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Dive into the research topics where Chima O. Oluigbo is active.

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Featured researches published by Chima O. Oluigbo.


Journal of Neurosurgery | 2010

Prevalence of cervical spine injury in infants with head trauma.

Joel S. Katz; Chima O. Oluigbo; C. Corbett Wilkinson; Sean A. McNatt; Michael H. Handler

OBJECTnThe incidence, type, and severity of pediatric cervical spine injuries (CSIs) are related to age and mechanism of injury. In this study, the authors assessed the prevalence of CSIs in infants with head trauma treated in their institution.nnnMETHODSnThe authors reviewed the medical records of children younger than 1 year of age who presented to The Childrens Hospital with head injuries between January 1993 and December 2007. They excluded infants with head injuries resulting from motor vehicle accidents and known falls from heights greater than 10 ft. For each patient, collected data included age, cause of injury, diagnosis, discharge disposition, and outcome. Relevant imaging data were reviewed, and when appropriate, autopsy reports were also reviewed.nnnRESULTSnNine hundred five infants with head trauma and without a major mechanism/cause were identified. Their mean age was 4.3 months. Of the 905 patients, only 2 cases of CSI were detected, giving a prevalence of 0.2%. The mechanism of injury in these 2 patients was nonaccidental trauma (NAT).nnnCONCLUSIONSnThe study revealed a very low prevalence of CSIs in infants with head trauma (0.2%). Routine cervical spine imaging in these infants, therefore, appears to have low diagnostic yield. The mechanism of head injury was NAT in the 2 patients who sustained an associated CSI. This supports the need for more stringent cervical spine imaging criteria for the infant with suspected NAT.


Journal of Neurosurgery | 2012

Comparison of outcomes following decompressive craniectomy in children with accidental and nonaccidental blunt cranial trauma

Chima O. Oluigbo; C. Corbett Wilkinson; Nicholas V. Stence; Laura Z. Fenton; Sean A. McNatt; Michael H. Handler

OBJECTnThe goal of this study was to compare clinical outcomes following decompressive craniectomy performed for intracranial hypertension in children with nonaccidental, blunt cranial trauma with outcomes of decompressive craniectomy in children injured by other mechanisms.nnnMETHODSnAll children in a prospectively acquired database of trauma admissions who underwent decompressive craniectomy over a 9-year span, beginning January 1, 2000, are the basis for this study. Clinical records and neuroimaging studies were systematically reviewed.nnnRESULTSnThirty-seven children met the inclusion criteria. Nonaccidental head trauma was the most common mechanism of injury (38%). The mortality rate in patients with abusive brain injury (35.7%) was significantly higher (p < 0.05) than in patients with other causes of traumatic brain injury (4.3%). Children with inflicted head injuries had a 12-fold increase in the odds of death and 3-fold increase in the odds of a poor outcome (Kings Outcome Scale for Closed Head Injury score of 1, 2, or 3).nnnCONCLUSIONSnChildren with nonaccidental blunt cranial trauma have significantly higher mortality following decompressive craniectomy than do children with other mechanisms of injury. This understanding can be interpreted to mean either that the threshold for decompression should be lower in children with nonaccidental closed head injury or that decompression is unlikely to alter the path to a fatal outcome. If decompressive craniectomy is to be effective in reducing mortality in the setting of nonaccidental blunt cranial trauma, it should be done quite early.


Neuromodulation | 2016

Spinal Cord Stimulation (SCS) and Functional Magnetic Resonance Imaging (fMRI): Modulation of Cortical Connectivity With Therapeutic SCS

Milind Deogaonkar; Mayur Sharma; Chima O. Oluigbo; Dylan M. Nielson; Xiangyu Yang; Louis Vera-Portocarrero; Gregory F. Molnar; Amir M. Abduljalil; Per B. Sederberg; Michael V. Knopp; Ali R. Rezai

The neurophysiological basis of pain relief due to spinal cord stimulation (SCS) and the related cortical processing of sensory information are not completely understood. The aim of this study was to use resting state functional magnetic resonance imaging (rs‐fMRI) to detect changes in cortical networks and cortical processing related to the stimulator‐induced pain relief.


Journal of Neurosurgery | 2010

The role of lumboperitoneal shunts in the treatment of syringomyelia.

