Optimal Screening for Prediction of Referral and Outcome (OSPRO) for Musculoskeletal Pain Conditions: Results From the Validation Cohort.
Steven Z George, Jason M Beneciuk, Trevor A Lentz and 4 others
PMID 29629615WHAT IT FOUND
The 10-item OSPRO-YF and 10-item OSPRO-ROS improved prediction of some 12-month outcomes only slightly after demographic, clinical and baseline scores were considered.
Use them as adjuncts, not stand-alone decision tools.
Key findings
01The 10-item OSPRO-YF explained variance beyond baseline scores, and the 10-item OSPRO-ROS explained additional variance only for mental quality-of-life scores; the added amounts were small (increments from 0.01 to 0.07).
02The 4-week change in the 10-item OSPRO-YF explained additional variance in 12-month pain, disability and quality of life (increments from 0.04 to 0.07).
03For 12-month comorbidity change, the baseline number of comorbidities explained the most additional variance, and only the 13 additional OSPRO-ROS+ items explained variance.
STILL TO COME
How it was doneWhat they foundWhat it means for PTs
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What it does not show
The sample was a convenience sample from 9 clinics, and 275 of 440 participants came from the Southeast, so the results may not apply to other regions or clinic settings. Only 279 of 440 participants completed 12-month follow-up (63.4%), which was lower than anticipated. Participants who completed follow-up were more likely to be younger, have higher income and more education, and have lower pain, lower region-specific disability and lower OSPRO-YF scores than those who did not complete follow-up. Those who did not complete follow-up were more likely to be uninsured, on disability, covered by Medicaid or worker compensation, and to have higher pain and pain-associated distress, so the models may need adjustment for these groups. All outcomes were self-reported, and 12-month comorbidity was not verified against medical records. The models did not include specific medical diagnoses, injury severity or individual treatment parameters. The OSPRO tools added small amounts of variance (0.01 to 0.07 at baseline; 0.04 to 0.07 for change), and the authors state that clinical relevance is limited. The study tested prediction, not whether using the tools changes treatment decisions or patient outcomes. Prediction of comorbidity outcomes was most affected by loss to follow-up. The OSPRO-YF total score was not weighted by its components, so it is unclear which psychological domains drive prediction.
Declared interests
The authors report no financial, conflicting or competing interests.
The easy way to misread this
Do not read the prediction results as evidence that OSPRO screening will change care. The tools added only 0.01 to 0.07 of variance beyond baseline scores, and the study did not test whether using them changes treatment decisions or outcomes.