Evidence map›Paper›PMID 34674000›Full record

ArticleAnnals of hematology2022

Analysis of incidence and risk factors of the multidrug resistant gastrointestinal tract infection in children and adolescents undergoing allogeneic and autologous hematopoietic cell transplantation: a nationwide study.

Małgorzata Salamonowicz-Bodzioch, Jowita Frączkiewicz, Krzysztof Czyżewski, Olga Zając-Spychała, Ewa Gorczyńska, Grażyna Wróbel, Bernarda Kazanowska, Dorota Sęga-Pondel, Jadwiga Węcławek-Tompol, Marek Ussowicz and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Annals of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Pre-transplantCell transplantation
    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

18 authors.

Małgorzata Salamonowicz-BodziochDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland. msalamonowicz@poczta.onet.pl.ORCID http://orcid.org/0000-0003-1736-3177
Jowita FrączkiewiczDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland.
Krzysztof CzyżewskiDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
Olga Zając-SpychałaDepartment of Pediatric Oncology, Hematology and Transplantology, University of Medical Sciences, Poznan, Poland.
Ewa GorczyńskaDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland.
Grażyna WróbelDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland.
Bernarda KazanowskaDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland.
Dorota Sęga-PondelDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland.
Jadwiga Węcławek-TompolDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland.
Marek UssowiczDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland.
Krzysztof KałwakDepartment of Pediatric Stem Cell Transplantation, Hematology and Oncology, Wroclaw Medical University, ul. Borowska 213, 50-556, Wroclaw, Poland.
Mariusz WysockiDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
Magdalena DziedzicDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
Jacek WachowiakDepartment of Pediatric Oncology, Hematology and Transplantology, University of Medical Sciences, Poznan, Poland.
Agnieszka Zaucha-PrażmoDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, Medical University of Lublin, Lublin, Poland.
Jerzy KowalczykDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, Medical University of Lublin, Lublin, Poland.
Jolanta GoździkStem Cell Transplant Center, Department of Clinical Immunology and Transplantology, University Children's Hospital, Jagiellonian University Collegium Medicum, Krakow, Poland.
Jan StyczyńskiDepartment of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this multi-center study was to evaluate the incidence, clinical course, and risk factors for bacterial multidrug-resistant (MDR) gastrointestinal tract infections (GTI) among children undergoing allogeneic and autologous hematopoietic cell transplantation. A total number of 175 pediatric patients (aged 1-18 years), transplanted between January 2018 and December 2019, who were tested for bacterial colonization/infection were enrolled into this multi-center analysis. Episodes of MDR GTI occurred in 77/175 (44%) patients. In multivariate analysis for higher GTI incidence, the following factors were significant: matched-unrelated donor (MUD) transplantation, HLA mismatch, presence of graft-versus-host disease (GVHD), and gut GVHD. The most common GTI were Clostridium difficile (CDI), multidrug-resistant Enterobacteriaceae (Klebsiella pneumoniae, Escherichia coli extended-spectrum β-lactamase), and Enterococcus HLAR (high-level aminoglycoside-resistant). No MDR GTI-attributed deaths were reported. MDR GTI is a frequent complication after HCT among children, causes prolonged hospitalization, but rarely contributes to death. We identified risk factors of MDR GTI development in children, with focus on GVHD and unrelated donor and HLA mismatch. We conclude that the presence of Clostridiales plays an important anti-inflammatory homeostatic role and decreases incidence of GVHD or alleviate its course.

Indexed as

AdolescentBacterial InfectionsChildChild, PreschoolClostridioides difficileClostridium InfectionsDrug Resistance, Multiple, BacterialFemaleGastrointestinal DiseasesGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansIncidenceInfantMaleRisk FactorsAutologous transplantationClostridium difficileGastrointestinal tract infectionGram-negative multidrug-resistant bacteriaHematopoietic stem cell transplantationMalignant diseasesPediatric hematology and oncology

Identifiers

PMID34674000
PMCPMC8720737

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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.