Literature DB >> 23669872

Health-related quality of life in children and adolescents with cystic fibrosis: convergent validity with parent-reports and objective measures of pulmonary health.

Audrey Tluczek1, Tara Becker, Adam Grieve, Anita Laxova, Michael J Rock, William M Gershan, Christopher G Green, Philip M Farrell.   

Abstract

OBJECTIVE: This study examined the convergent validity of health-related quality of life (HRQOL) reported by patients with cystic fibrosis compared with their parents' reports and objective pulmonary measures across 3 time points.
METHODS: Ninety-two children (8-13 years) and adolescents (14-18 years) with cystic fibrosis and their parents completed Cystic Fibrosis Questionnaires to examine concordance with Wisconsin chest x-ray (WCXR) scores and pulmonary function tests, for example, forced expiratory volume at 1 second (FEV1), and parent-child/adolescent concordance across multiple HRQOL domains. Concordance was analyzed relative to patient age and gender.
RESULTS: Parent-reports were closely aligned with WCXR scores, whereas patient reports were more closely aligned with FEV1. Adolescents and parents of both age groups had more HRQOL domains concordant with pulmonary health measures than did child self-reports. Parent-child concordance was inversely related to child age, particularly with male adolescents. Children generally reported better HRQOL than parents. Male adolescents and their parents were more likely to have significantly discordant HRQOL scores than female adolescents and their parents. Male and female adolescents reported higher HRQOL than their parents reported for all but vitality and health perception domains. Younger male children showed concordance with their parents on 5 of 7 domains.
CONCLUSIONS: Parent-child/adolescent discordance on HRQOL was consistent with normative child development expectations. Findings underscore the value of enlisting perspectives from parents as well as children regarding HRQOL.

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Year:  2013        PMID: 23669872      PMCID: PMC3775595          DOI: 10.1097/DBP.0b013e3182905646

Source DB:  PubMed          Journal:  J Dev Behav Pediatr        ISSN: 0196-206X            Impact factor:   2.225


  28 in total

1.  Differences between adolescents' and parents' reports of health-related quality of life in cystic fibrosis.

Authors:  Maria T Britto; Uma R Kotagal; Thomas Chenier; Joel Tsevat; Harry D Atherton; Robert W Wilmott
Journal:  Pediatr Pulmonol       Date:  2004-02

2.  Wisconsin cystic fibrosis chest radiograph scoring system: validation and standardization for application to longitudinal studies.

Authors:  R E Koscik; M R Kosorok; P M Farrell; J Collins; M E Peters; A Laxova; C G Green; L Zeng; L S Rusakow; R C Hardie; P W Campbell; J W Gurney
Journal:  Pediatr Pulmonol       Date:  2000-06

3.  Issues in measuring quality of life in childhood cancer: measures, proxies, and parental mental health.

Authors:  Y H Vance; R C Morse; M E Jenney; C Eiser
Journal:  J Child Psychol Psychiatry       Date:  2001-07       Impact factor: 8.982

4.  The PedsQL in pediatric rheumatology: reliability, validity, and responsiveness of the Pediatric Quality of Life Inventory Generic Core Scales and Rheumatology Module.

Authors:  James W Varni; Michael Seid; Tara Smith Knight; Tasha Burwinkle; Joy Brown; Ilona S Szer
Journal:  Arthritis Rheum       Date:  2002-03

5.  Adolescents with cystic fibrosis: family reports of adolescent health-related quality of life and forced expiratory volume in one second.

Authors:  P M Powers; R Gerstle; A Lapey
Journal:  Pediatrics       Date:  2001-05       Impact factor: 7.124

Review 6.  Can parents rate their child's health-related quality of life? Results of a systematic review.

Authors:  C Eiser; R Morse
Journal:  Qual Life Res       Date:  2001       Impact factor: 4.147

7.  Longitudinal evaluation of bronchopulmonary disease in children with cystic fibrosis.

Authors:  Philip M Farrell; Zhanhai Li; Michael R Kosorok; Anita Laxova; Christopher G Green; Jannette Collins; Hui-Chuan Lai; Linda M Makholm; Michael J Rock; Mark L Splaingard
Journal:  Pediatr Pulmonol       Date:  2003-09

Review 8.  Medical decision-making and minors: issues of consent and assent.

Authors:  Tara L Kuther
Journal:  Adolescence       Date:  2003

9.  Validation of a disease-specific measure of health-related quality of life for children with cystic fibrosis.

Authors:  Avani C Modi; Alexandra L Quittner
Journal:  J Pediatr Psychol       Date:  2003-12

10.  An observational study of patient versus parental perceptions of health-related quality of life in children and adolescents with a chronic pain condition: who should the clinician believe?

Authors:  Thomas R Vetter; Cynthia L Bridgewater; Gerald McGwin
Journal:  Health Qual Life Outcomes       Date:  2012-07-23       Impact factor: 3.186

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  3 in total

1.  Parent-child agreement in different domains of child behavior and health.

Authors:  Tanja Poulain; Mandy Vogel; Christof Meigen; Ulrike Spielau; Andreas Hiemisch; Wieland Kiess
Journal:  PLoS One       Date:  2020-04-09       Impact factor: 3.240

2.  Social and economic costs and health-related quality of life in non-institutionalised patients with cystic fibrosis in the United Kingdom.

Authors:  Aris Angelis; Panos Kanavos; Julio López-Bastida; Renata Linertová; Elena Nicod; Pedro Serrano-Aguilar
Journal:  BMC Health Serv Res       Date:  2015-09-28       Impact factor: 2.655

3.  A systematic review of patient-reported outcome measures (PROMs) in cystic fibrosis.

Authors:  Irushi Ratnayake; Susannah Ahern; Rasa Ruseckaite
Journal:  BMJ Open       Date:  2020-10-01       Impact factor: 2.692

  3 in total

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