Chima O. Oluigbo; Karen Thacker; Graham Flint

OBJECT The role of thecoperitoneal shunts in the management of syringomyelia is not well defined. In this study, the authors analyze the outcome of lumboperitoneal shunt procedures carried out to treat syringomyelia in their institution. METHODS The authors retrospectively reviewed the medical records of 19 patients who underwent lumboperitoneal shunt procedures for syringomyelia. RESULTS The mean follow-up duration was 25 months (range 3-51 months). Of 16 cases followed up, only 5 patients reported clinical improvement in their preoperative symptoms, but of these, 2 had clear radiological evidence of improvement. Three of 6 patients with syringomyelia due to spinal arachnoiditis improved. CONCLUSIONS Lumboperitoneal shunts may lead to useful improvement in the symptoms of a patient with syringomyelia while avoiding the risk of neurological deterioration inherent in myelotomies required for syrinx shunting procedures.


Childs Nervous System | 2016

Resective surgery for focal cortical dysplasia in children: a comparative analysis of the utility of intraoperative magnetic resonance imaging (iMRI).

Matthew F. Sacino; Cheng-Ying Ho; Matthew T. Whitehead; Tesfaye Zelleke; Suresh N. Magge; John S. Myseros; Robert F. Keating; William D. Gaillard; Chima O. Oluigbo

PurposeSeizure freedom following resection of focal cortical dysplasia (FCD) correlates with complete resection of the dysplastic cortical tissue. However, difficulty with intraoperative identification of the lesion may limit the ability to achieve the surgical objective of complete extirpation of these lesions. Intraoperative magnetic resonance imaging (iMRI) may aid in FCD resections. The objective of this study is to compare rates of postoperative seizure freedom, completeness of resection, and need for reoperation in patients undergoing iMRI-assisted FCD resection versus conventional surgical techniques.MethodsWe retrospectively reviewed the medical records of pediatric subjects who underwent surgical resection of FCD at Children’s National Medical Center between March 2005 and April 2015.ResultsAt the time of the last postoperative follow-up, 11 of the 12 patients (92xa0%) in the iMRI resection group were seizure free (Engel Class I), compared to 14 of the 42 patients (33xa0%) in the control resection group (pxa0=xa00.0005). All 12 of the iMRI patients (100xa0%) achieved complete resection, compared to 24 of 42 patients (57xa0%) in the control group (pxa0=xa00.01). One (8xa0%) patient from the iMRI-assisted resection group has required reoperation, compared to 17 (40xa0%) patients in the control resection group.ConclusionOur results suggest that the utilization of iMRI during surgery for resection of FCD results in improved postoperative seizure freedom, completeness of lesion resection, and reduction in the need for reoperation.


Neurosurgery | 2006

Primary malignant melanoma of the cerebellopontine angle: a diagnostic dilemma: case report.

Chima O. Oluigbo; Cooke; Peter A. Flynn; Kishor A. Choudhari

OBJECTIVETo present a rare case of a primary malignant melanoma of the central nervous system presenting as a cerebellopontine angle (CPA) tumor and to delineate aspects of the clinical presentation and magnetic resonance imaging scan characteristics that may suggest this unusual condition. CLINICAL PRESENTATIONThe clinical presentation consisted of a short duration of right-sided sensorineural hearing loss, facial weakness, and ataxia in a previously healthy man. Brain magnetic resonance imaging scans showed a right-sided CPA tumor exhibiting shortening of T1 and T2 relaxation times, but overall neuroradiological features were not consistent with any commonly occurring CPA tumors. INTERVENTIONGross total excision of the lesion was accomplished via a right suboccipital craniectomy. Histological examination revealed a malignant melanoma. A detailed search excluded extracranial primary melanoma. CONCLUSIONCorrelation of clinical and imaging findings offer the most important clues in the diagnosis of such unusual primary malignant tumors of the CPA. A history of rapid onset of audiovestibular symptoms, presence of facial palsy, and shortening of T1 and T2 relaxation times on magnetic resonance imaging scans should arouse the clinicians suspicions.


Neuron | 2017

Loss of CLOCK Results in Dysfunction of Brain Circuits Underlying Focal Epilepsy.

