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一款用于客观监测退行性颈椎脊髓病患者功能结局的智能手机应用程序的可靠性:观察性研究。

Reliability of a Smartphone App to Objectively Monitor Performance Outcomes in Degenerative Cervical Myelopathy: Observational Study.

作者信息

Yanez Touzet Alvaro, Houhou Tatiana, Rahic Zerina, Kolias Angelos, Yordanov Stefan, Anderson David B, Laufer Ilya, Li Maggie, Grahovac Gordan, Kotter Mark Rn, Davies Benjamin M

机构信息

School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.

MoveMed Ltd., Cambridge, United Kingdom.

出版信息

JMIR Form Res. 2024 May 24;8:e56889. doi: 10.2196/56889.

Abstract

BACKGROUND

Developing new clinical measures for degenerative cervical myelopathy (DCM) is an AO Spine RECODE-DCM Research, an international and multi-stakeholder partnership, priority. Difficulties in detecting DCM and its changes cause diagnostic and treatment delays in clinical settings and heightened costs in clinical trials due to elevated recruitment targets. Digital outcome measures can tackle these challenges due to their ability to measure disease remotely, repeatedly, and more economically.

OBJECTIVE

The aim of this study is to assess the reliability of the MoveMed battery of performance outcome measures.

METHODS

A prospective observational study in decentralized secondary care was performed in England, United Kingdom. The primary outcome was to determine the test-retest reliability of the MoveMed performance outcomes using the intraclass correlation (ICC) of agreement . The secondary outcome was to determine the measurement error of the MoveMed performance outcomes using both the SE of the mean (SEM) of agreement and the smallest detectable change (SDC) of agreement . Criteria from the Consensus-Based Standards for the Selection of Health Measurement Instruments (COSMIN) manual were used to determine adequate reliability (ie, ICC of agreement ≥0.7) and risk of bias. Disease stability was controlled using 2 minimum clinically important difference (MCID) thresholds obtained from the literature on the patient-derived modified Japanese Orthopaedic Association (p-mJOA) score, namely, MCID ≤1 point and MCID ≤2 points.

RESULTS

In total, 7 adults aged 59.5 (SD 12.4) years who live with DCM and possess an approved smartphone participated in the study. All tests demonstrated moderate to excellent test-retest coefficients and low measurement errors. In the MCID ≤1 group, ICC of agreement values were 0.84-0.94 in the fast tap test, 0.89-0.95 in the hold test, 0.95 in the typing test, and 0.98 in the stand and walk test. SEM of agreement values were ±1 tap, ±1%-3% stability score points, ±0.06 keys per second, and ±10 steps per minute, respectively. SDC of agreement values were ±3 taps, ±4%-7% stability score points, ±0.2 keys per second, and ±27 steps per minute, respectively. In the MCID ≤2 group, ICC of agreement values were 0.61-0.91, 0.75-0.77, 0.98, and 0.62, respectively; SEM of agreement values were ±1 tap, ±2%-4% stability score points, ±0.06 keys per second, and ±10 steps per minute, respectively; and SDC of agreement values were ±3-7 taps, ±7%-10% stability score points, ±0.2 keys per second, and ±27 steps per minute, respectively. Furthermore, the fast tap, hold, and typing tests obtained sufficient ratings (ICC of agreement ≥0.7) in both MCID ≤1 and MCID ≤2 groups. No risk of bias factors from the COSMIN Risk of Bias checklist were recorded.

CONCLUSIONS

The criteria from COSMIN provide "very good" quality evidence of the reliability of the MoveMed tests in an adult population living with DCM.

摘要

背景

开发用于退行性脊髓型颈椎病(DCM)的新临床测量方法是AO脊柱RECODE - DCM研究的重点,该研究是一项国际多利益相关方合作项目。在临床环境中,检测DCM及其变化存在困难,这导致诊断和治疗延迟,并且由于提高了招募目标,临床试验成本增加。数字结局测量方法因其能够远程、重复且更经济地测量疾病,从而可以应对这些挑战。

目的

本研究旨在评估MoveMed性能结局测量组合的可靠性。

方法

在英国英格兰的分散式二级医疗中进行了一项前瞻性观察研究。主要结局是使用一致性组内相关系数(ICC)来确定MoveMed性能结局的重测可靠性。次要结局是使用一致性均值标准误(SEM)和一致性最小可检测变化(SDC)来确定MoveMed性能结局的测量误差。使用基于共识的健康测量工具选择标准(COSMIN)手册中的标准来确定足够的可靠性(即一致性ICC≥0.7)和偏倚风险。使用从关于患者衍生的改良日本骨科协会(p - mJOA)评分的文献中获得的2个最小临床重要差异(MCID)阈值来控制疾病稳定性,即MCID≤1分和MCID≤2分。

结果

共有7名年龄为59.5(标准差12.4)岁、患有DCM且拥有经批准智能手机的成年人参与了该研究。所有测试均显示出中度至优秀的重测系数和低测量误差。在MCID≤1组中,快速点击测试的一致性ICC值为0.84 - 0.94,保持测试为0.89 - 0.95,打字测试为0.95,站立和行走测试为0.98。一致性SEM值分别为±1次点击、±1% - 3%稳定性得分点、±0.06键/秒和±10步/分钟。一致性SDC值分别为±3次点击、±4% - 7%稳定性得分点、±0.2键/秒和±27步/分钟。在MCID≤2组中,一致性ICC值分别为0.61 - 0.91、0.75 - 0.77、0.98和0.62;一致性SEM值分别为±1次点击、±2% - 4%稳定性得分点、±0.06键/秒和±10步/分钟;一致性SDC值分别为±3 - 7次点击、±7% - 10%稳定性得分点、±0.2键/秒和±27步/分钟。此外,快速点击、保持和打字测试在MCID≤1和MCID≤2组中均获得了足够的评分(一致性ICC≥0.7)。未记录到COSMIN偏倚风险清单中的偏倚风险因素。

结论

COSMIN的标准为MoveMed测试在患有DCM的成年人群中的可靠性提供了“非常好”质量的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcf1/11161705/0e34a50a6373/formative_v8i1e56889_fig1.jpg

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