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递增运动试验期间不同强度下通过生物阻抗心动图测量的血流动力学参数的可靠性。

Reliability of hemodynamic parameters measured by bioimpedance cardiography at different intensities during incremental exercise testing.

作者信息

Schoch Raphael, Wagner Jonathan, Niemeyer Max, Bruggisser Fabienne, Infanger Denis, Carrard Justin, Gasser Benedikt, Schmidt-Trucksäss Arno, Knaier Raphael

机构信息

Department of Sport, Exercise and Health, Division Sports and Exercise Medicine, University of Basel, Basel, Switzerland.

Department Medicine, Training and Health, Institute of Sport Science and Motology, Philipps-University Marburg, Marburg, Germany.

出版信息

Front Cardiovasc Med. 2025 Apr 10;12:1531027. doi: 10.3389/fcvm.2025.1531027. eCollection 2025.

Abstract

BACKGROUND

Bioimpedance cardiography offers a non-invasive and time-efficient method to measure hemodynamic parameters. Previous studies only investigated its reliability under steady-state conditions and at maximum load but not at ventilatory thresholds (VTs). This is the first study that assesses the reliability of measured hemodynamic parameters at different exercise stages during cardiopulmonary exercise testing (CPET) using prespecified strict criteria to assess reliability.

METHODS

Data from 31 healthy, well-trained adults were analyzed. Each participant completed two CPETs, both following the same ramp protocol, with a 7-day interval between them. Hemodynamic parameters were measured with the PhysioFlow® (Manatec Biomedical, Poissy, France) at characteristic phases and thresholds [VT1, VT2, and peak oxygen uptake (V̇O)]. To ensure comparability, the wattage (power) corresponding to the thresholds in Test 1 (P, P, and P) was used for Test 2.

RESULTS

Heart rate, stroke volume, and cardiac output demonstrated good reliability on a group level (mean intraclass correlation >0.75) at both thresholds (0.91, 0.80, and 0.77 at P; 0.92, 0.80, and 0.77 at P) and at P (0.93, 0.82, and 0.80). For stroke volume at P, both individual differences (-39.0 to 36.9 mL for the women and -39.9 to 45.2 mL for the men) and mean detectable change (17.5 mL) were larger than the defined acceptable ranges of agreement (-3.6 to 3.8 mL for the women and -4.5 to 3.3 mL for the men).

CONCLUSION

The PhysioFlow® reliably measures heart rate, stroke volume, and cardiac output during CPET on a group level. However, as shown by the Bland-Altman plots, the reliability is too low to be used for individual comparisons.

摘要

背景

生物阻抗心动描记术提供了一种无创且省时的方法来测量血流动力学参数。以往的研究仅调查了其在稳态条件和最大负荷下的可靠性,而未涉及通气阈值(VT)时的情况。这是第一项使用预先设定的严格标准来评估可靠性的研究,该研究评估了心肺运动试验(CPET)期间不同运动阶段所测量的血流动力学参数的可靠性。

方法

分析了31名健康、训练有素的成年人的数据。每位参与者完成两次CPET,均遵循相同的递增方案,两次测试间隔7天。使用PhysioFlow®(法国普瓦西的马纳泰克生物医学公司)在特征阶段和阈值[VT1、VT2和峰值摄氧量(V̇O)]测量血流动力学参数。为确保可比性,将测试1中与阈值相对应的瓦数(功率)(P、P和P)用于测试2。

结果

在两个阈值(P时为0.91、0.80和0.77;P时为0.92、0.80和0.77)以及P时(0.93、0.82和0.80),心率、每搏输出量和心输出量在组水平上显示出良好的可靠性(组内相关系数均值>0.75)。对于P时的每搏输出量,个体差异(女性为-39.0至36.9 mL,男性为-39.9至45.2 mL)和平均可检测变化(17.5 mL)均大于定义的可接受一致性范围(女性为-3.6至3.8 mL,男性为-4.5至3.3 mL)。

结论

PhysioFlow®在组水平上能够可靠地测量CPET期间的心率、每搏输出量和心输出量。然而,正如布兰德-奥特曼图所示,其可靠性过低,无法用于个体比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d23/12018426/628beee6d93a/fcvm-12-1531027-g001.jpg

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