# No Impact of Vancomycin MIC, AUC, or AUC/MIC in Enterococcus faecium Bacteremia

## TL;DR

This study found no link between vancomycin levels or resistance and mortality in patients with a specific type of blood infection.

## Contribution

The study shows that vancomycin MIC, AUC, or AUC/MIC are not reliable predictors of mortality in Enterococcus faecium bacteremia.

## Key findings

- In-hospital mortality was not associated with vancomycin MIC or AUC/MIC in Enterococcus faecium bacteremia.
- Amoxicillin susceptibility did not significantly affect mortality outcomes.
- Retrospective studies on severe comorbidities may not determine vancomycin's PK/PD targets.

## Abstract

There is no clear pharmacokinetic and pharmacodynamic (PK/PD) target during vancomycin‐susceptible
Enterococcus faecium
bacteremia (EFB).

To investigate whether in‐hospital mortality was associated with susceptibility to amoxicillin or vancomycin minimum inhibitory concentration (MIC) of the strain and with area under the curve over 24 h (AUC) and AUC/MIC during EFBs.

All
E. faecium
strains isolated from blood cultures performed between January 1, 2017, and December 31, 2022, were included, and clinicobiological data were retrospectively extracted from corresponding medical records. The Vancomycin MICs were estimated using the VITEK 2 automated system. AUC was calculated among patients who received vancomycin during their first episode of EFB with available data.

Two hundred fifteen
E. faecium
strains not susceptible to amoxicillin had been isolated in 207 patients (125 male, median age 69 [1–98] years) with biliary and digestive tract diseases, hematologic malignancies, or COVID‐19 in 124 (59.9%), 35 (16.9%), and 17 (8.2%) cases, respectively. The median vancomycin MIC was 0.5 [0.5–2] mg/L, and 67 patients (32.3%) died during the hospitalization. In‐hospital mortality was not associated with susceptibility to amoxicillin (p = 0.14) or vancomycin MIC (p = 0.07) of the strain. Neither mean AUC (592.7 versus 521.7mgh/L) nor mean AUC/MIC ratio (1066.5 versus 1000.5) was associated with in‐hospital mortality (p = 0.17 and p = 0.54, respectively).

Besides amoxicillin susceptibility and vancomycin MIC of the strain, there was no significant association between in‐hospital mortality and vancomycin AUC or AUC/MIC. Retrospective observational studies focusing on in‐hospital mortality among patients with severe comorbidities may not be adequate for the determination of the PK/PD target of vancomycin.