Skip to main content
. 2021 Aug 10;25:289. doi: 10.1186/s13054-021-03706-2

Table 3.

Secondary safety outcomes

End point Beta-blocker (n = 93) No beta-blocker (n = 99) Crude RR (95% CI) P value Adjusted RRa (95% CI) P value
Cardiac intensive care unit length of stay greater than or equal to 7 days 31 (33%) 42 (42%) 0.79 (0.54–1.13) 0.19 0.71 (0.48–1.03) 0.07
Acute kidney injuryb 86 (96%) 85 (88%) 1.09 (1.00–1.19) 0.051 1.05 (0.92–1.21) 0.47
Arrhythmia requiring medical team interventionc 51 (55%) 41 (41%) 1.32 (0.98–1.78) 0.06 1.21 (0.89–1.65) 0.23
Atrial arrhythmia requiring medical team intervention 47 (51%) 32 (32%) 1.56 (1.10–2.22) 0.01 1.33 (0.92–1.91) 0.13
Ventricular arrhythmiad 11 (12%) 20 (20%) 0.59 (0.30–1.15) 0.12 0.59 (0.29–1.21) 0.15
Need for oral or intravenous anti-arrhythmic therapy 48 (52%) 36 (36%) 1.42 (1.02–1.97) 0.03 1.30 (0.92–1.85) 0.14
Need for uptitration or addition of vasopressor therapy 91 (98%) 96 (97%) 1.01 (0.96–1.06) 0.70 1.02 (0.86–1.21) 0.84

aAdjusted for age, sex, beta-blocker use, inotrope (dobutamine vs. milrinone), and history of atrial fibrillation; relative risk presented is for β(beta-blocker)

bPatients with a history of renal replacement therapy prior to randomization were excluded from analysis

cDefined as electrical/chemical cardioversion or any intravenous anti-arrhythmia medication administration

dDefined as monomorphic or polymorphic ventricular tachycardia greater than 30 s, or hemodynamically unstable ventricular arrhythmia requiring intervention, or ventricular fibrillation