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. 2023 Nov 2;6(2):100950. doi: 10.1016/j.jhepr.2023.100950

Table 5.

Adjusted probabilities for 3-month mortality in propensity-matched patients.

Risk factors 3-month mortality
Adjusted odds ratio (95% CI) p value
ABSI 1.11 (0.97–1.26) 0.122
SAPS II 1.04 (1.03–1.06) <0.001
Acute kidney injury 0.88 (0.37–2.00) 0.756
Acute respiratory distress syndrome 0.86 (0.33–2.18) 0.751
Cholestatic liver injury with ketamine ≥10,000 mg 9.92 (2.76–39.05) 0.001
No cholestatic liver injury with ketamine ≥10,000 mg 0.43 (0.02–2.64) 0.446
Cholestatic liver injury with ketamine <10,000 mg 0.90 (0.14–3.78) 0.894
Total sufentanil (mg): (0, 50] 1.77 (0.54–5.71) 0.340
Total sufentanil (mg): (50, 1,500] 0.58 (0.17–1.86) 0.367
Total sufentanil (mg): (1,500, 5,000] 0.42 (0.08–1.98) 0.281
Total sufentanil (mg): (5,000, Inf] 0.23 (0.04–1.36) 0.110
Total midazolam (mg): (0, 500] 1.97 (0.68–5.92) 0.216
Total midazolam (mg): (500, 1,500] 2.95 (0.61–14.37) 0.177
Total midazolam (mg): (1,500, Inf] 1.31 (0.21–8.08) 0.768
Observations 279

Patient were matched (full matching) on the probability of receiving ketamine dose >1,000 mg according to severity of illness (ABSI and SAPS II scores), and organ failure (acute kidney injury, acute respiratory syndrome, and septic shock). Risks were computed with multivariate logistic regression models. Cholestatic liver injury corresponded to an increase of ALP ≥1.5 × ULN with a concomitant increase of serum GGT ≥3 × ULN and TBIL >ULN. The SAPS II ranges from 0 to 163, with higher scores indicating greater severity of illness. The ABSI ranges from 0 to 18, with higher scores indicating a greater probability of death after the burn injury.

ABSI, abbreviated burn severity index; ALP, alkaline phosphatase; TBIL, total bilirubin; GGT, gamma glutamyl transferase; Inf, infinite; SAPS II, Simplified Acute Physiology Score II; ULN, upper limit of normal.