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	<title>Neurosurgery Blog &#187; Stereotactic neurosurgery</title>
	<atom:link href="http://www.neurosurgery-blog.com/archives/category/stereotactic-neurosurgery/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>Bilateral subthalamic deep brain stimulation using single track microelectrode recording</title>
		<link>http://www.neurosurgery-blog.com/archives/2644</link>
		<comments>http://www.neurosurgery-blog.com/archives/2644#comments</comments>
		<pubDate>Tue, 17 May 2011 22:00:07 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Accuracy]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Electrode positioning]]></category>
		<category><![CDATA[Microelectrode recording]]></category>
		<category><![CDATA[Targeting]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=2644</guid>
		<description><![CDATA[Acta Neurochir (2011) 153:1087–1095 DOI 10.1007/s00701-011-0953-1
Microelectrode recording (MER) is widely used during deep brain stimulation (DBS) procedures because MER can identify structural borders and eloquent structures, localize somatotopic arrangements, and provide an outline of the three-dimensional shapes of target nuclei. However, MER may cause intracranial hemorrhage. We performed single track MER during DBS procedures, analyzed [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/05/DBS-STN.jpg"><img class="alignleft size-thumbnail wp-image-2647" title="DBS-STN" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/05/DBS-STN-150x150.jpg" alt="" width="150" height="150" /></a>Acta Neurochir (2011) 153:1087–1095 DOI 10.1007/s00701-011-0953-1</strong></p>
<p style="text-align: justify;">Microelectrode recording (MER) is widely used during deep brain stimulation (DBS) procedures because MER can identify structural borders and eloquent structures, localize somatotopic arrangements, and provide an outline of the three-dimensional shapes of target nuclei. However, MER may cause intracranial hemorrhage. We performed single track MER during DBS procedures, analyzed the accuracy of electrode positioning with MRI, and compared the amount of air and the potential risk of intracranial hemorrhage.</p>
<p style="text-align: justify;">Method A total of 46 electrodes were placed in 23 patients who suffered from advanced Parkinson’s disease and who underwent bilateral subthalamic nucleus DBS using single track MER. Each patient’s Unified Parkinson’s Disease Rating Scale (UPDRS) score and levo-dopa equivalent dosage (LED) were estimated pre- and postoperatively. The accuracy of electrode positioning and fontal air thickness was measured by a pre- or postoperative magnetic resonance imaging (MRI) merging technique.</p>
<p style="text-align: justify;">Findings The mean electrode positioning error was 0.92 mm (0.3–2.94 mm). The mean frontal air thickness on postoperative MRI was 3.85 mm (0–10.3 mm), which did not affect the electrode accuracy statistically (p=0.730). A total of nine electrodes required repositioning after single-track MER because they affected microstimulation or because an abnormally short STN length was observed during MER. In this series, one patient suffered from an intracranial hemorrhage after surgery that appeared to be due to venous infarction rather than related to MER.</p>
<p style="text-align: justify;">Conclusions Although MER can facilitate accurate positioning of electrodes, multi-track MER may increase the risk of intracranial hemorrhage. The accuracy of electrode positioning appears to be acceptable under single track MER during STN DBS with careful electrophysiological and neurological monitoring. The risk of intracranial hemorrhage appears to be minimal, especially in elderly patients with atrophic brains.</p>
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		<item>
		<title>Are stereotactic sample biopsies still of value in the modern management of pineal region tumours? Lessons from a single-department, retrospective series</title>
		<link>http://www.neurosurgery-blog.com/archives/2577</link>
		<comments>http://www.neurosurgery-blog.com/archives/2577#comments</comments>
		<pubDate>Tue, 03 May 2011 04:00:19 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Patient management]]></category>
		<category><![CDATA[Pineal tumour]]></category>
		<category><![CDATA[stereotactic biopsy]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=2577</guid>
		<description><![CDATA[Acta Neurochir (2011) 153:1111–1122. DOI 10.1007/s00701-010-0936-7
