Ceftazidime-Avibactam as a Salvage Treatment for Severely Infected Immunosuppressed Children

Lvchang Zhu1, Qiongyao Hu2, Lijun Liu1

  • 1Department of General Intensive Care Unit, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou City, Zhejiang Province, People's Republic of China.

Abstract

Insights

Ceftazidime-avibactam (CAZ/AVI) shows promise as a salvage treatment for multidrug-resistant Gram-negative bacterial infections in critically ill children. Clinical improvement was observed in 50% of cases, highlighting its potential, especially when bacteria are recovered.

Area of Science:

  • Infectious Diseases
  • Pediatric Critical Care
  • Antimicrobial Resistance

Background:

  • Multidrug-resistant Gram-negative bacteria (MDR-GNB) pose a growing global threat, with carbapenem resistance increasing.
  • Ceftazidime-avibactam (CAZ/AVI) offers a potential treatment option for MDR-GNB infections.
  • Limited clinical data exists on CAZ/AVI use in critically ill, immunosuppressed pediatric populations.

Purpose of the Study:

  • To evaluate the efficacy and safety of CAZ/AVI as a salvage therapy in severely infected, immunosuppressed children.
  • To compare outcomes of CAZ/AVI treatment with other antibiotic regimens in a matched cohort.
  • To identify factors influencing treatment response and mortality in this vulnerable patient group.

Main Methods:

  • Retrospective analysis of critically ill immunosuppressed children with confirmed GNB infections treated with CAZ/AVI from September 2019 to July 2022.
  • Matching CAZ/AVI treated patients with those receiving alternative antibiotics.
  • Assessment of clinical improvement, microbiological outcomes, and mortality rates.

Main Results:

  • Twenty-five children received CAZ/AVI, primarily with hematologic diseases and sepsis.
  • Clinical improvement occurred in 50% of CAZ/AVI courses.
  • Positive microbiological cultures, including carbapenem-resistant GNB, were found in 48% of patients.
  • Clinical response was significantly higher when GNB was recovered (66.7% vs. 23.1%).
  • Mortality rates were 24% at 14 days and 28% at 30 days, correlated with lack of GNB recovery and hospital-acquired pneumonia.
  • No significant difference in major outcomes was observed between CAZ/AVI and other antibiotics.

Conclusions:

  • CAZ/AVI can be considered a salvage treatment option for immunosuppressed children with GNB infections.
  • Careful consideration is advised when using CAZ/AVI in patients without confirmed GNB recovery.
  • Further research is needed to optimize CAZ/AVI use in pediatric critical care settings.

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