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	<title>Neurosurgery Blog &#187; Functional</title>
	<atom:link href="http://www.neurosurgery-blog.com/archives/category/functional/feed" rel="self" type="application/rss+xml" />
	<link>http://www.neurosurgery-blog.com</link>
	<description>Daily bibliographic and video review of the Neurosurgery Department. La Fe University Hospital. Valencia, Spain</description>
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		<title>Localization of Primary Language Areas by Arcuate Fascicle Fiber Tracking</title>
		<link>http://www.neurosurgery-blog.com/archives/3721</link>
		<comments>http://www.neurosurgery-blog.com/archives/3721#comments</comments>
		<pubDate>Mon, 23 Jan 2012 23:00:07 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Surgical technique]]></category>
		<category><![CDATA[Arcuate fascicle]]></category>
		<category><![CDATA[Broca]]></category>
		<category><![CDATA[Fiber tracking]]></category>
		<category><![CDATA[Neuronavigation]]></category>
		<category><![CDATA[Wernicke]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3721</guid>
		<description><![CDATA[Neurosurgery 70:56–65, 2012 DOI: 10.1227/NEU.0b013e31822cb882
To reduce the risk of disabling postoperative functional deficit in patients with lesions in the dominant hemisphere, information about the localization of eloquent language areas is mandatory.
OBJECTIVE: To demonstrate the feasibility of arcuate fascicle (AF) tractography for proper localization of eloquent language areas in the superior temporal (STG) and inferior frontal [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Localization_of_Primary_Language_Areas_by_Arcuate-1.jpg"><img class="alignleft size-thumbnail wp-image-3725" title="Localization_of_Primary_Language_Areas_by_Arcuate-1" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/Localization_of_Primary_Language_Areas_by_Arcuate-1-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 70:56–65, 2012 DOI: 10.1227/NEU.0b013e31822cb882</strong></p>
<p style="text-align: justify;">To reduce the risk of disabling postoperative functional deficit in patients with lesions in the dominant hemisphere, information about the localization of eloquent language areas is mandatory.</p>
<p style="text-align: justify;">OBJECTIVE: To demonstrate the feasibility of arcuate fascicle (AF) tractography for proper localization of eloquent language areas in the superior temporal (STG) and inferior frontal gyrus (IFG).</p>
<p style="text-align: justify;">METHODS: Between January and June 2010, we performed surgery in 13 patients with highly eloquent lesions with close spatial relationship to the primary language areas. All of them received preoperative diffusion tensor imaging for AF tractography. The STG and IFG were delineated at the ends of the AF. Five patients underwent functional magnetic resonance imaging of the primary language areas. The results were compared with tractography.</p>
<p style="text-align: justify;">RESULTS: Tractography of the AF without prior knowledge of the localization of the STG and IFG was feasible in all cases. In the cases with functional magnetic resonance imaging, the activation maps matched the tractography results. In all but 1 patient, preservation of the primary language areas was possible, proven by the good neurological outcome. One patient suffered from a language dysfunction caused by a lesion in the medial and inferior temporal gyrus along the surgical pathway.</p>
<p style="text-align: justify;">CONCLUSION: Tractography of the AF is a useful tool for identification of parts of the main primary language areas. Using tractography as a localization procedure to determine the primary language areas aids in the delineation of the STG and IFG and thus may help reduce the risk of postoperative permanent neurological deficit.</p>
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		<title>Transcranial magnetic resonance imaging–guided focused ultrasound: noninvasive central lateral thalamotomy for chronic neuropathic pain</title>
		<link>http://www.neurosurgery-blog.com/archives/3627</link>
		<comments>http://www.neurosurgery-blog.com/archives/3627#comments</comments>
		<pubDate>Wed, 04 Jan 2012 23:00:26 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Pain]]></category>
		<category><![CDATA[central lateral thalamotomy]]></category>
		<category><![CDATA[neuropathic or neurogenic pain]]></category>
		<category><![CDATA[transcranial magnetic resonance imaging–guided focused ultrasound]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3627</guid>
		<description><![CDATA[Neurosurgical Focus Jan 2012 / Vol. 32 / No. 1 / Page E1. DOI: 10.3171/2011.10.FOCUS11248
