CRRT (n = 2175) | IHD (n = 367) | Unadjusted analysis | Adjusted analysisa | |||
---|---|---|---|---|---|---|
Effect estimate (95% CI) | p value | Effect estimate (95% CI) | p value | |||
Primary outcome | ||||||
RRT dependence at day 28—no. (%) | 320 (14.7) | 113 (30.8) | SHR, 0.75 (0.67 to 0.83) | < 0.001 | SHR, 0.96 (0.84 to 1.10) | 0.570 |
Death before the event | 618 (28.4) | 95 (25.9) | ||||
Secondary outcomes | ||||||
RRT dependence at day 60—no. (%) | 145 (6.8) | 49 (13.7) | SHR, 0.75 (0.62 to 0.90) | 0.002 | SHR, 1.04 (0.85 to 1.28) | 0.670 |
Death before the event | 673 (31.3) | 109 (30.4) | ||||
RRT-free days at day 28 | 0.0 (0.0–22.0) | 0.0 (0.0–17.0) | COR, 1.38 (1.11 to 1.71) | 0.004 | COR, 1.45 (1.12 to 1.88) | 0.005 |
Mean ± SD | 9.1 ± 10.9 | 7.2 ± 10.2 | ||||
ICU length of stay, days | 9.0 (4.0–19.0) | 13.0 (7.0–25.0) | SHR, 0.82 (0.72 to 0.94)* | 0.003 | SHR, 1.03 (0.87 to 1.21)* | 0.750 |
In survivors | 11.0 (6.0–21.0) | 13.0 (7.0–25.0) | ||||
Hospital length of stay, days | 19.0 (9.0–36.0) | 25.0 (15.0–41.0) | SHR, 0.69 (0.60 to 0.81)* | < 0.001 | SHR, 0.81 (0.68 to 0.97)* | 0.025 |
In survivors | 28.0 (17.0–47.0) | 30.0 (18.0–44.0) | ||||
ICU mortality—no. (%) | 848 (39.0) | 108 (29.4) | OR, 1.53 (1.21 to 1.95) | < 0.001 | OR, 0.96 (0.71 to 1.29) | 0.778 |
Hospital mortality—no. (%) | 1016 (46.7) | 121 (33.0) | OR, 1.78 (1.41 to 2.26) | < 0.001 | OR, 1.14 (0.86 to 1.52) | 0.361 |
28-day mortality—no. (%) | 875 (40.2) | 114 (31.1) | HR, 1.38 (1.13 to 1.68)** | 0.001 | HR, 0.90 (0.72 to 1.12)** | 0.343 |
60-day mortality—no. (%) | 1005 (46.7) | 143 (39.4) | HR, 1.28 (1.07 to 1.52)** | 0.006 | HR, 0.92 (0.75 to 1.13)** | 0.434 |
Sensitivity analysis | ||||||
Among survivors at the longest follow-up—no. (%) | ||||||
RRT dependence at day 28 | 232 (20.9) | 90 (40.9) | OR, 0.38 (0.28 to 0.52) | < 0.001 | OR, 0.54 (0.37 to 0.80) | 0.002 |
RRT dependence at day 60 | 136 (12.3) | 49 (22.6) | OR, 0.48 (0.33 to 0.70) | < 0.001 | OR, 0.76 (0.48 to 1.22) | 0.261 |