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1.
J Neurooncol ; 136(2): 413-419, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29273890

ABSTRACT

We aimed to assess the efficacy of stereotactic irradiation for patients with recurrent high-grade glioma (HGG) and identify predictive factors of progression-free survival (PFS) and overall survival (OS) following reirradiation. We identified 32 patients with recurrent brain HGG who had been treated with either single-dose (stereotactic radiosurgery) or fractionated stereotactic radiotherapy between April 2008 and October 2015. Median follow up was 21.4 months (range 12.9-23.2) and median PFS was and 3.3 months (95% CI [2.3-4.7]), respectively. OS was 90.40% (95% CI [73.09-96.80]) at 6 months and 79.55% (95% CI [59.9-90.29]) at 12 months. Univariate analysis showed that biological effective dose at isocenter ≤ 76 Gy was a poor prognostic factor for both OS (83.33 vs. 100% at 6 months, p = 0.032) and median PFS (2.7 vs. 4.7 months, p = 0.025), as was gross tumor volume (GTV) above 1 cm3 for OS (86.15 vs. 94.12% at 6 months, p = 0.043). Contact with the subventricular zone (SVZ) was also a poor prognostic factor for median PFS (2.3 vs. 4.7 months, p = 0.002). Multivariate analysis showed that SVZ contact remained a poor prognostic factor for PFS (hazard ratio = 3.44, 95% CI [1.21-9.82], p = 0.021). Results suggest that reirradiation is a safe and effective treatment option for recurrent HGG in patients with a good Karnosfsky Performance Scale score, a long progression-free interval since first radiation and limited GTV, and that contact to SVZ is a strong prognostic factor for PFS.


Subject(s)
Brain Neoplasms/diagnosis , Brain Neoplasms/radiotherapy , Glioma/diagnosis , Glioma/radiotherapy , Lateral Ventricles/radiation effects , Neoplasm Recurrence, Local/diagnosis , Neoplasm Recurrence, Local/radiotherapy , Re-Irradiation , Adolescent , Adult , Aged , Aged, 80 and over , Dose Fractionation, Radiation , Humans , Kaplan-Meier Estimate , Middle Aged , Neoplasm Grading , Prognosis , Progression-Free Survival , Radiosurgery , Young Adult
2.
Brain Inj ; 26(13-14): 1636-45, 2012.
Article in English | MEDLINE | ID: mdl-22823462

ABSTRACT

OBJECTIVES: In the adult human brain, neurogenesis occurs in the SVZ and the dentate gyrus of the hippocampus, but it is still unclear whether persistent neural progenitor/stem cells are also present in other brain areas. The present work studies the possibility of obtaining neural progenitor/stem cells from the temporal lobe and investigates their potential to differentiate into neuronal cells. METHODS: Human biopsies from the temporal lobe of epileptic patients were used to isolate potential neural progenitors. Differentiation was induced in the presence of different agents (NGF, NT3, RA) and immunocytochemistry was then performed for quantitative analysis. RESULTS: It was shown that a significant number of cells in the temporal lobe are also capable of expansion and multi-potency. These cells can be amplified as neurospheres and have the potential to differentiate naturally in vitro into neurons, astrocytes and oligodendrocytes. Quantitative analyses show that the progenitor cells of the temporal lobe exhibit a better rate of neuronal differentiation in vitro than the cells from the SVZ, particularly in the presence of NGF. CONCLUSION: This study indicates that neural progenitors are also present in the human temporal lobe. Studying them could be of great interest for cell therapy in neurological disorders.


Subject(s)
Cell Differentiation , Epilepsy, Temporal Lobe/metabolism , Neurodegenerative Diseases/metabolism , Stem Cells/metabolism , Stroke/metabolism , Temporal Lobe/pathology , Adult , Cell Adhesion , Epilepsy, Temporal Lobe/physiopathology , Female , Humans , Immunohistochemistry , Male , Middle Aged , Neurodegenerative Diseases/physiopathology , Stroke/physiopathology
3.
Explore (NY) ; 17(3): 197-202, 2021.
Article in English | MEDLINE | ID: mdl-33262082

ABSTRACT

Meditation has been deemed a miracle cure for a wide range of neurological disorders. However, it is unclear whether meditation practice would be beneficial for patients suffering from epilepsy. Here we report on the comparison of the effects of focused-attention meditation and a control task on electroencephalographic (EEG) activity in a patient undergoing stereoencephalographic (SEEG) investigation for drug-resistant epilepsy. The patient routinely practiced focused-attention meditation and reported that she found it beneficial. During the SEEG investigation, intracerebral EEG data were recorded during meditation as well as during mind-wandering task. The EEG data were analyzed for type of electrical activity (labeled) by two expert epileptologists. We found that the proportion of EEG segments containing activity classified as interictal epileptiform discharges (IEDs; abnormal electrical activity that occurs between seizures) increased significantly during meditation practice. Although the finding was surprising, this increase in IEDs may not correlate with an increase in seizure frequency, and the patient might still benefit from practicing meditation. The finding does, however, warrant further studies on the influence of meditation on epileptic activity.