Recent technological developments open the field of therapeutic application of focused ultrasound to the brain through the intact cranium. The goal of this study was to apply the new transcranial magnetic resonance imaging–guided focused ultrasound (tcMRgFUS) technology to perform noninvasive central [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/MRI-US.gif"><img class="alignleft size-thumbnail wp-image-3631" title="MRI-US" src="http://www.neurosurgery-blog.com/wp-content/uploads/2012/01/MRI-US-150x150.gif" alt="" width="150" height="150" /></a><a href="http://thejns.org/action/showCoverGallery?journalCode=foc">Neurosurgical Focus</a> Jan 2012 / Vol. 32 / No. 1 / Page E1. DOI: 10.3171/2011.10.FOCUS11248</strong></p>
<p style="text-align: justify;">Recent technological developments open the field of therapeutic application of focused ultrasound to the brain through the intact cranium. The goal of this study was to apply the new transcranial magnetic resonance imaging–guided focused ultrasound (tcMRgFUS) technology to perform noninvasive central lateral thalamotomies (CLTs) as a treatment for chronic neuropathic pain.</p>
<p style="text-align: justify;">METHODS</p>
<p style="text-align: justify;">In 12 patients suffering from chronic therapy-resistant neuropathic pain, tcMRgFUS CLT was proposed. In 11 patients, precisely localized thermal ablations of 3–4 mm in diameter were produced in the posterior part of the central lateral thalamic nucleus at peak temperatures between 51°C and 64°C with the aid of real-time patient monitoring and MR imaging and MR thermometry guidance. The treated neuropathic pain syndromes had peripheral (5 patients) or central (6 patients) origins and covered all body parts (face, arm, leg, trunk, and hemibody).</p>
<p style="text-align: justify;">RESULTS</p>
<p style="text-align: justify;">Patients experienced mean pain relief of 49% at the 3-month follow-up (9 patients) and 57% at the 1-year follow-up (8 patients). Mean improvement according to the visual analog scale amounted to 42% at 3 months and 41% at 1 year. Six patients experienced immediate and persisting somatosensory improvements. Somatosensory and vestibular clinical manifestations were always observed during sonication time because of ultrasound-based neuronal activation and/or initial therapeutic effects. Quantitative electroencephalography (EEG) showed a significant reduction in EEG spectral overactivities. Thermal ablation sites showed sharply delineated ellipsoidal thermolesions surrounded by short-lived vasogenic edema. Lesion reconstructions (18 lesions in 9 patients) demonstrated targeting precision within a millimeter for all 3 coordinates. There was 1 complication, a bleed in the target with ischemia in the motor thalamus, which led to the introduction of 2 safety measures, that is, the detection of a potential cavitation by a cavitation detector and the maintenance of sonication temperatures below 60°C.</p>
<p style="text-align: justify;">CONCLUSIONS</p>
<p style="text-align: justify;">The authors assert that tcMRgFUS represents a noninvasive, precise, and radiation-free neurosurgical technique for the treatment of neuropathic pain. The procedure avoids mechanical brain tissue shift and eliminates the risk of infection. The possibility of applying sonication thermal spots free from trajectory restrictions should allow one to optimize target coverage. The real-time continuous MR imaging and MR thermometry monitoring of targeting accuracy and thermal effects are major factors in optimizing precision, safety, and efficacy in an outpatient context.</p>
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		<title>Accuracy of Frame-Based Stereotactic Magnetic Resonance Imaging vs Frame-Based Stereotactic Head Computed Tomography Fused With Recent Magnetic Resonance Imaging for Postimplantation Deep Brain Stimulator Lead Localization</title>
		<link>http://www.neurosurgery-blog.com/archives/3510</link>
		<comments>http://www.neurosurgery-blog.com/archives/3510#comments</comments>
		<pubDate>Wed, 14 Dec 2011 23:00:37 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Accuracy]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Postimplantation intraoperative computed tomography]]></category>
		<category><![CDATA[Postimplantation intraoperative magnetic resonance imaging]]></category>
		<category><![CDATA[Stereotactic surgery]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3510</guid>
		<description><![CDATA[Neurosurgery 69:1299–1306, 2011 DOI: 10.1227/NEU.0b013e31822b7069
Introduction of the portable intraoperative CT scanner provides for a precise and cost-effective way of fusing head CT images with high-tesla MRI for the exquisite definition of soft tissue needed for stereotactic targeting.
