» Articles » PMID: 34730449

Validation of a Spanish Version of the Leicester Cough Questionnaire in Cystic Fibrosis

Overview
Publisher Sage Publications
Date 2021 Nov 3
PMID 34730449
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Cough is a main symptom in cystic fibrosis (CF). We aim to validate a Spanish version of the Leicester Cough Questionnaire (LCQ-Sp) to measure the impact of cough in CF bronchiectasis. A prospective longitudinal multicentre study was performed. Internal consistency and score changes over a 15-day period in stable state were assessed to analyse reliability. Concurrent validity was analysed by correlation with Saint George's Respiratory Questionnaire (SGRQ) and convergent validity by assessing the association with clinical variables. Changes in scores between stable state and the first exacerbation were assessed to analyse responsiveness. 132 patients (29.73 ± 10.52 years) were enrolled in four hospitals. Internal consistency was high for the total score and good for the three domains (Cronbach's α 0.81-0.93). The test-retest reliability showed an intraclass correlation coefficient of 0.86 for the total score. The correlation between LCQ-Sp and SGRQ scores was -0.74. The LCQ-Sp score negatively correlated with sputum volume, and the mean score decreased at the beginning of exacerbations (16.04±3.81 vs 13.91±4.29) with a large effect size. The LCQ-Sp is a reliable, repeatable and responsive instrument to assess the impact of cough in CF bronchiectasis and is responsive to change in the event of exacerbations.

Citing Articles

A systematic literature review of the clinical and socioeconomic burden of bronchiectasis.

Chalmers J, Mall M, McShane P, Nielsen K, Shteinberg M, Sullivan S Eur Respir Rev. 2024; 33(173).

PMID: 39231597 PMC: 11372470. DOI: 10.1183/16000617.0049-2024.


Study on the Therapeutic Effect of Azithromycin Combined with Glucocorticoid on Pulmonary Function and Inflammatory Response in Children with Pneumonia.

Zhao Q, Yang J, Sheng Y, Zhuang M, Qi M J Healthc Eng. 2022; 2022:5288148.

PMID: 35388320 PMC: 8977326. DOI: 10.1155/2022/5288148.

References
1.
Goss C, Burns J . Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis. Thorax. 2007; 62(4):360-7. PMC: 2092469. DOI: 10.1136/thx.2006.060889. View

2.
Munoz G, Buxo M, De Gracia J, Olveira C, Martinez-Garcia M, Giron R . Validation of a Spanish version of the Leicester Cough Questionnaire in non-cystic fibrosis bronchiectasis. Chron Respir Dis. 2016; 13(2):128-36. PMC: 5734594. DOI: 10.1177/1479972316632005. View

3.
Moss R, Flume P, Elborn J, Cooke J, Rowe S, McColley S . Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trial. Lancet Respir Med. 2015; 3(7):524-33. PMC: 4641035. DOI: 10.1016/S2213-2600(15)00201-5. View

4.
Birring S, Prudon B, Carr A, Singh S, Morgan M, Pavord I . Development of a symptom specific health status measure for patients with chronic cough: Leicester Cough Questionnaire (LCQ). Thorax. 2003; 58(4):339-43. PMC: 1746649. DOI: 10.1136/thorax.58.4.339. View

5.
Gee L, Abbott J, Conway S, Etherington C, Webb A . Development of a disease specific health related quality of life measure for adults and adolescents with cystic fibrosis. Thorax. 2000; 55(11):946-54. PMC: 1745639. DOI: 10.1136/thorax.55.11.946. View