Chen Tsinsue, Mirzadeh Zaman, Ponce Francisco A
Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.
Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.
World Neurosurg. 2017 Sep;105:191-198. doi: 10.1016/j.wneu.2017.05.042. Epub 2017 May 16.
Although performing deep brain stimulation (DBS) with the patient under general anesthesia without microelectrode recording (MER) or intraoperative test stimulation (ITS) for movement disorders ("asleep" DBS) has become increasingly popular, its feasibility is based on the untested assumption that stereotactic accuracy correlates with positive clinical outcomes. To investigate outcomes after asleep DBS without MER or neurophysiological testing, we reviewed the medical literature on the topic.
We searched PubMed to identify all studies reporting clinical outcomes for patients who underwent DBS without MER or ITS for Parkinson disease (PD) or essential tremor (ET).
We identified 9 studies with level 3b (n = 3) or level 4 evidence (n = 6). Eight PD studies (220 patients) reported asleep placement of 431 electrodes (341 subthalamic nucleus, 90 globus pallidus interna). Unified Parkinson Disease Rating Scale motor examination-III scores for 208 patients demonstrated significant improvement (40.2%-65%) at 6-12 months. The levodopa equivalent daily dose for 115 patients was significantly reduced (14%-49.3%) at 6-12 months in 103 patients. Two studies with a comparison cohort undergoing "awake" DBS with MER found no differences in postoperative Unified Parkinson Disease Rating Scale-III improvement or levodopa equivalent daily dose reduction. One study of asleep DBS for ET found no difference in functional outcomes between 17 patients undergoing asleep ventral intermediate nucleus DBS and 40 patients undergoing awake placement with ITS.
Initial evidence suggests that asleep DBS can be performed safely for PD and ET with good clinical outcomes. Long-term follow-up, larger cohorts, and double-armed studies are needed to validate these initial results.
尽管在全身麻醉下对运动障碍患者进行无微电极记录(MER)或术中测试刺激(ITS)的深部脑刺激(DBS)(“睡眠中”DBS)越来越普遍,但其可行性基于未经检验的假设,即立体定向准确性与良好的临床结果相关。为了研究无MER或神经生理学测试的睡眠中DBS后的结果,我们回顾了关于该主题的医学文献。
我们在PubMed上进行搜索,以识别所有报告了无MER或ITS的帕金森病(PD)或特发性震颤(ET)患者接受DBS的临床结果的研究。
我们确定了9项具有3b级(n = 3)或4级证据(n = 6)的研究。8项PD研究(220例患者)报告了431个电极的睡眠中植入(341个丘脑底核,90个内侧苍白球)。208例患者的统一帕金森病评定量表运动检查III评分在6至12个月时显示出显著改善(40.2%-65%)。103例患者中115例患者的左旋多巴等效日剂量在6至12个月时显著降低(14%-49.3%)。两项对有MER的“清醒”DBS比较队列的研究发现,术后统一帕金森病评定量表III改善或左旋多巴等效日剂量降低方面无差异。一项对ET的睡眠中DBS研究发现,17例接受睡眠中腹中间核DBS的患者与40例接受清醒植入并进行ITS的患者在功能结果上无差异。
初步证据表明,睡眠中DBS可安全用于PD和ET,临床结果良好。需要长期随访、更大的队列和双臂研究来验证这些初步结果。