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Published on: February 17, 2023
Clinical and Microbiologic Outcomes of Tigecycline in Pediatric Patients With Multidrug-resistant Gram-negative
Narut Suphap1,2, Prachayawat Kongtawelert3, Lucksanapon Pitikawinwong2
1From the Division of Infectious Diseases, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Insights
Tigecycline shows promise as a salvage therapy for children with multidrug-resistant Gram-negative bacterial infections, offering a good safety profile despite some resistance. Further research is needed to optimize dosing for younger patients.
Area of Science:
- Pediatric infectious diseases
- Antimicrobial resistance
- Pharmacology
Background:
- The rising incidence of multidrug-resistant Gram-negative bacteria (MDR-GNB) necessitates effective treatments in pediatric populations.
- Limited pediatric-specific data exist for tigecycline, a crucial antibiotic for MDR-GNB infections.
Purpose of the Study:
- To assess the clinical and microbiologic outcomes of tigecycline treatment in pediatric patients with MDR-GNB infections.
- To evaluate the susceptibility patterns and safety of tigecycline in this demographic.
- To identify factors influencing treatment success in children.
Main Methods:
- A retrospective observational study was conducted between January 2015 and December 2024.
- Included were pediatric patients (≤18 years) receiving tigecycline for at least 48 hours for confirmed MDR-GNB infections.
- Clinical and microbiologic outcomes, susceptibility, and adverse events were analyzed.
Main Results:
- Forty-six treatment episodes in 43 children were analyzed, with ventilator-associated pneumonia being the primary indication.
- Clinical improvement was observed in 73.9% of cases, with microbiologic eradication in 60.9%.
- Despite 45.7% of isolates showing non-susceptibility, tigecycline demonstrated clinical efficacy. Adverse events were mild and mostly gastrointestinal.
Conclusions:
- Tigecycline serves as a viable salvage therapy for severe pediatric MDR-GNB infections with a manageable safety profile.
- The study highlights a significant mortality rate (23.9%) and moderate microbiologic eradication rates, indicating treatment complexity.
- There is a critical need for pharmacokinetic data to optimize tigecycline dosing in younger children due to sparse evidence.
Background:
Increasing prevalence of multidrug-resistant Gram-negative bacteria (MDR-GNB) necessitates the use of tigecycline in children, yet pediatric-specific data are limited.
Objectives:
To evaluate the clinical and microbiologic outcomes, susceptibility patterns and safety profile of tigecycline in pediatric MDR-GNB infections.
Methods:
A retrospective observational study was conducted at a tertiary university hospital from January 2015 to December 2024. We included patients aged ≤18 years who received tigecycline for ≥48 hours for confirmed MDR-GNB infections.
Results:
Forty-six treatment episodes were identified in 43 patients (median age: 16 months; interquartile range, 2-100). The majority (91.3%) required intensive care, with ventilator-associated pneumonia (56.5%) being the primary indication. Causative pathogens were carbapenem-resistant Acinetobacter baumannii (69.6%), carbapenem-resistant Enterobacterales (23.9%) and Stenotrophomonas maltophilia (6.5%). Clinical improvement was achieved in 73.9% of episodes, and microbiologic eradication in 60.9%. Although 45.7% of isolates were nonsusceptible to tigecycline (minimum inhibitory concentration >2 mg/L), clinical success remained high. Higher improvement rates were observed in children aged ≥8 years and those receiving a loading dose, though statistical significance was not reached. Adverse events were mild and predominantly gastrointestinal; no treatment discontinuations due to toxicity were reported.
Conclusions:
Tigecycline is a viable salvage therapy for severe pediatric MDR-GNB infections, demonstrating a manageable safety profile. However, the mortality rate of 23.9% and relatively modest microbiologic eradication rates underscore the complexity of such infections and emphasize the pressing need for pharmacokinetic data to refine dosing in younger children, where evidence remains sparse.
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