Recurrent ESBL Escherichia coli Urosepsis in a Pediatric Renal Transplant Patient Treated With Antibiotics and Bacteriophage Therapy.


Journal

The Pediatric infectious disease journal
ISSN: 1532-0987
Titre abrégé: Pediatr Infect Dis J
Pays: United States
ID NLM: 8701858

Informations de publication

Date de publication:
01 01 2023
Historique:
pubmed: 7 10 2022
medline: 15 12 2022
entrez: 6 10 2022
Statut: ppublish

Résumé

Treating recurrent multidrug resistant (MDR) urosepsis in pediatric transplant recipients can be challenging. Particularly when antibiotics fail to prevent future occurrence and the nidus is seemingly undiscoverable. While there is an increasing amount of data on phage therapy, to our knowledge, there are no published cases involving pediatric renal transplant recipients. Therefore, we present a challenging clinical case in which phage therapy was used in a pediatric renal transplant recipient who developed recurrent MDR urosepsis with an unclear source. Our patient was a 17-year-old female who initially developed urosepsis caused by extended-spectrum β-lactamase (ESBL) Escherichia coli , while being treated with an immunosuppressant regimen because of kidney rejection secondary to poor immunosuppression therapy compliance. She was admitted to our hospital intermittently for 4 months with 4 episodes of urosepsis caused by ESBL E. coli . She received multiple courses of antibiotics (mainly ertapenem) and underwent a fecal material transplant to eradicate her ESBL E. coli colonized gastrointestinal tract. Because of recurrent development of urosepsis after antibiotic treatment, she later underwent treatment with a phage cocktail consisting of 2 isolate-specific phages. After a prolonged antibiotic course and subsequent 3-week intravenous phage treatment, she had no ESBL E. coli in her urinary cultures for 4 years post-treatment. This case highlights the challenges of treating recurrent ESBL E. coli infections in a pediatric renal transplant patient and provides evidence that phage therapy may prove useful in such cases.

Identifiants

pubmed: 36201671
doi: 10.1097/INF.0000000000003735
pii: 00006454-202301000-00012
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

43-46

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

Références

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Auteurs

Andrew B Gainey (AB)

From the Department of Pharmacy, Division of Pediatric Infectious Diseases, Prisma Health Children's Hospital-Midlands, Columbia, South Carolina.

Robert Daniels (R)

From the Department of Pharmacy, Division of Pediatric Infectious Diseases, Prisma Health Children's Hospital-Midlands, Columbia, South Carolina.

Anna-Kathryn Burch (AK)

Department of Pediatrics, Division of Pediatric Infectious Diseases, Prisma Health Children's Hospital-Midlands, Columbia, South Carolina.

Jason Hawn (J)

Department of Pediatrics, Division of General and Hospital Pediatrics, Prisma Health Children's Hospital-Midlands, Columbia, South Carolina.

Joseph Fackler (J)

Adaptive Phage Therapeutics, Gaithersburg, Maryland.

Biswajit Biswas (B)

Department of Genomics & Bioinformatics, Biological Defense Research Directorate, Naval Medical Research Center, Frederick, Maryland.

Michael J Brownstein (MJ)

Adaptive Phage Therapeutics, Gaithersburg, Maryland.

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