英国特发性肺纤维化:来自英国胸科学会英国特发性肺纤维化登记处的发现。

IF 3.4 3区 医学 Q1 RESPIRATORY SYSTEM
Ahmed Fahim, Maria Loughenbury, Iain Stewart, Sarah Agnew, Howard Almond, Leo Casimo, Nazia Chaudhuri, Sophie V Fletcher, Sarah Haney, Ling-Pei Ho, Clare Hodkinson, Paul Minnis, Evelyn Palmer, Andrew M Wilson
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引用次数: 0

摘要

目的:特发性肺纤维化(IPF)是一种进行性间质性肺疾病(ILD),是最常见的特发性间质性肺炎。英国IPF登记处成立于2013年,收集有关临床特征、治疗方法和结果的数据。从2023年2月起,登记范围扩大到包括任何有纤维化证据的ILD。设计:英国IPF登记是一个全国性的、多中心的观察性登记,包括IPF患者在二级或三级护理中的前瞻性和回顾性数据。符合纳入条件的病例是自2013年1月起在参与中心就诊的诊断为IPF的患者。结果:2013年1月至2023年2月,64个参与中心共登记了5052例IPF病例。男性居多(77.8%),平均±SD年龄为74±8.1岁,66%为戒烟者,76%至少有一种合并症。超过三分之一(36.7%)的患者在首次就诊前出现症状超过24个月。大多数病例在多学科小组(MDT)会议上讨论,最常见的影像学表现为可能的(54.6%)和确定的(42.7%)通常的间质性肺炎。手术肺活检的比例从2013年的14%下降到2022年的5.5%。抗纤维化治疗处方从2013年的36.0%上升到2023年的55.9%。尼达尼布(2016年1月由美国国家临床卓越研究所批准)的使用率从2013年的6.7%上升到2022年的31.5%,吡非尼酮(2013年4月批准)最初用于约三分之一的病例,在尼达尼布被批准后下降到16.8%至24.9%之间。结论:这些数据反映了整个英国的临床实践,它的目的是数据将在告知IPF护理的未来和提供基准模型的作用,最终增加知识和改善这种毁灭性疾病的临床护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Idiopathic pulmonary fibrosis in the UK: findings from the British Thoracic Society UK Idiopathic Pulmonary Fibrosis Registry.

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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来源期刊
BMJ Open Respiratory Research
BMJ Open Respiratory Research RESPIRATORY SYSTEM-
CiteScore
6.60
自引率
2.40%
发文量
95
审稿时长
12 weeks
期刊介绍: BMJ Open Respiratory Research is a peer-reviewed, open access journal publishing respiratory and critical care medicine. It is the sister journal to Thorax and co-owned by the British Thoracic Society and BMJ. The journal focuses on robustness of methodology and scientific rigour with less emphasis on novelty or perceived impact. BMJ Open Respiratory Research operates a rapid review process, with continuous publication online, ensuring timely, up-to-date research is available worldwide. The journal publishes review articles and all research study types: Basic science including laboratory based experiments and animal models, Pilot studies or proof of concept, Observational studies, Study protocols, Registries, Clinical trials from phase I to multicentre randomised clinical trials, Systematic reviews and meta-analyses.
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