From the Centre d'Investigation Clinique, Department of Neurology (H.P.-C., T.R., P. Damier), Department of Medical Evaluation and Epidemiology (J.-M.N.), and Department of Neurosurgery (S.R.), CHU Nantes, INSERM; Hôpital Neurologique (S.T., C.L., P.M.), Hospices Civils de Lyon, Université de Lyon 1; Centre d'Investigation Clinique, Department of Neurology (C.B.-C., F.O.-M., O.R.), CHU Toulouse, INSERM; Departments of Psychiatry (I.C.) and Neurology (P. Derost, M.U.), CHU Clermont-Ferrand; Departments of Neurosurgery (E.C.) and Neurology (D.G., P.B.), Bordeaux CHU; and the Departments of Neurology (A.E., T.W.) and Neurosurgery (J.R.), Assistance Publique Hôpitaux de Marseille, France.
Neurology. 2016 Feb 16;86(7):651-9. doi: 10.1212/WNL.0000000000002370. Epub 2016 Jan 20.
To confirm the efficacy and safety of deep brain stimulation (DBS) of the internal part of the globus pallidus in improving severe tardive dyskinesia (TD).
Nineteen patients with severe pharmacoresistant TD were included. All were assessed at baseline and at 3, 6 (main outcome measure), and 12 months, and in the long term (6-11 years) for 14 patients, after bilateral pallidal DBS, using motor scales (Extrapyramidal Symptoms Rating Scale [ESRS], Abnormal Involuntary Movement Scale [AIMS]), cognitive scales, and a psychiatric assessment. At 6 months, a double-blind ESRS evaluation was performed in the stimulation "on" and stimulation "off" conditions.
At 6 months, all patients had a decrease of more than 40% on the ESRS. The efficacy of the procedure was confirmed by a double-blind evaluation. This improvement was maintained at 12 months (ESRS: decrease of 58% [21%-81%];
decrease of 50% [7%-77%]) and in the long term (ESRS: decrease of 60% [22%-90%];
decrease of 63% [14%-94%], n = 14). All the subscores of the ESRS (parkinsonism, dystonia, and chorea) and of the AIMS (facial, oral, extremities, and trunk movements) improved. Despite psychiatric comorbidities at baseline, cognitive and psychiatric tolerability of the procedure was excellent. No cognitive decline was observed and mood was improved in most of the patients.
Pallidal DBS procedure should be considered as a therapeutic option in disabling TD refractory to medical treatment.
This study provides Class II evidence that in patients with severe pharmacoresistant TD with implanted pallidal leads, the stimulation "on" condition significantly improved ESRS scores compared to the stimulation "off" condition.
确认深部脑刺激(DBS)内侧苍白球对改善严重迟发性运动障碍(TD)的疗效和安全性。
纳入 19 例严重药物难治性 TD 患者。所有患者均在基线时以及 3、6 个月(主要观察指标)、12 个月以及 14 例患者的长期(6-11 年)进行双侧苍白球 DBS 后进行评估,使用运动量表(锥体外系症状评定量表[ESRS]、不自主运动量表[AIMS])、认知量表和精神科评估。在 6 个月时,在刺激“开”和刺激“关”条件下进行双盲 ESRS 评估。
6 个月时,所有患者的 ESRS 评分均下降超过 40%。该程序的疗效通过双盲评估得到证实。这种改善在 12 个月时得到维持(ESRS:下降 58%[21%-81%];AIMS:下降 50%[7%-77%]),并在长期(ESRS:下降 60%[22%-90%];AIMS:下降 63%[14%-94%],n=14)。ESRS 的所有亚评分(帕金森病、肌张力障碍和舞蹈病)和 AIMS(面部、口腔、四肢和躯干运动)均有所改善。尽管基线时存在精神共病,但该程序的认知和精神耐受性仍极佳。大多数患者的认知能力没有下降,情绪也得到改善。
对于药物难治性、致残性 TD 患者,应考虑苍白球 DBS 作为一种治疗选择。
这项研究提供了 II 级证据,表明在植入苍白球导联的严重药物难治性 TD 患者中,与刺激“关”相比,刺激“开”显著改善了 ESRS 评分。