Department of Neurology, Hospital Universitario Burgos, Spain; University of Burgos, Spain.
Department of Neurology, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, USA.
Parkinsonism Relat Disord. 2021 Dec;93:85-88. doi: 10.1016/j.parkreldis.2021.11.016. Epub 2021 Nov 19.
The minimal clinically important difference (MCID) describes the smallest change in an outcome that is considered clinically meaningful. The Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) is the most frequently rating scale assessing the efficacy of deep brain stimulation therapy (DBS) for dystonia. To expand our understanding, we evaluated the MCID thresholds for the BFMDRS motor subscale (MS) using physician-reported outcomes.
We assessed the MCID thresholds for the BFMDRS using movement disorder specialist ratings of videotapes from patients with genetically determined dystonia (Tor1A and THAP1) who underwent bilateral globus pallidum internum (GPi) DBS. We calculated the effect size of the BFMDRS-MS change and determined the MCID thresholds using the Clinical Global Impression of Change (CGIC).
Twelve participants with a median age at DBS of 44.5 (range:27-68) had baseline and follow-up BFMDRS-MS with a median post-DBS follow-up of 5.5 years. Based on descriptive analysis, patients with good improvement after DBS according to the CGIC [8/12 (67%)] had a median BFMDRS-MS score reduction of 77% [Interquartile range (IQR):66.2;91.0) with an effect size of 0.39, and those with non-improvement [4/12 (33%)], had a median BFMDRS-MS score reduction of 62% (IQR:36.6;83.6).
Our MCID estimates can be utilized in clinical practice in judging clinical relevance. However, further larger, powered studies are needed to simultaneously determine and compare MCID using patient and physician-reported outcomes in segmental and generalized dystonia in genetic and non-genetic populations.
最小临床重要差异(MCID)描述了结果中被认为具有临床意义的最小变化。 Burke-Fahn-Marsden 肌张力障碍评定量表(BFMDRS)是评估深部脑刺激疗法(DBS)治疗肌张力障碍疗效最常用的评定量表。为了扩大我们的理解,我们使用医生报告的结果评估了 BFMDRS 运动分量表(MS)的 MCID 阈值。
我们使用运动障碍专家对接受双侧苍白球内侧(GPi)DBS 的遗传性肌张力障碍(Tor1A 和 THAP1)患者的录像带进行评估,计算了 BFMDRS-MS 变化的效应量,并使用临床总体印象变化量表(CGIC)确定了 MCID 阈值。
12 名参与者的 DBS 中位年龄为 44.5 岁(范围:27-68 岁),基线和随访时均有 BFMDRS-MS,DBS 后中位随访时间为 5.5 年。根据描述性分析,根据 CGIC 评估为 DBS 后改善良好的患者[8/12(67%)],BFMDRS-MS 评分降低中位数为 77%[四分位距(IQR):66.2;91.0),效应量为 0.39,而改善不佳的患者[4/12(33%)],BFMDRS-MS 评分降低中位数为 62%(IQR:36.6;83.6)。
我们的 MCID 估计值可用于临床实践,以判断临床相关性。然而,需要进一步进行更大、更有力的研究,以同时使用患者和医生报告的结果,在遗传和非遗传人群的节段性和全身性肌张力障碍中确定和比较 MCID。