Idiopathic pulmonary fibrosis in the UK: findings from the British Thoracic Society UK Idiopathic Pulmonary Fibrosis Registry

被引:0
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作者
Fahim, Ahmed [1 ]
Loughenbury, Maria [2 ]
Stewart, Iain [3 ]
Agnew, Sarah [4 ]
Almond, Howard [2 ]
Casimo, Leo [5 ]
Chaudhuri, Nazia [6 ]
Fletcher, Sophie, V [7 ,8 ,9 ]
Haney, Sarah [10 ]
Ho, Ling-Pei [11 ,12 ]
Hodkinson, Clare [13 ]
Minnis, Paul [14 ]
Palmer, Evelyn [15 ]
Wilson, Andrew M. [16 ,17 ]
British Thorac Soc
机构
[1] Royal Wolverhampton NHS Trust, New Cross Hosp, Wolverhampton, England
[2] British Thorac Soc, London, England
[3] Imperial Coll London, Natl Heart & Lung Inst, London, England
[4] Liverpool Univ Hosp NHS Fdn Trust, Aintree Hosp, Liverpool Interstitial Lung Dis Serv, Liverpool, England
[5] SarcoidosisUK, London, England
[6] Ulster Univ, Sch Biomed Sci, Genom Med Res Grp, Coleraine, Londonderry, North Ireland
[7] Univ Hosp Southampton NHS Fdn Trust, Southampton, England
[8] NIHR Southampton Resp Biomed Res Ctr, Southampton, England
[9] Univ Southampton, Sch Clin & Expt Sci, Faulty Med, Southampton, England
[10] Northumbria Healthcare NHS Fdn Trust, Northumberland, England
[11] Univ Oxford, Weatherall Inst Mol Med, MRC Translat Immune Discovery Unit, Oxford, England
[12] NIHR Oxford Biomed Res Ctr, Oxford, England
[13] Act Pulm Fibrosis, Peterborough, England
[14] Northern Hlth & Social Care Trust, Antrim Area Hosp, Antrim, North Ireland
[15] Newcastle Upon Tyne NHS Hosp Fdn Trust, Royal Victoria Infirm, Newcastle Upon Tyne, England
[16] Univ East Anglia, Norwich Med Sch, Norwich, England
[17] NHS Fdn Trust, Norfolk & Norwich Univ Hosp, Norwich, England
关键词
Interstitial Fibrosis; Idiopathic Pulmonary Fibrosis; CLINICAL-PRACTICE; DIAGNOSIS; SURVIVAL; IPF;
D O I
10.1136/bmjresp-2024-002773
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Objectives Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease (ILD) and the most common idiopathic interstitial pneumonia. The UK IPF Registry was established in 2013 to collect data pertaining to clinical features, therapeutic approaches and outcomes. From February 2023, the Registry expanded to include any ILD with evidence of fibrosis.Design The UK IPF Registry is a national, multicentre observational registry, including both prospective and retrospective data of patients with IPF in secondary or tertiary care. Cases eligible for inclusion were those with a diagnosis of IPF, presenting at participating centres from January 2013.Results Between January 2013 and February 2023, 5052 IPF cases were registered from 64 participating centres. There was a male preponderance (77.8%) with mean +/- SD age of 74 +/- 8.1 years, 66% were ex-smokers and 76% had at least one comorbidity. Over a third (36.7%) experienced symptoms for more than 24 months prior to their first clinic visit. The majority of cases were discussed at a multidisciplinary team (MDT) meeting and the most common radiological patterns at presentation were probable (54.6%) and definite (42.7%) usual interstitial pneumonia. There was a reduction in surgical lung biopsies from 14% in 2013 to 5.5% in 2022. Antifibrotic therapy prescription rose from 36.0% in 2013 to 55.9% in 2023. The use of nintedanib (approved by National Institute of Clinical Excellence in January 2016) rose from 6.7% in 2013 to 31.5% in 2022 and pirfenidone (approved in April 2013) was initially used in around a third of cases before dropping to between 16.8% and 24.9% after nintedanib was approved.Conclusion These data reflect clinical practice across the UK and it is intended the data will have a role in informing the future of IPF care and providing a model for benchmarking, ultimately increasing knowledge and improving clinical care for this devastating disease.
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