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Intracranial Neurostimulation for Epilepsy

Published online by Cambridge University Press:  02 December 2014

A. Parrent
A. Parrent*
Affiliation:
Epilepsy Program, Western University, University Hospital, London, Ontario, Canada
*
Epilepsy Programme, Western University, London Health Sciences Centre, 339 Windermere Rd, London, Ontario, N6A5A5, Canada
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Abstract

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Type
Research Article
Information
Canadian Journal of Neurological Sciences , Volume 39 , Issue S6 , November 2012 , pp. S14 - S19
Copyright
Copyright © The Canadian Journal of Neurological 2012

References

1. Benabid, AL, Pollak, P, Henry, S, de Rougemont, J. Combined (thalamotomy and stimulation) stereotactic surgery of the VIM thalamic nucleus for bilateral Parkinson disease. Appl. Neurophysiol. 1987;50(1-6):244–6.Google Scholar
2. Cooper, IS, Amin, I, Gilman, . The effect of chronic cerebellar stimulation upon epilepsy in man. Trans Am Neurol Assoc. 1973;98:192–6.Google Scholar
3. Laxer, KD, Robertson, LT, Julien, RM, Dow, RS. Phenytoin: relationship between cerebellar function and epileptic discharges. Adv Neurol. 1980;27:415–27.Google Scholar
4. Krauss, GL, Koubeissi, MZ. Cerebellar and thalamic stimulation treatment for epilepsy. Acta Neurochir Suppl. 2007;97(Pt. 2):347–56.Google Scholar
5. Wright, GD, McLellan, DL, Brice, JG. A double-blind trial of chronic cerebellar stimulation in twelve patients with severe epilepsy. J Neurol Neurosurg Psychiatry. 1984;47:769–74.Google Scholar
6. Van Buren, JM, Wood, JH, Oakley, J, Hambrecht, F. Preliminary evaluation of cerebellar stimulation and biological criteria in the treatment of epilepsy. J Neurosurg. 1978;48:407–16.Google Scholar
7. Davis, R, Emmonds, SE. Cerebellar stimulation for seizure control: 17-year study. Stereotact Funct Neurosurg. 1992;58:200–8.CrossRefGoogle ScholarPubMed
8. Cooper, IS. Twenty-five years of experience with physiological neurosurgery. Neurosurgery. 1981;9:190–200.CrossRefGoogle ScholarPubMed
9. Velasco, F, Carrillo-Ruiz, JD, Brito, F, et al. Double-blind, randomized controlled pilot study of bilateral cerebellar stimulation for treatment of intractable motor seizures. Epilepsia. 2005;46(7):1071–81.Google Scholar
10. Bidzinski, J, Bacia, T, Ostrowski, K. Effect of cerebellar cortex electrostimulation on the frequency of seizures in drug-resistant epilepsy. Neurol Neurochir Pol. 1981;31:605–9.Google Scholar
11. Davis, R. Cerebellar stimulation for cerebral palsy spasticity, function, and seizures. Arch Med Res. 2000;31:290–9.Google Scholar
12. La, GruttaV, Sabatino, M, Gravante, G, Morici, G, Ferraro, G, Lagrutta, G. A study of caudate inhibition on an epileptic focus in the cat hippocampus. Arch Int Physiol Biochim. 1988;96:113–20.Google Scholar
13. La Grutta, V, Amato, G, Zagami, MT. The importance of the caudate nucleus in the control of convulsive activity in the amygdaloid complex and the temporal cortex of the cat. Electroencephalogr Clin Neurophysiol. 1971;31:57–69.Google Scholar
14. La Grutta, V, Sabatino, M, Gravante, G, La Grutta, G. Effects of caudate nucleus on paroxysmal activity in hippocampus of cat. Electroencephalogr. Clin. Neurophysiol. 1985;61:416–21.Google Scholar
15. Psatta, DM. Control of chronic experimental focal epilepsy by feedback caudatum stimulations. Epilepsia. 1983;24:444–54.Google Scholar
16. Sorbera, F, Crescimanno, G, Amato, G, La Grutta, V. [Effects of conditioning stimulation of the substantia nigra on the epileptic activity of the cat amygdala]. Boll Soc Ital Biol Sper. 1981;57:1901–4.Google ScholarPubMed
17. Chkhenkeli, SA, Sramka, M, Lortkipanidze, GS, et al. Electrophysiological effects and clinical results of direct brain stimulation for intractable epilepsy. Clin Neurol Neurosurg. 2004;106(4):318–29.Google Scholar
