PATIENT INFO

Directions

The hospital where we would be admitting and performing Deep Brain Stimulation and Advanced Neuromodulation surgery is one of the best and maintains world standard in Health care.

Hotels & Accomodation

In Pakistan we have 5 star hotels for accomodation like Pearl Continental & Avari Hotel.

Nearest place to our hospital is a 4 star Hotel Park Plaza which is at a walking distance and its administration gives special discount and priority to ANFN patients admitted for DBS surgery

International Patients

Lahore has an International airport and entry needs Visa for most of the countries.

Our office will help in getting visa and immigration to ANFN patients as special guests of Lahore making your travelling comfortable.

PIA our international airline has been very kind to extend special rebate to all patients travelling as ANFN patients along with their attendents and relatives accompanying the patients.

Getting started

Call us at +92-322-99-9900 and we will take care of all your traveling arrangements and stay in Lahore at very reasonable prices and give you all information about requirements to enter in Lahore.

FAQ

I. FAQ for Patients: Deep Brain Stimulation for Parkinson’s Disease

 

When should one consider surgical therapy?
What are the different types of surgery for Parkinson’s disease?
What are the possible brain targets for DBS?
How does DBS work?
How is the surgery performed?
What are the cosmetic considerations with DBS surgery?
Why must patients be awake for part of DBS surgery?
Would both sides of the brain be done at once, or only one side? 
What are the benefits of DBS surgery?
What are the risks of DBS surgery?
What makes a patient a good candidate for DBS for Parkinson’s disease?
Where is the surgery performed?
What are the results and complications of DBS ?
What determines the choice of STN versus GPi as the target?
What tests are needed prior to surgery?
How should the patient prepare for surgery?
What type of follow-up is needed after surgery? Who will program the DBS unit? 
How long does it take before the full benefit of DBS is apparent?
Can patients control the DBS device themselves?
Are there any restrictions on a person’s activity after a DBS system is implanted? 
Can I have an MRI scan after DBS surgery?
Summary

 

II. FAQ for Patients: Deep Brain Stimulation for Dystonia
History of surgery for dystonia
What type of brain surgery is best for dystonia?
Is DBS for dystonia a standard, widely accepted therapy?
Who should consider having surgery for dystonia?
How is the surgery performed?
Can children have surgery for dystonia?
“What are the risks of surgery?
What are the benefits of surgery?
What are the cosmetic considerations with DBS surgery
What tests are needed prior to surgery?
How should the patient prepare for surgery? 
What type of follow-up is needed after surgery? Who will program the DBS unit?
How long does it take before the full benefit of DBS is apparent?
Summary

 

I. FAQ for Patients: Deep Brain Stimulation for Parkinson’s Disease

When should one consider surgical therapy?

For patients with early Parkinson’s disease, levodopa (sinemet) and other antiparkinsonian medications are usually effective for maintaining a good quality of life. As the disorder progresses, however, medications can produce disabling side effects. Many patients on long-term levodopa develop troublesome dyskinesias, excessive movements that often cause the limbs and body to writhe or jump. In addition, their dose of levodopa no longer lasts as long as it once did. This may lead to “on-off fluctuations,” a condition in which the ability to move changes unpredictably between a mobile (“on”), state when medication seem to work, and an immobile (“off”) state in which little effect of medication is apparent and normal movement is very difficult. When patients no longer have an acceptable quality of life due to these shortcomings of medical therapy, surgical treatment should be considered.

What are the different types of surgery for Parkinson’s disease? 

There are several different types of surgery for Parkinson’s disease. The first surgical procedures developed were the ablative, or brain lesioning, procedures. Examples of lesioning surgery include thalamotomy and pallidotomy. Lesioning surgery involves the precisely controlled destruction, using a heat probe, of a small region of brain tissue that is abnormally active. It produces a permanent effect on the brain. In general, it is not safe to perform lesioning on both sides of the brain.

We continue to perform some lesioning surgeries for patients who desire it, although in our practice lesioning has been largely replaced by deep brain stimulation (DBS). DBS surgery involves placing a thin metal electrode (about the diameter of a piece of spaghetti) into one of several possible brain targets and attaching it to a computerized pulse generator, which is implanted under the skin in the chest (much like a heart pacemaker). All parts of the stimulator system are internal; there are no wires coming out through the skin. To achieve maximal relief of symptoms, the stimulation can be adjusted during a routine office visit by a physician or nurse using a programming computer held next to the skin over the pulse generator. Unlike lesioning, DBS does not destroy brain tissue. Instead, it reversibly alters the abnormal function of the brain tissue in the region of the stimulating electrode. DBS is the procedure most often recommended by our Movement Disorders Surgery Program. Although deep brain stimulation is a major new advance, it is a relatively complicated therapy that may demand considerable time and patience before its effects are optimized.