Subject(s)
Epilepsy, Temporal Lobe , Epilepsy , Meditation , Electroencephalography , Epilepsy, Temporal Lobe/therapy , Female , Humans , Seizures/therapy
4.
Cancer Radiother ; 23(2): 147-150, 2019 Apr.
Article in French | MEDLINE | ID: mdl-30904418

ABSTRACT

Whereas immune checkpoint inhibitors of serine/threonine protein kinase B-raf therapy dramatically changed metastatic outcomes of patients with melanoma, they remain at high risk of brain extension. Additional local treatment can be offered in this situation such as surgery and or stereotactic radiotherapy. In this review article, we describe the different options with published data and their optimal timing.


Subject(s)
Brain Neoplasms/secondary , Brain Neoplasms/therapy , Melanoma/secondary , Melanoma/therapy , Antineoplastic Agents, Immunological/therapeutic use , Brain/pathology , Brain Neoplasms/pathology , CTLA-4 Antigen/antagonists & inhibitors , Dose Fractionation, Radiation , Humans , Melanoma/pathology , Mutation , Necrosis/etiology , Necrosis/prevention & control , Programmed Cell Death 1 Receptor/antagonists & inhibitors , Proto-Oncogene Proteins B-raf/genetics , Radiosurgery , Skin Neoplasms/pathology
5.
Neurochirurgie ; 54(3): 453-65, 2008 May.
Article in French | MEDLINE | ID: mdl-18466930

ABSTRACT

We report here the results of the first survey on epilepsy surgery activity in France. Data from a questionnaire sent to 17 centers practicing epilepsy surgery were analyzed. All centers responded; however, all items were not completely documented. Over 50 years, more than 5000 patients have been operated on for drug-resistant epilepsy and more than 3000 patients underwent some invasive monitoring, most often SEEG. Currently, nearly 400 patients (including more than 100 children) are operated on yearly for epilepsy in France. Over a study period varying among centers (from two to 20 years; mean, 9.5 years), results from more than 2000 patients including one-third children were analyzed. Important differences between adults and children, respectively, were observed in terms of location (temporal: 72% versus 4.3%; frontal: 12% versus 28%; central: 2% versus 11%), etiology (hippocampal sclerosis: 41% versus 2%; tumors 20% versus 61%); and procedures (cortectomy: 50% versus 23%; lesionectomy: 8% versus 59%), although overall results were identical (seizure-free rates following temporal lobe surgery: 80.6% versus 79%; following extratemporal surgery: 65.9% versus 65%). In adults, the best results were observed following temporomesial (TM) resection associated with hippocampal sclerosis or other lesions (class I: 83% and 79%, respectively), temporal neocortical (TNC) lesional (82%), while resections for cryptogenic temporal resections were followed by 69% (TM) and 63% (TNC) class I outcome. Extratemporal lesional resections were associated with 71% class I outcome and cryptogenic 43%. In children, the best results were obtained in tumor-associated epilepsy regardless of location (class I: 80%). A surgical complication occurred in 8% after resective surgery - with only 2.5% permanent morbidity - and 4.3% after invasive monitoring (mostly hemorrhagic). Overall results obtained by epilepsy surgery centers were in the higher range of those reported in the literature, along with a low rate of major surgical complications. Growing interest for epilepsy surgery is clearly demonstrated in this survey and supports further development to better satisfy the population's needs, particularly children. Activity should be further evaluated, while existing epilepsy surgery centers as well as healthcare networks should be expanded.


