4.7 Article

Long-term effects of pallidal deep brain stimulation in tardive dystonia: a follow-up of 5-14 years

期刊

JOURNAL OF NEUROLOGY
卷 269, 期 7, 页码 3563-3568

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00415-022-10965-8

关键词

Dystonia; Tardive; Pallidal DBS; Long-term effects; DBS and quality of life

资金

  1. German Research Foundation (DFG) [SFB TRR 295, 424778381]
  2. Charite Lydia Rabinowitsch grant
  3. BIH

向作者/读者索取更多资源

This observational study evaluates the long-term effects of deep brain stimulation of the globus pallidus internus (GPi-DBS) in patients with treatment-refractory tardive syndromes. The results show that GPi-DBS is a safe and effective long-term treatment for tardive dyskinesia and tardive dystonia, with significant improvements in involuntary movements and dystonia. Furthermore, three patients were able to stop stimulation after several years without relapse.
Introduction Pallidal DBS is an established treatment for severe isolated dystonia. However, its use in disabling and treatment-refractory tardive syndromes (TS) including tardive dyskinesia and tardive dystonia (TD) is less well investigated and long-term data remain sparse. This observational study evaluates long-term effects of deep brain stimulation (DBS) of the globus pallidus internus (GPi) in patients with medically refractory TS. Methods We retrospectively analyzed a cohort of seven TD patients with bilateral GPi-DBS. Involuntary movements, dystonia and disability were rated at long-term follow-up (LT-FU) after a mean of 122 +/- 33.2 SD months (range 63-171 months) and compared to baseline (BL), short-term (ST-FU; mean 6 +/- 2.0 SD months) and 4-year follow-up (4y-FU; mean 45 +/- 12.3 SD months) using the Abnormal Involuntary Movement Scale (AIMS) and the Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS), respectively. Quality of life and mood were evaluated using the SF36 and Beck Depression Index (BDI) questionnaires, respectively. Results At LT-FU patients had improved by 73% +/- 14.2 SD in involuntary movements and 90% +/- 1.0 SD in dystonia. Mood had improved significantly whereas quality of life remained unchanged compared to baseline. No serious long-lasting stimulation-related adverse events (AEs) were observed. Three patients of this cohort presented without active stimulation and ongoing symptom relief at long-term follow-up after 3-10 years of continuous DBS. Conclusion Pallidal DBS is a safe and effective long-term TD treatment. Even more interesting, three of our patients could stop stimulation after several years of DBS without serious relapse. Larger studies need to explore the phenomenon of ongoing symptom relief after DBS cessation.

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