Evidence map›Paper›PMID 34502196›Full record

ReviewInternational journal of molecular sciences2021

Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: A Translational Perspective for the Clinician-Scientist.

Dania Kallas, Avani Lamba, Thomas M Roston, Alia Arslanova, Sonia Franciosi, Glen F Tibbits, Shubhayan Sanatani

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. 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
–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

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

  1. Guideline
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Novel causativeFrontiers in genetics · 2025
    Article
  9. Review
  10. Novel variants inLife science alliance · 2024
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. 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

7 authors.

Dania KallasBritish Columbia Children's Hospital Heart Center, 1F9-4480 Oak St., Vancouver, BC V6H 3V4, Canada.ORCID 0000-0002-7438-0873
Avani LambaBritish Columbia Children's Hospital Heart Center, 1F9-4480 Oak St., Vancouver, BC V6H 3V4, Canada.
Thomas M RostonBritish Columbia Children's Hospital Heart Center, 1F9-4480 Oak St., Vancouver, BC V6H 3V4, Canada.
Alia ArslanovaCellular and Regenerative Medicine Centre, British Columbia Children's Hospital Research Institute, 938 W 28th Ave, Vancouver, BC V5Z 4H4, Canada.
Sonia FranciosiBritish Columbia Children's Hospital Heart Center, 1F9-4480 Oak St., Vancouver, BC V6H 3V4, Canada.
Glen F TibbitsCellular and Regenerative Medicine Centre, British Columbia Children's Hospital Research Institute, 938 W 28th Ave, Vancouver, BC V5Z 4H4, Canada.
Shubhayan SanataniBritish Columbia Children's Hospital Heart Center, 1F9-4480 Oak St., Vancouver, BC V6H 3V4, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and potentially lethal inherited arrhythmia disease characterized by exercise or emotion-induced bidirectional or polymorphic ventricular tachyarrhythmias. The median age of disease onset is reported to be approximately 10 years of age. The majority of CPVT patients have pathogenic variants in the gene encoding the cardiac ryanodine receptor, or calsequestrin 2. These lead to mishandling of calcium in cardiomyocytes resulting in after-depolarizations, and ventricular arrhythmias. Disease severity is particularly pronounced in younger individuals who usually present with cardiac arrest and arrhythmic syncope. Risk stratification is imprecise and long-term prognosis on therapy is unknown despite decades of research focused on pediatric CPVT populations. The purpose of this review is to summarize contemporary data on pediatric CPVT, highlight knowledge gaps and present future research directions for the clinician-scientist to address.

Indexed as

ExerciseMutationChildEmotionsHumansPolymorphic Catecholaminergic Ventricular TachycardiaRyanodine Receptor Calcium Release ChannelTachycardia, VentricularRyanodine Receptor Calcium Release Channelcatecholaminergic polymorphic ventricular tachycardiainherited arrhythmiapediatric electrophysiologyprimary electrical diseaseryanodine receptorsudden cardiac deathventricular tachycardia

Identifiers

PMID34502196
PMCPMC8431429

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.