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Chapter 3 - Surgical placement of deep brain stimulating leads for the treatment of movement disorders – intraoperative aspects: physiological mapping, test stimulation, and patient evaluation

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

Feger, J, Hassani, O, Mouroux, M. The subthalamic nucleus and its connections. New electrophysiological and pharmacological data. Adv Neurol 1997;74:3143.Google ScholarPubMed
DeLong, M. Primate models of movement disorders of basal ganglia origin. Trends Neurosci 1990;13:281–85.CrossRefGoogle ScholarPubMed
Wichmann, T, Bergman, H, DeLong, M. The primate subthalamic nucleus. I. Functional properties in intact animals. J Neurophysiol 1994;72(2):494506.Google ScholarPubMed
Robledo, P, Feger, J. Excitatory influence of rat subthalamic nucleus to substantia nigra pars reticulata and the pallidal complex: electrophysiological data. Brain Res 1990;51(8):4754.CrossRefGoogle Scholar
Kita, H, Kitai, S. Intracellular study of rat globus pallidus neurons: membrane properties and responses to neostriatal, subthalamic and nigral stimulation. Brain Res 1991;564:296305.CrossRefGoogle ScholarPubMed
Hammond, C, Deniau, J, Rizk, A, Feger, J. Electrophysiological demonstration of an excitatory subthalamonigral pathway in the rat. Brain Res 1978;151:235–44.CrossRefGoogle ScholarPubMed
Monakow, KH, Akert, K, Kunzle, H. Projections of the precentral motor cortex and other cortical areas of the frontal lobe to the subthalamic nucleus in the monkey. Exp Brain Res 1978;33:395403.CrossRefGoogle ScholarPubMed
Nambu, A, Takada, M, Inase, M, et al. Dual somatotopical representations in the primate subthalamic nucleus: evidence for ordered but reversed body-map transformations from the primary motor cortex and the supplementary motor area. J Neurosci 1996;16:2671–83.Google ScholarPubMed
Romanelli, P, Heit, G, Hill, BC, et al. Microelectrode recording revealing a somatotopic body map in the subthalamic nucleus in humans with Parkinson disease. J Neurosurg 2004;100:611–18.CrossRefGoogle ScholarPubMed
Miller, W, DeLong, M. Altered tonic activity of neurons in the globus pallidus and subthalamic nucleus in the primate MPTP model of parkinsonism. Carpenter, MB, Jayaraman, A, eds. The Basal Ganglia II. Structure and Function – Current Concepts. New York: Plenum Press, 1987.Google Scholar
Filion, M, Tremblay, L. Abnormal spontaneous activity of globus pallidus neurons in monkeys with MPTP-induced parkinsonism. Brain Res 1991;547:142–51.Google ScholarPubMed
Bergman, H, Wichmann, T, Karmon, B, DeLong, M. The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of parkinsonism. J Neurophysiol 1994;72:507–20.Google ScholarPubMed
Bergman, H, Wichmann, T, DeLong, M. Reversal of experimental parkinsonism by lesions of the subthalamic nucleus. Science 1990;249:1436–38.CrossRefGoogle ScholarPubMed
Lozano, A, Hutchison, W, Kiss, Z, et al. Methods for microelectrode-guided posteroventral pallidotomy. J Neurosurg 1996;84:192202.CrossRefGoogle ScholarPubMed
Vitek, J, Bakay, R, Hashimoto, T, et al. Microelectrode-guided pallidotomy: technical approach and its application in medically intractable Parkinson's disease. J Neurosurg 1998;88:1027–43.CrossRefGoogle ScholarPubMed
Bezard, E, Boraud, T, Bioulae, B, Gross, C. Presymptomatic revelation of experimental Parkinsonism. Neuro Rep 1997;8:435–38.Google ScholarPubMed
Lenz, FA, Tasker, RR, Kwan, HC, et al. Single unit analysis of the human ventral thalamic nuclear group: correlation of thalamic “tremor cells” with the 3–6 Hz component of parkinsonian tremor. J Neurosci 1988;8:754–64.Google ScholarPubMed
Brown, P. Oscillatory nature of human basal ganglia activity: relationship to the pathophysiology of Parkinson's disease. Mov Disord 2003;18(4):357–63.CrossRefGoogle ScholarPubMed
Bronte-Stewart, H, Barberini, C, Miller Koop, M, et al. The STN beta band profile in Parkinson's disease is stationary and shows prolonged attenuation after deep brain stimulation. Exp Neurol 2009;215:2028.CrossRefGoogle ScholarPubMed
