Evidence map›Paper›PMID 35798233›Full record

ArticleTransplantation and cellular therapy2022

Clinical Characteristics and Outcomes of COVID-19 in Pediatric and Early Adolescent and Young Adult Hematopoietic Stem Cell Transplant Recipients: A Cohort Study.

Neel S Bhatt, Akshay Sharma, Andrew St Martin, Muhammad Bilal Abid, Valerie I Brown, Miguel Angel Diaz Perez, Haydar Frangoul, Shahinaz M Gadalla, Megan M Herr, Maxwell M Krem and 13 more

Abstract read
In one paragraph

Article in Transplantation and cellular therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Risk Factors for Pediatric Critical COVID-19: A Systematic Review and Meta-Analysis.Journal of the Pediatric Infectious Diseases Society · 2024
    Pooled it
  2. Pre-existing Immunocompromising Conditions and Outcomes of Acute COVID-19 Patients Admitted for Pediatric Intensive Care.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
    Article
  3. Risk Factors for Pediatric Critical COVID-19: A Systematic Review and Meta-Analysis.medRxiv : the preprint server for health sciences · 2024
    Article
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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

23 authors.

Neel S BhattClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington. Electronic address: nbhatt@fredhutch.org.
Akshay SharmaDepartment of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee.
Andrew St MartinCIBMTR (Center for International Blood and Marrow Transplant Research), Milwaukee, Wisconsin.
Muhammad Bilal AbidDivisions of Hematology/Oncology & Infectious Diseases, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Valerie I BrownPenn State Children's Hospital and Penn State College of Medicine, Hershey, Pennsylvania.
Miguel Angel Diaz PerezHospital Infantil Universitario "Niño Jesus," Madrid, Spain.
Haydar FrangoulSarah Cannon Research Institute, Nashville, Tennessee.
Shahinaz M GadallaDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
Megan M HerrRoswell Park Comprehensive Cancer Center, Buffalo, New York.
Maxwell M KremKansas City VA Medical Center, Kansas City, Missouri.
Hillard M LazarusCase Western Reserve University, Cleveland, Ohio.
Michael J MartensCIBMTR (Center for International Blood and Marrow Transplant Research), Milwaukee, Wisconsin; Division of Biostatistics, Medical College of Wisconsin, Milwaukee, Wisconsin.
Parinda A MehtaCincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Taiga NishihoriMoffitt Cancer Center, Tampa, Florida.
Tim PrestidgeStarship Hospital University of Auckland, Auckland, New Zeeland.
Michael A PulsipherPrimary Children's Hospital and the Huntsman Cancer Institute at the University of Utah, Salt Lake City, Utah.
Hemalatha G RangarajanNationwide Children's Hospital, Columbus, Ohio.
Kirsten M WilliamsDepartment of Pediatrics, Emory University and the Children's Healthcare of Atlanta, Atlanta, Georgia.
Lena E WinestoneDivision of Allergy, Immunology, and BMT, UCSF Benioff Children's Hospitals, San Francisco, California.
Dwight E YinDivision of Infectious Diseases, Department of Pediatrics, Children's Mercy Kansas City and University of Missouri at Kansas City School of Medicine, Kansas City, Missouri.
Marcie L RichesIQVIA Biotech, Morrisville, North Carolina.
Christopher E DandoyCase Western Reserve University, Cleveland, Ohio.
Jeffery J AulettaNationwide Children's Hospital, Columbus, Ohio; National Marrow Donor Program/Be The Match, Minneapolis, Minnesota.

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

Adult hematopoietic stem cell transplantation (HSCT) recipients are at a high risk of adverse outcomes after COVID-19. Although children have had better outcomes after COVID-19 compared to adults, data on risk factors and outcomes of COVID-19 among pediatric HSCT recipients are lacking. We describe outcomes of HSCT recipients who were ≤21 years of age at COVID-19 diagnosis and were reported to the Center for International Blood and Marrow Transplant Research between March 27, 2020, and May 7, 2021. The primary outcome was overall survival after COVID-19 diagnosis. We determined risk factors of COVID-19 as a secondary outcome in a subset of allogeneic HSCT recipients. A total of 167 pediatric HSCT recipients (135 allogeneic; 32 autologous HSCT recipients) were included. Median time from HSCT to COVID-19 was 15 months (interquartile range [IQR] 7-45) for allogeneic HSCT recipients and 16 months (IQR 6-59) for autologous HSCT recipients. Median follow-up from COVID-19 diagnosis was 53 days (range 1-270) and 37 days (1-179) for allogeneic and autologous HSCT recipients, respectively. Although COVID-19 was mild in 87% (n = 146/167), 10% (n = 16/167) of patients required supplemental oxygen or mechanical ventilation. The 45-day overall survival was 95% (95% confidence interval [CI], 90-99) and 90% (74-99) for allogeneic and autologous HSCT recipients, respectively. Cox regression analysis showed that patients with a hematopoietic cell transplant comorbidity index (HCT-CI) score of 1-2 were more likely to be diagnosed with COVID-19 (hazard ratio 1.95; 95% CI, 1.03-3.69, P = .042) compared to those with an HCT-CI of 0. Pediatric and early adolescent and young adult HSCT recipients with pre-HSCT comorbidities were more likely to be diagnosed with COVID-19. Overall mortality, albeit higher than the reported general population estimates, was lower when compared with previously published data focusing on adult HSCT recipients.

Indexed as

COVID-19Hematopoietic Stem Cell TransplantationAdolescentChildCohort StudiesCOVID-19 TestingHumansOxygenYoung AdultOxygenCovid-19Early adolescent and young adultHematopoietic stem cellPediatricTransplantation

Identifiers

PMID35798233
PMCPMC9251957

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.