Related Experiment Video
Updated: Jul 9, 2026

Reverse Total Shoulder Arthroplasty
Published on: July 5, 2011
Significant Heterogeneity in Pooled Patient Acceptable Symptom State Threshold for Shoulder Pain: A Systematic Review
Ozge Ozkutlu1, Aysenur Erekdag2, Sahra Sirvan Tongar3
1Gulhane Faculty of Physiotherapy and Rehabilitation, University of Health Sciences, Ankara, Türkiye.
Purpose:
To identify studies reporting patient acceptable symptom state (PASS) thresholds in diverse shoulder pain populations and to investigate whether patient-reported outcome measurements measuring shoulder pain severity provide similar estimates of the PASS across groups of people experiencing shoulder pain.
Methods:
Web of Science, Scopus, CENTRAL, and OVID (MEDLINE) databases were searched for studies on PASS related to shoulder pain using terms for PASS, shoulder pathologies, and pain-related patient-reported outcome measurements. Risk of bias (RoB) was categorized using a modified the Quality in Prognosis Studies Tool. The meta-analysis applied random effects models, with heterogeneity assessed via I2 and Cochran's Q-test. Subgroup analysis was performed, with bias evaluated using funnel plots and the Egger test.
Results:
Twenty-one studies were included, involving 8.992 participants with an average age of 50.55 years. The PASS thresholds for shoulder pain varied across the interventions and follow-up periods. The pooled PASS estimate was 20.18 (95% confidence interval 16.63-23.73, prediction interval 2.98 to 37.38), with significant heterogeneity (I2 = 97%). Surgical interventions had lower PASS thresholds than nonsurgical approaches. Studies with longer follow-up duration and moderate RoB had lower PASS thresholds. A significant publication bias was identified.
Conclusions:
This systematic review and meta-analysis established a pooled PASS threshold for shoulder pain, highlighting substantial heterogeneity and significant differences in PASS thresholds across RoB levels, follow-up durations, and types of intervention.
Level Of Evidence:
Level IV, systematic review and meta-analysis of Level II-IV studies.
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