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Dive into the research topics where Katherine Holland-Bouley is active.

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Featured researches published by Katherine Holland-Bouley.


Annals of Neurology | 2013

Everolimus treatment of refractory epilepsy in tuberous sclerosis complex

Darcy A. Krueger; Angus A. Wilfong; Katherine Holland-Bouley; Anne E. Anderson; Karen Agricola; Cindy Tudor; Maxwell Mays; Christina Lopez; Mi-Ok Kim; David Neal Franz

Epilepsy is a major manifestation of tuberous sclerosis complex (TSC). Everolimus is an mammalian target of rapamycin complex 1 inhibitor with demonstrated benefit in several aspects of TSC. We report the first prospective human clinical trial to directly assess whether everolimus will also benefit epilepsy in TSC patients.


Epilepsia | 2012

Resection of ictal high-frequency oscillations leads to favorable surgical outcome in pediatric epilepsy

Hisako Fujiwara; Hansel M. Greiner; Ki Hyeong Lee; Katherine Holland-Bouley; Joo Hee Seo; Todd M. Arthur; Francesco T. Mangano; James L. Leach; Douglas F. Rose

Purpose:  Intracranial electroencephalography (EEG) is performed as part of an epilepsy surgery evaluation when noninvasive tests are incongruent or the putative seizure‐onset zone is near eloquent cortex. Determining the seizure‐onset zone using intracranial EEG has been conventionally based on identification of specific ictal patterns with visual inspection. High‐frequency oscillations (HFOs, >80 Hz) have been recognized recently as highly correlated with the epileptogenic zone. However, HFOs can be difficult to detect because of their low amplitude. Therefore, the prevalence of ictal HFOs and their role in localization of epileptogenic zone on intracranial EEG are unknown.


Annals of Neurology | 2015

Everolimus for subependymal giant cell astrocytoma: 5-year final analysis.

David Neal Franz; Karen Agricola; Maxwell Mays; Cindy Tudor; Marguerite M. Caré; Katherine Holland-Bouley; Noah Berkowitz; Sara Miao; Severine Peyrard; Darcy A. Krueger

To analyze the cumulative efficacy and safety of everolimus in treating subependymal giant cell astrocytomas (SEGA) associated with tuberous sclerosis complex (TSC) from an open‐label phase II study (NCT00411619). Updated data became available from the conclusion of the extension phase and are presented in this ≥5‐year analysis.


Epilepsy Research | 2012

Ictal MEG onset source localization compared to intracranial EEG and outcome: improved epilepsy presurgical evaluation in pediatrics.

Hisako Fujiwara; Hansel M. Greiner; Nat Hemasilpin; Ki Hyeong Lee; Katherine Holland-Bouley; Todd M. Arthur; Diego Morita; Sejal V. Jain; Francesco T. Mangano; Ton J. deGrauw; Douglas F. Rose

PURPOSE Magnetoencephalography (MEG) has been shown a useful diagnostic tool for presurgical evaluation of pediatric medically intractable partial epilepsy as MEG source localization has been shown to improve the likelihood of seizure onset zone (SOZ) sampling during subsequent evaluation with intracranial EEG (ICEEG). We investigated whether ictal MEG onset source localization further improves results of interictal MEG in defining the SOZ. METHODS We identified 20 pediatric patients with one habitual seizure during MEG recordings between October 2007 and April 2011. MEG was recorded with sampling rates of 600Hz and 4000Hz for 10 and 2min respectively. Continuous head localization (CHL) was applied. Source localization analyses were applied using multiple algorithms, both at the beginning of ictal onset and for interictal MEG discharges. Ictal MEG onsets were identified by visual inspection and power spectrum using short-time Fourier transform (STFT). Source localizations were compared with ICEEG, surgical procedure and outcome. KEY FINDINGS Eight patients met all inclusion criteria. Five of the 8 patients (63%) had concordant ictal MEG onset source localization and interictal MEG discharge source localizations in the same lobe, but the source of ictal MEG onset was closer to the SOZ defined by ICEEG. SIGNIFICANCE Although the capture of seizures during MEG recording is challenging, the source localization for ictal MEG onset proved to be a useful tool for presurgical evaluation in our pediatric population with medically intractable epilepsy.