Many patients inquire about the “restorative” therapies, a category of procedures which includes transplantation of fetal cells or stem cells, growth factor infusion, or gene therapy. These procedures attempt to correct the basic chemical defect of Parkinson’s disease by increasing the production of dopamine in the brain. In the future, restorative therapies will hopefully emerge as effective and possibly curative interventions for Parkinson’s disease.

What are the possible brain targets for DBS?

There are now four possible target sites in the brain that may be selected for placement of stimulating electrodes: the internal segment of the globus pallidus (GPi), the subthalamic nucleus (STN), the pedunculopontine nucleus (PPN), and a subdivision of the thalamus referred to as Vim (ventro-intermediate nucleus). These structures are small clusters of nerve cells that play critical roles in the control of movement. Thalamic (Vim) stimulation is only effective for tremor, not for the other symptoms of PD. Stimulation of the globus pallidus or subthalamic nucleus, in contrast, may benefit not only tremor but also other parkinsonian symptoms such as rigidity (muscle stiffness), bradykinesia (slow movement), gait problems, and dyskinesias. All of three of these targets are now approved by the U.S. Food and Drug Administration, which oversees medical devices. The PPN is a new, investigational target that may be appropriate for patients with gait freezing, but there are currently few clinical studies of this. For most patients with Parkinson’s disease, DBS of the globus pallidus or subthalamic nucleus is the most appropriate choice because stimulation at these targets affects a broad range of symptoms.

How does DBS work? 

The theoretical basis for DBS of the GPi or STN in PD was worked out in the late 1980’s and early 1990’s. In Parkinson’s disease, loss of dopamine-producing cells leads to excessive and abnormally patterned activity in both the GPi and the STN. “Pacing” of these nuclei with a constant, steady-frequency electrical pulse corrects this excessive and abnormal activity. DBS does not act directly on dopamine producing cells and does not affect brain dopamine levels. Instead, it compensates for one of the major secondary effects of dopamine loss, the excessive and abnormally patterned electrical discharge in the GPi or the STN. The exact mechanism by which the constant frequency stimulation pulse affects nearby brain cells has not been determined.

How is the surgery performed?

There are several available surgical methods. In the most common method, implantation of the brain electrode is performed with the patient awake, using only local anesthetic and occasional sedation. The basic surgical method is called stereotaxis, a method useful for approaching deep brain targets though a small skull opening. For stereotactic surgery, a rigid frame is attached to the patient’s head just before surgery, after the skin is anesthetized with local anesthetic. A brain imaging study (MRI or CT) is obtained with the frame in place. The images of the brain and frame are used to calculate the position of the desired brain target and guide instruments to that target with minimal trauma to the brain. After frame placement, MRI/CT, and calculation of the target coordinates on a computer, the patient is taken to the operating room. At that point an intravenous sedative is given, a Foley catheter is placed in the bladder, the stereotactic frame is rigidly fixed to the operating table, a patch of hair on top of the head is shaved, and the scalp is washed. After giving local anesthetic to the scalp to make it completely numb, an incision is made on top of the head behind the hairline and a small opening (1.5 centimeters, about the size of a nickel) is made in the skull. At this point, all intravenous sedatives are turned off so that the patient becomes fully awake.

To maximize the precision of the surgery, we employ a “brain mapping” procedure in which fine microelectrodes are used to record brain cell activity in the region of the intended target to confirm that it is correct, or to make very fine adjustments of 1 or 2 millimeters in the intended brain target if the initial target is not exactly correct. The brain mapping produces no sensation for the patients, but the patient must be calm, cooperative, and silent during the mapping or else the procedure must be stopped. The brain’s electrical signals are played on an audio monitor so that the surgical team can hear the signals and assess their pattern. The electronic equipment is fairly noisy, and the members of the surgical team often discuss the signals being obtained so as to be sure to interpret them correctly. Since each person’s brain is different, the time it takes for the mapping varies from about 30 minutes to up to 2 hours for each side of the brain. The neurological status of the patient (such as strength, vision, and improvement of motor function) is monitored frequently during the operation, by the surgeon or by the neurologist.

