Neuromonitoring in Cervical Spine Surgery: When Is a Signal Drop Clinically Significant?

Joshua Decruz, Arun-Kumar Kaliya-Perumal, Kevin Ho-Yin Wong, Dinesh Shree Kumar, Eugene Weiren Yang, Jacob Yoong-Leong Oh
2020 Asian Spine Journal  
Retrospective cohort study. To identify the clinical significance of different patterns of intraoperative neuromonitoring (IONM) signal alerts. IONM is a long-established valuable adjunct to complex spine surgeries. IONM for cervical spine surgery is in the form of somatosensory evoked potential (SSEP) and motor evoked potential (MEP). The efficacy of both modalities (individually or in combination) to detect clinically significant neurological compromise is constantly being debated and
more » ... debated and requires conclusive suggestions. Clinical and neuromonitoring data of 207 consecutive adult patients who underwent cervical spine surgeries at multiple surgical centers using bimodal IONM were analyzed. Signal changes were divided into three groups. Group 0 had transient signal changes in either MEPs or SSEPs, group 1 had sustained unimodal changes, and group 2 had sustained changes in both MEPs and SSEPs. The incidences of true neurological deficits in each group were recorded. A total of 25% (52/207) had IONM signal alerts. Out of these signal drops, 96% (50/52) were considered to be false positives. Groups 0 and 1 had no incidence of neurological deficits, while group 2 had a 29% (2/7) rate of true neurological deficits. The sensitivities of both MEP and SSEP were 100%. SSEP had a specificity of 96.6%, while MEP had a lower specificity at 76.6%. C5 palsy rate was 6%, and there was no correlation with IONM signal alerts (p=0.73). This study shows that we can better predict its clinical significance by dividing IONM signal drops into three groups. A sustained, bimodal (MEP and SSEP) signal drop had the highest risk of true neurological deficits and warrants a high level of caution. There were no clear risk factors for false-positive alerts but there was a trend toward patients with cervical myelopathy.
doi:10.31616/asj.2020.0074 pmid:33260284 fatcat:yf7lecwczbai7of4twe4lzz6rm