Evidence map›Paper›PMID 30383912›Full record

ArticleTransfusion2019

The burden of invasive infections in neutropenic patients: incidence, outcomes, and use of granulocyte transfusions.

Tanja Netelenbos, Edwin Massey, Liesbeth C de Wreede, Kay Harding, Angela Hamblin, Mallika Sekhar, Anna Li, Paula F Ypma, Lynn Ball, Jaap Jan Zwaginga and 1 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Transfusion, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 37 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Tanja NetelenbosDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0002-6708-0995
Edwin MasseyUniversity Hospitals Bristol NHS Foundation Trust and NHS Blood and Transplant Bristol, Bristol, United Kingdom.
Liesbeth C de WreedeMedical Statistics Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, the Netherlands.
Kay HardingUniversity Hospitals Bristol NHS Foundation Trust and NHS Blood and Transplant Bristol, Bristol, United Kingdom.
Angela HamblinOxford University Hospitals NHS Foundation Trust & Oxford BRC Hematology Theme Oxford, Oxford, United Kingdom.
Mallika SekharDepartment of Hematology, Royal Free Hospital London, London, United Kingdom.
Anna LiDepartment of Hematology, Royal Free Hospital London, London, United Kingdom.
Paula F YpmaDepartment of Hematology, HAGA Hospital, The Hague, the Netherlands.
Lynn BallDepartment of Pediatrics, Leiden University Medical Center, Leiden, the Netherlands.
Jaap Jan ZwagingaDepartment of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, the Netherlands.
Simon J StanworthOxford University Hospitals NHS Foundation Trust & Oxford BRC Hematology Theme Oxford, Oxford, United Kingdom.
Leiden University Medical Center · NLNHS Blood and Transplant · GBThe Royal Free Hospital · GBUniversity of Oxford · GBHaga Hospital · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with prolonged neutropenia caused by chemotherapy or underlying marrow disorders are at risk of invasive bacterial and fungal infections. New treatment options alongside targeted antimicrobial therapy that might improve outcomes include granulocyte transfusions (GTX). To inform the research agenda, a prospective observational cohort study was performed in the Netherlands and United Kingdom. The aim was to describe the incidence, characteristics, and outcomes of patients developing invasive infections and assess patients fulfilling criteria for GTX. STUDY DESIGN AND

methodsAll patients receiving myeloablative chemotherapy and anticipated to develop 7 or more days of neutropenia (<0.5 × 10

resultsA total of 471 patients enrolled at six hematology-oncology departments were followed for 569 neutropenic episodes. Overall, 32.5% of patients developed invasive infections during their first episode. Significant baseline risk factors for developing infections were high comorbidity scores (WHO performance status ≥ 2, hazard ratio [HR], 2.6 [1.7-3.9]; and hematopoietic cell transplantation-comorbidity index score ≥ 2 HR 1.3 [0.9-1.8]). Infections were bacterial (59.4%) and fungal (22.3%). Despite 34 patients (6.3% of all episodes) appearing to meet criteria to receive GTX, only nine patients received granulocytes. The HR for death was 5.8 (2.5-13.0) for patients with invasive infections.

conclusionThis study documents that invasive infections are associated with significant mortality. There is a need for new strategies to prevent and treat infections, which may include better understanding of use GTX.

Indexed as

AdolescentAdultAgedAged, 80 and overAlgorithmsChildChild, PreschoolFemaleGranulocytesHumansIncidenceInfantInfant, NewbornLeukocyte TransfusionMaleMiddle Aged

Identifiers

PMID30383912
PMCPMC7379528
OpenAlexW2899042416

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.