Febrile neutropenia management and outcomes in hematopoietic cell transplantation for chronic granulomatous disease.


Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Apr 2022
Historique:
revised: 02 02 2022
received: 06 12 2021
accepted: 07 02 2022
pubmed: 23 2 2022
medline: 8 4 2022
entrez: 22 2 2022
Statut: ppublish

Résumé

We analyzed events and therapies related to febrile neutropenia in patients receiving hematopoietic cell transplantation (HCT) for chronic granulomatous disease (CGD). Three protocols for HCT were used to extract the relation between conditioning and infectious complications during transplantation for CGD, especially the relation of fever and neutropenia to microbiological events and antibiotic therapy. Sixty-nine recipients received either reduced intensity conditioning with matched related or unrelated donors or conditioning specific to haploidentical-related donors utilizing posttransplant cyclophosphamide. Fever prior to neutropenia was common (52) and in eight recipients, Gram negative bacterial infection occurred prior to neutropenia, and in nine during neutropenia. Alemtuzumab as conditioning was associated with preneutropenic infection. Empiric therapy (noncarbapenem) by institutional guideline was given in 40. Carbapenems were given before neutropenia (8) or as empiric therapy in neutropenia (18), or a switch to a carbapenem (n = 22) occurred in 48 cases. No deaths related to infection associated with neutropenia occurred. The management of febrile neutropenia in HCT for CGD led to no deaths related to infection associated with neutropenia. Bacteremias occurred both prior to neutropenia and during neutropenia. Bacteria isolated may have represented the recrudescence of prior infection, representing the population transplanted and the platform for HCT. The treatment of prior infections may have had an influence on the necessity of carbapenem use as either empiric or directed therapy for bacterial infections.

Identifiants

pubmed: 35191140
doi: 10.1111/tid.13815
pmc: PMC11024981
mid: NIHMS1980595
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13815

Subventions

Organisme : CCR NIH HHS
ID : HHSN261200800001C
Pays : United States
Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States
Organisme : Intramural NIH HHS
ID : Z01 AI000989
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA AI000989
Pays : United States

Informations de copyright

© 2022 Wiley Periodicals LLC. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

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Auteurs

Mark Parta (M)

Clinical Research Directorate, Frederick National Laboratory for Cancer Research, Bethesda, Maryland, USA.

Jennifer Cuellar-Rodriguez (J)

National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.

Juan Gea-Banacloche (J)

National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.

Jing Qin (J)

Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.

Corin Kelly (C)

National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.

Christa S Zerbe (CS)

National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.

Steven M Holland (SM)

National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.

Harry L Malech (HL)

National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.

Elizabeth M Kang (EM)

National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.

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