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What proportion of patients with Idiopathic pulmonary fibrosis fall outside UK prescribing criteria for anti-fibrotic treatment? A UK specialist centre review

What proportion of patients with Idiopathic pulmonary fibrosis fall outside UK prescribing criteria for anti-fibrotic treatment? A UK specialist centre review
What proportion of patients with Idiopathic pulmonary fibrosis fall outside UK prescribing criteria for anti-fibrotic treatment? A UK specialist centre review
Background: anti-fibrotic therapies have transformed the care of patients with Idiopathic Pulmonary Fibrosis (IPF). Within the United Kingdom, prescribing criteria set by NICE (National Institute for Health and Care Excellence) restrict anti-fibrotic prescription to patients with an FVC of 50-80% predicted, potentially excluding a significant proportion of patients with IPF from receiving anti-fibrotic treatment.

Aims and objectives: to investigate the proportion of patients with IPF that do not meet UK NICE prescribing criteria for anti-fibrotic treatment.

Methods: this is a retrospective specialist centre cohort study. Consecutive patients with an MDT diagnosis of IPF and a minimum of 12 months follow up were included in the analysis.

Results: 194 patients with IPF were identified. 150 (77%) were male and 120 (62%) were ex-smokers. Mean age at diagnosis was 73 years (SD=8 years). The most common comorbidity was GORD (n=73, 38%) while 36 (19%) had a background of ischaemic heart disease. At diagnosis mean FVC was 75% predicted (SD=20%) and mean TLCO was 47% predicted (SD=16%). 150 patients (77%) were eligible for anti-fibrotic treatment on diagnosis. 29 (15%) patients were not eligible for anti-fibrotics when assessed by NICE criteria, with 20 having an FVC>80% predicted while 9 had an FVC80% have subsequently received anti-fibrotic treatment following FVC decline.

Conclusions: 15% of patients with IPF referred for specialist centre care were ineligible for anti-fibrotic treatment as a consequence of the NICE FVC prescribing criteria.
0903-1936
Brereton, Christopher J.
14b6396e-9e2c-4313-b337-71df6e0d8c8d
Pontoppidan, Katarina
efb2a238-0091-4a9f-bdaf-1a200839b48b
Wallis, Tim
54714e60-8bbc-45cc-90ce-215c8d074718
Richeldi, Luca
89f3b3b9-2dc9-4803-a190-3d4facabd8c2
Jones, Mark G.
119d23fa-c777-482a-8eb4-69d3bd499791
Fletcher, Sophie V.
d05721e8-8943-4f13-a1f5-4ba183741c89
Brereton, Christopher J.
14b6396e-9e2c-4313-b337-71df6e0d8c8d
Pontoppidan, Katarina
efb2a238-0091-4a9f-bdaf-1a200839b48b
Wallis, Tim
54714e60-8bbc-45cc-90ce-215c8d074718
Richeldi, Luca
89f3b3b9-2dc9-4803-a190-3d4facabd8c2
Jones, Mark G.
119d23fa-c777-482a-8eb4-69d3bd499791
Fletcher, Sophie V.
d05721e8-8943-4f13-a1f5-4ba183741c89

Brereton, Christopher J., Pontoppidan, Katarina, Wallis, Tim, Richeldi, Luca, Jones, Mark G. and Fletcher, Sophie V. (2019) What proportion of patients with Idiopathic pulmonary fibrosis fall outside UK prescribing criteria for anti-fibrotic treatment? A UK specialist centre review. European Respiratory Journal, 54 (Suppl 63), [PA1348]. (doi:10.1183/13993003.congress-2019.PA1348).

Record type: Meeting abstract

Abstract

Background: anti-fibrotic therapies have transformed the care of patients with Idiopathic Pulmonary Fibrosis (IPF). Within the United Kingdom, prescribing criteria set by NICE (National Institute for Health and Care Excellence) restrict anti-fibrotic prescription to patients with an FVC of 50-80% predicted, potentially excluding a significant proportion of patients with IPF from receiving anti-fibrotic treatment.

Aims and objectives: to investigate the proportion of patients with IPF that do not meet UK NICE prescribing criteria for anti-fibrotic treatment.

Methods: this is a retrospective specialist centre cohort study. Consecutive patients with an MDT diagnosis of IPF and a minimum of 12 months follow up were included in the analysis.

Results: 194 patients with IPF were identified. 150 (77%) were male and 120 (62%) were ex-smokers. Mean age at diagnosis was 73 years (SD=8 years). The most common comorbidity was GORD (n=73, 38%) while 36 (19%) had a background of ischaemic heart disease. At diagnosis mean FVC was 75% predicted (SD=20%) and mean TLCO was 47% predicted (SD=16%). 150 patients (77%) were eligible for anti-fibrotic treatment on diagnosis. 29 (15%) patients were not eligible for anti-fibrotics when assessed by NICE criteria, with 20 having an FVC>80% predicted while 9 had an FVC80% have subsequently received anti-fibrotic treatment following FVC decline.

Conclusions: 15% of patients with IPF referred for specialist centre care were ineligible for anti-fibrotic treatment as a consequence of the NICE FVC prescribing criteria.

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e-pub ahead of print date: 21 November 2019

Identifiers

Local EPrints ID: 486025
URI: http://eprints.soton.ac.uk/id/eprint/486025
ISSN: 0903-1936
PURE UUID: 4bfa25d4-caaf-4544-a85b-9e1f2cc14230

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Date deposited: 05 Jan 2024 18:03
Last modified: 17 Mar 2024 06:42

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Contributors

Author: Christopher J. Brereton
Author: Katarina Pontoppidan
Author: Tim Wallis
Author: Luca Richeldi
Author: Mark G. Jones
Author: Sophie V. Fletcher

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