韩国特发性肺纤维化患者肺康复现状及对预后的影响

IF 2.1 3区 医学 Q3 RESPIRATORY SYSTEM
Journal of thoracic disease Pub Date : 2024-12-31 Epub Date: 2024-12-11 DOI:10.21037/jtd-24-1165
Jung Hyun Nam, Kyung Joo Kim, Chin Kook Rhee, Joon Young Choi, Yong Suk Jo
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引用次数: 0

摘要

背景:肺康复(PR)对特发性肺纤维化(IPF)患者的益处仅限于改善呼吸困难、运动能力和生活质量(QoL)。本研究旨在评估PR的现状及其对预后的影响。方法:本研究使用全国韩国健康保险审查和评估服务(HIRA)数据库。分析了自2016年以来PR纳入健康保险后的年度PR执行率。IPF病例的定义采用国际疾病分类第十版(ICD-10)代码和罕见难治性疾病(RID)代码。分析IPF患者合并或不合并PR的急性加重(AE)风险及死亡率。结果:在4228例IPF患者中,只有205例(4.85%)接受了PR治疗。PR组患者比非PR组更频繁地使用吡非尼酮和全身类固醇治疗。在接受类固醇治疗的患者中,无论使用何种PR,死亡风险都增加,风险比(HR)为1.63[95%置信区间(CI): 1.26-2.10],结论:PR仅用于少数IPF患者。它没有成功地降低AE的风险或死亡率。考虑到IPF疾病本身的进行性,需要针对早期患者的前瞻性研究来评估PR的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current status of pulmonary rehabilitation and impact on prognosis of patients with idiopathic pulmonary fibrosis in South Korea.

Background: The benefits of pulmonary rehabilitation (PR) for patients with idiopathic pulmonary fibrosis (IPF) have been limited to improving dyspnea, exercise capacity, and quality of life (QoL). This study aimed to assess the current status of PR and its effect on prognosis.

Methods: The Nationwide Korean Health Insurance Review and Assessment Service (HIRA) database was used in this study. Annual PR implementation rate since 2016 following its coverage in the health insurance was analyzed. IPF cases were defined using the International Classification of Diseases 10th Revision (ICD-10) codes and rare intractable diseases (RID) codes. Risk of acute exacerbation (AE) and mortality of IPF patients with or without PR were analyzed.

Results: Of the 4,228 patients with IPF, only 205 (4.85%) received PR. Patients in the PR group were more frequently treated with pirfenidone and systemic steroids than non-PR group. In patients treated with steroids, mortality risk increased regardless of PR application, with hazard ratio (HR) of 1.63 [95% confidence interval (CI): 1.26-2.10, P<0.001] in the PR group and 1.38 (95% CI: 1.21-1.57, P<0.001) in the non-PR group, compared to those not treated with steroids. Additionally, PR did not significant affect mortality risk in patients not receiving steroids (HR, 1.49, 95% CI: 0.87-2.54, P=0.15). Similar patterns were seen for the risk of AE.

Conclusions: PR was applied in only a minority of patients with IPF. It did not succeed in reducing the risk of AE or mortality. A prospective study targeting early-stage patients is needed to evaluate the impact of PR considering the progressive nature of IPF disease itself.

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来源期刊
Journal of thoracic disease
Journal of thoracic disease RESPIRATORY SYSTEM-
CiteScore
4.60
自引率
4.00%
发文量
254
期刊介绍: The Journal of Thoracic Disease (JTD, J Thorac Dis, pISSN: 2072-1439; eISSN: 2077-6624) was founded in Dec 2009, and indexed in PubMed in Dec 2011 and Science Citation Index SCI in Feb 2013. It is published quarterly (Dec 2009- Dec 2011), bimonthly (Jan 2012 - Dec 2013), monthly (Jan. 2014-) and openly distributed worldwide. JTD received its impact factor of 2.365 for the year 2016. JTD publishes manuscripts that describe new findings and provide current, practical information on the diagnosis and treatment of conditions related to thoracic disease. All the submission and reviewing are conducted electronically so that rapid review is assured.
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