Ellis 1982 (chole).
Study characteristics | ||
Methods | Parallel, 5 days | |
Participants | PCA 15, control 17 (third group receiving sublingual buprenorphine not reported here) Cholecystectomy | |
Interventions | PCA: meperidine. Bolus/lockout/4 h limit: NR Control: IM morphine 10 mg prn according to usual practice of nursing staff |
|
Outcomes | Pain intensity, opioid consumption, pulmonary function tests, sedation, nausea, patient satisfaction and preference | |
Source of funding | Not reported | |
Notes | QS = 2 (R = 1, DB = 0, W = 1) | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not described |
Allocation concealment (selection bias) | Unclear risk | Not mentioned |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Not explicitly stated, but appears to be unblinded |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Appears that all participants completed the study (although not explicitly stated) |
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 |