McIntyre, CC, Grill, WM, Sherman, DL, et al. Cellular effects of deep brain stimulation: model-based analysis of activation and inhibition. J Neurophysiol 2004;91:1457–69.CrossRefGoogle Scholar
Ondo, W, Bronte-Stewart, H. The North American survey of placement and adjustment strategies for deep brain stimulation. Stereotact Funct Neurosurg 2005;83(4):142–47.CrossRefGoogle ScholarPubMed
Holloway, KL, Gaede, SE, Starr, PA, et al. Frameless stereotaxy using bone fiducial markers for deep brain stimulation. J Neurosurg 2005;103(3):404–13.CrossRefGoogle ScholarPubMed
Svennilson, E, Torvik, A, Lowe, R, Leksell, L. Treatment of Parkinsonism by stereotactic thermolesions in the pallidal region. Acta Psychiat Scand 1960;35:358–77.CrossRefGoogle Scholar
Vitek, J, Bakay, R, DeLong, M. Microelectrode-guided pallidotomy for medically intractable Parkinson's disease. Adv Neurol 1997;74:183–98.Google ScholarPubMed
Gross, R, Lombardi, W, Lang, A, et al. Relationship of lesion location to clinical outcome following microelectrode-guided pallidotomy for Parkinson's disease. Brain 1999;122:405–16.CrossRefGoogle ScholarPubMed
Eskandar, E, Cosgrove, G, Shinobu, L, Penney, J. The importance of accurate lesion placement in posteroventral pallidotomy: report of two cases. J Neurosurg 1998;89:630–34.CrossRefGoogle ScholarPubMed
Bronte-Stewart, H, Hill, B, Molander, M, et al. Lesion location predicts clinical outcome of pallidotomy. Mov Disord 1998;13:300.Google Scholar
Romanelli, P, Bronte-Stewart, HM, Heit, G, Schaal, DW, Vincenzo, E. The functional organization of the sensorimotor region of the subthalamic nucleus. Stereotact Funct Neurosurg 2004;82:222–29.Google ScholarPubMed
Haynes, WIA, Haber, SN. The organization of prefrontal–subthalamic inputs in primates provides an anatomical substrate for both functional specificity and integration: implications for basal ganglia models and deep brain stimulation. J Neurosci 2013;33(11):4804–14.CrossRefGoogle ScholarPubMed
Starr, PA, Vitek, JL, DeLong, M, Bakay, RA. Magnetic resonance imaging-based stereotactic localization of the globus pallidus and subthalamic nucleus. Neurosurgery 1999;44(2):303–13.CrossRefGoogle ScholarPubMed
Bejjani, BP, Dormont, D, Pidoux, B, et al. Bilateral subthalamic stimulation for Parkinson's disease by using three-dimensional stereotactic magnetic resonance imaging and electrophysiological guidance. J Neurosurg 2000;92(4):615–25.CrossRefGoogle ScholarPubMed
Cuny, E, Grehl, D, Burbaud, P, et al. Lack of agreement between direct magnetic resonance imaging and statistical determination of a subthalamic target: the role of electrophysiological guidance. J Neurosurg 2002;97:591–97.CrossRefGoogle ScholarPubMed
Okun, MS, Vitek, JL. Lesion therapy for Parkinson's disease and other movement disorders: update and controversies. Mov Disord 2004;19(4):375–89.CrossRefGoogle ScholarPubMed
The 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. New Engl J Med 2001;345:956–63.PubMed
Binder, DK, Rau, GM, Starr, PA. Risk factors for hemorrhage during microelectrode-guided deep brain stimulator implantation for movement disorders. Neurosurgery 2005;6(4):722–32.Google Scholar
Miller Koop, M, Andrzejewski, A, Hill, BC, Heit, G, Bronte-Stewart, HM. Improvement in a quantitative measure of bradykinesia after microelectrode recording in patients with Parkinson's disease during deep brain stimulation surgery. Mov Disord 2006;21(5):673–78.Google Scholar
Bejjani, B, Damier, P, Arnulf, I, et al. Pallidal stimulation for Parkinson's disease. Two targets? Neurology 1997;49:1564–69.CrossRefGoogle ScholarPubMed
Pollak, P, Benabid, AL, Krack, P, et al. Deep brain stimulation. In Jancovic, J, ed., Parkinson's Disease and Movement Disorders. Baltimore: Williams and Wilkins, 1998.Google ScholarPubMed
Okun, MS, Tagliati, M, Pourfar, M, et al. Management of referred deep brain stimulation failures: a retrospective analysis from 2 movement disorders centers. Arch Neurol 2005;62(8):1250–55.CrossRefGoogle ScholarPubMed

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