Outcomes | Group | Hazard ratio | 95% CI | p value |
---|
90-days mortality |
Crude | Non-AF | Ref | | |
| New-onset AF | 1.41 | 1.30–1.52 | < 0.001 |
Model 1 | Non-AF | Ref | | |
| New-onset AF | 1.33 | 1.22–1.44 | < 0.001 |
Model 2 | Non-AF | Ref | | |
| New-onset AF | 1.37 | 1.26–1.50 | < 0.001 |
Crude | Pre-existing AF | Ref | | |
| New-onset AF | 0.81 | 0.75–0.89 | < 0.001 |
Model 1 | Pre-existing AF | Ref | | |
| New-onset AF | 1.21 | 1.11–1.33 | < 0.001 |
Model 2 | Pre-existing AF | Ref | | |
| New-onset AF | 1.12 | 1.02–1.23 | 0.019 |
- Model 1 was adjusted by: age, gender, type of intensive care unit, hypertension, diabetes, coronary heart diseases, congestive heart failure, hyperlipidemia, chronic obstructive pulmonary disease (COPD), cerebral infarction, pulmonary embolism, sepsis, and hypothyroidism; Model 2 was adjusted by: except variables in model 1, the following have been added: Sequential Organ Failure Assessment(SOFA) score, laboratory tests performed on admission, including white blood cells (WBC), hemoglobin (HB), serum creatinine (Scr), and medications during hospitalization, including β blockers, statin, amiodarone, Non-dihydropyridine calcium channel blocker (CCB), digoxin, warfarin
- AF atrial fibrillation, Ref reference