Use of cefuroxime for women with community-onset acute pyelonephritis caused by cefuroxime-susceptible or -resistant Escherichia coli.
10.3904/kjim.2016.31.1.145
- Author:
U Im CHANG
1
;
Hyung Wook KIM
;
Seong Heon WIE
Author Information
1. Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea. wiesh@chol.com
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Cefuroxime;
Acute pyelonephritis;
Escherichia coli
- MeSH:
Administration, Intravenous;
Aged;
Anti-Bacterial Agents/administration & dosage/adverse effects/*therapeutic use;
Cefuroxime/administration & dosage/adverse effects/*therapeutic use;
Community-Acquired Infections/diagnosis/*drug therapy/microbiology/urine;
Databases, Factual;
*Drug Resistance, Bacterial;
Escherichia coli/*drug effects/isolation & purification;
Escherichia coli Infections/diagnosis/*drug therapy/microbiology/urine;
Female;
Hospitalization;
Humans;
Microbial Sensitivity Tests;
Middle Aged;
Pyelonephritis/diagnosis/*drug therapy/microbiology/urine;
Remission Induction;
Retrospective Studies;
Time Factors;
Treatment Outcome;
Urinalysis;
Urinary Tract Infections/diagnosis/*drug therapy/microbiology/urine;
Urine/microbiology
- From:The Korean Journal of Internal Medicine
2016;31(1):145-155
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND/AIMS: Efforts to decrease the use of extended-spectrum cephalosporins are required to prevent the selection and transmission of multi-drug resistant pathogens, such as extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae. The objectives of this study were to assess the clinical efficacy of intravenous cefuroxime as an empirical antibiotic for the treatment of hospitalized women with acute pyelonephritis (APN) caused by Escherichia coli. METHODS: We analyzed the clinical and microbiologic database of 328 hospitalized women with community-onset APN. RESULTS: Of 328 women with APN, 22 patients had cefuroxime-resistant E. coli APN, and 306 patients had cefuroxime-susceptible E. coli APN. The early clinical success rates were significantly higher (p = 0.001) in the cefuroxime-susceptible group (90.8%, 278/306) than in the cefuroxime-resistant group (68.2%, 15/22) at 72 hours. The clinical cure rates at 4 to 14 days after completing antimicrobial therapy were not significantly different in the cefuroxime-resistant or -susceptible groups, with 88.2% (15/17) and 97.8% (223/228; p = 0.078), respectively. The microbiological cure rates were not significantly different and were 90.9% (10/11) and 93.4% (128/137), respectively (p =0.550). The median duration of hospitalization in the cefuroxime-resistant and -susceptible groups was 10 days (interquartile range [IQR], 8 to 13) and 10 days (IQR, 8 to 14), respectively (p =0.319). CONCLUSIONS: Cefuroxime, a second-generation cephalosporin, can be used for the initial empirical therapy of community-onset APN if tailored according to uropathogen identification and susceptibility results, especially in areas where the prevalence rate of ESBL-producing uropathogens is low.
