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Dive into the research topics where James W. Wheless is active.

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Featured researches published by James W. Wheless.


Neurology | 1998

Vagus nerve stimulation therapy for partial-onset seizures A randomized active-control trial

Adrian Handforth; Christopher M. DeGiorgio; Steven C. Schachter; Basim M. Uthman; Dean K. Naritoku; Evelyn S. Tecoma; Thomas R. Henry; S. D. Collins; Bradley V. Vaughn; R. C. Gilmartin; Douglas Labar; George L. Morris; Martin Salinsky; Ivan Osorio; Ruzica Ristanovic; David M. Labiner; John C. Jones; J. Murphy; G. C. Ney; James W. Wheless

Objective: The purpose of this multicenter, add-on, double-blind, randomized, active-control study was to compare the efficacy and safety of presumably therapeutic (high) vagus nerve stimulation with less (low) stimulation. Background: Chronic intermittent left vagus nerve stimulation has been shown in animal models and in preliminary clinical trials to suppress the occurrence of seizures. Methods: Patients had at least six partial-onset seizures over 30 days involving complex partial or secondarily generalized seizures. Concurrent antiepileptic drugs were unaltered. After a 3-month baseline, patients were surgically implanted with stimulating leads coiled around the left vagus nerve and connected to an infraclavicular subcutaneous programmable pacemaker-like generator. After randomization, device initiation, and a 2-week ramp-up period, patients were assessed for seizure counts and safety over 3 months. The primary efficacy variable was the percentage change in total seizure frequency compared with baseline. Results: Patients receiving high stimulation (94 patients, ages 13 to 54 years) had an average 28% reduction in total seizure frequency compared with a 15% reduction in the low stimulation group (102 patients, ages 15 to 60 year; p = 0.04). The high-stimulation group also had greater improvements on global evaluation scores, as rated by a blinded interviewer and the patient. High stimulation was associated with more voice alteration and dyspnea. No changes in physiologic indicators of gastric, cardiac, or pulmonary functions occurred. Conclusions: Vagus nerve stimulation is an effective and safe adjunctive treatment for patients with refractory partial-onset seizures. It represents the advent of a new, nonpharmacologic treatment for epilepsy.


Epilepsia | 2000

Prospective Long-Term Study of Vagus Nerve Stimulation for the Treatment of Refractory Seizures

Christopher M. DeGiorgio; Steven C. Schachter; Adrian Handforth; Martin Salinsky; J. Thompson; Basim M. Uthman; Robin Reed; S. Collin; Evelyn S. Tecoma; George L. Morris; Bradley V. Vaughn; Dean K. Naritoku; Thomas R. Henry; D. Labar; R. C. Gilmartin; D. Labiner; Ivan Osorio; R. Ristanovic; Jana E. Jones; Jerome V. Murphy; G. C. Ney; James W. Wheless; P. Lewis; C. Heck

Summary: Purpose: To determine the long‐term efficacy of vagus nerve stimulation (VNS) for refractory seizures. VNS is a new treatment for refractory epilepsy. Two short‐term double‐blind trials have demonstrated its safety and efficacy, and one long‐term study in 114 patients has demonstrated a cumulative improvement in efficacy at 1 year. We report the largest prospective long‐term study of VNS to date.


Genetics in Medicine | 2007

Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States.

Kit Sing Au; Aimee T. Williams; E. Steve Roach; Lori Batchelor; Steven Sparagana; Mauricio R. Delgado; James W. Wheless; James E. Baumgartner; Benjamin B. Roa; Carolyn M. Wilson; Teresa K. Smith-Knuppel; Min Yuen C Cheung; Vicky Whittemore; Terri M. King; Hope Northrup

Tuberous sclerosis complex is an autosomal dominant neurocutaneous disorder marked by hamartoma growth in multiple organ systems. We performed mutational analyses on 325 individuals with definite tuberous sclerosis complex diagnostic status. We identified mutations in 72% (199/257) of de novo and 77% (53/68) of familial cases, with 17% of mutations in the TSC1 gene and 50% in the TSC2 gene. There were 4% unclassified variants and 29% with no mutation identified. Genotype/phenotype analyses of all observed tuberous sclerosis complex findings in probands were performed, including several clinical features not analyzed in two previous large studies. We showed that patients with TSC2 mutations have significantly more hypomelanotic macules and learning disability in contrast to those with TSC1 mutations, findings not noted in previous studies. We also observed results consistent with two similar studies suggesting that individuals with mutations in TSC2 have more severe symptoms. On performing meta-analyses of our data and the other two largest studies in the literature, we found significant correlations for several features that individual studies did not have sufficient power to conclude. Male patients showed more frequent neurologic and eye symptoms, renal cysts, and ungual fibromas. Correlating genotypes with phenotypes should facilitate the disease management of tuberous sclerosis complex.