When the correct target site is confirmed with the microelectrode, the permanent DBS electrode is inserted and tested for about 20 minutes. The testing does not focus on relief of parkinsonian signs but rather on unwanted stimulation-induced side effects. This is because the beneficial effects of stimulation may take hours or days to develop, whereas any unwanted effects will be present immediately. For the testing, we deliberately turn the device up to a higher intensity than is normally used, in order to deliberately produce unwanted stimulation-induced side effects (such as tingling in the arm or leg, difficulty speaking, a pulling sensation in the tongue or face, or flashing lights). The sensations produced at high intensities of stimulation during this testing are experienced as strange but not painful. We thus confirm that the stimulation intensity needed to produce such effects is higher than the intensity normally used during long-term function of the device.

Once the permanent DBS electrode is inserted and tested, intravenous sedation is resumed to make the patient sleepy, the electrode is anchored to the skull with a plastic cap, and the scalp is closed with sutures. The stereotactic headframe is removed. The patient then receives a general anesthetic to be completely asleep for the placement of the pulse generator in the chest and the tunneling of the connector wire between the brain electrode and the pulse generator unit. This part of the proce

What are the cosmetic considerations with DBS surgery? 

Complete shaving of the head is not necessary for surgery. However, patches of hair on top of the head and behind the ear are shaved immediately before surgery when the patient is sedated. Many patients elect to get a short haircut after surgery (must be at least 2 weeks afterwards) so that the hair grows in evenly.

There are generally 3 incisions made on each side for DBS surgery: a 5 cm (2 inch) incision on top of the head, a 2.5 cm (1 inch) incision behind the ear, and a 6 cm (2.5 inches) incision in the chest just under the clavicle. For patients with receding hairlines, a slight scar from an incision will be visible on top of the head, but is not especially prominent. The cap used to anchor the DBS electrode (under the scalp) forms a slight bump, which again may be visible in the case of a receding hairline.

There is often puffiness around the eyes for a few days after surgery, but this goes away rapidly.

All parts of the device are internal (under the skin), so there are no wires sticking out. In a thin person, the connecting wire running down the neck may be visible as a slight bulge when the head is turned all the way to the opposite side. The incision for the pulse generator in the chest is closed with particular attention to minimize scar formation; this incision would be visible with the shirt off, or in a swimsuit, or in a low-cut evening gown. In thin persons, the pulse generator itself forms a bulge under the skin in the pectoral area that may be apparent if the area is uncovered, but is not visible through clothing.

Why must patients be awake for part of DBS surgery? 

Using the standard, microelectrode guided technique for DBS surgery, brain mapping is performed using microelectrodes. The brain mapping procedure is much harder to do if the patient is under a general anesthetic or strong sedative. In addition, the procedure is safer if the patient’s neurological function (speech and voluntary movement) can be checked periodically during the procedure, which is only possible in an awake patient. For patients undergoing surgery in our investigational interventional MRI protocol, general anesthesia is used for the whole procedure, as the MR images take the place of electrical mapping and monitoring of neurological function.

Would both sides of the brain be done at once, or only one side?

DBS on one side of the brain mainly affects symptoms on the opposite side of the body. Most patients have symptoms on both sides of the body and thus require both sides of the brain to be implanted for maximal benefit. In the first several years of our DBS program, most implant surgeries were “staged,” that is each side done in a separate surgery separated by several months. As this surgery has become more rapid and routine, we are now offering “simultaneous bilateral” procedures, or implantation of both leads in a single surgery, to many patients. The brain side opposite the most affected body side is implanted first. Then, if the patient and anesthesiologist agree to proceed, the second side is then implanted. For elderly patients, or patients concerned about a longer operation, it may be best to stage the procedures several months apart.

What are the benefits of DBS surgery? 

The major benefit of DBS surgery for PD is that it makes movement in the off-medication state more like the movement in the on-medication state. In addition, it reduces levodopa-induced dyskinesias, either by a direct suppressive effect or indirectly by allowing some reduction in medication dose. Thus, the procedure is most beneficial for Parkinson’s patients who cycle between states of immobility (“off” state) and states of better mobility (“on” state). DBS smoothes out these fluctuations so that there is better function during more of the day. Any symptom that can improve with levodopa (slowness, stiffness, tremor, gait disorder) can also improve with DBS. Symptoms that do not respond at all to levodopa usually do not improve significantly with DBS. Following DBS, there may be a reduction, but not elimination, of anti-Parkinsonian medications. At present, we believe that DBS only suppresses symptoms and does not alter the underlying progression of Parkinson’s disease.

