The Role of Microelectrode Recording in Deep Brain Stimulation Surgery for Parkinson’s Disease: A Systematic Review and Meta-Analysis

帕金森病 脑深部刺激 神经科学 微电极 医学 荟萃分析 物理医学与康复 疾病 心理学 内科学 化学 电极 物理化学
作者
Saman Vinke,Martin Geerlings,Ashok K. Selvaraj,Dejan Georgiev,Bastiaan R. Bloem,Rianne A.J. Esselink,Ronald Bartels
出处
期刊:Journal of Parkinson's disease [IOS Press]
卷期号:12 (7): 2059-2069 被引量:22
标识
DOI:10.3233/jpd-223333
摘要

Background: STN-DBS is a cornerstone in the treatment of advanced Parkinson’s disease (PD). The traditional approach is to use an awake operative technique with microelectrode recording (MER). However, more centers start using an asleep MRI-guided technique without MER. Objective: We systematically reviewed the literature to compare STN-DBS surgery with and without MER for differences in clinical outcome. Methods: We systematically searched PubMed, Embase, MEDLINE, and Web of Science databases for randomized clinical trials and consecutive cohort studies published between 01-01-2000 and 26-08-2021, that included at least 10 PD patients who had received bilateral STN-DBS. Results: 2,129 articles were identified. After abstract screening and full-text review, 26 studies were included in the final analysis, comprising a total of 34 study groups (29 MER and 5 non-MER). The standardized mean difference (SMD) in change in motor symptoms between baseline (OFF medication) and 6–24 months follow-up (OFF medication and ON stimulation) was 1.64 for the MER group and 1.87 for non-MER group ( p = 0.59). SMD in change in levodopa equivalent daily dose (LEDD) was 1.14 for the MER group and 0.65 for non-MER group ( p < 0.01). Insufficient data were available for comparative analysis of PDQ-39 and complications. Conclusion: The change in motor symptoms from baseline to follow-up did not differ between studies that used MER and those that did not. The postoperative reduction in LEDD from baseline to follow-up was greater in the MER-group. In the absence of high-quality studies comparing both methods, there is a clear need for a well-designed comparative trial.
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