Department of Rehabilitation Medicine, Erasmus MC University Medical Center Rotterdam, Doctor Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Rijndam Rehabilitation, Rotterdam, The Netherlands.
J Neuroeng Rehabil. 2022 Feb 11;19(1):16. doi: 10.1186/s12984-022-00996-7.
Many diagnostic robotic devices have been developed to quantify viscoelastic properties and spasticity of patients with upper motor neuron lesions. However, in clinical practice, subjective and nonvalid clinical scales are still commonly used. To understand the limited use of diagnostic robotic devices assessing viscoelastic joint properties and spasticity in clinical practice, we evaluate the diagnostic level of evidence of studies on these devices.
A systematic literature review was performed using multiple databases. Two of the authors independently screened all articles. Studies investigating human subjects diagnosed with stroke or cerebral palsy, measured with a mechanical device to assess viscoelastic joint properties and/or spasticity of an extremity. All articles were assigned a diagnostic level of evidence, which was established with a classification strategy based on the number of participants and the design of the study, from a Level 0 (less than 10 subjects) to a Level IV, reporting the long-term clinical consequences in daily care.
Fifty-nine articles were included. Most studies measured the upper limb (64%) in stroke patients (81%). The highest level of evidence found was Level IIa (53%); these studies correlated the test values of the robotic device with a clinical test or within subgroups. Level 0 (30%) and Level I (17%; determining the range of values of the robotic test) were also common. None of the studies tested their device for diagnostic accuracy (Level III), clinical added value (Level IV).
The diagnostic evidence needed for implementing robotic devices in clinical practice is lacking. Our findings indicate that more effort should be invested in studying diagnostic accuracy (Level III) or added value for clinical care (Level IV); only these studies can provide clinicians with evidence that robotic devices have added value above the currently-used clinical scales.
许多诊断机器人设备已经被开发出来,以量化上运动神经元损伤患者的粘弹性特性和痉挛程度。然而,在临床实践中,仍然普遍使用主观的和未经验证的临床量表。为了了解在临床实践中评估粘弹性关节特性和痉挛程度的诊断机器人设备的使用受限,我们评估了这些设备的研究的诊断证据水平。
使用多个数据库进行了系统的文献回顾。两位作者独立筛选了所有文章。研究对象为被诊断为中风或脑瘫的人类患者,使用机械设备评估肢体的粘弹性关节特性和/或痉挛程度。所有文章都根据参与者数量和研究设计的分类策略被分配了诊断证据水平,从 0 级(少于 10 名受试者)到 4 级,报告了在日常护理中对长期临床后果的影响。
共纳入 59 篇文章。大多数研究测量了中风患者的上肢(64%)(81%)。发现的最高证据水平是 IIa 级(53%);这些研究将机器人设备的测试值与临床测试或亚组进行了相关性分析。0 级(30%)和 I 级(17%;确定机器人测试的范围值)也很常见。没有一项研究测试他们的设备的诊断准确性(III 级)或临床附加值(IV 级)。
在临床实践中实施机器人设备所需的诊断证据不足。我们的研究结果表明,应该投入更多的努力来研究诊断准确性(III 级)或对临床护理的附加值(IV 级);只有这些研究才能为临床医生提供证据,证明机器人设备具有高于目前使用的临床量表的附加值。