DEEP BRAIN STIMULATION (DBS) is a standard treatment

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1 1320 ORIGINAL ARTICLE Fast-Track Programming and Rehabilitation Model: A Novel Approach to Postoperative Deep Brain Stimulation Patient Care David B. Cohen, MD, Michael Y. Oh, MD, Susan M. Baser, MD, Cindy Angle, RN, Alex Whiting, Catherine Birk, MD, Donald M. Whiting, MD ABSTRACT. Cohen DB, Oh MY, Baser SM, Angle C, Whiting A, Birk C, Whiting DM. Fast-track programming and rehabilitation model: a novel approach to postoperative deep brain stimulation patient care. Arch Phys Med Rehabil 2007; 88: Objective: To propose a new model of integrated, multidisciplinary postoperative care of the patients with deep brain stimulation (DBS). Design: Observational cohort study with follow-up at 3 months and 1 year. Setting: Academic medical center movement disorder clinic. Participants: Seventy-three consecutive patients with medically refractory Parkinson s disease underwent bilateral DBS. Patients were then transferred directly to an inpatient rehabilitation facility. Intervention: DBS and inpatient programming and rehabilitation. Simultaneous programming and rehabilitation was carried out by a multidisciplinary team. Main Outcome Measures: The FIM instrument, Unified Parkinson Disease Rating Scale (UPDRS), and levodopa dosage. Results: The average rehabilitation stay was 17.3 days, with a mean of 6.2 stimulator adjustments during that time. FIM scores improved from 62.1 (admission) to 98.5 (discharge), an average improvement of 36.4 (58.6%). Average UPDRS scores improved from 52.5 (preoperative off) and 30.1 (preoperative on) to 20.4 (3mo postoperative on-medication, on-stimulation), a 32.2% improvement from the preoperative on score. Levodopa dosages decreased by an average of 48.3% (all P.001). Conclusions: We describe our fast-track protocol, which allows for rapid DBS programming and tapering of Parkinson s medications. It also provides for treatment of concomitant medical and psychologic problems and optimized physical performance. Key Words: Brain stimulation, deep; Neurosurgery; Parkinson disease; Rehabilitation by the American Congress of Rehabilitation Medicine and the American Academy of Physical Medicine and Rehabilitation DEEP BRAIN STIMULATION (DBS) is a standard treatment for movement disorders that are refractory to medical management. Among all movement disorders, DBS has been most widely used and comprehensively studied for Parkinson s disease. Targets include the subthalamic nucleus (STN), nucleus ventro-intermedius of the thalamus, or globus pallidus interna (GPi), with the choice of stimulation site dependent on the patient s individual symptom complex. 1 Whichever site is used for stimulation, much effort is expended postoperatively for programming of the stimulator, adjustment of Parkinson s disease medications, and for rehabilitation of these functionally impaired patients. 2 In addition, medication adjustments and stimulator changes interact in complex ways to affect the patients symptoms and functional capabilities. The traditional model of postoperative DBS patient care in the United States involves neurosurgeons and movement disorder neurologists spending many months after surgery to fine-tune DBS programming and medication management. 3 This process can extend the time involved for the patient to realize the beneficial clinical effect of DBS. It also requires patients to make multiple office visits for programming, because clinical changes after programming adjustments often are not evident for hours or even days. To maximize both efficiency of programming and patients functional outcome, we developed a multidisciplinary, integrated program for the postoperative management of Parkinson s disease patients. Neurosurgery, movement disorder neurology, physiatry, physical therapy, speech therapy, occupational therapy, and psychiatry all participate in an intensive 2- to 3-week program that incorporates inpatient rehabilitation with up-to-daily DBS programming and rapid medication titration. This study describes the methods and results of this integrated approach to postoperative DBS patient care. METHODS Seventy-three consecutive patients with Parkinson s disease underwent DBS surgery and then entered fast-track programming and rehabilitation. Institutional review board approval was not required because we examined existing, deidentified data collected during the course of routine patient care. From the Department of Neurosurgery, Division of Neuromodulation (Cohen, Oh, Angle, Whiting, Whiting) and Department of Neurology, Movement Disorder and Spasticity Center (Baser), Allegheny General Hospital, Pittsburgh, PA; and Health- South Harmarville Rehabilitation Hospital, Pittsburgh, PA (Birk). A commercial party having a direct financial interest in the results of the research supporting this article has conferred or will confer a financial benefit upon the author or 1 or more of the authors. Oh and DM Whiting are consultants for Medtronic Inc. Birk has served as a speaker for Medtronic Inc. No funding was received for the performance of this study. Reprint requests to Donald M. Whiting, MD, Dept of Neurosurgery, Allegheny General Hospital, 420 E North Ave, Ste 302, Pittsburgh, PA 15212, /07/ $32.00/0 doi: /j.apmr Preoperative Evaluation All patients underwent evaluation by a movement disorder neurologist and received the best possible medical treatment. Patients selected for DBS were those who showed dopamine sensitivity but who required escalating doses and/or were developing significant side effects (ie, dyskinesias) and had disabling symptoms. These symptoms included freezing, tremor, and rigidity. Neuropsychologic testing was performed prior to surgery, with a score of 130 on the Mattis Dementia Rating Scale being the minimum cutoff for cognitive performance. The entire test battery included the Mini-Mental State Examination, clock drawing test, Disability Rating Scale, Wechsler Adult Intelligence Scale III, Wechsler Memory Scale III, Hopkins Verbal Learning Test, verbal fluency, Boston naming,

2 FAST-TRACK DEEP BRAIN STIMULATION REHABILITATION, Cohen 1321 Trail-Making Test Parts A and B, and Geriatric Depression Scale. Video assessment and Unified Parkinson Disease Rating Scale (UPDRS) scores are determined with the patient in onand off-medication states. For the off-medication state, patients hold their medications for at least 10 hours prior to testing, which occurs in the morning. Patients then take their normal morning medications and wait until they are on for on-medication testing. Patients are considered for surgery if they show at least a 25% improvement in on versus off UPDRS motor scores. Patients then have a brain magnetic resonance imaging (MRI) under general anesthesia to rule out other lesions or significant atrophy. This same MRI is then fused with a framebased stereotactic brain computed tomography (CT) on the day of surgery. Contraindications to the procedure included irreversible coagulopathy or other general medical condition that would preclude surgery, lack of response to dopamine, or poor neuropsychologic testing performance (Mattis Dementia Rating Scale score 130). Perioperative Details Patients receive implants in the STN or GPi. The surgery is performed in 2 stages. In stage I, quadripolar DBS electrodes (model 3389) a are implanted bilaterally using CT and MRI fusion and microelectrode recording for electrophysiologic target confirmation. Our surgical technique followed closely the methods for microrecording and electrode implantation that have been published elsewhere. 4-9 Stage I was performed under local anesthesia with minimal intravenous sedation. Dopamine agonists were held for 2 weeks before the procedure to allow for washout of these medications. If patients were taking the extended-release form of carbidopa-levodopa, they were changed to the regular form. Postoperatively, a brain CT was obtained to check for intracranial hemorrhage. MRI was not routinely performed to examine electrode position; it was only performed in the event of lack of benefit from the stimulator. Patients were observed in the hospital overnight and then discharged to home the next day. The following week, patients returned for stage II, in which bilateral extensions and pulse generators (Soletra) a were implanted in subcutaneous pockets in the chest under general anesthesia. If patients showed improvement in their symptoms after stage I due to lesioning effect, stage II was delayed until the lesioning effect abates. After the stage II procedure, patients were observed for several hours in the postanesthesia and ambulatory care units. As long as there were no complications, the patients were then transferred, on the afternoon of surgery, directly to an inpatient rehabilitation facility for our fast-track program. Fast-Track Programming and Rehabilitation Information obtained from the intraoperative mapping is shared with the physiatrists to facilitate initial programming. Specifically, the location of the