Health-related quality of life (HRQOL) in children and adolescents with congenital heart disease: a cross-sectional survey from South India

被引:7
|
作者
Raj, Manu [1 ]
Sudhakar, Abish [2 ]
Roy, Rinku [2 ]
Champaneri, Bhavik [3 ]
Sudevan, Remya [4 ]
Kabali, Conrad [5 ]
Kumar, Raman Krishna [6 ]
机构
[1] Amrita Inst Med Sci, Res Ctr, Pediatr & Pediat Cardiol, Cochin, Kerala, India
[2] Amrita Inst Med Sci, Paediatr Cardiol, Kochi, Kerala, India
[3] Mehta Inst Cardiol & Res Ctr, Pediatr Cardiol, Ahmadabad, Gujarat, India
[4] Amrita Inst Med Sci & Res Ctr, Med Res, Cochin, Kerala, India
[5] Univ Toronto Dalla Lana Sch Publ Hlth, Div Epidemiol, Toronto, ON, Canada
[6] Amrita Inst Med Sci & Res Ctr, Dept Pediat Cardiol, Cochin, Kerala, India
关键词
cardiology; congenital abnormalities; patient perspective; paediatric practice; adolescent health; OUTCOMES; ADULTS; PEDSQL(TM)-4.0; TRANSPOSITION; RELIABILITY; TETRALOGY; SURGERY; FALLOT;
D O I
10.1136/bmjpo-2018-000377
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective There are limited data on health-related quality of life (HRQOL) for children and adolescents with uncorrected congenital heart disease (CHD) from low-income and middle-income countries where late presentation is common. We sought to compare HRQOL of children and adolescents with uncorrected CHD to that of controls using the Pediatric Quality of Life Inventory (PedsQL 4.0). Methods The study design is a cross-sectional analytical survey. The study setting was (1) Hospital-based survey of patients with CHD and their parents. (2) Community survey of controls and their parents. Subjects included (1) Children/adolescents with CHD between the ages of 2 years and 18 years and their parents enrolled in a previous study (n=308). (2) Unmatched community controls (719 children/adolescents, aged 2-18 years) and their parents. Participants were given PedsQL 4.0 to fill out details. Parents assisted children 5-7 years of age in filling the questionnaires. Children younger than 5 years had only parent-reported HRQOL and those above 5 years had both self-reported and parent-reported HRQOL. Results The median (IQR) total generic HRQOL from self-reports for CHD subjects and controls were 71.7 (62.0, 84.8) and 91.3 (82.6, 95.7), respectively. The corresponding figures for parent-reports were 78.3 (63.0, 90.5) and 92.4 (87.0, 95.7) respectively. The adjusted median difference was -20.6 (99% CI -24.9 to -16.3, p<0.001) for self-reported and -14.1 (99% CI -16.7 to -11.6, p<0.001) for parent-reported total HRQOL between patients with CHD and controls. Cardiac-specific HRQOL by self-reports was 75.0 (53.6, 92.9) for heart problems, 95.0 (73.8, 100.0) for treatment barriers, 83.3 (66.7, 100.0) for physical appearance, 87.5 (62.5, 100.0) for treatment-related anxiety, 91.7 (68.8, 100.0) for cognitive problems and 83.3 (66.7, 100.0) for communication. The values for parent-reports were 71.4 (53.6, 85.7), 100.0 (75.0, 100.0), 100.0 (75.0, 100.0), 81.3 (50.0, 100.0), 100.0 (81.2, 100.0) and 83.3 (50.0, 100.0), respectively. Conclusions Children and adolescents with uncorrected CHD reported significant reductions in overall quality of life compared with controls.
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页数:11
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