Evidence map›Paper›PMID 29243008›Full record

ArticleJournal of genetic counseling2018

Examining the Psychosocial Impact of Genetic Testing for Cardiomyopathies.

Julia Wynn, David T Holland, Jimmy Duong, Priyanka Ahimaz, Wendy K Chung

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of genetic counseling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. 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

5 authors at 2 institutions in 1 country.

Julia WynnDepartment of Pediatrics, Division of Molecular Genetics, Columbia University Medical Center, New York, NY, USA.ORCID 0000-0002-5220-6022
David T HollandDepartment of Pediatrics, Division of Molecular Genetics, Columbia University Medical Center, New York, NY, USA.
Jimmy DuongDepartment of Sociomedical Sciences, Mailman School of Public Health, Columbia University, New York, NY, USA.
Priyanka AhimazDepartment of Pediatrics, Division of Molecular Genetics, Columbia University Medical Center, New York, NY, USA.
Wendy K ChungDepartment of Pediatrics, Division of Molecular Genetics, Columbia University Medical Center, New York, NY, USA. Wkc15@columbia.edu.
Columbia University Irving Medical Center · USColumbia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited cardiomyopathies, including hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM), are the most common monogenic cause of cardiac disease and can rarely lead to sudden cardiac death (SCD). They are characterized by incomplete and age-dependent penetrance and are usually initially symptomatic in adulthood yet can present in childhood as well. Over 20 genes have been identified to cause HCM, and more than 40 genes are known to cause DCM. Genetic testing for these genes has been integrated into medical care; however, the psychological impact of genetic testing and the impact of the uncertainty that comes with receiving these results have not been well studied. This study surveyed 90 adult probands and relatives with a personal or family history of cardiomyopathy from a single hospital-based cardiac genetic program to determine the psychosocial impact of genetic testing for cardiomyopathies. Standardized psychological instruments including an adapted Multidimensional Impact of Cancer Risk Assessment (aMICRA), Impact of Event Scale (IES), and Satisfaction with Decision (SWD) scales were utilized. Patients with positive genetic test results had higher scores for intrusive thoughts, avoidance, and distress when compared to those with negative genetic test results and were also more likely to make or plan to make life changes because of the results of their genetic testing. Satisfaction with the decision to undergo genetic testing was similar regardless of genetic test results. The results of this study provide insight into the patient experience of genetic testing for cardiomyopathies and how these experiences are associated with genetic test results and cardiac history.

Indexed as

AdultCardiomyopathiesCardiomyopathy, HypertrophicCross-Sectional StudiesFamilyFemaleGenetic CounselingGenetic Predisposition to DiseaseGenetic TestingHumansMaleRisk FactorsCardiomyopathyGeneticsImpact of Events ScaleLife changesMultidimensional Impact of Cancer Risk Assessment (MICRA)Satisfaction with Decision Scale

Identifiers

PMID29243008
OpenAlexW2771885997

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.