AI Article Synopsis

  • The study aimed to explore how the concentration of chlorhexidine gluconate (CHG) on the skin affects microbial colonization, particularly in adult patients in medical ICUs across several hospitals.
  • By collecting skin swab samples and measuring CHG concentration, researchers found that higher CHG levels correlated with fewer detections of gram-positive bacteria and specific species, while gram-negative bacteria were less affected.
  • The findings suggest that increasing CHG skin concentrations could enhance infection control for certain pathogens, although no specific threshold level was identified for reducing microbial detection.

Article Abstract

Objective: To characterize the relationship between chlorhexidine gluconate (CHG) skin concentration and skin microbial colonization.

Design: Serial cross-sectional study.

Setting/participants: Adult patients in medical intensive care units (ICUs) from 7 hospitals; from 1 hospital, additional patients colonized with carbapenemase-producing Enterobacterales (CPE) from both ICU and non-ICU settings. All hospitals performed routine CHG bathing in the ICU.

Methods: Skin swab samples were collected from adjacent areas of the neck, axilla, and inguinal region for microbial culture and CHG skin concentration measurement using a semiquantitative colorimetric assay. We used linear mixed effects multilevel models to analyze the relationship between CHG concentration and microbial detection. We explored threshold effects using additional models.

Results: We collected samples from 736 of 759 (97%) eligible ICU patients and 68 patients colonized with CPE. On skin, gram-positive bacteria were cultured most frequently (93% of patients), followed by species (26%) and gram-negative bacteria (20%). The adjusted odds of microbial recovery for every twofold increase in CHG skin concentration were 0.84 (95% CI, 0.80-0.87; < .001) for gram-positive bacteria, 0.93 (95% CI, 0.89-0.98; = .008) for species, 0.96 (95% CI, 0.91-1.02; = .17) for gram-negative bacteria, and 0.94 (95% CI, 0.84-1.06; = .33) for CPE. A threshold CHG skin concentration for reduced microbial detection was not observed.

Conclusions: On a cross-sectional basis, higher CHG skin concentrations were associated with less detection of gram-positive bacteria and species on the skin, but not gram-negative bacteria, including CPE. For infection prevention, targeting higher CHG skin concentrations may improve control of certain pathogens.

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Source
http://dx.doi.org/10.1017/ice.2024.81DOI Listing

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