<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Neurosurgery Blog &#187; Trauma</title>
	<atom:link href="http://www.neurosurgery-blog.com/archives/category/trauma/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>
	<lastBuildDate>Thu, 09 Feb 2012 23:00:45 +0000</lastBuildDate>
	<generator>http://wordpress.org/?v=2.9.1</generator>
	<language>en</language>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
			<item>
		<title>Traumatic brain injury in pediatric patients: evidence for the effectiveness of decompressive surgery</title>
		<link>http://www.neurosurgery-blog.com/archives/3466</link>
		<comments>http://www.neurosurgery-blog.com/archives/3466#comments</comments>
		<pubDate>Tue, 29 Nov 2011 23:00:37 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Pediatrics]]></category>
		<category><![CDATA[Trauma]]></category>
		<category><![CDATA[Clinical Trial]]></category>
		<category><![CDATA[decompressive surgery]]></category>
		<category><![CDATA[pediatric]]></category>
		<category><![CDATA[Traumatic brain injury]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=3466</guid>
		<description><![CDATA[Neurosurg Focus 31 (5):E5, 2011. DOI: 10.3171/2011.8.FOCUS11177
Traumatic brain injury (TBI) is the current leading cause of death in children over 1 year of age. Adequate management and care of pediatric patients is critical to ensure the best functional outcome in this population.
In their controversial trial, Cooper et al. concluded that decompressive craniectomy following TBI did [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/11/traumatic_brain_injury.jpg"><img class="alignleft size-thumbnail wp-image-3467" title="traumatic_brain_injury" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/11/traumatic_brain_injury-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurg Focus 31 (5):E5, 2011. DOI: 10.3171/2011.8.FOCUS11177</strong></p>
<p style="text-align: justify;">Traumatic brain injury (TBI) is the current leading cause of death in children over 1 year of age. Adequate management and care of pediatric patients is critical to ensure the best functional outcome in this population.</p>
<p style="text-align: justify;">In their controversial trial, Cooper et al. concluded that decompressive craniectomy following TBI did not improve clinical outcome of the analyzed adult population. While the study did not target pediatric populations, the results do raise important and timely clinical questions regarding the effectiveness of decompressive surgery in pediatric patients. There is still a paucity of evidence regarding the effectiveness of this therapy in a pediatric population, and there is an especially noticeable knowledge gap surrounding age-stratified interventions in pediatric trauma.</p>
<p style="text-align: justify;">The purposes of this review are to first explore the anatomical variations between pediatric and adult populations in the setting of TBI. Second, the authors assess how these differences between adult and pediatric populations could translate into differences in the impact of decompressive surgery following TBI.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/3466/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Increased incidence of nonaccidental head trauma in infants associated with the economic recession</title>
		<link>http://www.neurosurgery-blog.com/archives/3079</link>
		<comments>http://www.neurosurgery-blog.com/archives/3079#comments</comments>
		<pubDate>Thu, 25 Aug 2011 22:00:46 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Pediatrics]]></category>
		<category><![CDATA[Trauma]]></category>
		<category><![CDATA[economic recession]]></category>
		<category><![CDATA[Glasgow Coma Scale]]></category>
		<category><![CDATA[nonaccidental head trauma]]></category>
		<category><![CDATA[unemployment]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/archives/3079</guid>
		<description><![CDATA[J Neurosurg Pediatrics 8:171-176, 2011.DOI: 10.3171/2011.5.PEDS1139
Nonaccidental head trauma (NAHT) is a major cause of death in infants. During the current economic recession, the authors noticed an anecdotal increase in infants with NAHT without an increase in the overall number of infants admitted with traumatic injuries. An analysis was performed to determine whether there was an [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/08/Nonaccidental-head-trauma-rates-rise-during-economic-recession.jpg"><img class="alignleft size-thumbnail wp-image-3078" title="Nonaccidental head trauma rates rise during economic recession" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/08/Nonaccidental-head-trauma-rates-rise-during-economic-recession-150x150.jpg" alt="" width="150" height="150" /></a>J Neurosurg Pediatrics 8:171-176, 2011.DOI: 10.3171/2011.5.PEDS1139</strong></p>
