Assessment of Inter-Instrument Reliability for Dominant Handgrip Dynamometry and Spirometry

IF 0.5 Q4 HEALTH CARE SCIENCES & SERVICES
Nnamdi Mgbemena, A. Jones, A. Leicht
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Abstract

Purpose: The aim of this study was to determine the inter-instrument reliability of different dynamometers and spirometers commonly used in clinical practice. Methods: The study involved 113 healthy volunteers across three facility sites. At each site, dominant handgrip strength (DHGS), and lung function (forced expiratory volume in one second [FEV1], forced vital capacity [FVC] and peak expiratory flow rate [PEFR]), were compared using a local and reference device. Assessments were randomized with five minutes rest between measurements. Significant differences between devices were assessed using paired t-test while relative reliability between devices was determined via intra-class correlations (ICC). Accuracy index and variability between measurements were assessed using the technical error of measurement (TEM%) and coefficient of variation (CV), respectively. Agreement between devices was determined using the Bland Altman’s plot with limits of agreement (LOA). Results: The local devices recorded significantly (p1 (3.1%-8.4%), FVC (3.1%-13%) compared to the reference devices. Good-excellent correlations (ICC=0.89-0.96), unacceptable CV (5.8-9.9%) and TEM% (6.6-9.9%), and large mean biases (3-9kg) and LOA (3-23kg) were identified between the local and reference dynamometers. Excellent correlations (ICC=0.91-0.99), and mostly unacceptable CV and TEM% were identified between the local and reference spirometers for FVC and PEFR. Compared to the reference device, all local spirometers showed unacceptable (-0.134 to -0.536 liters) and acceptable (-0.12 to 0.05 liters/second) mean biases for FVC and PEFR, respectively. Conclusion: Unacceptable inter-instrument reliability was identified between local and reference dynamometers and spirometers for measuring DHGS and all lung function indices, respectively. Across clinical settings, comparing DHGS and lung function between different brands of devices may lead to the reporting of erroneous results with corrective adjustments required for clinical practice.
优势握力测定仪和肺活量测定仪间可靠性评估
目的:本研究的目的是确定临床常用的不同测力计和肺活量计的仪器间可靠性。方法:研究涉及三个设施站点的113名健康志愿者。在每个部位,使用局部和参考装置比较优势握力(DHGS)和肺功能(一秒钟用力呼气量[FEV1]、用力肺活量[FVC]和呼气峰值流速[PEFR])。评估随机进行,每次评估之间休息5分钟。使用配对t检验评估设备之间的显著差异,而通过类内相关性(ICC)确定设备之间的相对可靠性。分别用测量技术误差(TEM%)和变异系数(CV)评估准确度指数和测量间的变异性。采用带有一致性限制(LOA)的Bland Altman图确定设备之间的一致性。结果:与参比装置相比,局部装置的p1(3.1% ~ 8.4%)、FVC(3.1% ~ 13%)有显著性差异。本地测功机和参考测功机之间存在良好的相关性(ICC=0.89-0.96),不可接受的CV(5.8-9.9%)和TEM%(6.6-9.9%),以及较大的平均偏差(3-9kg)和LOA (3-23kg)。在FVC和PEFR的本地肺活量计和参考肺活量计之间发现了极好的相关性(ICC=0.91-0.99),但CV和TEM%大多不可接受。与参考装置相比,所有本地肺活量计的FVC和PEFR的平均偏差分别为不可接受(-0.134至-0.536升)和可接受(-0.12至0.05升/秒)。结论:在测量DHGS和所有肺功能指标时,局部测功机和参考测功机、肺活量计的仪器间可靠性均不理想。在整个临床环境中,比较不同品牌器械之间的DHGS和肺功能可能导致报告错误的结果,需要临床实践进行纠正调整。
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
自引率
25.00%
发文量
18
审稿时长
35 weeks
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