Evidence map›Paper›PMID 28405885›Full record

ArticleForensic science, medicine, and pathology2017

Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications.

Cristian D'Ovidio, Aldo Carnevale, Vincenzo M Grassi, Enrica Rosato, Bernat Del Olmo, Monica Coll, Oscar Campuzano, Anna Iglesias, Ramon Brugada, Antonio Oliva

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Forensic science, medicine, and pathology, 2017. 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
0.5field-weighted citation impact, top 31% 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, 9 citations in OpenAlex.

  1. Review
  2. 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

10 authors at 4 institutions in 2 countries.

Cristian D'OvidioSection of Legal Medicine, Department of Medicine and Aging Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
Aldo CarnevaleSection of Legal Medicine, Department of Medicine and Aging Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
Vincenzo M GrassiInstitute of Public Health, Legal Medicine Section, Catholic University, School of Medicine, Largo Francesco Vito 1, 00168, Rome, Italy.
Enrica RosatoSection of Legal Medicine, Department of Medicine and Aging Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
Bernat Del OlmoCardiovascular Genetics Centre, University of Girona-IDIBGI, Girona, Spain.
Monica CollCardiovascular Genetics Centre, University of Girona-IDIBGI, Girona, Spain.
Oscar CampuzanoCardiovascular Genetics Centre, University of Girona-IDIBGI, Girona, Spain.
Anna IglesiasCardiovascular Genetics Centre, University of Girona-IDIBGI, Girona, Spain.
Ramon BrugadaCardiovascular Genetics Centre, University of Girona-IDIBGI, Girona, Spain.
Antonio OlivaInstitute of Public Health, Legal Medicine Section, Catholic University, School of Medicine, Largo Francesco Vito 1, 00168, Rome, Italy. antonio.oliva@unicatt.it.
Institut d'Investigació Biomèdica de Girona · ESUniversity of Chieti-Pescara · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Girona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This paper discusses the case of a young boy who died suddenly during a football match. The victim's personal and family medical histories were negative for cardiac events. He had undergone a cardiological investigation some months before his death, enabling him to participate in competitive sports. Only post-mortem molecular analysis allowed for a clearer determination of the most plausible cause of death, which was identified as inherited arrhythmogenic heart disease, known as catecholaminergic polymorphic ventricular tachycardia. It was possible to detect a novel, previously undescribed, variant in the RYR2 gene. This case report highlights the importance of a meaningful forensic multidisciplinary investigation in such cases, and also discusses possible medical malpractice claims.

Indexed as

Amino Acid SubstitutionMutation, MissenseAdolescentDeath, Sudden, CardiacEchocardiography, StressElectrocardiography, AmbulatoryHumansMalePolymorphic Catecholaminergic Ventricular TachycardiaRyanodine Receptor Calcium Release ChannelTachycardia, VentricularRyanodine Receptor Calcium Release ChannelCatecholaminergic polymorphic ventricular tachycardiaProvocation testRare variantStress electrocardiogramSudden cardiac death

Identifiers

PMID28405885
OpenAlexW2606676848

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.