Neurology | 2016

Long-term treatment of epilepsy with everolimus in tuberous sclerosis

Darcy A. Krueger; Angus A. Wilfong; Maxwell Mays; Christina M. Talley; Karen Agricola; Cindy Tudor; Jamie K. Capal; Katherine Holland-Bouley; David Neal Franz

Objective: To evaluate the long-term benefit and safety of everolimus for the treatment of medically refractory epilepsy in patients with tuberous sclerosis complex (TSC). Methods: Everolimus was titrated over 4 weeks and continued an additional 8 weeks in a prospective, open-label, phase I/II clinical trial design. Participants demonstrating initial benefit continued treatment until study completion (48 months). The primary endpoint was percentage of patients with a ≥50% reduction in seizure frequency compared to baseline. Secondary endpoints assessed absolute seizure frequency, adverse events (AEs), behavior, and quality of life. Results: Of the 20 participants who completed the initial study phase, 18 continued extended treatment. Fourteen of 18 (78%) participants completed the study, all but 1 of whom reported ≥50% reduction in seizure frequency at 48 months. All participants reported at least 1 AE, the vast majority (94%) of which were graded mild or moderate severity. Improvements in behavior and quality of life were also observed, but failed to achieve statistical significance at 48 months. Conclusions: Improved seizure control was maintained for 4 years in the majority of patients with TSC with medically refractory epilepsy treated with everolimus. Long-term treatment with everolimus is safe and well-tolerated in this population. Everolimus may be a therapeutic option for refractory epilepsy in TSC. Classification of evidence: This study provides Class IV evidence that for patients with TSC with medically refractory epilepsy everolimus improves seizure control.


Frontiers in Neurology | 2013

Focal Peak Activities in Spread of Interictal-Ictal Discharges in Epilepsy with Beamformer MEG: Evidence for an Epileptic Network?

Douglas F. Rose; Hisako Fujiwara; Katherine Holland-Bouley; Hansel M. Greiner; Todd M. Arthur; Francesco T. Mangano

Non-invasive studies to predict regions of seizure onset are important for planning intracranial grid locations for invasive cortical recordings prior to resective surgery for patients with medically intractable epilepsy. The neurosurgeon needs to know both the seizure onset zone (SOZ) and the region of immediate cortical spread to determine the epileptogenic zone to be resected. The immediate zone of spread may be immediately adjacent, on a nearby gyrus, in a different lobe, and sometimes even in the contralateral cerebral hemisphere. We reviewed consecutive simultaneous EEG/MEG recordings on 162 children with medically intractable epilepsy. We analyzed the MEG signals in the bandwidth 20–70 Hz with a beamformer algorithm, synthetic aperture magnetometry, at a 2.5 mm voxel spacing throughout the brain (virtual sensor locations, VSLs) with the kurtosis statistic (g2) to determine presence of excess kurtosis (γ2) consistent with intermittent increased high frequency spikiness of the background. The MEG time series was reconstructed (virtual sensor signals) at each of these VSLs. The VS signals were further examined with a relative peak amplitude spike detection algorithm. The time of VS spike detection was compared to the simultaneous EEG and MEG sensor signals for presence of conventional epileptiform spike morphology in the latter signals. The time of VS spike detection was compared across VSLs to determine earliest and last VSL to show a VS spike. Seven subjects showed delay in activation across VS locations detectable on visual examination. We compared the VS locations that showed earliest and later VS spikes with the locations on intracranial grid locations by electrocorticography (ECoG) that showed spikes and both onset and spread of seizures. We compared completeness of resection of VS locations to postoperative outcome. The VS locations for spike onset and spread were similar to locations for ictal onset and spread by ECoG.


Acta Neurologica Scandinavica | 2013

Selecting anti-epileptic drugs: a pediatric epileptologist's view, a computer's view

John Pestian; Pawel Matykiewicz; Katherine Holland-Bouley; Shannon M. Standridge; M. Spencer; Tracy A. Glauser

To identify which clinical characteristics are important to include in clinical decision support systems developed for Antiepileptic Drug (AEDs) selection.


