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Table 3 Comparison of characteristics by 30-day mortality

From: Pharmacokinetic/pharmacodynamic parameters of vancomycin for predicting clinical outcome of enterococcal bacteremia

 

Survival (n = 56)

Death (n = 9)

Odds ratio (95% CI)

p-value

Adjusted odds ratio (95% CI)

p-value

Demographics

 Age (year)

59 (53, 70)

64 (52, 71)

 

0.864

  

 Male sex

39 (69.6%)

7 (77.8%)

1.53 (0.29–8.12)

> 0.999

  

 Body mass index (kg/m2)

22.1 (20.1, 24.1)

22.4 (18.7, 23.3)

 

0.488

  

Comorbidities

 Diabetes mellitus

5 (8.9%)

3 (33.3%)

5.10 (0.97–26.89)

0.074

5.58 (0.90–38.55)

0.064

 Liver cirrhosis

5 (8.9%)

0 (0.0%)

N/A

> 0.999

  

 Solid organ transplant

7 (12.5%)

1 (11.1%)

0.88 (0.09–8.09)

> 0.999

  

 Solid cancer

33 (58.9%)

3 (33.3%)

0.35 (0.07–1.54)

0.278

  

 Hematologic cancer

26 (46.4%)

2 (22.2%)

0.33 (0.06–1.73)

0.280

  

 Charlson comorbidity index

5 (3, 6)

8 (3, 9)

 

0.276

  

Source of bacteremia

      

 Intraabdominal infection

29 (51.8%)

4 (44.4%)

1.34 (0.33–5.53)

0.733

  

 Urinary tract infection

4 (7.1%)

0 (0.0%)

N/A

> 0.999

  

 Primary bacteremia

19 (33.9%)

4 (44.4%)

1.56 (0.37–6.49)

0.709

  

 Others

4 (7.1%)

1 (11.1%)

1.63 (0.16–16.44)

0.536

  

Severity of infection

 Pitt bacteremia score

0 (0, 1)

2 (0, 2)

 

0.134

  

 ICU admission at the onset of bacteremia

2 (3.7%)

0 (0.0%)

N/A

> 0.999

  

 AKI at the onset of bacteremia

5 (8.9%)

3 (33.3%)

5.10 (0.97–26.89)

0.074

  

Laboratory test results

 Neutropenia

21 (37.5%)

0 (0.0%)

N/A

0.026

  

 White blood cell count (× 103/μL)

3.00 (0.22, 10.31)

11.08 (7.97, 13.68)

 

0.024

1.04 (1.00–1.16)

0.072

 C-reactive protein (mg/dL)

8.9 (5.4, 12.9)

8.9 (4.9, 12.5)

 

0.643

  

 Creatinine clearance (mL/min)

96.4 (64.8, 125.6)

98.6 (57.8, 106.4)

 

0.857

  

Factors related to vancomycin treatment

 

 Use of vancomycin loading dose

44 (78.6%)

7 (77.8%)

0.95 (0.18–5.21)

> 0.999

  

 Average AUC24 during initial 72 h (mg/L)

531 (435, 603)

616 (562, 706)

 

0.016

  

 Average AUC24/MIC during initial 72 h

564 (435, 658)

616 (561, 1053)

 

0.043

  

 Average AUC24/MIC ≥ 504

34 (60.7%)

9 (100.0%)

 

0.023

  

 Average trough during initial 72 h (μg/mL)

12.52 (10.14, 15.14)

15.88 (14.94, 17.86)

 

0.013

  

 Average trough ≥ 13.94 μg/mL

20 (35.7%)

8 (88.9%)

14.40 (1.68–123.56)

0.004

8.40 (1.60–86.62)

0.010

 Duration of vancomycin treatment (days)

11 (8, 14)

7 (7, 10)

 

0.034

  

 Nephrotoxicity

10 (17.9%)

4 (44.4%)

3.68 (0.84–16.20)

0.091

  

Other factors potentially related to prognosis

 

 Bloodstream infection due to other microorganism(s) within a month

24 (42.9%)

3 (33.3%)

0.67 (0.15–2.94)

0.724

  

 Source control indicated

21 (37.5%)

5 (55.6%)

2.08 (0.50–8.63)

0.465

  

 Source control performed (n = 26)

10 (47.6%)

2 (40.0%)

0.73 (0.10–5.33)

> 0.999

  

 Consult with infectious disease expert

17 (30.4%)

3 (33.3%)

1.15 (0.26–5.13)

> 0.999

  
  1. Logistic regression with backward selection (threshold p < 0.10) was used for the multivariable model
  2. CI, confidence interval; ICU, intensive care unit; AKI, acute kidney injury; AUC24, area under the curve during 24 h; MIC, minimum inhibitory concentration; N/A, not applicable
  3. *Amikacin was the only aminoglycoside in all patients who received aminoglycoside concurrently with vancomycin