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. 2020 Dec 16;9(12):915.
doi: 10.3390/antibiotics9120915.

Impact of Antibiotic Prescribing Patterns on Susceptibilities of Uropathogens in Children below 24 Months Old

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Impact of Antibiotic Prescribing Patterns on Susceptibilities of Uropathogens in Children below 24 Months Old

Ji Young Park et al. Antibiotics (Basel). .

Abstract

Monitoring regional antibiotic resistance patterns of uropathogens are important for deciding suitable empirical antibiotics for urinary tract infections (UTIs) in children. This study aimed to investigate regional differences in antimicrobial susceptibility patterns of E. coli and Klebsiella spp. in children below 24 months old, diagnosed with their first episode of UTI, and to find factors associated with an increased risk for UTI caused by extended-spectrum β-lactamase (ESBL)-producing uropathogens. This was a retrospective cohort study of children diagnosed between 2011 and 2017 in four different hospitals located in four different regions of South Korea; regions A, B, C, and D. The government's big data repository was used to acquire data on regional antibiotic prescriptions. The pooled antimicrobial susceptibilities of E. coli and Klebsiella spp. (n = 2044) were as follows: ampicillin-sulbactam (61.0%), 3rd generation cephalosporin (3C) (82.8%), and trimethoprim-sulfamethoxazole (72.0%). Multivariate analysis showed that children diagnosed at hospital A (OR, 1.8; 95% confidence interval [CI], 1.2-2.6; P = 0.002) and every year that increased in the study period (OR, 1.1; 95% CI, 1.1-1.2; P < 0.001) were factors associated with an increased risk for UTIs with ESBL-producers. Regions A and B had significantly higher amounts of oral 3Cs prescribed compared to regions C and D (P = 0.009), which correlate with hospitals in the regions that had higher proportions of UTIs with ESBL-producing uropathogens (A and B vs. C and D, P < 0.001). Therefore, children in certain regions are at a higher risk for UTIs caused by ESBL-producers compared to other regions, which correlate with regions that had higher amounts of oral 3Cs prescribed.

Keywords: extended-spectrum β-lactamase; resistance; urinary tract infections.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flow chart of the patients included in this study. A total of 2159 patients below 24 months old were included in the study.
Figure 2
Figure 2
The pooled antimicrobial susceptibilities of (a) patients diagnosed with urinary tract infections (UTIs) in all four hospitals, and (b) in each of the four hospitals, A to D. AMP, ampicillin; AMP/SBT, ampicillin–sulbactam; PIP/TAZ, piperacillin–tazobactam; 1st CEPHA, 1st generation cephalosporin; 3rd CEPHA, 3rd generation cephalosporin; 4 CEPHA, 4 generation cephalosporin; GM, gentamicin; AMK, amikacin; IMI, imipenem; MERO, meropenem; CIPRO, ciprofloxacin; TMP/SMX, trimethoprim–sulfamethoxazole.
Figure 3
Figure 3
Trends showing (a) the proportions of UTIs caused by ESBL-producing uropathogens in hospitals A, B, C, and D. Hospitals A and B had significantly higher proportions of ESBL producers compared to hospitals C and D. (b) The average number of oral BL doses prescribed in regions A, B, C, and D. Regions C and B had higher oral BLs prescribed per 100,000 children per day compared to regions D and A. (c) The average number of oral 3C doses prescribed in regions A, B, C, and D. Regions A and B had higher oral 3Cs prescribed per 100,000 children per day compared to regions C and D. P < 0.05 are shown with an asterisk. BL, β-lactam; ESBL, extended-spectrum β-lactamase; 3C, third-generation cephalosporin.

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