<p style="text-align: justify;">Nonaccidental head trauma (NAHT) is a major cause of death in infants. During the current economic recession, the authors noticed an anecdotal increase in infants with NAHT without an increase in the overall number of infants admitted with traumatic injuries. An analysis was performed to determine whether there was an association between economic recession and NAHT.</p>
<p style="text-align: justify;">Methods. With Institutional Review Board approval, the trauma database was searched for NAHT in infants 0–2 years old during nonrecession (December 2001 to November 2007) and recession (December 2007 to June 2010) periods. Incidence is reported as infants with NAHT per month summarized over time periods. Continuous variables were compared using Mann-Whitney U-tests, and proportions were compared using the Fisher exact test.</p>
<p style="text-align: justify;">Results. Six hundred thirty-nine infant traumas were observed during the study time period. From the nonrecession to the recession period, there was an 8.2% reduction in all traumas (458 in 72 months [6.4 /month] vs 181 in 31 months [5.8/month]) and a 3.5% reduction in accidental head traumas (142 in 72 months [2.0/month] vs 59 in 31 months [1.9/month]). Nonaccidental head trauma accounted for 14.6% of all traumas (93/639). The median patient age was 4.0 months and 52% were boys. There were no significant differences in the representative counties of referral or demographics between nonrecession and recession populations (all p &gt; 0.05). The monthly incidence rates of NAHT doubled from nonrecession to recession periods (50 in 72 months [0.7/month] vs 43 in 31 months [1.4/month]; p = 0.01). During this recession, at least 1 NAHT was reported in 68% of the months compared with 44% of the months during the nonrecession period (p = 0.03). The severity of NAHTs also increased, with a greater proportion of deaths (11.6% vs 4%, respectively; p = 0.16) and severe brain injury (Glasgow Coma Scale score ≤ 8: 19.5% vs 4%, respectively; p = 0.06) during the recession.</p>
<p style="text-align: justify;">Conclusions. In the context of an overall reduction in head trauma, the significant increase in the incidence of NAHT appears coincident with economic recession. Although the cause is likely multifactorial, a full analysis of the basis of this increase is beyond the scope of this study. This study highlights the need to protect vulnerable infants during challenging economic times.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/3079/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>O-Arm–Guided Balloon Kyphoplasty: Prospective Single-Center Case Series of 54 Consecutive Patients</title>
		<link>http://www.neurosurgery-blog.com/archives/2735</link>
		<comments>http://www.neurosurgery-blog.com/archives/2735#comments</comments>
		<pubDate>Tue, 07 Jun 2011 22:00:31 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Neuronavigation]]></category>
		<category><![CDATA[Spine]]></category>
		<category><![CDATA[Trauma]]></category>
		<category><![CDATA[Balloon kyphoplasty]]></category>
		<category><![CDATA[Minimal invasive spinal surgery]]></category>
		<category><![CDATA[O-arm intraoperative system]]></category>
		<category><![CDATA[Radiation exposure]]></category>
		<category><![CDATA[Vertebral compression fractures]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=2735</guid>
		<description><![CDATA[Neurosurgery 68[ONS Suppl 2]:ons250–ons256, 2011 DOI: 10.1227/NEU.0b013e31821421b9
Balloon kyphoplasty is widely used to treat vertebral compression fractures. Procedure outcome and safety are directly linked to precise radiological imaging requiring 1 or 2 C arms to allow correct visualization throughout the procedure. This minimally invasive spinal surgery is associated with radiation exposure for both patient and surgeon. [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/06/O_Arm_Guided_Balloon_Kyphoplasty__Prospective1.jpg"><img class="alignleft size-thumbnail wp-image-2739" title="O_Arm_Guided_Balloon_Kyphoplasty__Prospective" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/06/O_Arm_Guided_Balloon_Kyphoplasty__Prospective1-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 68[ONS Suppl 2]:ons250–ons256, 2011 DOI: 10.1227/NEU.0b013e31821421b9</strong></p>
