Prospective Cohort Study Investigating the Safety and Efficacy of Ambulatory Treatment With Oral Cefuroxime-Axetil in Febrile Children With Urinary Tract Infection

被引:2
作者
Hennaut, Elise [1 ]
Duong, Hong P. [1 ]
Chiodini, Benedetta [1 ]
Adams, Brigitte [1 ]
Lolin, Ksenija [1 ]
Blumental, Sophie [2 ]
Wissing, Karl M. [3 ]
Ismaili, Khalid [1 ]
机构
[1] Univ Libre Bruxelles, Hop Univ Enfants Reine Fabiola, Dept Pediat Nephrol, Brussels, Belgium
[2] Univ Libre Bruxelles, Hop Univ Enfants Reine Fabiola, Dept Infect Dis, Brussels, Belgium
[3] Vrije Univ Brussel, Univ Ziekenhuis Brussel, Dept Nephrol, Brussels, Belgium
关键词
urinary tract infection; oral treatment; children; uropathogens; Escherichia coli; antibiotic resistance; urine culture; RANDOMIZED-TRIAL; PYELONEPHRITIS; MANAGEMENT; DIAGNOSIS; BACTERIA;
D O I
10.3389/fped.2018.00237
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aims: To assess the safety and efficacy of ambulatory oral cefuroxime-axetil treatment in children presenting with first febrile urinary tract infection (UTI) in terms of resolution of fever, antibiotics tolerance, bacterial resistance, and loss to ambulatory follow-up. Methods: Two-year prospective single-center evaluation of the local protocol of oral ambulatory treatment of children presenting first febrile urinary tract infection (UTI). Results: From October 2013 to October 2015, 82 children were treated ambulatory with oral cefuroxime-axetil. The median age was 8 months. When analyzing those 82 children treated orally, 51 (62%) completed oral treatment, 14 (17%) missed their scheduled follow-up visits (3 patients at day 2 and 11 patients at week 2), and 17 (21%) were switched to IV therapy for the following reasons: vomiting in 9, persistent fever in 5, antibiotic resistance in 2 and bacteremia in 1. Six children (8%) presented recurrent UTI after a median of 5 months of follow-up. Conclusions: This 2-year evaluation suggests that oral treatment with cefuroxime-axetil in febrile UTI is feasible but should be implemented with caution. Home-treated children require reevaluation during treatment since 21% of our cohort had to be temporarily switched to parenteral therapy and 17% did not attend scheduled follow-up visits during oral treatment.
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页数:7
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