Chan 1995 (laminectomy).
Study characteristics | ||
Methods | Parallel, 48 h | |
Participants | PCA 24, control 20 (laminectomy) | |
Interventions | PCA: morphine. Bolus/lockout/4 h limit: 1.5 to 2 mg/5 to 10 min/NR Control: IM morphine 0.15 to 0.2 mg/kg every 4 h prn |
|
Outcomes | Pain relief, satisfaction with analgesia, nursing time spent on each participant, time to ambulation, resumption of activities of daily living, return of bowel function, return of oral feeding, tolerance of oral analgesia, LOS | |
Source of funding | Abbott Laboratories | |
Notes | QS = 3 (R = 2, DB = 0, W = 1) | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer‐generated |
Allocation concealment (selection bias) | Unclear risk | Not mentioned |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Not blinded |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Appears that all participants completed study, but not stated. Imputation methods not described |
Selective reporting (reporting bias) | Low risk | All outcomes described in Methods section are reported in Results section |
Other bias | High risk | Very small sample size |