Table 2.
Etomidate | Other Agent | Crude Relative Risk (95% CI) |
Adjusted Relative Risk (95% CI)* |
|
---|---|---|---|---|
Hospital mortality, no. (%) | 175 (38.7) | 108 (29.0) | 1.33 (1.09–1.62) | 1.20 (0.99–1.45) |
Diagnosis of CIRCI following intubation, no. (%)† | 140 (62.5) | 74 (47.1) | 1.33 (1.09–1.61) | 1.37 (1.12–1.66) |
Non-responsiveness‡ to cosyntropin following intubation, no. (%)§ | 127 (56.4) | 57 (36.0) | 1.59 (1.25–2.01) | 1.59 (1.26–2.00) |
Adjusted for age, sex, and Simplified Acute Physiology Score (SAPS II).
Restricted to the 412 subjects whose adrenal function was tested within the 48 hours following intubation, of whom 31 had baseline cortisol ≥ 10 μg/dL and Δ max of ≤ 9 μg/dL but were missing data for their 60-min post-stimulation reading, precluding definitive diagnosis of CIRCI. We omitted those subjects. Including them by using their 30-min result provided an adjusted relative risk of 1.37 (95% CI 1.12–1.68).
Non-responsiveness was defined as a Δ max of ≤ 9 μg/dL following administration of cosyntropin.
Restricted to the 412 subjects whose adrenal function was tested within the 48 hours following intubation, of whom 29 subjects had 30-min results of ≤ 9 μg/dL but were missing data for their 60-min post-stimulation reading, precluding definitive diagnosis of non-responsiveness. We omitted those subjects. Including them by using their 30-min result provided an adjusted relative risk of 1.46 (95% CI 1.19–1.78).
CIRCI = critical illness-related corticosteroid insufficiency, defined as a random total cortisol < 10 μg/dL and/or a Δ max cortisol following cosyntropin administration of < 9 μg/dL