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Chapter 12 - Assessing patient outcome and troubleshooting deep brain stimulation

Published online by Cambridge University Press:  05 September 2015

William J. Marks, Jr
Affiliation:
University of California, San Francisco
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Publisher: Cambridge University Press
Print publication year: 2015

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References

Okun, MS, Tagliati, M, Pourfar, M, et al. Management of referred deep brain stimulation failures: a retrospective analysis from 2 movement disorders centers. Archives of Neurology. 2005;62(8):1250–55.CrossRefGoogle ScholarPubMed
Goetz, CG, Fahn, S, Martinez-Martin, P, et al. Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): Process, format, and clinimetric testing plan. Movement Disorders: Official Journal of the Movement Disorder Society. 2007;22(1):4147.CrossRefGoogle ScholarPubMed
Morishita, T, Rahman, M, Foote, KD, et al. DBS candidates that fall short on a levodopa challenge test: alternative and important indications. The Neurologist. 2011;17(5):263–68.CrossRefGoogle ScholarPubMed
Defer, GL, Widner, H, Marie, RM, Remy, P, Levivier, M. Core assessment program for surgical interventional therapies in Parkinson's disease (CAPSIT-PD). Movement Disorders: Official Journal of the Movement Disorder Society. 1999;14(4):572–84.3.0.CO;2-C>CrossRefGoogle ScholarPubMed
Germano, IM, Gracies, JM, Weisz, DJ, et al. Unilateral stimulation of the subthalamic nucleus in Parkinson disease: a double-blind 12-month evaluation study. Journal of Neurosurgery. 2004;101(1):3642.CrossRefGoogle ScholarPubMed
Loher, TJ, Burgunder, JM, Pohle, T, et al. Long-term pallidal deep brain stimulation in patients with advanced Parkinson disease: 1-year follow-up study. Journal of Neurosurgery. 2002;96(5):844–53.CrossRefGoogle ScholarPubMed
Weaver, F, Follett, K, Hur, K, Ippolito, D, Stern, M. Deep brain stimulation in Parkinson disease: a metaanalysis of patient outcomes. Journal of Neurosurgery. 2005;103(6):956–67.CrossRefGoogle ScholarPubMed
Williams, NR, Foote, KD, Okun, MS. STN vs. GPi deep brain stimulation: translating the rematch into clinical practice. Movement Disorders Clinical Practice. 2014;1(1):2435.CrossRefGoogle ScholarPubMed
Blomstedt, P, Hariz, GM, Hariz, MI, Koskinen, LO. Thalamic deep brain stimulation in the treatment of essential tremor: a long-term follow-up. British Journal of Neurosurgery. 2007;21(5):504–09.CrossRefGoogle ScholarPubMed
Koller, WC, Lyons, KE, Wilkinson, SB, Troster, AI, Pahwa, R. Long-term safety and efficacy of unilateral deep brain stimulation of the thalamus in essential tremor. Movement Disorders: Official Journal of the Movement Disorder Society. 2001;16(3):464–68.CrossRefGoogle ScholarPubMed
Vickrey, BG. Getting oriented to patient-oriented outcomes. Neurology. 1999;53(4):662–63.CrossRefGoogle ScholarPubMed
Guyatt, GH, Bombardier, C, Tugwell, PX. Measuring disease-specific quality of life in clinical trials. CMAJ: Canadian Medical Association journal = journal de l'Association medicale canadienne. 1986;134(8):889–95.Google ScholarPubMed
Doward, LC, McKenna, SP. Defining patient-reported outcomes. Value in Health: The Journal of the International Society for Pharmacoeconomics and Outcomes Research. 2004;7(Suppl 1):S48.CrossRefGoogle ScholarPubMed
Hayes, V, Morris, J, Wolfe, C, Morgan, M. The SF-36 health survey questionnaire: is it suitable for use with older adults? Age and Ageing. 1995;24(2):120–25.CrossRefGoogle ScholarPubMed
Hill, S, Harries, U, Popay, J. Is the short form 36 (SF-36) suitable for routine health outcomes assessment in health care for older people? Evidence from preliminary work in community based health services in England. Journal of Epidemiology and Community Health. 1996;50(1):9498.CrossRefGoogle ScholarPubMed
Hobson, JP, Meara, RJ. Is the SF-36 health survey questionnaire suitable as a self-report measure of the health status of older adults with Parkinson's disease? Quality of Life Research : An International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation. 1997;6(3):213–16.CrossRefGoogle ScholarPubMed
Ware, JE Jr., Sherbourne, CD. The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Medical Care. 1992;30(6):473–83.CrossRefGoogle ScholarPubMed
Hunt, SM, McKenna, SP, McEwen, J, Williams, J, Papp, E. The Nottingham Health Profile: subjective health status and medical consultations. Social Science & Medicine Part A, Medical Sociology. 1981;15(3 Pt 1):221–29.CrossRefGoogle ScholarPubMed
Kind, P, Carr-Hill, R. The Nottingham health profile: a useful tool for epidemiologists? Social Science & Medicine. 1987;25(8):905–10.CrossRefGoogle ScholarPubMed
Bergner, M, Bobbitt, RA, Carter, WB, Gilson, BS. The Sickness Impact Profile: development and final revision of a health status measure. Medical Care. 1981;19(8):787805.CrossRefGoogle ScholarPubMed
Welsh, M, McDermott, MP, Holloway, RG, et al. Development and testing of the Parkinson's disease quality of life scale. Movement Disorders: Official Journal of the Movement Disorder Society. 2003;18(6):637–45.CrossRefGoogle ScholarPubMed
Kuehler, A, Henrich, G, Schroeder, U, et al. A novel quality of life instrument for deep brain stimulation in movement disorders. Journal of Neurology, Neurosurgery, and Psychiatry. 2003;74(8):1023–30.CrossRefGoogle ScholarPubMed
Devlin, N, Williams, A. Valuing quality of life: results for New Zealand health professionals. The New Zealand Medical Journal. 1999;112(1083):6871.Google ScholarPubMed
Hobson, P, Holden, A, Meara, J. Measuring the impact of Parkinson's disease with the Parkinson's Disease Quality of Life questionnaire. Age and Ageing. 1999;28(4):341–46.CrossRefGoogle ScholarPubMed
Jenkinson, C, Fitzpatrick, R, Argyle, M. The Nottingham Health Profile: an analysis of its sensitivity in differentiating illness groups. Social Science & Medicine. 1988;27(12):1411–14.CrossRefGoogle ScholarPubMed
Wiklund, I. The Nottingham Health Profile – a measure of health-related quality of life. Scandinavian Journal of Primary Health Care Supplement. 1990;1:1518.Google ScholarPubMed
Hagell, P, Whalley, D, McKenna, SP, Lindvall, O. Health status measurement in Parkinson's disease: validity of the PDQ-39 and Nottingham Health Profile. Movement Disorders: Official Journal of the Movement Disorder Society. 2003;18(7):773–83.CrossRefGoogle ScholarPubMed
Hunt, SM, McKenna, SP. Validating the SF-36. BMJ. 1992;305(6854):645; author reply 6.CrossRefGoogle ScholarPubMed
Sullivan, M, Karlsson, J, Ware, JE Jr. The Swedish SF-36 Health Survey – I. Evaluation of data quality, scaling assumptions, reliability and construct validity across general populations in Sweden. Social Science & Medicine. 1995;41(10):1349–58.CrossRefGoogle ScholarPubMed
Den Oudsten, BL, Van Heck, GL, De Vries, J. The suitability of patient-based measures in the field of Parkinson's disease: a systematic review. Movement Disorders: Official Journal of the Movement Disorder Society. 2007;22(10):1390–401.CrossRefGoogle ScholarPubMed
Thorsen, H, McKenna, S, Tennant, A, Holstein, P. Nottingham health profile scores predict the outcome and support aggressive revascularisation for critical ischaemia. European Journal of Vascular and Endovascular Surgery: The Official Journal of the European Society for Vascular Surgery. 2002;23(6):495–99.CrossRefGoogle ScholarPubMed
