Summary of findings and quality of evidence assessment
Summary of findings | Quality of evidence assessment (GRADE) | ||||||||
Outcome | No. of studies | No. of participants | Risk of bias | Inconsistency | Indirectness | Imprecision | Other considerations | Level of evidence | Importance |
Depressive symptoms | |||||||||
Pain intensity | 14 | 9466 | Very serious* | Very serious† | Very serious‡ | Very serious§ | Reporting bias detected¶ | Very low | Critical |
Disability | 12 | 9350 | Very serious* | Very serious† | Very serious‡ | Very serious§ | Reporting bias detected¶ | Very low | Critical |
Anxiety | |||||||||
Pain intensity | 11 | 6344 | Very serious* | Very serious† | Very serious‡ | Very serious§ | Reporting bias detected¶ | Very low | Critical |
Disability | 8 | 6169 | Very serious* | Very serious† | Very serious‡ | Very serious§ | Reporting bias detected¶ | Very low | Critical |
Emotional distress | |||||||||
Pain intensity | 7 | 5336 | Very serious* | Very serious† | Very serious‡ | Very serious§ | Reporting bias detected¶ | Very low | Critical |
Disability | 7 | 5336 | Very serious* | Serious† | Very serious‡ | Very serious§ | Reporting bias detected¶ | Very low | Critical |
Self-efficacy | |||||||||
Pain intensity | 4 | 1297 | Serious* | Serious† | Very serious‡ | Serious§ | N/A | Very low | Critical |
Disability | 3 | 1240 | Serious* | Serious† | Very serious‡ | Serious§ | N/A | Very low | Critical |
Expectations of recovery | |||||||||
Pain intensity | 5 | 1802 | Very serious* | Very serious† | Very serious‡ | Very serious§ | Reporting bias detected¶ | Very low | Critical |
Disability | 7 | 2115 | Very serious* | Very serious† | Very serious‡ | Very serious§ | Reporting bias detected¶ | Very low | Critical |
Pain catastrophising | |||||||||
Pain intensity | 6 | 918 | Very serious* | Serious† | Serious‡ | Very serious§ | N/A | Very low | Critical |
Disability | 4 | 833 | Serious* | Very serious† | Very serious‡ | Serious§ | Reporting bias detected¶ | Very low | Critical |
*Randomised trials (lack of allocation concealment; lack of blinding; incomplete accounting of patients and outcomes events; selective outcome reporting bias; other limitations; observational studies (failure to develop and apply appropriate eligibility criteria; flawed measurement of both exposure and outcome; failure to adequate control confounding; incomplete follow-up; non-presence of an unexposed cohort).
†Point estimates vary widely across studies; CIs show minimal or no overlap.
‡ Differences in population, differences in intervention, differences in outcome, indirect comparison.
§ Optimal information size (OIS) criterion is not met and the sample size is small; OIS criterion is met but the 95% CI around an effect does not exclude 1.0 (wide CIs); 95% CI is not reported.
¶ Outcome data not included in the predictive model.
N/A, not available.