Comparison between Perianal Swab and Stool Specimens for Detecting Colonization with Extended-Spectrum

Jeffrey M Kubiak1,2, Michael Hovan3, Emily Davidson3

  • 1Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.

Insights

Perianal swabs offer a rapid and reliable alternative to stool samples for detecting antimicrobial-resistant bacteria in the gut. This study shows high agreement between swab and stool results for ESBL-E and FQRE.

Area of Science:

  • Clinical Microbiology
  • Infectious Diseases
  • Healthcare Epidemiology

Background:

  • Stool specimens are standard for detecting gastrointestinal antimicrobial-resistant enteric bacteria but are slow to collect.
  • Perianal swabs offer faster collection but their utility for this surveillance is not well-established.
  • Hematopoietic cell transplant recipients and acute leukemia patients are at high risk for resistant infections.

Purpose of the Study:

  • To evaluate the suitability of perianal swabs versus stool specimens for detecting specific antimicrobial-resistant bacteria.
  • To assess the diagnostic accuracy of perianal swabs for extended-spectrum β-lactamase-producing Enterobacterales (ESBL-E) and fluoroquinolone-resistant Enterobacterales (FQRE).

Main Methods:

  • Paired perianal swab and stool specimens were collected from at-risk patients.
  • Selective culture was used to identify ESBL-E and FQRE in both specimen types.
  • Positive percent agreement and concordance between specimen types were calculated.

Main Results:

  • Stool cultures detected ESBL-E in 7.6% and FQRE in 26% of patients.
  • Perianal swabs showed 95% positive percent agreement for both ESBL-E and FQRE compared to stool.
  • Overall concordance between perianal swabs and stool specimens was high at 98%.

Conclusions:

  • Perianal swabs are a reliable and efficient specimen type for surveillance of gastrointestinal colonization with ESBL-E and FQRE.
  • This finding supports the use of perianal swabs to expedite the detection of key antimicrobial-resistant organisms.

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