Troster, AI, Pahwa, R, Fields, JA, Tanner, CM, Lyons, KE. Quality of life in Essential Tremor Questionnaire (QUEST): development and initial validation. Parkinsonism & Related Disorders. 2005;11(6):367–73.CrossRefGoogle ScholarPubMed
Damiano, AM, Snyder, C, Strausser, B, Willian, MK. A review of health-related quality-of-life concepts and measures for Parkinson's disease. Quality of Life Research: An International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation. 1999;8(3):235–43.CrossRefGoogle ScholarPubMed
Diamond, A, Jankovic, J. The effect of deep brain stimulation on quality of life in movement disorders. Journal of Neurology, Neurosurgery, and Psychiatry. 2005;76(9):1188–93.CrossRefGoogle ScholarPubMed
Schulzer, M, Mak, E, Calne, SM. The psychometric properties of the Parkinson's Impact Scale (PIMS) as a measure of quality of life in Parkinson's disease. Parkinsonism & Related Disorders. 2003;9(5):291–94.CrossRefGoogle ScholarPubMed
Calne, SM, Mak, E, Hall, J, et al. Validating a quality-of-life scale in caregivers of patients with Parkinson's disease: Parkinson's Impact Scale (PIMS). Advances in Neurology. 2003;91:115–22.Google ScholarPubMed
Jenkinson, C, Fitzpatrick, R, Peto, V, Greenhall, R, Hyman, N. The Parkinson's Disease Questionnaire (PDQ-39): development and validation of a Parkinson's disease summary index score. Age and Ageing. 1997;26(5):353–57.CrossRefGoogle ScholarPubMed
Peto, V, Jenkinson, C, Fitzpatrick, R, Greenhall, R. The development and validation of a short measure of functioning and well being for individuals with Parkinson's disease. Quality of Life Research: An International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation. 1995;4(3):241–48.CrossRefGoogle Scholar
Blahak, C, Wohrle, JC, Capelle, HH, et al. Health-related quality of life in segmental dystonia is improved by bilateral pallidal stimulation. Journal of Neurology. 2008;255(2):178–82.CrossRefGoogle ScholarPubMed
Halbig, TD, Gruber, D, Kopp, UA, et al. Pallidal stimulation in dystonia: effects on cognition, mood, and quality of life. Journal of Neurology, Neurosurgery, and Psychiatry. 2005;76(12):1713–16.CrossRefGoogle ScholarPubMed
Mueller, J, Skogseid, IM, Benecke, R, et al. Pallidal deep brain stimulation improves quality of life in segmental and generalized dystonia: results from a prospective, randomized sham-controlled trial. Movement Disorders: Official Journal of the Movement Disorder Society. 2008;23(1):131–34.CrossRefGoogle ScholarPubMed
Skogseid, IM. Pallidal deep brain stimulation is effective, and improves quality of life in primary segmental and generalized dystonia. Acta Neurologica Scandinavica Supplementum. 2008;188:5155.CrossRefGoogle ScholarPubMed
Vingerhoets, G, Lannoo, E, van der Linden, C, et al. Changes in quality of life following unilateral pallidal stimulation in Parkinson's disease. Journal of Psychosomatic Research. 1999;46(3):247–55.CrossRefGoogle ScholarPubMed
Castelli, L, Perozzo, P, Zibetti, M, et al. Chronic deep brain stimulation of the subthalamic nucleus for Parkinson's disease: effects on cognition, mood, anxiety and personality traits. European Neurology. 2006;55(3):136–44.CrossRefGoogle ScholarPubMed
Funkiewiez, A, Ardouin, C, Caputo, E, et al. Long term effects of bilateral subthalamic nucleus stimulation on cognitive function, mood, and behaviour in Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 2004;75(6):834–39.CrossRefGoogle ScholarPubMed
Voon, V, Moro, E, Saint-Cyr, JA, Lozano, AM, Lang, AE. Psychiatric symptoms following surgery for Parkinson's disease with an emphasis on subthalamic stimulation. Advances in Neurology. 2005;96:130–47.Google ScholarPubMed
Odekerken, VJ, van Laar, T, Staal, MJ, et al. Subthalamic nucleus versus globus pallidus bilateral deep brain stimulation for advanced Parkinson's disease (NSTAPS study): a randomised controlled trial. Lancet Neurology. 2013;12(1):3744.CrossRefGoogle ScholarPubMed
Mink, JW, Walkup, J, Frey, KA, et al. Patient selection and assessment recommendations for deep brain stimulation in Tourette syndrome. Movement Disorders: Official Journal of the Movement Disorder Society. 2006;21(11):1831–38.CrossRefGoogle ScholarPubMed
Rodriguez, RL, Fernandez, HH, Haq, I, Okun, MS. Pearls in patient selection for deep brain stimulation. The Neurologist. 2007;13(5):253–60.CrossRefGoogle ScholarPubMed
Contarino, MF, Daniele, A, Sibilia, AH, et al. Cognitive outcome 5 years after bilateral chronic stimulation of subthalamic nucleus in patients with Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 2007;78(3):248–52.Google ScholarPubMed
Dujardin, K, Defebvre, L, Krystkowiak, P, Blond, S, Destee, A. Influence of chronic bilateral stimulation of the subthalamic nucleus on cognitive function in Parkinson's disease. Journal of Neurology. 2001;248(7):603–11.CrossRefGoogle ScholarPubMed
Moretti, R, Torre, P, Antonello, RM, et al. Neuropsychological changes after subthalamic nucleus stimulation: a 12 month follow-up in nine patients with Parkinson's disease. Parkinsonism & Related Disorders. 2003;10(2):7379.CrossRefGoogle ScholarPubMed
Schroeder, U, Kuehler, A, Haslinger, B, et al. Subthalamic nucleus stimulation affects striato-anterior cingulate cortex circuit in a response conflict task: a PET study. Brain: A Journal of Neurology. 2002;125(Pt 9):19952004.CrossRefGoogle Scholar
Schupbach, WM, Chastan, N, Welter, ML, et al. Stimulation of the subthalamic nucleus in Parkinson's disease: a 5 year follow up. Journal of Neurology, Neurosurgery, and Psychiatry. 2005;76(12):1640–44.CrossRefGoogle ScholarPubMed
Alegret, M, Junque, C, Valldeoriola, F, et al. Effects of bilateral subthalamic stimulation on cognitive function in Parkinson disease. Archives of Neurology. 2001;58(8):1223–27.CrossRefGoogle ScholarPubMed
Morrison, CE, Borod, JC, Perrine, K, et al. Neuropsychological functioning following bilateral subthalamic nucleus stimulation in Parkinson's disease. Archives of Clinical Neuropsychology: The Official Journal of the National Academy of Neuropsychologists. 2004;19(2):165–81.CrossRefGoogle ScholarPubMed
Saint-Cyr, JA, Trepanier, LL, Kumar, R, Lozano, AM, Lang, AE. Neuropsychological consequences of chronic bilateral stimulation of the subthalamic nucleus in Parkinson's disease. Brain: A Journal of Neurology. 2000;123(Pt 10):2091–108.CrossRefGoogle ScholarPubMed
Gironell, A, Kulisevsky, J, Rami, L, et al. Effects of pallidotomy and bilateral subthalamic stimulation on cognitive function in Parkinson disease. A controlled comparative study. Journal of Neurology. 2003;250(8):917–23.CrossRefGoogle ScholarPubMed
De Gaspari, D, Siri, C, Di Gioia, M, et al. Clinical correlates and cognitive underpinnings of verbal fluency impairment after chronic subthalamic stimulation in Parkinson's disease. Parkinsonism & Related Disorders. 2006;12(5):289–95.CrossRefGoogle ScholarPubMed
De Gaspari, D, Siri, C, Landi, A, et al. Clinical and neuropsychological follow up at 12 months in patients with complicated Parkinson's disease treated with subcutaneous apomorphine infusion or deep brain stimulation of the subthalamic nucleus. Journal of Neurology, Neurosurgery, and Psychiatry. 2006;77(4):450–53.CrossRefGoogle ScholarPubMed
Williams, AE, Arzola, GM, Strutt, AM, et al. Cognitive outcome and reliable change indices two years following bilateral subthalamic nucleus deep brain stimulation. Parkinsonism & Related Disorders. 2011;17(5):321–27.CrossRefGoogle ScholarPubMed
Folstein, MF, Folstein, SE, McHugh, PR. “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research. 1975;12(3):189–98.Google Scholar
