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Table 3 Primary and secondary outcomes

From: Initiating angiotensin II at lower vasopressor doses in vasodilatory shock: an exploratory post-hoc analysis of the ATHOS-3 clinical trial

Primary outcome, 28-day survival in the Low-NED (≤ 0.25 µg/kg/min) subgroup

Placebo (n = 48)

AT II (n = 56)

HR (95% CI)

p-value

48% (33%–61%)

64% (50%–75%)

0.51 (0.27, 0.95)

0.03

Secondary outcome, 28-day survival in the High-NED (> 0.25 µg/kg/min) subgroup

Placebo (n = 110)

AT II (n = 107)

HR (95% CI)

p-value

45% (36–54%)

49% (39–58%)

0.93 (0.64, 1.35)

0.71

  1. Values are expressed as median (IQR)
  2. AT II, angiotensin II; NED, norepinephrine-equivalent dose