Table 2.
Group | Comparison | HR (95% CI) |
---|---|---|
Ventricular tachycardia | ||
HFrEF | HFrEF vs no HF | 7.00 (6.10-8.02) |
HFpEF | HFpEF vs no HF | 1.99 (1.70-2.32) |
Taking D or S | Taking D or S vs not taking D or S | 2.47 (1.89-3.23) |
HFrEF taking D or S | HFrEF taking D or S vs HFrEF not taking D or S | 1.53 (1.07-2.20) |
HFpEF taking D or S | HFpEF taking D or S vs HFpEF not taking D or S | 2.34 (1.11-4.95) |
Sudden cardiac arrest | ||
HFrEF | HFrEF vs no HF | 5.19 (4.10-6.57) |
HFpEF | HFpEF vs no HF | 2.53 (1.98-3.23) |
Taking D or S | Taking D or S vs not taking D or S | 1.39 (0.70-2.76) |
HFrEF taking D or S | HFrEF taking D or S vs HFrEF not taking D or S | 1.82 (0.60-5.52) |
HFpEF taking D or S | HFpEF taking D or S vs HFpEF not taking D or S | 0.86 (0.33-2.24) |
D = dofetilide; S = sotalol; other abbreviations as in Table 1.
The multinomial propensity scoremethod was used to select potential covariates (listed in Supplemental Tables 7 and 8), and any characteristics with SMDs larger than 0.1 (listed in Supplemental Tables 7 and 8) were incorporated into the final model for double adjustment. The inverse probability of treatment weighting was used to stabilize the covariates-induced differences and survival analysis for the recurrent events model was performed. HFrEF, HFpEF, and taking D or S are the main effects, and HFrEF taking D or S and HFpEF taking D or S are the interaction terms in the model.