Health-related quality-of-life in children with cystic fibrosis aged 5-years and associations with health outcomes

被引:15
作者
Cheney, Joyce [1 ,2 ]
Vidmar, Suzanna [3 ,4 ]
Gailer, Nicholas [1 ]
Wainwright, Claire [1 ,2 ]
Douglas, Tonia A. [1 ,2 ]
机构
[1] Queensland Childrens Hosp, Dept Resp & Sleep Med, Brisbane, Qld, Australia
[2] Univ Queensland, Ctr Childrens Hlth Res, Sch Med, Brisbane, Qld, Australia
[3] Murdoch Childrens Res Inst, Clin Epidemiol & Biostat Unit, Melbourne, Vic, Australia
[4] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
Cystic fibrosis; Preschool; Children; Health-related quality of life; Pulmonary; Exacerbations; Lung function; REPORTED OUTCOMES; UNITED-STATES; ADOLESCENTS; EXACERBATIONS; QUESTIONNAIRE; INSTRUMENTS; VALIDATION;
D O I
10.1016/j.jcf.2020.02.022
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: The impact of early cystic fibrosis (CF) on health-related quality-of-life (HRQOL) in preschool children is poorly characterised, and data on relationships between HRQOL and health outcomes in young children with CF are limited. We aimed to characterise and compare parent-proxy and child-reported HRQOL and evaluate relationships with clinical outcomes at age 5-years. Methods: Subjects were participating in the multi-centre Australasian Cystic Fibrosis Bronchoalveolar Lavage (ACFBAL) trial investigating BAL-directed versus standard CF therapy. Children aged 5-years and their parents rated HRQOL using the Pediatric Quality of Life Inventory (PedsQL (TM)) and Cystic Fibrosis Questionnaire-Revised (CFQ-R) questionnaires. Results: PedsQL and CFQ-R questionnaires were completed by 141 primary caregivers and 135 and 130 children, respectively. There were no differences in HRQOL between children randomised to BAL-directed versus standard CF therapy. Children with CF rated worse HRQOL than healthy children and there was poor parent-child concordance across HRQOL domains. Nutritional status, CF-CT scan score, forced expiratory volume in 1-second (FEV1), and pulmonary exacerbations correlated with HRQOL at age 5-years. FEV1 z-scores positively correlated with parent-proxy HRQOL in CFQ-R Respiratory (p = 0.018), Physical (<0.001), Emotional (p = 0.007) subscales and PedsQL Total-score (p = 0.021), Physical (p = 0.019) domains. Pulmonary exacerbation rates were inversely associated with parent-proxy CFQ-R Respiratory (p = 0.004), Physical (p = 0.022), PedsQL Total (p = 0.009) and Physical (p = 0.009) scores. Conclusion: Parent-reported HRQOL is a meaningful clinical endpoint to evaluate interventions in young children. Parent and child HRQOL reports provide different, complementary information. A preschool version of the CFQ-R is needed to assess relationships between HRQOL and clinical outcomes in young children. (C) 2020 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:483 / 491
页数:9
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