Evidence map›Paper›PMID 39113112›Full record

ArticleJournal of hematology & oncology2024

Prevalence of fungal DNAemia mediated by putatively non-pathogenic fungi in immunocompromised patients with febrile neutropenia: a prospective cohort study.

Chantal Lucini, Klára Obrová, Isabella Krickl, Filomena Nogueira, Iva Kocmanová, Susanne Herndlhofer, Karoline V Gleixner, Wolfgang R Sperr, Tijana Frank, Nuno Andrade and 18 more

Abstract readLetter
In one paragraph

Article in Journal of hematology & oncology, 2024. 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
–field-weighted citation impact
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. 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

28 authors.

Chantal Lucini *St. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Klára Obrová *St. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Isabella KricklSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Filomena NogueiraSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Iva KocmanováDepartment of Clinical Microbiology and Immunology, University Hospital Brno, Brno, Czech Republic.
Susanne HerndlhoferDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Karoline V GleixnerDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Wolfgang R SperrDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Tijana FrankSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Nuno AndradeSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Christina PetersSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Gernot EngstlerDepartment of Pediatrics, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.
Michael DworzakSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Andishe AttarbaschiSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Martine van GrotelPrincess Máxima Centre for Paediatric Oncology, Utrecht, the Netherlands.
Marry M van den Heuvel-EibrinkPrincess Máxima Centre for Paediatric Oncology, Utrecht, the Netherlands.
Ivan S MoiseevRM Gorbacheva Children Research Institute, Pavlov University, Saint Petersburg, Russian Federation.
Yuliya RogachevaRM Gorbacheva Children Research Institute, Pavlov University, Saint Petersburg, Russian Federation.
Ludmilla ZubarovskayaRM Gorbacheva Children Research Institute, Pavlov University, Saint Petersburg, Russian Federation.
Natalia ZubarovskayaDepartment of Pediatrics, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.
Herbert PichlerDepartment of Pediatrics, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.
Anita LawitschkaSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria.
Elisabeth Koller3rd Medical Dept, Hanusch Hospital, Vienna, Austria.
Felix KeilLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
Jiří MayerDepartment of Internal Medicine-Haematology and Oncology, University Hospital Brno, Brno, Czech Republic.
Barbora WeinbergerováDepartment of Internal Medicine-Haematology and Oncology, University Hospital Brno, Brno, Czech Republic.
Peter ValentDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Thomas LionSt. Anna Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, Vienna, A-1090, Austria. thomas.lion@ccri.at.

Funding

7th Framework Programme (FP7) of the EU (Project FUNGITECT) 602125
6 · The paper itself

Abstract

Invasive fungal disease (IFD) presents a life-threatening condition in immunocompromised patients, thus often prompting empirical administration of antifungal treatment, without adequate mycological evidence. Over the past years, wide use of antifungal prophylaxis resulted in decreased occurrence of IFD but has contributed to changes in the spectrum of fungal pathogens, revealing the occurrence of previously rare fungal genera causing breakthrough infections. The expanding spectrum of clinically relevant fungal pathogens required the implementation of screening approaches permitting broad rather than targeted fungus detection to support timely onset of pre-emptive antifungal treatment. To address this diagnostically important aspect in a prospective setting, we analyzed 935 serial peripheral blood (PB) samples from 195 pediatric and adult patients at high risk for IFD, involving individuals displaying febrile neutropenia during treatment of hematological malignancies or following allogeneic hematopoietic stem cell transplantation. Two different panfungal-PCR-screening methods combined with ensuing fungal genus identification by Sanger sequencing were employed. In the great majority of PB-specimens displaying fungal DNAemia, the findings were transient and revealed fungi commonly regarded as non-pathogenic or rarely pathogenic even in the highly immunocompromised patient setting. Hence, to adequately exploit the diagnostic potential of panfungal-PCR approaches for detecting IFD, particularly if caused by hitherto rarely observed fungal pathogens, it is necessary to confirm the findings by repeated testing and to identify the fungal genus present by ensuing analysis. If applied appropriately, panfungal-PCR-screening can help prevent unnecessary empirical therapy, and conversely, contribute to timely employment of effective pre-emptive antifungal treatment strategies.

Indexed as

DNA, FungalFebrile NeutropeniaImmunocompromised HostAdolescentAdultAgedAntifungal AgentsChildChild, PreschoolFemaleFungiHematologic NeoplasmsHematopoietic Stem Cell TransplantationHumansInvasive Fungal InfectionsMaleAntifungal AgentsDNA, FungalAntifungal therapyAntifungal treatmentFungal diagnosticInvasive fungal diseasepanfungal-PCR

Identifiers

PMID39113112
PMCPMC11304904

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.