What are the risks of DBS surgery?

The most serious potential risk of the surgical procedures is bleeding in the brain, producing a stroke. This risk varies from patient to patient, depending on the overall medical condition, but the average risk is about 2%. If stroke occurs, it usually occurs during, or within a few hours of, surgery. The effects of stroke can range from mild weakness that recovers in a few weeks or months to severe, permanent weakness, intellectual impairment, or death. The second most serious risk is infection, which occurs in about 4% of patients. If an infection occurs, it is usually not life threatening, but it may require removal of the entire DBS system. In most cases, a new DBS system can be re-implanted when the infection is eradicated. Finally, hardware may break or erode through the skin with normal usage, requiring it to be replaced.

In the first few days after surgery, it is normal to have some temporary swelling of the brain tissue around the electrode. This may produce no symptoms, but it can produce mild disorientation, sleepiness, or personality change that lasts for up to 1-2 weeks.

What makes a patient a good candidate for DBS for Parkinson’s disease? 

In determining whether a patient is a good candidate for surgery, we look for the following:

  1. Intact intellectual function and memory. Dementia (significantly impaired memory or thinking) is a major contraindication to surgery, since such patients have great difficulty tolerating the surgery, may have further loss of intellectual function due to the surgery, deal poorly with the complexity of DBS therapy, and realize little overall functional benefit.
  2. History of significant benefit from taking levodopa (Sinemet). Good mobility, with the ability to walk, in the best “on-medication” state is important for a good outcome. In general, surgery makes the “off” medication state more like the “on” state but rarely does better than the best “on” state, so a patient with poor function in best “on” (for example, unable to walk at any time) is a poor surgical candidate
  3. Certainty of diagnosis. A number of neurological illnesses can mimic the symptoms of Parkinson’s disease but do not respond significantly to levodopa. Such illnesses are often called “atypical parkinsonism” or “Parkinson’s plus syndromes.” These illnesses are different from classic Parkinson’s disease, and they do not respond to DBS surgery. If there is a strong possibility that the patient has atypical parkinsonism rather than classic Parkinson’s disease, surgery should not be performed.
  4. Lack of other untreated or inadequately treated illnesses. Serious cardiac disease, uncontrolled hypertension, or any major other chronic systemic illness increases the risk and decreases the benefit of surgery.
  5. Realistic expectations. People who expect a sudden miracle are disappointed with the results, and they may have difficulty with the complexity of the therapy.
  6. Patient age. The benefits of DBS for PD decline with advancing age, and the risks go up. We rarely offer surgery to a person over 80 and would only consider it if they are in otherwise excellent health, are cognitively intact, and have good function in the on state. For patients over 75, the benefits are likely to be modest.
  7. MRI of the brain should be free of severe vascular disease, extensive atrophy, or signs of atypical parkinsonism.
  8. Degree of disability. DBS is a poor procedure to rescue someone with end stage Parkinson’s disease who is wheelchair bound or in a nursing home, although these are the most desperate patients. It is an excellent procedure for Parkinson’s patients who are still employed but may be just at the point where disability would stop them from working.
  9. Ability to remain calm and cooperative during an awake neurosurgical procedure lasting 2-3 hours per brain side.

Where is the surgery performed? 

For patients referred to the Movement Disorders SurgeryProgram. Our surgical team  performs DBS surgery at one of the finest centers.

What are the results and complications of DBS ? 

For bilateral DBS, the evaluations showed a 45-70% improvement in the scores on standard rating scales, off of medication, as a result of DBS. The risk of stroke is 1.6%, the risk of severe stroke with death or permanent major disability is 0.5%, and the risk of device infection that requires further surgery for device removal is 4%.

What determines the choice of STN versus GPi as the target? 

In the future, the target choice will be made based upon what will give the best result for an individual patient’s symptoms. At this time, data show that both STN and GPi DBS are effective for most symptoms, and it is not clear if one is a better target. For patients who were enrolled in our formal clinical trial of DBS for PD, the choice of STN or GPi is determined by randomization. If not enrolled in the trial, the target choice is made largely by preference of the patient and referring neurologist.

What tests are needed prior to surgery? 

