Evidence map›Paper›PMID 26433939›Full record

ArticlePediatric cardiology2016

Exploring the Discussion of Risk of Sudden Cardiac Death.

Kristin Anne Wiley, Erin M Demo, Peggy Walker, C Osborne Shuler

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric cardiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Finding a new rhythm: child health-related quality of life, parent psychological distress, and unmet needs among families of children with cardiac channelopathies.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2026
    Article
  2. Article
  3. Phenotypic Variability of a PathogenicFrontiers in cardiovascular medicine · 2021
    Article
  4. 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.

Kristin Anne WileyWake Forest Baptist Medical Center, OCCC 4TH Floor, Medical Center Blvd, Winston-Salem, NC, USA. kristinannewiley@gmail.com.
Erin M DemoPediatric Cardiology, Sibley Heart Center Cardiology, 2835 Brandywine Road, Suite 300, Atlanta, GA, 30341, USA.
Peggy WalkerGenetic Counseling Program, University of South Carolina School of Medicine, Two Medical Park, Suite 103, Columbia, SC, 29203, USA.
C Osborne ShulerUniversity Specialty Clinics, University of South Carolina, 9 Medical Park, Ste. 110, Columbia, SC, 29203, USA.
University of South Carolina · USAtrium Health Wake Forest Baptist · USBrandywine Photonics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sudden arrhythmic death syndrome (SADS), where death is secondary to cardiac arrhythmia, is associated with several cardiac ion channelopathies, including long QT syndrome and Brugada syndrome, as well as cardiomyopathies such as hypertrophic cardiomyopathy and dilated cardiomyopathy. Many of these conditions often present in childhood or adolescence. This study investigates how diagnoses of cardiac diseases associated with SADS are communicated within families. A questionnaire was distributed through cardiac disease-focused support groups and organizations. Data from 114 parents who have a child with a SADS condition were used for analysis. Based on the responses, parents explained the risk of SADS in a straightforward manner and related the risk to the importance of compliance with the prescribed treatment. Participants also found it difficult to determine and enforce lifestyle modifications, manage individuals' emotional reactions, convey the seriousness of the information without scaring their children, and discuss the risk of SADS during these conversations. Concerns regarding disease progression, length and quality of life, and treatment failures were also expressed. Healthcare providers, the Internet, other affected people, visual aids, and personal experience were all reported to be helpful for facilitating these discussions. Services and resources requested by participants included children's support groups, a counselor or psychologist, and child-oriented materials. Increased understanding of how families discuss children's diagnosis of SADS conditions will equip healthcare providers with the information to address parental concerns and help facilitate meaningful and informative discussions within families.

Indexed as

AdolescentAdultAgedCardiomyopathy, DilatedCardiomyopathy, HypertrophicChildChild, PreschoolCommunicationDeath, Sudden, CardiacFemaleHumansInfantInfant, NewbornLong QT SyndromeMaleMiddle AgedCommunicationFamilyGeneticsLQTSRiskSADS

Identifiers

PMID26433939
OpenAlexW2213607538

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.