Evidence map›Paper›PMID 36849806›Full record

ArticleBone marrow transplantation2023

Risk factors for a severe disease course in children with SARS-COV-2 infection following hematopoietic cell transplantation in the pre-Omicron period: a prospective multinational Infectious Disease Working Party from the European Society for Blood and Marrow Transplantation group (EBMT) and the Spanish Group of Hematopoietic Stem Cell Transplantation (GETH) study.

Dina Averbuch, Rafael de la Camara, Gloria Tridello, Nina Simone Knelange, Tatiana A Bykova, Marianne Ifversen, Veronika Dobsinska, Mouhab Ayas, Amir Ali Hamidieh, Herbert Pichler and 17 more

Open access · bronzeAbstract read
In one paragraph

Article in Bone marrow transplantation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Risk Factors for Pediatric Critical COVID-19: A Systematic Review and Meta-Analysis.Journal of the Pediatric Infectious Diseases Society · 2024
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  8. Risk Factors for Pediatric Critical COVID-19: A Systematic Review and Meta-Analysis.medRxiv : the preprint server for health sciences · 2024
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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

27 authors at 20 institutions in 16 countries.

Dina AverbuchFaculty of Medicine, Hebrew University of Jerusalem, Pediatric Infectious Diseases, Hadassah Medical Center, Jerusalem, Israel. adiana@hadassah.org.il.ORCID 0000-0001-9614-7274
Rafael de la CamaraHematology Department, Hospital Universitario de La Princesa, Madrid, Spain.ORCID 0000-0002-8189-5779
Gloria TridelloPediatric Hematology Oncology, Department of Mother and Child, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Nina Simone KnelangeEBMT - Leiden Study Unit, Leiden, Netherlands.
Tatiana A BykovaRM Gorbacheva Research Institute, Pavlov University, St. Petersburg, Russia.ORCID 0000-0002-4456-2369
Marianne IfversenDepartment of Children and Adolescents Medicine, Stem Cell Transplant Unit, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0002-2558-1935
Veronika DobsinskaDepartment of Pediatric Hematology and Oncology, Comenius University, Bratislava, Slovakia.
Mouhab AyasPediatric Hematology/Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.ORCID 0000-0002-5740-1302
Amir Ali HamidiehPediatric Cell and Gene Therapy Research Center, Gene, Cell & Tissue Research Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-8935-079X
Herbert PichlerDepartment of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-5107-5123
Antonio Perez-MartinezDepartment of Pediatric Hematology and Oncology, Hospital Universitario La Paz, Madrid, Spain.ORCID 0000-0002-6436-9195
Simone CesaroPediatric Hematology Oncology, Department of Mother and Child, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.ORCID 0000-0002-8698-9547
Mikael SundinSection of Pediatric Hematology, Immunology and HCT, Astrid Lindgren Children's Hospital, Karolinska University Hospital and Division of Pediatrics, CLINTEC, Karolinska Institutet, Stockholm, Sweden.
Isabel BadellPediatric BMT Unit, Hospital Santa Creu i Sant Pau, Universitat Autonoma de Barcelona, Barcelona, Spain.
Peter BaderUniversitaetsklinikum Frankfurt Goethe-Universitaet, Frankfurt Main, Germany.ORCID 0000-0003-4554-0265
Jan-Erik JohanssonSahlgrenska University Hospital, Goeteborg, Sweden.
Oana Mirci-DanicarBMT Unit, Bristol Royal Hospital for Children, Bristol, UK.
Petr SedlacekHSCT Unit, Department of Paediatric Haematology and Oncology, University Hospital Motol, Prague, Czech Republic.ORCID 0000-0001-7895-2886
Catherine PaillardPediatric Hematology Oncology, Hautepierre Hospital, Strasbourg University, Strasbourg, France.
Brenda GibsonDepartment of Haematology, Royal Hospital for Children, Glasgow, UK.
Sarah LawsonDepartment of Haematology, Birmingham Children's Hospital, Birmingham, UK.
Nicolaus KroegerDepartment of Stem Cell Transplantation, University Hospital Eppendorf, Hamburg, Germany.ORCID 0000-0001-5103-9966
Selim CorbaciogluDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, University of Regensburg, Regensburg, Germany.
Malgorzata MikulskaDivision of Infectious Diseases, University of Genova, Ospedale Policlinco San Martino, Genova, Italy.ORCID 0000-0002-5535-4602
Jose Luis PiñanaHospital Clinico Universitario de Valencia. Fundación de investigación INCLIVA, Hospital Clinico Universitario de Valencia, Valencia, Spain.ORCID 0000-0001-8533-2562
Jan StyczynskiPediatric Hematology and Oncology, University Hospital, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.ORCID 0000-0002-3158-119X
Per LjungmanDepartment of Cellular Therapy and Allogeneic Stem Cell Transplantation, Karolinska Comprehensive Cancer Center, Karolinska University Hospital Huddinge, Division of Hematology, Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-8281-3245
Azienda Ospedaliera Universitaria Integrata Verona · ITKarolinska University Hospital · SEBirmingham Children's Hospital · GBBristol Royal Hospital for Children · GBCopenhagen University Hospital · DKEuropean Society for Blood and Marrow Transplantation · NLFirst Pavlov State Medical University of St. Petersburg · RUGoethe University Frankfurt · DEHebrew University of Jerusalem · ILHôpital d'Hautepierre · FRHospital Clínico Universitario de Valencia · ESHospital Universitario de La Princesa · ESHospital Universitario La Paz · ESKing Faisal Specialist Hospital & Research Centre · SANational Institute of Cardiovascular Diseases · SKNicolaus Copernicus University · PLOspedale Policlinico San Martino · ITRoyal Hospital for Children · GBSahlgrenska University Hospital · SESt Anna Children's Hospital · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Risk factors for severe SARS-Cov-2 infection course are poorly described in children following hematopoietic cell transplantation (HCT). In this international study, we analyzed factors associated with a severe course (intensive care unit (ICU) admission and/or mortality) in post-HCT children. Eighty-nine children (58% male; median age 9 years (min-max 1-18)) who received an allogeneic (85; 96%) or an autologous (4; 4%) HCT were reported from 28 centers (18 countries). Median time from HCT to SARS-Cov-2 infection was 7 months (min-max 0-181). The most common clinical manifestations included fever (37; 42%) and cough (26; 29%); 37 (42%) were asymptomatic. Nine (10%) children following allo-HCT required ICU care. Seven children (8%) following allo-HCT, died at a median of 22 days after SARS-Cov-2 diagnosis. In a univariate analysis, the probability of a severe disease course was higher in allo-HCT children with chronic GVHD, non-malignant disease, immune suppressive treatment (specifically, mycophenolate), moderate immunodeficiency score, low Lansky score, fever, cough, coinfection, pulmonary radiological findings, and high C-reactive protein. In conclusion, SARS-Cov-2 infection in children following HCT was frequently asymptomatic. Despite this, 10% needed ICU admission and 8% died in our cohort. Certain HCT, underlying disease, and SARS-Cov-2 related factors were associated with a severe disease course.

Indexed as

Communicable DiseasesCOVID-19Hematopoietic Stem Cell TransplantationBone MarrowChildCoughCOVID-19 TestingDisease ProgressionFemaleHumansMaleProspective StudiesRisk FactorsSARS-CoV-2Transplantation, Homologous

Identifiers

PMID36849806
PMCPMC9969031
OpenAlexW4322217322

What OpenQuestion holds

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Registered trials

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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.