electrode contacts relative to the borders of the nucleus (determined by intraoperative microrecording) is communicated to the physiatrists to provide a physiologically defined starting point for programming. Physiatrists receive special training in DBS programming, and all programming is done in consultation with the movement disorder neurologist. Baseline FIM instrument scores are obtained on admission to the rehabilitation facility by a physiatrist certified in its administration, along with a complete physical examination. Programming is started on the second day, with all parkinsonian medications having been held since the prior evening. FIM scores are repeated at discharge, and the average number of stimulator adjustments made during the inpatient stay is recorded. UPDRS scores are repeated at 3 months and 12 months in the on-medication, on-stimulation condition. Comparing these scores with the preoperative on-medication score provides a good measure of stimulation effect, because the presence of stimulation is the only difference between the preoperative and postoperative condition. The FIM score is composed of 18 items, with the score on each item ranging from 1 (total assistance) to 7 (complete independence). The composite score ranges from 18 (lowest level of independence) to 126 (highest level of independence). The total score is composed of motor and cognitive components. The motor subscore contains 13 items (maximum score 91), whereas the cognitive subscore contains 5 items (maximum score 35). The FIM score is the most commonly used functional assessment scale and is designed to measure severity of disability and assess response to rehabilitation. The FIM describes patient s abilities and limits with relation to activities involved in everyday life, and reflects a patient s usual performance instead of their optimal performance. It has been shown to be both reliable, valid, and responsive. 10 The UPDRS was developed to provide a single comprehensive rating scale for Parkinson s disease patients. It consists of 4 subsections: behavior, activities of daily living, motor examination, and complications of therapy. We used the motor subsection to evaluate our patients. The motor subsection contains 14 items concerning various aspects of the clinical examination (eg, tremor, rigidity, bradykinesia, speech) with the score for each item ranging from 0 (normal function) to 4 (most severe symptoms). The overall scores on this subsection range from 0 to 56. Initial stimulation parameters are a frequency of 130Hz and a pulse width of 60 s. Stimulation is first carried out in a unipolar mode (ie, using 1 of the 4 contacts on each electrode). Each electrode is tested for efficacy and threshold for side effects. Selection of which contact to use is made based on the contact(s) which give the greatest degree of symptomatic improvement at the lowest voltage without inducing side effects. After the initial electrode settings have been found, the stimulators are usually set to 1.0 to 1.5V. After holding all parkinsonian medications since the prior evening, on the morning that programming begins the patients levodopa-carbidopa dose (Sinemet CR) is decreased by 50% from the preoperative baseline. The dose is then further adjusted as necessary at the discretion of the movement disorder neurologist. During the inpatient stay, the DBS parameters are titrated every 1 to 2 days, depending on symptom response and the presence of dyskinesia. Patient Care While the patient undergoes inpatient programming, routine medical and postoperative wound care takes place. Residual functional and physical problems are managed in the context of a comprehensive therapy program. Physical, occupational, and speech therapists provide care individualized to each patient s needs, and cognitive function is reassessed postoperatively. Nutritional counseling is provided to help patients manage the frequent weight gain that occurs after DBS. Psychologic counseling is available to help patients adjust to their greater degree of independence and autonomy and to help caregiving relatives cope with their changing role. Psychologists also provide assistance with alterations in patients moods following medication adjustments. Case managers help with insurance coverage and coordination of postdischarge therapy or care. Patients are discharged from the rehabilitation facility at the discretion of the physiatrist and movement disorder neurologist when they are judged to have obtained the maximum acute benefit from surgery.