Gardner, R Jr., Oliver-Munoz, S, Fisher, L, Empting, L. Mattis Dementia Rating Scale: internal reliability study using a diffusely impaired population. Journal of Clinical Neuropsychology. 1981;3(3):271–75.CrossRefGoogle ScholarPubMed
D W. Wechsler Adult Intelligence Scale (WAIS-3R). Third ed. San Antonio, TX: Harcourt Assessment; 1997.Google Scholar
Lhermitte, F, Pillon, B, Serdaru, M. Human autonomy and the frontal lobes. Part I: Imitation and utilization behavior: a neuropsychological study of 75 patients. Annals of Neurology. 1986;19(4):326–34.CrossRefGoogle ScholarPubMed
Nelson, HE. A modified card sorting test sensitive to frontal lobe defects. Cortex; A Journal Devoted to the Study of the Nervous System and Behavior. 1976;12(4):313–24.CrossRefGoogle ScholarPubMed
Giovagnoli, AR, Del Pesce, M, Mascheroni, S, et al. Trail making test: normative values from 287 normal adult controls. Italian Journal of Neurological Sciences. 1996;17(4):305–09.CrossRefGoogle ScholarPubMed
Miner, T, Ferraro, FR. The role of speed of processing, inhibitory mechanisms, and presentation order in trail-making test performance. Brain and Cognition. 1998;38(2):246–53.CrossRefGoogle ScholarPubMed
Tombaugh, TN, Kozak, J, Rees, L. Normative data stratified by age and education for two measures of verbal fluency: FAS and animal naming. Archives of Clinical Neuropsychology: The Official Journal of the National Academy of Neuropsychologists. 1999;14(2):167–77.Google ScholarPubMed
Benton, AL, Hamsher, K. Multilingual Aphasia Examination. Iowa City, IA: AJA Associates; 1989.Google Scholar
Amodio, P, Wenin, H, Del Piccolo, F, et al. Variability of trail making test, symbol digit test and line trait test in normal people. A normative study taking into account age-dependent decline and sociobiological variables. Aging Clinical and Experimental Research. 2002;14(2):117–31.CrossRefGoogle ScholarPubMed
Arbuthnott, K, Frank, J. Trail making test, part B as a measure of executive control: validation using a set-switching paradigm. Journal of Clinical and Experimental Neuropsychology. 2000;22(4):518–28.CrossRefGoogle ScholarPubMed
Mascolo, MF, Hirtle, SC. Verbal coding and the elimination of Stroop interference in a matching task. The American Journal of Psychology. 1990;103(2):195215.CrossRefGoogle Scholar
Van der Elst, W, Van Boxtel, MP, Van Breukelen, GJ, Jolles, J. Detecting the significance of changes in performance on the Stroop Color-Word Test, Rey's Verbal Learning Test, and the Letter Digit Substitution Test: the regression-based change approach. Journal of the International Neuropsychological Society: JINS. 2008;14(1):7180.CrossRefGoogle ScholarPubMed
Flowers, KA, Robertson, C. The effect of Parkinson's disease on the ability to maintain a mental set. Journal of Neurology, Neurosurgery, and Psychiatry. 1985;48(6):517–29.CrossRefGoogle ScholarPubMed
Wechsler Memory Scale. San Antonio, TX: The Psychological Corporation; 1997.Google Scholar
Owen, AM, Beksinska, M, James, M, et al. Visuospatial memory deficits at different stages of Parkinson's disease. Neuropsychologia. 1993;31(7):627–44.CrossRefGoogle ScholarPubMed
Cooper, JA, Sagar, HJ, Jordan, N, Harvey, NS, Sullivan, EV. Cognitive impairment in early, untreated Parkinson's disease and its relationship to motor disability. Brain: A Journal of Neurology. 1991;114(Pt 5):2095–122.CrossRefGoogle ScholarPubMed
Tombaugh, TN. A comprehensive review of the Paced Auditory Serial Addition Test (PASAT). Archives of Clinical Neuropsychology: The Official Journal of the National Academy of Neuropsychologists. 2006;21(1):5376.CrossRefGoogle ScholarPubMed
Wiens, AN, Fuller, KH, Crossen, JR. Paced Auditory Serial Addition Test: adult norms and moderator variables. Journal of Clinical and Experimental Neuropsychology. 1997;19(4):473–83.CrossRefGoogle ScholarPubMed
Frank, RM, Byrne, GJ. The clinical utility of the Hopkins Verbal Learning Test as a screening test for mild dementia. International Journal of Geriatric Psychiatry. 2000;15(4):317–24.3.0.CO;2-7>CrossRefGoogle ScholarPubMed
Shapiro, AM, Benedict, RH, Schretlen, D, Brandt, J. Construct and concurrent validity of the Hopkins Verbal Learning Test-revised. The Clinical Neuropsychologist. 1999;13(3):348–58.CrossRefGoogle ScholarPubMed
Poreh, A. Analysis of mean learning of normal participants on the Rey Auditory–Verbal Learning Test. Psychological Assessment. 2005;17(2):191–99.CrossRefGoogle ScholarPubMed
Ryan, JJ, Geisser, ME. Validity and diagnostic accuracy of an alternate form of the Rey Auditory Verbal Learning Test. Archives of Clinical Neuropsychology: The Official Journal of the National Academy of Neuropsychologists. 1986;1(3):209–17.CrossRefGoogle ScholarPubMed
Pillon, B, Deweer, B, Agid, Y, Dubois, B. Explicit memory in Alzheimer's, Huntington's, and Parkinson's diseases. Archives of Neurology. 1993;50(4):374–79.CrossRefGoogle ScholarPubMed
Cockburn, J. Performance on the Tower of London test after severe head injury. Journal of the International Neuropsychological Society: JINS. 1995;1(6):537–44.CrossRefGoogle ScholarPubMed
Delis, DC, Kramer, JH, Kaplan, E, Holdnack, J. Reliability and validity of the Delis-Kaplan Executive Function System: an update. Journal of the International Neuropsychological Society: JINS. 2004;10(2):301–03.CrossRefGoogle ScholarPubMed
Homack, S, Lee, D, Riccio, CA. Test review: Delis–Kaplan executive function system. Journal of Clinical and Experimental Neuropsychology. 2005;27(5):599609.CrossRefGoogle ScholarPubMed
Calero, MD, Arnedo, ML, Navarro, E, Ruiz-Pedrosa, M, Carnero, C. Usefulness of a 15-item version of the Boston Naming Test in neuropsychological assessment of low-educational elders with dementia. The Journals of Gerontology Series B, Psychological Sciences and Social Sciences. 2002;57(2):P187–91.Google ScholarPubMed
Kent, PS, Luszcz, MA. A review of the Boston Naming Test and multiple-occasion normative data for older adults on 15-item versions. The Clinical Neuropsychologist. 2002;16(4):555–74.CrossRefGoogle ScholarPubMed
Tombaugh, TN, Hubley, AM. The 60-item Boston Naming Test: norms for cognitively intact adults aged 25 to 88 years. Journal of Clinical and Experimental Neuropsychology. 1997;19(6):922–32.CrossRefGoogle ScholarPubMed
Gladsjo, JA, Schuman, CC, Evans, JD, et al. Norms for letter and category fluency: demographic corrections for age, education, and ethnicity. Assessment. 1999;6(2):147–78.CrossRefGoogle ScholarPubMed
Sunderland, T, Hill, JL, Mellow, AM, et al. Clock drawing in Alzheimer's disease. A novel measure of dementia severity. Journal of the American Geriatrics Society. 1989;37(8):725–29.CrossRefGoogle ScholarPubMed
Janvin, C, Aarsland, D, Larsen, JP, Hugdahl, K. Neuropsychological profile of patients with Parkinson's disease without dementia. Dementia and Geriatric Cognitive Disorders. 2003;15(3):126–31.CrossRefGoogle ScholarPubMed
Warrington, EK, James, M. The Visual Object and Space Perception Battery. Bury St Edmunds: Thames Valley Test Company; 1991.Google Scholar
Mason, CF, Ganzler, H. Adult norms for the Shipley Institute of Living Scale and Hooper Visual Organization Test based on age and education. Journal of Gerontology. 1964;19:419–24.CrossRefGoogle ScholarPubMed
Merten, T, Beal, C. An analysis of the Hooper Visual Organization Test with neurological patients. The Clinical Neuropsychologist. 1999;13(4):521–9.CrossRefGoogle ScholarPubMed
