Cargando…
Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature
BACKGROUND: Rare movement disorders (RMDs) throw remarkable challenges to their appropriate management particularly when they are medically refractory. We studied the outcome of functional neurosurgery among patients with RMDs. METHODS: Retrospective chart-review from 2006 to 2021 of patients with R...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ubiquity Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231568/ https://www.ncbi.nlm.nih.gov/pubmed/35811746 http://dx.doi.org/10.5334/tohm.693 |
_version_ | 1784735373933412352 |
---|---|
author | Dhar, Debjyoti Holla, Vikram Venkappayya Kamble, Nitish Yadav, Ravi Srinivas, Dwarakanath Pal, Pramod Kumar |
author_facet | Dhar, Debjyoti Holla, Vikram Venkappayya Kamble, Nitish Yadav, Ravi Srinivas, Dwarakanath Pal, Pramod Kumar |
author_sort | Dhar, Debjyoti |
collection | PubMed |
description | BACKGROUND: Rare movement disorders (RMDs) throw remarkable challenges to their appropriate management particularly when they are medically refractory. We studied the outcome of functional neurosurgery among patients with RMDs. METHODS: Retrospective chart-review from 2006 to 2021 of patients with RMDs who underwent either Deep brain Stimulation (DBS) or lesional surgeries in the department of Neurology and Neurosurgery at a tertiary care centre. RESULTS: Seventeen patients were included. Generalized dystonia (11 patients, 64.7%) and tremor (5 patients, 29.4%) were the most common indication for surgery whereas, Wilson’s disease (8 patients, 47.1%) and Neurodegeneration with brain iron accumulation (5 patients, 29.4%) were the most common aetiology. Sixteen patients (94.1%) had objective clinical improvement. Significant improvement was noted in the dystonia motor scores both at 6-months and 12-months follow-up (n = 11, p-value of <0.01 and 0.01 respectively). Comparison between DBS and lesional surgery showed no significant difference in the outcomes (p = 0.95 at 6-months and p = 0.53 at 12-months), with slight worsening of scores in the DBS arm at 12-months. Among five patients of refractory tremor with Wilson’s disease, there was remarkable improvement in the tremor scores by 85.0 ± 7.8% at the last follow-up. Speech impairment was the main complication observed with most of the other adverse events either transient or reversible. DISCUSSION: Surgical options should be contemplated among patients with disabling medically refractory RMDs irrespective of the aetiology. Key to success lies in appropriate patient selection. In situations when DBS is not feasible, lesional surgeries can offer an excellent alternative with comparable efficacy and safety. |
format | Online Article Text |
id | pubmed-9231568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Ubiquity Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92315682022-07-08 Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature Dhar, Debjyoti Holla, Vikram Venkappayya Kamble, Nitish Yadav, Ravi Srinivas, Dwarakanath Pal, Pramod Kumar Tremor Other Hyperkinet Mov (N Y) Article BACKGROUND: Rare movement disorders (RMDs) throw remarkable challenges to their appropriate management particularly when they are medically refractory. We studied the outcome of functional neurosurgery among patients with RMDs. METHODS: Retrospective chart-review from 2006 to 2021 of patients with RMDs who underwent either Deep brain Stimulation (DBS) or lesional surgeries in the department of Neurology and Neurosurgery at a tertiary care centre. RESULTS: Seventeen patients were included. Generalized dystonia (11 patients, 64.7%) and tremor (5 patients, 29.4%) were the most common indication for surgery whereas, Wilson’s disease (8 patients, 47.1%) and Neurodegeneration with brain iron accumulation (5 patients, 29.4%) were the most common aetiology. Sixteen patients (94.1%) had objective clinical improvement. Significant improvement was noted in the dystonia motor scores both at 6-months and 12-months follow-up (n = 11, p-value of <0.01 and 0.01 respectively). Comparison between DBS and lesional surgery showed no significant difference in the outcomes (p = 0.95 at 6-months and p = 0.53 at 12-months), with slight worsening of scores in the DBS arm at 12-months. Among five patients of refractory tremor with Wilson’s disease, there was remarkable improvement in the tremor scores by 85.0 ± 7.8% at the last follow-up. Speech impairment was the main complication observed with most of the other adverse events either transient or reversible. DISCUSSION: Surgical options should be contemplated among patients with disabling medically refractory RMDs irrespective of the aetiology. Key to success lies in appropriate patient selection. In situations when DBS is not feasible, lesional surgeries can offer an excellent alternative with comparable efficacy and safety. Ubiquity Press 2022-06-20 /pmc/articles/PMC9231568/ /pubmed/35811746 http://dx.doi.org/10.5334/tohm.693 Text en Copyright: © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dhar, Debjyoti Holla, Vikram Venkappayya Kamble, Nitish Yadav, Ravi Srinivas, Dwarakanath Pal, Pramod Kumar Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature |
title | Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature |
title_full | Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature |
title_fullStr | Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature |
title_full_unstemmed | Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature |
title_short | Surgical Outcomes in Rare Movement Disorders: A Report of Seventeen Patients from India and Review of Literature |
title_sort | surgical outcomes in rare movement disorders: a report of seventeen patients from india and review of literature |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231568/ https://www.ncbi.nlm.nih.gov/pubmed/35811746 http://dx.doi.org/10.5334/tohm.693 |
work_keys_str_mv | AT dhardebjyoti surgicaloutcomesinraremovementdisordersareportofseventeenpatientsfromindiaandreviewofliterature AT hollavikramvenkappayya surgicaloutcomesinraremovementdisordersareportofseventeenpatientsfromindiaandreviewofliterature AT kamblenitish surgicaloutcomesinraremovementdisordersareportofseventeenpatientsfromindiaandreviewofliterature AT yadavravi surgicaloutcomesinraremovementdisordersareportofseventeenpatientsfromindiaandreviewofliterature AT srinivasdwarakanath surgicaloutcomesinraremovementdisordersareportofseventeenpatientsfromindiaandreviewofliterature AT palpramodkumar surgicaloutcomesinraremovementdisordersareportofseventeenpatientsfromindiaandreviewofliterature |