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A core domain set for hidradenitis suppurativa trial outcomes: an international Delphi process

  • L. Thorlacius*
  • , J. R. Ingram
  • , B. Villumsen
  • , S. Esmann
  • , J. S. Kirby
  • , A. B. Gottlieb
  • , J. F. Merola
  • , R. Dellavalle
  • , S. M. Nielsen
  • , R. Christensen
  • , A. Garg
  • , G. B.E. Jemec
  • , on behalf of the HIdradenitis SuppuraTiva cORe outcomes set International Collaboration (HISTORIC)
  • *Corresponding author af dette arbejde

Publikation: Bidrag til tidsskriftArtikelForskningpeer review

Abstract

Background: There is no consensus on core outcome domains for hidradenitis suppurativa (HS). Heterogeneous outcome measure instruments in clinical trials likely leads to outcome-reporting bias and limits the ability to synthesize evidence. Objectives: To achieve global multistakeholder consensus on a core outcome set (COS) of domains regarding what to measure in clinical trials for HS. Methods: Six stakeholder groups participated in a Delphi process that included five anonymous e-Delphi rounds and four face-to-face consensus meetings to reach consensus on the final COS. The aim was for a 1 : 1 ratio of patients to healthcare professionals (HCPs). Results: A total of 41 patients and 52 HCPs from 19 countries in four continents participated in the consensus process, which yielded a final COS that included five domains: pain, physical signs, HS-specific quality of life, global assessment and progression of course. A sixth domain, symptoms, was highly supported by patients and not by HCPs but is recommended for the core domain set. Conclusions: Routine adoption of the COS in future HS trials should ensure that core outcomes of importance to both patients and HCPs are collected.

OriginalsprogEngelsk
Sider (fra-til)642-650
Antal sider9
TidsskriftBritish Journal of Dermatology
Vol/bind179
Udgave nummer3
DOI
StatusUdgivet - sep. 2018

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