Study characteristics |
Methods |
Double‐blind, randomized, placebo‐controlled |
Participants |
On‐pump CABG only |
Interventions |
Landiolol vs. placebo |
Outcomes |
AF lasting at least 5 minutes or requiring intervention for hemodynamic compromise; Stroke; Mortality; CV Mortality; LOS; Cost |
Follow‐Up |
7 days |
Concurrent Antiarrhythmic Medications |
None |
Notes |
|
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Low risk |
Randomization by lottery method |
Allocation concealment (selection bias) |
Unclear risk |
Concealment methods not described |
Blinding of participants and personnel (performance bias)
All outcomes |
Low risk |
Double‐blind |
Blinding of outcome assessment (detection bias)
All outcomes |
Low risk |
Double‐blind |
Incomplete outcome data (attrition bias)
All outcomes |
Low risk |
|
Selective reporting (reporting bias) |
Low risk |
|
Intention‐to‐treat analysis |
High risk |
No |