Schretlen, DJ, Pearlson, GD, Anthony, JC, Yates, KO. Determinants of Benton Facial Recognition Test performance in normal adults. Neuropsychology. 2001;15(3):405–10.CrossRefGoogle ScholarPubMed
Starkstein, SE, Mayberg, HS, Preziosi, TJ, et al. Reliability, validity, and clinical correlates of apathy in Parkinson's disease. The Journal of Neuropsychiatry and Clinical Neurosciences. 1992;4(2):134–39.Google ScholarPubMed
Sockeel, P, Dujardin, K, Devos, D, et al. The Lille apathy rating scale (LARS), a new instrument for detecting and quantifying apathy: validation in Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 2006;77(5):579–84.CrossRefGoogle Scholar
Bruss, GS, Gruenberg, AM, Goldstein, RD, Barber, JP. Hamilton Anxiety Rating Scale Interview guide: joint interview and test-retest methods for interrater reliability. Psychiatry Research. 1994;53(2):191202.CrossRefGoogle ScholarPubMed
Leentjens, AF, Verhey, FR, Lousberg, R, Spitsbergen, H, Wilmink, FW. The validity of the Hamilton and Montgomery–Asberg depression rating scales as screening and diagnostic tools for depression in Parkinson's disease. International Journal of Geriatric Psychiatry. 2000;15(7):644–49.3.0.CO;2-L>CrossRefGoogle ScholarPubMed
Weintraub, D, Oehlberg, KA, Katz, IR, Stern, MB. Test characteristics of the 15-item geriatric depression scale and Hamilton depression rating scale in Parkinson disease. The American Journal of Geriatric Psychiatry: Official Journal of the American Association for Geriatric Psychiatry. 2006;14(2):169–75.CrossRefGoogle ScholarPubMed
Visser, M, Leentjens, AF, Marinus, J, Stiggelbout, AM, van Hilten, JJ. Reliability and validity of the Beck depression inventory in patients with Parkinson's disease. Movement Disorders: Official Journal of the Movement Disorder Society. 2006;21(5):668–72.CrossRefGoogle ScholarPubMed
Ertan, FS, Ertan, T, Kiziltan, G, Uygucgil, H. Reliability and validity of the Geriatric Depression Scale in depression in Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 2005;76(10):1445–47.CrossRefGoogle ScholarPubMed
Biggs, JT, Wylie, LT, Ziegler, VE. Validity of the Zung Self-rating Depression Scale. The British Journal of Psychiatry: The Journal of Mental Science. 1978;132:381–85.CrossRefGoogle ScholarPubMed
Thurber, S, Snow, M, Honts, CR. The Zung Self-Rating Depression Scale: convergent validity and diagnostic discrimination. Assessment. 2002;9(4):401–05.CrossRefGoogle ScholarPubMed
Young, RC, Biggs, JT, Ziegler, VE, Meyer, DA. A rating scale for mania: reliability, validity and sensitivity. The British Journal of Psychiatry: The Journal of Mental Science. 1978;133:429–35.CrossRefGoogle ScholarPubMed
Steiner, M, Streiner, DL. Validation of a revised visual analog scale for premenstrual mood symptoms: results from prospective and retrospective trials. Canadian Journal of Psychiatry: Revue canadienne de psychiatrie. 2005;50(6):327–32.CrossRefGoogle ScholarPubMed
Goodman, WK, Price, LH, Rasmussen, SA, et al. The Yale–Brown Obsessive Compulsive Scale. II. Validity. Archives of General Psychiatry. 1989;46(11):1012–16.Google ScholarPubMed
Goodman, WK, Price, LH, Rasmussen, SA, et al. The Yale–Brown Obsessive Compulsive Scale. I. Development, use, and reliability. Archives of General Psychiatry. 1989;46(11):1006–11.Google ScholarPubMed
Kim, SW, Dysken, MW, Kuskowski, M. The Yale–Brown Obsessive–Compulsive Scale: a reliability and validity study. Psychiatry Research. 1990;34(1):99106.CrossRefGoogle Scholar
Cummings, JL, Mega, M, Gray, K, et al. The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia. Neurology. 1994;44(12):2308–14.CrossRefGoogle ScholarPubMed
Brandstaedter, D, Spieker, S, Ulm, G, et al. Development and evaluation of the Parkinson Psychosis Questionnaire. A screening-instrument for the early diagnosis of drug-induced psychosis in Parkinson's disease. Journal of Neurology. 2005;252(9):1060–66.Google Scholar
Okun, MS, Foote, KD. A mnemonic for Parkinson disease patients considering DBS: a tool to improve perceived outcome of surgery. The Neurologist. 2004;10(5):290.CrossRefGoogle ScholarPubMed
Okun, MS, Rodriguez, RL, Foote, KD, et al. A case-based review of troubleshooting deep brain stimulator issues in movement and neuropsychiatric disorders. Parkinsonism & Related Disorders. 2008;14(7):532–38.CrossRefGoogle ScholarPubMed
Rughani, AI, Hodaie, M, Lozano, AM. Acute complications of movement disorders surgery: effects of age and comorbidities. Movement Disorders: Official Journal of the Movement Disorder Society. 2013;28(12):1661–67.CrossRefGoogle ScholarPubMed
Mikos, A, Pavon, J, Bowers, D, et al. Factors related to extended hospital stays following deep brain stimulation for Parkinson's disease. Parkinsonism & Related Disorders. 2010;16(5):324–28.CrossRefGoogle ScholarPubMed
Beric, A, Kelly, PJ, Rezai, A, et al. Complications of deep brain stimulation surgery. Stereotactic and Functional Neurosurgery. 2001;77(1–4):7378.CrossRefGoogle ScholarPubMed
Fenoy, AJ, Simpson, RK Jr. Risks of common complications in deep brain stimulation surgery: management and avoidance. Journal of Neurosurgery. 2014;120(1):132–39.CrossRefGoogle ScholarPubMed
Franzini, A, Cordella, R, Messina, G, et al. Deep brain stimulation for movement disorders. Considerations on 276 consecutive patients. Journal of Neural Transmission. 2011;118(10):1497–510.CrossRefGoogle ScholarPubMed
Hariz, MI. Complications of deep brain stimulation surgery. Movement Disorders: Official Journal of the Movement Disorder Society. 2002;17(Suppl 3):S162–66.CrossRefGoogle ScholarPubMed
Hariz, MI, Fodstad, H. Do microelectrode techniques increase accuracy or decrease risks in pallidotomy and deep brain stimulation? A critical review of the literature. Stereotactic and Functional Neurosurgery. 1999;72(2–4):157–69.CrossRefGoogle ScholarPubMed
Oh, MY, Abosch, A, Kim, SH, Lang, AE, Lozano, AM. Long-term hardware-related complications of deep brain stimulation. Neurosurgery. 2002;50(6):1268–74; discussion 74–76.Google ScholarPubMed
Seijo, FJ, Alvarez-Vega, MA, Gutierrez, JC, Fdez-Glez, F, Lozano, B. Complications in subthalamic nucleus stimulation surgery for treatment of Parkinson's disease. Review of 272 procedures. Acta Neurochirurgica. 2007;149(9):867–75; discussion 76.CrossRefGoogle ScholarPubMed
Umemura, A, Jaggi, JL, Hurtig, HI, et al. Deep brain stimulation for movement disorders: morbidity and mortality in 109 patients. Journal of Neurosurgery. 2003;98(4):779–84.CrossRefGoogle ScholarPubMed
Voges, J, Volkmann, J, Allert, N, et al. Bilateral high-frequency stimulation in the subthalamic nucleus for the treatment of Parkinson disease: correlation of therapeutic effect with anatomical electrode position. Journal of Neurosurgery. 2002;96(2):269–79.CrossRefGoogle ScholarPubMed
Inci, S, Erbengi, A, Berker, M. Pulmonary embolism in neurosurgical patients. Surgical neurology. 1995;43(2):123–8; discussion 8–9.CrossRefGoogle ScholarPubMed
Voges, J, Hilker, R, Botzel, K, et al. Thirty days complication rate following surgery performed for deep-brain-stimulation. Movement Disorders: Official Journal of the Movement Disorder Society. 2007;22(10):1486–89.CrossRefGoogle ScholarPubMed
Krack, P, Batir, A, Van Blercom, N, et al. Five-year follow-up of bilateral stimulation of the subthalamic nucleus in advanced Parkinson's disease. The New England Journal of Medicine. 2003;349(20):1925–34.CrossRefGoogle ScholarPubMed
Volkmann, J, Allert, N, Voges, J, et al. Safety and efficacy of pallidal or subthalamic nucleus stimulation in advanced PD. Neurology. 2001;56(4):548–51.CrossRefGoogle ScholarPubMed
