Literature DB >> 27817810

Patient eligibility for anti-fibrotic therapy in idiopathic pulmonary fibrosis can be altered by use of different sets of reference values for calculation of FVC percent predicted.

Katie Ward1, Lydia Spurr2, Nina R Goldman2, George A Margaritopoulos2, Maria Kokosi2, Elizabetta Renzoni2, Felix Chua2, Toby M Maher3, Simon Ward2, Athol U Wells2.   

Abstract

Antifibrotic drugs for idiopathic pulmonary fibrosis patients in England and Scotland are only available to those with FVC percent predicted (FVC%pred) less than or equal to 80%. The prescribing guidance does not state which set of reference values should be used and we show that a patient's FVC%pred can change by 4-6% depending on the choice of reference. We calculated FVC%pred for a group of 528 IPF patients using three different sets of reference values. 90% of patients with FVC%pred 80-85% calculated using European Community Coal and Steel (ECSC) reference values fall into the eligible range when NHANES reference values are used.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Idiopathic pulmonary fibrosis; Interstitial lung disease; Respiratory function tests

Mesh:

Year:  2016        PMID: 27817810     DOI: 10.1016/j.rmed.2016.10.007

Source DB:  PubMed          Journal:  Respir Med        ISSN: 0954-6111            Impact factor:   3.415


  2 in total

1.  Antifibrotic Drug Use in Patients with Idiopathic Pulmonary Fibrosis. Data from the IPF-PRO Registry.

Authors:  Margaret L Salisbury; Craig S Conoscenti; Daniel A Culver; Eric Yow; Megan L Neely; Shaun Bender; Nadine Hartmann; Scott M Palmer; Thomas B Leonard
Journal:  Ann Am Thorac Soc       Date:  2020-11

2.  Putting lung function reference equations into context.

Authors:  Brigitte M Borg; Bruce R Thompson
Journal:  Breathe (Sheff)       Date:  2021-09
  2 in total

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