Volume 23, Issue 5 pp. 498-506
Original Article

Phenotypic characteristics associated with slow gait speed in idiopathic pulmonary fibrosis

Claire M. Nolan

Corresponding Author

Claire M. Nolan

Harefield Pulmonary Rehabilitation and Muscle Research Group, Royal Brompton and Harefield NHS Foundation Trust, London, UK

National Heart and Lung Institute, Imperial College London, London, UK

Correspondence: Claire M. Nolan, Harefield Pulmonary Rehabilitation and Muscle Research Group, Royal Brompton and Harefield NHS Foundation Trust, Harefield Hospital, Middlesex UB9 6JH, UK. Email: [email protected]

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Matthew Maddocks

Matthew Maddocks

Division of Palliative Care, Policy and Rehabilitation, King’s College London, Cicely Saunders Institute, London, UK

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Toby M. Maher

Toby M. Maher

Interstitial Lung Disease Unit, Royal Brompton and Harefield NHS Foundation Trust, London, UK

Fibrosis Research Group, National Heart and Lung Institute, Imperial College London, London, UK

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Jane L. Canavan

Jane L. Canavan

Harefield Pulmonary Rehabilitation and Muscle Research Group, Royal Brompton and Harefield NHS Foundation Trust, London, UK

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Sarah E. Jones

Sarah E. Jones

Harefield Pulmonary Rehabilitation and Muscle Research Group, Royal Brompton and Harefield NHS Foundation Trust, London, UK

National Heart and Lung Institute, Imperial College London, London, UK

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Ruth E. Barker

Ruth E. Barker

Harefield Pulmonary Rehabilitation and Muscle Research Group, Royal Brompton and Harefield NHS Foundation Trust, London, UK

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Suhani Patel

Suhani Patel

Harefield Pulmonary Rehabilitation and Muscle Research Group, Royal Brompton and Harefield NHS Foundation Trust, London, UK

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Joseph Jacob

Joseph Jacob

Fibrosis Research Group, National Heart and Lung Institute, Imperial College London, London, UK

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Paul Cullinan

Paul Cullinan

Department of Occupational and Environmental Medicine, Imperial College London, London, UK

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William D.-C. Man

William D.-C. Man

Harefield Pulmonary Rehabilitation and Muscle Research Group, Royal Brompton and Harefield NHS Foundation Trust, London, UK

National Heart and Lung Institute, Imperial College London, London, UK

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First published: 14 November 2017
Citations: 25
(Associate Editor: Jeffrey Horowitz; Senior Editor: Lutz Beckert)

ABSTRACT

Background and objective

Usual gait speed over 4 m (4MGS) is an established functional performance measure in older adults that consistently predicts adverse health outcomes, but few data exist in idiopathic pulmonary fibrosis (IPF). We assessed the reliability of 4MGS, its relationship with established outcome measures and its responsiveness to pulmonary rehabilitation.

Methods

In four prospective IPF cohorts, 4MGS inter-observer (n = 46) and test–retest (n = 46) reliability, concurrent validity (n = 65 and n = 62) and responsiveness (n = 60) were determined. The phenotypic characteristics of all patients stratified according to slow 4MGS (<0.8 m/s) were compared, including lung function parameters, HRCT of the chest, 6-min walking distance (6MWD), Medical Respiratory Council (MRC) dyspnoea score, King’s Brief Interstitial Lung Disease (KBILD) questionnaire and Gender, Age and lung Physiology (GAP) prognostic index.

Results

Intra-class correlation coefficients for inter-observer and test–retest reliability were 0.996 and 0.983, respectively. There was a strong association between 4MGS and 6MWD (r = 0.76; P < 0.0001) and moderate correlations with MRC (r = −0.56), KBILD (r = 0.44) and GAP index (r = −0.41); all P < 0.005. 4MGS improved significantly with pulmonary rehabilitation (mean (95% CI) change: 0.16 (0.12–0.20) m/s), effect size 0.65. Patients with slow 4MGS had significantly worse exercise performance (6MWD: −167 (−220 to −133) m), dyspnoea, health status and prognosis index than those with preserved 4MGS, despite similar lung function and HRCT parameters.

Conclusion

4MGS is a simple, reliable, valid and responsive tool that may detect a patient phenotype with worse exercise performance, dyspnoea, health status and prognosis index in stable IPF.

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