Patients should have a brain imaging study (MRI or CT) to determine if there are problems in the brain that would pose excessive risk for surgery, unless one has been done within 1 year. Most patients should have a formal neurological exam in the off-medication condition, following by re-assessment after a test dose of medication, by one of our neurologists or by the referring neurologist. For any patient with a question of cognitive dysfunction, we request formal neuropsychological evaluation. All patients must have a blood test (mainly for blood clotting ability) and visit with the anesthesiologists in the week prior to surgery. For patients interested in the interventional MRI implantation protocol, the patients must have an “on medication, off medication” test once before surgery and then again approximately 6 months after surgery.

How should the patient prepare for surgery? 

For 10 days prior to surgery, patients must not take aspirin, any aspirin containing drugs, related drugs such as ibuprofen (Advil, Motrin) or naproxen (Naprosyn), or Vitamin E. These drugs can increase the risk of bleeding. The evening before surgery, patients should wash their head, neck, and chest with hibiclens (or other soap containing chlorhexidine) in the shower. The morning of surgery, the patient should not take their antiparkinsonian medications. However, the patient should take any medications they normally take for other problems, such as high blood pressure. Patients should inform the surgeon if they develop a cold, cough, or any type of infection in the days prior to the surgery. Patients should hydrate (drink a lot of non-alcoholic, non-caffeinated drinks) prior to surgery.

What type of follow-up is needed after surgery? Who will program the DBS unit? 

Patients normally leave the hospital two days after surgery. We ask patients to return to our clinic 1 week later for suture removal and check of the incisions by our DBS nursing specialist, and approximately 4 weeks later to see the surgeon and neurologist in the Movement Disorders Surgery Clinic. The initial programming is done by us  usually at the one-week postoperative visit. Some patients have temporary disorientation or sleepiness for a few days after surgery due to temporary brain swelling, and if this occurs programming is deferred until the mental state completely returns to baseline. For subsequent programming needs after the initial stimulator activation, the patient is welcome to continue in our Movement Disorders Clinic. For patients who have neurologists outside of our center who are comfortable with programming, it is often most convenient to return to their regular neurologist. We are happy to advise referring neurologists regarding programming strategies, and we have close working relationships with our major referring doctors.

In the first month or two following DBS implantation, some patients may develop an infection of the device or of the skin over the device. This would present as drainage, increasing redness, increasing swelling, or increasing pain starting a few days to a few weeks post-surgery. It is very important to let our office know IMMEDIATELY if such signs are noted, since early wound care may be effective at salvaging the device. If such symptoms are ignored for even a few days, however, the patient will usually have to have all of the hardware removed.

Patients will typically require replacement of the pulse generator after 3-4 years, depending on the exact settings of the device. This is an outpatient procedure that takes about 30 minutes.

How long does it take before the full benefit of DBS is apparent? 

For reasons that are not fully understood, the improvement in parkinsonisan symptoms my take a few hour or days to reach its maximal level following a programming change. Some problems may respond more quickly than others. In addition, to realize the full benefit of DBS, medication changes and multiple programming sessions may be needed. Thus it is usually a few months after surgery before the final degree of benefit is actually realized.

Can patients control the DBS device themselves? 

Following surgery, the patient is given the Medtronic Access Review unit, a hand-held battery-operated unit that can be used to determine if the device is on or off, to turn it on or off, and to check battery life. In addition, the newer pulse generator allows some patient control over the stimulation level. Normally, in DBS for Parkinson’s disease, the device is left on all the time.

Are there any restrictions on a person’s activity after a DBS system is implanted? 

For at least 4 days after surgery, the patient should refrain from flying in commercial aircraft. For one week after surgery, the incisions should be kept dry, so for showering in the first week incisions must be covered with an occlusive dressing. Tight clothing or tightly fitting hats should be avoided in the two weeks after surgery. After the incisions are completely healed (2-3 weeks), the patient may return to all normal activities, including exercise. Normal physical activities will not harm the device. Security devices (such as those in airports or stores) will not harm the device or the patient, although in rare cases they may activate the on-off switch, thus turning off a DBS system that had been on. The loss of benefit to the patient may take minutes or hours to be apparent. When traveling extensively away from home, patients should carry their Medtronic Access Review unit so that they can easily re-activate the DBS system if it is de-activated by a security device.

Can I have an MRI scan after DBS?
After DBS implantation, patients should avoid most types of MRI exams, as the exam may produce heating of the brain electrode. We have developed a specialized, low-energy protocol for brain MRI, allowing us to perform postoperative brain MRI safely. However, we do not recommend any other forms of MRI (such as spine or chest MRI), because safe conditions for performing these have not been worked out.

