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用于评估腰痛患者腰椎前屈活动度的BROM II型和EDI - 320型腰椎测角器的效标效度研究

Criterion validity study of lumbar goniometers BROM II and EDI-320 for range of motion of lumbar flexion of low back pain patients.

作者信息

Tousignant M, Morissette J, Murphy M

机构信息

Gerontology and Geriatrics Research Center, Sherbrooke Geriatric University Institute, Quebec, Canada.

出版信息

J Back Musculoskelet Rehabil. 2002 Jan 1;16(4):159-67. doi: 10.3233/bmr-2002-16407.

Abstract

PURPOSE

The purpose was to estimate the criterion validity of the Back Range of Motion (BROM II) and Electronic Digital Inclinometer (EDI-320) devices. METHODS. This study compared the range of motion measurements of low back pain (LBP) patients taken with the BROM II and EDI-320 with measurements using the double inclinometer (DI) method as the gold standard. Forty subjects with LBP volunteered for the study. The subjects were asked to do three forward flexion movements. A measurement was taken with each of the three different devices for each movement.

RESULTS

The BROM II demonstrated good linear relationship (Pearson r = 0.78; 95% CI: 0.78-0.94) and the EDI-320 very good linear relationship (Pearson r = 0.88; 95% CI: 0.62-0.89) with the gold standard, the DI.

CONCLUSIONS

The Pearson correlation value indicates good validity of the EDI-320 in our sample of LBP patients. Although a good correlation was established for the BROM II, the significant difference of the mean ROM reported for this instrument compared to the gold standard data suggests that the BROM II actually measures ROM differently. Our results suggest that the EDI 320 is clinically useful in providing objective and valid data for outcome measures in a population with LBP. More research is needed on the BROM II before we can make final conclusion on its use in clinical settings as an outcome measure.

摘要

目的

评估背部活动范围测量仪(BROM II)和电子数字倾角仪(EDI - 320)的标准效度。方法:本研究将BROM II和EDI - 320测量的腰痛(LBP)患者的活动范围与采用双倾角仪(DI)法测量的结果进行比较,以双倾角仪法作为金标准。40名LBP患者自愿参与本研究。要求受试者进行三次前屈动作。每次动作使用三种不同设备分别进行测量。结果:BROM II与金标准DI显示出良好的线性关系(Pearson r = 0.78;95%置信区间:0.78 - 0.94),EDI - 320与金标准DI显示出非常好的线性关系(Pearson r = 0.88;95%置信区间:0.62 - 0.89)。结论:Pearson相关值表明EDI - 320在我们的LBP患者样本中具有良好的效度。虽然BROM II也建立了良好的相关性,但该仪器报告的平均活动范围与金标准数据存在显著差异,这表明BROM II实际测量活动范围的方式有所不同。我们的结果表明,EDI - 320在为LBP人群的结局测量提供客观有效数据方面具有临床实用性。在我们能够就BROM II在临床环境中作为结局测量工具的使用得出最终结论之前,还需要对其进行更多研究。

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