Literature DB >> 20304545

[Validation of the Spanish version of the Revised Cystic Fibrosis Quality of Life Questionnaire in adolescents and adults (CFQR 14+ Spain)].

Gabriel Olveira1, Casilda Olveira, Inmaculada Gaspar, Ivette Cruz, Antonio Dorado, Estela Pérez-Ruiz, Nuria Porras, Federico Soriguer.   

Abstract

BACKGROUND: The aim of this study was to assess the validity and reliability of the Spanish version of the revised disease-specific health related quality of life questionnaire for adolescents and adults with cystic fibrosis (CFQR 14+ Spain).
METHODS: A total of 43 cystic fibrosis (CF) patients completed the CFQR 14+ Spain. Forced expiratory volume in 1 second, in percentage of predicted - FEV(1) (%)-, number of respiratory exacerbations, 6-minute walk test, Bhalla score (based on computerized tomography of the chest), fat-free mass index, body mass index (BMI), faecal fat and St George's Respiratory Questionnaire were included as measurements of health status.
RESULTS: Ten out of the twelve scales had alpha coefficients above 0.70. Test-retest correlations (Spearman) ranged from 0.49 to 0.95 and they were significant in all scales. Intraclass correlations ranged from 0.47 to 0.95 (ten out of the twelve scales were >0.70) forty out of the fifty ítems have correlations between items and scale above 0.70. All the CFQR+14 scales, except the digestive symptoms scale, discriminated significantly between patients with mild, moderate and severe disease (according to FEV(1) (%)). Other respiratory parameters also discriminated significantly between patients with mild-moderate and severe disease. Only some scales discriminated significantly between nourished and malnourished patients. All of the scales met standards for floor effects (<15% of the responders with the lowest score) but not for ceiling effects (only five out of the twelve).
CONCLUSION: The Spanish CFQR14+ (Spain) is a reliable and valid instrument for measuring the health-related quality of life in Spanish adolescents and adults with CF, though with the exception of a few of its subscales. Copyright (c) 2009 SEPAR. Published by Elsevier Espana. All rights reserved.

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Year:  2010        PMID: 20304545     DOI: 10.1016/j.arbres.2010.01.006

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


  7 in total

1.  Depression and anxiety symptoms in bronchiectasis: associations with health-related quality of life.

Authors:  Casilda Olveira; Gabriel Olveira; Inmaculada Gaspar; Antonio Dorado; Ivette Cruz; Federico Soriguer; Alexandra L Quittner; Francisco Espildora
Journal:  Qual Life Res       Date:  2012-04-29       Impact factor: 4.147

2.  Objective and Subjective Sleep Efficiency in Adult Patients with Cystic Fibrosis and Impact on Quality of Life.

Authors:  Marta Íscar-Urrutia; Claudia Janeth Madrid-Carbajal; Gemma Rubinos-Cuadrado; Ramón Fernández-Álvarez; María José Vázquez-López; Cristina Hernández-González; Ana Isabel Enríquez-Rodríguez; Marta García-Clemente
Journal:  Lung       Date:  2018-10-03       Impact factor: 2.584

3.  Validation of a Quality of Life Questionnaire for Bronchiectasis: psychometric analyses of the Spanish QOL-B-V3.0.

Authors:  Casilda Olveira; Gabriel Olveira; Francisco Espildora; Rosa-Maria Giron; Gerard Muñoz; Alexandra L Quittner; Miguel-Angel Martinez-Garcia
Journal:  Qual Life Res       Date:  2013-10-19       Impact factor: 4.147

4.  Chest CT abnormalities and quality of life: relationship in adult cystic fibrosis.

Authors:  Aoife Kilcoyne; Lisa P Lavelle; Colin J McCarthy; Sinead H McEvoy; Hannah Fleming; Annika Gallagher; Martine Loeve; Harm Tiddens; Edward McKone; Charles C Gallagher; Jonathan D Dodd
Journal:  Ann Transl Med       Date:  2016-03

Review 5.  Impact of Pseudomonas aeruginosa Infection on Patients with Chronic Inflammatory Airway Diseases.

Authors:  Marta Garcia-Clemente; David de la Rosa; Luis Máiz; Rosa Girón; Marina Blanco; Casilda Olveira; Rafael Canton; Miguel Angel Martinez-García
Journal:  J Clin Med       Date:  2020-11-24       Impact factor: 4.241

6.  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

7.  Quality of life amongst adolescents and young adults with cystic fibrosis: correlations with clinical outcomes.

Authors:  Daniela W Gancz; Maristela T Cunha; Claudio Leone; Joaquim C Rodrigues; Fabíola V Adde
Journal:  Clinics (Sao Paulo)       Date:  2018-10-18       Impact factor: 2.365

  7 in total

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