Psychological Symptoms and Physical Limitations With Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is a genetic disease of myocytes caused by a mutation in genes encoding for sarcomere proteins resulting in alterations in cardiac structure, hence affecting its function.1 It is believed that most deaths in patients living with HCM are cardiac –related, with 16% be...
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Veröffentlicht in: | The American journal of cardiology 2022-07, Vol.174, p.179-180 |
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creator | Asbeutah, Abdul Aziz A. Ingram, Eva Mouksian, Kristina Wilbanks, David Alexander, John Bath, Anandbir Salberg, Lisa Jefferies, John L. |
description | Hypertrophic cardiomyopathy (HCM) is a genetic disease of myocytes caused by a mutation in genes encoding for sarcomere proteins resulting in alterations in cardiac structure, hence affecting its function.1 It is believed that most deaths in patients living with HCM are cardiac –related, with 16% being sudden cardiac death (SCD).2 HCM is a chronic condition that creates physical limitations and affects the psychological and emotional well-being of patients. A recent study in China concluded that depression in patients with HCM was independently associated with an increased risk of SCD and heart failure events.3 Hence, we aimed to estimate the prevalence of anxiety and depression-related symptoms and physical limitations in adults living with HCM and implantable cardioverter-defibrillators (ICDs) in the United States. [...]incorporating a multidisciplinary approach by including psychologists and social workers early to assist and identify the psychological and social needs of patients with HCM is imperative. |
doi_str_mv | 10.1016/j.amjcard.2022.03.031 |
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A recent study in China concluded that depression in patients with HCM was independently associated with an increased risk of SCD and heart failure events.3 Hence, we aimed to estimate the prevalence of anxiety and depression-related symptoms and physical limitations in adults living with HCM and implantable cardioverter-defibrillators (ICDs) in the United States. [...]incorporating a multidisciplinary approach by including psychologists and social workers early to assist and identify the psychological and social needs of patients with HCM is imperative.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/j.amjcard.2022.03.031</identifier><identifier>PMID: 35504746</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anxiety ; Cardiomyopathy ; Congestive heart failure ; COVID-19 ; Defibrillators ; Genetic disorders ; Mental depression ; Mutation ; Myocytes ; Quality of life ; Signs and symptoms</subject><ispartof>The American journal of cardiology, 2022-07, Vol.174, p.179-180</ispartof><rights>2022 Elsevier Inc.</rights><rights>2022. 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A recent study in China concluded that depression in patients with HCM was independently associated with an increased risk of SCD and heart failure events.3 Hence, we aimed to estimate the prevalence of anxiety and depression-related symptoms and physical limitations in adults living with HCM and implantable cardioverter-defibrillators (ICDs) in the United States. 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subjects | Anxiety Cardiomyopathy Congestive heart failure COVID-19 Defibrillators Genetic disorders Mental depression Mutation Myocytes Quality of life Signs and symptoms |
title | Psychological Symptoms and Physical Limitations With Hypertrophic Cardiomyopathy |
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