Outcome of Antimicrobial Therapy of Pediatric Urinary Tract Infections Caused by Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae
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Background: The purpose of this study was to compare the outcome of carbapenem versus non-carbapenem antimicrobial therapyfor pediatric urinary tract infections (UTIs) caused by extended-spectrum β-lactamase (ESBL) producing Enterobacteriaceae. Materials and Methods: From 2006 to 2011, 42 episodes of UTI caused by ESBL-producing Enterobacteriaceae were diagnosed atSeoul National University Children’s Hospital. Patients were grouped according to the antimicrobials they received into a carbapenemgroup and a non-carbapenem group. Medical records were retrospectively reviewed to assess treatment outcome, time to defervescenceafter initiation of treatment, and relapse rate. Results: There were 36 children with 42 episodes of UTI caused by ESBL-producing Enterobacteriaceae. Twenty-seven cases (64%)had an underlying urologic disease, 28 (67%) cases were caused by Escherichia coli , and 14 (33%) cases were caused by Klebsiellapneumoniae . Four (10%) cases were treated with carbapenem, 23 cases (55%) were treated with non-carbapenem, and 15 (36%)cases were treated by switching from a carbapenem to a non-carbapenem and vice versa. There was no treatment failure at the timeof antimicrobial discontinuation. Between the carbapenem and the non-carbapenem treatment groups, there were no significant differencesin bacterial etiology (P = 0.59), time to defervescence after the initiation of antimicrobials (P = 0.28), and relapse rate (P = 0.50). In vitro susceptibility to non-carbapenem antimicrobials did not affect the time to defervescence after the initiation of antimicrobialtreatment, and the relapse rate in the non-carbapenem group. Conclusions: This study found no significant difference in the treatment outcome between pediatric patients treated with carbapenemand those treated with non-carbapenem antimicrobials for UTI caused by ESBL-producing Enterobacteriaceae. Therefore,the initially administered non-carbapenem can be maintained in UTI patients showing clinical improvement.
Abstract
Background: The purpose of this study was to compare the outcome of carbapenem versus non-carbapenem antimicrobial therapyfor pediatric urinary tract infections (UTIs) caused by extended-spectrum β-lactamase (ESBL) producing Enterobacteriaceae. Materials and Methods: From 2006 to 2011, 42 episodes of UTI caused by ESBL-producing Enterobacteriaceae were diagnosed atSeoul National University Children’s Hospital. Patients were grouped according to the antimicrobials they received into a carbapenemgroup and a non-carbapenem group. Medical records were retrospectively reviewed to assess treatment outcome, time to defervescenceafter initiation of treatment, and relapse rate. Results: There were 36 children with 42 episodes of UTI caused by ESBL-producing Enterobacteriaceae. Twenty-seven cases (64%)had an underlying urologic disease, 28 (67%) cases were caused by Escherichia coli , and 14 (33%) cases were caused by Klebsiellapneumoniae . Four (10%) cases were treated with carbapenem, 23 cases (55%) were treated with non-carbapenem, and 15 (36%)cases were treated by switching from a carbapenem to a non-carbapenem and vice versa. There was no treatment failure at the timeof antimicrobial discontinuation. Between the carbapenem and the non-carbapenem treatment groups, there were no significant differencesin bacterial etiology (P = 0.59), time to defervescence after the initiation of antimicrobials (P = 0.28), and relapse rate (P = 0.50). In vitro susceptibility to non-carbapenem antimicrobials did not affect the time to defervescence after the initiation of antimicrobialtreatment, and the relapse rate in the non-carbapenem group. Conclusions: This study found no significant difference in the treatment outcome between pediatric patients treated with carbapenemand those treated with non-carbapenem antimicrobials for UTI caused by ESBL-producing Enterobacteriaceae. Therefore,the initially administered non-carbapenem can be maintained in UTI patients showing clinical improvement.
