Ceftazidime–Avibactam Use in a Case Series of Difficult-to-Treat or Recurrent Infections in Pediatric Patients with Complex Chronic Conditions: Effectiveness and Absence of Resistance Development

Author:

García-Boyano Miguel12ORCID,Alós Díez María23,Fernández Tomé Lorena23ORCID,Escosa-García Luis124ORCID,Moreno Ramos Francisco25ORCID,Schuffelmann-Gutiérrez Cristina6ORCID,Cendejas Bueno Emilio27,Calvo Cristina124ORCID,Baquero-Artigao Fernando124ORCID,Frauca Remacha Esteban23

Affiliation:

1. Pediatric Infectious Disease Department, La Paz University Hospital, 28046 Madrid, Spain

2. La Paz Research Institute—IdiPAZ, 28046 Madrid, Spain

3. ERN-TransplantChild, Pediatric Hepatology Service, La Paz University Hospital, 28046 Madrid, Spain

4. Área de Enfermedades Infecciosas del Centro de Investigación Biomédica en Red del Instituto de Salud Carlos III (CIBERINFEC), Instituto de Salud Carlos III, 28029 Madrid, Spain

5. Department of Pharmacy, La Paz University Hospital, 28046 Madrid, Spain

6. Pediatric Intensive Care Unit, La Paz University Hospital, 28046 Madrid, Spain

7. Clinical Microbiology Department, La Paz University Hospital, 28046 Madrid, Spain

Abstract

The prevalence of multidrug-resistant Gram-negative infections, particularly carbapenem-resistant strains, has become a significant global health concern. Ceftazidime–avibactam (CZA) has emerged as a promising treatment option. However, data on its efficacy and safety in children are scarce, necessitating further investigation. We conducted a descriptive case series at a tertiary hospital in Spain from February 2019 to January 2022. Pediatric patients (<16 years) treated with CZA for confirmed or suspected multidrug-resistant Gram-negative infections were included. The clinical and microbiological characteristics, treatment approaches, and outcomes were examined. Eighteen children received CZA treatment. All had complex chronic conditions, with the most frequent underlying main diseases being liver transplantation (n = 8) and biliary atresia (n = 4). The predominant type of infection for which they received CZA was intra-abdominal infection caused or suspected to be caused by OXA-48-producing Klebsiella pneumoniae. CZA was generally well tolerated. Within the first month of starting CZA therapy, two patients died, with one case directly linked to the infection’s fatal outcome. Some patients needed repeated courses of therapy due to recurrent infections, yet no resistance development was noted. In summary, the use of CZA showed effectiveness and safety, while the lack of resistance development highlights CZA’s potential as a primary treatment option against OXA-48-producing infections.

Funder

Instituto de Salud Carlos III, Acción Estratégica en Salud

Publisher

MDPI AG

Reference41 articles.

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