18. Chkhenkeli, SA, Chkhenkeli, IS. Effects of therapeutic stimulation of nucleus caudatus on epileptic electrical activity of brain in patients with intractable epilepsy. Stereotact Funct Neurosurg. 1997;69(1-4 Pt. 2):221–4.Google Scholar
19. Sramka, M, Fritz, G, Galanda, M, Nadvornik, P. Some observations in treatment stimulation of epilepsy. Acta Neurochir (Wien.) 1976;23(Suppl.):257–62.Google Scholar
20. Rasmussen, T. The neurosurgical treatment of epilepsy. In: Niedermeyer, E, editor. Modern Problems of Pharma-copsychiatry. New York: Karger; 1970. p. 306–25.Google Scholar
21. Krauss, GL, Fisher, RS. Cerebellar and thalamic stimulation for epilepsy. Adv Neurol. 1993;63:231–45.Google ScholarPubMed
22. Jasper, HH. Current evaluation of the concepts of centrencephalic and cortico-reticular seizures. Electroencephalogr Clin Neurophysiol. 1991;78:2–11.CrossRefGoogle ScholarPubMed
23. Jasper, HH, Droogglever-Furtuyn, J. Experimental studies on the functional anatomy of petit mal epilepsy. Assoc Res Nerv Ment Dis. 1947;26:272–98.Google Scholar
24. Williams, D. a study of thalamic and cortical rhythms in petit mal. Brain. 1953;76:50–69.Google Scholar
25. Kostopoulos, GK. Involvement if the thalamocortical system in epileptic loss of consciousness. Epilepsia. 2001;42(Suppl. 3):13–9.CrossRefGoogle ScholarPubMed
26. Hunter, J, Jasper, HH. Effects of thalamic stimulation in unanesthetized animals. The arrest reaction and petit mal like seizure activation patterns and generalized convulsions. Electroencephalogr Clin Neurophysiol. 1949;1:305–24.Google Scholar
27. Starzl, TE, Taylor, CW, Magoun, HW. Ascending conduction in reticular activating system, with special reference to the diencephalon. J Neurophysiol. 1951;14:461–77.CrossRefGoogle Scholar
28. Velasco, M, Velasco, F. State related brain stem regulation of cortical and motor excitability: effects on experimental focal motor seizures. In: Sterman, MB, Passouant, P, editors. Sleep and Epilepsy. New York: Academic Press; 1982. p. 53–61.Google Scholar
29. Velasco, F, Velasco, M, Ogarrio, C, Fanghanel, G. Electrical stimulation of the centromedian thalamic nucleus in the treatment of convulsive seizures: a preliminary report. Epilepsia. 1987;28:421–30.Google Scholar
30. Velasco, F. Velasco, M, Velasco, AL, Jiminez, F, Marquez, I, Rise, M. Electrical stimulation of the centromedian thalamic nucleus in control of seizures: long-term studies. Epilepsia. 1995;26:63–71.Google Scholar
31. Velasco, F, Velasco, M, Jiminez, F, et al. Predictors in the treatment of difficult-to-control seizures by electrical stimulation of the centromedian thalamic nucleus. Neurosurgery. 2000;47:295–304.Google Scholar
32. Velasco, M, Velasco, F, Velasco, AL. Centromedian-thalamic and hippocampal electrical stimulation for the control of intractable epileptic seizures. J Clin Neurophysiol. 2001;18:495–513.Google Scholar
33. Fisher, RS, Uematsu, S, Krauss, GL, et al. Placebo-controlled pilot study of centromedian thalamic stimulation in treatment of intractable seizures. Epilepsia. 1992;33:841–51.Google Scholar
34. Mirski, MA, Ferrendelli, JA. Andterio thalamic mediation of generalized pentylenetetrazol seizures. Brain Res. 1986;399:212–23.CrossRefGoogle ScholarPubMed
35. Mirski, MA, Rossell, LA, Terry, JB, Fisher, RS. Anticonvulsant effect of anterior thalamic high frequency electrical stimulation in the rat. Epilepsy Res. 1997;28:89–100.Google Scholar
36. Mirski, MA, Ferrendelli, JA. Selective metabolic activation of the mammillary bodies and their connection during ethosuximide-induced suppression of pentylenetetrazol seizures. Epilepsia. 1986;27:194–203.Google Scholar
37. Mirski, MA, Fisher, RS. Electrical stimulation of the mammillary nuclei increases seizure threshold to pentylenetetrazol in rats. Epilepsia. 1994;35:1309–16.CrossRefGoogle ScholarPubMed
38. Mirski, MA, Ferrendelli, JA. Interruption of the mammillothalamic tract prevents seizures in guinea pigs. Science. 1984;226:72–4.CrossRefGoogle ScholarPubMed
