Table 2

Primary and secondary outcomes in the intention-to-treat analysis

OutcomeBeta-blockers (n=34 253)
Events/100 patient-years (incidence rate)
No beta-blockers (n=9365)
Events/100 patient-years (incidence rate)
Hazard ratio
(95% CI) for beta-blockers (unadjusted)
Hazard ratio
(95% CI) for beta-blockers (adjusted)
Primary composite outcome6475/1709 (3.8)2028/414 (4.9)0.76 (0.73 to 0.80)0.99 (0.93 to 1.04)
 All-cause mortality2872/1733 (1.7)945/420 (2.3)0.72 (0.67 to 0.78)1.00 (0.92 to 1.09)
 Myocardial infarction2598/1733 (1.5)787/420 (1.9)0.82 (0.76 to 0.89)1.00 (0.91 to 1.09)
 Unscheduled revascularisation1415/1709 (0.8)372/414 (0.9)0.95 (0.84 to 1.06)0.96 (0.85 to 1.09)
 Heart failure hospitalisation462/1733 (0.3)145/420 (0.4)0.78 (0.65 to 0.94)1.05 (0.85 to 1.31)
Other secondary outcomes
 Cardiovascular mortality760/1481 (0.5)270/355 (0.8)0.68 (0.59 to 0.78)0.98 (0.83 to 1.14)
 Stroke1136/1704 (0.7)318/412 (0.8)0.88 (0.78 to 1.00)1.02 (0.89 to 1.17)
Negative control outcome
 Pneumonia1314/1707 (0.8)375/414 (0.9)0.86 (0.77 to 0.97)1.07 (0.94 to 1.22)
  • The primary composite outcome was a composite of all-cause mortality, myocardial infarction, hospitalisation for heart failure and unscheduled coronary revascularisation. Person time and incidence rate is given in 100 person-years. Hazard ratios are given with 95% confidence intervals. The no beta-blockers group is the reference group.