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尼达尼布治疗特发性肺纤维化患者的高氧输送以维持运动能力。HOPE-IPF 研究的方法学。

High Oxygen Delivery to Preserve Exercise Capacity in Patients with Idiopathic Pulmonary Fibrosis Treated with Nintedanib. Methodology of the HOPE-IPF Study.

机构信息

1 Department of Medicine.

2 Centre for Heart Lung Innovation, University of British Columbia and St. Paul's Hospital, Vancouver, British Columbia, Canada.

出版信息

Ann Am Thorac Soc. 2016 Sep;13(9):1640-7. doi: 10.1513/AnnalsATS.201604-267OC.

Abstract

RATIONALE

Pulmonary rehabilitation improves dyspnea and exercise capacity in idiopathic pulmonary fibrosis (IPF); however, it is unknown whether breathing high amounts of oxygen during exercise training leads to further benefits.

OBJECTIVES

Herein, we describe the design of the High Oxygen Delivery to Preserve Exercise Capacity in IPF Patients Treated with Nintedanib study (the HOPE-IPF study). The primary objective of this study is to determine the physiological and perceptual impact of breathing high levels of oxygen during exercise training in patients with IPF who are receiving antifibrotic therapy.

METHODS

HOPE-IPF is a two-arm double-blind multicenter randomized placebo-controlled trial of 88 patients with IPF treated with nintedanib. Patients will undergo 8 weeks of three times weekly aerobic cycle exercise training, breathing a hyperoxic gas mixture with a constant fraction of 60% inhaled oxygen, or breathing up to 40% oxygen as required to maintain an oxygen saturation level of at least 88%.

MEASUREMENTS AND MAIN RESULTS

End points will be assessed at baseline, postintervention (Week 8), and follow-up (Week 26). The primary analysis will compare the between-group baseline with post-training change in endurance time during constant work rate cycle exercise tests. Additional analyses will evaluate the impact of training with high oxygen delivery on 6-minute walk distance, dyspnea, physical activity, and quality of life.

CONCLUSIONS

The HOPE-IPF study will lead to a comprehensive understanding of IPF exercise physiology, with the potential to change clinical practice by indicating the need for increased delivery of supplemental oxygen during pulmonary rehabilitation in patients with IPF. Clinical trial registered with www.clinicaltrials.gov (NCT02551068).

摘要

背景

肺康复可改善特发性肺纤维化(IPF)患者的呼吸困难和运动能力;然而,运动训练时吸入高浓度氧气是否会带来进一步的益处尚不清楚。

目的

本研究旨在描述尼达尼布治疗的 IPF 患者接受高氧输送以维持运动能力(HOPE-IPF 研究)的设计。该研究的主要目的是确定 IPF 患者在接受抗纤维化治疗的同时,在运动训练中吸入高浓度氧气对生理和感知的影响。

方法

HOPE-IPF 是一项针对尼达尼布治疗的 88 例 IPF 患者的双盲、双臂、随机、安慰剂对照的 2 期临床试验。患者将接受 8 周每周 3 次的有氧循环运动训练,吸入恒定分数为 60%的吸氧混合气体,或根据需要吸入高达 40%的氧气,以维持血氧饱和度至少 88%。

测量和主要结果

终点将在基线、干预后(第 8 周)和随访(第 26 周)进行评估。主要分析将比较恒功自行车运动试验中两组间的基线与训练后耐力时间的变化。额外的分析将评估高氧输送对 6 分钟步行距离、呼吸困难、体力活动和生活质量的影响。

结论

HOPE-IPF 研究将全面了解特发性肺纤维化的运动生理学,有可能通过表明特发性肺纤维化患者肺康复期间需要增加补充氧气的输送来改变临床实践。该临床试验已在 www.clinicaltrials.gov 注册(NCT02551068)。

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