Literature DB >> 12628062

Parkinson's Disease: Surgical Options.

Helen Bronte-Stewart1.   

Abstract

Surgical therapy for Parkinson's disease (PD) has been a treatment option for over 100 years. Advances in the knowledge of basal ganglia physiology and in techniques of stereotactic neurosurgery and neuroimaging have allowed more accurate placement of lesions or "brain pacemakers" in the sensorimotor regions of target nuclei. This, in turn, has led to improved efficacy with fewer complications than in the past. Currently, bilateral deep brain stimulation (DBS) of the subthalamic nucleus (STN) or the internal segment of the globus pallidus (GPi) is the preferred option (and is approved by the US Food and Drug Administration) for the surgical treatment of PD. The most important predictors for outcome for DBS for PD are patient selection and electrode location. Patients should have a documented preoperative improvement from dopaminergic medication of at least 30% in the patient's Unified Parkinson's Disease Rating Scale motor disability scores. A levodopa challenge may be needed to document the best "on" state. Dementia or active cognitive decline must be excluded. Active psychiatric disease should be treated preoperatively. Patients should be motivated, with good support systems, and committed to the postoperative management of DBS therapy. Deep brain stimulation should be considered when the patient begins to experience dyskinesia and on-off fluctuations despite optimal medical therapy. Deep brain stimulation is not a good option at the final stages of the disease because of the increased incidence of dementia and severe comorbidity. The DBS electrode should be placed in the sensorimotor region of the GPi or STN. Subthalamic nucleus and GPi DBS can improve all motor aspects of PD, as well as predictable "on" time, without dyskinesia or fluctuations. On average, STN DBS results in a greater reduction of dopaminergic medication compared with GPi DBS. Because of the smaller size of the target region, the pulse generator battery life is longer with STN then with GPi DBS. Deep brain stimulation programming is a skill that is readily learned and may be required of all neurologists in the future. Emerging surgical therapies are restorative, and they aim to replace or regenerate degenerating dopaminergic neurons. These include embryonic mesencephalic tissue transplantation, human embryonic stem cell transplantation, and gene-derived methods of intracerebral implantation of growth factors and dopamine- producing cell lines. It will be important to determine whether DBS, if performed before the onset of motor response complications to medical therapy, may prevent this stage of disease altogether or delay it for a significant period of time. The same question applies to the future with restorative therapy.

Entities:  

Year:  2003        PMID: 12628062     DOI: 10.1007/s11940-003-0004-1

Source DB:  PubMed          Journal:  Curr Treat Options Neurol        ISSN: 1092-8480            Impact factor:   3.598


  121 in total

1.  Cognitive functioning after subthalamic nucleotomy for refractory Parkinson's disease.

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Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-07       Impact factor: 10.154

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Journal:  J Neurosurg       Date:  1992-01       Impact factor: 5.115

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Journal:  Brain Res       Date:  1990-06-04       Impact factor: 3.252

5.  Improvement of severe postural cerebellar tremor in multiple sclerosis by chronic thalamic stimulation.

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Journal:  Mov Disord       Date:  1996-09       Impact factor: 10.338

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Journal:  N Engl J Med       Date:  2000-06-08       Impact factor: 91.245

Review 7.  Posteroventral medial pallidotomy in Parkinson's disease.

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Journal:  J Neurol       Date:  1999-09       Impact factor: 4.849

8.  Neuropsychological outcome of GPi pallidotomy and GPi or STN deep brain stimulation in Parkinson's disease.

Authors:  L L Trépanier; R Kumar; A M Lozano; A E Lang; J A Saint-Cyr
Journal:  Brain Cogn       Date:  2000-04       Impact factor: 2.310

9.  Behavioral and cellular protection of rat dopaminergic neurons by an adenoviral vector encoding glial cell line-derived neurotrophic factor.

Authors:  D L Choi-Lundberg; Q Lin; T Schallert; D Crippens; B L Davidson; Y N Chang; Y L Chiang; J Qian; L Bardwaj; M C Bohn
Journal:  Exp Neurol       Date:  1998-12       Impact factor: 5.330

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  3 in total

1.  Parkinson's disease and motor fluctuations.

Authors:  Vanessa K Hinson
Journal:  Curr Treat Options Neurol       Date:  2010-05       Impact factor: 3.598

2.  Considerations regarding the etiology and future treatment of autosomal recessive versus idiopathic Parkinson disease.

Authors:  Tohru Kitada; Julianna J Tomlinson; Hei Sio Ao; David A Grimes; Michael G Schlossmacher
Journal:  Curr Treat Options Neurol       Date:  2012-06       Impact factor: 3.598

Review 3.  Long term motor complications of levodopa: clinical features, mechanisms, and management strategies.

Authors:  B R Thanvi; T C N Lo
Journal:  Postgrad Med J       Date:  2004-08       Impact factor: 2.401

  3 in total

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