Christopher Skidmore
Thomas Jefferson University
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Publication
Featured researches published by Christopher Skidmore.
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.
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
Scott Mintzer; Christopher Skidmore; Caitlin J. Abidin; Megan C. Morales; Inna Chervoneva; David M. Capuzzi; Michael R. Sperling
The widely prescribed anticonvulsants phenytoin and carbamazepine are potent inducers of cytochrome P450 enzymes, which are involved in cholesterol synthesis. We sought to determine whether these drugs have an effect on cholesterol and other serological markers of vascular risk.
Epilepsia | 2016
Joon Y. Kang; Chengyuan Wu; Joseph I. Tracy; Matthew Lorenzo; James J. Evans; Maromi Nei; Christopher Skidmore; Scott Mintzer; Ashwini Sharan; Michael R. Sperling
To describe mesial temporal lobe ablated volumes, verbal memory, and surgical outcomes in patients with medically intractable mesial temporal lobe epilepsy (mTLE) treated with magnetic resonance imaging (MRI)–guided stereotactic laser interstitial thermal therapy (LiTT).
Epilepsia | 2012
Carla LoPinto-Khoury; Michael R. Sperling; Christopher Skidmore; Maromi Nei; James J. Evans; Ashwini Sharan; Scott Mintzer
Purpose: Fluorodeoxyglucose positron emission computed tomography (FDG‐PET) hypometabolism is important for surgical planning in patients with temporal lobe epilepsy (TLE), but its significance remains unclear in patients who do not have evidence of mesial temporal sclerosis (MTS) on magnetic resonance imaging (MRI). We examined surgical outcomes in a group of PET‐positive, MRI‐negative patients and compared them with those of patients with MTS.
Neurosurgery Clinics of North America | 2002
Christopher Skidmore; John Andrefsky
This article introduces the basic epidemiology of intracerebral hemorrhage (ICH) and discusses the current available literature on the pathophysiology of primary ICH, hematoma enlargement, and cerebral edema. The article also includes a brief presentation of the basic steps regarding initial ICH management is presented as a framework for patient care.
Epilepsia | 2013
Sophia Pan Wang; Scott Mintzer; Christopher Skidmore; Tingting Zhan; Erika Stuckert; Maromi Nei; Michael R. Sperling
Purpose: Studies of seizure outcome in patients undergoing serial antiepileptic drug trials have all been uncontrolled, with no account made for the spontaneous changes in disease state that could confound the elucidation of drug effects. In addition, no study has ever looked at outcome following antiepileptic drug switch in seizure‐free patients, despite the fact that this is done routinely in clinical practice. We aimed to address both of these issues using a matched case‐cohort design.
Epilepsia | 2015
Gaelle Eve Doucet; Robert Rider; Nathan Taylor; Christopher Skidmore; Ashwini Sharan; Michael R. Sperling; Joseph I. Tracy
This study determined the ability of resting‐state functional connectivity (rsFC) graph‐theory measures to predict neurocognitive status postsurgery in patients with temporal lobe epilepsy (TLE) who underwent anterior temporal lobectomy (ATL).
Brain Topography | 2015
Gaelle Eve Doucet; Ashwini Sharan; Dorian Pustina; Christopher Skidmore; Michael R. Sperling; Joseph I. Tracy
Temporal lobe epilepsy (TLE) is associated with abnormalities which extend into the entire brain. While the age of seizure onset (SO) has a large impact on brain plasticity, its effect on brain connectivity at rest remains unclear, especially, in interaction with factors such as the presence of mesial temporal sclerosis (MTS). In this context, we investigated whole-brain and regional functional connectivity (FC) organization in 50 TLE patients who underwent a resting-state fMRI scan, in comparison to healthy controls, using graph-theory measures. We first classified TLE patients according to the presence of MTS or not. Then, we categorized the patients based on their age of SO into two subgroups (early or late age of SO). Results revealed whole-brain differences with both reduced functional segregation and increased integration in the patients, regardless of the age of SO and MTS, relative to the controls. At a local level, we revealed that the connectivity of the ictal hippocampus remains the most impaired for an early SO, even in the absence of MTS. Importantly, we showed that the impact of age of SO on whole-brain and regional resting-state FC depends on the presence of MTS. Overall, our results highlight the importance of investigating the effect of age of SO when examining resting-state activity in TLE, as this factor leads different perturbations of network modularity and connectivity at the global and local level, with different implications for regional plasticity and adaptive organization.
The Neurologist | 2011
Ritu Bagla; Christopher Skidmore
Background and ObjectiveFrontal lobe epilepsy is the second most common localization-related or focal epilepsy. Frontal lobe seizures are challenging to diagnose as the clinical manifestations are diverse due to the complexity and variability of the patterns of epileptic discharges, and the scalp electroencephalograph (EEG) can often be normal or misleading. This review focuses on the clinical and EEG features of seizures arising from the frontal lobe. Review SummaryThe clinical manifestations in patients with frontal lobe epilepsy are varied. Frontal lobe seizures can be divided into perirolandic, supplementary sensorimotor area, dorsolateral, orbitofrontal, anterior frontopolar, opercular, and cingulate types. Seizures originating from the perirolandic and supplementary sensorimotor areas are clinically distinct, characterized by motor activity or asymmetric tonic posturing with preserved awareness. Seizures arising from dorsolateral, orbitofrontal, frontopolar, and cingulate areas are not as well characterized and have more variable clinical manifestations. Scalp EEG recording is sometimes helpful in localization but is usually normal or misleading in frontal lobe epilepsy. The treatment is similar to other localization-related or focal epilepsies. Medications are the first line of therapy, and surgery is considered for patients who fail to respond to medications. The surgical outcome in frontal lobe resections is less favorable than in anterior temporal lobectomies due to the challenge in locating the epileptogenic zone and the presence of functional areas (eloquent cortex) that can limit the resection. ConclusionsFrontal lobe seizures are characterized by diverse behavioral manifestations. Only a few well-described frontal lobe syndromes exist. The variety of clinical manifestations reflects both the varying sites of seizure origin and propagation routes that seizures may take. Although this review provides a framework for the understanding of these seizures, one should remain cautious in diagnosing seizure localization based on clinical or EEG description. Only a few patients have well-described syndromes and can be diagnosed with confidence. For most patients, new diagnostic methods and genetic testing may help improve our ability to diagnose and treat the conditions discussed in this study.