Successful Use of Cefiderocol to Treat a Multidrug-resistant Stenotrophomonas maltophilia Ventilator-associated Pneumonia in an Extremely Preterm Neonate

Author:

Koirala Archana1234ORCID,Krishnappa Bharath5,Banh Caroline16,Brandenburg Ulrike5,Findlay Michael16,Williams Phoebe C. M.2347ORCID

Affiliation:

1. Department of Infectious Diseases, Nepean Hospital, Kingswood, New South Wales, Australia

2. National Centre for Immunisation Research and Surveillance, Westmead, New South Wales, Australia

3. School of Public Health, Faculty of Medicine and Health, University of Sydney, Camperdown, New South Wales, Australia

4. Sydney Infectious Diseases Institute, The University of Sydney, Sydney, New South Wales, Australia

5. Department of Neonatal Services, Nepean Hospital, Kingswood, New South Wales, Australia

6. Department of Microbiology, New South Wales Health Pathology, Kingswood, New South Wales, Australia

7. Department of Infectious Diseases, Sydney Children Hospital, New South Wales, Australia.

Abstract

Background: Ventilator-associated pneumonia (VAP) caries a morbidity and mortality risk in the preterm neonate, particularly in the context of rising global antimicrobial resistance driving infections due to multidrug-resistant Gram-negative bacteria. Cefiderocol, a siderophilic cephalosporin, has broad Gram-negative antimicrobial activity and central nervous system penetration and is used for the treatment of hospital-acquired pneumonia or VAP in adults. Scarce data exists on its use in neonates. Case: A female neonate born at 26 + 6 weeks developed VAP at 21 days of life. She was commenced on corticosteroids, vancomycin and ceftazidime but continued to deteriorate. Sputum cultures yielded Stenotrophomonas maltophilia resistant to trimethoprim/sulfamethoxazole, ciprofloxacin and ceftazidime, with potential susceptibility to cefiderocol. Cerebrospinal fluid showed an elevated white cell count. In view of worsening respiratory and hemodynamic status, antibiotic treatment was changed to cefiderocol monotherapy at 30 mg/kg/dose every 8 hours. Within 72 hours of commencing cefiderocol, the neonate was successfully extubated to variable-flow continuous positive airway pressure and showed ongoing clinical improvement. Conclusions: Cefiderocol was integral for the care of our neonate without any immediate adverse safety consequences. We relied on dosing data from a conference abstract, due to the paucity of evidence on the use of novel antimicrobials. This lack of evidence is particularly concerning given preterm neonates are particularly vulnerable to infections with multidrug-resistant Gram-negative organisms due to their immature immune systems, prolonged hospital stay, repeated interventions and antimicrobial exposure.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Microbiology (medical),Pediatrics, Perinatology and Child Health

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