使用了改进的德尔菲法。在对从Medline检索的过去五年的相关文献进行全面审查后,制定了建议的初步文本,并在专家之间寻求共识。这份共识包括了超过80%的专家同意的声明。本文提出了最终制定的24项共识建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
4.00
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102
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