OBJECTIVE: To evaluate the accuracy of stereotactic electrode placement in patients undergoing deep brain stimulation (DBS) by comparing frame-based [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/12/Accuracy_of_Frame_Based_Stereotactic_Magnetic.jpg"><img class="alignleft size-thumbnail wp-image-3515" title="Accuracy_of_Frame_Based_Stereotactic_Magnetic" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/12/Accuracy_of_Frame_Based_Stereotactic_Magnetic-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 69:1299–1306, 2011 DOI: 10.1227/NEU.0b013e31822b7069</strong></p>
<p style="text-align: justify;">Introduction of the portable intraoperative CT scanner provides for a precise and cost-effective way of fusing head CT images with high-tesla MRI for the exquisite definition of soft tissue needed for stereotactic targeting.</p>
<p style="text-align: justify;">OBJECTIVE: To evaluate the accuracy of stereotactic electrode placement in patients undergoing deep brain stimulation (DBS) by comparing frame-based postimplantation intraoperative CT (iCT) images fused to a recent 3T-MRI with frame-based postimplantation intraoperative MRI (iMRI) alone.</p>
<p style="text-align: justify;">METHODS: Frame-based DBS surgeries of 46 targets performed from February 8, 2007 to April 28, 2008 in 26 patients with the use of immediate postimplantation iMRI for target localization were compared with frame-based immediate postimplantation iCT fused with a recent 3T brain MRI for DBS localization of 50 targets performed from August 13, 2008 to February 18, 2010 in 26 patients. Pre- and postoperative mid anterior commissure-posterior commissure line coordinates and XYZ coordinates for preoperatively calculated DBS targets (intended target) and for the permanent DBS lead tips were determined. The differences between preoperative DBS target and postoperative permanent DBS lead-tip coordinates based on postimplantation intraoperative MRI for the MRI-alone group and based on postimplantation intraoperative CT fused to recent preoperative MRI in the CTMRI group were measured. The t test and Yuen test were used for comparison.</p>
<p style="text-align: justify;">RESULTS: No statistically significant differences were found between the 2 groups when comparing the pre- and postperative changes in mid anterior commissure-posterior commissure line coordinates and XYZ coordinates.</p>
<p style="text-align: justify;">CONCLUSION: Postimplantation DBS lead localization and therefore targeting accuracy was not significantly different between frame-based stereotactic 1.5T-MRI and framebased stereotactic head CT fused with recent 3T-MRI.</p>
]]></content:encoded>
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		<title>Discrepancies between the MRI and the electrophysiologically defined subthalamic nucleus</title>
		<link>http://www.neurosurgery-blog.com/archives/3499</link>
		<comments>http://www.neurosurgery-blog.com/archives/3499#comments</comments>
		<pubDate>Sun, 11 Dec 2011 23:00:58 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Brain shift]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Microelectrode recording]]></category>
		<category><![CDATA[Subthalamic nucleus]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3499</guid>
		<description><![CDATA[Acta Neurochir (2011) 153:2307–2318. DOI 10.1007/s00701-011-1081-7
The aim of our study was to evaluate discrepancies between the electrophysiologically and MRI-defined subthalamic nucleus (STN) in order to contribute to the ongoing debate of whether or not microelectrode recording (MER) provides additional information to imageguided targeting in deep brain stimulation.