Summary
 
There are more medical and surgical treatment options for patients with Parkinson’s disease than ever before. Deep brain stimulation surgery offers important symptomatic relief in patients with moderate disability from Parkinson’s disease who still retain some benefit from antiparkinsonian medications and who are cognitively intact. Patients who fluctuate between “on medication” and “off medication” states are usually good surgical candidates, as are those who have troublesome dyskinesias. The major risk is a 2% risk of stroke, due to bleeding in the brain. DBS is a relatively complex therapy requiring regular neurological follow-up and battery changes every 3-4 years. It reduces, but does not eliminate, symptoms of Parkinson’s disease. The time to consider DBS surgery is when quality of life is no longer acceptable on optimal medical therapy as administered by a movement disorders neurologist.

 

II. FAQ for Patients: Deep Brain Stimulation for Dystonia

History of surgery for dystonia

Brain operations to treat various forms of dystonia were first performed 40-50 years ago. The operations involved a precisely controlled lesioning (destruction) of deep structures in the brain involved in movement control. Two different deep structures, called the thalamus and the globus pallidus, were operated upon. Lesioning was performed by freezing or coagulation. Surgical techniques were much less advanced in that era than they are today, so the results were not consistent and complications were frequent.

In the last 5 years there has been a resurgence of interest in the surgical treatment of dystonia. There are several reasons for this:

  1. Techniques for operating on deep brain structures have become much more precise and safe.
  2. In addition to the older technique of brain lesioning, there is a new technique, deep brain stimulation (DBS), which involves placing a stimulation electrode rather than performing a brain lesion. DBS can alter the function of abnormal brain tissue in a way that improves movement, but it is reversible if there is an unwanted effect, and it can be adjusted during a routine office visit to optimize the degree of benefit. Thus it is somewhat safer than lesioning.
  3. Patients with other, more common movement disorders are increasingly undergoing surgical treatment. These other movement disorders include tremor and Parkinson’s disease. Success with these movement disorders has stimulated greater interest in surgery for more rare movement disorders such as dystonia.
  4. Since 1995, a small number of publications in neurology and neurosurgery journals have shown that pallidal surgery for several forms of dystonia, using modern techniques, can be effective

What type of brain surgery is best for dystonia?

Evidence is starting to accumulate that the best brain region for surgery for generalized dystonia (dystonia affecting the whole body) is the globus pallidus. This is a peanut-sized structure deep in the brain whose electrical activity is abnormal in dystonia. For dystonias affecting mainly the neck and face, hower, the optimal target is less clear. Although DBS of the globus pallidus often improves the dystonia, there can also be subtle impairments (slowing down) of previously normal limbs with this techniques. Therefore, for patients with dystonia affecting mainly the neck and face, we are offering enrollment in a clinical trial of subthalamic nucleus DBS. This target may prove to be better tolerated for neck dystonia, but the the clinical study is not complete.

While the older lesioning technique and the newer DBS technique can both be effective, we usually prefer DBS over lesioning because it is reversible and adjustable, and does not permanently destroy any part of the brain. Thus, pallidal or subthalamic DBS is our preferred surgery for dystonia at this time.

Is DBS for dystonia a standard, widely accepted therapy? 
About 500 cases of DBS for dystonia have been described in the world medical literature, and the longest time any patient has had this therapy is about 10 years. Thus it is considered a standard therapy.

Who should consider having surgery for dystonia? 

Patients should consider deep brain stimulation for dystonia if they meet the following criteria:

  1. The patient has been evaluated and treated by a qualified movement disorders neurologist who has clearly diagnosed the type of dystonia, and excluded other neurological problems.
  2. The dystonia adversely affects quality of life by interfering significantly with normal activities or causing social isolation.
  3. The patient’s neurologist has attempted treatment with a variety of medications, which should at least include sinemet and anticholingergic medications such as trihexyphenydil (Artane). Baclofen and muscle relaxants such as clonazepam are also often tried before considering surgery.
  4. The dystonia affects too large a body area to be treated effectively with injections of botulinum toxin (botox); or attempts at injection with botox have been tried and failed.
  5. The patient and family clearly understand the nature and complexity of DBS therapy as well as the fact that the therapy is too new to guarantee successful treatment in any individual case.

In addition to the above considerations, DBS for dystonia appears to be more effective for certain forms of dystonia than others. Primary dystonias (patients without brain abnormality on MRI) are more likely to benefit than those with secondary dystonia (patients with brain abnormalities seen on MRI that are causing the dystonia).

How is the surgery performed? 

