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	<title>Neurosurgery Blog &#187; Movement Disorders</title>
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	<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>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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		<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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		<item>
		<title>A role of diffusion tensor imaging in movement disorder surgery</title>
		<link>http://www.neurosurgery-blog.com/archives/1416</link>
		<comments>http://www.neurosurgery-blog.com/archives/1416#comments</comments>
		<pubDate>Wed, 18 Aug 2010 04:00:57 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Movement Disorders]]></category>
		<category><![CDATA[Stereotactic neurosurgery]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[diffusion tensor imaging]]></category>
		<category><![CDATA[Fiber tractography]]></category>
		<category><![CDATA[GPi]]></category>
		<category><![CDATA[STN]]></category>
		<category><![CDATA[ViM]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1416</guid>
		<description><![CDATA[Acta Neurochir DOI 10.1007/s00701-010-0742-2
The safe and reversible nature of deep brain stimulation (DBS) has allowed movement disorder neurosurgery to become commonplace throughout the world. Fundamental understanding of individual patient’s anatomy is critical for optimizing the effects and side effects of DBS surgery. Three patients undergoing stereotactic surgery for movement disorders, at the institution’s intraoperative magnetic [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/08/DTI.jpg"><img class="alignleft size-full wp-image-1417" title="DTI" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/08/DTI.jpg" alt="" width="114" height="99" /></a>Acta Neurochir DOI 10.1007/s00701-010-0742-2</p>
<p style="text-align: justify;">The safe and reversible nature of deep brain stimulation (DBS) has allowed movement disorder neurosurgery to become commonplace throughout the world. Fundamental understanding of individual patient’s anatomy is critical for optimizing the effects and side effects of DBS surgery. Three patients undergoing stereotactic surgery for movement disorders, at the institution’s intraoperative magnetic resonance imaging operating suite, were studied with fiber tractography. Stereotactic targets and fiber tractography were determined on preoperative magnetic resonance imagings using the Schaltenbrand–Wahren atlas for definition in the BrainLab iPlan software (BrainLAB Inc., Feldkirchen, Germany). Subthalamic nucleus, globus pallidus interna, and ventral intermediate nucleus targets were studied. Diffusion tensor imaging parameters used ranged from 2 to 8 mm for volume of interest in the x/y/z planes, fiber length was kept constant at 30 mm, and fractional anisotropy threshold varied from 0.20 to 0.45. Diffusion tensor imaging tractography allowed reliable and reproducible visualization and correlation between frontal eye field, premotor, primary motor, and primary sensory cortices via corticospinal tracts and corticopontocerebellar tracts. There is an apparent increase in the number of cortical regions targeted by the fiber tracts as the region of interest is enlarged. This represents a possible mechanism of the increased effects and side effects observed with higher stimulation voltages. Currently available diffusion tensor imaging techniques allow potential methods to characterize the effects and side effects of DBS. This technology has the potential of being a powerful tool to optimize DBS neurosurgery</p>
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		<item>
		<title>Microvascular decompression for treating hemifacial spasm: lessons learned from a prospective study of 1,174 operations</title>
		<link>http://www.neurosurgery-blog.com/archives/1271</link>
		<comments>http://www.neurosurgery-blog.com/archives/1271#comments</comments>
		<pubDate>Thu, 15 Jul 2010 04:00:30 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Movement Disorders]]></category>
		<category><![CDATA[Outcome]]></category>
		<category><![CDATA[Surgical technique]]></category>
		<category><![CDATA[Hemifacial spasm]]></category>
		<category><![CDATA[Lessons]]></category>
		<category><![CDATA[Microvascular decompression]]></category>
		<category><![CDATA[Neurophysiological monitoring]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1271</guid>
		<description><![CDATA[Neurosurg Rev (2010) 33:325–334.DOI 10.1007/s10143-010-0254-9
The authors critically analyzed a large series of patients with hemifacial spasm (HFS) and who underwent microvascular decompression (MVD) under a prospective protocol. We describe several “lessons learned” that are required for achieving successful surgery and proper postoperative management.
The purpose of this study is to report on our experience during the [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/07/MVD.jpg"><img class="alignleft size-thumbnail wp-image-1272" title="MVD" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/07/MVD-150x150.jpg" alt="" width="105" height="105" /></a>Neurosurg Rev (2010) 33:325–334.DOI 10.1007/s10143-010-0254-9</p>
<p style="text-align: justify;">The authors critically analyzed a large series of patients with hemifacial spasm (HFS) and who underwent microvascular decompression (MVD) under a prospective protocol. We describe several “lessons learned” that are required for achieving successful surgery and proper postoperative management.</p>
<p style="text-align: justify;">The purpose of this study is to report on our experience during the previous 10 years with this procedure and we also discuss various related topics.</p>
<p style="text-align: justify;">From April 1997 to June 2009, over 1,200 consecutive patients underwent MVD for HFS. Among them, 1,174 patients who underwent MVD for HFS with a minimum 1 year follow-up were enrolled in the study. The median follow-up period was 3.5 years (range, 1-9.3 years). Based on the operative and medical records, the intraoperative findings and the postoperative outcomes were obtained and then analyzed. At the 1- year follow-up examination, 1,105 (94.1%) patients of the total 1,174 patients exhibited a “cured” state, and 69 (5.9%) patients had residual spasms. In all the patients, the major postoperative complications included transient hearing loss in 31 (2.6%), permanent hearing loss in 13 (1.1%), transient facial weakness in 86 (7.3%), permanent facial weakness in 9 (0.7%), cerebrospinal fluid leak in three (0.25%) and cerebellar infarction or hemorrhage in two (0.17%). There were no operative deaths.</p>
<p style="text-align: justify;">Microvascular decompression is a very effective, safe modality of treatment for hemifacial spasm. MVD is not sophisticated surgery, but having a basic understanding of the surgical procedures is required to achieve successful surgery</p>
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		<item>
		<title>Effect of subthalamic deep brain stimulation on postural abnormality in Parkinson disease</title>
		<link>http://www.neurosurgery-blog.com/archives/1145</link>
		<comments>http://www.neurosurgery-blog.com/archives/1145#comments</comments>
		<pubDate>Tue, 22 Jun 2010 04:00:24 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Movement Disorders]]></category>
		<category><![CDATA[camptocormia]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Parkinson disease]]></category>
		<category><![CDATA[Pisa syndrome]]></category>
		<category><![CDATA[postural abnormality]]></category>
		<category><![CDATA[Subthalamic nucleus]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1145</guid>
		<description><![CDATA[J Neurosurg 112:1283–1288, 2010.DOI: 10.3171/2009.10.JNS09917
Parkinson disease (PD) is often accompanied by various postural abnormalities such as camptocormia (bent spine) or Pisa syndrome (lateral flexion). The authors studied the effect of subthalamic nucleus deep brain stimulation (STN DBS) on postural abnormality in patients with PD.
