University of Hertfordshire

Documents

  • Atul Mehta
  • David Kuter
  • N Belmatoug
  • B Bembi
  • J Bright
  • S Vom Dahl
  • F Deodato
  • M Di Rocco
  • O Goker-Alpan
  • DA Hughes
  • EA Lukina
  • M Machaczka
  • E Mengel
  • A Nagral
  • K Nakamura
  • A Narita
  • B Oliveri
  • G Pastores
  • J Pérez-López
  • U Ramaswami
  • IV Schwartz
  • J Szer
  • NJ Weinreb
  • A Zimran
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Original languageEnglish
Number of pages14
Pages (from-to)578-591
JournalInternal Medicine Journal
Journal publication date1 May 2019
Volume49
Issue5
Early online date10 Nov 2018
DOIs
Publication statusPublished - 1 May 2019

Abstract

Background: Gaucher disease (GD) presents with a range of signs and symptoms. Physicians can fail to recognize the early stages of GD owing to a lack of disease awareness, which can lead to significant diagnostic delays and sometimes irreversible but avoidable morbidities.
Aims: The Gaucher Earlier Diagnosis Consensus (GED‐C) initiative aimed to identify signs and co‐variables considered most indicative of early type 1 and type 3 GD, to help non‐specialists identify ‘at‐risk’ patients who may benefit from diagnostic testing.
Methods: An anonymous, three‐round Delphi consensus process was deployed among a global panel of 22 specialists in GD (median experience 17.5 years, collectively managing almost 3000 patients). The rounds entailed data gathering, then importance ranking and establishment of consensus, using 5‐point Likert scales and scoring thresholds defined a priori.
Results: For type 1 disease, seven major signs (splenomegaly, thrombocytopenia, bone‐related manifestations, anaemia, hyperferritinaemia, hepatomegaly, and gammopathy) and two major co‐variables (family history of GD and Ashkenazi‐Jewish ancestry) were identified. For type 3 disease, nine major signs (splenomegaly, oculomotor disturbances, thrombocytopenia, epilepsy, anaemia, hepatomegaly, bone pain, motor disturbances, and kyphosis) and one major co‐variable (family history of Gaucher disease) were identified. Lack of disease awareness, overlooking mild early signs, and failure to consider GD as a diagnostic differential were considered major barriers to early diagnosis.
Conclusions: The signs and co‐variables identified in the GED‐C initiative as potentially indicative of early GD will help to guide non‐specialists and raise their index of suspicion in identifying patients potentially suitable for diagnostic testing for GD.

Notes

© 2018 The Authors. Internal Medicine Journal by Wiley Publishing Asia Pty Ltd on behalf of Royal Australasian College of Physicians.

ID: 16444843