Epilepsia | 2002

Vagus Nerve Stimulation in Children with Refractory Seizures Associated with Lennox–Gastaut Syndrome

Michael Frost; John R. Gates; Sandra L. Helmers; James W. Wheless; Paul Levisohn; Carmelo Tardo; Joan A. Conry

Summary: u2002Purpose: Vagus nerve stimulation (VNS) is approved for use for refractory partial seizures. Nevertheless, information regarding VNS therapy for special populations, including Lennox–Gastaut syndrome (LGS) is limited. We discuss the effectiveness, tolerability, and safety of VNS therapy in patients with LGS.


Epilepsia | 1999

A Comparison of Magnetoencephalography, MRI, and V-EEG in Patients Evaluated for Epilepsy Surgery

James W. Wheless; L. J. Willmore; Joshua I. Breier; M. Kataki; Joseph R. Smith; Don W. King; Kimford J. Meador; Y. D. Park; David W. Loring; Guy L. Clifton; James E. Baumgartner; A. Thomas; J. E. C. Constantinou; Andrew C. Papanicolaou

Summary: Purpose: To determine the efficacy and relative contribution of several diagnostic methods [ictal and interictal scalp and intracranial EEG, magnetic resonance imaging (MRI), and magnetoencephalography (MEG)] in identifying the epileptogenic zone for resection.


Journal of Child Neurology | 2001

Vagus nerve stimulation therapy in pediatric patients with refractory epilepsy: retrospective study.

Sandra L. Helmers; James W. Wheless; Michael Frost; John Gates; Paul Levisohn; Carmelo Tardo; Joan A. Conry; Dilek Yalnızoğlu; Joseph R. Madsen

This six-center, retrospective study evaluated the effectiveness, tolerability, and safety of vagus nerve stimulation in children. Data were available for 125 patients at baseline, 95 patients at 3 months, 56 patients at 6 months, and 12 patients at 12 months. The typical patient, aged 12 years, had onset of seizures at age 2 years and had tried nine anticonvulsants before implantation. Collected data included preimplant history, seizures, implant, device settings, quality of life, and adverse events. Average seizure reduction was 36.1% at 3 months and 44.7% at 6 months. Common adverse events included voice alteration and coughing during stimulation. Rare adverse events, unique to this age group, included increased drooling and increased hyperactivity. Quality of life improved in alertness, verbal communication, school performance, clustering of seizures, and postictal periods. We concluded that vagus nerve stimulation is an effective treatment for medically refractory epilepsy in children. (J Child Neurol 2001;16:843—848).


Neurology | 1999

Language dominance determined by magnetic source imaging A comparison with the Wada procedure

Joshua I. Breier; Panagiotis G. Simos; George Zouridakis; James W. Wheless; L. J. Willmore; Jules E. C. Constantinou; William W. Maggio; Andrew C. Papanicolaou

Objective: To evaluate the validity of data derived from magnetic source imaging (MSI) regarding cerebral dominance for language in patients with intractable seizure disorder.Method:— The authors performed functional imaging of the receptive language cortex using a whole-head neuromagnetometer in 26 consecutive epilepsy patients who also underwent the intracarotid amobarbital (Wada) procedure. During MSI recordings, patients engaged in a word recognition task. This task was shown previously to activate language areas in normal adults as well as in patients who undergo intraoperative language mapping, allowing confirmation of MSI findings. Language laterality indices were formed for both the Wada and the MSI procedures. In addition, clinical judgments regarding cerebral dominance for language were made using the two methods by independent raters. Results: Cluster analysis indicated excellent agreement between the quantitative MSI and Wada indices. Rater judgments showed almost complete agreement as well. Conclusion: MSI is a promising method for determining cerebral dominance for language.