Recent improvements in imaging-based diagnosis, the broader application of neuroendoscopic techniques and advances in open surgery techniques mean that the need for stereotactic biopsies in the management of pineal region tumours must be reevaluated. The primary aim of this retrospective study was to establish whether stereotactic biopsy is still of [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/05/Surgical-planning.jpg"><img class="alignleft size-thumbnail wp-image-2579" title="Surgical planning" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/05/Surgical-planning-150x150.jpg" alt="" width="150" height="150" /></a>Acta Neurochir (2011) 153:1111–1122. DOI 10.1007/s00701-010-0936-7</strong></p>
<p style="text-align: justify;">Recent improvements in imaging-based diagnosis, the broader application of neuroendoscopic techniques and advances in open surgery techniques mean that the need for stereotactic biopsies in the management of pineal region tumours must be reevaluated. The primary aim of this retrospective study was to establish whether stereotactic biopsy is still of value in the modern management of pineal region tumours.</p>
<p style="text-align: justify;">Methods From 1985 to 2009, 88 consecutive patients underwent a stereotactic biopsy in our institution (51 males and 37 females; median age at presentation 30; range 2–74).</p>
<p style="text-align: justify;">Results Accurate tissue diagnoses were obtained in all but one case (i.e. 99%). In one case (1%), three distinct stereotactic procedures were necessary to obtain a tissue diagnosis. There was no mortality or permanent morbidity associated with stereotactic biopsy. One patient (1%) presented an intra-parenchymal hematoma but no related clinical symptoms. Five patients (6%) presented transient morbidity, which lasted for between 2 days and 3 weeks after the biopsy.</p>
<p style="text-align: justify;">Conclusions To guide subsequent treatment, we believe that histological diagnosis is paramount. Stereotactic biopsies are currently the safest and the most efficient way of obtaining this essential information. Recent improvements in stereotactic technology (particularly robotic techniques) appear to be very valuable, with almost no permanent morbidity or mortality risk and no decrease in the accuracy rate. In our opinion, other available neurosurgical techniques (such as endoscopic neurosurgery, stereotactic neurosurgery and open microsurgery) are complementary and not competitive.</p>
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		<title>Intraoperative Computed Tomography for Deep Brain Stimulation Surgery: Technique and Accuracy Assessment</title>
		<link>http://www.neurosurgery-blog.com/archives/2291</link>
		<comments>http://www.neurosurgery-blog.com/archives/2291#comments</comments>
		<pubDate>Mon, 07 Mar 2011 05:00:37 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Neuronavigation]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Technology]]></category>
		<category><![CDATA[Computed tomography]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Intraoperative imaging]]></category>
		<category><![CDATA[Lead location]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=2291</guid>
		<description><![CDATA[Neurosurgery 68[ONS Suppl 1]:ons114–ons124, 2011. DOI: 10.1227/NEU.0b013e31820781bc
The efficacy of deep brain stimulation (DBS) is highly dependent on the accuracy of lead placement.
OBJECTIVE: To describe the use of intraoperative computed tomography (iCT) to confirm lead location before surgical closure and to study the accuracy of this technique.
METHODS: Fifteen patients underwent awake microelectrode-guided DBS surgery in a [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/03/iCT-DBS.jpg"><img class="alignleft size-thumbnail wp-image-2295" title="iCT-DBS" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/03/iCT-DBS-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 68[ONS Suppl 1]:ons114–ons124, 2011. DOI: 10.1227/NEU.0b013e31820781bc</strong></p>
<p style="text-align: justify;">The efficacy of deep brain stimulation (DBS) is highly dependent on the accuracy of lead placement.</p>
<p style="text-align: justify;">OBJECTIVE: To describe the use of intraoperative computed tomography (iCT) to confirm lead location before surgical closure and to study the accuracy of this technique.</p>
<p style="text-align: justify;">METHODS: Fifteen patients underwent awake microelectrode-guided DBS surgery in a stereotactic frame. A portable iCT scanner (Medtronic O-arm) was positioned around the patient’s head throughout the procedure and was used to confirm lead location before fixation of the lead to the skull. Images were computationally fused with preoperative magnetic resonance imaging (MRI), and lead tip coordinates with respect to the midpoint of the anterior commissure-posterior commissure line were measured. Tip coordinates were compared with those obtained from postoperative MRI.</p>
