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Development of a Patient-Reported Outcome Measure (PROM) in Bony Facial Trauma Patients.
Kent Curran1, Alayna Panzer2, Thomas Guterbock2
1Department of Otolaryngology University of Virginia Health System Charlottesville Virginia USA.
Laryngoscope Investigative Otolaryngology
|April 9, 2026
Summary
Researchers developed a new patient-reported outcome measure (PROM) for bony facial trauma. This tool assesses crucial functional and psychosocial concerns, improving quality-of-life evaluations for affected individuals.
Area of Science:
- Trauma Surgery
- Patient-Reported Outcomes
- Quality of Life Measurement
Background:
- Currently, no validated patient-reported outcome measures (PROMs) specifically assess quality of life for patients with bony facial trauma.
- Existing measures do not adequately capture the unique functional and psychosocial challenges faced by this patient population.
Purpose of the Study:
- To identify and investigate the functional and psychosocial concerns of patients with bony facial trauma.
- To develop a novel, clinically applicable patient-reported outcome measurement tool tailored to this population.
Main Methods:
- Semi-structured interviews were conducted with 10 facial trauma experts to identify key concerns.
- A preliminary PROM instrument was developed based on expert feedback.
- Cognitive debriefing interviews with 15 patients experiencing bony facial trauma refined the PROM instrument.
Main Results:
- The finalized PROM includes critical functional concerns like nasal obstruction, persistent facial numbness, vision issues, and limited jaw mobility.
- Key psychosocial concerns identified encompass difficulty with personal tasks, depression, anxiety, and social withdrawal.
- The developed PROM effectively captures relevant patient-identified issues.
Conclusions:
- A standardized approach using expert and patient input successfully created a PROM specific to bony facial trauma.
- The new PROM addresses both functional and psychosocial aspects crucial for evaluating patient well-being.
- Future multi-institutional validation with a larger patient cohort is planned to confirm the PROM's efficacy.