<p style="text-align: justify;">Balloon kyphoplasty is widely used to treat vertebral compression fractures. Procedure outcome and safety are directly linked to precise radiological imaging requiring 1 or 2 C arms to allow correct visualization throughout the procedure. This minimally invasive spinal surgery is associated with radiation exposure for both patient and surgeon. In our center, we switched from using a C-arm to an O-arm image guidance system to perform balloon kyphoplasty. Our preliminary experience is reported in Acta Neurochirurgica, and the encouraging results led us to study this subject more extensively. This article presents our complete results. To the best of our knowledge, there is no comparable clinical series describing O-arm use in kyphoplasty procedures published in the literature. OBJECTIVE: To report our complete results of using the O-arm guidance system to perform balloon kyphoplasty.</p>
<p style="text-align: justify;">METHODS: We prospectively evaluated O-arm–guided kyphoplasty procedure in 54 consecutive patients and measured x-ray exposure and fluoroscopy time.</p>
<p style="text-align: justify;">RESULTS: The mean surgical time for the procedure was 38 minutes with a mean fluoroscopy procedure time of 3.1 minutes. The mean fluoroscopy time by level was 2.5 minutes. Mean irradiation dose by procedure was 220 mGy and by level was 166 mGy. There was a significant reduction in fluoroscopy time and x-ray exposure from 5.1 minutes with classic C-arm use to 3.1 minutes when with O-arm use without additional time required for positioning the system.</p>
<p style="text-align: justify;">CONCLUSION: With this new intraoperative system, the overall surgical and fluoroscopy times can be further reduced in the near future.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/2735/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Risk Factors for Conversion to Permanent Ventricular Shunt in Patients Receiving Therapeutic Ventriculostomy for Traumatic Brain Injury</title>
		<link>http://www.neurosurgery-blog.com/archives/2018</link>
		<comments>http://www.neurosurgery-blog.com/archives/2018#comments</comments>
		<pubDate>Tue, 04 Jan 2011 05:00:35 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Trauma]]></category>
		<category><![CDATA[hydrocephalus]]></category>
		<category><![CDATA[Hemorrhage]]></category>
		<category><![CDATA[shunt]]></category>
		<category><![CDATA[Ventriculostomy]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=2018</guid>
		<description><![CDATA[Neurosurgery 68:85–88, 2011 DOI: 10.1227/NEU.0b013e3181fd85f4
Intracranial pressure is routinely monitored in patients with severe traumatic brain injury (TBI). Patients with TBI sometimes develop hydrocephalus, requiring permanent cerebrospinal fluid (CSF) diversion. OBJECTIVE: To quantify the need for permanent CSF diversion in patients with TBI. METHODS: Patients who received a ventriculostomy after TBI between June 2007 and July [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2011/01/TBI1.jpg"><img class="alignleft size-thumbnail wp-image-2022" title="TBI" src="http://www.neurosurgery-blog.com/wp-content/uploads/2011/01/TBI1-150x150.jpg" alt="" width="150" height="150" /></a>Neurosurgery 68:85–88, 2011 DOI: 10.1227/NEU.0b013e3181fd85f4</strong></p>
<p style="text-align: justify;">Intracranial pressure is routinely monitored in patients with severe traumatic brain injury (TBI). Patients with TBI sometimes develop hydrocephalus, requiring permanent cerebrospinal fluid (CSF) diversion. OBJECTIVE: To quantify the need for permanent CSF diversion in patients with TBI. METHODS: Patients who received a ventriculostomy after TBI between June 2007 and July 2008 were identified, and their medical records were abstracted to a database. RESULTS: Sixteen of 71 patients (22.5%) receiving a ventriculostomy required a ventriculoperitoneal or ventriculoatrial shunt before discharge from the hospital. The average number of days between ventriculostomy and shunt was 18.3. Characteristics that predispose these patients to require permanent CSF diversion include the need for craniotomy within 48 hours of admission (odds ratio, 5.20; 95% confidence interval, 1.48-18.35) and history of culture-positive CSF (odds ratio, 5.52; 95% confidence interval, 1.19-25.52). Length of stay was increased in patients receiving permanent CSF diversion (average length of stay, 61 vs 31 days; P = .04). Patient discharge disposition was similar between shunted and nonshunted patients. CONCLUSION: In this retrospective study, 22% of TBI patients who required a ventriculostomy eventually needed permanent CSF diversion. Patients with TBI should be assessed for the need for permanent CSF diversion before discharge from the hospital. Care must be taken to prevent ventriculitis. Future studies are needed to evaluate more thoroughly the risk factors for the need for permanent CSF diversion in this patient population.