<p style="text-align: justify;">RESULTS: iCT was integrated into standard frame-based microelectrode-guided DBS surgery with a minimal increase in surgical time or complexity. Technically adequate 2-dimensional and 3-dimensional images were obtained in all cases. Head positioning and fixation techniques that allow unobstructed imaging are described. Lead tip measurements on iCT fused with preoperative MRI were statistically indistinguishable from those obtained with postoperative MRI.</p>
<p style="text-align: justify;">CONCLUSION: iCT can be easily incorporated into standard DBS surgery, replaces the need for C-arm fluoroscopy, and provides accurate intraoperative 3-dimensional confirmation of electrode tip locations relative to preoperative images and surgical plans. iCT fused to preoperative MRI may obviate the need for routine postoperative MRI in DBS surgery. Technical nuances that must be mastered for the efficient use of iCT during DBS implantation are described.</p>
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		<item>
		<title>Stereotactic versus endoscopic surgery in periventricular lesions</title>
		<link>http://www.neurosurgery-blog.com/archives/2279</link>
		<comments>http://www.neurosurgery-blog.com/archives/2279#comments</comments>
		<pubDate>Thu, 03 Mar 2011 05:00:11 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Endoscopy]]></category>
		<category><![CDATA[Oncology]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Neuroendoscopy]]></category>
		<category><![CDATA[Periventricular lesion]]></category>
		<category><![CDATA[Stereotactic surgery]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=2279</guid>
		<description><![CDATA[Acta Neurochir (2011) 153:517–526.DOI 10.1007/s00701-010-0933-x
Endoscopic and stereotactic surgery have gained widespread acceptance as minimally invasive tools for the diagnosis of intracerebral pathologies. We investigated the specific advantages and disadvantages of each technique in the assessment of periventricular lesions.
Method This study included a retrospective series of 70 patients with periventricular lesions. Endoscopic surgery was performed in [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/03/Thalamic_tumor.jpg"><img class="alignleft size-thumbnail wp-image-2283" title="Thalamic_tumor" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/03/Thalamic_tumor-150x150.jpg" alt="" width="150" height="150" /></a>Acta Neurochir (2011) 153:517–526.DOI 10.1007/s00701-010-0933-x</strong></p>
<p style="text-align: justify;">Endoscopic and stereotactic surgery have gained widespread acceptance as minimally invasive tools for the diagnosis of intracerebral pathologies. We investigated the specific advantages and disadvantages of each technique in the assessment of periventricular lesions.</p>
<p style="text-align: justify;">Method This study included a retrospective series of 70 patients with periventricular lesions. Endoscopic surgery was performed in 17 patients (mean age, 37 years; range, 4 months–78 years) and stereotactic biopsy in 55 patients (mean age, 63 years; range, 23–80 years), including two patients who underwent both procedures.</p>
<p style="text-align: justify;">Results Hydrocephalus was present in 13/17 patients in the endoscopic group (77%) and in 11/55 patients in the stereotactic group (20%). Diagnosis was achieved in all patients in the endoscopic group and in all but one patient in the stereotactic group, in whom histological diagnosis was obtained by endoscopic biopsy during a second operation. In the endoscopic group, additional procedures performed included ventriculostomy (2/17), cyst fenestration (3/17), endoscopic shunt revision (3/17) and placement of Rickham reservoirs or external cerebrospinal fluid drains (6/17). Adverse events occurred in one patient after endoscopy (chronic subdural hematoma) and in two patients after stereotactic surgery (one mild hemiparesis and one transitory paresis of the contralateral leg).</p>
<p style="text-align: justify;">Conclusions Endoscopic and stereotactic surgery have distinct advantages and disadvantages in approaching periventricular lesions. The advantages of endoscopy encompass the possibility to perform additional surgical procedures during the same session (e.g. tumour reduction, third ventriculostomy, fenestration of a cyst). The visual control reduces the hazard of injury to anatomical structures and allows for a better control of bleeding although there is a considerable blind-out in such situations. The advantages of stereotactic surgery include a smaller approach and precise planning of the trajectory. It is usually performed under local anaesthesia. Both methods provide a safe and efficient therapeutic option in periventricular lesions with low surgical-related morbidity.</p>
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		<item>
		<title>An Assessment of Current Brain Targets for Deep Brain Stimulation Surgery With Susceptibility- Weighted Imaging at 7 Tesla</title>