참고문헌 (28)
- Zorc JJ, "Diagnosis and managementof pediatric urinary tract infections", Clin Microbiol Rev, 18, pp.417~422 (2005)
- Knothe H, "Transferable resistance to cefotaxime, cefoxitin, cefamandoleand cefuroxime in clinical isolates of Klebsiella pneumoniaeand Serratia marcescens", Infection, 11, pp.315~317 (1983)
- Bauernfeind A, "Novel R-factor borne beta-lactamaseof Escherichia coli confering resistance to cephalosporins", Infection, 15, pp.257~259 (1987)
- Lee J, "Control of extended-spectrum beta-lactamase-producing Escherichiacoli and Klebsiella pneumoniae in a children’s hospital bychanging antimicrobial agent usage policy", J AntimicrobChemother, 60, pp.629~637 (2007)
- Briongos-Figuero LS, "Epidemiology, risk factors and comorbidityfor urinary tract infections caused by extended-spectrumbeta-lactamase (ESBL)-producing enterobacteria", Int JClin Pract, 66, pp.891~896 (2012)
- Yamasaki K, "Laboratory surveillance for prospectiveplasmid-mediated AmpC beta-lactamases in the Kinkiregion of Japan", J Clin Microbiol, 48, pp.3267~3273 (2010)
- Titelman E, "Efficacy of pivmecillinamfor treatment of lower urinary tract infectioncaused by extended-spectrum beta-lactamase-producingEscherichia coli and Klebsiella pneumoniae", Microb DrugResist, 18, pp.189~192 (2012)
- Neuner EA, "Experiencewith fosfomycin for treatment of urinary tract infectionsdue to multidrug-resistant organisms", Antimicrob AgentsChemother, 56, pp.5744~5748 (2012)
- Doi A, "The efficacyof cefmetazole against pyelonephritis caused by extended-spectrum beta-lactamase-producing Enterobacteriaceae", Int J Infect Dis, 17, pp.e159~e163 (2012)
- Tinelli M, "Epidemiologyand genetic characteristics of extended-spectrum betalactamase-producing Gram-negative bacteria causing urinarytract infections in long-term care facilities", J AntimicrobChemother, 67, pp.2982~2987 (2012)
- Kizilca O, "Risk factors for community-acquired urinarytract infection caused by ESBL-producing bacteria inchildren", Pediatr Int, 54, pp.858~862 (2012)
- Azap OK, "Risk factors for extendedspectrum beta-lactamase positivity in uropathogenic Escherichia coli isolated from community-acquired urinary tract infections", Clin Microbiol Infect, 16, pp.147~151 (2010)
- Topaloglu R, "Risk factors in community-acquired urinary tract infections caused by ESBL-producingbacteria in children", Pediatr Nephrol, 25, pp.919~925 (2010)
- 김남희, "Extended-Spectrum β - Lactamase 생성 Escherichia coli에 의한 소아 요로감염의 위험인자", Korean Journal of Pediatrics, 47(2), pp.164~169 (2004), 대한소아과학회
- Lee CH, "Treatment of ESBL-producingKlebsiella pneumoniae bacteraemia with carbapenemsor flomoxef: a retrospective study and laboratoryanalysis of the isolates", J Antimicrob Chemother, 58, pp.1074~1077 (2006)
- Apisarnthanarak A, "Carbapenem-resistant Gram-negative bacteria: howto prioritize infection prevention and control interventionsin resource-limited settings", Expert Rev Anti InfectTher, 11, pp.147~157 (2013)
- Clinical and Laboratory Standards Institute, "Performancestandards for antimicrobial susceptibility testing; 19th InformationalSupplement. CLSI document M100-S19", Clinical and Laboratory Standards Institute, ~ (2009)
- Jarlier V, "Extendedbroad-spectrum beta-lactamases conferring transferableresistance to newer beta-lactam agents in Enterobacteriaceae:hospital prevalence and susceptibility patterns", RevInfect Dis, 10, pp.867~878 (1988)
- Thomson KS, "Detection of extended-spectrumbeta-lactamases in members of the family Enterobacteriaceae:comparison of the double-disk and threedimensionaltests", Antimicrob Agents Chemother, 36, pp.1877~1882 (1992)
- Dalgic N, "Ertapenemfor the treatment of urinary tract infections causedby extended-spectrum beta-lactamase-producing bacteriain children", Scand J Infect Dis, 43, pp.339~343 (2011)
- Nordmann P, "Global spread of Carbapenemase-producing Enterobacteriaceae", Emerg Infect Dis, 17, pp.1791~1798 (2011)
- Heritier C, "Contributionof acquired carbapenem-hydrolyzing oxacillinases to carbapenemresistance in Acinetobacter baumannii", AntimicrobAgents Chemother, 49, pp.3198~3202 (2005)
- Poirel L, "Carbapenem resistance in Acinetobacterbaumannii: mechanisms and epidemiology", ClinMicrobiol Infect, 12, pp.826~836 (2006)
- Pai H, "Carbapenemresistance mechanisms in Pseudomonas aeruginosacl inical isolates", Ant imicrob Agents Chemother, 45, pp.480~484 (2001)
- Shilo S, "Risk factors for bacteriuriawith carbapenem-resistant Klebsiella pneumoniae and itsimpact on mortality: a case-control study", Infection, 41, pp.503~509 (2013)
- Jacoby GA, "The new beta-lactamases", NEngl J Med, 352, pp.380~391 (2005)
- Lee NY, "Cefepime therapy for monomicrobial bacteremia causedby cefepime-susceptible extended-spectrum eeta-lactamase?producing enterobacteriaceae: MIC matters", ClinInfect Dis, 56, pp.488~495 (2013)
- Vardakas KZ, "Carbapenemsversus alternative antibiotics for the treatmentof bacteraemia due to Enterobacteriaceae producing extended-spectrum β-lactamases: a systematic review andmeta-analysis", J Antimicrob Chemother, 67, pp.2793~2803 (2012)
