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Genetic testing for inherited heart diseases: longitudinal impact on health-related quality of life

Overview of attention for article published in Genetics in Medicine, May 2012
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Title
Genetic testing for inherited heart diseases: longitudinal impact on health-related quality of life
Published in
Genetics in Medicine, May 2012
DOI 10.1038/gim.2012.47
Pubmed ID
Authors

Jodie Ingles, Laura Yeates, Lisa O’Brien, Julie McGaughran, Paul A. Scuffham, John Atherton, Christopher Semsarian

Abstract

Purpose:A genetic diagnosis is an extremely useful tool in the management and care of families with inherited heart diseases, particularly in allowing clarification of risk status of asymptomatic family members. The psychosocial consequences of genetic testing in this group are poorly understood. This longitudinal pilot study sought to determine changes in health-related quality of life in patients and asymptomatic family members undergoing genetic testing for inherited heart diseases.Methods:Individuals attending two specialized multidisciplinary cardiac genetic clinics in Australia were invited to participate. Patients undergoing proband or predictive genetic testing for an inherited cardiomyopathy or primary arrhythmogenic disorder were eligible. The Medical Outcomes Short Form-36 (version 2) was administered before the genetic result was given, and follow-up surveys were completed 1-3, 6, and 12 months after the result was given.Results:A total of 54 individuals with hypertrophic cardiomyopathy, familial dilated cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, and long QT syndrome completed baseline and at least one follow-up survey, including 33 probands and 21 asymptomatic relatives. Physical and mental component scores analyzed at baseline and 1-3 months were found to be unchanged in all groups. Furthermore, no significant differences were observed up to 12 months after result.Conclusion:In this longitudinal pilot study, no change in health-related quality of life was observed up to 12 months after the result was given in patients and their asymptomatic family members undergoing genetic testing for an inherited heart disease.Genet Med 2012 advance online publication 3 May 2012.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 55 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 2%
Unknown 54 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 10 18%
Student > Master 9 16%
Student > Bachelor 7 13%
Student > Ph. D. Student 7 13%
Other 3 5%
Other 7 13%
Unknown 12 22%
Readers by discipline Count As %
Medicine and Dentistry 12 22%
Biochemistry, Genetics and Molecular Biology 8 15%
Nursing and Health Professions 4 7%
Psychology 3 5%
Physics and Astronomy 2 4%
Other 11 20%
Unknown 15 27%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 08 May 2012.
All research outputs
#17,364,523
of 25,482,409 outputs
Outputs from Genetics in Medicine
#2,604
of 2,954 outputs
Outputs of similar age
#115,556
of 176,076 outputs
Outputs of similar age from Genetics in Medicine
#17
of 24 outputs
Altmetric has tracked 25,482,409 research outputs across all sources so far. This one is in the 21st percentile – i.e., 21% of other outputs scored the same or lower than it.
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