Evidence map›Paper›PMID 37614574›Full record

ArticleJACC. CardioOncology2023

Extensive Cardiac Function Analyses Using Contemporary Echocardiography in Childhood Cancer Survivors: A DCCSS LATER Study.

Remy Merkx, Jan M Leerink, E Lieke A M Feijen, Esmée C de Baat, Louise Bellersen, Dorine Bresters, Elvira C van Dalen, Eline van Dulmen-den Broeder, Margriet van der Heiden-van der Loo, Marry M van den Heuvel-Eibrink and 18 more

Open access · goldAbstract read
In one paragraph

Article in JACC. CardioOncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  5. Observational
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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

28 authors at 9 institutions in 3 countries.

Remy MerkxMedical Imaging/Radiology, Medical UltraSound Imaging Centre, Radboud Institute for Health Sciences, Radboud university medical center, the Netherlands.
Jan M LeerinkClinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
E Lieke A M FeijenPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Esmée C de BaatPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Louise BellersenCardiology, Radboud university medical center, Nijmegen, the Netherlands.
Dorine BrestersPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Elvira C van DalenPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Eline van Dulmen-den BroederPediatric Oncology, Amsterdam UMC, VU University, Amsterdam, the Netherlands.
Margriet van der Heiden-van der LooTrial- and Data Center, Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Marry M van den Heuvel-EibrinkPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Judith L KokPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Marloes LouwerensInternal Medicine, Leiden University Medical Center, Leiden, the Netherlands.
Angela H E M MaasCardiology, Radboud university medical center, Nijmegen, the Netherlands.
Sebastian J C M M NeggersMedicine, Erasmus University Medical Center Rotterdam, Rotterdam, the Netherlands.
Cécile M RonckersPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Jop C TeepenPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Arco J TeskeCardiology, University Medical Center Utrecht, Utrecht, the Netherlands.
Wim J E TissingPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Andrica C H de VriesPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Gert WeijersMedical Imaging/Radiology, Medical UltraSound Imaging Centre, Radboud Institute for Health Sciences, Radboud university medical center, the Netherlands.
Chris L de KorteMedical Imaging/Radiology, Medical UltraSound Imaging Centre, Radboud Institute for Health Sciences, Radboud university medical center, the Netherlands.
Jacqueline LoonenHematology, Radboud university medical center, Nijmegen, the Netherlands.
Annelies M C Mavinkurve-GroothuisPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Helena J H van der PalPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Leontien C M KremerPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Wouter E M KokClinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Livia KapustaPediatrics, Pediatric Cardiology Unit, Tel Aviv Sourasky Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Dutch LATER Study Group
Princess Máxima Center · NLRadboud University Nijmegen · NLUniversity Medical Center Utrecht · NLAmsterdam UMC Location Vrije Universiteit Amsterdam · NLAmsterdam University Medical Centers · NLErasmus MC · NLJohannes Gutenberg University Mainz · DELeiden University Medical Center · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Childhood cancer survivors (CCS) are at risk for cardiotoxicity. Objectives: We sought to assess how cardiac dysfunction measurements in CCS overlap and are differentially influenced by risk factors. Methods: This cross-sectional Dutch Childhood Cancer Survivor Study evaluated echocardiograms of 1,397 ≥5-year CCS and 277 siblings. Of CCS, n = 1,254 received cardiotoxic (anthracyclines/mitoxantrone/radiotherapy involving the heart region [RT Results: CCS were a median of 26.7 years after diagnosis; 49% were women. Abnormal left ventricular ejection fraction (LVEF) (defined as <52% in men, <54% in women) occurred most commonly in CCS treated with anthracyclines and RT Conclusions: Abnormal LVEF and GLS constitute complementary measures of systolic dysfunction among long-term CCS. Their diagnostic value may differ according to cardiotoxic exposures. Also, CCS have residual, unexplained risk of cardiac dysfunction. (Early Detection of Cardiac Dysfunction in Childhood Cancer Survivors, a DCOG LATER study; NTR7481).

Indexed as

cancer survivorscardiotoxicitychildechocardiographyglobal longitudinal strainleft ventricular dysfunction

Identifiers

PMID37614574
PMCPMC10443197
OpenAlexW4385830342

What Socratic 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 Socratic graph.