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Resistance to antibacterial therapy in pediatric febrile urinary tract infections-a single-center analysis
Thomas Raupach1, Jürgen Held2, Hans-Ulrich Prokosch3
1Department of Pediatrics and Adolescent Medicine, University Hospital Erlangen, Erlangen, Germany.
Insights
Febrile urinary tract infections (UTIs) in children are common. Aminopenicillin/β-lactamase-inhibitor (BLI) combinations show satisfactory treatment response for acute pyelonephritis, despite some resistance patterns.
Area of Science:
- Pediatric infectious diseases
- Clinical microbiology
- Antimicrobial stewardship
Background:
- Febrile urinary tract infections (UTIs) are serious childhood infections requiring prompt diagnosis and treatment.
- Optimal antibacterial therapy for pediatric UTIs remains uncertain, with evolving resistance patterns.
- Microbiological resistance does not always correlate with clinical treatment failure in pediatric UTIs.
Purpose of the Study:
- To analyze uropathogens and their resistance patterns in children with acute pyelonephritis.
- To evaluate the response to antibacterial treatment in pediatric UTIs.
- To assess the efficacy of first-line therapy for febrile UTIs in children.
Main Methods:
- Retrospective analysis of 907 inpatients aged 0-18 years with febrile UTIs (2009-2018) using billing codes.
- Microbial results and treatment regimens were analyzed from laboratory data.
- Treatment response was assessed in a subgroup of children, focusing on clinical markers.
Main Results:
- Escherichia coli was the most common pathogen (60.8%) in 590 detected uropathogens.
- 81.0% of E. coli isolates showed susceptibility or intermediate resistance to aminopenicillin/β-lactamase-inhibitor (BLI) combinations.
- In cases of E. coli resistance to initial aminopenicillin/BLI therapy, treatment changes did not significantly impact clinical markers after 3 days.
Conclusions:
- This study presents the spectrum of uropathogens and susceptibility data for pediatric UTIs in a tertiary care setting.
- Findings support the use of aminopenicillin/β-lactamase-inhibitor (BLI) combinations as a satisfactory first-line therapy.
- Further research may refine treatment guidelines for pediatric UTIs based on local resistance data.
Background:
Febrile urinary tract infections (UTIs) are common serious bacterial infections in childhood and require early diagnosis and antibacterial therapy. However, considerable uncertainty exists regarding the optimal antibacterial agent for primary treatment of pediatric UTIs. Additionally, patterns of susceptibility and resistance change over time and microbiological in vitro resistance is not necessarily associated with treatment failure. Here, we analyzed uropathogens, their resistance patterns, and response to antibacterial treatment in children with acute pyelonephritis.
Methods:
We used billing codes (international classification of diseases) to identify all inpatients aged 0-18 years with febrile UTIs in a German university tertiary care center from 2009 until 2018. Microbial results were retrieved from the laboratory information system for all children, and treatment regimen and treatment response were analyzed in a subgroup of children.
Results:
We identified 907 children with acute pyelonephritis; in 590 cases (65%) an uropathogen was detected. Escherichia coli (60.8%), Enterococcus faecalis (13.2%), Klebsiella pneumoniae (7.0%), Proteus spp. (5.2%), and Pseudomonas aeruginosa (4.2%) were the most common pathogens. 353 of 436 E.coli isolates (81.0%) were susceptible or intermediate to aminopenicillin/β-lactamase-inhibitor (BLI) combinations. We examined 52 cases where E. coli was resistant to initial therapy with aminopenicillin/BLI combinations: Therapy was changed in 35 cases (67%) and left unchanged in 17 cases (33%), and we found no significant differences in C-reactive protein and leucocyte count in blood and urine between both groups after 3 days.
Conclusions:
We present the spectrum of uropathogens and susceptibility test results in pediatric UTIs in a tertiary care center. Our findings suggest a satisfactory response to first-line therapy with aminopenicillin/BLI combinations.
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