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两种人体成分监测仪的生物阻抗法液体状态差异。

Differences in bioimpedance-derived fluid status between two versions of the Body Composition Monitor.

机构信息

Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria.

Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria; Department of Epidemiology, Center for Public Health, Medical University of Vienna, Vienna, Austria.

出版信息

Nutrition. 2023 Oct;114:112131. doi: 10.1016/j.nut.2023.112131. Epub 2023 Jun 14.

DOI:10.1016/j.nut.2023.112131
PMID:37467529
Abstract

OBJECTIVES

The Body Composition Monitor (BCM) (Fresenius Medical Care) measures body impedances in alternating currents to subsequently calculate fat and lean tissue mass, fluid compartments, and overhydration (OH). The aim of this study was to investigate differences between two versions of the BCM (an older version, 3.2.5, and a newer version, 3.3.3).

METHODS

Between September 2021 and December 2021, 28 hemodialysis patients were included to undergo BCM measurements before each of 14 consecutive dialysis sessions with versions 3.2.5 and 3.3.3 devices. Measurements were performed according to instructions provided by the manufacturer. Differences between BCM devices were tested for statistical significance using paired Wilcoxon tests, neglecting clustering.

RESULTS

A total of 288 measurement pairs of 27 patients were left after exclusion of 43 flawed data points. The mean difference in OH between both BCM devices was 0.548 L (higher for version 3.2.5). Analysis of impedance data revealed differences in the high-frequency spectrum, quantifiable by the intracellular resistance, R (median R = 1750.3 Ω; R = 1612.45 Ω; P < 0.001), and the time delay, T (median T = 1.85 ns; T = 8.88 nanoseconds; P < 0.001).

CONCLUSIONS

This study finds that results between the two versions of the BCM differed in a clinically meaningful fashion and that the newer version 3.3.3 device had a bias toward less OH. Circulating BCM devices should be checked for versions and only devices of the same version should be used for each patient to ensure better within-patient consistency.

摘要

目的

体成分监测仪(BCM)(费森尤斯医疗保健)通过测量交流电中的身体阻抗,随后计算脂肪和瘦组织质量、体液腔室和过度水化(OH)。本研究的目的是比较两种 BCM 版本(旧版本 3.2.5 和新版本 3.3.3)之间的差异。

方法

2021 年 9 月至 2021 年 12 月,纳入 28 名血液透析患者,在 14 次连续透析治疗前,分别使用 3.2.5 版和 3.3.3 版设备进行 BCM 测量。测量按照制造商提供的说明进行。使用配对 Wilcoxon 检验忽略聚类来检验两种 BCM 设备之间的差异是否具有统计学意义。

结果

在排除 43 个有缺陷的数据点后,共有 27 名患者的 288 对测量值。两种 BCM 设备之间 OH 的平均差异为 0.548 L(3.2.5 版更高)。对阻抗数据的分析显示,高频谱存在差异,可通过细胞内电阻 R(中位数 R=1750.3 Ω;R=1612.45 Ω;P <0.001)和时间延迟 T(中位数 T=1.85 ns;T=8.88 纳秒;P <0.001)进行量化。

结论

本研究发现,两种 BCM 版本的结果存在有临床意义的差异,新版本 3.3.3 设备的 OH 结果偏低。应检查循环使用的 BCM 设备的版本,并且应为每位患者使用相同版本的设备,以确保更好的患者内一致性。

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