		<link>http://www.neurosurgery-blog.com/archives/1942</link>
		<comments>http://www.neurosurgery-blog.com/archives/1942#comments</comments>
		<pubDate>Fri, 17 Dec 2010 05:00:59 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Movement Disorders]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[neurorradiology]]></category>
		<category><![CDATA[7-Tesla]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Globus pallidum]]></category>
		<category><![CDATA[Subthalamic]]></category>
		<category><![CDATA[Susceptibility-weighted]]></category>
		<category><![CDATA[Thalamus]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1942</guid>
		<description><![CDATA[Neurosurgery 67:1745–1756, 2010 DOI: 10.1227/NEU.0b013e3181f74105
Deep brain stimulation (DBS) surgery is used for treating movement disorders, including Parkinson disease, essential tremor, and dystonia. Successful DBS surgery is critically dependent on precise placement of DBS electrodes into target structures. Frequently, DBS surgery relies on normalized atlas-derived diagrams that are superimposed on patient brain magnetic resonance imaging (MRI) [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/12/7T1.jpg"><img class="alignleft size-thumbnail wp-image-1946" title="7T" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/12/7T1-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 67:1745–1756, 2010 DOI: 10.1227/NEU.0b013e3181f74105</strong></p>
<p style="text-align: justify;">Deep brain stimulation (DBS) surgery is used for treating movement disorders, including Parkinson disease, essential tremor, and dystonia. Successful DBS surgery is critically dependent on precise placement of DBS electrodes into target structures. Frequently, DBS surgery relies on normalized atlas-derived diagrams that are superimposed on patient brain magnetic resonance imaging (MRI) scans, followed by microelectrode recording and macrostimulation to refine the ultimate electrode position. Microelectrode recording carries a risk of hemorrhage and requires active patient participation during surgery.</p>
<p style="text-align: justify;">OBJECTIVE: To enhance anatomic imaging for DBS surgery using high-field MRI with the ultimate goal of improving the accuracy of anatomic target selection.</p>
<p style="text-align: justify;">METHODS: Using a 7-T MRI scanner combined with an array of acquisition schemes using multiple image contrasts, we obtained high-resolution images of human deep nuclei in healthy subjects.</p>
<p style="text-align: justify;">RESULTS: Superior image resolution and contrast obtained at 7 T in vivo using susceptibility-weighted imaging dramatically improved anatomic delineation of DBS targets and allowed the identification of internal architecture within these targets. A patient-specific, 3-dimensional model of each target area was generated on the basis of the acquired images.</p>
<p style="text-align: justify;">CONCLUSION: Technical developments in MRI at 7 T have yielded improved anatomic resolution of deep brain structures, thereby holding the promise of improving anatomicbased targeting for DBS surgery. Future study is needed to validate this technique in improving the accuracy of targeting in DBS surgery.</p>
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		<item>
		<title>Is MRI a reliable tool to locate the electrode after deep brain stimulation surgery? Comparison study of CT and MRI for the localization of electrodes after DBS</title>
		<link>http://www.neurosurgery-blog.com/archives/1908</link>
		<comments>http://www.neurosurgery-blog.com/archives/1908#comments</comments>
		<pubDate>Thu, 09 Dec 2010 05:00:49 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[neurorradiology]]></category>
		<category><![CDATA[CT]]></category>
		<category><![CDATA[DBS]]></category>
		<category><![CDATA[Electrode localization]]></category>
		<category><![CDATA[Image fusion]]></category>
		<category><![CDATA[MRI]]></category>
		<category><![CDATA[Parkinson's disease]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1908</guid>
		<description><![CDATA[Acta Neurochir (2010) 152:2029–2036. DOI 10.1007/s00701-010-0779-2
MRI has been utilized to localize the electrode after deep brain stimulation, but its accuracy has been questioned due to image distortion. Under the hypothesis that MRI is not adequate for evaluation of electrode position after deep brain stimulation, this study is aimed at validating the accuracy of MRI in [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/12/3D-STN.jpg"><img class="alignleft size-thumbnail wp-image-1911" title="3D-STN" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/12/3D-STN-150x150.jpg" alt="" width="150" height="150" /></a>Acta Neurochir (2010) 152:2029–2036. DOI 10.1007/s00701-010-0779-2</strong></p>
