P-1345. Risk Factors for Ceftriaxone Resistant <i>E. coli</i> or <i>K. pneumoniae</i> Infections in Floor Patients

Abstract Background In 2019, 1.3 million deaths worldwide were linked to antimicrobial resistant organisms. Resistant organisms are associated with poor outcomes including increased mortality and length of stay (LOS). Identification of local risk factors predisposing for resistant organisms can lead to rapid antimicrobial optimization. Patient Population Methods In this retrospective, single center, observational cohort study, floor patients with ceftriaxone (CRO) resistant E. coli or K. pneumoniae via broth microdilution were screened from January 2022 to October 2023. Exclusion criteria included urine isolates, extended spectrum beta-lactamase (ESBL) or CRO resistant E. coli or K. pneumoniae isolate within 6 months of index culture, and intensive care unit (ICU) admission at time of index culture. The primary outcome was to identify risk factors for CRO resistant E. coli and K. pneumoniae in floor patients. Secondary outcomes included 14-day all-cause mortality, ICU admission rate, hospital LOS, and 30-day readmission rate. A list of patients was generated via MedMined™. REDCap™ was used for data collection. All statistical analyses were performed using IBM SPSS™. Significance was defined at p&amp;lt; 0.05. Multivariate Logistical Regression Results 118 patients were included in the statistical analyses. The following risk factors found to be statistically significant were: fluoroquinolone (FQ) (p&amp;lt; 0.01), ceftriaxone (CRO) (p&amp;lt; 0.01), or sulfamethoxazole-trimethoprim (SMX-TMP) (p&amp;lt; 0.01) use within 90-days of index culture; chronic obstructive pulmonary disease (p=0.01); ventilator or tracheostomy use at admission (p=0.03); active hematologic malignancy (p=0.01); poor functional status at admission (p=0.02); percutaneous endoscopic gastrostomy tube at admission (p=0.01); admission from a skilled nursing facility (SNF) (p=0.01). The significant risk factors were included in the multivariate logistic regression. FQ use (95% CI 0.98-16.35, p=0.05), SMX-TMP use (95% CI 2.08-29.24, p&amp;lt; 0.01), hematologic malignancy (95% CI 1.40-129.36, p=0.02), and admission from a SNF (95% CI 1.29-36.27, p=0.02) were found to meet statistical significance. Conclusion FQ use and SMX-TMP use within 90-days of index culture, hematologic malignancy, and admission from a SNF were found to be independently associated with ceftriaxone resistance. Disclosures All Authors: No reported disclosures

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Journal
Open Forum Infectious Diseases
Published
2025-01-29
DOI
https://doi.org/10.1093/ofid/ofae631.1522
Primary Topic
Antibiotic Use and Resistance
Type
article
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article

P-1345. Risk Factors for Ceftriaxone Resistant E. coli or K. pneumoniae Infections in Floor Patients

H. Westerkamp, Jenna Adams, Olivia C. Knack, Fritzie S Albarillo
Open Forum Infectious Diseases
Antibiotic Use and Resistance
article

P-1345. Risk Factors for Ceftriaxone Resistant E. coli or K. pneumoniae Infections in Floor Patients

H. Westerkamp, Jenna Adams, Olivia C. Knack, Fritzie S Albarillo
article en

Abstract

Abstract Background In 2019, 1.3 million deaths worldwide were linked to antimicrobial resistant organisms. Resistant organisms are associated with poor outcomes including increased mortality and length of stay (LOS). Identification of local risk factors predisposing for resistant organisms can lead to rapid antimicrobial optimization. Patient Population Methods In this retrospective, single center, observational cohort study, floor patients with ceftriaxone (CRO) resistant E. coli or K. pneumoniae via broth microdilution were screened from January 2022 to October 2023. Exclusion criteria included urine isolates, extended spectrum beta-lactamase (ESBL) or CRO resistant E. coli or K. pneumoniae isolate within 6 months of index culture, and intensive care unit (ICU) admission at time of index culture. The primary outcome was to identify risk factors for CRO resistant E. coli and K. pneumoniae in floor patients. Secondary outcomes included 14-day all-cause mortality, ICU admission rate, hospital LOS, and 30-day readmission rate. A list of patients was generated via MedMined™. REDCap™ was used for data collection. All statistical analyses were performed using IBM SPSS™. Significance was defined at p&amp;lt; 0.05. Multivariate Logistical Regression Results 118 patients were included in the statistical analyses. The following risk factors found to be statistically significant were: fluoroquinolone (FQ) (p&amp;lt; 0.01), ceftriaxone (CRO) (p&amp;lt; 0.01), or sulfamethoxazole-trimethoprim (SMX-TMP) (p&amp;lt; 0.01) use within 90-days of index culture; chronic obstructive pulmonary disease (p=0.01); ventilator or tracheostomy use at admission (p=0.03); active hematologic malignancy (p=0.01); poor functional status at admission (p=0.02); percutaneous endoscopic gastrostomy tube at admission (p=0.01); admission from a skilled nursing facility (SNF) (p=0.01). The significant risk factors were included in the multivariate logistic regression. FQ use (95% CI 0.98-16.35, p=0.05), SMX-TMP use (95% CI 2.08-29.24, p&amp;lt; 0.01), hematologic malignancy (95% CI 1.40-129.36, p=0.02), and admission from a SNF (95% CI 1.29-36.27, p=0.02) were found to meet statistical significance. Conclusion FQ use and SMX-TMP use within 90-days of index culture, hematologic malignancy, and admission from a SNF were found to be independently associated with ceftriaxone resistance. Disclosures All Authors: No reported disclosures

Open Forum Infectious DiseasesVol. 12(Supplement_1)
Loyola University Medical Center (US), University of Illinois Chicago (US), Duke University Hospital (US)
Openalex Percentile: Top 97%
Antibiotic Use and Resistance
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