Dy 1998.
Methods | RCT, parallel design | |
Participants |
Total number of randomized participants: 135 Inclusion criteria: scheduled for isolated CABG Exclusion criteria: ejection fraction < 30%, prior atrial or ventricular arrhythmias, severe COPD, serum creatinine > 2.0, severe bradycardia Type of surgery: elective CABG Baseline characteristics not reported in abstract Country: USA Setting: not reported in abstract |
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Interventions |
Intervention group (metoprolol)
Control group (placebo)
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Outcomes |
Outcomes measured/reported by study authors: AF (period of observation is unclear) Outcomes relevant to the review: AF |
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Notes |
Funding/declarations of interest: not reported Study dates: January 1995‐May 1997 Notes:
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not specified |
Allocation concealment (selection bias) | Unclear risk | Not specified |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Randomized, placebo‐controlled, double‐blind trial |
Blinding of outcome assessors (detection bias) All outcomes | Unclear risk | Not specified |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No apparent losses |
Selective reporting (reporting bias) | Unclear risk | Study authors did not report prospective clinical trial registration or publication of a protocol. It was not feasible to effectively assess risk of reporting bias |
Other bias | Unclear risk | Limited detail in abstract. Not feasible to assess other risks of bias from this report |