Peijun Li; Xiaoqin Fu; Nathan A. Smith; Julie Ziobro; Julian Curiel; Milagros J. Tenga; Brandon S. Martin; Samuel Freedman; Christian A. Cea-Del Rio; Livio Oboti; Tammy N. Tsuchida; Chima O. Oluigbo; Amanda L. Yaun; Suresh N. Magge; Brent O’Neill; Amy Kao; Tesfaye Zelleke; Dewi Depositario-Cabacar; Svetlana Ghimbovschi; Susan Knoblach; Chen-Ying Ho; Joshua G. Corbin; Howard P. Goodkin; Stefano Vicini; Molly M. Huntsman; William D. Gaillard; Gregorio Valdez; Judy S. Liu

Because molecular mechanisms underlying refractory focal epilepsy are poorly defined, we performed transcriptome analysis on human epileptogenic tissue. Compared with controls, expression of Circadianxa0Locomotor Output Cycles Kaput (CLOCK) is decreased in epileptogenic tissue. To define the function of CLOCK, we generated and tested thexa0Emx-Cre; Clockflox/flox and PV-Cre; Clockflox/flox mouse lines with targeted deletions of the Clock gene in excitatory and parvalbumin (PV)-expressing inhibitory neurons, respectively. The Emx-Cre; Clockflox/flox mouse line alone has decreased seizure thresholds, but no laminar or dendritic defects in the cortex. However, excitatory neurons from the Emx-Cre; Clockflox/flox mouse have spontaneous epileptiform discharges. Both neurons from Emx-Cre; Clockflox/flox mouse and human epileptogenic tissue exhibit decreased spontaneous inhibitory postsynaptic currents. Finally, video-EEG of Emx-Cre; Clockflox/flox mice reveals epileptiform discharges during sleep and also seizures arising from sleep. Altogether, these data show that disruption of CLOCK alters cortical circuits and may lead to generation of focal epilepsy.


Epilepsia | 2017

Temporal lobe epilepsy and focal cortical dysplasia in children: A tip to find the abnormality

Luca Bartolini; Matthew T. Whitehead; Cheng-Ying Ho; Leigh N. Sepeta; Chima O. Oluigbo; Kathryn Havens; Emily R. Freilich; John M. Schreiber; William D. Gaillard

To demonstrate an association between magnetic resonance imaging (MRI) findings and pathologic characteristics in children who had surgery for medically refractory epilepsy due to focal cortical dysplasia (FCD).


Journal of Clinical Neuroscience | 2015

Successful subthalamic nucleus deep brain stimulation therapy after significant lead displacement from a subdural hematoma

Esmiralda Yeremeyeva Henderson; Timothy Goble; Pierre-François D’Haese; Srivatsan Pallavaram; Chima O. Oluigbo; Punit Agrawal; Milind Deogaonkar; Ali R. Rezai

A 57-year-old man with a 21 year history of Parkinsons disease underwent bilateral subthalamic nucleus deep brain stimulation (DBS) placement. One week postoperatively he developed an acute left subdural hematoma from a fall with significant displacement of the DBS leads. It was promptly evacuated, the patient slowly recovered neurologically, and the leads again moved near to the original position. Six months of stimulation therapy attained 50% reduction in symptoms. This case report demonstrates the movement of DBS leads due to brain shift and their ability to come back to previous location once the brain shift is corrected.


Childs Nervous System | 2017

Considerations in deep brain stimulation (DBS) for pediatric secondary dystonia

Deki Tsering; Laura Tochen; Bennett Lavenstein; Srijaya K. Reddy; Yael Granader; Robert F. Keating; Chima O. Oluigbo

PurposeThere is a paucity of effective long-term medication treatment for secondary dystonias. In situations where significantly impairing secondary dystonias fail to respond to typical enteral medications and intrathecal (or even intraventricular) baclofen, consideration should be given to the use of deep brain stimulation (DBS). While Level I evidence and long-term follow-up clearly demonstrate the efficacy of DBS for primary dystonia, the evidence for secondary dystonia remains mixed and unclear. In this study, we report our experience with pediatric subjects who have undergone DBS for secondary dystonia.MethodsWe discuss the indications and outcomes of DBS procedures completed at our center. We also present a detailed discussion of the considerations in the management of these patients as well as a literature review.ResultsOf the four cases retrospectively examined here, all subjects experienced reductions in the severity of their dystonia (ranging from 0 to 100% on both the Barry-Albright Dystonia (BAD) and Burke-Fahn-Marsden Dystonia Rating Scale-Motor (BFMDRS-M) scales).ConclusionsPallidal DBS should be considered among children with functionally debilitating, medication-resistant secondary dystonia. Patients without fixed skeletal deformities who have experienced a short duration of symptoms are most likely to benefit from this intervention.

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Robert F. Keating

Children's National Medical Center

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William D. Gaillard

George Washington University

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Judy S. Liu

Children's National Medical Center

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Matthew F. Sacino

Children's National Medical Center

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Suresh N. Magge

Children's National Medical Center

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Albert K. Oh

George Washington University

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Bennett Lavenstein

Children's National Medical Center

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C. Corbett Wilkinson

University of Colorado Denver

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