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/2018/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>“In-window” craniotomy and “bridgelike” duraplasty: an alternative to decompressive hemicraniectomy</title>
		<link>http://www.neurosurgery-blog.com/archives/1857</link>
		<comments>http://www.neurosurgery-blog.com/archives/1857#comments</comments>
		<pubDate>Fri, 26 Nov 2010 05:00:14 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Surgical technique]]></category>
		<category><![CDATA[Trauma]]></category>
		<category><![CDATA[brain trauma]]></category>
		<category><![CDATA[cerebral venous sinus thrombosis]]></category>
		<category><![CDATA[cranioplasty]]></category>
		<category><![CDATA[decompressive hemicraniectomy]]></category>
		<category><![CDATA[duraplasty]]></category>
		<category><![CDATA[in-window craniotomy]]></category>
		<category><![CDATA[malignant cerebral ischemia]]></category>
		<category><![CDATA[Stroke]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1857</guid>
		<description><![CDATA[J Neurosurg 113:982–989, 2010. DOI: 10.3171/2009.11.JNS09674
The object of this study was to propose an alternative procedure to the classic decompressive hemicraniectomy using an “in-window” craniotomy and a “bridgelike” duraplasty.
Methods. The authors performed a large, almost rectangular craniotomy involving the frontal, temporal, and parietal bones and part of the occipital squama in 5 patients. The dura [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/11/inwindowcranio.jpg"><img class="alignleft size-thumbnail wp-image-1859" title="inwindowcranio" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/11/inwindowcranio-150x150.jpg" alt="" width="120" height="120" /></a><strong>J Neurosurg 113:982–989, 2010. DOI: 10.3171/2009.11.JNS09674</strong></p>
<p style="text-align: justify;">The object of this study was to propose an alternative procedure to the classic decompressive hemicraniectomy using an “in-window” craniotomy and a “bridgelike” duraplasty.</p>
<p style="text-align: justify;">Methods. The authors performed a large, almost rectangular craniotomy involving the frontal, temporal, and parietal bones and part of the occipital squama in 5 patients. The dura mater is opened and its area is enlarged using a rectangular dural patch of the surgeon’s choice in the form of a bridge between the anterior and posterior dural edges. With a vertical cut, the bone flap is divided into 2 similarly sized pieces that function as “window lids.” The outer frontal and occipital sides of the bone are tied to the skull border at 2 points to function as a hinge joint. The angle of the bone cut must be beveled outward (inclination ~ 45° of the bone drill or saw) to allow the bone flap to rest on the adjacent skull and prevent its slippage toward the intracranial cavity.</p>
<p style="text-align: justify;">Results. The above procedures were performed with effective control of intracranial hypertension due to cerebral venous sinus thrombosis, brain trauma, intracerebral hematoma, or malignant cerebral ischemia.</p>
<p style="text-align: justify;">Conclusions. Decompressive surgery, which uses an in-window craniotomy that gradually opens according to the intracranial pressure, is an alternative solution for deploying autologous material. The procedure has the advantage of obviating the need for a second surgical procedure to close the bone defect, and thus preventing the metabolic cerebral impairment associated with the absence of an overlying skull.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/1857/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Dysfunction of hypothalamic-hypophysial axis after traumatic brain injury in adults</title>
		<link>http://www.neurosurgery-blog.com/archives/1591</link>
		<comments>http://www.neurosurgery-blog.com/archives/1591#comments</comments>
