Surveillance strategies and impact of vancomycin-resistant enterococcal colonization and infection in critically ill patients

C W Hendrix, J M Hammond, S M Swoboda, W G Merz, S M Harrington, T M Perl, J D Dick, D M Borschel, P W Halczenko, R K Pelz, L E Rocco, J E Conway, R G Brower, P A Lipsett, C W Hendrix, J M Hammond, S M Swoboda, W G Merz, S M Harrington, T M Perl, J D Dick, D M Borschel, P W Halczenko, R K Pelz, L E Rocco, J E Conway, R G Brower, P A Lipsett

Abstract

Objective: To determine the optimal site and frequency for vancomycin-resistant enterococci (VRE) surveillance to minimize the number of days of VRE colonization before identification and subsequent isolation.

Summary background data: The increasing prevalence of VRE and the limited therapeutic options for its treatment demand early identification of colonization to prevent transmission.

Methods: The authors conducted a 3-month prospective observational study in medical and surgical intensive care unit (ICU) patients with a stay of 3 days or more. Oropharyngeal and rectal swabs, tracheal and gastric aspirates, and urine specimens were cultured for VRE on admission to the ICU and twice weekly until discharge.

Results: Of 117 evaluable patients, 23 (20%) were colonized by VRE. Twelve patients (10%) had VRE infection. Of nine patients who developed infections after ICU admission, eight were colonized before infection. The rectum was the first site of colonization in 92% of patients, and positive rectal cultures preceded 89% of infections acquired in the ICU. This was supported by strain delineations using pulsed-field gel electrophoresis. Twice-weekly rectal surveillance alone identified 93% of the maximal estimated VRE-related patient-days; weekly or admission-only surveillance was less effective. As a test for future VRE infection, rectal surveillance culture twice weekly had a negative predictive value of 99%, a positive predictive value of 44%, and a relative risk for infection of 34.

Conclusions: Twice-weekly rectal VRE surveillance of critically ill patients is an effective strategy for early identification of colonized patients at increased risk for VRE transmission, infection, and death.

Figures

https://www.ncbi.nlm.nih.gov/pmc/articles/instance/1421209/bin/16FF1.jpg
Figure 1. Schematic of vancomycin-resistant enterococci events. The denominator for the percentages is the number in the branch immediately above the percentage.
https://www.ncbi.nlm.nih.gov/pmc/articles/instance/1421209/bin/16FF2.jpg
Figure 2. Pulsed-field gel electrophoresis (PFGE) of colonization/infection pairs. PFGE of SmaI DNA digests of paired vancomycin-resistant enterococci isolates from nine patients with infection acquired in the intensive care unit. First colonizing rectal isolates are designated 1R to 9R. The corresponding first-infected site isolate from the same patient is designated 1I to 9I. End lanes contain NotI-digested Enterococcus faecalis OGIRF molecular weight marker. Band sizes are shown to the left in kilobase (kb) pairs. Patients 1 to 4 are in panel A, patients 5 to 9 in panel B.

Source: PubMed

3
Subskrybuj