Literature DB >> 18281919

Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy.

Jodie Ingles1, Joanne M Lind, Philayrath Phongsavan, Christopher Semsarian.   

Abstract

PURPOSE: The diagnosis of hypertrophic cardiomyopathy, an autosomal dominant chronic heart disease, can have significant implications, including increased risk of sudden death, exercise limitations, and risk of transmission to offspring. This study sought to describe the psychosocial factors associated with attending a specialty cardiac genetic clinic, and to determine whether these may be predictors of comorbid anxiety and depression in this population.
METHODS: Questionnaires were sent to 184 individuals attending the Royal Prince Alfred Hospital Hypertrophic Cardiomyopathy Clinic. Questionnaires were anonymous and comprised demographics, the Hospital Anxiety and Depression Scale, Patient Experience Scales, and Patient Satisfaction Scales.
RESULTS: Completed questionnaires were returned by 109 participants (59.2% response rate), of which 76.9% had a diagnosis of hypertrophic cardiomyopathy, while 23.1% were at-risk relatives attending for clinical screening. Patient satisfaction scores were generally high to very high across all groups, though only 24% of HCM patients showed good adjustment to hypertrophic cardiomyopathy and 10% had low worry about hypertrophic cardiomyopathy scores. Within the disease group, logistic regression analysis adjusting for age, gender, and education revealed adjustment to hypertrophic cardiomyopathy and worry about hypertrophic cardiomyopathy scores to be significantly associated with anxiety, while adjustment scores and location of patient follow-up (i.e., Hypertrophic Cardiomyopathy clinic or another cardiologist) to be significantly associated with depression scores.
CONCLUSION: HCM patients who attend specialized cardiac genetic clinics are better adjusted and worry less, than those who do not attend. An integrated approach, including a genetic counselor, is important in the management of HCM families.

Entities:  

Mesh:

Year:  2008        PMID: 18281919     DOI: 10.1097/GIM.0b013e3181612cc7

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  28 in total

1.  Attitudes, knowledge and consequences of uncertain genetic findings in hypertrophic cardiomyopathy.

Authors:  Charlotte Burns; Laura Yeates; Catherine Spinks; Christopher Semsarian; Jodie Ingles
Journal:  Eur J Hum Genet       Date:  2017-05-03       Impact factor: 4.246

2.  Impediments to DNA testing and cascade screening for hypertrophic cardiomyopathy and Long QT syndrome: a qualitative study of patient experiences.

Authors:  Andrew Smart
Journal:  J Genet Couns       Date:  2010-08-03       Impact factor: 2.537

3.  Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification.

Authors:  Chloe Reuter; Megan E Grove; Kate Orland; Katherine Spoonamore; Colleen Caleshu
Journal:  J Genet Couns       Date:  2017-12-12       Impact factor: 2.537

Review 4.  At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease.

Authors:  Ana Morales; Dawn C Allain; Patricia Arscott; Emily James; Gretchen MacCarrick; Brittney Murray; Crystal Tichnell; Amy R Shikany; Sara Spencer; Sara M Fitzgerald-Butt; Jessica D Kushner; Christi Munn; Emily Smith; Katherine G Spoonamore; Harikrishna S Tandri; W Aaron Kay
Journal:  J Genet Couns       Date:  2017-03-10       Impact factor: 2.537

Review 5.  Genetic Testing in Inherited Heart Diseases: Practical Considerations for Clinicians.

Authors:  Melanie Care; Vijay Chauhan; Danna Spears
Journal:  Curr Cardiol Rep       Date:  2017-08-16       Impact factor: 2.931

6.  Minding the Genes: a Multidisciplinary Approach towards Genetic Assessment of Cardiovascular Disease.

Authors:  Ashley Rhodes; Lindsey Rosman; John Cahill; Jodie Ingles; Brittney Murray; Crystal Tichnell; Cynthia A James; Samuel F Sears
Journal:  J Genet Couns       Date:  2016-09-30       Impact factor: 2.537

7.  A toolkit for incorporating genetics into mainstream medical services: Learning from service development pilots in England.

Authors:  Catherine L Bennett; Sarah E Burke; Hilary Burton; Peter A Farndon
Journal:  BMC Health Serv Res       Date:  2010-05-14       Impact factor: 2.655

8.  Parental knowledge and attitudes toward hypertrophic cardiomyopathy genetic testing.

Authors:  Sara M Fitzgerald-Butt; Lindsey Byrne; Cynthia A Gerhardt; Kathryn Vannatta; Timothy M Hoffman; Kim L McBride
Journal:  Pediatr Cardiol       Date:  2009-12-01       Impact factor: 1.655

9.  2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families.

Authors:  Martin K Stiles; Arthur A M Wilde; Dominic J Abrams; Michael J Ackerman; Christine M Albert; Elijah R Behr; Sumeet S Chugh; Martina C Cornel; Karen Gardner; Jodie Ingles; Cynthia A James; Jyh-Ming Jimmy Juang; Stefan Kääb; Elizabeth S Kaufman; Andrew D Krahn; Steven A Lubitz; Heather MacLeod; Carlos A Morillo; Koonlawee Nademanee; Vincent Probst; Elizabeth V Saarel; Luciana Sacilotto; Christopher Semsarian; Mary N Sheppard; Wataru Shimizu; Jonathan R Skinner; Jacob Tfelt-Hansen; Dao Wu Wang
Journal:  Heart Rhythm       Date:  2020-10-19       Impact factor: 6.343

10.  Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population.

Authors:  Anniken Hamang; Geir Egil Eide; Karin Nordin; Berit Rokne; Cathrine Bjorvatn; Nina Øyen
Journal:  BMC Med Genet       Date:  2010-02-17       Impact factor: 2.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.