4.7 Article

A Core Outcome Set for Seamless, Standardized Evaluation of Innovative Surgical Procedures and Devices (COHESIVE) A Patient and Professional Stakeholder Consensus Study

Journal

ANNALS OF SURGERY
Volume 277, Issue 2, Pages 238-245

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/SLA.0000000000004975

Keywords

core outcome set; Delphi technique; device approval; operative; outcome assessment; surgical procedures

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This study aims to develop a COS, an agreed minimum set of outcomes to measure and report in studies evaluating novel surgical techniques. Currently, there is a lack of agreement on key outcomes for safe and efficient surgical innovation. The study generated a list of outcome domains, prioritized them through a Delphi survey, and reached consensus through a meeting involving international stakeholders.
Objective:To develop a COS, an agreed minimum set of outcomes to measure and report in all studies evaluating the introduction and evaluation of novel surgical techniques. Summary of Background Data:Agreement on the key outcomes to measure and report for safe and efficient surgical innovation is lacking, hindering transparency and risking patient harm. Methods:(I) Generation of a list of outcome domains from published innovation-specific literature, policy/regulatory body documents, and surgeon interviews; (II) Prioritization of identified outcome domains using an international, multi-stakeholder Delphi survey; (III) Consensus meeting to agree the final COS. Participants were international stakeholders, including patients/public, surgeons, device manufacturers, regulators, trialists, methodologists, and journal editors. Results:A total of 7972 verbatim outcomes were identified, categorized into 32 domains, and formatted into survey items/questions. Four hundred ten international participants (220 professionals, 190 patients/public) completed at least one round 1 survey item, of which 153 (69.5%) professionals and 116 (61.1%) patients completed at least one round 2 item. Twelve outcomes were scored consensus in (very important by >= 70% of patients and professionals) and 20 no consensus. A consensus meeting, involvingcontext: modifications, unexpected disadvantages, device problems, technical procedure completion success, patients' experience relating to the procedure being innovative, surgeons'/operators' experience. Other domains relate to intended benefits, whether the overall desired effect was achieved and expected disadvantages. Conclusions:The COS is recommended for use in all studies before definitive randomized controlled trial evaluation to promote safe, transparent, and efficient surgical innovation.

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