3 1322 FAST-TRACK DEEP BRAIN STIMULATION REHABILITATION, Cohen Table 1: Patient Characteristics Characteristics Average Age (range), y 60.6 (43 80) Sex, n (%) Male 50 (68.5) Female 23 (31.5) Implant site, n (%) STN 71 (97.3) GPi 2 (2.7) Chief complaint, n (%) Freezing 24 (32.9) Tremor 22 (30.1) Dyskinesia 15 (20.5) Rigidity 11 (15.1) Bradykinesia 1 (1.4) Duration of disease (range), y 13.6 (3 27) Statistical Analysis The changes in FIM scores from rehabilitation admission to discharge, including subanalysis of the motor and cognitive components, as well as the change in UPDRS scores from preoperative to postoperative and the change in daily levodopa dose, were statistically compared using a paired t test. RESULTS The average age of the 73 patients was 60.6 years. There were 50 men (68.5%) and 23 women (31.5%). Seventy-one (97.3%) patients were implanted in STN and 2 in GPi (2.7%). Demographic information is shown in table 1, and procedural details can be found in table 2. FIM scores standard deviation at admission to the rehabilitation facility averaged , and improved to an average of at discharge, yielding an average improvement of 36.4 (58.6%) (P.001) (fig 1). The motor component of the FIM score increased from at admission to at discharge, an average improvement of 29.0 (78.0%) (P.001). The cognitive subscore increased from at admission to at discharge, an average improvement of 4.5 (19.4%) (P.001). The average number of stimulator adjustments during the rehabilitation stay was From discharge from rehabilitation until 3 months postoperative, an average of further stimulator adjustments were made. Patients average daily dose of levodopa significantly decreased from 1084mg preoperatively to 560mg at 3 months postoperatively, for an average reduction of 524mg (48.3%) (P.001). The average length of stay in the rehabilitation facility was days. Average UPDRS scores improved from (preoperative off score) and (preoperative on score) to Table 2: Operating Department Data Data Operating room time* Surgical time* Microrecording time (left side)* Microrecording time (right side)* Microelectrode tracks (left side) Microelectrode tracks (right side) *In minutes. Average (Range) ( ) (75 303) 35.6 (10 103) 26.9 (8 100) 1.3 (1 3) 1.5 (1 5) Fig 1. UPDRS and FIM scores before and after DBS. *P<.001 between pre- and postoperative; P<.001 between admission and discharge from fast-track rehabilitation (3-mo postoperative score), an improvement of 9.7 (32.2%) from the preoperative on score (P.001) (see fig 1). Although the sample size in whom 12-month postoperative UPDRS scores were available was limited (27 patients), there was evidence of maintenance of benefit, with an average UP- DRS score of (P.001 in comparison with preoperative on score). The 3-month and 12-month postoperative scores did not differ significantly (P.94). DISCUSSION The process of programming after DBS surgery is complicated and time-intensive. 2,3 The time involved to observe clinical effects after a programming change contributes to the many months that it often takes, using traditional methods, to realize full clinical benefit from DBS. As noted by Volkmann et al, 11 the response of bradykinesia and tremor to stimulation adjustments may be variable, and some complications of DBS may not occur for hours after a programming adjustment. Therefore, the time of day that a patient can safely undergo adjustment in the outpatient setting is generally limited to the morning. In contrast, in an inpatient setting, with constant supervision by and availability of the treating physician, programming changes can be made throughout the day. This could potentially allow for expediting the programming process. The goal of our fast-track method of inpatient programming and rehabilitation of the DBS patient is to allow for rapid initial programming of the devices, prompt identification and treatment of medical complications, and early restoration of function. It also provides patients tools to quickly adapt to their improved level of function and lifestyle. A recent consensus report acknowledged that there is a lack of studies in the literature addressing immediate postoperative care and little information on medication management after surgery. 12 In this initial report, we provide a description of our methods and the favorable results we have obtained using it, and adds to the literature on patient management following DBS; we do not claim superiority to traditional methods of postoperative care. We have obtained rapid improvement in motor symptoms in our patients with this method as measured with UPDRS scores. The UPDRS, however, is not ideal at measuring overall functional improvement after surgical interventions. Other limitations of the UPDRS are the subjective nature of rigidity measurement 13 and poor interrater reliability of some aspects of the motor section. 14 For this study, the FIM score was felt to