<p style="text-align: justify;">MRI has been utilized to localize the electrode after deep brain stimulation, but its accuracy has been questioned due to image distortion. Under the hypothesis that MRI is not adequate for evaluation of electrode position after deep brain stimulation, this study is aimed at validating the accuracy of MRI in electrode localization in comparison with CT scan. Methods Sixty one patients who had undergone STN DBS were enrolled for the analysis. Using mutual information technique, CT and MRI taken at 6 months after the operation were fused. The x and y coordinates of the centers of electrodes shown of CT and MRI were compared in the fused images to calculate average difference at five different levels. The difference of the tips of the electrodes, designated as the z coordinate, was also calculated. Results The average of the distance between the centers of the electrodes in the five levels estimated in the fused image of brain CT and MRI taken at least 6 months after STN DBS was 1.33 mm (0.1–5.8 mm). The average discrepancy of x coordinates for all five levels between MRI and CT was 0.56±0.54 mm (0–5.7 mm), the discrepancy of y coordinates was 1.06±0.59 mm (0–3.5 mm), and for the z coordinate, it was 0.98±0.52 mm (0–3.1 mm) (all p values &lt;0.001). Notably, the average discrepancy of x coordinates at 3.5 mm below AC–PC level, i.e., at the STN level between MRI and CT, was 0.59±0.42 mm (0–2.4 mm); the discrepancy of y coordinates was 0.81±0.47 mm (0–2.9 mm) (p values&lt;0.001). Conclusions The results suggest that there was significant discrepancy between the centers of electrodes estimated by CT and MRI after STN DBS surgery.</p>
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		<title>Bilateral Deep Brain Stimulation for Cervical Dystonia: Long-term Outcome in a Series of 10 Patients</title>
		<link>http://www.neurosurgery-blog.com/archives/1742</link>
		<comments>http://www.neurosurgery-blog.com/archives/1742#comments</comments>
		<pubDate>Thu, 28 Oct 2010 04:00:39 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Movement Disorders]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Cervical dystonia]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Globus pallidus internus]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1742</guid>
		<description><![CDATA[Neurosurgery 67:957–963, 2010 DOI: 10.1227/NEU.0b013e3181ec49c7
Bilateral globus pallidus internus (GPi) deep brain stimulation (DBS) was shown to be effective in cervical dystonia refractory to medical treatment in several small short-term and 1 long-term follow-up series. Optimal stimulation parameters and their repercussions on the cost/benefit ratio still need to be established.
OBJECTIVE: To report our long-term outcome with [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/10/Bilateral-GPi.jpg"><img class="alignleft size-thumbnail wp-image-1744" title="Bilateral-GPi" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/10/Bilateral-GPi-150x150.jpg" alt="" width="120" height="120" /></a>Neurosurgery 67:957–963, 2010 DOI: 10.1227/NEU.0b013e3181ec49c7</strong></p>
<p style="text-align: justify;">Bilateral globus pallidus internus (GPi) deep brain stimulation (DBS) was shown to be effective in cervical dystonia refractory to medical treatment in several small short-term and 1 long-term follow-up series. Optimal stimulation parameters and their repercussions on the cost/benefit ratio still need to be established.</p>
<p style="text-align: justify;">OBJECTIVE: To report our long-term outcome with bilateral GPi deep brain stimulation in cervical dystonia.</p>
<p style="text-align: justify;">METHODS: The Toronto Western Spasmodic Torticollis Rating Scale was evaluated in 10 consecutive patients preoperatively and at last follow-up. The relationship of improvement in postural severity and pain was analyzed and stimulation parameters noted and compared with those in a similar series in the literature.</p>
<p style="text-align: justify;">RESULTS: The mean (standard deviation) follow-up was 37.6 (16.9) months. Improvement in the total Toronto Western Spasmodic Torticollis Rating Scale score as evaluated at latest follow-up was 68.1% (95% confidence interval: 51.5-84.6). In 4 patients, there was dissociation between posture severity and pain improvement. Prevalently bipolar stimulation settings and high pulse widths and amplitudes led to excellent results at the expense of battery life.</p>
<p style="text-align: justify;">CONCLUSION: Improvement in all 3 subscale scores of the Toronto Western Spasmodic Torticollis Rating Scale with bilateral GPi deep brain stimulation seems to be the rule. Refinement of stimulation parameters might have a significant impact on the cost/ benefit ratio of the treatment. The dissociation of improvement in posture severity and pain provides tangible evidence of the complex nature of cervical dystonia and offers interesting insight into the complex functional organization of the GPi.</p>
