1. Incidence and Prognostic Significance of Hypoxemia in Fibrotic Interstitial Lung Disease: An International Cohort Study.
- Author
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Khor YH, Gutman L, Abu Hussein N, Johannson KA, Glaspole IN, Guler SA, Funke-Chambour M, Geiser T, Goh NSL, and Ryerson CJ
- Subjects
- Australia epidemiology, Canada epidemiology, Disease Progression, Humans, Incidence, Oxygen Inhalation Therapy methods, Predictive Value of Tests, Prognosis, Registries statistics & numerical data, Risk Assessment methods, Risk Factors, Switzerland epidemiology, Walk Test methods, Hypoxia etiology, Hypoxia physiopathology, Hypoxia therapy, Idiopathic Pulmonary Fibrosis blood, Idiopathic Pulmonary Fibrosis diagnosis, Idiopathic Pulmonary Fibrosis mortality, Idiopathic Pulmonary Fibrosis surgery, Lung Transplantation statistics & numerical data, Physical Exertion physiology, Rest physiology
- Abstract
Background: Hypoxemia is a cardinal feature of fibrotic interstitial lung disease (ILD). The incidence, progression, and prognostic significance of hypoxemia in patients with fibrotic ILD currently is unknown., Research Question: What are the epidemiologic features of hypoxemia and its additive prognostic value in a current risk prediction model of fibrotic ILD?, Methods: We identified 848 patients with fibrotic ILD (258 with idiopathic pulmonary fibrosis [IPF]) in five prospective ILD registries from Australia, Canada, and Switzerland. Cumulative incidence of exertional and resting hypoxemia from the time of diagnosis was estimated at 1-year intervals in patients with baseline 6-min walk tests, adjusted for competing risks of death and lung transplantation. Likelihood ratio tests were used to determine the prognostic significance of exertional and resting hypoxemia for 1-year mortality or transplantation when added to the ILD-GAP model. The cohort was divided into derivation and validation subsets to evaluate performance characteristics of the extended model (the ILD-GAP-O
2 model), which included oxygenation status as a predictor., Results: The 1-, 2-, and 5-year overall cumulative incidence was 6.1%, 17.3%, and 40.1%, respectively, for exertional hypoxemia and 2.4%, 5.6%, and 16.5%, respectively, for resting hypoxemia, which were significantly higher in patients with IPF compared with patients without IPF (P < .001 for both). Addition of exertional or resting hypoxemia to the ILD-GAP model improved 1-year mortality and transplantation prediction (P < .001 for both). The ILD-GAP-O2 model showed improved discrimination (C-index, 0.80 vs 0.75) and model fit (Akaike information criteria, 400 vs 422) in the validation cohort, with comparable calibration., Interpretation: Patients with IPF have higher cumulative incidence of exertional and resting hypoxemia than patients without IPF. The extended ILD-GAP-O2 model provides additional risk stratification for 1-year prognosis in fibrotic ILD., (Copyright © 2021 American College of Chest Physicians. All rights reserved.)- Published
- 2021
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