Digital clubbing predicts the efficacy of antifibrotic drugs in patients with idiopathic pulmonary fibrosis.

4区 医学 Q2 Nursing
Hiroyoshi Yamauchi, Masashi Bando, Akiko Okuyama, Toshikazu Takasaki, Shu Hisata, Masayuki Nakayama, Naoko Mato, Makoto Maemondo
{"title":"Digital clubbing predicts the efficacy of antifibrotic drugs in patients with idiopathic pulmonary fibrosis.","authors":"Hiroyoshi Yamauchi, Masashi Bando, Akiko Okuyama, Toshikazu Takasaki, Shu Hisata, Masayuki Nakayama, Naoko Mato, Makoto Maemondo","doi":"10.21037/apm-24-177","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The introduction of antifibrotic drugs elicited a significant paradigm shift in the treatment of fibrosing interstitial lung diseases such as idiopathic pulmonary fibrosis (IPF). However, it remains unclear which clinical characteristics of IPF patients predicts therapeutic efficacy, and there has been limited investigation of the relationship between physical findings. The aim of this study was to investigate whether various clinical factors, including physical findings at the initiation of antifibrotic therapy, had an impact on the clinical response to treatment.</p><p><strong>Methods: </strong>We retrospectively examined baseline clinical characteristics of IPF patients to identify features associated with better responses to antifibrotic drugs. We identified 257 consecutive patients with progressive pulmonary fibrosis who received antifibrotic therapy between March 2009 and May 2021, including 153 patients treated with pirfenidone and 104 patients treated with nintedanib. Of these, 66 patients with IPF had comprehensive baseline data recorded at the time of therapy initiation, including gender, age, smoking history, symptoms, physical findings including digital clubbing, biomarkers, and pulmonary function. Based on pulmonary function at 6 months after initiation of treatment, these patients were classified into a non-deterioration group and a deterioration group. Baseline data at the initiation of antifibrotic therapy were compared between these two groups.</p><p><strong>Results: </strong>Twenty-two patients were classified into the deterioration group and 44 into the non-deterioration group. The annualized change in forced vital capacity (FVC) was -385.8±363.3 mL in the deterioration group and 94.1±207.0 mL in the non-deterioration group. The only significant difference in baseline characteristics between the groups was the presence of digital clubbing, observed in 5 of 22 patients (22.7%) in the deterioration group and in 22 of 44 patients (50.0%) in the non-deterioration group (P=0.04). Our findings indicate that IPF patients with digital clubbing experienced a smaller annual decline in FVC following antifibrotic therapy compared to those without digital clubbing.</p><p><strong>Conclusions: </strong>These findings suggest that the presence or absence of digital clubbing in IPF patients may predict the annual rate of FVC decline following antifibrotic therapy. Antifibrotic drugs may be more effective in IPF patients who present with digital clubbing.</p>","PeriodicalId":7956,"journal":{"name":"Annals of palliative medicine","volume":"14 3","pages":"231-238"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of palliative medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.21037/apm-24-177","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Nursing","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The introduction of antifibrotic drugs elicited a significant paradigm shift in the treatment of fibrosing interstitial lung diseases such as idiopathic pulmonary fibrosis (IPF). However, it remains unclear which clinical characteristics of IPF patients predicts therapeutic efficacy, and there has been limited investigation of the relationship between physical findings. The aim of this study was to investigate whether various clinical factors, including physical findings at the initiation of antifibrotic therapy, had an impact on the clinical response to treatment.

Methods: We retrospectively examined baseline clinical characteristics of IPF patients to identify features associated with better responses to antifibrotic drugs. We identified 257 consecutive patients with progressive pulmonary fibrosis who received antifibrotic therapy between March 2009 and May 2021, including 153 patients treated with pirfenidone and 104 patients treated with nintedanib. Of these, 66 patients with IPF had comprehensive baseline data recorded at the time of therapy initiation, including gender, age, smoking history, symptoms, physical findings including digital clubbing, biomarkers, and pulmonary function. Based on pulmonary function at 6 months after initiation of treatment, these patients were classified into a non-deterioration group and a deterioration group. Baseline data at the initiation of antifibrotic therapy were compared between these two groups.

Results: Twenty-two patients were classified into the deterioration group and 44 into the non-deterioration group. The annualized change in forced vital capacity (FVC) was -385.8±363.3 mL in the deterioration group and 94.1±207.0 mL in the non-deterioration group. The only significant difference in baseline characteristics between the groups was the presence of digital clubbing, observed in 5 of 22 patients (22.7%) in the deterioration group and in 22 of 44 patients (50.0%) in the non-deterioration group (P=0.04). Our findings indicate that IPF patients with digital clubbing experienced a smaller annual decline in FVC following antifibrotic therapy compared to those without digital clubbing.

Conclusions: These findings suggest that the presence or absence of digital clubbing in IPF patients may predict the annual rate of FVC decline following antifibrotic therapy. Antifibrotic drugs may be more effective in IPF patients who present with digital clubbing.

数字俱乐部预测抗纤维化药物对特发性肺纤维化患者的疗效。
背景:抗纤维化药物的引入引发了纤维化间质性肺疾病(如特发性肺纤维化(IPF))治疗的重大范式转变。然而,目前尚不清楚IPF患者的哪些临床特征可以预测治疗效果,并且对身体检查结果之间关系的研究也很有限。本研究的目的是探讨各种临床因素,包括抗纤维化治疗开始时的身体检查结果,是否对治疗的临床反应有影响。方法:我们回顾性检查了IPF患者的基线临床特征,以确定与抗纤维化药物更好反应相关的特征。我们确定了2009年3月至2021年5月期间连续接受抗纤维化治疗的257例进行性肺纤维化患者,其中153例接受吡非尼酮治疗,104例接受尼达尼布治疗。其中,66例IPF患者在治疗开始时有全面的基线数据记录,包括性别、年龄、吸烟史、症状、体征(包括数字棍棒)、生物标志物和肺功能。根据治疗开始后6个月的肺功能,将这些患者分为非恶化组和恶化组。比较两组开始抗纤维化治疗时的基线数据。结果:分为恶化组22例,非恶化组44例。用力肺活量(FVC)年化变化,恶化组为-385.8±363.3 mL,未恶化组为94.1±207.0 mL。两组之间基线特征的唯一显著差异是出现了数字杵状反应,恶化组22例患者中有5例(22.7%)出现了数字杵状反应,非恶化组44例患者中有22例(50.0%)出现了数字杵状反应(P=0.04)。我们的研究结果表明,与没有数字棒化的IPF患者相比,有数字棒化的IPF患者在抗纤维化治疗后FVC的年下降幅度较小。结论:这些研究结果表明,IPF患者中是否存在数字棍棒可以预测抗纤维化治疗后FVC的年下降率。抗纤维化药物可能更有效的IPF患者谁目前的数字棍棒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Annals of palliative medicine
Annals of palliative medicine Medicine-Anesthesiology and Pain Medicine
自引率
0.00%
发文量
231
期刊介绍: Annals of Palliative Medicine (Ann Palliat Med; Print ISSN 2224-5820; Online ISSN 2224-5839) is an open access, international, peer-reviewed journal published quarterly with both online and printed copies since 2012. The aim of the journal is to provide up-to-date and cutting-edge information and professional support for health care providers in palliative medicine disciplines to improve the quality of life for patients and their families and caregivers.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信