Exploring Consumer and Clinician Attitudes towards Patient Reported Outcome Measures (PROMs) in an Australian Inpatient Musculoskeletal Rehabilitation Unit: A Qualitative Pilot Study
Published November 13, 2024


This pilot qualitative study explores consumers’ and clinicians’ perspectives about the relevance and utility of patient reported outcome measures (PROMs) in an Australian inpatient rehabilitation unit. Methods: Two focus groups, were recruited via convenience sampling, comprising English speaking rehabilitation clinicians (n = 5) and consumers (n = 6) who had recent experience of inpatient musculoskeletal rehabilitation in a large, privately funded, rehabilitation hospital in Melbourne Australia, in 2020. The focus groups were conducted via videoconference, moderated by two experienced rehabilitation clinician-researchers, following semi-structured interview guides. Focus group recordings were professionally transcribed for coding and thematic analysis by two researchers, with consensus reached about final themes. Results: Rehabilitation clinicians and consumers identified potential utility in measuring PROs at the patient level to improve patient-centred care and team coordination, and at the system level through quality improvement, benchmarking and research. Benefits were viewed as contingent on a clearly articulated rationale for measurement, careful selection of PRO instruments and specific application in target populations, with doubts expressed over their specific utility in musculoskeletal rehabilitation. Risks associated with PROMs were also identified, including procedural burden, emotional distress, psychological safety, incomplete forms and opportunity-cost. Clinicians and consumers expressed concern over the validity, reliability and representativeness of PROM data. Conclusions: While the potential benefits of PROMs were recognised, numerous risks and logistical challenges were also identified. The current lack of confidence from both clinicians and consumers in the inherent value of PROM data and its ability to improve patient care or quality standards will likely impede successful incorporation into routine rehabilitation care.
Related content
-
Policy & Measurement
Policy & Measurement: The Impact of Patient & Family Involvement
Published September 10, 2024

By Rosie Bartel This is the sixth blog in a series of eight by The Beryl Institute’s Global Patient & Family Advisory Board (GPFAB). The intent of this series is to present our perspective on patients’ and families’ lived experience through each of the strategic lenses of The Beryl Institute’s Experience Framework. The Experience Framework
Learn more -
Policy & Measurement
Enhancing Post-Visit Communication: A Quality Improvement Initiative
Published August 18, 2024

With grant funding from The Beryl Institute, Briargate Outpatient Specialty Care Clinic at Children’s Hospital Colorado launched a quality improvement project to tackle the decline in patient and family experience scores concerning post-visit communication. By implementing targeted interventions, the clinic increased the percentage of families who felt well-informed about handling questions after visits from 72%
Learn more -
Patient Family & Community Engagement | Policy & Measurement | Staff & Provider Engagement
Signals to Action: Northwestern Medicine’s Journey to Humanizing Healthcare Experiences
Published December 19, 2023

Complimentary – In an effort to (re)build trust post-pandemic, many health systems are experiencing the pressure to modernize methods used to engage patients and the workforce who care for them. This trend towards an improvement-focused understanding is reflected in the greater conversations happening across our industry, including the evolved shift in understanding from “Patient” to
Learn more