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DEEP BRAIN STIMULATION
Philip A. Hanna, MD
Parkinson's Disease and Movement Disorders Center
New Jersey Neuroscience Institute
Edison, New Jersey

Essential tremor (ET) and Parkinson's disease (PD) are the two most common disorders with severe tremor. Despite optimal medical therapy, a number of patients continue to have disabling tremor, and these patients may be candidates for surgical intervention. Until recently, thalamotomy was the neurosurgical treatment of choice in such cases. In this procedure, after making an incision in the scalp and an opening in the skull on the side opposite of the most tremulous limb(s), the surgeon advances an electrode into the thalamus, which contains "pacemakers", or group of nerve cells involved in generating tremor. The surgeon then passes a current through the tip of the electrode thus creating a lesion and stopping the tremor on the opposite side of the body. Although effective, tremor recurs in about 20% of patients, and there is a risk of weakness, numbness, and incoordination on the other side of the body, and changes in speech. 
In the late 1980's Prof. A. Benabid and colleagues in France discovered that tremor can also be relieved by high frequency stimulation of the thalamus and other areas of the brain. This technique, called deep brain stimulation (DBS), involves 1.) a DBSTM lead with four electrodes that are surgically inserted and fixed at the skull, 2.) a wire passing from the scalp area under the skin to 3.) an implantable pulse generator (IPG), a pacemaker-like device, which has adjustable parameters, and which is placed just under the skin in the upper chest area. The patient can turn the DBS system "on" or "off" by placing a magnet over the IPG.
In a recent publication (Ondo et al) patients with ET and PD demonstrated an 83% and 82% reduction, respectively, in contralateral arm tremor. In the ET patients, functional testing and disability scores significantly improved. While similar improvement was seen in tremor in the patients with PD, functional aspects of the disease were not notably improved, likely because thalamic DBS helps tremor but other features of PD such as rigidity, slowness of movement, and gait difficulty. DBS into the subthalamic nucleus and globus pallidus has shown beneficial results not only with regards to these other parkinsonian features, but also in reducing levodopa-related complications such as dyskinesias and fluctuations. 
The major advantage of DBS over lesioning procedures, such as thalamotomy, is that the electrode parameters are adjustable, and thus can be customized to the needs of the individual patient. Additionally, side effects, if they occur, are usually reversible and bilateral stimulation is possible with much reduced risk of speech or swallowing difficulties, compared with bilateral thalamotomy. 

Ondo W, Jankovic J, Schwartz K, Almaguer M, Simpson RK. Unilateral thalamic deep brain stimulation for refractory essential tremor and Parkinson's disease tremor. Neurology 1998;51:1063-1068.

Pollak P, Benabid AL, Krack P, Limousin P, Benazzouz A. Deep brain stimulation. In: Jankovic J, Tolosa E, eds. Parkinson's Disease and Movement Disorders, 3rd edition, Williams and Wilkins, Baltimore, Maryland, 1998:1085-1102.

Hanna PA, Jankovic J. Comparison of mouse bioassay and immunoprecipitation assay for botulinum toxin antibodies. J Neurol Neurosurg Psychiatry 1999;66:612-616.

Hanna PA, Kwak CH, Jankovic J. Botulinum toxin in the treatment of tics. 3rd International Scientific Symposium on Tourette Syndrome. New York, NY, June 4-6, 1999. 

Hanna PA, Jankovic J. Mouse bioassay versus western blot assay for botulinum toxin antibodies: correlation with clinical response. Neurology 1998;50:1624-1629.

Jankovic J. Use of botulinum toxin in neurology. In: Kennard C, ed. Recent Advances in Clinical Neurology. Vol. 8, Churchill Livingstone, London, 1995:89-110.