39. Hamani, C, Ewerton, FI, Bonilha, SM, Ballester, G, Mello, LE, Lozano, AM. Bilateral anterior thalamic nucleus lesions and high-frequency stimulation are protective against pilocarpine-induced seizures and status epilepticus. Neurosurgery 2004;54:191–5.Google Scholar
40. Hamani, C, Hodaie, M, Chiang, J, et al. Deep brain stimulation of the anterior nucleus of the thalamus: effects of electrical stimulation on pilocarpine-induced seizures and status epilepticus. Epilepsy Res. 2008;78(2-3):117–23.Google Scholar
41. Rosenow, J, Das, K, Rovit, RL, Couldwell, WT. Irving S. Cooper and his role in intracranial stimulation for movement disorders and epilepsy. Stereotact Funct Neurosurg. 2002;78:95–112.Google Scholar
42. Sussman, NM, Goldman, HW, Jackel, RA, et al. Anterior thalamic stimulation in medically intractable epilepsy. Part II: Preliminary clinical results (abstract). Epilepsia. 1988;29(5):677.Google Scholar
43. Hodaie, M, Wennberg, RA, Dostrovsky, JO, Lozano, AM. Chronic anterior thalamus stimulation for intractable epilepsy. Epilepsia. 2002;43(6):603–8.CrossRefGoogle ScholarPubMed
44. Andrade, DM, Zumsteg, D, Hamani, C, et al. Neurology. 2006;66 (10):1571–3.CrossRefGoogle Scholar
45. Fisher, R, Salanova, V, Witt, T, et al. Electrical stimulation of the anterior nucleus of the thalamus for treatment of refractory epilepsy. Epilepsia. 2010;51(5):1528–67.Google Scholar
46. Iadarola, MJ, Gale, K. Substantia nigra: site of anticonvulsant activity mediated by gamma-aminobutyric acid. Science. 1982;218:1237–40.Google Scholar
47. Garant, DS, Gale, K. Substantia nigra-mediated anticonvulsant actions: role of nigral output pathways. Exp Neurol. 1987;97:143–59.Google Scholar
48. Chevalier, G, Vacher, S, Deniau, JM, Desban, M. Disinhibition as a basic process in the expression of striatal functions. I. The striato-nigral influence on tecto-spinal/tecto-diencephalic neurons. Brain Res. 1985;334:215–26.Google Scholar
49. Dean, P, Gale, K. Anticonvulsant action of GABA receptor blockade in the nigrotectal target region. Brain Res. 1989;477:391–95.Google Scholar
50. Redgrave, P, Simkins, M, Overton, P, Dean, P. Anticonvulsant role of nigrotectal projection in the maximal electroshock model of epilepsy-I. Mapping of dorsal midbrain with bicuculline. Neuroscience. 1992;46:379–90.CrossRefGoogle ScholarPubMed
51. Shehab, S, Simkins, M, Dean, P, Redgrave, P. Regional distribution of the anticonvulsant and behavioural effects of muscimol injected into the substantia nigra of rats. Eur J Neurosci. 1996;8:749–57.Google Scholar
52. Cavalheiro, EA, Turski, L. Intrastriatal N-methyl-D-aspartate prevents amygdala kindled seizures in rats. Brain Res. 1986;377:173–6.CrossRefGoogle ScholarPubMed
53. Cavalheiro, EA, Bortolotto, ZA, Turski, L. Microinjections of the gamma-aminobutyrate antagonist, bicuculline methiodide, into the caudate-putamen prevent amygdala-kindled seizures in rats. Brain Res. 1987;411:370–2.Google Scholar
54. Deransart, C, Le, BT, Marescaux, C, Depaulis, A. Role of the subthalamo-nigral input in the control of amygdala-kindled seizures in the rat. Brain Res. 1998;807(1-2):78–83.Google Scholar
55. Deransart, C, Marescaux, C, Depaulis, A. Involvement of nigral glutamatergic inputs in the control of seizures in a genetic model of absence epilepsy in the rat. Neuroscience. 1996;71:721–8.Google Scholar
56. Vercueil, L, Benazzouz, A, Deransart, C et al. High-frequency stimulation of the subthalamic nucleus suppresses absence seizures in the rat: comparison with neurotoxic lesions. Epilepsy Res. 1998;31:39–46.Google Scholar
57. Usui, N, Maesawa, S, Kajita, Y, Endo, O, Takebayashi, S, Yoshida, J. Suppression of secondary generalization of limbic seizures by stimulation of subthalamic nucleus in rats. J Neurosurg. 2005;102:1122–9.Google Scholar
58. Lado, FA, Velísek, L, Moshé, SL. The effect of electrical stimulation of the subthalamic nucleus on seizures is frequency dependent. Epilepsia. 2003;44:157–64.Google Scholar