Epilepsy Research | 1999

Safety of rapid intravenous infusion of valproate loading doses in epilepsy patients

Vijay Venkataraman; James W. Wheless

IV valproate may be given to patients requiring rapid elevation of serum valproate or for patients unable to take oral medication. Previously we established the loading dose of IV valproate needed to achieve serum concentrations of > 100 ug/ml. This study evaluated the safety of rapid infusion of valproate to achieve high therapeutic levels. Twenty-four infusions of IV valproate were carried out electively in twenty-one patients with epilepsy (ages 2-54 years). The dose ranged from 21-28 mg/kg (mean 24.2 mg/kg). Target infusion rates were 3 or 6 mg/kg per min, yielding an infusion duration of 4.17 or 8.34 min. ECG was monitored; blood pressure was measured before and after infusion. Post infusion serum valproate concentrations were 64-204.1 ug/ml (mean 132.6). There were no significant changes in blood pressure and no ECG abnormalities observed. Transient pain occurred at the site of injection in five patients, associated with redness in two. This appeared to related to the concentration of valproic acid in the infusion fluid. We conclude that a loading dose of IV valproate can be administered safely and rapidly. This finding enables further studies evaluating IV valproate as a non-sedative anticonvulsant in the management of status epilepticus.


Neurology | 2004

Does magnetoencephalography add to scalp video-EEG as a diagnostic tool in epilepsy surgery?

Ekaterina Pataraia; Panagiotis G. Simos; E. M. Castillo; Rebecca L. Billingsley; Shirin Sarkari; James W. Wheless; Vijay Maggio; William W. Maggio; James E. Baumgartner; Paul R. Swank; Joshua I. Breier; Andrew C. Papanicolaou

Objective: The authors evaluated the sensitivity and selectivity of interictal magnetoencephalography (MEG) versus prolonged ictal and interictal scalp video-electroencephalography (V-EEG) in order to identify patient groups that would benefit from preoperative MEG testing. Methods: The authors evaluated 113 consecutive patients with medically refractory epilepsy who underwent surgery. The epileptogenic region predicted by interictal and ictal V-EEG and MEG was defined in relation to the resected area as perfectly overlapping with the resected area, partially overlapping, or nonoverlapping. Results: The sensitivity of a 30-minute interictal MEG study for detecting clinically significant epileptiform activity was 79.2%. Using MEG, we were able to localize the resected region in a greater proportion of patients (72.3%) than with noninvasive V-EEG (40%). MEG contributed to the localization of the resected region in 58.8% of the patients with a nonlocalizing V-EEG study and 72.8% of the patients for whom V-EEG only partially identified the resected zone. Overall, MEG and V-EEG results were equivalent in 32.3% of the cases, and additional localization information was obtained using MEG in 40% of the patients. Conclusion: MEG is most useful for presurgical planning in patients who have either partially or nonlocalizing V-EEG results.


Neuroreport | 2000

Brain mechanisms for reading : the role of the superior temporal gyrus in word and pseudoword naming

Panagiotis G. Simos; Joshua I. Breier; James W. Wheless; William W. Maggio; Jack M. Fletcher; Eduardo M. Castillo; Andrew C. Papanicolaou

The purpose of this study was to test the neurological validity of a dual-route model of reading by asking patients, who were undergoing electrocortical stimulation mapping, to read words with irregular print-to-sound correspondences and pseudowords. Brain activation profiles were also obtained from these patients during an auditory and a visual word recognition task using whole-head magnetic source imaging. We demonstrated that reading is subserved by at least two brain mechanisms that are anatomically dissociable. One mechanism subserves assembled phonology and depends on the activity of the posterior part of the left superior temporal gyrus (STGp), whereas the second is responsible for addressed phonology and does not necessarily involve this region. The contribution of STGp to reading appears to be based on its specialization for phonological analysis operations, involved in the processing of both spoken and written language.

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Joshua I. Breier

University of Texas Health Science Center at Houston

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James E. Baumgartner

University of Texas Health Science Center at Houston

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Jules E. C. Constantinou

University of Texas Health Science Center at Houston

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Eduardo M. Castillo

University of Texas Health Science Center at Houston

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William W. Maggio

University of Texas Health Science Center at Houston

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Bonnie L. Brookshire

University of Texas Health Science Center at Houston

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L. J. Willmore

University of Texas Health Science Center at Houston

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Azreena B. Thomas

University of Texas Health Science Center at Houston

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