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Dive into the research topics where Hiroshi Otsubo is active.

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Featured researches published by Hiroshi Otsubo.


Annals of Neurology | 1999

Magnetoencephalographic localization in pediatric epilepsy surgery: Comparison with invasive intracranial electroencephalography

Berge A. Minassian; Hiroshi Otsubo; Shelly K. Weiss; Irene Elliott; James T. Rutka; O. Carter Snead

The object of this study was to determine the concordance of the anatomical location of interictal magnetoencephalographic (MEG) spike foci with the location of ictal onset zones identified by invasive ictal intracranial electroencephalographic recordings in children undergoing evaluation for epilepsy surgery. MEG was performed in 11 children with intractable, nonlesional, extratemporal, localization‐related epilepsy. Subsequently, chronic invasive intracranial electroencephalographic monitoring was performed by using subdural electrodes to localize the ictal onset zone and eloquent cortex. Based on the invasive monitoring data, all children had excision of, or multiple subpial transections through, ictal onset cortex and surrounding irritative zones. In 10 of 11 patients, the anatomical location of the epileptiform discharges as determined by MEG corresponded to the ictal onset zone established by ictal intracranial recordings. In all children, the anatomical location of the somatosensory hand area, determined by functional mapping through the subdural electrode array, was the same as that delineated by MEG. Nine of 11 patients became either seizure‐free or had a greater than 90% reduction in seizures after surgery, with a mean follow‐up of 24 months. MEG is a powerful and accurate tool in the presurgical evaluation of children with refractory nonlesional extratemporal epilepsy.


Epilepsia | 2007

Dynamic Changes of Ictal High‐Frequency Oscillations in Neocortical Epilepsy: Using Multiple Band Frequency Analysis

Ayako Ochi; Hiroshi Otsubo; Elizabeth J. Donner; Irene Elliott; Ryoichi Iwata; Takanori Funaki; Yoko Akizuki; Tomoyuki Akiyama; Katsumi Imai; James T. Rutka; O. Carter Snead

Summary:  Purpose: To characterize the spatial and temporal course of ictal high‐frequency oscillations (HFOs) recorded by subdural EEG in children with intractable neocortical epilepsy.


Epilepsia | 2002

MEG predicts epileptic zone in lesional extrahippocampal epilepsy: 12 pediatric surgery cases.

Hiroshi Otsubo; Ayako Ochi; Irene Elliott; Sylvester H. Chuang; James T. Rutka; Venita Jay; Maung Aung; David F. Sobel; O. Carter Snead

Summary:  Purpose: To discover whether the spatial distribution of spike sources determined by magnetoencephalography (MEG) provides reliable information for planning surgery and predicting outcomes in pediatric patients with lesional extrahippocampal epilepsy.


Epilepsia | 2011

Focal resection of fast ripples on extraoperative intracranial EEG improves seizure outcome in pediatric epilepsy

Tomoyuki Akiyama; Bláthnaid McCoy; Cristina Go; Ayako Ochi; Irene Elliott; Mari Akiyama; Elizabeth J. Donner; Shelly K. Weiss; O. Carter Snead; James T. Rutka; James M. Drake; Hiroshi Otsubo

Purpose:  High‐frequency oscillations (HFOs), termed ripples at 80–200 Hz and fast ripples (FRs) at >200/250 Hz, recorded by intracranial electroencephalography (EEG), may be a valuable surrogate marker for the localization of the epileptogenic zone. We evaluated the relationship of the resection of focal brain regions containing high‐rate interictal HFOs and the seizure‐onset zone (SOZ) determined by visual EEG analysis with the postsurgical seizure outcome, using extraoperative intracranial EEG monitoring in pediatric patients and automated HFO detection.


Epilepsia | 2007

MEG Predicts Outcome Following Surgery for Intractable Epilepsy in Children with Normal or Nonfocal MRI Findings

Rajesh RamachandranNair; Hiroshi Otsubo; Manohar Shroff; Ayako Ochi; Shelly K. Weiss; James T. Rutka; O. Carter Snead

Summary:  Purpose: To identify the predictors of postsurgical seizure freedom in children with refractory epilepsy and normal or nonfocal MRI findings.


Neurology | 2004

Dysembryoplastic neuroepithelial tumors in childhood Long-term outcome and prognostic features

M. A. Nolan; R. Sakuta; N. Chuang; Hiroshi Otsubo; James T. Rutka; O. C. Snead; Cynthia Hawkins; Shelly K. Weiss

Background: Dysembryoplastic neuroepithelial tumors (DNTs) are associated with medically intractable epilepsy and a favorable prognosis after surgical resection. The authors describe the clinical, radiologic, and pathologic characteristics and outcomes in children after surgical resection of pathologically confirmed DNT to ascertain prognostic features for seizure recurrence following surgery. Methods: Neurology, neurosurgery, and pathology databases from 1993 to 2002 at the Hospital for Sick Children were searched to retrospectively identify children with confirmed DNT and presentation with seizures. Risk factors for postoperative seizure recurrence were examined with respect to seizure outcome at 12 months and long-term follow-up. Results: Of the 26 children identified (mean age at surgery 10.0 years) seizure outcome was good in 22 children (85%) at 12 months (Class 1). At longer follow-up (mean 4.3, range 1.0 to 11.0 years) only 16 (62%) remained seizure-free. Residual DNT was evident in 15 of the 24 children with available postoperative MRI. Three children demonstrated recurrence of tumor. At 12 months follow-up, older age (>10 years) and longer duration of epilepsy (>2 years) were associated with seizure recurrence. The presence of residual tumor was a risk factor for seizure recurrence at long-term follow-up (p = 0.02). Conclusions: Children with DNT and epilepsy may benefit from surgical management; however, seizure outcome is not always favorable. Although the majority of children remain seizure free after surgical excision of DNT, a considerable number have recurrent seizures. Short-term outcome is influenced by older age at surgery and longer duration of epilepsy. Residual tumor is a significant risk factor for poor seizure outcome. Recurrent tumor can occur.


