Vicenta Salanova
Indiana University
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Publication
Featured researches published by Vicenta Salanova.
Epilepsia | 2010
Robert S. Fisher; Vicenta Salanova; Thomas C. Witt; Robert Worth; Thomas R. Henry; Robert E. Gross; Kalarickal J. Oommen; Ivan Osorio; Jules M. Nazzaro; Douglas Labar; Michael G. Kaplitt; Michael R. Sperling; Evan Sandok; John H. Neal; Adrian Handforth; John M. Stern; Antonio DeSalles; Steve Chung; Andrew G. Shetter; Donna Bergen; Roy A. E. Bakay; Jaimie M. Henderson; Jacqueline A. French; Gordon H. Baltuch; William E. Rosenfeld; Andrew Youkilis; William J. Marks; Paul A. Garcia; Nicolas Barbaro; Nathan B. Fountain
Purpose: We report a multicenter, double‐blind, randomized trial of bilateral stimulation of the anterior nuclei of the thalamus for localization‐related epilepsy.
Epilepsia | 2014
Christianne Heck; David King-Stephens; Andrew Massey; Dileep Nair; Barbara C. Jobst; Gregory L. Barkley; Vicenta Salanova; Andrew J. Cole; Michael C. Smith; Ryder P. Gwinn; Christopher Skidmore; Paul C. Van Ness; Yong D. Park; Ian Miller; Eric B. Geller; Paul Rutecki; Richard S. Zimmerman; David C. Spencer; Alica Goldman; Jonathan C. Edwards; James W. Leiphart; Robert E. Wharen; James Fessler; Nathan B. Fountain; Gregory A. Worrell; Robert E. Gross; Stephan Eisenschenk; Robert B. Duckrow; Lawrence J. Hirsch; Carl W. Bazil
To demonstrate the safety and effectiveness of responsive stimulation at the seizure focus as an adjunctive therapy to reduce the frequency of seizures in adults with medically intractable partial onset seizures arising from one or two seizure foci.
Epilepsia | 2002
Vicenta Salanova; Omkar N. Markand; Robert M. Worth
Summary: Purpose: We studied the surgical outcome, complications, and the late mortality rate in a large group of patients with medically refractory temporal lobe epilepsy (TLE).
Neurology | 2015
Martha J. Morrell; Eli M. Mizrahi; Alica Goldman; David King-Stephens; Dileep Nair; Shraddha Srinivasan; Barbara C. Jobst; Robert E. Gross; Donald C. Shields; Gregory L. Barkley; Vicenta Salanova; Piotr W. Olejniczak; Andrew J. Cole; Sydney S. Cash; Katherine H. Noe; Robert E. Wharen; Gregory A. Worrell; Anthony M. Murro; Jonathan C. Edwards; Michael Duchowny; David C. Spencer; Michael C. Smith; Eric B. Geller; Ryder P. Gwinn; Christopher Skidmore; Stephan Eisenschenk; Michel J. Berg; Christianne Heck; Paul C. Van Ness; Nathan B. Fountain
Objective: The long-term efficacy and safety of responsive direct neurostimulation was assessed in adults with medically refractory partial onset seizures. Methods: All participants were treated with a cranially implanted responsive neurostimulator that delivers stimulation to 1 or 2 seizure foci via chronically implanted electrodes when specific electrocorticographic patterns are detected (RNS System). Participants had completed a 2-year primarily open-label safety study (n = 65) or a 2-year randomized blinded controlled safety and efficacy study (n = 191); 230 participants transitioned into an ongoing 7-year study to assess safety and efficacy. Results: The average participant was 34 (±11.4) years old with epilepsy for 19.6 (±11.4) years. The median preimplant frequency of disabling partial or generalized tonic-clonic seizures was 10.2 seizures a month. The median percent seizure reduction in the randomized blinded controlled trial was 44% at 1 year and 53% at 2 years (p < 0.0001, generalized estimating equation) and ranged from 48% to 66% over postimplant years 3 through 6 in the long-term study. Improvements in quality of life were maintained (p < 0.05). The most common serious device-related adverse events over the mean 5.4 years of follow-up were implant site infection (9.0%) involving soft tissue and neurostimulator explantation (4.7%). Conclusions: The RNS System is the first direct brain responsive neurostimulator. Acute and sustained efficacy and safety were demonstrated in adults with medically refractory partial onset seizures arising from 1 or 2 foci over a mean follow-up of 5.4 years. This experience supports the RNS System as a treatment option for refractory partial seizures. Classification of evidence: This study provides Class IV evidence that for adults with medically refractory partial onset seizures, responsive direct cortical stimulation reduces seizures and improves quality of life over a mean follow-up of 5.4 years.
