Development of a New Patient-reported Outcome Instrument to Evaluate Treatments for Scars: The SCAR-Q.

Journal Article (Journal Article)

BACKGROUND: Every year millions of individuals acquire scars. A literature review of patient-reported outcome (PRO) instruments identified content limitations in existing scar-specific measures. The aim of this study was to develop a new PRO instrument called SCAR-Q for children and adults with surgical, traumatic, and burn scars. METHODS: We performed a secondary analysis of the qualitative datasets used in the development of PRO instruments for plastic and reconstructive surgery, that is, BREAST-Q, FACE-Q, BODY-Q, and CLEFT-Q. The keyword "scar*" was used to extract scar-specific text. Data were analyzed to identify concepts of interest and to form a comprehensive item pool. Scales were developed and refined through multiple rounds of cognitive interviews with patients and with input from international clinical experts between July 2015 and December 2016. RESULTS: A total of 52 children and 192 adults from the qualitative datasets provided between 1 and 34 scar-specific codes (n = 1,227). The analysis led to the identification of 3 key domains for which scales were developed: scar appearance (eg, size, color, contour), scar symptoms (eg, painful, tight, itchy), and psychosocial impact (eg, feeling self-conscious, bothered by scar). Cognitive interviews with 25 adults and 20 pediatric participants with scars, plus feedback from 27 clinical experts, led to rewording and removal of items, and new items added. These steps ensured content validity for SCAR-Q in a broad range of scars. CONCLUSIONS: The SCAR-Q is now being field-tested. Once completed, we anticipate SCAR-Q will be used in clinical practice and in clinical trials to test different scar therapies.

Full Text

Duke Authors

Cited Authors

  • Klassen, AF; Ziolkowski, N; Mundy, LR; Miller, HC; McIlvride, A; DiLaura, A; Fish, J; Pusic, AL

Published Date

  • April 2018

Published In

Volume / Issue

  • 6 / 4

Start / End Page

  • e1672 -

PubMed ID

  • 29876160

Pubmed Central ID

  • PMC5977950

International Standard Serial Number (ISSN)

  • 2169-7574

Digital Object Identifier (DOI)

  • 10.1097/GOX.0000000000001672


  • eng

Conference Location

  • United States