Pediatric Neurosurgery | 1997

Combined utility of functional MRI, cortical mapping, and frameless stereotaxy in the resection of lesions in eloquent areas of brain in children.

Simon R. Stapleton; Elaine Kiriakopoulos; David J. Mikulis; James M. Drake; Harold J. Hoffman; Robin P. Humphreys; Paul A. Hwang; Hiroshi Otsubo; Stephanie Holowka; William J. Logan; James T. Rutka

We studied 16 children with lesions in the eloquent brain to determine if the amalgamation of information from functional magnetic resonance imaging (fMRI), frameless stereotaxy, and direct cortical mapping and recording could facilitate the excision of these lesions while minimizing potential neurological deficits. The mean age of the children was 10 years. Fourteen children presented with seizures. All lesions were located in or near eloquent cerebral cortex. fMRI was successful in all patients in delineating the relationship between the lesion and regions of task-activated cortex. The ISG wand was utilized in all cases for scalp and bone flap placement, and for intraoperative localization of the lesion. Direct cortical stimulation or recording of phase reversals with somatosensory evoked potentials helped delineate the central sulcus and language cortex in patients with lesions near the motor or language cortex. Intraoperative electrocorticography (ECoG) was utilized in all patients who presented with seizures to guide the extent of resection of the epileptiform cortex. Ten children had benign cerebral neoplasms, nine of which were totally resected. The other diagnoses included vascular malformations, Sturge-Weber, tuberous sclerosis, Rasmussens encephalitis, and primitive neuroectodermal tumor. Only 1 patient with a left Rolandic AVM developed a new neurological deficit postoperatively. Thirteen of fourteen patients who presented with seizure disorders were rendered either seizure free or improved in terms of seizure control postoperatively. Follow-up has ranged from 12 to 18 months, with a mean follow-up of 15 months. We conclude that the techniques of fMRI, frameless stereotaxy, direct cortical stimulation and recording can be utilized in sequence to accurately localize intracerebral lesions in eloquent brain, and to reduce the morbidity of resecting these lesions in children.


Epilepsia | 2002

Epileptic Spikes: Magnetoencephalography versus Simultaneous Electrocorticography

Makoto Oishi; Hiroshi Otsubo; Shigeki Kameyama; Nobuhito Morota; Hiroshi Masuda; Masaomi Kitayama; Ryuichi Tanaka

Summary:  Purpose: To test the sensitivity of extracranial magnetoencephalography (MEG) for epileptic spikes in different cerebral sites.


Epilepsia | 2006

Single and Multiple Clusters of Magnetoencephalographic Dipoles in Neocortical Epilepsy: Significance in Characterizing the Epileptogenic Zone

Makoto Oishi; Shigeki Kameyama; Hiroshi Masuda; Jun Tohyama; Osamu Kanazawa; Mutsuo Sasagawa; Hiroshi Otsubo

Summary:  Purpose: To characterize the epileptogenic zone in neocortical epilepsy (NE) by using magnetoencephalography (MEG).


Neurosurgery | 2006

Temporal lobe surgery for intractable epilepsy in children: an analysis of outcomes in 126 children.

Mony Benifla; Hiroshi Otsubo; Ayako Ochi; Shelly K. Weiss; Elizabeth J. Donner; Manohar Shroff; Sylvester H. Chuang; Cynthia Hawkins; James M. Drake; Irene Elliott; Mary Lou Smith; Snead Oc rd; James T. Rutka

OBJECTIVETemporal lobectomy is a well-established neurosurgical procedure for temporal lobe epilepsy. In this study, we conducted a retrospective review of children with drug-resistant temporal lobe epilepsy to evaluate seizure outcome after temporal lobe surgery. METHODSWe reviewed the medical records of 126 children who had surgery for temporal lobe epilepsy at The Hospital for Sick Children between 1983 and 2003. The records were examined for preoperative and intraoperative factors that could predict patient outcome after surgery. RESULTSThe mean age at seizure onset was 5.9 years. The mean seizure duration before surgery was 5.6 years. All patients had preoperative computed tomographic scans, magnetic resonance imaging scans, or both. The mean age at the time of surgery was 13.5 years. Sixty-two patients underwent left temporal resections and 64 patients underwent right temporal resections. The histopathology of the temporal resections revealed low-grade brain tumors in 65 children (52%) and cavernous malformations in four children. Ganglioglioma and astrocytoma were the most common tumors encountered. Mesial temporal sclerosis was found in 16 patients (13%), astrogliosis in 15 patients (12%), and cortical dysplasia in eight patients (7%). Postoperative follow-up of at least 2 years was available for 106 patients and ranged up to 13.0 years. Seventy-four percent of patients had an Engel Class I or II outcome. Patients with temporal lobe lesions had better outcomes compared with those without lesions (P < 0.05). Patients without a history of secondary generalization of seizures also had a better outcome when compared with those with secondary generalization. Complications in the form of contralateral homonymous hemianopsia, dysphasia, and infection were found in 5% of patients. Twelve patients had a second temporal lobe procedure for intractable recurrent seizures. After a second procedure, seven patients returned to a seizure-free state. CONCLUSIONTemporal lobe resections for epilepsy in children are effective and safe procedures, with a favorable impact on seizure control. Repeat temporal resections for recurrent seizures may also be effective in restoring a seizure-free outcome to children.

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