Deep-Brain Stimulation for Parkinson's Disease Study Group. Deep-brain stimulation of the subthalamic nucleus or the pars interna of the globus pallidus in Parkinson's disease. The New England Journal of Medicine. 2001;345(13):956–63.Google Scholar
Benabid, AL, Koudsie, A, Benazzouz, A, Le Bas, JF, Pollak, P. Imaging of subthalamic nucleus and ventralis intermediate of the thalamus. Movement Disorders: Official Journal of the Movement Disorder Society. 2002;17(Suppl 3):S123–29.CrossRefGoogle Scholar
Hamani, C, Richter, E, Schwalb, JM, Lozano, AM. Bilateral subthalamic nucleus stimulation for Parkinson's disease: a systematic review of the clinical literature. Neurosurgery. 2005;56(6):1313–21; discussion 21–24.CrossRefGoogle ScholarPubMed
Medtronic. Deep Brain Stimulation 3387/89 Lead Kit: Implant Manual. Minneapolis, MN: Medtronic, Inc.; 2000.Google Scholar
Lyons, KE, Wilkinson, SB, Overman, J, Pahwa, R. Surgical and hardware complications of subthalamic stimulation: a series of 160 procedures. Neurology. 2004;63(4):612–16.CrossRefGoogle ScholarPubMed
Schwalb, JM, Riina, HA, Skolnick, B, et al. Revision of deep brain stimulator for tremor. Technical note. Journal of Neurosurgery. 2001;94(6):1010–12.CrossRefGoogle ScholarPubMed
Sherif, C, Dorfer, C, Kalteis, K, et al. Deep brain pulse-generator and lead-extensions: subjective sensations related to measured parameters. Movement Disorders: Official Journal of the Movement Disorder Society. 2008;23(7):1036–40.CrossRefGoogle ScholarPubMed
Alesch, F, Pinter, MM, Helscher, RJ, et al. Stimulation of the ventral intermediate thalamic nucleus in tremor dominated Parkinson's disease and essential tremor. Acta Neurochirurgica. 1995;136(1–2):7581.CrossRefGoogle ScholarPubMed
Albanese, A, Nordera, GP, Caraceni, T, Moro, E. Long-term ventralis intermediate thalamic stimulation for parkinsonian tremor. Italian Registry for Neuromodulation in Movement Disorders. Advances in Neurology. 1999;80:631–34.Google Scholar
Kumar, K, Kelly, M, Toth, C. Deep brain stimulation of the ventral intermediate nucleus of the thalamus for control of tremors in Parkinson's disease and essential tremor. Stereotactic and Functional Neurosurgery. 1999;72(1):4761.CrossRefGoogle ScholarPubMed
Limousin, P, Speelman, JD, Gielen, F, Janssens, M. Multicentre European study of thalamic stimulation in parkinsonian and essential tremor. Journal of Neurology, Neurosurgery, and Psychiatry. 1999;66(3):289–96.CrossRefGoogle ScholarPubMed
Benabid, AL, Pollak, P, Gao, D, et al. Chronic electrical stimulation of the ventralis intermediate nucleus of the thalamus as a treatment of movement disorders. Journal of Neurosurgery. 1996;84(2):203–14.CrossRefGoogle Scholar
Deuschl, G, Herzog, J, Kleiner-Fisman, G, et al. Deep brain stimulation: postoperative issues. Movement Disorders: Official Journal of the Movement Disorder Society. 2006;21(Suppl 14):S219–37.CrossRefGoogle ScholarPubMed
Limousin-Dowsey, P, Pollak, P, Van Blercom, N, et al. Thalamic, subthalamic nucleus and internal pallidum stimulation in Parkinson's disease. Journal of Neurology. 1999;246(Suppl 2):II4245.CrossRefGoogle ScholarPubMed
Kleiner-Fisman, G, Fisman, DN, Sime, E, et al. Long-term follow up of bilateral deep brain stimulation of the subthalamic nucleus in patients with advanced Parkinson disease. Journal of Neurosurgery. 2003;99(3):489–95.CrossRefGoogle ScholarPubMed
Tavella, A, Bergamasco, B, Bosticco, E, et al. Deep brain stimulation of the subthalamic nucleus in Parkinson's disease: long-term follow-up. Neurological Sciences: Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2002;23(Suppl 2):S111–12.CrossRefGoogle ScholarPubMed
Valldeoriola, F, Pilleri, M, Tolosa, E, et al. Bilateral subthalamic stimulation monotherapy in advanced Parkinson's disease: long-term follow-up of patients. Movement Disorders: Official Journal of the Movement Disorder Society. 2002;17(1):125–32.CrossRefGoogle ScholarPubMed
Kadowaki, T, Hashimoto, K, Suzuki, K, Watanabe, Y, Hirata, K. Case report: recurrent parkinsonism–hyperpyrexia syndrome following discontinuation of subthalamic deep brain stimulation. Movement Disorders: Official Journal of the Movement Disorder Society. 2011;26(8):1561–62.CrossRefGoogle ScholarPubMed
Hocker, S, Kenney, DL, Ramar, K. Parkinsonism Hyperpyrexia Syndrome. Neurology Clinical Practice. 2013;3(6):535–38.CrossRefGoogle ScholarPubMed
Herzog, J, Volkmann, J, Krack, P, et al. Two-year follow-up of subthalamic deep brain stimulation in Parkinson's disease. Movement Disorders: Official Journal of the Movement Disorder Society. 2003;18(11):1332–37.CrossRefGoogle ScholarPubMed
Hariz, MI, Johansson, F, Shamsgovara, P, et al. Bilateral subthalamic nucleus stimulation in a parkinsonian patient with preoperative deficits in speech and cognition: persistent improvement in mobility but increased dependency: a case study. Movement Disorders: Official Journal of the Movement Disorder Society. 2000;15(1):136–39.3.0.CO;2-5>CrossRefGoogle Scholar
Doshi, PK, Chhaya, N, Bhatt, MH. Depression leading to attempted suicide after bilateral subthalamic nucleus stimulation for Parkinson's disease. Movement Disorders: Official Journal of the Movement Disorder Society. 2002;17(5):1084–85.CrossRefGoogle ScholarPubMed
Houeto, JL, Mesnage, V, Mallet, L, et al. Behavioural disorders, Parkinson's disease and subthalamic stimulation. Journal of Neurology, Neurosurgery, and Psychiatry. 2002;72(6):701–07.CrossRefGoogle ScholarPubMed
Holmberg, B, Corneliusson, O, Elam, M. Bilateral stimulation of nucleus subthalamicus in advanced Parkinson's disease: no effects on, and of, autonomic dysfunction. Movement Disorders: Official Journal of the Movement Disorder Society. 2005;20(8):976–81.CrossRefGoogle ScholarPubMed
Ostergaard, K, Sunde, N, Dupont, E. Effects of bilateral stimulation of the subthalamic nucleus in patients with severe Parkinson's disease and motor fluctuations. Movement Disorders: Official Journal of the Movement Disorder Society. 2002;17(4):693700.CrossRefGoogle ScholarPubMed
Rodriguez-Oroz, MC, Obeso, JA, Lang, AE, et al. Bilateral deep brain stimulation in Parkinson's disease: a multicentre study with 4 years follow-up. Brain: A Journal of Neurology. 2005;128(Pt 10):2240–49.CrossRefGoogle ScholarPubMed
Krause, M, Fogel, W, Heck, A, et al. Deep brain stimulation for the treatment of Parkinson's disease: subthalamic nucleus versus globus pallidus internus. Journal of Neurology, Neurosurgery, and Psychiatry. 2001;70(4):464–70.CrossRefGoogle ScholarPubMed
Voon, V, Hassan, K, Zurowski, M, et al. Prevalence of repetitive and reward-seeking behaviors in Parkinson disease. Neurology. 2006;67(7):1254–57.CrossRefGoogle ScholarPubMed
Romito, LM, Scerrati, M, Contarino, MF, et al. Long-term follow up of subthalamic nucleus stimulation in Parkinson's disease. Neurology. 2002;58(10):1546–50.CrossRefGoogle ScholarPubMed
Kumar, R, Lang, AE, Rodriguez-Oroz, MC, et al. Deep brain stimulation of the globus pallidus pars interna in advanced Parkinson's disease. Neurology. 2000;55(12 Suppl 6):S3439.Google ScholarPubMed
Sobstyl, M, Zabek, M, Kmiec, T, Slawek, J, Budohoski, KP. Status dystonicus due to internal pulse generator depletion in a patient with primary generalized dystonia. Movement Disorders: Official Journal of the Movement Disorder Society. 2014;29(2):188–89.CrossRefGoogle Scholar
Boviatsis, EJ, Stavrinou, LC, Themistocleous, M, Kouyialis, AT, Sakas, DE. Surgical and hardware complications of deep brain stimulation. A seven-year experience and review of the literature. Acta Neurochirurgica. 2010;152(12):2053–62.CrossRefGoogle ScholarPubMed
