Mapping EQ5D utilities from forced vital capacity and diffusing capacity in fibrotic interstitial lung disease
Fibrotic interstitial lung disease (ILD) includes a large group of conditions that lead to scarring of the lungs. The lack of available 5-level EuroQol 5D (EQ5D) data has limited the ability to conduct economic evaluations in ILD. The purpose of this study was to develop and validate a mapping algor...
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Published in | PloS one Vol. 18; no. 3; p. e0283110 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
31.03.2023
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | Fibrotic interstitial lung disease (ILD) includes a large group of conditions that lead to scarring of the lungs. The lack of available 5-level EuroQol 5D (EQ5D) data has limited the ability to conduct economic evaluations in ILD. The purpose of this study was to develop and validate a mapping algorithm that predicts EQ5D utilities from commonly collected pulmonary function measurements (forced vital capacity [FVC] and diffusing capacity of the lung for carbon monoxide [DLCO]) in fibrotic ILDs.
EQ5D utility and pulmonary function measurements from the Canadian Registry for Pulmonary Fibrosis were included. Ordinary least squares (OLS), beta regression, two-part, and tobit models were used to map EQ5D utilities from FVC or DLCO. Model performance was assessed by comparing the predicted and observed utilities. Subgroup analyses were also conducted to test how well models performed across different patient characteristics. The models were then externally validated in the Australian Idiopathic Pulmonary Fibrosis Registry.
The OLS model performed as well as other more complex models (root mean squared error: 0.17 for FVC and 0.16 for DLCO). As with the other models, the OLS algorithm performed well across the different subgroups (except for EQ5D utilities < 0.5) and in the external validation cohort.
We developed a mapping algorithm that predicts EQ5D utilities from FVC and DLCO, with the intent that this algorithm can be applied to clinical trial populations and real-world cohorts that have not prioritized collection of health-related utilities. The mapping algorithm can be used in future economic evaluations of potential ILD therapies. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: Drs. Wong, Johannson, Marcoux, Assayag, Manganas, Kolb, Ryerson report personal fees and/or grants from Boehringer Ingelheim, outside the submitted work. Drs. Marcoux, Assayag, Kolb, and Ryerson report grants and/or personal fees from Roche Canada, outside the submitted work. Dr. Marcoux reports grants from AstraZeneca, outside the submitted work. Drs. Wong and Assayag report personal fees from AstraZeneca, outside the submitted work. Dr. Johannson reports grants from The Chest Foundation, University of Calgary Cumming School of Medicine, Pulmonary Fibrosis Society of Calgary, UCB Biopharma SPRL and personal fees from Blade Therapeutics, Theravance, Three Lakes Foundation, Pliant Therapeutics, and Hoffman-La Roche Ltd., outside the submitted work. Dr. Manganas reports grants from Galapagos, outside the submitted work. Dr. Kolb reports grants from Canadian Pulmonary Fibrosis Foundation, grants from Canadian Institute for Health Research, grants and personal fees from Prometic, other from European Respiratory Journal, personal fees from Third Pole, MitoImmune, Abbvie, DevPro Biopharma, Horizon, Algernon, CSL Behring, and grants and personal fees from Pieris, outside the submitted work. Dr. Ryerson reports personal fees from Pliant Therapeutics and Veracyte, outside the submitted work;. Drs. Sun, Cox, Fisher, Khalil, Palmer, de Graaff, Walters, Hopkins, Zappala, Goh, Moodley, Navaratnam, Corte, and Zhang report nothing to disclose. This does not alter our adherence to PLOS ONE policies on sharing data and materials. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0283110 |