Subject(s)
Epilepsy/surgery , Neurosurgical Procedures/statistics & numerical data , Adult , Brain/pathology , Child , Electroencephalography , Epilepsy/epidemiology , Epilepsy/pathology , France/epidemiology , Health Care Surveys , Humans , Monitoring, Intraoperative , Neurosurgical Procedures/adverse effects , Postoperative Complications/epidemiology , Surveys and Questionnaires , Treatment Outcome
6.
Neurochirurgie ; 64(4): 303-309, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29909974

ABSTRACT

INTRODUCTION: Hirayama disease is a rare cervical myelopathy predominantly affecting young adults and mainly found in Asia. It results in a pure motor distal lesion of the upper limbs with slow progression. Dynamic magnetic resonance imaging (MRI), which allows the diagnosis to be made, shows a typical appearance of anterior compression of the cervical spinal cord associated with enlargement of the posterior epidural spaces due to a dilated venous plexus. Surgery is considered when conservative treatment has failed. However, the type of surgery is not well standardized in this compressive myelopathy. METHODS: We report on three patients with Hirayama disease operated using an original method: cervical decompressive laminectomy and coagulation of the posterior epidural plexus without fixation. The clinical, radiological and surgical data of these three patients were analyzed. Each patient underwent postoperative MR imaging. RESULTS: The mean age at diagnosis was 18.6 years (16-20 years) with a history of progressive symptoms lasting 1 to 4 years before treatment. Follow-up was 21 to 66 months after surgery. Neurological and electrophysiological improvement was noted in two patients; the third had stabilized. Postoperative MRI confirmed normalization of flexion imaging on MRI. None of the three patients complained of disabling neck pain. CONCLUSION: Posterior cervical decompression with coagulation of epidural venous plexus is a technique that seems effective in Hirayama disease in young subjects. It effectively treats patients by avoiding permanent cervical fixation.


Subject(s)
Cervical Vertebrae/surgery , Laminectomy , Spinal Cord Compression/surgery , Spinal Muscular Atrophies of Childhood/surgery , Adolescent , Decompression, Surgical/methods , Humans , Laminectomy/adverse effects , Magnetic Resonance Imaging/methods , Male , Neck/pathology , Spinal Cord Diseases/surgery , Spinal Muscular Atrophies of Childhood/diagnosis , Treatment Outcome , Young Adult
7.
Acta Neurochir Suppl ; 97(Pt 2): 37-44, 2007.
Article in English | MEDLINE | ID: mdl-17691287

ABSTRACT

Since the initial publication of Tsubokawa in 1991, epidural motor cortex stimulation (MCS) is increasingly reported as an effective surgical option for the treatment of refractory neuropathic pain although its mechanism of action remains poorly understood. The authors review the extensive literature published over the last 15 years on central and neuropathic pain. Optimal patient selection remains difficult and the value of pharmacological tests or transcranial magnetic stimulation in predicting the efficacy of MCS has not been established. Pre-operative functional magnetic resonance imaging (fMRI), 3-dimensional volume MRI, neuronavigation and intra-operative neurophysiological monitoring have contributed to improvements in the technique for identifying the precise location of the targeted motor cortical area and the correct placement of the electrode array. MCS should be considered as the treatment of choice in post-stroke pain, thalamic pain or facial anesthesia dolorosa. In brachial plexus avulsion pain, it is preferable to propose initially dorsal root entry zone (DREZ)-tomy; MCS may be offered after DREZotomy has failed to control the pain. In our experience, the results of MCS on phantom limb pain are promising. In general, the efficacy of MCS depends on: a) the accurate placement of the stimulation electrode over the appropriate area of the motor cortex, and b) on sophisticated programming of the stimulation parameters. A better understanding of the MCS mechanism of action will probably make it possible to adjust better the stimulation parameters. The conclusions of multicentered randomised studies, now in progress, will be very useful and are likely to promote further research and clinical applications in this field.


Subject(s)
Electric Stimulation Therapy , Motor Cortex/physiopathology , Neuralgia/therapy , Electric Stimulation Therapy/adverse effects , Follow-Up Studies , Humans , Magnetic Resonance Imaging/methods , Monitoring, Intraoperative , Motor Cortex/radiation effects , Neuralgia/pathology , Neuralgia/physiopathology , Neuronavigation/methods , Retrospective Studies , Review Literature as Topic
8.
Cell Transplant ; 15(2): 121-33, 2006.
Article in English | MEDLINE | ID: mdl-16719046

ABSTRACT

Implantation of adrenal medullary bovine chromaffin cells (BCC), which synthesize and secrete a combination of pain-reducing neuroactive compounds including catecholamines and opioid peptides, has been proposed for the treatment of intractable cancer pain. Macro- or microencapsulation of such cells within semipermeable membranes is expected to protect the transplant from the host's immune system. In the present study, we report the viability and functionality of BCC encapsulated into microcapsules of alginate-poly-L-lysine (PLL) with a liquefied inner core. The experiment was carried out during 44 days. Empty microcapsules were characterized in terms of morphology, permeability, and mechanical resistance. At the same time, the viability and functionality of both encapsulated and nonencapsulated BCC were evaluated in vitro. We obtained viable BCC with excellent functionality: immunocytochemical analysis revealed robust survival of chromaffin cells 30 days after isolation and microencapsulation. HPLC assay showed that encapsulated BCC released catecholamines basally during the time course study. Taken together, these results demonstrate that viable BCC can be successfully encapsulated into alginate-PLL microcapsules with a liquefied inner core.


