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. 2016 Feb 23;36(3):235–243. doi: 10.3343/alm.2016.36.3.235

Table 6. Univariate analysis of predictors for 30-day mortality in patients with SAP.

Characteristics 30-day mortality (+)
(N=5) (%)
30-day mortality (-)
(N=34) (%)
P
Age (mean, yr) 58.8±16.9 67.9 ± 13.9 NS
Old age (≥ 65 yr) 2 (40.0) 23 (67.6) NS
Male 4 (80.0) 23 (67.6) NS
Vancomycin MIC ≥ 1.5 µg/mL 4 (80.0) 19 (55.9) NS
Teicoplanin MIC ≥ 4 µg/mL 3 (60.0) 11 (32.4) NS
MRSA (+) 3 (60.0) 24 (70.6) NS
hVISA* (+) 3 (60.0) 14 (41.2) NS
Duration of hospital stay before SAP onset 21.0 ± 24.2 7.2 ± 11.5 0.0391
Mode of transmission
 Hospital-acquired 2 (40.0) 9 (26.5) NS
Comorbidity
 Solid cancer 2 (40.0) 5 (14.7) NS
 Hematologic malignancy 0 (-) 4 (11.8) NS
 Diabetes mellitus 2 (40.0) 9 (26.5) NS
 Cerebrovascular accident 3 (60.0) 6 (17.6) NS
 Congestive heart failure 0 (-) 4 (11.8) NS
 Chronic liver disease 0 (-) 2 (5.9) NS
 Chronic respiratory disease 0 (-) 7 (20.6) NS
 Chronic kidney disease 2 (40.0) 7 (20.6) NS
Previous treatment
 Previous surgery 2 (40.0) 7 (20.6) NS
 Cancer chemotherapy 1 (20.0) 4 (12.8) NS
 Immunosuppressive therapy 0 (-) 2 (5.9) NS
 Prior vancomycin therapy 2 (40.0) 10 (29.4) NS
Appropriate empirical therapy 2 (40.0) 22 (64.7) NS

Categorical variables were compared using Fisher's exact test, and continuous variables were compared using Mann-Whitney U test.

*The hVISA phenotype was identified by macromethod E test.

Abbreviations: SAP, S. aureus pneumonia; MRSA, methicillin-resistant S. aureus; hVISA, heterogeneous vancomycin-intermediate S. aureus; MIC, minimum inhibitory concentration; NS, not significant.