Methods: Forty-four STNs in 22 patients with Parkinson’s disease [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/12/Discrepancies-between-theMRI-and-the-electrophysiologically-defined-subthalamic-nucleus.jpg"><img class="alignleft size-thumbnail wp-image-3500" title="Discrepancies between theMRI- and the electrophysiologically defined subthalamic nucleus" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/12/Discrepancies-between-theMRI-and-the-electrophysiologically-defined-subthalamic-nucleus-150x150.jpg" alt="" width="150" height="150" /></a>Acta Neurochir (2011) 153:2307–2318. DOI 10.1007/s00701-011-1081-7</strong></p>
<p style="text-align: justify;">The aim of our study was to evaluate discrepancies between the electrophysiologically and MRI-defined subthalamic nucleus (STN) in order to contribute to the ongoing debate of whether or not microelectrode recording (MER) provides additional information to imageguided targeting in deep brain stimulation.</p>
<p style="text-align: justify;">Methods: Forty-four STNs in 22 patients with Parkinson’s disease were investigated. The three-dimensional MRI-defined STN was derived from segmentations of axial and coronal T2-weighted images. The electrophysiological STNs were generated from intraoperative MERs in 1,487 locations. The stereotactical coordinates of positive and negative STN recordings were re-imported to the planning software, where a three-dimensional reconstruction of the electrophysiological STN was performed and fused to the MRI data set. The estimated borders of the MRI- and MERSTN were compared. For statistical analysis Student&#8217;s t, Mann-Whitney rank sum and Fisher&#8217;s exact tests were used.</p>
<p style="text-align: justify;">Results: MER-STN volumes, which were found outside the MRI-STN, ranged from 0 mm3 to 87 mm3 (mean: 45 mm3). A mean of 44% of the MER-STN volumes exceeded the MRI-STN (maximum: 85.1%; minimum: 15.1 %); 53.4% (n=793) of the microelectrode recordings were concordant and 46.6% (n=694) discordant with the MRI-defined anatomical STN. Regarding the dorsal borders, we found discrepancies between the MER- and MRI-STN of 0.27 mm (= mean; SD: 0.51 mm) on the first operated side and 1.51 mm (SD: 1.5 mm) on the second (p=0.010, t-test).</p>
<p style="text-align: justify;">Conclusions: MER provides additional information to highresolution anatomical MR images and may help to detect the amount and direction of brain shift.</p>
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		<title>Expanding applications of deep brain stimulation: a potential therapeutic role in obesity and addiction management</title>
		<link>http://www.neurosurgery-blog.com/archives/3443</link>
		<comments>http://www.neurosurgery-blog.com/archives/3443#comments</comments>
		<pubDate>Wed, 23 Nov 2011 23:00:24 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[meta-analysis]]></category>
		<category><![CDATA[Addiction]]></category>
		<category><![CDATA[Binge eating]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[hypothalamus]]></category>
		<category><![CDATA[Nucleus accumbens]]></category>
		<category><![CDATA[obesity]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3443</guid>
		<description><![CDATA[Acta Neurochir (2011) 153:2293–2306. DOI 10.1007/s00701-011-1166-3
The indications for deep brain stimulation (DBS) are expanding, and the feasibility and efficacy of this surgical procedure in various neurologic and neuropsychiatric disorders continue to be tested.
This review attempts to provide background and rationale for applying this therapeutic option to obesity and addiction. We review neural targets currently under [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/11/Expanding-applications-of-deep-brain-stimulation-a-potential-therapeutic-role-in-obesity-and-addiction-management.jpg"><img class="alignleft size-thumbnail wp-image-3444" title="Expanding applications of deep brain stimulation- a potential therapeutic role in obesity and addiction management" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/11/Expanding-applications-of-deep-brain-stimulation-a-potential-therapeutic-role-in-obesity-and-addiction-management-150x150.jpg" alt="" width="150" height="150" /></a>Acta Neurochir (2011) 153:2293–2306. DOI 10.1007/s00701-011-1166-3</strong></p>
<p style="text-align: justify;">The indications for deep brain stimulation (DBS) are expanding, and the feasibility and efficacy of this surgical procedure in various neurologic and neuropsychiatric disorders continue to be tested.</p>
