Clinical Utility of Bronchoalveolar Lavage in Pediatric Oncology Patients.


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 11 2022
Historique:
pubmed: 28 7 2022
medline: 15 10 2022
entrez: 27 7 2022
Statut: ppublish

Résumé

Lower airway sampling is important in the assessment of lower respiratory tract infection in children with cancer or posthematopoietic stem cell transplant and can be done via bronchoalveolar lavage (BAL). Clinicians can struggle with balancing the benefits of BAL against the risks. This study aimed to define the diagnostic and clinical utility of BAL in this population. A single-center retrospective review of BAL performed in children with cancer or posthematopoietic stem cell transplant. Data extracted included demographics, BAL method and results and antimicrobial treatment. Variables significantly associated with diagnostic yield, diagnostic impact (confirmation or exclusion of infection), and clinical impact (any change in antimicrobial or nonantimicrobial therapy) were assessed in both univariate and multivariate analysis. Seventy-three BAL episodes were included. In 26 (35.6%) episodes, a pathogen was identified on BAL. Forty-nine (67%) BAL episodes had a diagnostic impact and 15 (21%) had a clinical impact. Late BAL (>72 hours) compared with early BAL (odds ratio 3.27; 95% CI: 1.03-10.86), and flexible bronchoscopy compared with nonbronchoscopic lavage (odds ratio 6.10; 95% CI: 1.90-24.0), were more likely to have a diagnostic impact on multivariate analysis. No associations were found for clinical impact. One-third of BAL episodes identified a pathogen, two-thirds had a diagnostic impact, and almost a quarter of episodes impacted antimicrobial prescribing. The method and timing of BAL may be important, with flexible bronchoscopy 6-fold more likely and late BAL 3-fold more likely to have a diagnostic impact.

Sections du résumé

BACKGROUND
Lower airway sampling is important in the assessment of lower respiratory tract infection in children with cancer or posthematopoietic stem cell transplant and can be done via bronchoalveolar lavage (BAL). Clinicians can struggle with balancing the benefits of BAL against the risks. This study aimed to define the diagnostic and clinical utility of BAL in this population.
METHODS
A single-center retrospective review of BAL performed in children with cancer or posthematopoietic stem cell transplant. Data extracted included demographics, BAL method and results and antimicrobial treatment. Variables significantly associated with diagnostic yield, diagnostic impact (confirmation or exclusion of infection), and clinical impact (any change in antimicrobial or nonantimicrobial therapy) were assessed in both univariate and multivariate analysis.
RESULTS
Seventy-three BAL episodes were included. In 26 (35.6%) episodes, a pathogen was identified on BAL. Forty-nine (67%) BAL episodes had a diagnostic impact and 15 (21%) had a clinical impact. Late BAL (>72 hours) compared with early BAL (odds ratio 3.27; 95% CI: 1.03-10.86), and flexible bronchoscopy compared with nonbronchoscopic lavage (odds ratio 6.10; 95% CI: 1.90-24.0), were more likely to have a diagnostic impact on multivariate analysis. No associations were found for clinical impact.
CONCLUSIONS
One-third of BAL episodes identified a pathogen, two-thirds had a diagnostic impact, and almost a quarter of episodes impacted antimicrobial prescribing. The method and timing of BAL may be important, with flexible bronchoscopy 6-fold more likely and late BAL 3-fold more likely to have a diagnostic impact.

Identifiants

pubmed: 35895881
doi: 10.1097/INF.0000000000003648
pii: 00006454-990000000-00139
doi:

Substances chimiques

Anti-Bacterial Agents 0
Anti-Infective Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

899-903

Informations de copyright

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

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to disclose.

Références

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Auteurs

Shivanthan Shanthikumar (S)

From the Respiratory and Sleep Medicine, Royal Children's Hospital, Parkville, VIC, Australia.
Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Murdoch Children's Research Institute, Parkville, VIC, Australia.

Samuel Colenutt (S)

From the Respiratory and Sleep Medicine, Royal Children's Hospital, Parkville, VIC, Australia.

Theresa Cole (T)

Allergy and Immunology, Royal Children's Hospital, Parkville, VIC, Australia.

Rachel Conyers (R)

Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Murdoch Children's Research Institute, Parkville, VIC, Australia.
Children's Cancer Centre, Royal Children's Hospital, Parkville, VIC, Australia.

Tom Rozen (T)

Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Murdoch Children's Research Institute, Parkville, VIC, Australia.
Intensive Care Unit, Royal Children's Hospital, Parkville, VIC, Australia.
Department of Critical Care, University of Melbourne, Parkville, VIC, Australia.

Jo Harrison (J)

From the Respiratory and Sleep Medicine, Royal Children's Hospital, Parkville, VIC, Australia.
Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Murdoch Children's Research Institute, Parkville, VIC, Australia.

Philip Robinson (P)

From the Respiratory and Sleep Medicine, Royal Children's Hospital, Parkville, VIC, Australia.
Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Murdoch Children's Research Institute, Parkville, VIC, Australia.

Gabrielle M Haeusler (GM)

Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Murdoch Children's Research Institute, Parkville, VIC, Australia.
Infection Diseases Unit, Department of General Medicine, Royal Children's Hospital, Parkville, VIC, Australia.
Department of Infectious Diseases, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Sir Peter MacCallum Department of Oncology, NHMRC National Centre for Infections in Cancer, University of Melbourne, Parkville, VIC, Australia.
The Paediatric Integrated Cancer Service, Parkville, VIC, Australia.

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