Evidence map›Paper›PMID 39104518›Full record

ArticleEuropean heart journal. Case reports2024

A rare case report of catecholaminergic polymorphic ventricular tachycardia with an uncommon

Kimberly R Ding, Angelo L de la Rosa, Duc Do, Sonia Shah

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in European heart journal. Case reports, 2024. 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
–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

2 citing papers in PubMed.

  1. Article
  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

4 authors.

Kimberly R DingDepartment of Internal Medicine, Harbor-UCLA Medical Center, 1000 W Carson St, Torrance, CA 90509, USA.ORCID https://orcid.org/0000-0002-3971-6941
Angelo L de la RosaDepartment of Cardiology, Harbor-UCLA Medical Center, Torrance, CA, USA.
Duc DoDepartment of Electrophysiology, Ronald-Reagan UCLA Medical Center, Los Angeles, CA, USA.
Sonia ShahDepartment of Cardiology, Harbor-UCLA Medical Center, Torrance, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a primary arrhythmia disorder characterized by syncope or sudden cardiac death and typically caused by a gain-of-function of the Ryanodine Receptor Type 2 ( Case summary: A 21-year-old female with autism was brought to the ED following cardiac arrest. Bidirectional ventricular tachycardia was captured on electrocardiogram. Propranolol was initiated, and patient had no further episodes of ventricular arrhythmia. A subcutaneous implantable cardioverter defibrillator (ICD) was implanted, and further genetics testing was done. Rapid Whole Genome Sequencing (PGnome®-RAPID) resulted heterozygous variant of uncertain significance in Discussion: To the authors' knowledge, this is the third known record of such mutation in accordance with the International Calmodulin Registry (

Indexed as

Bidirectional ventricular tachycardiaCardiac arrestCase reportCatecholaminergic polymorphic ventricular tachycardia

Identifiers

PMID39104518
PMCPMC11299022

What OpenQuestion holds

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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.