<p style="text-align: justify;">This review attempts to provide background and rationale for applying this therapeutic option to obesity and addiction. We review neural targets currently under clinical investigation for DBS—the hypothalamus and nucleus accumbens—in conditions such as cluster headache and obsessive-compulsive disorder. These brain regions have also been strongly implicated in obesity and addiction. These disorders are frequently refractory, with very high rates of weight regain or relapse, respectively, despite the best available treatments.</p>
<p style="text-align: justify;">Methods We performed a structured literature review of the animal studies of DBS, which revealed attenuation of food intake, increased metabolism, or decreased drug seeking. We also review the available radiologic evidence in humans, implicating the hypothalamus and nucleus in obesity and addiction.</p>
<p style="text-align: justify;">Results The available evidence of the promise of DBS in these conditions combined with significant medical need, support pursuing pilot studies and clinical trials of DBS in order to decrease the risk of dietary and drug relapse.</p>
<p style="text-align: justify;">Conclusions Well-designed pilot studies and clinical trials enrolling carefully selected patients with obesity or addiction should be initiated.</p>
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		<title>Epidural Cortical Stimulation of the Left Dorsolateral Prefrontal Cortex for Refractory Major Depressive Disorder</title>
		<link>http://www.neurosurgery-blog.com/archives/3399</link>
		<comments>http://www.neurosurgery-blog.com/archives/3399#comments</comments>
		<pubDate>Tue, 15 Nov 2011 23:00:23 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Clinical Trial]]></category>
		<category><![CDATA[Functional]]></category>
		<category><![CDATA[Pain]]></category>
		<category><![CDATA[cortical stimulation]]></category>
		<category><![CDATA[DLPFC]]></category>
		<category><![CDATA[Major depressive disorder]]></category>
		<category><![CDATA[Neuromodulation]]></category>
		<category><![CDATA[PET]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3399</guid>
		<description><![CDATA[Neurosurgery 69:1015–1029, 2011 DOI: 10.1227/NEU.0b013e318229cfcd
A significant number of patients with major depressive disorder are unresponsive to conventional therapies. For these patients, neuromodulation approaches are being investigated.
OBJECTIVE: To determine whether epidural cortical stimulation at the left dorsolateral prefrontal cortex is safe and efficacious for major depressive disorder through a safety and feasibility study.
METHODS: Twelve patients were [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/11/Epidural_Cortical_Stimulation_of_the_Left.jpg"><img class="alignleft size-thumbnail wp-image-3400" title="Epidural_Cortical_Stimulation_of_the_Left" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/11/Epidural_Cortical_Stimulation_of_the_Left-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 69:1015–1029, 2011 DOI: 10.1227/NEU.0b013e318229cfcd</strong></p>
<p style="text-align: justify;">A significant number of patients with major depressive disorder are unresponsive to conventional therapies. For these patients, neuromodulation approaches are being investigated.</p>
<p style="text-align: justify;">OBJECTIVE: To determine whether epidural cortical stimulation at the left dorsolateral prefrontal cortex is safe and efficacious for major depressive disorder through a safety and feasibility study.</p>
<p style="text-align: justify;">METHODS: Twelve patients were recruited in this randomized, single-blind, shamcontrolled study with a 104-week follow-up period. The main outcome measures were Hamilton Depression Rating Scale-28 (HDRS), Montgomery-Asberg Depression Rating Scale (MADRS), Global Assessment of Function (GAF), and Quality of Life Enjoyment and Satisfaction (QLES) questionnaire. An electrode was implanted over Brodmann area 9/46 in the left hemisphere. The electrode provided long-term stimulation to this target via its connections to an implanted neurostimulator in the chest.</p>
<p style="text-align: justify;">RESULTS: During the sham-controlled phase, there was no statistical difference between sham and active stimulation, although a trend toward efficacy was seen with the active stimulation group. In the open-label phase, we observed a significant improvement in outcome scores for the HDRS, MADRS, and GAF but not the QLES (HDRS: df = 7, F = 7.72, P &lt; .001; MADRS: df = 7, F = 8.2, P &lt; .001; GAF: df = 5, F = 16.87, P &lt; .001; QLES: df = 5, F = 1.32, P . .2; repeated measures ANOVA). With regard to the HDRS, 6 patients had ≥40% improvement, 5 patients had ≥ 50% improvement, and 4 subjects achieved remission (HDRS , 10) at some point during the study.</p>