Biomedical Informatics Insights | 2016

Methodological Issues in Predicting Pediatric Epilepsy Surgery Candidates Through Natural Language Processing and Machine Learning

Kevin Bretonnel Cohen; Benjamin Glass; Hansel M. Greiner; Katherine Holland-Bouley; Shannon Standridge; Ravindra Arya; Robert Faist; Diego Morita; Francesco T. Mangano; Brian Connolly; Tracy A. Glauser; John Pestian

Objective: We describe the development and evaluation of a system that uses machine learning and natural language processing techniques to identify potential candidates for surgical intervention for drug-resistant pediatric epilepsy. The data are comprised of free-text clinical notes extracted from the electronic health record (EHR). Both known clinical outcomes from the EHR and manual chart annotations provide gold standards for the patients status. The following hypotheses are then tested: 1) machine learning methods can identify epilepsy surgery candidates as well as physicians do and 2) machine learning methods can identify candidates earlier than physicians do. These hypotheses are tested by systematically evaluating the effects of the data source, amount of training data, class balance, classification algorithm, and feature set on classifier performance. The results support both hypotheses, with F-measures ranging from 0.71 to 0.82. The feature set, classification algorithm, amount of training data, class balance, and gold standard all significantly affected classification performance. It was further observed that classification performance was better than the highest agreement between two annotators, even at one year before documented surgery referral. The results demonstrate that such machine learning methods can contribute to predicting pediatric epilepsy surgery candidates and reducing lag time to surgery referral.


Epilepsy Research | 2016

Resection of ictal high frequency oscillations is associated with favorable surgical outcome in pediatric drug resistant epilepsy secondary to tuberous sclerosis complex

Hisako Fujiwara; James L. Leach; Hansel M. Greiner; Katherine Holland-Bouley; Douglas F. Rose; Todd M. Arthur; Francesco T. Mangano

Resective epilepsy surgery can improve seizures when the epileptogenic zone (EZ) is limited to a well-defined region. High frequency oscillations (HFO) have been recognized as having a high association with the seizure onset zone. Therefore, we retrospectively identified ictal HFOs and determined their relationship to specific intracranial features of cortical tubers in children with TSC who underwent resective surgery. We identified 14 patients with drug resistant epilepsy secondary to TSC who underwent subdural grid and strip implantation for presurgical evaluation and subsequent resection with adequate post-surgical follow-up. We aimed to determine the relationship between ictal HFOs, post-resection outcome and neuroimaging features in this population. The largest tuber was identified in all 14 patients (100%). Four patients (29%) had unusual tubers. HFOs were observed at ictal onset in all 14 patients. Seven of 10 patients with complete resection of HFOs were seizure free. The better seizure outcome (ILAE=1-3) was achieved with complete HFO resection regardless of the unique TSC structural features (p=0.0140). Our study demonstrates the presence of ripple and fast ripple range HFOs at ictal onset in children with TSC. Our study showed that complete HFO resection led to the better surgical outcome, independent of MR imaging findings.


international conference on complex medical engineering | 2012

Patient-specific spectrum power determination for source localization of ictal MEG

Hisako Fujiwara; Hansel M. Greiner; Nat Hemasilpin; Katherine Holland-Bouley; Todd M. Arthur; Diego Morita; Sejal V. Jain; Francesco T. Mangano; Douglas F. Rose

Magnetoencephalography (MEG) has been shown to be a useful diagnostic tool for presurgical evaluation of pediatric medically intractable partial epilepsy. MEG source localization has been shown to improve the likelihood of seizure onset zone (SOZ) sampling during subsequent evaluation with intracranial EEG (ICEEG). We investigated whether frequency-dependent ictal MEG onset source localization further improves results of interictal MEG in defining the SOZ. Source localization analyses were applied using multiple algorithms, both at the beginning of ictal onset and for interictal MEG discharges. Ictal MEG onsets were identified by visual inspection and power spectrum using short-time Fourier transform (STFT). Source localizations were compared with ICEEG, surgical procedure and outcome. Eight patients were included in this study. Five of the 8 patients (63%) had concordant ictal MEG onset source localization and interictal MEG discharge source localizations in the same lobe, but the source of ictal MEG onset was closer to the SOZ defined by ICEEG. The source localization for the earliest ictal MEG onset with patient-specific frequency change proved to be a useful tool for presurgical evaluation in our pediatric population with medically intractable epilepsy.

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Francesco T. Mangano

Cincinnati Children's Hospital Medical Center

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Hansel M. Greiner

Cincinnati Children's Hospital Medical Center

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Douglas F. Rose

Cincinnati Children's Hospital Medical Center

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Hisako Fujiwara

Cincinnati Children's Hospital Medical Center

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Todd M. Arthur

Cincinnati Children's Hospital Medical Center

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Darcy A. Krueger

Cincinnati Children's Hospital Medical Center

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David Neal Franz

Cincinnati Children's Hospital Medical Center

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Karen Agricola

Cincinnati Children's Hospital Medical Center

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Cindy Tudor

Cincinnati Children's Hospital Medical Center

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Diego Morita

Cincinnati Children's Hospital Medical Center

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