Table 3.
Sensitivity analyses of the primary outcome: time to resolution of shock
| Metaraminol and norepinephrine* | Norepinephrine* | P value† | HR (95% CI)‡ | SHR (95% CI)§ |
| Full sample (n=286) | ||||
| 44 (28 to 66) | 27 (14 to 63) | <0.01 | 1.24 (0.96 to 1.60) | 1.16 (0.90 to 1.49) |
| Subset with sepsis (n=131) | ||||
| 50 (31 to 76) | 41 (21 to 75) | 0.15 | 1.09 (0.74 to 1.60) | 1.04 (0.71 to 1.51) |
| Subset without other concurrent vasopressors or inotropes (n=201) | ||||
| 41 (26 to 60) | 22 (13 to 41) | <0.01 | 1.55 (1.16 to 2.07) | 1.54 (1.14 to 2.09) |
| Subset with sepsis and without other concurrent vasopressors or inotropes (n=86) | ||||
| 45 (29 to 61) | 26 (14 to 58) | 0.02 | 1.32 (0.84 to 2.07) | 1.42 (0.90 to 2.23) |
*Reported as median (IQR) hours from Kaplan-Meier analysis.
†Wilcoxon test.
‡HR from Cox regression.
§Sub-hazard ratio with death as a competing risk.