Subject(s)
Alginates , Biocompatible Materials , Cell Transplantation/methods , Chromaffin Cells/transplantation , Polylysine/analogs & derivatives , Animals , Blotting, Western , Capsules , Catecholamines/metabolism , Cattle , Cell Survival/physiology , Cells, Cultured , Chromaffin Cells/metabolism , Chromaffin Cells/ultrastructure , Chromatography, High Pressure Liquid , Immunohistochemistry , Implants, Experimental , Microscopy, Confocal , Microscopy, Electron, Scanning , Neoplasms/complications , Pain Management , Permeability , Time Factors
9.
Cell Transplant ; 14(6): 353-65, 2005.
Article in English | MEDLINE | ID: mdl-16180654

ABSTRACT

Chromaffin cells from the adrenal gland secrete a combination of neuroactive compounds including catecholamines, opioid peptides, and growth factors that have strong analgesic effects, especially when administered intrathecally. Preclinical studies of intrathecal implantation with xenogeneic bovine chromaffin cells in rats have provided conflicting data with regard to analgesic effects, and recent concern over risk of prion transmission has precluded their use in human clinical trials. We previously developed a new, safer source of adult adrenal chromaffin cells of porcine origin and demonstrated an in vivo antinociceptive effect in the formalin test, a rodent model of tonic pain. The goal of the present study was to confirm porcine chromaffin cell analgesic effects at the molecular level by evaluating neural activity as reflected by spinal cord c-Fos protein expression. To this end, the expression of c-Fos in response to intraplantar formalin injection was evaluated in animals following intrathecal grafting of 10(6) porcine or bovine chromaffin cells. For the two species, adrenal chromaffin cells significantly reduced the tonic phases of the formalin response. Similarly, c-Fos-like immunoreactive neurons were markedly reduced in the dorsal horns of animals that had received injections of xenogeneic chromaffin cells. This reduction was observed in both the superficial (I-II) and deep (V-VI) lamina of the dorsal horn. The present study demonstrates that both xenogeneic porcine and bovine chromaffin cells transplanted into the spinal subarachnoid space of the rat can suppress formalin-evoked c-Fos expression equally, in parallel with suppression of nociceptive behaviors in the tonic phase of the test. These findings confirm previous reports that adrenal chromaffin cells may produce antinociception by inhibiting activation of nociceptive neurons in the spinal dorsal horn. Taken together these results support the concept that porcine chromaffin cells may offer an alternative xenogeneic cell source for transplants delivering pain-reducing neuroactive substances.


Subject(s)
Chromaffin Cells/metabolism , Fixatives/toxicity , Formaldehyde/toxicity , Pain/metabolism , Proto-Oncogene Proteins c-fos/biosynthesis , Spinal Cord/metabolism , Animals , Behavior, Animal/drug effects , Cattle , Chromaffin Cells/transplantation , Male , Pain/chemically induced , Pain Management , Pain Measurement/methods , Posterior Horn Cells/metabolism , Rats , Rats, Sprague-Dawley , Transplantation, Heterologous
10.
Biomaterials ; 58: 46-53, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25941781

ABSTRACT

With the ever increasing incidence of brain injury, developing new tissue engineering strategies to promote neural tissue regeneration is an enormous challenge. The goal of this study was to design and evaluate an implantable scaffold capable of directing neurite and axonal growth for neuronal brain tissue regeneration. We have previously shown in cell culture conditions that engineered micropatterned PDMS surface with straight microchannels allow directed neurite growth without perturbing cell differentiation and neurite outgrowth. In this study, the micropatterned PDMS device pre-seeded with hNT2 neuronal cells were implanted in rat model of primary motor cortex lesion which induced a strong motor deficit. Functional recovery was assessed by the forelimb grip strength test during 3 months post implantation. Results show a more rapid and efficient motor recovery with the hNT2 neuroimplants associated with an increase of neuronal tissue reconstruction and cell survival. This improvement is also hastened when compared to a direct cell graft of ten times more cells. Histological analyses showed that the implant remained structurally intact and we did not see any evidence of inflammatory reaction. In conclusion, PDMS bioimplants with guided neuronal cells seem to be a promising approach for supporting neural tissue reconstruction after central brain injury.


