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1101


Neurofibromatosis: advances in molecular genetics, diagnosis, and treatment. Introduction

Devinsky, Orrin
PMID: 19587629
ISSN: 1949-4378
CID: 100631

Refractory epilepsy in tuberous sclerosis: Vagus nerve stimulation with or without subsequent resective surgery

Elliott, Robert E; Carlson, Chad; Kalhorn, Stephen P; Moshel, Yaron A; Weiner, Howard L; Devinsky, Orrin; Doyle, Werner K
OBJECTIVE: The goal of the work described here was to assess the efficacy and safety of vagus nerve stimulation in a cohort of patients with tuberous sclerosis complex with refractory epilepsy. Furthermore, we examined the impact of vagus nerve stimulation failure on the ultimate outcome following subsequent intracranial epilepsy surgery. METHODS: A retrospective review was performed on 19 patients with refractory epilepsy and TSC who underwent vagus nerve stimulator (VNS) implantation. There were 11 (58%) females and 8 (42%) males aged 2 to 44 years when the VNS was implanted (mean: 14.7+/-12 years). Twelve patients underwent primary VNS implantation after having failed a mean of 7.1 antiepileptic drugs. Two patients (17%) had generalized epilepsy, one had a single seizure focus, three (25%) had multifocal epilepsy, and six (50%) had multifocal and generalized epilepsy. Seven patients were referred for device removal and evaluation for intracranial procedures. One patient in the primary implantation group was lost to follow-up and excluded from outcome analysis. RESULTS: All implantations and removals were performed without permanent complications. The duration of treatment for primary VNS implants varied from 8.5 months to 9.6 years (mean: 4.9 years). Mean seizure frequency significantly improved following VNS implantation (mean reduction: 72%, P<0.002). Two patients had Engel Class I (18%), one had Class II (9%), seven had Class III (64%), and one had Class IV (9%) outcome. Three patients with poor response to vagus nerve stimulation therapy at our center underwent resection of one or more seizure foci (Engel Class I, two patients; Engel Class III, one patient). Seven patients referred to our center for VNS removal and craniotomy underwent seizure focus resection (6) or corpus callosotomy (1) (Engel Class II: 2, Engel III: 2; Engel IV: 3). In total, 8 of 10 (80%) patients experienced improved seizure control following intracranial surgery (mean reduction: 65%, range: 0-100%, P<0.05). CONCLUSIONS: VNS is a safe and effective treatment option for medically refractory epilepsy in patients with tuberous sclerosis complex. Nine of 11 patients (82%) experienced at least a 67% reduction in seizure burden. Lack of response to vagus nerve stimulation does not preclude subsequent improvement in seizure burden with intracranial epilepsy surgery
PMID: 19767244
ISSN: 1525-5069
CID: 105245

AANTERIOR TEMPORAL LOBECTOMY & RADICAL AMYGDALOHIPPOCAMPECTOMY (ATLRA) FOR MESIAL TEMPORAL SCLEROSIS: PREOPERATIVE RISK FACTORS FOR LONG-TERM SEIZURE CONTROL IN A HIGHLY SELECTED POPULATION [Meeting Abstract]

Bollo, RJ; Elliott, RE; Berliner, JL; Silverberg, A; Geller, EB; Devinsky, O; Doyle, WK
ISI:000270550500937
ISSN: 0013-9580
CID: 106074

QUANTITATIVE MAGNETIC RESONANCE IMAGING FINDINGS IN IDIOPATHIC GENERALIZED EPILEPSY [Meeting Abstract]

Carlson, C; DuBois, J; Marcuse, L; Kuzniecky, R; Devinsky, O; Boo, C; Mikhly, M; Blumberg, M; Thesen, T
ISI:000270550500989
ISSN: 0013-9580
CID: 106075

STRUCTURAL BRAIN ABNORMALITIES IN POSTICTAL PSYCHOSIS [Meeting Abstract]

DuBois, J; Carlson, C; Kuzniecky, R; Devinsky, O; Alper, K; Blumberg, M; Mikhly, M; Starner, K; Thesen, T
ISI:000270550501002
ISSN: 0013-9580
CID: 106076

VAGUS NERVE STIMULATION IN PATIENTS WITH TUBEROUS SCLEROSIS COMPLEX: EFFICACY OF NEW IMPLANTATIONS AND ASSOCIATION OF DEVICE INEFFICACY WITH SUBSEQUENT OUTCOME OF INTRACRANIAL EPILEPSY SURGERY [Meeting Abstract]

Kalhorn, SP; Elliott, R; Carlson, C; Moshel, Y; Weiner, H; Devinsky, O; Doyle, W
ISI:000270550501022
ISSN: 0013-9580
CID: 106077

VAGUS NERVE STIMULATION FOR REFRACTORY EPILEPSY: SINGLE SURGEON EXPERIENCE OF OVER 700 CONSECUTIVE OPERATIONS [Meeting Abstract]

Elliott, RE; Morsi, A; Kalhorn, S; Marcus, J; Sellin, J; Kang, M; Silverberg, A; Carlson, C; Geller, E; Devinsky, O; Doyle, W
ISI:000270550501096
ISSN: 0013-9580
CID: 106078

Translations from history: Epilepsy and behavior [Editorial]

Devinsky, Orrin
PMID: 19341978
ISSN: 1525-5069
CID: 134084

Remembrance. In memoriam: Ed Bromfield, M.D., 1951-2009 [Editorial]

Devinsky, Orrin
PMID: 19643673
ISSN: 1525-5069
CID: 111660

The human K-complex represents an isolated cortical down-state

Cash, Sydney S; Halgren, Eric; Dehghani, Nima; Rossetti, Andrea O; Thesen, Thomas; Wang, Chunmao; Devinsky, Orrin; Kuzniecky, Ruben; Doyle, Werner; Madsen, Joseph R; Bromfield, Edward; Eross, Lorand; Halasz, Peter; Karmos, George; Csercsa, Richard; Wittner, Lucia; Ulbert, Istvan
The electroencephalogram (EEG) is a mainstay of clinical neurology and is tightly correlated with brain function, but the specific currents generating human EEG elements remain poorly specified because of a lack of microphysiological recordings. The largest event in healthy human EEGs is the K-complex (KC), which occurs in slow-wave sleep. Here, we show that KCs are generated in widespread cortical areas by outward dendritic currents in the middle and upper cortical layers, accompanied by decreased broadband EEG power and decreased neuronal firing, which demonstrate a steep decline in network activity. Thus, KCs are isolated 'down-states,' a fundamental cortico-thalamic processing mode already characterized in animals. This correspondence is compatible with proposed contributions of the KC to sleep preservation and memory consolidation
PMCID:3715654
PMID: 19461004
ISSN: 1095-9203
CID: 114449