Abstract
Background: Urinary tract infections (UTIs) are commonly treated in the emergency department (ED), and unfortunately, resistance to first-line agents is increasing. Objectives: To characterize treatment of pyelonephritis in a nationally representative sample of ED patients and to identify patient- and treatment-specific factors associated with receiving initial inactive antibiotics. Methods: We conducted a multicentre, observational cohort study utilizing the Emergency Medicine PHARMacotherapy Research NETwork (EMPHARM-NET), comprising 15 geographically diverse US EDs. All patients ≥18 ...years of age with a diagnosis of pyelonephritis between 2018 and 2020 were included. The primary endpoint was the proportion of patients who received initial inactive empirical antibiotic therapy and to identify predictive factors of inactive antibiotic therapy. Results: Of the 3714 patients evaluated, 223 had culture-positive pyelonephritis. Median patient age was 50.1 ...years and patients were mostly female (78.3%). Overall, 40.4% of patients received an IV antibiotic, most commonly ceftriaxone (86.7%). The most frequently prescribed antibiotics were cefalexin (31.8%), ciprofloxacin (14.3%), cefdinir (13.5%) and trimethoprim/sulfamethoxazole (12.6%). Overall, 10.3% of patients received initial inactive therapy. After adjustment in a multivariable analysis, long-acting IV antibiotic was predictive of inactive therapy (OR 0.23, 95% CI 0.07-0.83). Conclusions: In our prospective, multicentre observational study, we found that only 40.4% of patients with pyelonephritis received empirical IV antibiotics in the ED, contributing to inactive therapy. Receipt of long-acting IV antibiotics was independently associated with a decreased rate of initial inactive therapy. This reinforces guideline recommendations to administer long-acting IV antibiotics empirically in the ED upon suspicion of pyelonephritis.
| Original language | English |
|---|---|
| Pages (from-to) | 1038-1044 |
| Number of pages | 7 |
| Journal | Journal of Antimicrobial Chemotherapy |
| Volume | 79 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 1 2024 |
Bibliographical note
Publisher Copyright:© 2024 The Author(s). Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. All rights reserved. For commercial re-use, please contact [email protected] for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site - for further information please contact [email protected].
Funding
We thank: Keith Burrell, University of Iowa; Devin Spolsdoff, MS, University of Iowa; Joann Huynh, PharmD Candidate (2022), University of Illinois at Chicago College of Pharmacy; Kevin Johns, PharmD Candidate (2022), University of Illinois at Chicago College of Pharmacy; Danielle Garza, PharmD; Monica Frauhiger, PharmD; Lyudmila Garbovsky, PharmD, BCPS, BCCCP, Hospital of the University of Pennsylvania, Philadelphia, PA; David Gajdosik, PharmD, BCPS, Hospital of the University of Pennsylvania, Philadelphia, PA; Rachel Lam, Stritch School of Medicine, Loyola University Chicago; and Mollie Shutter, Stritch School of Medicine, Loyola University Chicago. Spero Therapeutics provided an unrestricted research grant via its investigator-initiated research programme. The REDCap database was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award Number UL1TR002537. This study was partially funded by a research grant from the Mayo Midwest Pharmacy Research Committee. Spero Therapeutics provided an unrestricted research grant via its investigator-initiated research programme. The REDCap database was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award Number UL1TR002537. This study was partially funded by a research grant from the Mayo Midwest Pharmacy Research Committee.
| Funders | Funder number |
|---|---|
| Loyola University of Chicago | |
| University of Illinois Hospital & Health Sciences System | |
| Mayo Midwest Pharmacy Research Committee | |
| National Center for Advancing Translational Sciences (NCATS) | |
| Iowa Environmental Mesonet at Iowa State University | 2022 |
| National Institutes of Health (NIH) | UL1TR002537 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
ASJC Scopus subject areas
- Pharmacology
- Microbiology (medical)
- Pharmacology (medical)
- Infectious Diseases
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