Development of a core outcome set for research and audit studies in reconstructive breast surgery

Shelley Potter(University of Bristol), Chris Holcombe(Royal Liverpool and Broadgreen University Hospital NHS Trust), Joseph Ward(University of Bristol), Jane Blazeby(University Hospitals Bristol NHS Foundation Trust), Sara Brookes(University of Bristol), S. Cawthorn(North Bristol NHS Trust), Diana Harcourt(University of the West of England), Rhiannon Macefield(University of Bristol), Robert Warr(North Bristol NHS Trust), Eva Weiler-Mithoff(Canniesburn Hospital), Paula Williamson(University of Liverpool), Sandra Wilson(North Bristol NHS Trust)
British journal of surgery
July 15, 2015
Cited by 141Open Access
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Abstract

BACKGROUND: Appropriate outcome selection is essential if research is to guide decision-making and inform policy. Systematic reviews of the clinical, cosmetic and patient-reported outcomes of reconstructive breast surgery, however, have demonstrated marked heterogeneity, and results from individual studies cannot be compared or combined. Use of a core outcome set may improve the situation. The BRAVO study developed a core outcome set for reconstructive breast surgery. METHODS: A long list of outcomes identified from systematic reviews and stakeholder interviews was used to inform a questionnaire survey. Key stakeholders defined as individuals involved in decision-making for reconstructive breast surgery, including patients, breast and plastic surgeons, specialist nurses and psychologists, were sampled purposively and sent the questionnaire (round 1). This asked them to rate the importance of each outcome on a 9-point Likert scale from 1 (not important) to 9 (extremely important). The proportion of respondents rating each item as very important (score 7-9) was calculated. This was fed back to participants in a second questionnaire (round 2). Respondents were asked to reprioritize outcomes based on the feedback received. Items considered very important after round 2 were discussed at consensus meetings, where the core outcome set was agreed. RESULTS: A total of 148 items were combined into 34 domains within six categories. Some 303 participants (51·4 per cent) (215 (49·5 per cent) of 434 patients; 88 (56·4 per cent) of 156 professionals) completed and returned the round 1 questionnaire, and 259 (85·5 per cent) reprioritized outcomes in round 2. Fifteen items were excluded based on questionnaire scores and 19 were carried forward to the consensus meetings, where a core outcome set containing 11 key outcomes was agreed. CONCLUSION: The BRAVO study has used robust consensus methodology to develop a core outcome set for reconstructive breast surgery. Widespread adoption by the reconstructive community will improve the quality of outcome assessment in effectiveness studies. Future work will evaluate how these key outcomes should best be measured.


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