Umemura, A, Oka, Y, Yamamoto, K, et al. Complications of subthalamic nucleus stimulation in Parkinson's disease. Neurologia Medico-Chirurgica. 2011;51(11):749–55.CrossRefGoogle ScholarPubMed
Palur, RS, Berk, C, Schulzer, M, Honey, CR. A metaanalysis comparing the results of pallidotomy performed using microelectrode recording or macroelectrode stimulation. Journal of Neurosurgery. 2002;96(6):1058–62.CrossRefGoogle ScholarPubMed
Binder, DK, Rau, GM, Starr, PA. Risk factors for hemorrhage during microelectrode-guided deep brain stimulator implantation for movement disorders. Neurosurgery. 2005;56(4):722–32; discussion 732.CrossRefGoogle ScholarPubMed
Sansur, CA, Frysinger, RC, Pouratian, N, et al. Incidence of symptomatic hemorrhage after stereotactic electrode placement. Journal of Neurosurgery. 2007;107(5):9981003.CrossRefGoogle ScholarPubMed
Gorgulho, A, De Salles, AA, Frighetto, L, Behnke, E. Incidence of hemorrhage associated with electrophysiological studies performed using macroelectrodes and microelectrodes in functional neurosurgery. Journal of Neurosurgery. 2005;102(5):888–96.CrossRefGoogle Scholar
Broderick, J, Connolly, S, Feldmann, E, et al. Guidelines for the management of spontaneous intracerebral hemorrhage in adults: 2007 update: a guideline from the American Heart Association/American Stroke Association Stroke Council, High Blood Pressure Research Council, and the Quality of Care and Outcomes in Research Interdisciplinary Working Group. Stroke; A Journal of Cerebral Circulation. 2007;38(6):2001–23.CrossRefGoogle ScholarPubMed
van den Bergh, WM, van der Schaaf, I, van Gijn, J. The spectrum of presentations of venous infarction caused by deep cerebral vein thrombosis. Neurology. 2005;65(2):192–96.CrossRefGoogle ScholarPubMed
Morcos, Z. The spectrum of presentations of venous infarction caused by deep cerebral vein thrombosis. Neurology. 2006;66(8):1284; author reply.CrossRefGoogle ScholarPubMed
Morishita, T, Okun, MS, Burdick, A, Jacobson, CE, Foote, KD. Cerebral venous infarction: a potentially avoidable complication of deep brain stimulation surgery. Neuromodulation: Journal of the International Neuromodulation Society. 2013;16(5):407–13; discussion 413.CrossRefGoogle ScholarPubMed
Ferro, JM, Canhao, P. Acute treatment of cerebral venous and dural sinus thrombosis. Current Treatment Options in Neurology. 2008;10(2):126–37.CrossRefGoogle ScholarPubMed
Masuhr, F, Einhaupl, K. Treatment of cerebral venous and sinus thrombosis. Frontiers of Neurology and Neuroscience. 2008;23:132–43.Google ScholarPubMed
Zeng, L, Derex, L, Maarrawi, J, et al. Lifesaving decompressive craniectomy in ‘malignant’ cerebral venous infarction. European Journal of Neurology: The Official Journal of the European Federation of Neurological Societies. 2007;14(1):e2788.CrossRefGoogle ScholarPubMed
Ferro, JM, Canhao, P, Bousser, MG, et al. Early seizures in cerebral vein and dural sinus thrombosis: risk factors and role of antiepileptics. Stroke; A Journal of Cerebral Circulation. 2008;39(4):1152–58.CrossRefGoogle ScholarPubMed
Muir, KW. The PREVAIL trial and low-molecular-weight heparin for prevention of venous thromboembolism. Stroke; A Journal of Cerebral Circulation. 2008;39(7):2174–76.CrossRefGoogle ScholarPubMed
Lee, AY, Levine, MN, Baker, RI, et al. Low-molecular-weight heparin versus a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer. The New England Journal of Medicine. 2003;349(2):146–53.CrossRefGoogle ScholarPubMed
Patrono, C, Baigent, C, Hirsh, J, Roth, G, American College of Chest Physicians. Antiplatelet drugs: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition). Chest. 2008;133(6 Suppl):199S233S.CrossRefGoogle ScholarPubMed
Marik, PE. Aspiration pneumonitis and aspiration pneumonia. The New England Journal of Medicine. 2001;344(9):665–71.CrossRefGoogle ScholarPubMed
Gologorsky, Y, Ben-Haim, S, Moshier, EL, et al. Transgressing the ventricular wall during subthalamic deep brain stimulation surgery for Parkinson disease increases the risk of adverse neurological sequelae. Neurosurgery. 2011;69(2):294–99; discussion 299–300.CrossRefGoogle ScholarPubMed
Bronstein, JM, Tagliati, M, Alterman, RL, et al. Deep brain stimulation for Parkinson disease: an expert consensus and review of key issues. Archives of Neurology. 2011;68(2):165.CrossRefGoogle ScholarPubMed
Sillay, KA, Larson, PS, Starr, PA. Deep brain stimulator hardware-related infections: incidence and management in a large series. Neurosurgery. 2008;62(2):360–66; discussion 366–367.CrossRefGoogle Scholar
Levy, RM, Lamb, S, Adams, JE. Treatment of chronic pain by deep brain stimulation: long term follow-up and review of the literature. Neurosurgery. 1987;21(6):885–93.Google ScholarPubMed
Seal, LA, Paul-Cheadle, D. A systems approach to preoperative surgical patient skin preparation. American Journal of Infection Control. 2004;32(2):5762.CrossRefGoogle ScholarPubMed
Miyagi, Y, Shima, F, Ishido, K. Implantation of deep brain stimulation electrodes in unshaved patients. Technical note. Journal of Neurosurgery. 2002;97(6):1476–78.CrossRefGoogle ScholarPubMed
Masterson, TM, Rodeheaver, GT, Morgan, RF, Edlich, RF. Bacteriologic evaluation of electric clippers for surgical hair removal. American Journal of Surgery. 1984;148(3):301–02.CrossRefGoogle ScholarPubMed
Hariz, MI, Johansson, F. Hardware failure in parkinsonian patients with chronic subthalamic nucleus stimulation is a medical emergency. Movement Disorders: Official Journal of the Movement Disorder Society. 2001;16(1):166–68.3.0.CO;2-S>CrossRefGoogle ScholarPubMed
Blomstedt, P, Hariz, MI. Hardware-related complications of deep brain stimulation: a ten year experience. Acta Neurochirurgica. 2005;147(10):1061–64; discussion 1064.CrossRefGoogle ScholarPubMed
Baizabal Carvallo, JF, Mostile, G, Almaguer, M, et al. Deep brain stimulation hardware complications in patients with movement disorders: risk factors and clinical correlations. Stereotactic and Functional Neurosurgery. 2012;90(5):300–06.CrossRefGoogle ScholarPubMed
Fernandez, FS, Alvarez Vega, MA, Antuna Ramos, A, Fernandez Gonzalez, F, Lozano Aragoneses, B. Lead fractures in deep brain stimulation during long-term follow-up. Parkinson's Disease. 2010;2010:409356.CrossRefGoogle ScholarPubMed
Panov, F, Gologorsky, Y, Connors, G, et al. Deep brain stimulation in DYT1 dystonia: a 10-year experience. Neurosurgery. 2013;73(1):8693; discussion.CrossRefGoogle Scholar
Tagliati, M, Krack, P, Volkmann, J, et al. Long-term management of DBS in dystonia: response to stimulation, adverse events, battery changes, and special considerations. Movement Disorders: Official Journal of the Movement Disorder Society. 2011;26(Suppl 1):S5462.CrossRefGoogle ScholarPubMed
Servello, D, Sassi, M, Gaeta, M, Ricci, C, Porta, M. Tourette syndrome (TS) bears a higher rate of inflammatory complications at the implanted hardware in deep brain stimulation (DBS). Acta Neurochirurgica. 2011;153(3):629–32.CrossRefGoogle Scholar
Machado, AG, Hiremath, GK, Salazar, F, Rezai, AR. Fracture of subthalamic nucleus deep brain stimulation hardware as a result of compulsive manipulation: case report. Neurosurgery. 2005;57(6):E1318; discussion.CrossRefGoogle ScholarPubMed
Cardoso, AF, Almeida, GM. Twiddler syndrome. Arquivos Brasileiros de Cardiologia. 2008;90(2):e15.CrossRefGoogle ScholarPubMed
