Yang 2008.
Methods | RCT, parallel design | |
Participants |
Total number of randomized participants: 102 Inclusion criteria: non‐cardiac surgery (major abdominal) with risk or at high risk of coronary artery disease Exclusion criteria: chronic metoprolol use Type of surgery: non‐cardiac surgery (major abdominal) Baseline characteristics Intervention group (metoprolol)
Control group (standard care)
Country: China Setting: single centre; hospital |
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Interventions |
Intervention group (metoprolol)
Control group (standard care)
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Outcomes |
Outcomes measured/reported by study authors: changes in HR, levels of creatine kinase (CK‐MB), mortality, acute MI, stroke Outcomes relevant to the review: mortality, acute MI, stroke |
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Notes |
Funding/declarations of interest: not reported Study dates: January 2006‐October 2007
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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 | High risk | Open‐label trial |
Blinding of outcome assessors (detection bias) All outcomes | High risk | Open‐label trial |
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 | Low risk | Not detected |