Evidence map›Paper›PMID 37577706›Full record

ArticlemedRxiv : the preprint server for health sciences2023

Critical Illness Risk and Long-Term Outcomes Following Intensive Care in Pediatric Hematopoietic Cell Transplant Recipients.

Matt S Zinter, Ruta Brazauskas, Joelle Strom, Stella Chen, Stephanie Bo-Subait, Akshay Sharma, Amer Beitinjaneh, Dimana Dimitrova, Greg Guilcher, Jaime Preussler and 19 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 19 institutions in 3 countries.

Matt S ZinterDepartment of Pediatrics, Division of Critical Care Medicine, University of California, San Francisco, San Francisco, CA, USA.
Ruta BrazauskasMedical College of Wisconsin, Milwaukee, WI, USA.
Joelle StromMedical College of Wisconsin, Milwaukee, WI, USA.
Stella ChenMedical College of Wisconsin, Milwaukee, WI, USA.
Stephanie Bo-SubaitMedical College of Wisconsin, Milwaukee, WI, USA.
Akshay SharmaSt. Jude Children's Research Hospital, Memphis, TN, USA.
Amer BeitinjanehUniversity of Miami, Miami, FL, USA.
Dimana DimitrovaNational Institutes of Health, National Cancer Institute, Bethesda, MD, USA.
Greg GuilcherAlberta Children's Hospital, Alberta, Canada.
Jaime PreusslerNational Marrow Donor Program/Be The Match, Minneapolis, MN, USA.
Kasiani MyersCincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Neel S BhattFred Hutchinson Cancer Center, Seattle, WA, USA.
Olle RingdenKarolinska Institutet, Karolinska University Hospital, Huddinge, The Netherlands.
Peiman HemattiMedical College of Wisconsin, Milwaukee, WI, USA.
Robert J HayashiWashington University in St. Louis, St. Louis, MO, USA.
Sagar PatelHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Satiro Nakamura De OliveiraUniversity of California, Los Angeles, Los Angeles, CA, USA.
Seth RotzCleveland Clinic, Cleveland, OH, USA.
Sherif M BadawyNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
Taiga NishihoriMoffitt Cancer Center, Tampa, FL, USA.
David BuchbinderChildren's Hospital of Orange County, Orange, CA, USA.
Betty HamiltonCleveland Clinic, Cleveland, OH, USA.
Bipin SavaniVanderbilt University Medical Center, Nashville, TN, USA.
Hélène SchoemansUniversity Hospital Gasthuisberg, Leuven, Belgium.
Mohamed SorrorFred Hutchinson Cancer Center, Seattle, WA, USA.
Lena WinestoneDepartment of Pediatrics, Division of Allergy, Immunology, and BMT, University of California, San Francisco, San Francisco, CA, USA.
Christine DuncanDana Farber Cancer Center, Boston, MA, USA.
Rachel PhelanMedical College of Wisconsin, Milwaukee, WI, USA.
Christopher C DvorakDepartment of Pediatrics, Division of Allergy, Immunology, and BMT, University of California, San Francisco, San Francisco, CA, USA.
Medical College of Wisconsin · USUniversity of California, San Francisco · USCleveland Clinic · USFred Hutch Cancer Center · USAlberta Children's Hospital · CAChildren's Hospital of Orange County · USCincinnati Children's Hospital Medical Center · USDana-Farber Cancer Institute · USMoffitt Cancer Center · USNational Institutes of Health · USNational Marrow Donor Program · USNorthwestern University · USSt. Jude Children's Research Hospital · USUniversitair Ziekenhuis Leuven · BEUniversity of California, Los Angeles · USUniversity of Miami · USUniversity of Utah · USVanderbilt University Medical Center · USWashington University in St. Louis · US

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Pathobiologic Transcriptional Signatures of Pulmonary Complications in Pediatric Hematopoietic Cellular TransplantationK23HL146936 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZINTER, MATTHEW SCOTT · 2020 to 2024
$980k
NCI NIH HHS U24 CA076518NHLBI NIH HHS K23 HL146936
6 · The paper itself

Abstract

Background: Allogeneic hematopoietic cell transplantation (HCT) can be complicated by the development of organ toxicity and infection necessitating intensive care. Risk factors for intensive care admission are unclear due to heterogeneity across centers, and long-term outcome data after intensive care are sparse due to a historical paucity of survivors. Methods: The Center for International Blood and Marrow Transplant Research (CIBMTR) was queried to identify patients age ≤21 years who underwent a 1 Result: We identified 6,995 pediatric HCT patients from 69 HCT centers, of whom 1,067 required post-HCT intensive care. The cumulative incidence of PICU admission was 8.3% at day +100, 12.8% at 1 year, and 15.3% at 5 years post HCT. PICU admission was linked to younger age, lower median zip code income, Black or multiracial background, pre-transplant organ toxicity, pre-transplant CMV seropositivity, use of umbilical cord blood and/or HLA-mismatched allografts, and the development of post-HCT graft-versus-host disease or malignancy relapse. Among PICU patients, survival to ICU discharge was 85.7% but more than half of ICU survivors were readmitted to a PICU during the study interval. Overall survival from the time of 1 Conclusions: Intensive care management is common in pediatric HCT patients. Survival to ICU discharge is high, but ongoing complications necessitate recurrent ICU admission and lead to a poor 1-year outcome in many patients. Together, these data suggest an ongoing burden of toxicity in pediatric HCT patients that continues to limit long-term survival.

Identifiers

PMID37577706
PMCPMC10418579
OpenAlexW4385605972

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.