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      Clinical Pearls and Methods for Intraoperative Motor Mapping

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          Abstract

          Resection of brain tumors involving motor areas and pathways requires the identification and preservation of various cortical and subcortical structures involved in motor control at the time of the procedure, in order to maintain the patient's full motor capacities. The use of brain mapping techniques has now been integrated into clinical practice for many years, as they help the surgeon to identify the neural structures involved in motor functions. A common definition of motor function, as well as knowledge of its neural organization, has been continuously evolving, underlining the need for implementing intraoperative strategies at the time of the procedure. Similarly, mapping strategies have been subjected to continuous changes, enhancing the likelihood of preservation of full motor capacities. As a general rule, the motor mapping strategy should be as flexible as possible and adapted strictly to the individual patient and clinical context of the tumor. In this work, we present an overview of current knowledge of motor organization, indications for motor mapping, available motor mapping, and monitoring strategies, as well as their advantages and limitations. The use of motor mapping improves resection and outcomes in patients harboring tumors involving motor areas and pathways, and should be considered the gold standard in the resection of this type of tumor.

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          Most cited references62

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          SOMATIC MOTOR AND SENSORY REPRESENTATION IN THE CEREBRAL CORTEX OF MAN AS STUDIED BY ELECTRICAL STIMULATION

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            Impact of intraoperative stimulation brain mapping on glioma surgery outcome: a meta-analysis.

            Surgery for infiltrative gliomas aims to balance tumor removal with preservation of functional integrity. The usefulness of intraoperative stimulation mapping (ISM) has not been addressed in randomized trials. This study addresses glioma surgery outcome on the basis of a meta-analysis of observational studies. A systematic search retrieved 90 reports published between 1990 and 2010 with 8,091 adult patients who had resective surgery for supratentorial infiltrative glioma, with or without ISM. Quality criteria consisted of postoperative neurologic examination details and follow-up timing. New postoperative neurologic deficits were categorized on the basis of timing and severity. Meta-analysis with a Bayesian random effects model determined summary event rates of deficits as well as gross total resection rate and eloquent locations. Meta-regression analysis explored heterogeneity among studies. Late severe neurologic deficits were observed in 3.4% (95% CI, 2.3% to 4.8%) of patients after resections with ISM, and in 8.2% (95% CI, 5.7% to 11.4%) of patients after resections without ISM (adjusted odds ratio, 0.39; 95% CI, 0.23 to 0.64). The percentages of radiologically confirmed gross total resections were 75% (95% CI, 66% to 82%) with ISM and 58% (95% CI, 48% to 69%) without ISM. Eloquent locations were involved in 99.9% (95% CI, 99.9% to 100%) of resections with ISM and in 95.8% (95% CI, 73.1% to 99.8%) of resections without ISM. Relevant sources of heterogeneity among studies were ISM, continent, and academic setting. Glioma resections using ISM are associated with fewer late severe neurologic deficits and more extensive resection, and they involve eloquent locations more frequently. This indicates that ISM should be universally implemented as standard of care for glioma surgery.
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              Cortical mechanisms underlying the organization of goal-directed actions and mirror neuron-based action understanding.

              Our understanding of the functions of motor system evolved remarkably in the last 20 years. This is the consequence not only of an increase in the amount of data on this system but especially of a paradigm shift in our conceptualization of it. Motor system is not considered anymore just a "producer" of movements, as it was in the past, but a system crucially involved in cognitive functions. In the present study we review the data on the cortical organization underlying goal-directed actions and action understanding. Our review is subdivided into two major parts. In the first part, we review the anatomical and functional organization of the premotor and parietal areas of monkeys and humans. We show that the parietal and frontal areas form circuits devoted to specific motor functions. We discuss, in particular, the visuo-motor transformation necessary for reaching and for grasping. In the second part we show how a specific neural mechanism, the mirror mechanism, is involved in understanding the action and intention of others. This mechanism is located in the same parieto-frontal circuits that mediate goal-directed actions. We conclude by indicating future directions for studies on the mirror mechanism and suggest some major topics for forthcoming research.

                Author and article information

                Contributors
                Journal
                Neurosurgery
                Neurosurgery
                neurosurgery
                Neurosurgery
                Oxford University Press
                0148-396X
                1524-4040
                March 2021
                21 January 2021
                21 January 2021
                : 88
                : 3
                : 457-467
                Affiliations
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Laboratory of Motor Control, Department of Biotechnology and Translational Medicine, Università degli Studi di Milano Milano, Italy
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Laboratory of Motor Control, Department of Biotechnology and Translational Medicine, Università degli Studi di Milano Milano, Italy
                Laboratory of Motor Control, Department of Biotechnology and Translational Medicine, Università degli Studi di Milano Milano, Italy
                Laboratory of Motor Control, Department of Biotechnology and Translational Medicine, Università degli Studi di Milano Milano, Italy
                Laboratory of Motor Control, Department of Biotechnology and Translational Medicine, Università degli Studi di Milano Milano, Italy
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Neurosurgery , Department of Oncology and Hemato-Oncology, Università degli Studi di Milano , Milano, Italy
                Author notes
                Correspondence: Lorenzo Bello, Neurosurgery, Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, Via Francesco Sforza 35, 20122, Milano, Italy. E-mail: lorenzo.bello@ 123456unimi.it

                Marco Rossi and Tommaso Sciortino contributed equally to this work.

                Author information
                http://orcid.org/0000-0002-0196-2370
                http://orcid.org/0000-0001-7191-2822
                Article
                nyaa359
                10.1093/neuros/nyaa359
                7884143
                33476393
                f62b9a9a-93c8-4c20-beaa-41bcce847288
                Congress of Neurological Surgeons 2021.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@ 123456oup.com

                History
                : 07 February 2020
                : 26 April 2020
                Page count
                Pages: 11
                Categories
                Neuros/19
                Surgical Management of Eloquent Area Tumors
                AcademicSubjects/MED00930

                motor control,brain tumors,motor mapping techniques,monitoring techniques,motor area tumors,glioma,awake surgery,oncological balance

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