dc.contributor.author
Rosenstock, Tizian
dc.contributor.author
Tuncer, Mehmet Salih
dc.contributor.author
Münch, Max Richard
dc.contributor.author
Vajkoczy, Peter
dc.contributor.author
Picht, Thomas
dc.contributor.author
Faust, Katharina
dc.date.accessioned
2021-09-30T12:23:50Z
dc.date.available
2021-09-30T12:23:50Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/32128
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-31856
dc.description.abstract
Background The resection of a motor-eloquent glioma should be guided by intraoperative neurophysiological monitoring (IOM) but its interpretation is often difficult and may (unnecessarily) lead to subtotal resection. Navigated transcranial magnetic stimulation (nTMS) combined with diffusion-tensor-imaging (DTI) is able to stratify patients with motor-eloquent lesion preoperatively into high- and low-risk cases with respect to a new motor deficit. Objective To analyze to what extent preoperative nTMS motor risk stratification can improve the interpretation of IOM phenomena. Methods In this monocentric observational study, nTMS motor mapping with DTI fiber tracking of the corticospinal tract was performed before IOM-guided surgery for motor-eloquent gliomas in a prospectively collected cohort from January 2017 to October 2020. Descriptive analyses were performed considering nTMS data (motor cortex infiltration, resting motor threshold (RMT), motor evoked potential (MEP) amplitude, latency) and IOM data (transcranial MEP monitoring, intensity of monopolar subcortical stimulation (SCS), somatosensory evoked potentials) to examine the association with the postoperative motor outcome (assessed at day of discharge and at 3 months). Results Thirty-seven (56.1%) of 66 patients (27 female) with a median age of 48 years had tumors located in the right hemisphere, with glioblastoma being the most common diagnosis with 39 cases (59.1%). Three patients (4.9%) had a new motor deficit that recovered partially within 3 months and 6 patients had a persistent deterioration (9.8%). The more risk factors of the nTMS risk stratification model (motor cortex infiltration, tumor-tract distance (TTD) <= 8mm, RMTratio 110%) were detected, the higher was the risk for developing a new postoperative motor deficit, whereas no patient with a TTD >8mm deteriorated. Irreversible MEP amplitude decrease >50% was associated with worse motor outcome in all patients, while a MEP amplitude decrease <= 50% or lower SCS intensities <= 4mA were particularly correlated with a postoperative worsened motor status in nTMS-stratified high-risk cases. No patient had postoperative deterioration of motor function (except one with partial recovery) when intraoperative MEPs remained stable or showed only reversible alterations. Conclusions The preoperative nTMS-based risk assessment can help to interpret ambiguous IOM phenomena (such as irreversible MEP amplitude decrease <= 50%) and adjustment of SCS stimulation intensity.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
navigated transcranial magnetic stimulation (nTMS)
en
dc.subject
brain tumor surgery
en
dc.subject
motor outcome
en
dc.subject
diffusion tensor imaging
en
dc.subject
intraoperative neurophysiological monitoring (IOM)
en
dc.subject
motor-evoked potential (MEP)
en
dc.subject
subcortical stimulation
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Preoperative nTMS and Intraoperative Neurophysiology - A Comparative Analysis in Patients With Motor-Eloquent Glioma
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
676626
dcterms.bibliographicCitation.doi
10.3389/fonc.2021.676626
dcterms.bibliographicCitation.journaltitle
Frontiers in Oncology
dcterms.bibliographicCitation.originalpublishername
Frontiers Media SA
dcterms.bibliographicCitation.volume
11
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
34094981
dcterms.isPartOf.eissn
2234-943X