There are several available surgical methods. In the most common method, implantation of the brain electrode is performed with the patient awake, using only local anesthetic and occasional sedation. The basic surgical method is called stereotaxis, a method useful for approaching deep brain targets though a small skull opening. For stereotactic surgery, a rigid frame is attached to the patient’s head just before surgery and after the skin is anesthetized with local anesthetic. A brain imaging study (MRI or CT) is obtained with the frame in place. The images of the brain and frame are used to calculate the position of the desired brain target and guide instruments to that target with minimal trauma to the brain. After frame placement, MRI/CT, and calculation of the target coordinates on a computer, the patient is taken to the operating room. At that point an intravenous sedative is given, a Foley catheter is placed in the bladder, the stereotactic frame is rigidly fixed to the operating table, a patch of hair on top of the head is shaved, and the scalp is washed. After giving local anesthetic to the scalp to make it completely numb, an incision is made on top of the head behind the hairline and a small opening (1.5 centimeters, about the size of a nickel) is made in the skull. At this point, all intravenous sedatives are turned off so that the patient becomes fully awake.

To maximize the precision of the surgery, we employ a “brain mapping” procedure in which fine microelectrodes are used to record brain cell activity in the region of the intended target to confirm that it is correct, or to make very fine adjustments of 1 or 2 millimeters in the intended brain target if the initial target is not exactly correct. The brain mapping produces no sensation for the patients, but the patient must be calm, cooperative, and silent during the mapping or else the procedure must be stopped. The brain’s electrical signals are played on an audio monitor so that the surgical team can hear the signals and assess their pattern. The electronic equipment is fairly noisy, and the members of the surgical team often discuss the signals being obtained so as to be sure to interpret them correctly. Since each person’s brain is different, the time it takes for the mapping varies from about 30 minutes to up to 2 hours for each side of the brain. The neurological status of the patient (such as strength, vision, and improvement of motor function) is monitored frequently during the operation, by the surgeon or by the neurologist.

When the correct target site is confirmed with the microelectrode, the permanent DBS electrode is inserted and tested for about 20 minutes. The testing does not focus on relief of dystonia but rather on unwanted stimulation-induced side effects. This is because the beneficial effects of stimulation may take hours or days to develop, whereas any unwanted effects will be present immediately. For the testing, we deliberately turn the device up to a higher intensity than is normally used, in order to deliberately produce unwanted stimulation-induced side effects (such as tingling in the arm or leg, difficulty speaking, a pulling sensation in the tongue or face, or flashing lights). The sensations produced at high intensities of stimulation during this testing are experienced as strange but not painful. We thus confirm that the stimulation intensity needed to produce such effects is higher than the intensity normally used during long-term function of the device.

Once the permanent DBS electrode is inserted and tested, intravenous sedation is resumed to make the patient sleepy, the electrode is anchored to the skull with a plastic cap, and the scalp is closed with sutures. The stereotactic headframe is removed. The patient then receives a general anesthetic to be completely asleep for the placement of the pulse generator in the chest and the tunneling of the connector wire between the brain electrode and the pulse generator unit. This part of the procedure takes about 40 minutes.

Patients with dystonia on both sides of the body will usually require electrodes to be placed on both sides of the brain. We normally do the two implants as two separate surgical procedures spaced 3-6 months apart.

Can children have surgery for dystonia?

The most severe form of generalized dystonia often begins in childhood and may become severe by early teen years. These patients may be excellent candidates for surgery. We have implanted DBS devices in patients as young as five years old. For children under 16, the surgery is usually performed under general anesthesia, with no awake testing.

What are the risks of surgery?

The most serious potential risk of the surgical procedure is bleeding in the brain, producing a stroke. This risk varies from patient to patient, depending on other medical factors, but generally ranges from 1-3%. If stroke occurs, it usually occurs during or within a few hours of surgery. Another risk is infection, especially of the deep brain stimulating hardware, which occurs in about 4-5% of patients. If an infection occurs, it is usually not life threatening, but may require immediate removal of the entire DBS system.

What are the benefits of surgery? 

DBS surgery does not cure dystonia in any case. When the stimulator is turned off or if it malfunctions, the symptoms return. DBS can decrease the abnormal movements and postures of dystonia but usually does not totally eliminate them. The degree of benefit appears to vary with both the type of dystonia and the duration of the symptoms. Adolescents and young adults with inherited forms of dystonia appear to get very significant benefit. For patients with dystonia due to stroke or head trauma, the benefit may be only mild. Adults who have had dystonia for many years probably have less improvement than those with more recent onset of symptoms.