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		<title>Clinical Motor Outcome of Bilateral Subthalamic Nucleus Deep-Brain Stimulation for Parkinson’s Disease Using Image-Guided Frameless Stereotaxy</title>
		<link>http://www.neurosurgery-blog.com/archives/1665</link>
		<comments>http://www.neurosurgery-blog.com/archives/1665#comments</comments>
		<pubDate>Tue, 12 Oct 2010 04:00:30 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Neuronavigation]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Frameless stereotaxy]]></category>
		<category><![CDATA[Image-guided neurosurgery]]></category>
		<category><![CDATA[Parkinson’s disease]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1665</guid>
		<description><![CDATA[Neurosurgery 67:1088–1093, 2010 DOI: 10.1227/NEU.0b013e3181ecc887
Image-guided neuronavigation has largely replaced stereotactic frames when precise, real-time anatomic localization is required during neurosurgical procedures. However, some procedures, including placement of deep-brain stimulation (DBS) leads for the treatment of movement disorders, are still performed using frame-based stereotaxy. Despite the demonstration of comparable accuracy between frame-based and ‘‘frameless’’ image-guided approaches, [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/10/STN.DBS_1.jpg"><img class="alignleft size-thumbnail wp-image-1670" title="STN.DBS" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/10/STN.DBS_1-150x150.jpg" alt="" width="120" height="120" /></a>Neurosurgery 67:1088–1093, 2010 DOI: 10.1227/NEU.0b013e3181ecc887</strong></p>
<p style="text-align: justify;">Image-guided neuronavigation has largely replaced stereotactic frames when precise, real-time anatomic localization is required during neurosurgical procedures. However, some procedures, including placement of deep-brain stimulation (DBS) leads for the treatment of movement disorders, are still performed using frame-based stereotaxy. Despite the demonstration of comparable accuracy between frame-based and ‘‘frameless’’ image-guided approaches, the clinical efficacy of frameless DBS placement has never been reported.</p>
<p style="text-align: justify;">OBJECTIVE: To analyze the outcomes of subthalamic nucleus (STN) DBS using the frameless technique for the treatment of Parkinson’s disease (PD).</p>
<p style="text-align: justify;">METHODS: Of 31 subjects (20 men) with PD for 10 6 4 years, 28 had bilateral STN DBS and 3 had unilateral STN DBS. The Unified Parkinson’s Disease Rating Scale (UPDRS) motor scale (III) and total medication doses were assessed before surgery on and off medication and off medication/ON DBS (off/ON) after 6 to 12 months of STN DBS.</p>
<p style="text-align: justify;">RESULTS: There was a 58% improvement from bilateral STN DBS in the UPDRS III (40 6 16 preoperatively off, 17 6 11 off/ON) 9.6 6 1.9 months after surgery (P , .001). This compared favorably with the published outcomes using the frame-based technique. All motor subscores improved significantly (P , .01). The mean reduction in medication was 50%. No intraoperative complications occurred, but one subject with hypertension died of a delayed hemorrhage postoperatively. Two subjects developed postoperative infections that required lead removal and antibiotics.</p>
<p style="text-align: justify;">CONCLUSIONS: Bilateral STN DBS for PD performed by an experienced team using a frameless approach results in outcomes comparable to those reported with the use of the frame-based technique.</p>
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		<title>Direct visualization of deep brain stimulation targets in Parkinson disease with the use of 7-tesla magnetic resonance imaging</title>
		<link>http://www.neurosurgery-blog.com/archives/1500</link>
		<comments>http://www.neurosurgery-blog.com/archives/1500#comments</comments>
		<pubDate>Wed, 08 Sep 2010 04:00:00 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Surgical technique]]></category>
		<category><![CDATA[neurorradiology]]></category>
		<category><![CDATA[7-tesla magnetic resonance imaging]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[internal globus pallidus]]></category>
		<category><![CDATA[Parkinson disease]]></category>
		<category><![CDATA[Subthalamic nucleus]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1500</guid>
		<description><![CDATA[J Neurosurg 113:639–647, 2010.DOI: 10.3171/2010.3.JNS091385