Subject(s)
Motor Cortex/injuries , Motor Cortex/pathology , Neurons/metabolism , Tissue Scaffolds , Animals , Axons/metabolism , Behavior, Animal , Bioprosthesis , Brain Injuries/therapy , Dimethylpolysiloxanes/chemistry , Equipment Design , Glial Fibrillary Acidic Protein/chemistry , Humans , Immunohistochemistry , Male , Neurites/metabolism , Neurogenesis , Neurons/pathology , Prostheses and Implants , Rats , Rats, Sprague-Dawley , Regeneration , Tissue Engineering/methods
11.
Neurochirurgie ; 61 Suppl 1: S109-16, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25456442

ABSTRACT

BACKGROUND: Many studies have demonstrated the efficacy of spinal cord stimulation (SCS) for chronic neuropathic radicular pain over recent decades, but despite global favourable outcomes in failed back surgery syndrome (FBSS) with leg pain, the back pain component remains poorly controlled by neurostimulation. Technological and scientific progress has led to the development of new SCS leads, comprising a multicolumn design and a greater number of contacts. The efficacy of multicolumn SCS lead configurations for the treatment of the back pain component of FBSS has recently been suggested by pilot studies. However, a randomized controlled trial must be conducted to confirm the efficacy of new generation multicolumn SCS. Évaluation médico-économique de la STImulation MEdullaire mulTi-colonnes (ESTIMET) is a multicentre, randomized study designed to compare the clinical efficacy and health economics aspects of mono- vs. multicolumn SCS lead programming in FBSS patients with radicular pain and significant back pain. MATERIALS AND METHODS: FBSS patients with a radicular pain VAS score≥50mm, associated with a significant back pain component were recruited in 14 centres in France and implanted with multicolumn SCS. Before the lead implantation procedure, they were 1:1 randomized to monocolumn SCS (group 1) or multicolumn SCS (group 2). Programming was performed using only one column for group 1 and full use of the 3 columns for group 2. Outcome assessment was performed at baseline (pre-implantation), and 1, 3, 6 and 12months post-implantation. The primary outcome measure was a reduction of the severity of low back pain (bVAS reduction≥50%) at the 6-month visit. Additional outcome measures were changes in global pain, leg pain, paraesthesia coverage mapping, functional capacities, quality of life, neuropsychological aspects, patient satisfaction and healthcare resource consumption. TRIAL STATUS: Trial recruitment started in May 2012. As of September 2013, all 14 study centres have been initiated and 112/115 patients have been enrolled. Preliminary results are expected to be published in 2015. TRIAL REGISTRATION: Clinical trial registration information-URL: www.clinicaltrials.gov. Unique identifier NCT01628237.


Subject(s)
Failed Back Surgery Syndrome/complications , Failed Back Surgery Syndrome/therapy , Low Back Pain/etiology , Low Back Pain/therapy , Spinal Cord Stimulation/economics , Spinal Cord Stimulation/methods , Adolescent , Adult , Aged , Cost-Benefit Analysis , Electrodes, Implanted , Endpoint Determination , Failed Back Surgery Syndrome/economics , Female , Humans , Low Back Pain/economics , Male , Middle Aged , Neurosurgical Procedures/methods , Pain Measurement , Prospective Studies , Research Design , Young Adult
12.
Peptides ; 20(10): 1219-27, 1999.
Article in English | MEDLINE | ID: mdl-10573294

ABSTRACT

Degradation of neuropeptide FF (NPFF) and SQA-neuropeptide FF (SQA-NPFF) by mouse brain sections was investigated by using capillary electrophoresis with UV detection for the separation and the identification of the degradation products. The half disappearance time of SQA-NPFF was 2-fold greater than that of NPFF. NPFF was cleaved preferentially into an inactive metabolite, Gln-Arg-Phe-NH2, in the cerebrum slices. SQA-NPFF was hydrolyzed by an unidentified degrading activity to generate NPFF, and NPFF accounted for a larger part of SQA-NPFF degradation in the hindbrain and cervical spinal cord than in the cerebrum slices. These findings suggest that, depending on the brain regions, NPFF produced from SQA-NPFF could prolong the biologic effects of SQA-NPFF.


