Health status of cardiac genetic disease patients and their at-risk relatives

被引:34
|
作者
Ingles, Jodie [1 ,2 ]
Yeates, Laura [1 ]
Hunt, Lauren [3 ]
McGaughran, Julie [3 ,4 ]
Scuffham, Paul A. [5 ]
Atherton, John [4 ,6 ]
Semsarian, Christopher [1 ,2 ,7 ]
机构
[1] Centenary Inst, Agnes Ginges Ctr Mol Cardiol, Sydney, NSW, Australia
[2] Univ Sydney, Cent Clin Sch, Sydney, NSW 2006, Australia
[3] Brisbane & Womens Hosp, Genet Hlth Queensland, Brisbane, Qld, Australia
[4] Univ Queensland, Dept Med, Brisbane, Qld 4000, Australia
[5] Griffith Univ, Sch Med, Ctr Appl Hlth Econ, Brisbane, Qld 4111, Australia
[6] Royal Brisbane & Womens Hosp, Dept Cardiol, Brisbane, Qld, Australia
[7] Royal Prince Alfred Hosp, Dept Cardiol, Sydney, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Health status; Cardiac genetic disease; Physical function; Mental function; QUALITY-OF-LIFE; LONG QT SYNDROME; CARDIOMYOPATHY MUTATION CARRIERS; HYPERTROPHIC CARDIOMYOPATHY; PSYCHOLOGICAL CONSEQUENCES; HEART-FAILURE; SUDDEN-DEATH; SF-36; HOSPITALIZATION; MULTIMORBIDITY;
D O I
10.1016/j.ijcard.2011.08.083
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Health status is an important outcome measure that incorporates multiple dimensions of health, including symptoms, functional status, and psychosocial factors. While health status has been shown to be a predictor for hospital readmission, morbidity and mortality in the heart failure setting, there are limited data in cardiac genetic disease. We examined health status in a number of cardiac genetic disease groups compared to the general Australian population. Methods: A total of 409 individuals were assessed. Individuals with inherited cardiomyopathies [hypertrophic cardiomyopathy (HCM), familial dilated cardiomyopathy (FDC), arrhythmogenic right ventricular cardiomyopathy (ARVC)] and primary arrhythmogenic disorders [long QT syndrome (LQTS), catecholaminergic polymorphic ventricular tachycardia (CPVT)], as well as their first-degree relatives, completed the Medical Outcomes Survey Short Form-36 (SF-36). The physical and mental component scores (PCS and MCS) and SF-6D utility score were assessed. Results: Patients with HCM (p<0.001), FDC (p<0.05), and CPVT (p<0.05) were found to have a significantly lower PCS, while patients with LQTS (p<0.01) had a lower MCS. Individuals at risk of HCM (p<0.0001) and genotype positive-phenotype negative HCM patients (p<0.01) both had a higher PCS and utility scores compared to the clinically affected HCM population. Individuals at risk of LQTS had significantly higher PCS than those with a clinical diagnosis of LQTS (p<0.05) and similarly individuals at risk of FDC had significantly higher PCS than FDC patients (p<0.05). In HCM, female gender (p=0.002), presence of co-morbidities (p<0.0001) and higher NYHA functional class (p<0.0001) were predictors of a lower PCS. Conclusions: Patients with a clinical diagnosis of a genetic heart disease have an impaired health status, related to both physical andmental function. Clinical management strategies in such patient groups need to consider health status as an important outcome measure. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:448 / 453
页数:6
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