<p style="text-align: justify;">CONCLUSION: Epidural cortical stimulation of the left dorsolateral prefrontal cortex appears to be a safe and potentially efficacious neuromodulation approach for treatment- refractory major depressive disorder.</p>
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		<title>Diffusion Tensor Imaging and Colored Fractional Anisotropy Mapping of the Ventralis Intermedius Nucleus of the Thalamus</title>
		<link>http://www.neurosurgery-blog.com/archives/3341</link>
		<comments>http://www.neurosurgery-blog.com/archives/3341#comments</comments>
		<pubDate>Tue, 01 Nov 2011 23:00:57 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[diffusion tensor imaging]]></category>
		<category><![CDATA[Fiber tractography]]></category>
		<category><![CDATA[Fractional anisotropy]]></category>
		<category><![CDATA[Ventralis intermedius]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3341</guid>
		<description><![CDATA[Neurosurgery 69:1124–1130, 2011 DOI: 10.1227/NEU.0b013e3182296a42
The ventralis intermedius (VIM) nucleus of the thalamus is the primary surgical target for treatment of tremor. Most centers rely on indirect targeting based on atlas-defined coordinates rather than patient-specific anatomy, making intraoperative physiological mapping critical. Detailed identification of this target based on patientspecific anatomic features can help optimize the surgical [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/11/VIM-DTI.jpg"><img class="alignleft size-thumbnail wp-image-3342" title="VIM-DTI" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/11/VIM-DTI-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 69:1124–1130, 2011 DOI: 10.1227/NEU.0b013e3182296a42</strong></p>
<p style="text-align: justify;">The ventralis intermedius (VIM) nucleus of the thalamus is the primary surgical target for treatment of tremor. Most centers rely on indirect targeting based on atlas-defined coordinates rather than patient-specific anatomy, making intraoperative physiological mapping critical. Detailed identification of this target based on patientspecific anatomic features can help optimize the surgical treatment of tremor.</p>
<p style="text-align: justify;">OBJECTIVE: To study colored fractional anisotropic images and diffusion tensor imaging (DTI) tractography to identify characteristic magnetic resonance appearances of the VIM nucleus.</p>
<p style="text-align: justify;">METHODS: Four patients undergoing stereotactic surgery for essential tremor (ET) were retrospectively studied with analysis of magnetic resonance imaging-based colored fractional anisotropy (FA) images and fiber tractography. All were scanned with a 1.5-T magnetic resonance imaging unit, and all sequences were obtained before frame placement. Because the goal of this study was to identify the DTI characteristics of physiologically defined VIM nucleus, we selected and studied patients who had undergone DTI and had efficacious tremor control with intraoperative microlesioning effect and tremor reduction with less than 2.0-V stimulation.</p>
<p style="text-align: justify;">RESULTS: Analysis of color FA maps, which graphically illustrate fiber directionality, revealed consistent anatomic patterns. The region of the VIM nucleus can be seen as an intermediate region where there is a characteristic transition of color. Presumptive VIM nucleus interconnectivity with sensorimotor cortex and cerebellum was identified via the internal capsule and the superior cerebellar peduncle, respectively. FA maps could also be used to distinguish segments of gray matter, white matter, and gray-white matter boundaries.</p>
<p style="text-align: justify;">CONCLUSION: Analysis of DTI and FA maps on widely available 1.5-T magnetic resonance imaging yields clear identification of various structures key to neurosurgical targeting. Prospective evaluation of integrating DTI into neurosurgical planning may be warranted.</p>
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		<title>Dentatorubrothalamic tract in human brain: diffusion tensor tractography study</title>
		<link>http://www.neurosurgery-blog.com/archives/3301</link>
		<comments>http://www.neurosurgery-blog.com/archives/3301#comments</comments>
		<pubDate>Sun, 23 Oct 2011 22:00:15 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[neurorradiology]]></category>
		<category><![CDATA[Dentatorubrothalamic tract]]></category>
		<category><![CDATA[diffusion tensor imaging]]></category>
		<category><![CDATA[Diffusion tensor tractography]]></category>
		<category><![CDATA[Thalamus]]></category>
		<category><![CDATA[Ventrolateral nucleus]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/archives/3301</guid>
		<description><![CDATA[Neuroradiology (2011) 53:787–791.DOI 10.1007/s00234-011-0878-7