4 FAST-TRACK DEEP BRAIN STIMULATION REHABILITATION, Cohen 1323 provide a better measure for patients response to DBS and postoperative rehabilitation. For patients who live a long distance away from programming facilities, the initial inpatient programming and rehabilitation spares the patient and their family the burden of repeated long travel for adjustments. With our method, over 80% of stimulator adjustments are completed during the 2- to 3-week inpatient stay, as compared with the many weeks to months that are required for initial programming on an outpatient basis. This may allow patients to realize the benefit of DBS sooner than if they were programmed entirely in the outpatient setting. In our patients, most of the improvement in the FIM score was due to a large, statistically significant increase in the motor component. The functional improvement that we observed in our patients at discharge from fast-track rehabilitation and at 3-month follow-up was similar to the improvement noted at 3 months in 1 study 15 and at least equivalent to the typical 6-month outcomes reported in the literature. 16 The rapid tapering of medications also can often represent a substantial cost saving to the patient and their insurance carrier. For example, 60 tablets of Sinemet CR 25/100mg costs $ Our average patient took 1084mg/d preoperatively ($331.29/mo) and 560mg/d postoperatively ($171.78/mo). For patients taking frequent doses of multiple medications, rapid tapering can thus have economic benefit. A cost-effectiveness analysis of our fast-track model could be of use to balance the cost of inpatient rehabilitation against the savings resulting from medication tapering. Because Parkinson s disease frequently leads to a lifestyle of decreased physical activity, patients often present with muscle shortening and loss of joint range of motion (ROM), as well as varying degrees of deconditioning. The inpatient setting allows the physical therapist to tailor a stretching, ROM, and postural program to the needs of the patient. Ongoing gait and balance retraining occurs, and higher level gait and mobility skills that the patient may not have been able to manage prior to DBS can be undertaken. Occupational therapists are used to evaluate and treat the patients functional loss in activities of daily living, and assist with community re-entry. Physical conditioning and endurance activities are included in both the inpatient program and home instructions. A specific exercise program is given for use after discharge, to maintain physical gains. Speech and oral-motor symptoms are often less responsive to DBS. In these patients, speech therapists provide training to help the patient communicate more effectively. The speech therapist also examines the swallowing process, with the use of a modified barium swallow test in selected patients, to detect oral-motor problems and the risk of aspiration. Dietary modification to allow for easier food handling and to minimize the chances of aspiration is recommended if problems are found. The speech therapist also evaluates the cognitive aspects of language, and provides training to improve any deficits encountered. An audiologist is also available to screen hearing, and to make recommendations to improve auditory function. Patients undergoing DBS go through cognitive testing as part of their initial evaluation. The neurobehavioral specialist of the treatment team re-evaluates cognitive function to assess pre- and postimplantation cognitive processing. The neurobehaviorist also remains available if any unexpected thought process or behavioral problems arise postoperatively during programming, because changes in certain stimulation parameters are associated with specific alterations in cognitive performance. 18 We found that the cognitive component of the FIM score improved after DBS and fast-track rehabilitation. Although this change was relatively small (19.4%) compared with the motor improvement, it was statistically significant. The dynamics of family relationships may change following DBS, because patients realize a much greater degree of independence and autonomy. Psychologists provide counseling and training in coping and communication skills, and aid in the detection and treatment of any mood or affect changes. Changes in psychiatric symptoms have been noted after DBS, perhaps due to involvement of the limbic STN in mood disorders associated with Parkinson s disease. 22 Preoperative psychologic screening and postoperative psychologic and psychiatric care are important, especially because many postoperative psychiatric problems may actually be related to emergence of previously existing disorders that had not been noted preoperatively. 23 Although worsening of mood symptoms has been noted, antidepressant effects of DBS have been more commonly reported than depressant effects. 24 DBS has also been shown to result in an improved health-related quality of life for Parkinson s disease patients 25 and showed a trend toward significant improvement (P.15) in health-related quality of life over unilateral pallidotomy in a randomized study. 