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DOI: 10.1055/s-2005-915627
Association of Motor Deficits with Head Position during Awake Surgery for Resection of Medial Motor Area Brain Tumors
Publication History
Publication Date:
23 January 2006 (online)
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Abstract
Objective: Resection of tumors involving the motor area frequently results in postoperative motor deficits. In an attempt to prevent poor motor outcomes, our institution has utilized preoperative fMRI and tractography as well as intraoperative cortical mapping and continuous motor tasks during awake surgery in patients with motor area tumors. In one case, a patient demonstrated deterioration in continuous motor task performance before initiation of tumor resection. Thus, the goal of this study was to evaluate the relationship between head position and development of intraoperative or postoperative motor deficits in five patients with motor area tumors. Clinical Presentation: In four cases, the patient’s head was rotated 60 degrees from the supine position. In two cases, in which the tumor was located relatively medially, deterioration in continuous motor task function was noted prior to resection of the tumor. In the two other cases, in which the tumor was located relatively laterally, there was no deterioration of continuous motor task performance until resection of the tumor. Another patient, in whom the tumor was located relatively medially, underwent surgery with the head positioned straight and with the patient in a half-sitting position. This patient did not experience deterioration of continuous motor task performance during the surgery. Conclusion: These data suggest that head positioning can have a significant impact on motor function in patients with motor area tumors. Furthermore, the straight head position may be the preferred positioning, particularly for patients with tumors located on the medial side of motor area.
Key words
Head position - motor deficit - awake surgery
References
- 1 Yousry T A, Schmid U D, Jassoy A G, Schmidt D, Eisner W E, Reulen H J, Reiser M F, Lissner J. Topography of the cortical motor hand area: prospective study with functional MR imaging and direct motor mapping at surgery. Radiology. 1995; 195 23-29
- 2 Krings T, Reinges M HT, Erberich S, Kemeny S, Rohde V, Spetzger U, Korinth M, Willmes K, Gilsbach J M, Thron A. Functional MRI for presurgical planning: problems, artifacts, and solution strategies. J Neurol Neurosurg Psychiatry. 2001; 70 749-760
- 3 Guye M, Parker G JM, Symms M, Boulby P, Wheeler-Kingshott C AM, Salek-Haddadi A, Barker G J, Duncan J S. Combined functional MRI and tractography to demonstrate the connectivity of the human primary motor cortex in vivo. Neuroimage. 2003; 19 1349-1360
- 4 Taylor M D, Bernstein M. Awake craniotomy with brain mapping as the routine surgical approach to treating patients with supratentorial intraaxial tumors: a prospective trial of 200 cases. J Neurosurg. 1999; 90 35-41
- 5 Ebel H, Ebel M, Schillinger G, Klimek M, Sobesky J, Klug N. Surgery of intrinsic cerebral neoplasms in eloquent areas under local anesthesia. Minim Invas Neurosurg. 2000; 43 192-196
- 6 Reithmeier T, Krammer M, Gumprecht H, Gerstner W, Lumenta C B. Neuronavigation combined with electrophysiological monitoring for surgery of lesions in eloquent brain areas in 42 cases: a retrospective comparison of the neurological outcome and the quality of resection with a control group with similar lesions. Minim Invas Neurosurg. 2003; 46 65-71
- 7 Friston K J, Frith C D, Liddle P F, Frackowiak R S. Comparing functional (PET) images: the assessment significant change. J Cereb Blood Flow Metab. 1991; 11 690-699
- 8 Reese T G, Heid O, Weisskoff R M, Wedeen V J. Reduction of eddy-current-induced distortion in diffusion MRI using a twice-refocused spin echo. Magn Reson Med. 2003; 49 177-182
- 9 Lazar M, Weinstein O M, Tsuruda J S, Hasan K M, Arfanakis K, Meyerand M E, Badie B, Rowley H A, Haughton V, Field A. White matter tractography using diffusion tensor deflection. Hum Brain Mapp. 2003; 18 306-321
- 10 Conturo T E, Lori N F, Cull T S, Akbudak E, Snyder A Z, Shimoi J S, McKinstry R C, Burton H, Raichle M E. Tracking neuronal fiber pathways in the living human brain. Proc Natl Acad Sci USA. 1999; 96 10422-10427
- 11 Xue R, Zijl P C van, Crain B J, Solaiyappan M, Mori S. In vivo three-dimensional reconstruction of rat brain axonal projections by diffusion tensor imaging. Magn Reson Med. 1999; 42 1123-1127
- 12 Tongier W K, Joshi G P, Landers O F, Mickey B. Use of the laryngeal mask airway during awake craniotomy for tumor resection. J Clin Anesth. 2000; 12 592-594
- 13 Berger M S, Kincaid J, Ojemann G A, Lettich E. Brain mapping techniques to maximize resection, safety, and seizure control in children with brain tumors. Neurosurgery. 1989; 25 786-792
- 14 Ojemann G, Ojemann J, Lettich E, Berger M. Cortical language localization in left, dominant hemisphere. An electrical stimulation mapping investigation in 117 patients. J Neurosurg. 1989; 71 316-326
- 15 Hill D LG, Maurer C R, Maciunas R J, Barwise J A, Fitzpatrick J M, Matthew Y W. Measurement of intraoperative brain surface deformation under a craniotomy. Neurosurgery. 1998; 43 514-528
- 16 Whittle I R, Borthwick S, Haq N. Brain dysfunction following “awake” craniotomy, brain mapping and resection of glioma. Br J Neurosurg. 2003; 17 130-137
Nobusada Shinoura, M.D., D.Med.Sc.
Department of Neurosurgery · Komagome Metropolitan Hospital
3-18-22 Hon-Komagome
Bunkyo-ku
Tokyo 113-8677
Japan
Phone: +81-3-3823-2101 ·
Fax: +81-3-3824-1552
Email: shinoura@cick.jp