Literature DB >> 29788503

Visual analogue scales for interstitial lung disease: a prospective validation study.

H Yates1, H I Adamali2, N Maskell3, S Barratt2, C Sharp4.   

Abstract

BACKGROUND: Visual analogue scales (VAS) are simple symptom assessment tools which have not been validated in interstitial lung disease (ILD). Simple measures of ILD disease burden would be valuable for non-specialist clinicians monitoring disease away from ILD specialist centres.
OBJECTIVE: To validate VAS to assess change in dyspnoea, cough and fatigue in ILD, and to define the minimal clinically important difference (MCID) for change in these.
METHODS: Patients of 64 with ILD completed VAS for dyspnoea, cough and fatigue. Baseline King's Brief ILD questionnaire (K-BILD) scores, lung function and 6-min walk test results were collected. Tests were repeated 3-6 months later, in addition to a seven-point Likert scale. The MCID was estimated using median change in VAS in patients who reported 'small but just worthwhile change' in symptoms at follow-up. Methods were repeated in a validation cohort of 31 ILD patients to confirm findings.
RESULTS: VAS scores were significantly higher for patients who reported a 'small but just worthwhile change' in symptoms vs. 'no change' or 'not worthwhile change' (P < 0.01). The MCID for VAS Dyspnoea was estimated as 22.0 mm and 14.5 mm for VAS Fatigue. These results were reproducible in the validation cohort. Results were not significant for VAS Cough. Change in VAS Dyspnoea correlated with change in K-BILD (r = -0.51, P < 0.01), forced vital capacity (r = -0.32, P = 0.01) and 6-min walking distance (r = -0.37, P = 0.01).
CONCLUSION: The VAS is valid for assessing change in dyspnoea and fatigue in ILD. The MCID is estimated as 22.0 mm for dyspnoea and 14.5 mm for fatigue. This could be used to monitor disease in settings away from ILD specialist review. MESH DESCRIPTORS: Lung Diseases, Interstitial, Dyspnoea, Fatigue, Cough.
© The Author(s) 2018. Published by Oxford University Press on behalf of the Association of Physicians. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Mesh:

Year:  2018        PMID: 29788503     DOI: 10.1093/qjmed/hcy102

Source DB:  PubMed          Journal:  QJM        ISSN: 1460-2393


  4 in total

1.  The acute impact of resistance training on fatigue in patients with pulmonary sarcoidosis.

Authors:  Anita Grongstad; Nina Køpke Vøllestad; Line Merethe Oldervoll; Martijn Arthur Spruit; Anne Edvardsen
Journal:  Chron Respir Dis       Date:  2020 Jan-Dec       Impact factor: 2.444

2.  Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry.

Authors:  Wim A Wuyts; Caroline Dahlqvist; Hans Slabbynck; Marc Schlesser; Natacha Gusbin; Christophe Compere; Sofie Maddens; Shemra Rizzo; Klaus-Uwe Kirchgaessler; Karen Bartley; Benjamin Bondue
Journal:  Pulm Ther       Date:  2022-04-16

Review 3.  Cough in Idiopathic Pulmonary Fibrosis.

Authors:  Jennifer Mann; Nicole S L Goh; Anne E Holland; Yet Hong Khor
Journal:  Front Rehabil Sci       Date:  2021-10-18

4.  The use of online visual analogue scales in idiopathic pulmonary fibrosis.

Authors:  Catharina C Moor; Remy L M Mostard; Jan C Grutters; Paul Bresser; Marlies S Wijsenbeek
Journal:  Eur Respir J       Date:  2022-01-13       Impact factor: 16.671

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.