The dentatorubrothalamic tract (DRTT) originates from the dentate nucleus in the cerebellum and terminates in the contralateral ventrolateral nucleus (VL) of the thalamus after decussating to the contralateral red nucleus. Identification of the DRTT is difficult due to the fact that it is a long, multisynaptic, neural tract crossing to the opposite [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;"><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/10/DRTT.jpg"><img class="alignleft size-thumbnail wp-image-3318" title="DRTT" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/10/DRTT-150x150.jpg" alt="" width="150" height="150" /></a>Neuroradiology (2011) 53:787–791.DOI 10.1007/s00234-011-0878-7</strong><br />
The dentatorubrothalamic tract (DRTT) originates from the dentate nucleus in the cerebellum and terminates in the contralateral ventrolateral nucleus (VL) of the thalamus after decussating to the contralateral red nucleus. Identification of the DRTT is difficult due to the fact that it is a long, multisynaptic, neural tract crossing to the opposite hemisphere. In the current study, we attempted to identify the DRTT in the human brain using a probabilistic tractography technique of diffusion tensor imaging.<br />
Methods Diffusion tensor imaging was performed at 1.5-T using a synergy-L sensitivity encoding head coil. DRTTs were obtained by selection of fibers passing through three regions of interest (the dentate nucleus, the superior cerebellar peduncle, and the contralateral red nucleus) from 41 healthy volunteers. Probabilistic mapping was obtained from the highest probabilistic location at 2.3 mm above the anterior commissure–posterior commissure level.<br />
Results DRTTs of all subjects, which originated from the dentate nucleus, ascended through the junction of the superior cerebellar peduncle and the contralateral red nucleus and then terminated at the VL nucleus of the thalamus. The highest probabilistic location for the DRTT at the thalamus was compatible with the location of the VL nucleus.<br />
Conclusions We identified the DRTT in the human brain using probabilistic tractography. Our results could be useful in research on movement control.</p>
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		<title>Fiducial Registration With Spoiled Gradient-Echo Magnetic Resonance Imaging Enhances the Accuracy of Subthalamic Nucleus Targeting</title>
		<link>http://www.neurosurgery-blog.com/archives/3286</link>
		<comments>http://www.neurosurgery-blog.com/archives/3286#comments</comments>
		<pubDate>Wed, 19 Oct 2011 22:00:10 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[neurorradiology]]></category>
		<category><![CDATA[Deep brain stimulation (DBS)]]></category>
		<category><![CDATA[Microelectrode]]></category>
		<category><![CDATA[Parkinson disease]]></category>
		<category><![CDATA[Stereotactic surgery]]></category>
		<category><![CDATA[Subthalamic nucleus recording]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3286</guid>
		<description><![CDATA[Neurosurgery 69:870–875, 2011 DOI: 10.1227/NEU.0b013e318222ae33
A variety of imaging strategies may be used to derive reliable stereotactic coordinates when performing deep brain stimulation lead implants. No single technique has yet proved optimal.
OBJECTIVE: To compare the relative accuracy of stereotactic coordinates for the subthalamic nucleus (STN) derived either from fast spin echo/inversion recovery (FSE/IR) magnetic resonance imaging [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/10/Fiducial_Registration_With_Spoiled_Gradient_Echo.jpg"><img class="alignleft size-thumbnail wp-image-3287" title="Fiducial_Registration_With_Spoiled_Gradient_Echo" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/10/Fiducial_Registration_With_Spoiled_Gradient_Echo-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 69:870–875, 2011 DOI: 10.1227/NEU.0b013e318222ae33</strong></p>
<p style="text-align: justify;">A variety of imaging strategies may be used to derive reliable stereotactic coordinates when performing deep brain stimulation lead implants. No single technique has yet proved optimal.</p>
<p style="text-align: justify;">OBJECTIVE: To compare the relative accuracy of stereotactic coordinates for the subthalamic nucleus (STN) derived either from fast spin echo/inversion recovery (FSE/IR) magnetic resonance imaging MRI alone (group 1) or FSE/IR in conjunction with T1- weighted spoiled gradient-echo MRI (group 2).</p>
<p style="text-align: justify;">METHODS: A retrospective analysis of 145 consecutive STN deep brain stimulation lead placements (group 1, n = 72; group 2, n = 73) was performed in 81 Parkinson disease patients by 1 surgical team. From the operative reports, we recorded the number of microelectrode recording trajectories required to localize the desired STN target and the span of STN traversed along the implantation trajectory. In addition, we calculated the 3-dimensional vector difference between the initial MRI-derived coordinates and the final physiologically refined coordinates.</p>
