Feasibility of in-bed exercise testing using a clamp-on pedaling device: A single-center pragmatic study.

Neil K Jairath, Joshua Mijares, Kishore M Vora
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Abstract

Background: Exercise stress testing is the gold standard for evaluating peripheral arterial disease (PAD) and exercise-induced pulmonary hypertension, but traditional treadmill testing has operational limitations including need for patient transport, specialized facilities, and inability to perform invasive hemodynamic monitoring during exercise.

Methods: This prospective single-center feasibility study enrolled 54 consecutive patients undergoing ABI (n = 35) or RHC (n = 19) procedures at Owensboro Medical Practice. The Bedside Bike (Bedside Bike, LLC; 510(k)-exempt Class I device, product code ION) was integrated into routine vascular laboratory and catheterization laboratory workflows. Primary endpoints included exercise completion rates, data interpretability, and safety. Prespecified success criteria were: completion rate ⩾90% and interpretability ⩾80% for ABI; completion rate ⩾90% and interpretability ⩾70% for RHC; system usability ⩾80% for both.

Results: Exercise was attempted in 94.4% (51/54; 95% CI: 87.0-100%) of patients with a 94.1% (48/51; 95% CI: 86.3-100%) completion rate among those who attempted. Data interpretability was excellent: 97.1% (34/35; 95% CI: 91.4-100%) for ABI and 84.2% (16/19; 95% CI: 68.4-100%) for RHC. All prespecified feasibility criteria were met. System usability ratings were 85.7% (95% CI: 74.3-97.1%) for ABI and 89.5% (95% CI: 73.7-100%) for RHC. Adverse events were minor and occurred in 14.3% of ABI and 5.3% of RHC procedures. Among RHC patients with paired measurements, median cardiac output increased from 4.0 [IQR: 3.8-4.7] L/min at rest to 5.0 [4.8-6.5] L/min with exercise, with a median mPAP/CO slope of 8.26 [6.88-14.12] mmHg/L/min.

Conclusion: This feasibility study demonstrates that bedside exercise testing using a portable pedaling device is technically feasible, safe, and well-tolerated for both ABI and RHC procedures. These preliminary results support larger studies to evaluate diagnostic validity and clinical utility.

使用夹紧式踏板装置进行床上运动测试的可行性:一项单中心实用研究。
背景:运动应激试验是评估外周动脉疾病(PAD)和运动引起的肺动脉高压的金标准,但传统的跑步机试验存在操作上的局限性,包括需要患者转移、专门的设备,以及在运动过程中无法进行有创性血流动力学监测。方法:这项前瞻性单中心可行性研究纳入了54例连续在Owensboro Medical Practice接受ABI (n = 35)或RHC (n = 19)手术的患者。床边自行车(床边自行车有限责任公司;510(k)豁免I类设备,产品代码ION)被集成到常规血管实验室和导管实验室工作流程中。主要终点包括运动完成率、数据可解释性和安全性。预先指定的成功标准是:ABI的完成率大于或等于90%,可解释性大于或等于80%;RHC的完成率大于或等于90%,可解释性大于或等于70%;两者的系统可用性都大于等于80%结果:94.4% (51/54;95% CI: 87.0-100%)的患者尝试了运动,其中94.1% (48/51;95% CI: 86.3-100%)的患者尝试了运动。数据可解释性非常好:ABI为97.1% (34/35;95% CI: 91.4-100%), RHC为84.2% (16/19;95% CI: 68.4-100%)。所有预先规定的可行性标准均得到满足。ABI的系统可用性评分为85.7% (95% CI: 74.3-97.1%), RHC的系统可用性评分为89.5% (95% CI: 73.7-100%)。不良事件较少,14.3%的ABI和5.3%的RHC手术发生不良事件。在配对测量的RHC患者中,中位心输出量从静止时的4.0 [IQR: 3.8-4.7] L/min增加到运动时的5.0 [4.8-6.5]L/min,中位mPAP/CO斜率为8.26 [6.88-14.12]mmHg/L/min。结论:这项可行性研究表明,在ABI和RHC手术中,使用便携式踏板装置进行床边运动试验在技术上是可行的、安全的,并且耐受性良好。这些初步结果支持更大规模的研究来评估诊断的有效性和临床应用。
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
Global Cardiology Science & Practice
Global Cardiology Science & Practice Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.60
自引率
0.00%
发文量
20
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