Evidence map›Paper›PMID 35191140›Full record

ArticleTransplant infectious disease : an official journal of the Transplantation Society2022

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

Mark Parta, Jennifer Cuellar-Rodriguez, Juan Gea-Banacloche, Jing Qin, Corin Kelly, Christa S Zerbe, Steven M Holland, Harry L Malech, Elizabeth M Kang

Open access · greenAbstract read
In one paragraph

Article in Transplant infectious disease : an official journal of the Transplantation Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 42% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Mark PartaClinical Research Directorate, Frederick National Laboratory for Cancer Research, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-0534-6759
Jennifer Cuellar-RodriguezNational Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-5298-6463
Juan Gea-BanaclocheNational Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-0310-7172
Jing QinBiostatistics Research Branch, National Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-2817-6326
Corin KellyNational Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-9056-2661
Christa S ZerbeNational Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-4219-0503
Steven M HollandNational Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-3207-5464
Harry L MalechNational Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-5874-5775
Elizabeth M KangNational Institute of Allergy and Infectious Diseases/National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-4394-1831
National Institutes of Health · USFrederick National Laboratory for Cancer Research · US

Funding

Transgenic Animal Models Of Human Immune DefectsZIAAI000646 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HOLLAND, STEVEN · 2009 to 2025
$22.2M
Development and conduct of allogeneic stem cell transplant and autologous stem cell gene therapy for inherited immune deficienciesZIAAI000989 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KANG, ELIZABETH · 2009 to 2025
$12.4M
Gene Therapy Basic Research to Treat Inherited Primary Immune DeficienciesZIAAI000644 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MALECH, HARRY L · 2009 to 2025
$12.1M
Clinical Trials of Allogeneic Transplantation for Inherited Immune DeficienciesZ01AI000989 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI KANG, ELIZABETH · 2007 to 2008
$878k
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z01 AI000989Intramural NIH HHS ZIA AI000989NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

objectiveWe analyzed events and therapies related to febrile neutropenia in patients receiving hematopoietic cell transplantation (HCT) for chronic granulomatous disease (CGD).

methodsThree 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.

resultsSixty-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.

conclusionThe 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.

Indexed as

Febrile NeutropeniaGram-Negative Bacterial InfectionsGranulomatous Disease, ChronicHematopoietic Stem Cell TransplantationAnti-Bacterial AgentsHumansTransplantation ConditioningAnti-Bacterial Agentschronic granulomatous diseasefebrile neutropeniaGram negative bacteremiahematopoietic cell transplantationserotherapy

Identifiers

PMID35191140
PMCPMC11024981
OpenAlexW4212999633

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.