		<pubDate>Wed, 29 Sep 2010 04:00:52 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Outcome]]></category>
		<category><![CDATA[Trauma]]></category>
		<category><![CDATA[complications]]></category>
		<category><![CDATA[hypopituitarism]]></category>
		<category><![CDATA[hypothalamic-hypophysial axis]]></category>
		<category><![CDATA[Traumatic brain injury]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1591</guid>
		<description><![CDATA[J Neurosurg 113:581–584, 2010. DOI: 10.3171/2009.10.JNS09930
Traumatic brain injury (TBI) is a major cause of serious morbidity and mortality. The incidence is 100–500/100,000 inhabitants/year. Chronic pituitary dysfunction is increasingly recognized after TBI. To define the incidence of endocrine dysfunction and risk factors, the authors describe a prospectively assessed group of patients in whom they documented hormonal [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/09/homornaldeficits.jpg"><img class="alignleft size-thumbnail wp-image-1596" title="homornaldeficits" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/09/homornaldeficits-150x150.jpg" alt="" width="120" height="120" /></a>J Neurosurg 113:581–584, 2010. DOI: 10.3171/2009.10.JNS09930</strong></p>
<p style="text-align: justify;">Traumatic brain injury (TBI) is a major cause of serious morbidity and mortality. The incidence is 100–500/100,000 inhabitants/year. Chronic pituitary dysfunction is increasingly recognized after TBI. To define the incidence of endocrine dysfunction and risk factors, the authors describe a prospectively assessed group of patients in whom they documented hormonal functions, early diagnosis, and treatment of neuroendocrine dysfunction after TBI.</p>
<p style="text-align: justify;">Methods. Patients aged 18–65 years were prospectively observed from the time of injury to 1 year postinjury; the Glasgow Coma Scale score ranged from 3 to 14. Patients underwent evaluation of hormonal function at the time of injury and at 3, 6, and 12 months postinjury. Magnetic resonance imaging was also conducted at 1 year postinjury.</p>
<p style="text-align: justify;">Results. During the study period, 89 patients were observed. The mean age of the patients was 36 years, there were 23 women, and the median Glasgow Coma Scale score was 7. Nineteen patients (21%) had primary hormonal dysfunction. Major deficits included growth hormone dysfunction, hypogonadism, and diabetes insipidus. Patients in whom the deficiency was major had a worse Glasgow Outcome Scale score, and MR imaging demonstrated empty sella syndrome more often than in patients without a deficit.</p>
<p style="text-align: justify;">Conclusions. To the authors’ knowledge, this is the third largest study of its kind worldwide. The incidence of chronic hypopituitarism after TBI was higher than the authors expected. After TBI, patients are usually observed on the neurological and rehabilitative wards, and endocrine dysfunction can be overlooked. This dysfunction can be life threatening and other clinical symptoms can worsen the neurological deficit, extend the duration of physiotherapy, and lead to mental illness. The authors recommend routine pituitary hormone testing after moderate or severe TBI within 6 months and 1 year of injury.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/1591/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Management of Type II Odontoid Fractures in the Geriatric Population</title>
		<link>http://www.neurosurgery-blog.com/archives/1295</link>
		<comments>http://www.neurosurgery-blog.com/archives/1295#comments</comments>
		<pubDate>Wed, 21 Jul 2010 04:00:49 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Outcome]]></category>
		<category><![CDATA[Spine]]></category>
		<category><![CDATA[Trauma]]></category>
		<category><![CDATA[Cervical spine]]></category>
		<category><![CDATA[Elderly]]></category>
		<category><![CDATA[geriatric]]></category>
		<category><![CDATA[management]]></category>
		<category><![CDATA[nonoperative]]></category>
		<category><![CDATA[odontoid Type 2]]></category>
		<category><![CDATA[rigid cervical collar]]></category>
		<category><![CDATA[surgical]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1295</guid>
		<description><![CDATA[J Spinal Disord Tech 2010;23:317–320
Objective: To analyze geriatric patients with Type II odontoid fractures treated either with rigid cervical orthosis (CO) or surgery (Odontoid Screw or Transarticular screw).
