• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

特发性肺纤维化患者6分钟步行试验的短期和长期可靠性

Short- and Long-Term Reliability of the 6-Minute Walk Test in People With Idiopathic Pulmonary Fibrosis.

作者信息

Holland Anne E, Hill Catherine J, Dowman Leona, Glaspole Ian, Goh Nicole, Lee Annemarie L, McDonald Christine F

机构信息

Department of Physiotherapy

Department of Physiotherapy, La Trobe University, Melbourne, Australia.

出版信息

Respir Care. 2018 Aug;63(8):994-1001. doi: 10.4187/respcare.05875. Epub 2018 Jun 26.

DOI:10.4187/respcare.05875
PMID:29945909
Abstract

BACKGROUND

The aim of this work was to investigate the short- and long-term test-retest reliability of the 6-min walk distance (6MWD), peak heart rate, and nadir oxygen desaturation in idiopathic pulmonary fibrosis (IPF).

METHODS

A reliability study of 70 adults with IPF was undertaken within out-patient pulmonary rehabilitation programs at 2 tertiary hospitals. Participants completed 2 baseline 6-min walk tests using a standard protocol, with continuous measures of percutaneous S and heart rate via pulse oximetry. The 6-min walk test was completed immediately following an intervention period and 6 months after. Reproducibility was assessed by intraclass correlation coefficient and Bland-Altman analysis.

RESULTS

Participants with a mean ± SD diffusing capacity of the lung for carbon monoxide of 48 ± 14% were included. The reliability of the 6MWD was high (intraclass correlation coefficient = 0.96) with a mean learning effect of 21 m (95% CI 12-30 m). The learning effect persisted at 8 weeks (mean 14 m, 95% CI 5-23 m) but not 6 months (mean 15 m, 95% CI -1 to 30 m). Using the best (greatest) 6MWD significantly reduced the proportion of participants who were classified as having a clinically important response to rehabilitation compared with using the first 6MWD (40% vs 54%, = .002). Nadir S was reproducible, with a mean difference of 0.7 ± 2.2%, and limits of agreement of -4 to 5%. Peak heart rate was more variable, with mean difference 5 ± 9 beats/min and limits of agreement of -12 to 20 beats/min.

CONCLUSIONS

The 6MWD is a reproducible measure of exercise capacity in people with IPF. Whereas the nadir S may be accurately determined from one test, evaluating change in 6MWD with interventions may require 2 tests on each occasion. (ClinicalTrials.gov registration NCT0016828.).

摘要

背景

本研究旨在调查特发性肺纤维化(IPF)患者6分钟步行距离(6MWD)、心率峰值和最低氧饱和度的短期和长期重测信度。

方法

在两家三级医院的门诊肺康复项目中,对70例成年IPF患者进行了一项信度研究。参与者按照标准方案完成2次基线6分钟步行测试,通过脉搏血氧饱和度仪持续测量经皮血氧饱和度(S)和心率。在干预期结束后立即及6个月后再次完成6分钟步行测试。通过组内相关系数和Bland-Altman分析评估可重复性。

结果

纳入了一氧化碳肺弥散量平均±标准差为48±14%的参与者。6MWD的信度较高(组内相关系数=0.96),平均学习效应为21米(95%CI 12 - 30米)。学习效应在8周时持续存在(平均14米,95%CI 5 - 23米),但在6个月时不存在(平均15米,95%CI -1至30米)。与使用首次6MWD相比,使用最佳(最长)6MWD显著降低了被归类为对康复有临床重要反应的参与者比例(40%对54%,P = 0.002)。最低S是可重复的,平均差异为0.7±2.2%,一致性界限为-4%至5%。心率峰值变异性更大,平均差异为5±9次/分钟,一致性界限为-12至20次/分钟。

结论

6MWD是IPF患者运动能力的可重复测量指标。虽然最低S可通过一次测试准确测定,但评估干预后6MWD的变化可能每次都需要进行2次测试。(ClinicalTrials.gov注册号NCT0016828。)

