Literature DB >> 26163742

Validity of a Spanish Version of the Leicester Cough Questionnaire in Children With Cystic Fibrosis.

Tamara Del Corral1, Janaína Percegona2, Núria López3, Andrea Valiente3, María Garriga4, Melisa Seborga1, Jordi Vilaró5.   

Abstract

BACKGROUND: Cystic fibrosis (CF) patients present chronic cough as one of the main symptoms, which has an important effect on quality of life and social relations. Our goal was to validate the Spanish version of the Leicester Cough Questionnaire (LCQ) in a group of children and teenagers with CF.
METHODS: After adapting to Spanish by standardized translation and retro-translation methodology, a sample of 58 stable CF patients from 7 to 18 years were recruited from three CF specialized centers in Spain. The questionnaire was administered twice; the second administration (LCQ2) was performed between 2-4 weeks later than the first one (LCQ1), in order to analyse the reliability and validity of the Spanish version. To correlate results with health related quality of life (HRQoL) we used the Cystic Fibrosis Questionnaire-Revised (CFQ-R).
RESULTS: Population was composed by 62% male, age 11.7 ± 3.1 years and body mass index (BMI) 19 ± 3 kg/m(2). Total scores from LCQ were: LCQ1 19 (17.75-21) vs LCQ2 19 (16-21) (P=.199). Cronbach's Alpha coefficient was 0.83 for the LCQtotal and for each specific domain was: 0.82 LCQphysical; 0.74 LCQpsychological and 0.62 LCQsocial. Intraclass correlation coefficient was: 0.69 LCQphysical; 0.59 LCQpsychological; 0.45 LCQsocial and 0.71 LCQtotal (good reliability). Relations with CFQ-R showed moderated and significant results: for the LCQtotal: respiratory symptom domain r = 0,51 (P<.001) and physical capacity domain r = 0,62 (P<.05).
CONCLUSION: The Spanish version of the Leicester Cough Questionnaire is reliable and valid for children and adolescents with CF and it has good relations with health related quality of life in this population.
Copyright © 2014 SEPAR. Published by Elsevier Espana. All rights reserved.

Entities:  

Keywords:  Cough; Cough questionnaire and health related quality of life; Cuestionario de tos y calidad de vida relacionada con la salud; Cystic fibrosis; Fibrosis quística; Tos

Mesh:

Year:  2015        PMID: 26163742     DOI: 10.1016/j.arbres.2015.01.016

Source DB:  PubMed          Journal:  Arch Bronconeumol        ISSN: 0300-2896            Impact factor:   4.872


  3 in total

1.  Validation of a Spanish version of the Leicester Cough Questionnaire in cystic fibrosis.

Authors:  Gerard Muñoz; Javier de Gracia; Rosa Giron; Casilda Olveira; Antonio Alvarez; Maria Buxó; Surinder S Birring; Montserrat Vendrell
Journal:  Chron Respir Dis       Date:  2021 Jan-Dec       Impact factor: 2.444

2.  Psychometric properties of the German version of the Leicester Cough Questionnaire in sarcoidosis.

Authors:  Jonas Christian Schupp; Urs Alexander Fichtner; Björn Christian Frye; Katja Heyduck-Weides; Surinder S Birring; Wolfram Windisch; Carl-Peter Criée; Joachim Müller-Quernheim; Erik Farin
Journal:  PLoS One       Date:  2018-10-04       Impact factor: 3.240

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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