Lak Asad M, Segar David J, McDannold Nathan, White Phillip Jason, Cosgrove Garth Rees
Department of Neurosurgery, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States.
Department of Radiology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States.
Front Neurol. 2022 Feb 18;13:743649. doi: 10.3389/fneur.2022.743649. eCollection 2022.
MRgFUS thalamotomy has gained popularity as an FDA approved, non-invasive treatment for patients with Essential Tremor and tremor predominant Parkinson's Disease. We present our initial clinical experience with 160 consecutive cases of MRgFUS thalamotomy and describe the clinical outcomes with long term follow-up.
A retrospective chart review of all patients who underwent MRgFUS thalamotomy at our institution was performed. CRST Part A tremor scores were obtained pre-operatively and at each follow-up visit along with an assessment of side effects (SE). All patients had a post-operative MRI within 24 h to determine the location, size, and extent of the MRgFUS lesion.
One hundred and sixty unilateral MRgFUS Thalamotomies (Left, = 128; Right, = 32) were performed for medically refractory essential Tremor ( = 150) or tremor predominant Parkinson's disease ( = 10). Mean age at surgery was 75 Years (range: 48-93) and the mean skull density ratio (SDR) was 0.48 (range: 0.32-0.75; median: 0.46). In ET patients, both rest and postural tremor was abolished acutely and remained so at follow-up whereas intention tremor was reduced acutely by 93% below baseline, 87% at 3 months, 83.0% at 1-year, and 78% at 2 years. On post-operative day 1, the most common SE's included imbalance (57%), sensory disturbances (25%), and dysmetria (11%). All adverse events were rated as mild on the Clavien-Dindo Scale and improved over time. At 2-years follow-up, imbalance was seen in 18%, sensory disturbance in 10% and dysmetria in 8% patients. Mean clinical follow-up for all patients was 14 months (range: 1-48 months).
MRgFUS thalamotomy is a safe and effective procedure for long term improvement of unilateral tremor symptoms, with the most common side-effects being imbalance and sensory disturbance.
磁共振引导聚焦超声丘脑切开术已成为一种经美国食品药品监督管理局批准的、用于治疗特发性震颤和震颤为主型帕金森病患者的非侵入性治疗方法。我们介绍了连续160例磁共振引导聚焦超声丘脑切开术的初步临床经验,并描述了长期随访的临床结果。
对在我们机构接受磁共振引导聚焦超声丘脑切开术的所有患者进行回顾性病历审查。术前及每次随访时获取CRST A部分震颤评分,并评估副作用(SE)。所有患者在术后24小时内进行MRI检查,以确定磁共振引导聚焦超声损伤的位置、大小和范围。
对160例难治性特发性震颤(n = 150)或震颤为主型帕金森病(n = 10)患者进行了单侧磁共振引导聚焦超声丘脑切开术(左侧,n = 128;右侧,n = 32)。手术时的平均年龄为75岁(范围:48 - 93岁),平均颅骨密度比(SDR)为0.48(范围:0.32 - 0.75;中位数:0.46)。在特发性震颤患者中,静息和姿势性震颤在急性期消失,随访时仍保持消失,而意向性震颤在急性期比基线降低93%,3个月时降低87%,1年时降低83.0%,2年时降低78%。术后第1天,最常见的副作用包括平衡失调(57%)、感觉障碍(25%)和辨距不良(11%)。所有不良事件根据Clavien - Dindo量表评为轻度,并随时间改善。在2年随访时,18%患者出现平衡失调,10%患者出现感觉障碍,8%患者出现辨距不良。所有患者的平均临床随访时间为14个月(范围:1 - 48个月)。
磁共振引导聚焦超声丘脑切开术是一种安全有效的手术,可长期改善单侧震颤症状,最常见的副作用是平衡失调和感觉障碍。