Literature DB >> 29139195

Phenotypic characteristics associated with slow gait speed in idiopathic pulmonary fibrosis.

Claire M Nolan1,2, Matthew Maddocks3, Toby M Maher4,5, Jane L Canavan1, Sarah E Jones1,2, Ruth E Barker1, Suhani Patel1, Joseph Jacob5, Paul Cullinan6, William D-C Man1,2.   

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.
© 2017 Asian Pacific Society of Respirology.

Entities:  

Keywords:  gait; idiopathic pulmonary fibrosis; outcome assessment; phenotype; walking speed

Mesh:

Year:  2017        PMID: 29139195     DOI: 10.1111/resp.13213

Source DB:  PubMed          Journal:  Respirology        ISSN: 1323-7799            Impact factor:   6.424


  9 in total

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2.  The validity and reliability of four-meter gait speed test for stable interstitial lung disease patients: the prospective study.

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Review 5.  Management of Chronic Respiratory Failure in Interstitial Lung Diseases: Overview and Clinical Insights.

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6.  Validation of 4-meter-gait-speed test and 5-repetitions-sit-to-stand test in patients with pulmonary fibrosis: a clinimetric validation study.

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Review 7.  Which functional outcome measures can we use as a surrogate for exercise capacity during remote cardiopulmonary rehabilitation assessments? A rapid narrative review.

Authors:  Linzy Houchen-Wolloff; Enya Daynes; Amye Watt; Emma Chaplin; Nikki Gardiner; Sally Singh
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8.  Factors influencing self-selected walking speed in fibrotic interstitial lung disease.

Authors:  Gabriela Fischer; Francisco B de Queiroz; Danilo C Berton; Pedro Schons; Henrique B Oliveira; Marcelo Coertjens; Mathieu Gruet; Leonardo A Peyré-Tartaruga
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9.  Pulmonary Rehabilitation in Idiopathic Pulmonary Fibrosis and COPD: A Propensity-Matched Real-World Study.

Authors:  Claire M Nolan; Oliver Polgar; Susie J Schofield; Suhani Patel; Ruth E Barker; Jessica A Walsh; Karen A Ingram; Peter M George; Philip L Molyneaux; Toby M Maher; William D-C Man
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