Clinical implications of six-minute walk test in patients with idiopathic pulmonary fibrosis: a retrospective cohort study.

IF 3.3 3区 医学 Q2 RESPIRATORY SYSTEM Therapeutic Advances in Respiratory Disease Pub Date : 2024-01-01 DOI:10.1177/17534666241275329
Min Jee Kim, Steven D Nathan, Hyeon Hwa Kim, Ho Cheol Kim
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Abstract

Background: A six-minute walk test (6MWT) is a reproducible, easily performed test, and is widely used to determine functional exercise capacity in patients with idiopathic pulmonary fibrosis (IPF). However, there is currently a paucity of data on the clinical significance of baseline and serial 6-minute walk tests in patients with IPF, especially in Asian patients.

Objectives: We aimed to investigate the clinical significance of serial 6MWT in patients with IPF, especially in Asian patients.

Design: This is a single-center retrospective cohort study.

Methods: Clinical data of patients diagnosed with IPF at a tertiary center in Korea were retrospectively analyzed. IPF diagnosis was defined according to the clinical guidelines of the American Thoracic Society (ATS)/European Respiratory Society (ERS)/Japanese Respiratory Society/Latin American Thoracic Association.

Results: There were 216 patients diagnosed with IPF from December 2012 to January 2022, of whom 198 had a baseline of 6MWT data. The mean age of the cohort was 66.9 ± 8.6, and 89% were male. The non-survivors showed significantly lower six-minute walk distance (6MWD), minimum saturation of peripheral oxygen (SpO2) during 6MWT, forced vital capacity, and diffusing capacity of the lung for carbon monoxide than survivors at baseline. A multivariate Cox analysis demonstrated that lower minimum SpO2 was independently associated with increased mortality rates (Hazard ratio (HR): 1.081, 95% confidence interval (CI): 1.024-1.142, p = 0.005). Higher mortality rates were also associated with echocardiographic-determined pulmonary hypertension (HR: 2.466, 95% CI: 1.149-5.296, p = 0.021) at diagnosis. Among 144 patients with 6MWT results at 12 months, patients with a decline of 50 m or more in the 6MWD showed poorer overall survival than others (median survival: 45.0 months vs 58.0 months, p < 0.001).

Conclusions: Baseline lower minimum SpO2 during 6MWT was an independent prognostic factor in patients with IPF, and a decline in 6MWD in serial follow-up was also associated with a poorer prognosis. These findings suggest that both baseline 6MWT and follow-up data are important in the prognostication of patients with IPF.

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特发性肺纤维化患者六分钟步行测试的临床意义:一项回顾性队列研究。
背景:六分钟步行测试(6MWT)是一项可重复、易于进行的测试,被广泛用于确定特发性肺纤维化(IPF)患者的功能锻炼能力。然而,目前有关 IPF 患者(尤其是亚洲患者)基线和连续 6 分钟步行测试临床意义的数据却很少:我们旨在研究 IPF 患者(尤其是亚洲患者)连续 6 分钟步行测试的临床意义:这是一项单中心回顾性队列研究:方法:对韩国一家三级中心确诊的 IPF 患者的临床数据进行回顾性分析。IPF的诊断根据美国胸科学会(ATS)/欧洲呼吸学会(ERS)/日本呼吸学会/拉丁美洲胸科学会的临床指南进行定义:2012年12月至2022年1月期间,共有216名患者被诊断为IPF,其中198人有6MWT基线数据。患者的平均年龄为(66.9 ± 8.6)岁,89%为男性。非幸存者的六分钟步行距离(6MWD)、6MWT 期间外周血氧最低饱和度(SpO2)、强迫生命容量和肺部一氧化碳弥散容量均明显低于基线幸存者。多变量 Cox 分析表明,较低的最低 SpO2 与死亡率的增加有独立关联(危险比 (HR):1.081,95% 置信区间 (CI):1.024-1.142,P = 0.005)。诊断时超声心动图确定的肺动脉高压(HR:2.466,95% CI:1.149-5.296,p = 0.021)也会导致死亡率升高。在 144 名 6MWT 结果为 12 个月的患者中,6MWD 下降 50 米或以上的患者的总生存率低于其他患者(中位生存率:45.0 个月 vs 58.0 个月,P 结论:6MWD 下降 50 米或以上的患者的总生存率低于其他患者(中位生存率:45.0 个月 vs 58.0 个月):6MWT 期间较低的最小 SpO2 基线是 IPF 患者的一个独立预后因素,连续随访期间 6MWD 下降也与较差的预后有关。这些发现表明,基线 6MWT 和随访数据对 IPF 患者的预后都很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
57
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Respiratory Disease delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of respiratory disease.
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