Summary of Background Data: Our literature search did not yield any studies on the outcome of Type II odontoid fractures in geriatric population treated with the rigid CO. [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: left;"><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/07/TypeII.jpg"><img class="alignleft size-thumbnail wp-image-1296" title="TypeII" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/07/TypeII-124x150.jpg" alt="" width="99" height="120" /></a>J Spinal Disord Tech 2010;23:317–320</p>
<p style="text-align: justify;">Objective: To analyze geriatric patients with Type II odontoid fractures treated either with rigid cervical orthosis (CO) or surgery (Odontoid Screw or Transarticular screw).</p>
<p style="text-align: justify;">Summary of Background Data: Our literature search did not yield any studies on the outcome of Type II odontoid fractures in geriatric population treated with the rigid CO. We therefore designed a study to analyze geriatric patients with Type II odontoid fractures treated with either rigid cervical collar or surgery.</p>
<p style="text-align: justify;">Materials and Methods: This is a retrospective chart review of patients with Type II odontoid fractures between July 1998 and June 2006. Inclusion criteria consists of males and females of 70 years of age or older with Type II odontoid fractures who were treated with rigid cervical collar or surgery. Exclusion criteria were displacement &gt;4mm, posteriorly displaced fracture, neurologic compromise, multilevel cervical spine injury, and treatment in a halo vest. Medical comorbidities were assessed using the Modified Cumulative Illness Rating Scale for Geriatrics. Primary outcomes were mortality and fusion (union, stable nonunion, nonunion). Minimum of 3 months follow-up was acceptable.</p>
<p style="text-align: justify;">Results: One hundred eighty four odontoid fractures were identified in 8 years. Twenty patients met our inclusion criteria (9 treated in rigid collar and 11 treated surgically). Median follow-up was 5.5 months. Out of 20 patients, 4 patients died (1 treated in CO, 3 treated surgically). Cumulative Illness Rating Scale for Geriatrics index was highest in patient treated in CO. In the rigid collar group, 6 patients had union (66.6%), and 2 developed stable nonunion (22.2%); whereas in the surgically treated group, 7 patients had union (87.5%), and 1 patient developed nonunion (12.5%).</p>
<p style="text-align: justify;">Conclusions: Patients treated nonoperatively in rigid collar seem to have an overall favorable outcome. A well-designed prospective study, to compare the outcomes of surgical intervention with nonsurgical management of Type II odontoid in elderly is recommended</p>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/1295/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Transcranial Doppler Pulsatility Index: Not an Accurate Method to Assess Intracranial Pressure</title>
		<link>http://www.neurosurgery-blog.com/archives/1139</link>
		<comments>http://www.neurosurgery-blog.com/archives/1139#comments</comments>
		<pubDate>Mon, 21 Jun 2010 04:00:33 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Outcome]]></category>
		<category><![CDATA[Technology]]></category>
		<category><![CDATA[Trauma]]></category>
		<category><![CDATA[Blood flow velocity]]></category>
		<category><![CDATA[hydrocephalus]]></category>
		<category><![CDATA[intracranial pressure]]></category>
		<category><![CDATA[middle cerebral artery]]></category>
		<category><![CDATA[Pulsatility index]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1139</guid>
		<description><![CDATA[
Neurosurgery 66 (6):1050–1057.
DOI 10.1227/01.NEU.0000369519.35932.F2

Transcranial Doppler sonography (TCD) assessment of intracranial blood flow velocity has been suggested to accurately determine intracranial pressure (ICP).
OBJECTIVE: We attempted to validate this method in patients with communicating cerebrospinal fluid systems using predetermined pressure levels.
METHODS: Ten patients underwent a lumbar infusion test, applying 4 to 5 preset ICP levels. On each level, [...]]]></description>
			<content:encoded><![CDATA[<div id="ej-article-box-text1-article-box-text">
<div style="text-align: left;"><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/06/PI1.jpg"><img class="alignleft size-medium wp-image-1142" title="PI" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/06/PI1-300x279.jpg" alt="" width="113" height="104" /></a>Neurosurgery 66 (6):1050–1057.</div>
<div style="text-align: left;">DOI 10.1227/01.NEU.0000369519.35932.F2</div>
<div style="text-align: left;">
<p style="text-align: justify;">Transcranial Doppler sonography (TCD) assessment of intracranial blood flow velocity has been suggested to accurately determine intracranial pressure (ICP).</p>
<p style="text-align: justify;">OBJECTIVE: We attempted to validate this method in patients with communicating cerebrospinal fluid systems using predetermined pressure levels.</p>
<p style="text-align: justify;">METHODS: Ten patients underwent a lumbar infusion test, applying 4 to 5 preset ICP levels. On each level, the pulsatility index (PI) in the middle cerebral artery was determined by measuring the blood flow velocity using TCD. ICP was simultaneously measured with an intraparenchymal sensor. ICP and PI were compared using correlation analysis. For further understanding of the ICP-PI relationship, a mathematical model of the intracranial dynamics was simulated using a computer.</p>