Dursun, I, Yesildag, O, Soylu, K, et al. Late pacemaker twiddler syndrome. Clinical Research in Cardiology: Official Journal of the German Cardiac Society. 2006;95(10):547–49.CrossRefGoogle ScholarPubMed
Fahraeus, T, Hoijer, CJ. Early pacemaker twiddler syndrome. Europace: European Pacing, Arrhythmias, and Cardiac Electrophysiology: Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 2003;5(3):279–81.CrossRefGoogle ScholarPubMed
Geissinger, G, Neal, JH. Spontaneous twiddler's syndrome in a patient with a deep brain stimulator. Surgical Neurology. 2007;68(4):454–56; discussion 456.CrossRefGoogle Scholar
Farris, S, Vitek, J, Giroux, ML. Deep brain stimulation hardware complications: the role of electrode impedance and current measurements. Movement Disorders: Official Journal of the Movement Disorder Society. 2008;23(5):755–60.CrossRefGoogle ScholarPubMed
Benezet-Mazuecos, J, Benezet, J, Ortega-Carnicer, J. Pacemaker Twiddler syndrome. European Heart Journal. 2007;28(16):2000.CrossRefGoogle ScholarPubMed
Yianni, J, Nandi, D, Shad, A, et al. Increased risk of lead fracture and migration in dystonia compared with other movement disorders following deep brain stimulation. Journal of Clinical Neuroscience: Official Journal of the Neurosurgical Society of Australasia. 2004;11(3):243–45.CrossRefGoogle ScholarPubMed
Favre, J, Taha, JM, Steel, T, Burchiel, KJ. Anchoring of deep brain stimulation electrodes using a microplate. Technical note. Journal of Neurosurgery. 1996;85(6):1181–83.CrossRefGoogle ScholarPubMed
Fakhar, K, Hastings, E, Butson, CR, et al. Management of deep brain stimulator battery failure: battery estimators, charge density, and importance of clinical symptoms. PloS ONE. 2013;8(3):e58665.CrossRefGoogle ScholarPubMed
Montuno, MA, Kohner, AB, Foote, KD, Okun, MS. An algorithm for management of deep brain stimulation battery replacements: devising a web-based battery estimator and clinical symptom approach. Neuromodulation: Journal of the International Neuromodulation Society. 2013;16(2):147–53.CrossRefGoogle ScholarPubMed
Kiss, ZH, Anderson, T, Hansen, T, et al. Neural substrates of microstimulation-evoked tingling: a chronaxie study in human somatosensory thalamus. The European Journal of Neuroscience. 2003;18(3):728–32.CrossRefGoogle ScholarPubMed
Ashby, P, Kim, YJ, Kumar, R, Lang, AE, Lozano, AM. Neurophysiological effects of stimulation through electrodes in the human subthalamic nucleus. Brain: A Journal of Neurology. 1999;122(Pt 10):1919–31.CrossRefGoogle ScholarPubMed
Krack, P, Fraix, V, Mendes, A, Benabid, AL, Pollak, P. Postoperative management of subthalamic nucleus stimulation for Parkinson's disease. Movement Disorders: Official Journal of the Movement Disorder Society. 2002;17(Suppl 3):S188–97.CrossRefGoogle ScholarPubMed
Tamma, F, Caputo, E, Chiesa, V, et al. Anatomo-clinical correlation of intraoperative stimulation-induced side-effects during HF-DBS of the subthalamic nucleus. Neurological Sciences: Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2002;23(Suppl 2):S109–10.CrossRefGoogle ScholarPubMed
Baizabal-Carvallo, JF, Kagnoff, MN, Jimenez-Shahed, J, Fekete, R, Jankovic, J. The safety and efficacy of thalamic deep brain stimulation in essential tremor: 10 years and beyond. Journal of Neurology, Neurosurgery, and Psychiatry. 2014;85(5):567–72.CrossRefGoogle ScholarPubMed
Sriram, A, Ward, HE, Hassan, A, et al. Valproate as a treatment for dopamine dysregulation syndrome (DDS) in Parkinson's disease. Journal of Neurology. 2013;260(2):521–27.CrossRefGoogle ScholarPubMed
Martinez-Ramirez, D, Giugni, J, Vedam-Mai, V, et al. The “brittle response” to Parkinson's disease medications: characterization and response to deep brain stimulation. PloS ONE. 2014;9(4):e94856.CrossRefGoogle Scholar
Pinto, S, Gentil, M, Krack, P, et al. Changes induced by levodopa and subthalamic nucleus stimulation on parkinsonian speech. Movement Disorders: Official Journal of the Movement Disorder Society. 2005;20(11):1507–15.CrossRefGoogle ScholarPubMed
Ramig, LO, Sapir, S, Countryman, S, et al. Intensive voice treatment (LSVT) for patients with Parkinson's disease: a 2 year follow up. Journal of Neurology, Neurosurgery, and Psychiatry. 2001;71(4):493–98.CrossRefGoogle ScholarPubMed
Ramig, LO, Sapir, S, Fox, C, Countryman, S. Changes in vocal loudness following intensive voice treatment (LSVT) in individuals with Parkinson's disease: a comparison with untreated patients and normal age-matched controls. Movement Disorders: Official Journal of the Movement Disorder Society. 2001;16(1):7983.3.0.CO;2-H>CrossRefGoogle ScholarPubMed
Sapir, S, Ramig, LO, Hoyt, P, et al. Speech loudness and quality 12 months after intensive voice treatment (LSVT) for Parkinson's disease: a comparison with an alternative speech treatment. Folia Phoniatrica et Logopaedica: Official Organ of the International Association of Logopedics and Phoniatrics. 2002;54(6):296303.CrossRefGoogle ScholarPubMed
St George, RJ, Nutt, JG, Burchiel, KJ, Horak, FB. A meta-regression of the long-term effects of deep brain stimulation on balance and gait in PD. Neurology. 2010;75(14):1292–99.CrossRefGoogle ScholarPubMed
Felice, KJ, Keilson, GR, Schwartz, WJ. ‘Rubral’ gait ataxia. Neurology. 1990;40(6):1004–05.CrossRefGoogle ScholarPubMed
Limousin, P, Krack, P, Pollak, P, et al. Electrical stimulation of the subthalamic nucleus in advanced Parkinson's disease. The New England Journal of Medicine. 1998;339(16):1105–11.CrossRefGoogle ScholarPubMed
Voon, V, Kubu, C, Krack, P, Houeto, JL, Troster, AI. Deep brain stimulation: neuropsychological and neuropsychiatric issues. Movement Disorders: Official Journal of the Movement Disorder Society. 2006;21(Suppl 14):S305–27.CrossRefGoogle ScholarPubMed
Castrioto, A, Lhommee, E, Moro, E, Krack, P. Mood and behavioural effects of subthalamic stimulation in Parkinson's disease. Lancet Neurology. 2014;13(3):287305.CrossRefGoogle ScholarPubMed
Massano, J, Garrett, C. Deep brain stimulation and cognitive decline in Parkinson's disease: a clinical review. Frontiers in Neurology. 2012;3:66.CrossRefGoogle ScholarPubMed
Perestelo-Perez, L, Rivero-Santana, A, Perez-Ramos, J, et al. Deep brain stimulation in Parkinson's disease: meta-analysis of randomized controlled trials. Journal of Neurology. 2014;261:2051–60.CrossRefGoogle ScholarPubMed
Molinuevo, JL, Valldeoriola, F, Tolosa, E, et al. Levodopa withdrawal after bilateral subthalamic nucleus stimulation in advanced Parkinson disease. Archives of Neurology. 2000;57(7):983–88.CrossRefGoogle ScholarPubMed
Higuchi, MA, Tsuboi, Y, Inoue, T, et al. Predictors of the emergence of apathy after bilateral stimulation of the subthalamic nucleus in patients with Parkinson's disease. Neuromodulation: Journal of the International Neuromodulation Society. 2015;18:113–17.CrossRefGoogle ScholarPubMed
Kim, YE, Kim, HJ, Kim, HJ, et al. Impulse control and related behaviors after bilateral subthalamic stimulation in patients with Parkinson's disease. Journal of Clinical Neuroscience: Official Journal of the Neurosurgical Society of Australasia. 2013;20(7):964–69.CrossRefGoogle ScholarPubMed
Moum, SJ, Price, CC, Limotai, N, et al. Effects of STN and GPi deep brain stimulation on impulse control disorders and dopamine dysregulation syndrome. PloS ONE. 2012;7(1):e29768.CrossRefGoogle ScholarPubMed
Weintraub, D, Koester, J, Potenza, MN, et al. Impulse control disorders in Parkinson disease. A cross-sectional study of 3090 patients. Archives of Neurology. 2010;67(5):589–95.CrossRefGoogle ScholarPubMed
