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Table 1 Baseline characteristics of study subjects (n = 65)

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

Characteristic

Number (%) or median (IQR)

Demographics

 Age (years) (mean, SD)

60 (14)

 Male sex

46 (70.8%)

 Body mass index (kg/m2) (mean, SD)

22.2 (3.1)

Comorbidities

 Diabetes mellitus

8 (12.3%)

 Liver cirrhosis

5 (7.7%)

 Chronic kidney disease

0 (0.0%)

 Solid organ transplant

8 (12.3%)

 Solid cancer

29 (44.6%)

 Hematologic cancer

28 (43.1%)

 Immunocompromised

1 (1.5%)

 Charlson comorbidity index

5 (3, 7)

Source of bacteremia

 Intraabdominal infection

33 (50.8%)

 Urinary tract infection

4 (6.2%)

 Primary bacteremia

23 (35.4%)

 Others

5 (7.7%)

Severity of infection

 Pitt bacteremia score

0 (0, 2)

 ICU admission at the onset of bacteremia (n = 63*)

2 (3.1%)

 Acute kidney injury at the onset of bacteremia

8 (12.3%)

Laboratory test at the onset of bacteremia

 White blood cell count (× 103/μL)

5.83 (0.28, 12.03)

 Neutropenia

21 (32.3%)

 C-reactive protein (mg/dL) (n = 64**)

8.9 (5.4, 12.9)

 CLCr (mL/min)

96.7 (59.8, 123.9)

Microbiologic test results

 Enterococcus faecium isolated

62 (95.4%)

 Vancomycin MIC determined by broth microdilution (μg/mL)

1 (1, 1)

Factors related to vancomycin treatment

 Initiation of vancomycin as empiric antibiotic

62 (95.4%)

 Use of loading dose

14 (21.4%)

 Average AUC24 during initial 72 h (mg/L)

555 (443, 621)

 Average AUC24/MIC during initial 72 h

579 (453, 676)

 Average trough concentration (μg/mL) (mean, SD)

13.71 (4.48)

 Duration of treatment (days)

10 (7, 13)

Other factors potentially related to prognosis

 Bloodstream infection with other microorganism(s) within a month

27 (41.5%)

 Source control indicated

26 (40.0%)

 Source control performed (n = 26)

12 (18.5%)

 Infectious diseases consultation

45 (69.2%)

  1. IQR, interquartile range; SD, standard deviation; ICU, intensive care unit; CLCr, creatinine clearance; MIC, minimum inhibitory concentration; AUC24, area under the curve during 24 h; N/A, not applicable
  2. *Two patients who were already in the ICU at the onset of bacteremia were not included
  3. **One patient who did not have C-reactive protein measured at the onset of bacteremia was not included