A challenge associated with deep brain stimulation (DBS) in treating advanced Parkinson disease (PD) is the direct visualization of brain nuclei, which often involves indirect approximations of stereotactic targets. In the present study, the authors compared T2*-weighted images obtained using 7-T MR imaging with those obtained using 1.5- and 3-T MR [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/09/STN7t.jpg"><img class="alignleft size-full wp-image-1501" title="STN7t" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/09/STN7t.jpg" alt="" width="114" height="114" /></a>J Neurosurg 113:639–647, 2010.DOI: 10.3171/2010.3.JNS091385</strong></p>
<p style="text-align: justify;">A challenge associated with deep brain stimulation (DBS) in treating advanced Parkinson disease (PD) is the direct visualization of brain nuclei, which often involves indirect approximations of stereotactic targets. In the present study, the authors compared T2*-weighted images obtained using 7-T MR imaging with those obtained using 1.5- and 3-T MR imaging to ascertain whether 7-T imaging enables better visualization of targets for DBS in PD.</p>
<p style="text-align: justify;">Methods. The authors compared 1.5-, 3-, and 7-T MR images obtained in 11 healthy volunteers and 1 patient with PD.</p>
<p style="text-align: justify;">Results. With 7-T imaging, distinct images of the brain were obtained, including the subthalamic nucleus (STN) and internal globus pallidus (GPi). Compared with the 1.5- and 3-T MR images of the STN and GPi, the 7-T MR images showed marked improvements in spatial resolution, tissue contrast, and signal-to-noise ratio.</p>
<p style="text-align: justify;">Conclusions. Data in this study reveal the superiority of 7-T MR imaging for visualizing structures targeted for DBS in the management of PD. This finding suggests that by enabling the direct visualization of neural structures of interest, 7-T MR imaging could be a valuable aid in neurosurgical procedures.</p>
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		<title>Best surgical practices: a stepwise approach to the University of Pennsylvania deep brain stimulation protocol</title>
		<link>http://www.neurosurgery-blog.com/archives/1467</link>
		<comments>http://www.neurosurgery-blog.com/archives/1467#comments</comments>
		<pubDate>Tue, 31 Aug 2010 04:00:55 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Clinical Guide]]></category>
		<category><![CDATA[Functional]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Surgical technique]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[dystonia]]></category>
		<category><![CDATA[essential tremor]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1467</guid>
		<description><![CDATA[Neurosurg Focus 29 (2):E3, 2010. (DOI: 10.3171/2010.4.FOCUS10103)
Deep brain stimulation (DBS) is the treatment of choice for otherwise healthy patients with advanced Parkinson disease who are suffering from disabling dyskinesias and motor fluctuations related to dopaminergic therapy. As DBS is an elective procedure, it is essential to minimize the risk of morbidity. Further, precision in targeting [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/08/STXbestpractice.jpg"><img class="alignleft size-full wp-image-1468" title="STXbestpractice" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/08/STXbestpractice.jpg" alt="" width="136" height="132" /></a>Neurosurg Focus 29 (2):E3, 2010. (DOI: 10.3171/2010.4.FOCUS10103)</p>
<p style="text-align: justify;">Deep brain stimulation (DBS) is the treatment of choice for otherwise healthy patients with advanced Parkinson disease who are suffering from disabling dyskinesias and motor fluctuations related to dopaminergic therapy. As DBS is an elective procedure, it is essential to minimize the risk of morbidity. Further, precision in targeting deep brain structures is critical to optimize efficacy in controlling motor features. The authors have already established an operational checklist in an effort to minimize errors made during DBS surgery. Here, they set out to standardize a strict, step-by-step approach to the DBS surgery used at their institution, including preoperative evaluation, the day of surgery, and the postoperative course. They provide careful instruction on Leksell frame assembly and placement as well as the determination of indirect coordinates derived from MR images used to target deep brain structures. Detailed descriptions of the operative procedure are provided, outlining placement of the stereotactic arc as well as determination of the appropriate bur hole location, lead placement using electrophysiology, and placement of the internal pulse generator. The authors also include their approach to preventing postoperative morbidity. They believe that a strategic, step-by-step approach to DBS surgery combined with a standardized checklist will help to minimize operating room mistakes that can compromise targeting and increase the risk of complication.</p>
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