Albin, RL, Young, AB, Penney, JB. The functional anatomy of basal ganglia disorders. Trends in Neurosciences. 1989;12(10):366–75.CrossRefGoogle ScholarPubMed
Pazo, JH, Belforte, JE. Basal ganglia and functions of the autonomic nervous system. Cellular and Molecular Neurobiology. 2002;22(5–6):645–54.CrossRefGoogle ScholarPubMed
Sauleau, P, Raoul, S, Lallement, F, et al. Motor and non motor effects during intraoperative subthalamic stimulation for Parkinson's disease. Journal of Neurology. 2005;252(4):457–64.CrossRefGoogle ScholarPubMed
Kaufmann, H, Bhattacharya, KF, Voustianiouk, A, Gracies, JM. Stimulation of the subthalamic nucleus increases heart rate in patients with Parkinson disease. Neurology. 2002;59(10):1657–58.CrossRefGoogle ScholarPubMed
Ashkan, K, Samuel, M, Reddy, P, Ray Chaudhuri, K. The impact of deep brain stimulation on the nonmotor symptoms of Parkinson's disease. Journal of Neural Transmission. 2013;120(4):639–42.CrossRefGoogle ScholarPubMed
Hwynn, N, Ul Haq, I, Malaty, IA, et al. Effect of deep brain stimulation on Parkinson's nonmotor symptoms following unilateral DBS: a pilot study. Parkinson's Disease. 2011;2011:507416.CrossRefGoogle ScholarPubMed
Seif, C, Herzog, J, van der Horst, C, et al. Effect of subthalamic deep brain stimulation on the function of the urinary bladder. Annals of Neurology. 2004;55(1):118–20.CrossRefGoogle ScholarPubMed
Winge, K, Nielsen, KK. Bladder dysfunction in advanced Parkinson's disease. Neurourology and Urodynamics. 2012;31(8):1279–83.CrossRefGoogle ScholarPubMed
Fritsche, HM, Ganzer, R, Schlaier, J, et al. Acute urinary retention in two patients after subthalamic nucleus deep brain stimulation (STN-DBS) for the treatment of advanced Parkinson's disease. Movement Disorders: Official Journal of the Movement Disorder Society. 2009;24(10):1553–54.CrossRefGoogle ScholarPubMed
Thobois, S, Mertens, P, Guenot, M, et al. Subthalamic nucleus stimulation in Parkinson's disease: clinical evaluation of 18 patients. Journal of Neurology. 2002;249(5):529–34.Google ScholarPubMed
Esselink, RA, de Bie, RM, de Haan, RJ, et al. Unilateral pallidotomy versus bilateral subthalamic nucleus stimulation in PD: a randomized trial. Neurology. 2004;62(2):201–07.CrossRefGoogle ScholarPubMed
Troche, MS, Brandimore, AE, Foote, KD, Okun, MS. Swallowing and deep brain stimulation in Parkinson's disease: a systematic review. Parkinsonism & Related Disorders. 2013;19(9):783–88.CrossRefGoogle ScholarPubMed
Troche, MS, Brandimore, AE, Foote, KD, et al. Swallowing outcomes following unilateral STN vs. GPi surgery: a retrospective analysis. Dysphagia. 2014;29:425–31.CrossRefGoogle ScholarPubMed
Bejjani, BP, Gervais, D, Arnulf, I, et al. Axial parkinsonian symptoms can be improved: the role of levodopa and bilateral subthalamic stimulation. Journal of Neurology, Neurosurgery, and Psychiatry. 2000;68(5):595600.CrossRefGoogle ScholarPubMed
Castelli, L, Perozzo, P, Genesia, ML, et al. Sexual well being in parkinsonian patients after deep brain stimulation of the subthalamic nucleus. Journal of Neurology, Neurosurgery, and Psychiatry. 2004;75(9):1260–64.CrossRefGoogle ScholarPubMed
Romito, LM, Raja, M, Daniele, A, et al. Transient mania with hypersexuality after surgery for high frequency stimulation of the subthalamic nucleus in Parkinson's disease. Movement Disorders: Official Journal of the Movement Disorder Society. 2002;17(6):1371–74.CrossRefGoogle ScholarPubMed
Jimenez-Jimenez, FJ, Sayed, Y, Garcia-Soldevilla, MA, Barcenilla, B. Possible zoophilia associated with dopaminergic therapy in Parkinson disease. The Annals of Pharmacotherapy. 2002;36(7–8):1178–79.CrossRefGoogle ScholarPubMed
Klos, KJ, Bower, JH, Josephs, KA, Matsumoto, JY, Ahlskog, JE. Pathological hypersexuality predominantly linked to adjuvant dopamine agonist therapy in Parkinson's disease and multiple system atrophy. Parkinsonism & Related Disorders. 2005;11(6):381–86.CrossRefGoogle ScholarPubMed
Ivanco, LS, Bohnen, NI. Effects of donepezil on compulsive hypersexual behavior in Parkinson disease: a single case study. American Journal of Therapeutics. 2005;12(5):467–68.CrossRefGoogle ScholarPubMed
Barichella, M, Marczewska, AM, Mariani, C, et al. Body weight gain rate in patients with Parkinson's disease and deep brain stimulation. Movement Disorders: Official Journal of the Movement Disorder Society. 2003;18(11):1337–40.CrossRefGoogle ScholarPubMed
Macia, F, Perlemoine, C, Coman, I, et al. Parkinson's disease patients with bilateral subthalamic deep brain stimulation gain weight. Movement Disorders: Official Journal of the Movement Disorder Society. 2004;19(2):206–12.CrossRefGoogle ScholarPubMed
Montaurier, C, Morio, B, Bannier, S, et al. Mechanisms of body weight gain in patients with Parkinson's disease after subthalamic stimulation. Brain: A Journal of Neurology. 2007;130(Pt 7):1808–18.CrossRefGoogle ScholarPubMed
Kirschman, DL, Milligan, B, Wilkinson, S, et al. Pallidotomy microelectrode targeting: neurophysiology-based target refinement. Neurosurgery. 2000;46(3):613–22; discussion 622–24.CrossRefGoogle ScholarPubMed
Biousse, V, Newman, NJ, Carroll, C, et al. Visual fields in patients with posterior GPi pallidotomy. Neurology. 1998;50(1):258–65.CrossRefGoogle ScholarPubMed
Favilla, CG, Ullman, D, Wagle Shukla, A, et al. Worsening essential tremor following deep brain stimulation: disease progression versus tolerance. Brain: A Journal of Neurology. 2012;135(Pt 5):1455–62.CrossRefGoogle ScholarPubMed
Lang, AE, Houeto, JL, Krack, P, et al. Deep brain stimulation: preoperative issues. Movement Disorders: Official Journal of the Movement Disorder Society. 2006;21(Suppl 14):S171–96.CrossRefGoogle ScholarPubMed
Moro, E, Lang, AE. Criteria for deep-brain stimulation in Parkinson's disease: review and analysis. Expert Review of Neurotherapeutics. 2006;6(11):1695–705.CrossRefGoogle ScholarPubMed
Hughes, AJ, Daniel, SE, Ben-Shlomo, Y, Lees, AJ. The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. Brain: A Journal of Neurology. 2002;125(Pt 4):861–70.CrossRefGoogle Scholar
Charles, PD, Van Blercom, N, Krack, P, et al. Predictors of effective bilateral subthalamic nucleus stimulation for PD. Neurology. 2002;59(6):932–34.CrossRefGoogle ScholarPubMed
Schuepbach, WM, Rau, J, Knudsen, K, et al. Neurostimulation for Parkinson's disease with early motor complications. The New England Journal of Medicine. 2013;368(7):610–22.CrossRefGoogle ScholarPubMed
Mestre, TA, Shah, P, Marras, C, Tomlinson, G, Lang, AE. Another face of placebo: the lessebo effect in Parkinson disease: meta-analyses. Neurology. 2014;82(16):1402–09.CrossRefGoogle ScholarPubMed
Okun, MS, Fernandez, HH, Pedraza, O, et al. Development and initial validation of a screening tool for Parkinson disease surgical candidates. Neurology. 2004;63(1):161–63.CrossRefGoogle ScholarPubMed
Marjama-Lyons, J, Okun, MS. Parkinson Disease: Guide to Deep Brain Stimulation. Hagerstown, MD: National Parkinson Foundation; 2007.Google Scholar
Kronenbuerger, M, Fromm, C, Block, F, et al. On-demand deep brain stimulation for essential tremor: a report on four cases. Movement Disorders: Official Journal of the Movement Disorder Society. 2006;21(3):401–05.CrossRefGoogle ScholarPubMed
Guridi, J, Rodriguez-Oroz, MC, Alegre, M, Obeso, JA. Hardware complications in deep brain stimulation: electrode impedance and loss of clinical benefit. Parkinsonism & Related Disorders. 2012;18(6):765–69.CrossRefGoogle ScholarPubMed

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