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. 2019 Sep 23;2019(9):CD013435. doi: 10.1002/14651858.CD013435

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
Interventions Intervention group (metoprolol)
  • Randomized, n = 67; losses = 0; analysed, n = 67 (use of ITT analysis not reported)

  • Details: metoprolol given after extubation until 24 h before discharge. No additional details


Control group (placebo)
  • Randomized, n = 66; losses = 0; analysed, n = 66

  • Details: no details. We assume that the placebo was given the same as the intervention drug

Outcomes Outcomes measured/reported by study authors: AF (period of observation is unclear)
Outcomes relevant to the review: AF
Notes Funding/declarations of interest: not reported
Study dates: January 1995‐May 1997
Notes:
  • conference abstract. We attempted to contacted the study authors by email to request additional information or for a full‐text publication; this was unsuccessful

  • study includes an additional group (flecainide) which we did not include in the review

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