Subject(s)
Brain/metabolism , Oligopeptides/metabolism , Animals , Brain/enzymology , Brain/pathology , Carboxypeptidases/metabolism , Electrophoresis, Capillary , Kinetics , Leucine/analogs & derivatives , Leucine/pharmacology , Male , Mice
13.
Neurosurgery ; 49(5): 1145-56; discussion 1156-7, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11846909

ABSTRACT

OBJECTIVE: The aim of this article was to analyze the technical and methodological issues resulting from the use of functional magnetic resonance image (fMRI) data in a frameless stereotactic device for brain tumor or pain surgery (chronic motor cortex stimulation). METHODS: A total of 32 candidates, 26 for brain tumor surgery and six chronic motor cortex stimulation, were studied by fMRI scanning (61 procedures) and intraoperative cortical brain mapping under general anesthesia. The fMRI data obtained were analyzed with the Statistical Parametric Mapping 99 software, with an initial analysis threshold corresponding to P < 0.001. Subsequently, the fMRI data were registered in a frameless stereotactic neuronavigational device and correlated to brain mapping. RESULTS: Correspondence between fMRI-activated areas and cortical mapping in primary motor areas was good in 28 patients (87%), although fMRI-activated areas were highly dependent on the choice of paradigms and analysis thresholds. Primary sensory- and secondary motor-activated areas were not correlated to cortical brain mapping. Functional mislocalization as a result of insufficient correction of the echo-planar distortion was identified in four patients (13%). Analysis thresholds (from P < 0.0001 to P < 10(-12)) more restrictive than the initial threshold (P < 0.001) had to be used in 25 of the 28 patients studied, so that fMRI motor data could be matched to cortical mapping spatial data. These analysis thresholds were not predictable preoperatively. Maximal tumor resection was accomplished in all patients with brain tumors. Chronic motor cortex electrode placement was successful in each patient (significant pain relief >50% on the visual analog pain scale). CONCLUSION: In brain tumor surgery, fMRI data are helpful in surgical planning and guiding intraoperative brain mapping. The registration of fMRI data in anatomic slices or in the frameless stereotactic neuronavigational device, however, remained a potential source of functional mislocalization. Electrode placement for chronic motor cortex stimulation is a good indication to use fMRI data registered in a neuronavigational system and could replace somatosensory evoked potentials in detection of the central sulcus.


Subject(s)
Brain Neoplasms/surgery , Electric Stimulation Therapy/instrumentation , Electrodes, Implanted , Magnetic Resonance Imaging/methods , Motor Cortex/surgery , Pain/surgery , Stereotaxic Techniques , Surgery, Computer-Assisted/methods , Adolescent , Adult , Aged , Brain Mapping , Brain Neoplasms/diagnosis , Chronic Disease , Female , Humans , Imaging, Three-Dimensional , Male , Middle Aged
14.
J Neurosurg ; 95(5): 783-90, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11702868

ABSTRACT

OBJECT: Hydrocephalus associated with Chiari I malformation is a rare entity related to an obstruction in the flow of cerebrospinal fluid (CSF) in the foramen of Magendie. Like all forms of noncommunicating hydrocephalus. it can be treated by endoscopic third ventriculostomy (ETV). The object of this study is to report a series of five cases of hydrocephalus associated with Chiari I malformation and to evaluate the use of ETV in the treatment of this anomaly. METHODS: Five patients (four women and one man with a mean age of 29.6 years) underwent ETV for hydrocephalus associated with Chiari I malformation between April 1991 and February 1997. All patients had presented with paroxysmal headaches, which in two cases were associated with visual disorders. All patients had also presented with hydrocephalus (mean transverse diameter of the third ventricle 12.79 mm; mean sagittal diameter of the fourth ventricle 18.27 mm) with a mean herniation of the cerebellar tonsils at 13.75 mm below the basion-opisthion line. Surgery was performed in all patients by using a rigid endoscope. No complications occurred either during or after the procedure, except in one patient who experienced a wound infection that was treated by antibiotic medications. The mean duration of follow up in this study was 50.39 months. Four patients became completely asymptomatic and remained stable throughout the follow-up period. One patient required an additional third ventriculostomy after I year, due to secondary closure, and has remained stable since that time. Postoperative magnetic resonance images demonstrated a significant reduction in the extent of hydrocephalus in all patients (mean transverse diameter of the third ventricle 6.9 mm [p = 0.0035]; mean sagittal diameter of the fourth ventricle 10.32 mm [p = 0.007]), with a mean ascent of the cerebellar tonsils from 13.75 mm below the basion-opisthion line to 7.76 mm below it (p = 0.01). In addition, CSF flow was identified on either side of the orifice of the third ventriculostomy in all patients postoperatively. CONCLUSIONS: Results in this series confirm the efficacy of ETV in the treatment of hydrocephalus associated with Chiari I malformation. It is a reliable, minimally invasive technique that also provides a better understanding of the pathophysiology of this malformation.