26 Study Limitations There are several limitations of the present study. One weakness of this article is its retrospective nature, with all of the biases inherent in such a study design. Also, this initial report is intended only to serve as a description of our methods; we do not compare our results with a control group receiving usual care. The lack of a control group does not allow us to determine how much of the patients improvement is a result of our fast-track programming and rehabilitation protocol, and how much is simply a result of the DBS procedure itself. A randomized, controlled trial of fast-track programming and rehabilitation compared with usual care could provide stronger evidence for the efficacy of our method. Additionally, the inclusion of cost data in such a trial could prove the costeffectiveness of the fast-track method. Stratifying patients into subgroups based on factors such as age, comorbidities, etc, was not performed in this study due to the relatively small study size and resulting small size of subgroups. We believe that post hoc analysis would not be statistically or clinically valid in this situation. We also did not analyze patients average stimulation parameters at various time points, because one point of this study is to show that most programming is done during the initial rehabilitation stay, as opposed to presenting our overall results with DBS for Parkinson s disease. Finally, off-stimulation, off-medication UPDRS scores were not routinely obtained in our patients so as not to interfere with the intensive rehabilitation and programming protocol. Such scores would need to be included in a future study comparing our fast-track method with traditional programming methods. Clinical Implications Our fast-track, integrated inpatient rehabilitation and programming protocol, performed by a dedicated team, has several major benefits. First, the majority of initial programming can be accomplished over 2 to 3 weeks, instead of months. This study suggests that functional improvement is maximized after the inpatient stay and that there is little change noted at longterm follow-up. This expeditious programming may allow the patient to realize the benefits of DBS sooner than with traditional methods, although another, comparative study would need to be performed to prove this. Second, medications can be quickly tapered, resulting in cost savings to the patient and health system overall and reduction in medication side effects.

5 1324 FAST-TRACK DEEP BRAIN STIMULATION REHABILITATION, Cohen Both a retrospective study and a cost-effectiveness decision model have already provided evidence for overall cost savings from DBS, 27,28 but a prospective randomized study to demonstrate the cost-effectiveness of DBS would be a valuable contribution to the literature. Third, physical performance can be optimized in the timeliest manner possible by combining rehabilitation services with DBS programming. Last, the patient receives close medical attention in the postoperative period. Greater attention can be given to concomitant medical and psychologic problems as well as to wound care. All of these benefits allow the Parkinson s disease patient to address the myriad life changes that come with the rapid improvement in quality of life in a cohesive disease based fashion. CONCLUSIONS Our model of fast-track rehabilitation and programming after DBS for Parkinson s disease allows for rapid programming and tapering of Parkinson s medications. Concomitantly, patients physical performance can be optimized in a timely fashion. This protocol may represent a more efficient and efficacious method for postoperative DBS care. References 1. Okun MS, Foote KD. Subthalamic nucleus vs globus pallidus interna deep brain stimulation, the rematch. Arch Neurol 2005; 62: Volkmann J, Herzog J, Kopper F, Deuschl G. Introduction to the programming of deep brain stimulators. Mov Disord 2002;17: S Kumar R. Methods for programming and patient management with deep brain stimulation of the globus pallidus for the treatment of advanced Parkinson s disease and dystonia. Mov Disord 2002; 17:S Broggi G, Franzini A, Ferroli P, et al. Effect of bilateral subthalamic electrical stimulation in Parkinson s disease. Surg Neurol 2001;56:89-94; discussion Burchiel KJ, Anderson VC, Favre J, Hammerstad JP. Comparison of pallidal and subthalamic nucleus deep brain stimulation for advanced Parkinson s disease: results of a randomized, blinded pilot study. Neurosurgery 1999;45: Krause M, Fogel W, Heck A, et al. Deep brain stimulation for the treatment of Parkinson s disease: subthalamic nucleus versus globus pallidus internus. J Neurol Neurosurg Psychiatry 2001;70: Pahwa R, Wilkinson SB, Overman J, Lyons KE. Bilateral subthalamic stimulation in patients with Parkinson disease: long-term follow up. J Neurosurg 2003;99: Simuni T, Jaggi JL, Mulholland H, et al. Bilateral stimulation of the subthalamic nucleus in patients with Parkinson disease: a study of efficacy and safety. J Neurosurg 2002;96: Starr PA, Christine CW, Theodosopoulos PV, et al. Implantation of deep brain stimulators into the subthalamic nucleus: technical approach and magnetic resonance imaging-verified lead locations. 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