Methods. The authors retrospectively reviewed the clinical course of 18 patients who [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/06/camptocormia1.jpg"><img class="alignleft size-full wp-image-1173" title="camptocormia" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/06/camptocormia1.jpg" alt="" width="68" height="107" /></a>J Neurosurg 112:1283–1288, 2010.DOI: 10.3171/2009.10.JNS09917</p>
<p style="text-align: justify;">Parkinson disease (PD) is often accompanied by various postural abnormalities such as camptocormia (bent spine) or Pisa syndrome (lateral flexion). The authors studied the effect of subthalamic nucleus deep brain stimulation (STN DBS) on postural abnormality in patients with PD.</p>
<p style="text-align: justify;"><strong>Methods</strong>. The authors retrospectively reviewed the clinical course of 18 patients who suffered from significant postural abnormality and underwent bilateral STN DBS. Patients whose preoperative posture score (Unified Parkinson’s Disease Rating Scale III, item 28) was 2 or more in the “medication-on” state were enrolled in this study. Eight patients were considered to have camptocormia, and 10 patients were considered to have so-called Pisa syndrome. Nine patients showed apparent thoracolumbar spinal deformity on radiography. Most patients had significant motor fluctuations from levodopa.</p>
<p style="text-align: justify;"><strong>Results</strong>. In 13 patients with moderate postural abnormality (score of 2 on item 28), 9 patients improved soon after surgery, but 1 patient relapsed. Two patients improved gradually over a long period after surgery, whereas 2 patients did not improve at all. In 5 patients with severe postural abnormality (score of 3 or 4 on item 28), 2 patients improved slightly in the long-term follow-up period after surgery, but 3 patients did not improve at all.</p>
<p style="text-align: justify;"><strong>Conclusions</strong>. Postural abnormality in patients with PD could be ameliorated by STN DBS, and therefore surgery should be considered before irreversible spinal deformity develops</p>
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		<item>
		<title>Implantation of Deep Brain Stimulator Electrodes Using Interventional MRI</title>
		<link>http://www.neurosurgery-blog.com/archives/74</link>
		<comments>http://www.neurosurgery-blog.com/archives/74#comments</comments>
		<pubDate>Sat, 22 Aug 2009 21:50:45 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Functional]]></category>
		<category><![CDATA[Movement Disorders]]></category>
		<category><![CDATA[DBS]]></category>
		<category><![CDATA[Deep Brain Stimulation]]></category>
		<category><![CDATA[Interventional MRI]]></category>
		<category><![CDATA[Neurosurgery]]></category>
		<category><![CDATA[Parkinson disease]]></category>
		<category><![CDATA[Subthalamic nucleus]]></category>
		<category><![CDATA[Surgical methods]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=74</guid>
		<description><![CDATA[Philip A. Starr, MD, Alastair J.Martin, PhD, Paul S. Larson, MD
Neurosurgery Clinics of North America
Volume 20, Issue 2, Pages 207-217 (April 2009)
The authors describe a method for placement of deep brain stimulator electrodes using interventional MRI in conjunction with a skull-mounted aiming device (Medtronic Nexframe). This approach adapts the procedure to a standard-configuration 1.5-T diagnostic [...]]]></description>
			<content:encoded><![CDATA[<p>Philip A. Starr, MD, Alastair J.Martin, PhD, Paul S. Larson, MD</p>
<p>Neurosurgery Clinics of North America</p>
<p><span><span><a href="http://www.neurosurgery.theclinics.com/issues?Vol=20">Volume 20</a></span>, <span><a href="http://www.neurosurgery.theclinics.com/issues/contents?issue_key=S1042-3680%2809%29X0002-1">Issue 2</a></span>, Pages 207-217 (April 2009)</span></p>
<p>The authors describe a method for placement of deep brain stimulator electrodes using interventional MRI in conjunction with a skull-mounted aiming device (Medtronic Nexframe). This approach adapts the procedure to a standard-configuration 1.5-T diagnostic MRI scanner in a radiology suite. Preoperative imaging, device implantation, and postimplantation MRI are integrated into a single procedure performed under general anesthesia, providing real-time, high-resolution magnetic resonance confirmation of electrode position. The method is conceptually simpler than the current standard technique for deep brain stimulator placement, as it eliminates the stereotactic frame, the subsequent requirement for registration of the brain in stereotactic space, physiologic testing, and the need for patient cooperation. With further technical refinement, the interventional MRI method should improve the accuracy, safety, and speed of deep brain stimulator electrode placement.</p>

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