相似文献

1
Short- and Long-Term Reliability of the 6-Minute Walk Test in People With Idiopathic Pulmonary Fibrosis.特发性肺纤维化患者6分钟步行试验的短期和长期可靠性
Respir Care. 2018 Aug;63(8):994-1001. doi: 10.4187/respcare.05875. Epub 2018 Jun 26.
2
Clinical implications of six-minute walk test in patients with idiopathic pulmonary fibrosis: a retrospective cohort study.特发性肺纤维化患者六分钟步行试验的临床意义:一项回顾性队列研究。
Ther Adv Respir Dis. 2024 Jan-Dec;18:17534666241275329. doi: 10.1177/17534666241275329.
3
Six-Minute Walk Test: Clinical Role, Technique, Coding, and Reimbursement.六分钟步行试验:临床作用、技术、编码和报销。
Chest. 2020 Mar;157(3):603-611. doi: 10.1016/j.chest.2019.10.014. Epub 2019 Nov 2.
4
Validation of test performance characteristics and minimal clinically important difference of the 6-minute walk test in patients with idiopathic pulmonary fibrosis.特发性肺纤维化患者6分钟步行试验的测试性能特征及最小临床重要差异的验证
Respir Med. 2015 Jul;109(7):914-22. doi: 10.1016/j.rmed.2015.04.008. Epub 2015 Apr 24.
5
Cardiorespiratory adaptation during 6-Minute Walk Test in fibrotic idiopathic interstitial pneumonia patients who did or did not respond to pulmonary rehabilitation.纤维化特发性间质性肺炎患者在接受或未接受肺康复治疗后的 6 分钟步行试验中的心肺适应变化。
Eur J Phys Rehabil Med. 2019 Feb;55(1):103-112. doi: 10.23736/S1973-9087.18.05093-1. Epub 2018 Jun 14.
6
Minimal important difference and responsiveness of 2-minute walk test performance in people with COPD undergoing pulmonary rehabilitation.慢性阻塞性肺疾病患者接受肺康复治疗时2分钟步行试验表现的最小重要差异和反应性
Int J Chron Obstruct Pulmon Dis. 2017 Oct 9;12:2849-2857. doi: 10.2147/COPD.S143179. eCollection 2017.
7
Effect of Recombinant Human Pentraxin 2 vs Placebo on Change in Forced Vital Capacity in Patients With Idiopathic Pulmonary Fibrosis: A Randomized Clinical Trial.重组人 Pentraxin 2 与安慰剂对特发性肺纤维化患者用力肺活量变化的影响:一项随机临床试验。
JAMA. 2018 Jun 12;319(22):2299-2307. doi: 10.1001/jama.2018.6129.
8
Changes in physical activity in people with idiopathic pulmonary fibrosis before and after virtual pulmonary rehabilitation: a feasibility study.特发性肺纤维化患者在虚拟肺康复前后的身体活动变化:一项可行性研究。
BMC Pulm Med. 2024 May 2;24(1):215. doi: 10.1186/s12890-024-03030-9.
9
Multi-dimensional Assessment of IPF Across a Wide Range of Disease Severity.特发性肺纤维化疾病严重度范围的多维评估。
Lung. 2018 Dec;196(6):707-713. doi: 10.1007/s00408-018-0152-4. Epub 2018 Aug 27.
10
Six-minute-walk test in idiopathic pulmonary fibrosis: test validation and minimal clinically important difference.特发性肺纤维化六分钟步行试验:验证和最小临床重要差异。
Am J Respir Crit Care Med. 2011 May 1;183(9):1231-7. doi: 10.1164/rccm.201007-1179OC. Epub 2010 Dec 3.

引用本文的文献

1
A Real-World Multicenter Retrospective Observational Study on Polish Experience with Nintedanib Therapy in Patients with Idiopathic Pulmonary Fibrosis: The PolExNIB Study.一项关于尼达尼布治疗特发性肺纤维化患者的波兰经验的真实世界多中心回顾性观察研究:PolExNIB研究。
J Clin Med. 2023 Jul 12;12(14):4635. doi: 10.3390/jcm12144635.
2
Efficacy and safety of traditional Chinese medicine treatment for idiopathic pulmonary fibrosis: An exploratory, randomized, double-blinded and placebo controlled trial.中药治疗特发性肺纤维化的疗效与安全性:一项探索性、随机、双盲、安慰剂对照试验。
Front Pharmacol. 2022 Oct 28;13:1053356. doi: 10.3389/fphar.2022.1053356. eCollection 2022.
3
Derivation and validation of a simple multidimensional index incorporating exercise capacity parameters for survival prediction in idiopathic pulmonary fibrosis.
一个简单的多维指数的推导和验证,纳入运动能力参数,用于特发性肺纤维化的生存预测。
Thorax. 2023 Apr;78(4):368-375. doi: 10.1136/thoraxjnl-2021-218440. Epub 2022 Mar 24.
4
Longitudinal and Comparative Measures of Serum Chitotriosidase and YKL-40 in Patients With Idiopathic Pulmonary Fibrosis.特发性肺纤维化患者血清几丁质酶 3 样蛋白 1 和 YKL-40 的纵向和对比测量。
Front Immunol. 2022 Feb 10;13:760776. doi: 10.3389/fimmu.2022.760776. eCollection 2022.
5
Serial Measurements of Circulating KL-6, SP-D, MMP-7, CA19-9, CA-125, CCL18, and Periostin in Patients with Idiopathic Pulmonary Fibrosis Receiving Antifibrotic Therapy: An Exploratory Study.接受抗纤维化治疗的特发性肺纤维化患者循环中KL-6、SP-D、MMP-7、CA19-9、CA-125、CCL18和骨膜蛋白的系列测量:一项探索性研究
J Clin Med. 2021 Aug 28;10(17):3864. doi: 10.3390/jcm10173864.
6
A systematic comparison of exercise training protocols on animal models of cardiovascular capacity.系统比较心血管能力动物模型的运动训练方案。
Life Sci. 2019 Jan 15;217:128-140. doi: 10.1016/j.lfs.2018.12.001. Epub 2018 Dec 3.