Subject(s)
Arnold-Chiari Malformation/complications , Hydrocephalus/etiology , Hydrocephalus/surgery , Third Ventricle/surgery , Ventriculostomy , Adult , Arnold-Chiari Malformation/diagnosis , Endoscopy , Female , Humans , Hydrocephalus/diagnosis , Magnetic Resonance Imaging , Male , Middle Aged , Minimally Invasive Surgical Procedures
15.
Neurochirurgie ; 46(3): 203-8, 2000 Jun.
Article in French | MEDLINE | ID: mdl-10854980

ABSTRACT

According to the development of neurosurgical endoscopy (and especially for third ventriculostomy), the endoscopic anatomy in hydrocephalus should be well known and utilized for orientation. The endoscopic pictures are obtained with a 30; telescope, acquired by a digitalized camera and visualized on a video monitor. The pictures are then numerized on a DKR system. Endoscopic anatomy of the third ventricle is described with a particular focus on the anatomical landmarks and their variations around the foramen of Monro, the anterior and posterior walls of the third ventricle. The knowledge of this anatomy is essential for the safety and the reliability of intraventricular endoscopic procedures.


Subject(s)
Endoscopy , Third Ventricle/anatomy & histology , Humans , Neurosurgery/methods , Third Ventricle/pathology , Third Ventricle/surgery
16.
Neurochirurgie ; 50(1): 66-72, 2004 Mar.
Article in French | MEDLINE | ID: mdl-15097924

ABSTRACT

BACKGROUND: The script concordance test (SCT) is a new tool to assess clinical reasoning in a context of uncertainty. It was chosen for computer-based self-assessment training for neurosurgery residents. PURPOSE: The aim of this work is to describe the construction of a first series of questions and provide teachers practical information needed to build a SCT. METHOD: The theorical background of the SCT is explained. We review the steps we followed when writing of a series of more than two hundred questions. RESULTS: We present the different steps of our work, including writing clinical cases, validation of questions and elaboration of scoring systems. We explain the main difficulties we encountered. CONCLUSION: The script concordance test is an interesting easy-to-construct assessment tool useful for evaluating clinical competence. This work summarizes our experience in building a SCT, which should be helpful for teachers interested in this new assessment tool, especially in neurosurgery.


Subject(s)
Internship and Residency , Neurosurgery/education , Clinical Competence , Microcomputers , Specialization , Teaching Materials
17.
Neurochirurgie ; 44(3): 201-8, 1998 Sep.
Article in French | MEDLINE | ID: mdl-9827437

ABSTRACT

Direct intrathecal administration of baclofen in the treatment of severe spasticity was proposed in 1984 by Richard Penn with the objective to carry out a selective spinal distribution of the active principle thus avoiding supraspinal side effects. We presented our first results at the French Language Association of Neurosurgery in 1985 within the framework of a report on "Functional neurosurgery of cerebral palsy" (Neurochirurgie, 1985, 31 (suppl 1): 1-118). This study aims to specify the selection criteria and current indications of this method for the treatment of severe chronic diffused spasticity of spinal and cerebral origin in adults and in children. This report relates to our experience concerning 60 patients (10 children) that benefit from the use of a totally implantable system for chronic administration. The total follow-up of all patients was 48 months (from 3 to 140 months). The initial effective daily amount of baclofen was 156 micrograms/24 hours and progressed in time to reach in the long run 280 micrograms/24 hours, with a very broad interindividual variability from 36 to 1050 micrograms/24 hours. All the patients benefited from a reduction in muscular hypertonicity as well as painful muscular spasms. On the other hand, the functional improvement was very variable from one patient to another and depended primarily on the initial clinical state and the etiology of the spasticity. The results observed were more significant in post-traumatic paraplegia than those secondary to demyelination disease even if they were stabilized with regard to spasticity of spinal origin. This mode of administration currently plays a significant role in the treatment of spasticity of cerebral origin, in particular in children presenting a motor disorder of cerebral origin with spastic prevalence. The current limitations of this type of treatment are technical because of the frequent catheter malfunctions, but are due essentially to the importance and constraint of the multi-disciplinary organization needed for the out-patient follow-up.