What are the cosmetic considerations with DBS surgery? 

Complete shaving of the head is not necessary for surgery. However, a significant patch of hair from on top of the head to behind an ear is shaved immediately before surgery when the patient is sedated. Many patients elect to get a short haircut after surgery (must be at least 2 weeks afterwards) so that the hair grows in evenly. When hair grows back, incisions are not visible.

There is often puffiness around the eyes for a few days after surgery, but this goes away rapidly.

There are generally 3 incisions made for DBS surgery: a 5 cm (2 inch) incision on top of the head, a 2.5 cm (1 inch) incision behind the ear, and a 6 cm (2.5 inches) incision in the chest just under the clavicle. For adult patients with receding hairlines, a slight scar from an incision will be visible on top of the head, but is not especially prominent. The cap used to anchor the DBS electrode (under the scalp) forms a slight bump, which again may be visible but not prominent in the case of a receding hairline.

All parts of the device are internal (under the skin), so there are no wires sticking out. In a thin person, the connecting wire running down the neck may be visible as a slight bulge when the head is turned all the way to the opposite side. The incision for the pulse generator in the chest is closed with particular attention to minimize scar formation; this incision would be visible with the shirt off, or in a swimsuit, or in a low-cut evening gown. In thin persons, the pulse generator itself forms a bulge under the skin in the pectoral area that may be apparent if the area is uncovered, but is not visible through clothing.

What tests are needed prior to surgery? 

All patients must have had a brain MRI at some time since the onset of dystonia. All patients must have a detailed videotaped neurological evaluation, lasting several hours, to document the severity of dystonia. Some patients may require additional tests such as neuropsychological evaluation. Patients with dystonia that affects the neck usually require a cervical spine MRI prior to surgery.

How should the patient prepare for surgery?

For 10 days prior to surgery, patients must not take aspirin, any aspirin-containing drugs, related drugs such as ibuprofen (Advil, Motrin) or naproxen (Naprosyn), or Vitamin E. These drugs can increase the risk of bleeding. The evening before surgery, patients should wash their head, neck, and chest with hibiclens (or other soap containing chlorhexidine) in the shower. The morning of surgery, the patient should not take their anti-dystonia medications. However, the patient should take any medications they normally take for other problems, such as high blood pressure. Patients should inform the surgeon if they develop a cold, cough, or any type of infection in the days prior to the surgery.

What type of follow-up is needed after surgery? Who will program the DBS unit? 

Patients normally leave the hospital two days after surgery. We ask patients to return to our clinic 1 week later for suture removal and check of the incisions by our DBS nursing specialist, and approximately 4 weeks later to see the surgeon and neurologist in the Movement Disorders Surgery Clinic. The initial programming is done at the one-week postoperative visit. Some patients have temporary disorientation for a few days after surgery due to temporary brain swelling, and if this occurs programming is deferred until the mental state completely returns to baseline. For subsequent programming needs after the initial stimulator activation, the patient is encouraged to continue in our Movement Disorders Clinic. For patients who live at a distance  and have a neurologist with a DBS programmer, we are happy to advise other neurologists regarding optimal programming strategies for dystonia.

In the first month following DBS implantation, some patients may develop an infection of the device or of the skin over the device. This would present as drainage, increasing redness, increasing swelling, or increasing pain starting a few days to a few weeks post-surgery. It is very important to let our office know IMMEDIATELY if such signs are noted, since early wound care may be effective at salvaging the device. If such symptoms are ignored for even a few days, however, the patient will usually have to have all of the hardware removed.

Patients will typically require replacement of the pulse generator after 2-3 years, depending on the exact settings of the device. This is an outpatient procedure that takes about 30 minutes.
How long does it take before the full benefit of DBS is apparent?

For reasons that are not fully understood, it often takes several months for the full benefit of any particular programming setting to reach its maximum level.

Summary

There are more surgical treatment options for patients with dystonia than ever before. For patients with primary dystonia, without fixed (immobile) deformities of the skeleton or tendons, DBS offers significant relief of many symptoms. The major risk is a 2% risk of stroke, due to bleeding in the brain. DBS is a relatively complex therapy requiring regular neurological follow-up and battery changes every 2-3 years. The time to consider DBS surgery is when quality of life is no longer acceptable on optimal medical therapy as administered by a movement disorders neurologist. Secondary dystonias, such as those due to stroke, trauma, or cerebral palsy, may have modest benefit from DBS, but not as much benefit as primary dystonia.