Walter 2002.
Methods | Prospective randomized controlled trial | |
Participants | Patients undergoing elective cardiopulmonary bypass surgery Mean age (years): 1. 64.8 ± 1.7 2. 61.9 ± 2.0 Sample size (male): 1. 22(17); 2. 21(16) |
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Interventions | 1. oral 7.5 mg enalapril on the first day and oral 20 mg/d enalapril on the following days 2. placebo |
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Outcomes | All‐cause mortality; concentration of creatine kinase, MB form ; ST segment change or new Q wave in ECG test; hypotension | |
Notes | Participants in enalapril group were given 7.5 mg on the first day | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Random allocation, but no details available |
Allocation concealment (selection bias) | Unclear risk | No relevant description, and no further details available |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Double blind, but no details available |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No relevant description |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Information on dropouts specified |
Selective reporting (reporting bias) | Unclear risk | Protocol inaccessible |
Other bias | Low risk | No other source of bias found |
ACEIs: angiotensin‐converting enzyme inhibitors ARBs: angiotensin II type 1 receptor blockers CABG: coronary artery bypass graft surgery ECG: electrocardiograph IV: intravenous ST: the ST segment in electrocardiography