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MCG Neurosurgery: Movement Disorders Surgery Program
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Surgical Management of Movement Disorders

The Medical College of Georgia movement disorder program is a multidisciplinary program staffed by a neurosurgeon, neurologist, neuropsychologist, physician's assistant, nurse practitioner, and physical therapy with specialization in the care and rehabilitation of patients with movement disorders. The full spectrum of movement disorders is treated. The neurosurgery team has over 20 years experience in the surgical management of movement disorders.

Surgery is considered only after all attempts at conservative management have failed or have provided suboptimal results. The type of surgery varies depending upon the particular movement disorder. In general, significant reduction of abnormal movement and/or tone can be expected in 80% of cases. The incidence of significant postoperative complications is quite low.

The movement disorder staff works closely with referring physicians during evaluation and treatment to maximize continuity of care, particularly in the postoperative period.

In addition to surgery, selected patients with disorders involving localized increased muscle tone (e.g., hemifacial spasm, laryngeal dystonia, torticollis) may be treated with botulinum toxin (BoTox) injections.

Deep Brain Stimulation (DBS) and Parkinson's Disease (PD)
...view video

Currently, DBS is most commonly performed on drug-resistant Parkinson's disease (PD). PD is a degenerative disease of the nervous system. It is due to degeneration of nerve cells in a structure called the substantia nigra. This structure is part of an interconnected system of groups of nerve cells called the basal ganglia or basal nuclei. These structures form a part of the motor system which controls tone and posture. When the substantia nigra degenerates, there is a marked decrease in the neurotransmitter dopamine which is essential for proper function of the basal ganglia. Initially, the majority of PD cases respond well to L-DOPA (Sinement), the precursor of dopamine. However, after 5 or more years of use, patients often respond less consistently and for shorter periods of time. Side effects also begin to begin to appear, most noteably "on-stage" dyskinesias. These are abnormal involuntary movements which usually appear within an hour of the most recent dose of L-DOPA and subside gradually until the next dosage.

DBS of the subthalamic nucleus (STN) is becoming the most commonly performed operation for PD. It has recently been FDA approved. It is effective in alleviating the rigidity, slowness of movement, on stage dyskinesias, and tremor in about 80% of cases. It has also been effective in improving gait and gait freezing, but this usually requires bilateral (i.e., right and left) implants. It is more effective in younger and less disabled patients. It is not effective in cases that have not shown a good response to L-DOPA. In general, it improves signs and symptoms most that are present when a patient is in the "off-state" (the wearing off state of L-DOPA, nearing the time when the next dose is due). The exception to this is the "on-stage" dyskinesias which also improve after STN DBS. DBS patients reduce their dose of L-DOPA an average of 50%.

The surgery is performed under local anesthesia in order to allow testing of the patient during surgery. However, many of the preliminary portions of the operation, which do not require patient cooperation, are performed with patient receiving a rapid-acting intravenous sedative and narcotic in order to maximize comfort.

At MCG, state- of- the- art imaging (MRI), computer workstation, and microelectrode recording equipment is utilized. After sedation, a scalp block is performed and a stereotaxic basering together with a localizer is fixed to the patient's head. High resolution images of the target area are obtained and transferred via ethernet to the computer workstation, which is used to derive the target coordinates and pathway or trajectory for the recording and stimulating electrodes and DBS electrode.

The patient is then taken to the operating room where the basering is fixed to the operating table. The head is shaved, sterilized and draped. After injecting local anesthetic, a transverse frontal incision is made and right and left frontal bur holes (about 1/2 inch diameter) are made The aiming arc is then placed on the basering and the microelectrode guide is attached to it. An array of four microelectrodes is advanced to the right (and subsequently the left) targets with continuous recording of electrical activity. Typically, high frequency and amplitude electrical activity is recorded at the target point and this activity is further amplified with passive movement of the opposite arm. During the recording the patient is usually awake so that recordings from the target site are optimized.


After completion of the recordings, the DBS electrode is introduced to the target area. Proper positioning is confirmed with intraoperative fluoroscopy .Stimulation is performed after the implant to assure that no unwanted motor or speech responses are obtained. None of this is felt by the patient since the brain is not pain-sensitive. The DBS electrode is then locked in place with a silastic ring and ca, and fluoroscopy is repeated to assure proper electrode position. After that the other side is implanted similarly. The pictures below show postoperative MRIs with DBS electrodes in place.


After surgery, patients spend the first postoperative night in the ICU (intensive care unit) for precautionary purposes. They then transfer to a regular room, and usually are discharged home on the third postoperative day.

The patient then returns within one to two weeks to have the two pulse generators implanted as an outpatient procedure. Programming of the stimulators will begin after that.

Patients often notice alleviation of rigidity and bradykinesia (and tremor in cases with tremor) immediately after implantation, even before DBS is begun. Successful implantation not uncommonly leads to transient increase in dyskinesias in the immediate postoperative period. These will usually respond to a decrease in L-DOPA dose.

Other Movement Disorders and Operations
Deep Brain Stimulation (DBS) is also used for essential or familial tremor . This involves the permanent implantation of stimulating electrode (picture) into a different area of the brain called the thalamus. The basic technique is very similar to that of STN DBS. Patients with bilateral tremor will require bilateral implantation, which is done in stages. Depending on the patient's age and overall health the second operation is usually performed three to six months after the first.

Pallidotomy for the most part has been replaced by STN DBS in PD. The technique is similar to DBS except that a permanent lesion is made in a different location instead of implanting a DBS electrode. Pallidotomy has been used successfully for a condition referred to as dystonia which involves increased tone and associated abnormal posturing of trunk and/or limbs depending on the particular disorder. Depending on the etiology of the dystonia, as many as 80% of patients have significant reduction in their dystonia. Pictures 6a and 6b show a typical pallidotomy. Most recently, the FDA has approved pallidal DBS for treatment of certain dystonias.

Thalamotomy is rarely used since the introduction of DBS. Like pallidotomy, it is also a destructive procedure that requires coagulating an approximately six millimeter diameter area of the thalamus. It remains very effective in cases of drug resistant intention tremor that occur as a result of severe head trauma or multiple sclerosis. Gamma knife thalamotomy is a non-invasive technique that may be offered to patients with disabling tremor who are not candidates for open thalamotomy or DBS.

Selective Rhizotomy with or without peripheral nerve or muscle sectioning is used for medically refractory torticollis which is a cervical form of dystonia that involves static or repetitive rhythmic turning of the head.

The Movement Disorder Surgery Team
Joseph R. Smith, M.D., F.A.C.S., Director of Functional & Stereotaxic Neurosurgery

Kapil Sethi, M.D., Neurology, Chief, Section of Movement Disorders

John Morgan, M.D., P.h.D., Department of Neurology

Robbie Allen, Ph.D., Neurophysiologist, Southern Neurophysiology Associates

Caroline diDonato, Nurse Practitioner, Assistant Clinical Professor,
Movement Disorder Service

Gregory P. Lee, Ph.D. Neurology, Director of Neuropsychology Services

The program staff welcomes any inquiries or referrals and can be reached through MCG Physicians Direct at 1-800-733-1828.
 

   
  © 2003 MCG

Questions and Comments to Bill Hamilton 

 
 June 07, 2006


Department of Neurosurgery  |  Medical College of Georgia