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. 2021 Apr 17;160(5):1624–1633. doi: 10.1016/j.chest.2021.04.015

Table 4.

Association of PA Pathogen Characteristics and Mortality in Early Samples

PA Pathogen Characteristics, n = 156 30-d Mortality
90-d Mortality
Unadjusted
OR (95% CI)
Adjusteda
OR (95% CI)
Unadjusted
OR (95% CI)
Adjustedb
OR (95% CI)
Elastase activity, per SD 1.67 (1.17-2.38) 1.56 (1.10-2.23) 1.62 (1.12-2.34) 1.55 (1.08-2.22)
Protease activity, per SD 1.58 (1.14-2.20) 1.46 (1.04-2.07) 1.39 (1.01-1.92) 1.30 (0.92-1.86)
Biofilm production,c per SD 1.03 (0.77-1.38) 1.01 (0.75-1.36) 1.10 (0.82-1.47) 1.05 (0.77-1.44)
MDR/XDRc 0.98 (0.56-1.72) 0.83 (0.39-1.78) 0.86 (0.51-1.48 0.72 (0.34-1.51)
Polymicrobiald 0.41 (0.23-0.73) 0.57 (0.27-1.22) 0.66 (0.39-1.12) 0.91 (0.44-1.87)

A logistic regression model was used to determine the association between PA pathogen factors and 30-d and 90-d mortality in early samples collected between 0 and 3 days from the index ICU admission date. The early and late subgroups were determined using a finite mixture model. CCI = Charlson Co-morbidity Index; MDR = multidrug-resistant; mSOFA = modified sequential organ failure assessment score; XDR = extensively drug resistant.

a

The 30-d mortality model was adjusted for age, sex, and mSOFA.

b

The 90-d mortality model was adjusted for age, sex, mSOFA, and CCI. P < .05 are in bold.

c

n = 154 for Biofilm production and n = 153 for MDR/XDR.

d

n = 154 for polymicrobial.