» Articles » PMID: 31462235

Validation of the IPF-specific Version of St. George's Respiratory Questionnaire

Overview
Journal Respir Res
Specialty Pulmonary Medicine
Date 2019 Aug 30
PMID 31462235
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Patients with idiopathic pulmonary fibrosis (IPF) have impaired health-related quality of life (HRQL). To measure HRQL, an IPF-specific version of the St. George's Respiratory Questionnaire (SGRQ-I) was developed, but not sufficiently validated. This study aimed to assess the validity (i.a. known-groups validity and concurrent validity) and test-retest reliability of SGRQ-I in IPF patients with different disease durations.

Methods: Patients with IPF were consecutively recruited and completed SGRQ, SGRQ-I, King's Brief Interstitial Lung Disease questionnaire (K-BILD), University of California, San Diego Shortness of Breath Questionnaire (SOBQ) and Short Form-36 (SF-36) along with pulmonary function tests and a 6-min walk test (6MWT) at baseline. After two weeks, SGRQ-I and Global Rating of Change Scales (GRCS) were completed.

Results: At baseline and after two weeks, 150 and 134 patients completed the questionnaires, respectively. The internal consistency of SGRQ-I was high (Cronbach's α = 0.92). Good concurrent validity was demonstrated by high intraclass correlation coefficients (ICC = 0.97), Bland-Altman plots and moderate to strong correlations to K-BILD, SOBQ and SF-36 (r = - 0.46 to 0.80). High ICC (0.92) and a Bland-Altman plot indicated good test-retest reliability. SGRQ-I was good at discriminating between patients with different stages of disease (Δscore > 18.1, effect sizes > 0.10). Validity was similar across groups of different disease duration.

Conclusions: SGRQ-I proved to be valid at distinguishing between different disease severities, valid compared to other HRQL instruments, applicable across different disease durations and reliable upon repetition. SGRQ-I is a valid option for measuring HRQL in patients with IPF.

Trial Registration: The study was registered at clinicaltrials.org ( NCT02818712 ) on 15 June 2016.

Citing Articles

Autologous P63+ lung progenitor cell transplantation in idiopathic pulmonary fibrosis: a phase 1 clinical trial.

Zhang S, Zhou M, Shao C, Zhao Y, Liu M, Ni L Elife. 2025; 13.

PMID: 40036154 PMC: 11879106. DOI: 10.7554/eLife.102451.


Health-related quality of life and health state utility value in idiopathic pulmonary fibrosis: a systematic review and meta-analysis.

Zhao G, Lei S, Li Y, Feng Z, Li J Health Qual Life Outcomes. 2025; 23(1):3.

PMID: 39757157 PMC: 11702038. DOI: 10.1186/s12955-024-02326-y.


Assessment of quality of life in IPF Patients: a multicenter observational study.

Uzer F, Cilli A, Hanta I, Coskun F, Sevinc C, Ursavas A Sarcoidosis Vasc Diffuse Lung Dis. 2024; 41(3):e2024043.

PMID: 39315976 PMC: 11472669. DOI: 10.36141/svdld.v41i3.15805.


Divergent perspectives: exploring the relationships between St. George's Respiratory Questionnaire and outcome measures in systemic sclerosis-associated interstitial lung disease.

Basaran E, Temiz Karadag D, Cakir O, Gokcen N, Yazici A, Cefle A Clin Rheumatol. 2024; 43(5):1647-1656.

PMID: 38573479 DOI: 10.1007/s10067-024-06950-3.


Muco-Obstructive Lung Disease: A Systematic Review.

Singh G, Acharya S, Shukla S, Jain D Cureus. 2023; 15(10):e46866.

PMID: 37954759 PMC: 10637992. DOI: 10.7759/cureus.46866.


References
1.
Beaton D, Bombardier C, Guillemin F, Ferraz M . Guidelines for the process of cross-cultural adaptation of self-report measures. Spine (Phila Pa 1976). 2000; 25(24):3186-91. DOI: 10.1097/00007632-200012150-00014. View

2.
Wild D, Grove A, Martin M, Eremenco S, McElroy S, Verjee-Lorenz A . Principles of Good Practice for the Translation and Cultural Adaptation Process for Patient-Reported Outcomes (PRO) Measures: report of the ISPOR Task Force for Translation and Cultural Adaptation. Value Health. 2005; 8(2):94-104. DOI: 10.1111/j.1524-4733.2005.04054.x. View

3.
Tzanakis N, Samiou M, Lambiri I, Antoniou K, Siafakas N, Bouros D . Evaluation of health-related quality-of-life and dyspnea scales in patients with idiopathic pulmonary fibrosis. Correlation with pulmonary function tests. Eur J Intern Med. 2005; 16(2):105-112. DOI: 10.1016/j.ejim.2004.09.013. View

4.
Ware Jr J, Sherbourne C . The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care. 1992; 30(6):473-83. View

5.
Jones P, Quirk F, Baveystock C, Littlejohns P . A self-complete measure of health status for chronic airflow limitation. The St. George's Respiratory Questionnaire. Am Rev Respir Dis. 1992; 145(6):1321-7. DOI: 10.1164/ajrccm/145.6.1321. View