Evidence map›Paper›PMID 31484910›Full record

ArticleInternal medicine (Tokyo, Japan)2020

Pilsicainide Administration Unmasks a Phenotype of Brugada Syndrome in a Patient with Overlap Syndrome due to the E1784K SCN5A Mutation.

Hideyuki Hasebe, Tomoyo Yokoya, Nobuyuki Murakoshi, Nobutake Kurebayashi

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2020. 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, 4 citations in OpenAlex.

  1. Article
  2. Article
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 at 3 institutions in 1 country.

Hideyuki HasebeDivision of Arrhythmology, Shizuoka Saiseikai General Hospital, Japan.
Tomoyo YokoyaDivision of Arrhythmology, Shizuoka Saiseikai General Hospital, Japan.
Nobuyuki MurakoshiCardiovascular Division, Faculty of Medicine, University of Tsukuba, Japan.
Nobutake KurebayashiDivision of Cardiology, Chutoen General Medical Center, Japan.
Shizuoka Saiseikai General Hospital · JPMie Chuo Medical Center · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the cardiac sodium channel SCN5A can cause phenotypic overlap syndrome of long QT syndrome and Brugada syndrome. However, Brugada-type ST elevations in patients with overlap syndrome are often concealed, which creates a diagnostic challenge. A 38-year-old man was admitted due to ventricular fibrillation (VF). The 12-lead electrocardiogram showed a prolonged QT interval and saddleback-type ST elevation. Pilsicainide administration induced coved-type ST elevation and VF triggered by a single premature ventricular contraction. A genetic analysis showed an SCN5A c.5350G>A p.E1784K mutation. The present case suggests the importance of a drug administration test being performed in the clinical management of overlap syndrome.

Indexed as

Anti-Arrhythmia AgentsAdultBrugada SyndromeElectrocardiographyHumansLidocaineLong QT SyndromeMaleMutationNAV1.5 Voltage-Gated Sodium ChannelPhenotypeVentricular FibrillationAnti-Arrhythmia AgentsLidocaineNAV1.5 Voltage-Gated Sodium ChannelpilsicainideSCN5A protein, humanBrugada syndromeE1784Klong QT syndromeoverlap syndromeSCN5Asodium channel blocker

Identifiers

PMID31484910
PMCPMC6995720
OpenAlexW2972293461

What OpenQuestion 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 OpenQuestion graph.