Evidence map›Paper›PMID 36733348›Full record

ArticleFrontiers in oncology2022

Prior COVID-19 infection may increase risk for developing endothelial dysfunction following hematopoietic cell transplantation.

Sydney Ariagno, Dristhi Ragoonanan, Sajad Khazal, Kris M Mahadeo, Gabriel Salinas Cisneros, Matt S Zinter, Robyn A Blacken, Gopi Mohan, Leslie E Lehmann, Asmaa Ferdjallah and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 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
0.2field-weighted citation impact, top 54% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. 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

12 authors at 8 institutions in 1 country.

Sydney AriagnoPediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN, United States.
Dristhi RagoonananDivision of Pediatrics, Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Sajad KhazalDivision of Pediatrics, Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Kris M MahadeoDivision of Pediatrics, Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Gabriel Salinas CisnerosPediatric Hematology and Oncology, University of California San Francisco, San Francisco, CA, United States.
Matt S ZinterPediatric Critical Care Medicine, University of California San Francisco, San Francisco, CA, United States.
Robyn A BlackenCancer and Blood Disorders Center, Boston Children's Hospital, Boston, MA, United States.
Gopi MohanPediatric Critical Care, Massachusetts General Hospital, Boston, MA, United States.
Leslie E LehmannPediatric Stem Cell Transplant, Dana Farber Cancer Institute/Boston Children's Hospital, Boston, MA, United States.
Asmaa FerdjallahPediatric Hematology and Oncology, Mayo Clinic, Rochester, MN, United States.
Kristin C MaraDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.
Mira A KohorstPediatric Hematology and Oncology, Mayo Clinic, Rochester, MN, United States.
The University of Texas MD Anderson Cancer Center · USMayo Clinic in Arizona · USMayo Clinic in Florida · USBoston Children's Hospital · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · USMassachusetts General Hospital · USUniversity of California, San Francisco · USUniversity of California System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial dysfunction underlies many of the major complications following hematopoietic cell transplantation (HCT), including transplant-associated thrombotic microangiopathy (TA-TMA), veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS), and engraftment syndrome (ES). Emerging evidence similarly implicates endothelitis and microangiopathy in severe COVID-19-related multi-system organ dysfunction. Given the overlap in these two illness states, we hypothesize that prior COVID-19 infection may increase risk for HCT-related endotheliopathies. This retrospective, multicenter study included patients aged 0-25 years who underwent autologous or allogeneic HCT for any indication between January 1, 2020 and September 21, 2021, with close attention to those infected with COVID-19 in either the six months prior to transplant or twelve months following transplant. Incidences of TA-TMA, VOD/SOS, and ES were compared among patients with COVID-19 infection pre-HCT and post-HCT, as well as with historical controls who were never infected with SARS-CoV-2. Those who underwent HCT following COVID-19 infection displayed significantly increased rates of TA-TMA compared to those who were never infected. Additionally, our data suggests a similar trend for increased VOD/SOS and ES rates, although this did not reach statistical significance. Therefore, a history of COVID-19 infection prior to undergoing HCT may be a nonmodifiable risk factor for endothelial-related complications following HCT. Further studies are warranted to better clarify this relationship among larger cohorts and in the era of the Omicron SARS-CoV-2 variants.

Indexed as

COVID-19endothelial dysfunctionengraftment syndromehematopoietic cell transplantTA-TMAVOD/SOS

Identifiers

PMID36733348
PMCPMC9886674
OpenAlexW4316670106

What OpenQuestion holds

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LicenceCC BY
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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.