<p style="text-align: justify;">RESULTS: The proportion of implants completed with just 1 microelectrode recording trajectory was greater (81% vs 58%; P &lt; .001) and the 3-dimensional vector difference between the anatomically selected target and the microelectrode recording–refined target was smaller (0.6 ± 1.2 vs 0.9 ± 1.3; P = .04) in group 2 than in group 1. At the same time, the mean expanse of STN recorded along the implantation trajectory was 8% greater in group 2 (4.8 ± 0.6 vs 5.2 ± 0.6 mm; P &lt; .001).</p>
<p style="text-align: justify;">CONCLUSION: A combination of stereotactic FSE/IR and spoiled gradient-echo MRI yields more accurate coordinates for the STN than FSE/IR MRI alone.</p>
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		<item>
		<title>Intraoperative magnetic resonance imaging findings during deep brain stimulation surgery</title>
		<link>http://www.neurosurgery-blog.com/archives/3266</link>
		<comments>http://www.neurosurgery-blog.com/archives/3266#comments</comments>
		<pubDate>Thu, 13 Oct 2011 22:00:37 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[functional neurosurgery]]></category>
		<category><![CDATA[Intracranial hemorrhage]]></category>
		<category><![CDATA[intraoperative MR imaging]]></category>
		<category><![CDATA[Parkinson disease]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3266</guid>
		<description><![CDATA[J Neurosurg 115:852–857, 2011.DOI: 10.3171/2011.5.JNS101457
Deep brain stimulation (DBS) is an established neurosurgical technique used to treat a variety of neurological disorders, including Parkinson disease, essential tremor, dystonia, epilepsy, depression, and obsessive-compulsive disorder. This study reports on the use of intraoperative MR imaging during DBS surgery to evaluate acute hemorrhage, intracranial air, brain shift, and accuracy [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/10/Intraoperative-magnetic-resonance-imaging-findings-during-deep-brain-stimulation-surgery1.jpg"><img class="alignleft size-thumbnail wp-image-3271" title="Intraoperative magnetic resonance imaging findings during deep brain stimulation surgery" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/10/Intraoperative-magnetic-resonance-imaging-findings-during-deep-brain-stimulation-surgery1-150x150.jpg" alt="" width="150" height="150" /></a>J Neurosurg 115:852–857, 2011.DOI: 10.3171/2011.5.JNS101457</strong></p>
<p style="text-align: justify;">Deep brain stimulation (DBS) is an established neurosurgical technique used to treat a variety of neurological disorders, including Parkinson disease, essential tremor, dystonia, epilepsy, depression, and obsessive-compulsive disorder. This study reports on the use of intraoperative MR imaging during DBS surgery to evaluate acute hemorrhage, intracranial air, brain shift, and accuracy of lead placement.</p>
<p style="text-align: justify;">Methods. During a 46-month period, 143 patients underwent 152 DBS surgeries including 289 lead placements utilizing intraoperative 1.5-T MR imaging. Imaging was supervised by an MR imaging physicist to maintain the specific absorption rate below the required level of 0.1 W/kg and always included T1 magnetization-prepared rapid gradient echo and T2* gradient echo sequences with selected use of T2 fluid attenuated inversion recovery (FLAIR) and T2 fast spin echo (FSE). Retrospective review of the intraoperative MR imaging examinations was performed to quantify the amount of hemorrhage and the amount of air introduced during the DBS surgery.</p>
<p style="text-align: justify;">Results. Intraoperative MR imaging revealed 5 subdural hematomas, 3 subarachnoid hemorrhages, and 1 intraparenchymal hemorrhage in 9 of the 143 patients. Only 1 patient experiencing a subarachnoid hemorrhage developed clinically apparent symptoms, which included transient severe headache and mild confusion. Brain shift due to intracranial air was identified in 144 separate instances.</p>
<p style="text-align: justify;">Conclusions. Intraoperative MR imaging can be safely performed and may assist in demonstrating acute changes involving intracranial hemorrhage and air during DBS surgery. These findings are rarely clinically significant and typically resolve prior to follow-up imaging. Selective use of T2 FLAIR and T2 FSE imaging can confirm the presence of hemorrhage or air and preclude the need for CT examinations</p>
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