Evidence map›Paper›PMID 30539690›Full record

ArticleWestern journal of nursing research2019

Family Relationships Associated With Communication and Testing for Inherited Cardiac Conditions.

Lisa L Shah, Sandra Daack-Hirsch, Anne L Ersig, Anthony Paik, Ferhaan Ahmad, Janet Williams

Abstract read
In one paragraph

Article in Western journal of nursing research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
  3. Effectiveness of theCirculation · 2023
    Trial
  4. Article
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  9. Family genetic risk communication and reverse cascade testing in the BabySeq project.Genetics in medicine : official journal of the American College of Medical Genetics · 2025
    Article
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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

6 authors.

Lisa L ShahUniversity of Pittsburgh, PA, USA.ORCID 0000-0003-0671-3178
Sandra Daack-HirschThe University of Iowa, Iowa City, IA, USA.
Anne L ErsigUniversity of Wisconsin-Madison, WI, USA.
Anthony PaikUniversity of Massachusetts Amherst, MA, USA.
Ferhaan AhmadThe University of Iowa, Iowa City, IA, USA.
Janet WilliamsThe University of Iowa, Iowa City, IA, USA.

Funding

Targeting Research and Academic Training of Nurses in GenomicsT32NR009759 · NINR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CONLEY, YVETTE P · 2006 to 2025
$4.5M
Communication of Genetic Risk for Sudden Cardiac Death from Probands to RelativesF31NR014758 · NINR · UNIVERSITY OF IOWA · PI SHAH, LISA L · 2014 to 2016
$67k
NINR NIH HHS F31 NR014758NINR NIH HHS T32 NR009759
6 · The paper itself

Abstract

The purpose of this study was to identify characteristics of family relationships associated with communication of genetic risk and testing behaviors among at-risk relatives in families with an inherited cardiac condition. Data were collected from 53 patients and parents of children with an inherited cardiac condition through interviews, pedigrees, and surveys. Associations were examined among family relationship characteristics and whether at-risk relatives were informed about their risk and tested for disease. Of 1,178 at-risk relatives, 52.5% were informed about their risk and 52.1% of those informed were tested. Emotional closeness, relationship quality, and communication frequency had significant bivariate associations with genetic risk communication. Communication frequency was associated with genetic risk communication and testing in multivariate models. This study provides new insight into the extent of genetic risk communication and testing in families with inherited cardiac conditions. Family relationships, especially communication frequency, are critical factors in family communication of genetic risk.

Indexed as

CommunicationGenetic Predisposition to DiseaseGenetic TestingCross-Sectional StudiesFamilyHeart DiseasesHumansSurveys and Questionnairescardiomyopathycascade screeningdisclosure (mesh)genetic risk communicationhypertrophic (mesh)long QT syndrome (mesh)

Identifiers

PMID30539690
PMCPMC6561845

What OpenQuestion holds

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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.