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Fluoroquinolone-resistant Escherichia coli among the rectal flora is the predominant risk factor for severe infection after transrectal ultrasound-guided prostate biopsy: a prospective observational study
Linköping University, Faculty of Medicine and Health Sciences. Linköping University, Department of Biomedical and Clinical Sciences, Division of Surgery, Orthopedics and Oncology. Region Östergötland, Center for Surgery, Orthopaedics and Cancer Treatment, Department of Urology in Östergötland.
Linköping University, Department of Biomedical and Clinical Sciences. Linköping University, Faculty of Medicine and Health Sciences. Region Östergötland, Center for Surgery, Orthopaedics and Cancer Treatment, Department of Urology in Östergötland.
Linköping University, Department of Biomedical and Clinical Sciences, Division of Inflammation and Infection. Linköping University, Faculty of Medicine and Health Sciences, Forum Östergötland.ORCID iD: 0000-0003-3067-8587
Linköping University, Faculty of Medicine and Health Sciences. Linköping University, Department of Biomedical and Clinical Sciences, Division of Inflammation and Infection.
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2023 (English)In: Scandinavian journal of urology, ISSN 2168-1805, E-ISSN 2168-1813, Vol. 58, p. 32-37Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Infection of the prostate gland following biopsy, usually with Escherichia coli, is a common complication, despite the use of antimicrobial prophylaxis. A fluoroquinolone (FQ) is commonly prescribed as prophylaxis. Worryingly, the rate of fluoroquinolone-resistant (FQ-R) E. coli species has been shown to be increasing. OBJECTIVE: This study aimed to identify risk factors associated with infection after transrectal ultrasound-guided prostate biopsy (TRUS-Bx). METHODS: This was a prospective study on patients undergoing TRUS-Bx in southeast Sweden. Prebiopsy rectal and urine cultures were obtained, and antimicrobial susceptibility and risk-group stratification were determined. Multivariate analyses were performed to identify independent risk factors for post-biopsy urinary tract infection (UTI) and FQ-R E. coli in the rectal flora. RESULTS: In all, 283 patients were included, of whom 18 (6.4%) developed post-TRUS-Bx UTIs. Of these, 10 (3.5%) had an UTI without systemic inflammatory response syndrome (SIRS) and 8 (2.8%) had a UTI with SIRS. Being in the medium- or high-risk groups of infectious complications was not an independent risk factor for UTI with SIRS after TRUS-Bx, but low-level FQ-resistance (minimum inhibitory concentration (MIC): 0.125-0.25 mg/L) or FQ-resistance (MIC > 0.5 mg/L) among E. coli in the faecal flora was. Risk for SIRS increased in parallel with increasing degrees of FQ-resistance. Significant risk factor for harbouring FQ-R E.coli was travelling outside Europe within the previous 12 months. CONCLUSION: The predominant risk factor for UTI with SIRS after TRUS-Bx was FQ-R E. coli among the faecal flora. The difficulty in identifying this type of risk factor demonstrates a need for studies on the development of a general approach either with rectal swab culture for targeted prophylaxis, or prior rectal preparation with a bactericidal agent such as povidone-iodine before TRUS-Bx to reduce the risk of FQ-R E. coli-related infection.

Place, publisher, year, edition, pages
Medical Journals Sweden , 2023. Vol. 58, p. 32-37
Keywords [en]
Anti-Bacterial Agents; Antibiotic Prophylaxis; Biopsy; Drug Resistance, Bacterial; Escherichia coli; Escherichia coli Infections; Fluoroquinolones; Humans; Image-Guided Biopsy; Male; Prospective Studies; Prostate; Rectum; Risk Factors; Systemic Inflammatory Response Syndrome; Ultrasonography, Interventional; Urinary Tract Infections; antiinfective agent; quinolone derivative; antibiotic prophylaxis; antibiotic resistance; biopsy; Escherichia coli; Escherichia coli infection; human; image guided biopsy; interventional ultrasonography; male; pathology; prospective study; prostate; rectum; risk factor; systemic inflammatory response syndrome; urinary tract infection
National Category
Infectious Medicine
Identifiers
URN: urn:nbn:se:liu:diva-200771DOI: 10.2340/sju.v58.11920ISI: 001135085300015PubMedID: 37553957Scopus ID: 2-s2.0-85167371093OAI: oai:DiVA.org:liu-200771DiVA, id: diva2:1835885
Available from: 2024-02-07 Created: 2024-02-07 Last updated: 2024-12-02

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Holmbom, MartinForsberg, JonFredrikson, MatsNilsson, MaudNilsson, LennartHanberger, HåkanHällgren, Anita

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Holmbom, MartinForsberg, JonFredrikson, MatsNilsson, MaudNilsson, LennartHanberger, HåkanHällgren, Anita
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Faculty of Medicine and Health SciencesDivision of Surgery, Orthopedics and OncologyDepartment of Urology in ÖstergötlandDepartment of Biomedical and Clinical SciencesDivision of Inflammation and InfectionForum ÖstergötlandDepartment of Infectious Diseases
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