Boldt 1998.
Study characteristics | ||
Methods | Parallel, 72 h | |
Participants | PCA 30, control 30 First time elective cardiac surgery | |
Interventions | PCA: piritramide. Bolus/lockout/1 h limit: 2 mg/10 min/6 doses Control: IV piritramide 5 mg, on demand or as determined by nurse |
|
Outcomes | Pain intensity, sedation, patient satisfaction, pulmonary function, cortisol and troponin levels, O2 saturation, PaO2 and PaCO2, adverse events | |
Source of funding | Not reported | |
Notes | See Published notes for details regarding study retraction 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 blinded |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Number of participants completing study not reported, imputation methods not described |
Selective reporting (reporting bias) | Low risk | All outcomes described in Methods section are reported in Results section |
Other bias | Unclear risk | Small sample size |