Prevalence and prognostic impact of physical frailty in interstitial lung disease: A prospective cohort study.


Journal

Respirology (Carlton, Vic.)
ISSN: 1440-1843
Titre abrégé: Respirology
Pays: Australia
ID NLM: 9616368

Informations de publication

Date de publication:
07 2021
Historique:
revised: 11 03 2021
received: 18 12 2020
accepted: 06 04 2021
pubmed: 21 4 2021
medline: 1 10 2021
entrez: 20 4 2021
Statut: ppublish

Résumé

Physical frailty is associated with increased mortality and hospitalizations in older adults. We describe the prevalence of physical frailty and its prognostic impact in patients with a spectrum of fibrotic interstitial lung disease (ILD). Patients with fibrotic ILD at the McMaster University ILD programme were prospectively followed up from November 2015 to March 2020. Baseline data were used to classify patients as non-frail (score = 0), pre-frail (score = 1-2) or frail (score = 3-5) based on modified Fried physical frailty criteria. The association between physical frailty and mortality was assessed using time-to-event models, adjusted for age, sex, lung function and diagnosis using the ILD Gender-Age-Physiology (ILD-GAP) score. We included 463 patients (55% male, mean [SD] age 68 [11] years); 82 (18%) were non-frail, 258 (56%) pre-frail and 123 (26%) frail. The most common ILD diagnoses were idiopathic pulmonary fibrosis (n = 183, 40%) and connective tissue disease-associated-ILD (n = 79, 17%). Mean time since diagnosis was 2.7 ± 4.6 years. There were 56 deaths within the median follow-up of 1.71 (interquartile range [IQR] 1.24, 2.31) years. Both frail and pre-frail individuals had a higher risk of death compared to those categorized as non-frail at baseline (adjusted hazard ratio [aHR] 4.14, 95% CI 1.27-13.5 for pre-frail and aHR 4.41, 95% CI 1.29-15.1 for frail). Physical frailty is prevalent in patients with ILD and is independently associated with an increased risk of death. Assessment of physical frailty provides additional prognostic value to recognized risk scores such as the ILD-GAP score, and may present a modifiable target for intervention.

Sections du résumé

BACKGROUND AND OBJECTIVE
Physical frailty is associated with increased mortality and hospitalizations in older adults. We describe the prevalence of physical frailty and its prognostic impact in patients with a spectrum of fibrotic interstitial lung disease (ILD).
METHODS
Patients with fibrotic ILD at the McMaster University ILD programme were prospectively followed up from November 2015 to March 2020. Baseline data were used to classify patients as non-frail (score = 0), pre-frail (score = 1-2) or frail (score = 3-5) based on modified Fried physical frailty criteria. The association between physical frailty and mortality was assessed using time-to-event models, adjusted for age, sex, lung function and diagnosis using the ILD Gender-Age-Physiology (ILD-GAP) score.
RESULTS
We included 463 patients (55% male, mean [SD] age 68 [11] years); 82 (18%) were non-frail, 258 (56%) pre-frail and 123 (26%) frail. The most common ILD diagnoses were idiopathic pulmonary fibrosis (n = 183, 40%) and connective tissue disease-associated-ILD (n = 79, 17%). Mean time since diagnosis was 2.7 ± 4.6 years. There were 56 deaths within the median follow-up of 1.71 (interquartile range [IQR] 1.24, 2.31) years. Both frail and pre-frail individuals had a higher risk of death compared to those categorized as non-frail at baseline (adjusted hazard ratio [aHR] 4.14, 95% CI 1.27-13.5 for pre-frail and aHR 4.41, 95% CI 1.29-15.1 for frail).
CONCLUSION
Physical frailty is prevalent in patients with ILD and is independently associated with an increased risk of death. Assessment of physical frailty provides additional prognostic value to recognized risk scores such as the ILD-GAP score, and may present a modifiable target for intervention.

Identifiants

pubmed: 33876511
doi: 10.1111/resp.14066
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

683-689

Informations de copyright

© 2021 Asian Pacific Society of Respirology.

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Auteurs

Mohammed A Malik Farooqi (MAM)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.
Firestone Institute for Respiratory Health and St Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

Sachi O'Hoski (S)

School of Rehabilitation Science, McMaster University, Hamilton, Ontario, Canada.

Sarah Goodwin (S)

Firestone Institute for Respiratory Health and St Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

Nima Makhdami (N)

Firestone Institute for Respiratory Health and St Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

Afia Aziz (A)

Firestone Institute for Respiratory Health and St Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

Gerard Cox (G)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.
Firestone Institute for Respiratory Health and St Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

Joshua Wald (J)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.
Firestone Institute for Respiratory Health and St Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

Christopher J Ryerson (CJ)

Department of Medicine, University of British Columbia & Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, British Columbia, Canada.

Marla K Beauchamp (MK)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.
School of Rehabilitation Science, McMaster University, Hamilton, Ontario, Canada.

Nathan Hambly (N)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.
Firestone Institute for Respiratory Health and St Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

Martin Kolb (M)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.
Firestone Institute for Respiratory Health and St Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.

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