59. Benabid, AL, Minotti, L, Koudsie, A, de Saint, MA, Hirsch, E. Antiepileptic effect of high-frequency stimulation of the subthalamic nucleus (corpus luysi) in a case of medically intractable epilepsy caused by focal dysplasia: a 30-month follow-up: technical case report. Neurosurgery. 2002;50:1385–91.Google Scholar
60. Chabardes, S, Kahane, P, Minotti, L, Koudsie, A, Hirsch, E, Benabid, AL. Deep brain stimulation in epilepsy with particular reference to the subthalamic nucleus. Epileptic Disord. 2002;4(Suppl 3):S83–93.Google Scholar
61. Benabid, AL, Koudsie, A, Chabardes, S, et al. Subthalamic nucleus and substantia nigra pars reticularis stimulation: the Grenoble experience. In: Luders, HO, editor. Deep Brain Stimulation and Epilepsy. London: Martin Dunitz; 2004. p. 335–48.Google Scholar
62. Neme, S, Montgomery, EB, Rezai, A, Wilson, K, Luders, HO. Subthalamic nucleus stimulation in patients with intractable epilepsy: the Cleveland experience. In: Luders, HO, editor. Deep Brain Stimulation and Epilepsy. London: Martin Dunitz; 2004. p. 349–55.Google Scholar
63. Velasco, M, Velasco, F, Velasco, AL, et al. Subacute electrical stimulation of the hippocampus blocks intractable temporal lobe seizures and paroxysmal EEG activities. Epilepsia 2000;41:158–69.Google Scholar
64. Velasco, AL, Velasco, M, Velasco, F, et al. Subacute and chronic electrical stimulation of the hippocampus on intractable temporal lobe seizures: preliminary report. Arch Med Res. 2000;31:316–28.CrossRefGoogle ScholarPubMed
65. Vonck, K, Boon, P, Achten, E, De Reuck, J, Caemaert, J. Long-term amygdalohippocampal stimulation for refractory temporal lobe epilepsy. Ann Neurol. 2002;52:556–65.Google Scholar
66. Boon, P, Vonck, K, De Herdt, V, et al. Deep brain stimulation in patients with refractory temporal lobe epilepsy. Epilepsia. 2007;48:1551–60.Google Scholar
67. Velasco, AL, Velasco, F, Velasco, M, et al. Electrical stimulation of the hippocampal epileptic foci for seizure control: A double-blind, long-term follow-up study. Epilepsia. 2007;48(10):1895–1903.Google Scholar
68. Tellez-Zenteno, JF, McLachlan, RS, Parrent, A, Kubu, CS, Wiebe, S. Hippocampal electrical stimulation in mesial temporal lobe epilepsy. Neurology. 2006;66(10):1490–4.Google Scholar
69. McLachlan, RS, Pigott, S, Tellez-Zenteno, JF, Wiebe, S, Parrent, A. Bilateral hippocampal stimulation for intractable temporal lobe epilepsy: impact on seizures and memory. Epilepsia. 2010;51(2):304–7.Google Scholar
70. Lesser, RP, Kim, SH, Beyderman, L, Miglioretti, DL, Webber, WR, Bare, M, Cysyk, B, Krauss, G, Gordon, B. Brief bursts of pulse stimulation terminate afterdischarges caused by cortical stimulation. Neurology. 1999;53:2073–81.CrossRefGoogle ScholarPubMed
71. Yamamoto, J, Ikeda, A, Satow, T, et al. Low-frequency electric cortical stimulation has an inhibitory effect on epileptic focus in mesial temporal lobe epilepsy. Epilepsia. 2002;43:491–5.Google Scholar
72. Weiss, SR, Li, XL, Rosen, JB, Li, H, Heynen, T, Post, RM. Quenching: inhibition of development and expression of amygdala kindled seizures with low frequency stimulation. Neuroreport. 1995;6:2171–6.Google Scholar
73. Elisevich, K, Jenrow, K, Schuh, L, Smith, B. Long-term electrical stimulation-induced inhibition of partial epilepsy. J Neurosurg. 2006;105:894–7.Google Scholar
74. Kossoff, EH, Ritzl, EK, Politsky, JM et al. Effect of an external responsive neurostimulator on seizures and electrographic discharges during subdural electrode monitoring. Epilepsia. 2004;45:1560–7.Google Scholar
75. Osorio, I, Frei, MG, Sunderam, S et al. Automated seizure abatement in humans using electrical stimulation. Ann Neurol. 2005;57:258–68.Google Scholar
76. Morrell, MJ and the RNS System in Epilepsy Study Group. Responsive cortical stimulation for the treatment of medically intractable partial epilepsy. Neurology. 2011;77(13):1295–304.Google Scholar