Subject(s)
Baclofen/therapeutic use , Muscle Relaxants, Central/therapeutic use , Muscle Spasticity/drug therapy , Baclofen/administration & dosage , Child , Follow-Up Studies , Humans , Injections, Spinal , Muscle Relaxants, Central/administration & dosage , Muscle Spasticity/physiopathology , Time Factors , Treatment Outcome
18.
Neurochirurgie ; 46(5): 454-65, 2000 Nov.
Article in French | MEDLINE | ID: mdl-11084478

ABSTRACT

The durable effectiveness of intrathecal morphine administration is well established for the management of intractable cancer pain, after failure of systemic opioids, secondary to the persistence of non-reversible undesirable side effects. Many patients are referred to late in the disease course. This conservative method to control pain of malignant origin must not be reserved for last resort treatment for terminal patients. Intra-cerebro-ventricular morphine administration is a very effective and generally safe method for controlling intractable cancer pain. Because of the chronic implantation of an intra-ventricular catheter this method is somewhat invasive. Its indications remain a simple and effective alternative when the topography of nociceptive pain is diffuse or cephalic. In clinical practice, intrathecal and/or intra-cerebro-ventricular administration of opioids is limited by cost, the need for specialized maintenance and mechanical malfunctions if implantable drug delivery systems, or by the risk of bacterial contamination and ambulatory constraints when repeated daily injections via an intrathecal access port are used. To answer these limitations, cell therapy using intrathecal chromaffin cell allograft is a promising approach for the management of cancer pain refractory to traditional drug therapy and pain lesion surgery. The basic rationale and preclinical studies on experimental pain models have enabled starting prospective clinical trials. Prior to transplantation, handling and preparation of the chromaffin tissue is critical for allograft viability. The initial results of clinical trials with human chromaffin cell grafts from intractable cancer pain have reported long-lasting pain relief, in correlation with met-enkephalin release into the CSF. Convincing evidence will require controlled studies. The limitations of this innovative cell therapy and especially the lack of human adrenal gland availability point to the need for new sources of cells. Perspectives include xenogenic or engineered cell lines.


Subject(s)
Analgesics, Opioid/administration & dosage , Chromaffin Cells/transplantation , Morphine/administration & dosage , Neoplasms/complications , Pain, Intractable/etiology , Pain, Intractable/therapy , Chronic Disease , Humans , Injections, Spinal , Prospective Studies
19.
Neurochirurgie ; 59(4-5): 183-6, 2013.
Article in English | MEDLINE | ID: mdl-24176432

ABSTRACT

The origin of the middle meningeal artery (MMA) may vary although it can arise from the ophthalmic artery (OA) with a 0.5% prevalence. We report the exceptional bilateral asymmetric origin from the OAs that has not previously been reported in the literature. Surgeons should be aware of this variation as it could be crucial in the setting of an endovascular approach for meningeal lesions, as in our observation. A 50-year-old male underwent a preoperative cerebral digital subtracted angiography that incidentally revealed MMAs arising from the OA on both sides. In fact, the origin was asymmetric because it was complete on the right side with the anterior and posterior branches of the MMA arising from the OA, whereas it was partial on the left side, with only the anterior branch arising from the OA. The CT scan showed the absence of the foramen spinosum only on the right side. This paper discusses the unique anatomic variation in the light of MMA embryology and its different origins. Knowledge of this variation may have a practical impact in cases of cerebral embolization.


Subject(s)
Brain/blood supply , Cerebral Angiography , Embolization, Therapeutic , Meningeal Arteries/pathology , Ophthalmic Artery/pathology , Cerebral Angiography/methods , Embolization, Therapeutic/methods , Humans , Male , Middle Aged , Tomography Scanners, X-Ray Computed
20.
Neurochirurgie ; 59(4-5): 142-8, 2013.
Article in English | MEDLINE | ID: mdl-23953035

ABSTRACT

The operating room (OR) is a high-risk complex setting, where patient safety relies on the coordinated efforts of multiple team members. However, little attention has been paid to evaluating the strategies employed by OR practitioners to prevent and correct incidents that inevitably occur during surgery. Therefore, we were prompted to investigate human factor (HF) engineering methods that have been used in an innovative way in order to systematically observe and analyze the management of incidents in the neurosurgical OR of a French university hospital. A technical case report illustrates our approach that associates the following procedures: the recording of OR team member activities and behaviour by video cameras and direct observation of a HF researcher, with the description and the explicit demonstration of safety related procedures in self- and cross-confrontation interviews of OR team members. This technical report emphasizes complementary aspects of clinical performance related to safety skills. Moreover, individual and team performances rely on complementary abilities that associate practical knowledge, skills, and attitudes, which are engaged at various degrees to prevent and manage incidents. This report also enlightens new quality-improvement opportunities as well as further objectives for future studies.


Subject(s)
Brain Neoplasms/surgery , Operating Rooms , Video Recording , Aged , Female , Hospitals, University , Humans , Patient Care Team , Prospective Studies , Video Recording/methods
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