Evidence map›Paper›PMID 34017071›Full record

ArticleBone marrow transplantation2021

Association of persistent tachycardia with early myocardial dysfunction in children undergoing allogeneic hematopoietic cell transplantation.

Jason F Goldberg, Emily J Peters, Elizabeth A Tolley, Mazal N Hagler, Vijaya M Joshi, Shelby E Wallace, Simonne S Nouer, Gary S Beasley, Hugo R Martinez, Kaitlin A Ryan and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Review
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

14 authors at 2 institutions in 1 country.

Jason F GoldbergDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA. jgoldbe4@uthsc.edu.ORCID http://orcid.org/0000-0001-8351-6376
Emily J PetersDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Elizabeth A TolleyDepartment of Preventive Medicine, University of Tennessee Health Sciences Center, Memphis, TN, USA.ORCID http://orcid.org/0000-0002-6820-817X
Mazal N HaglerDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Vijaya M JoshiDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Shelby E WallaceDepartment of Preventive Medicine, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Simonne S NouerDepartment of Preventive Medicine, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Gary S BeasleyDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Hugo R MartinezDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Kaitlin A RyanDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Mohammed A AbsiDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Jenny R StrelsinDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Jeffrey A TowbinDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Brandon M TriplettDepartment of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.ORCID http://orcid.org/0000-0001-8220-9980
St. Jude Children's Research Hospital · USUniversity of Tennessee Health Science Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer survivors who have undergone hematopoietic cell transplantation (HCT) are at risk for myocardial dysfunction. Children who receive allogenic HCT encounter systemic inflammation resulting in tachycardia and hypertension. The effect of these abnormalities on myocardial function is not known. The aim of this study was to determine whether cardiac dysfunction early after HCT can be predicted by tachycardia or hypertension, within a retrospective single-center sample of pediatric HCT recipients. Early tachycardia or hypertension was defined as a majority of values taken from infusion date to 90 days post-infusion being abnormal. Ejection fraction <53% determined systolic dysfunction. A composite score of accepted pediatric diastolic abnormalities determined diastolic dysfunction. Among 80 subjects (median age 8 years), early tachycardia, systolic dysfunction, and diastolic dysfunction were present in 64%, 25%, and 48% of the sample, respectively. In multivariable models, early tachycardia was an independent predictor of early systolic dysfunction (OR = 12.6 [1.4-112.8], p = 0.024) and diastolic dysfunction (OR = 3.9 [1.3-11.5], p = 0.013). Tachycardia and cardiac dysfunction are common and associated with one another in the early period after pediatric HCT. Future studies may elucidate the role of tachycardia and myocardial dysfunction early after HCT as important predictors of future cardiovascular dysfunction.

Indexed as

CardiomyopathiesHematopoietic Stem Cell TransplantationChildHumansRetrospective StudiesTachycardiaTransplant Recipients

Identifiers

PMID34017071
OpenAlexW3162858375

What OpenQuestion holds

Textmetadata
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.