Table 5.
Association between autoimmune disease and 30-day mortality, accounting for chronic DMARD and prednisone use | Sepsis cohort | Septic shock cohort | ||
---|---|---|---|---|
OR (95% CI) | P value | OR (95% CI) | P value | |
All potential confounders adjusteda | ||||
No autoimmune disease presence | ||||
No chronic DMARD/prednisone usage | 1.00 | Reference | 1.00 | Reference |
Autoimmune disease presence | ||||
No chronic DMARD or prednisone usage | 0.82 (0.58–1.16) | 0.272 | 0.76 (0.50–1.14) | 0.186 |
Chronic DMARD or prednisone usage | 0.89 (0.65–1.20) | 0.452 | 0.87 (0.62–1.22) | 0.428 |
SOFA score adjusted | ||||
No autoimmune disease presence | ||||
No chronic DMARD/prednisone usage | 1.00 | Reference | 1.00 | Reference |
Autoimmune disease presence | ||||
No chronic DMARD or prednisone usage | 0.80 (0.57–1.11) | 0.190 | 0.73 (0.49–1.07) | 0.114 |
Chronic DMARD or prednisone usage | 0.84 (0.62–1.12) | 0.231 | 0.77 (0.55–1.07) | 0.121 |
Sepsis cohort—ICU patients with sepsis as defined by Martin criteria. Septic shock cohort—ICU patients with sepsis as defined by Martin criteria and three consecutive mean arterial blood pressure readings below 65 mmHg in a 30-min period or at least one dose of vasopressors during the ICU stay
OR odds ratio, CI confidence interval, DMARD disease-modifying antirheumatic drug, SOFA Sequential Organ Failure Assessment
aOR adjusted for age, sex, race, SOFA score at ICU admission, Elixhauser comorbidity index, pre-admission chronic DMARD or prednisone use, ICU care unit, documented bacteremia, and infection site