<p style="text-align: justify;">RESULTS: The ICP-PI regression equation was based on data from 8 patients. For 2 patients, no audible Doppler signal was obtained. The equation was ICP = 23*PI + 14 (R2 = 0.22, P &lt; .01, N = 35). The 95% confidence interval for a mean ICP of 20 mm Hg was −3.8 to 43.8 mm Hg. Individually, the regression coefficients varied from 42 to 90 and the offsets from −32 to +3. The mathematical simulations suggest that variations in vessel compliance, autoregulation, and arterial pressure have a serious effect on the ICP-PI relationship.</p>
<p style="text-align: justify;">CONCLUSIONS: The in vivo results show that PI is not a reliable predictor of ICP. Mathematical simulations indicate that this is caused by variations in physiological parameters.</p>
</div>
</div>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/1139/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Interhemispheric hygroma after decompressive craniectomy: does it predict posttraumatic hydrocephalus?</title>
		<link>http://www.neurosurgery-blog.com/archives/1073</link>
		<comments>http://www.neurosurgery-blog.com/archives/1073#comments</comments>
		<pubDate>Wed, 02 Jun 2010 04:00:08 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Outcome]]></category>
		<category><![CDATA[Trauma]]></category>
		<category><![CDATA[hydrocephalus]]></category>
		<category><![CDATA[decompressive craniectomy]]></category>
		<category><![CDATA[Head injury]]></category>
		<category><![CDATA[subdural hygroma]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=1073</guid>
		<description><![CDATA[Journal of Neurosurgery, June 2010. DOI: 10.3171/2010.4.JNS10132


The aim of this study was to determine the incidence of posttraumatic hydrocephalus in severely head-injured patients who required decompressive craniectomy (DC). Additional objectives were to determine the relationship between hydrocephalus and several clinical and radiological features, with special attention to subdural hygromas as a sign of distortion of the [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/06/jns10132f21.jpg"><img class="alignleft size-medium wp-image-1077" title="jns10132f2" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/06/jns10132f21-300x251.jpg" alt="" width="124" height="118" /></a>Journal of Neurosurgery, June 2010. DOI: 10.3171/2010.4.JNS10132</p>
<div>
<div>
<p style="text-align: justify;">The aim of this study was to determine the incidence of posttraumatic hydrocephalus in severely head-injured patients who required decompressive craniectomy (DC). Additional objectives were to determine the relationship between hydrocephalus and several clinical and radiological features, with special attention to subdural hygromas as a sign of distortion of the CSF circulation.</p>
<p style="text-align: justify;">Methods The authors conducted a retrospective study of 73 patients with severe head injury who required DC. The patients were admitted to the authors&#8217; department between January 2000 and January 2006. Posttraumatic hydrocephalus was defined as: 1) modified frontal horn index greater than 33%, and 2) the presence of Gudeman CT criteria. Hygromas were diagnosed based on subdural fluid collection and classified according to location of the craniectomy.</p>
<p style="text-align: justify;">Results Hydrocephalus was diagnosed in 20 patients (27.4%). After uni- and multivariate analysis, the presence of interhemispheric hygromas (IHHs) was the only independent prognostic factor for development of posttraumatic hydrocephalus (p &lt; 0.0001). More than 80% of patients with IHHs developed hydrocephalus within the first 50 days of undergoing DC. In all cases the presence of hygromas preceded the diagnosis of hydrocephalus. The IHH predicts the development of hydrocephalus after DC with 94% sensitivity and 96% specificity. The presence of an IHH showed an area under the receiver-operator characteristic of 0.951 (95% CI 0.87–1.00; p &lt; 0.0001).</p>
<p style="text-align: justify;">Conclusions Hydrocephalus was observed in 27.4% of the patients with severe traumatic brain injury who required DC. The presence of IHHs was a predictive radiological sign of hydrocephalus development within the first 6 months of DC in patients with severe head injury.</p>
</div>
</div>
<p><!-- /abstract content --></p>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/1073/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Exacerbation of Perihematomal Edema and Sterile Meningitis With Intraventricular Administration of Tissue Plasminogen Activator in Patients With Intracerebral Hemorrhage</title>
		<link>http://www.neurosurgery-blog.com/archives/802</link>
		<comments>http://www.neurosurgery-blog.com/archives/802#comments</comments>
		<pubDate>Fri, 02 Apr 2010 04:00:43 +0000</pubDate>
		<dc:creator>cba</dc:creator>
				<category><![CDATA[Trauma]]></category>
		<category><![CDATA[Vascular]]></category>
		<category><![CDATA[complications]]></category>
		<category><![CDATA[Edema]]></category>
		<category><![CDATA[Hemorrhage]]></category>
		<category><![CDATA[Intraventricular]]></category>
		<category><![CDATA[Tissue plasminogen activator]]></category>

		<guid isPermaLink="false">http://www.neurosurgery-blog.com/?p=802</guid>
		<description><![CDATA[
Neurosurgery 66:631-638, 2010. DOI: 10.1227/01.NEU.0000367634.89384.4B
Intraventricular hemorrhage (IVH) is associated with a poor outcome. External ventricular drainage together with clot lysis through intrathecal tissue plasminogen activator (IT-tPA) has been proposed as a promising therapy. However, recent experimental work has implicated tissue plasminogen activator (tPA) in the pathogenesis of cerebral edema.