Annals of Neurology | 2009
Nicholas M. Barbaro; Mark Quigg; Donna K. Broshek; Mariann M. Ward; Kathleen R. Lamborn; Kenneth D. Laxer; David A. Larson; William D. Dillon; Lynn Verhey; Paul A. Garcia; Ladislau Steiner; Christine Heck; Douglas Kondziolka; Robert L. Beach; William C. Olivero; Thomas C. Witt; Vicenta Salanova; Robert R. Goodman
The safety, efficacy, and morbidity of radiosurgery (RS) must be established before it can be offered as an alternative to open surgery for unilateral mesial temporal lobe epilepsy. We report the 3‐year outcomes of a multicenter, prospective pilot study of RS.
Epilepsia | 2000
Omkar N. Markand; Vicenta Salanova; Eileen Whelihan; Christine L. Emsley
Summary: Purpose: A prospective study to investigate health‐related quality of life (HRQOL) outcome in patients with temporal lobe epilepsy treated with anterior temporal lobectomy (ATL).
Epilepsia | 1999
Vicenta Salanova; Omkar N. Markand; Robert M. Worth
Summary: Purpose: There are few studies of prolonged longitudinal follow‐up after temporal resections.
Acta Neurologica Scandinavica | 2004
Vicenta Salanova; Omkar N. Markand; Robert M. Worth
Objectives – To determine the frequency and types of dual pathology in patients with temporal lobe epilepsy (TLE) and to analyze the clinical manifestations and surgical outcome.
Acta Neurologica Scandinavica | 2005
Vicenta Salanova; Omkar N. Markand; Robert M. Worth
Purpose – To analyze failures and reoperations in temporal lobe epilepsy (TLE), and compare these patients with those seizure‐free, and to determine any significant differences between the groups.
Acta Neurologica Scandinavica | 1997
Omkar N. Markand; Vicenta Salanova; Robert M. Worth; H. M. Park; H. N. Wellman
Objective – To compare the sensitivity of ictal 99mTc‐HMPAO single photon emission computed tomography (SPECT) with interictal 18F‐fluorodeoxyglucose positron emission tomography (PET) in localization of the epileptogenic focus in patients with medically intractable complex partial seizures (MI‐CPS). Material and methods – Retrospective analysis was performed on patients with MI‐CPS who underwent anterior temporal lobectomy from January 1993 onwards when PET became available to us for clinical studies at the Indiana University Medical Center. There were 38 female and 29 male patients (total=67) with MI‐CPS, 10 to 55.5 years of age (mean 31) and duration of their epilepsy from 1‐46 years (mean 21). Interictal PET was evaluated for evidence of focal hypometabolism and ictal SPECT for focal perfusion abnormality (hyperperfusion or hypoperfusion) by visual analysis. Results – Both Ictal SPECT and interictal FDG‐PET studies were obtained in 36 patients with MI‐CPS. PET showed definite hypometabolism in 30 and questionable hypometabolism in an additional two patients. Ictal SPECT correctly localized the seizure focus in 27 patients by demonstrating ictal hyperperfusion whereas in one the hyperperfusion was falsely localized. In an additional seven patients the ictal SPECT provided probable localization by demonstrating ictal hypoperfusion in the appropriate temporal lobe. The sensitivity of ictal SPECT and interictal PET was 34/36 and 32/36, respectively, the difference was not statistically significant (χ2y=0.18, DF=1, P=0.67). In six of the 36 patients the two tests were complementary to each other in providing localizing information. Conclusion – Ictal SPECT and interictal PET are equally sensitive and reliable techniques in localizing the epileptogenic focus in patients with MI‐CPS. They play a critical role in providing localization in MRI negative patients allowing surgical resection to be undertaken in many without additional invasive electrographic monitoring.