METHODS: We reviewed the records of all [...]]]></description>
			<content:encoded><![CDATA[<div id="ej-article-box-text1-article-box-text">
<p><a href="http://www.neurosurgery-blog.com/wp-content/uploads/2010/04/ICH.jpg"><img class="alignleft size-full wp-image-810" title="ICH" src="http://www.neurosurgery-blog.com/wp-content/uploads/2010/04/ICH.jpg" alt="" width="87" height="99" /></a>Neurosurgery 66:631-638, 2010. DOI: 10.1227/01.NEU.0000367634.89384.4B</p>
<p style="text-align: justify;">Intraventricular hemorrhage (IVH) is associated with a poor outcome. External ventricular drainage together with clot lysis through intrathecal tissue plasminogen activator (IT-tPA) has been proposed as a promising therapy. However, recent experimental work has implicated tissue plasminogen activator (tPA) in the pathogenesis of cerebral edema.</p>
<p id="P15" style="text-align: justify;">METHODS: We reviewed the records of all patients with IVH caused by primary supratentorial intracerebral hemorrhage who underwent external ventricular drainage without surgical evacuation between January 2001 and June 2008. Of these 30 patients, we identified 13 who received IT-tPA. The remaining 17 patients served as controls. Hemorrhage, edema volume, and IVH score were determined on admission and by follow-up computed tomographic scans for 96 hours after admission. Discharge outcome was evaluated using the modified Rankin Scale.</p>
<p id="P16" style="text-align: justify;">RESULTS: There were no significant differences between the treatment and controls in terms of age, Glasgow Coma Scale score, Graeb and LeRoux IVH scores, or intracerebral hemorrhage volume on admission. IT-tPA resulted in more rapid clearance of IVH as determined by the 96-hour decrease in both the Graeb IVH score (tPA, 3.00 ± .55; control, 1.00 ± 0.57; <em>P</em> = .05) and the LeRoux IVH score (tPA, 6.2 ± 0.80; control, 2.25 ± 1.32; <em>P</em> = .05). Patients treated with IT-tPA demonstrated significantly larger peak ratios of edema to intracerebral hemorrhage volume (1.24 ± 0.14 vs 0.70 ± 0.08 in controls; <em>P</em> = .002). Additionally, increased rates of sterile meningitis (46% vs 12%; <em>P</em> = .049) and a trend toward shunt dependence (38% vs 6%; <em>P</em> = .06) were observed in the tPA cohort. Nevertheless, no significant differences in outcome at discharge or length of hospital stay were observed between cohorts.</p>
<p id="P17" style="text-align: justify;">CONCLUSION: Although IT-tPA hastens the resolution of IVH, it may worsen perihematomal edema formation. Larger prospective studies are required to confirm these findings and to determine whether outcome is adversely affected by IT-tPA administration.</p>
</div>
]]></content:encoded>
			<wfw:commentRss>http://www.neurosurgery-blog.com/archives/802/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
	</channel>
</rss>

