- Research article
- Open Access
- Open Peer Review
Intraoperative neuromonitoring for function-guided resection differs for supratentorial motor eloquent gliomas and metastases
© Obermueller et al. 2015
- Received: 15 October 2014
- Accepted: 15 October 2015
- Published: 20 October 2015
Recent data show differences in intraoperative neuromonitoring (IOM) in relation to the operated brain lesion. Due to the recently shown infiltrative nature of cerebral metastases, this work investigates the differences of IOM for cerebral metastases and glioma resection concerning sensitivity, specificity, and predictive values when aiming on preservation of motor function.
Between 2006 and 2011 we resected 171 eloquently located tumors (56 metastases, 115 gliomas) associated with the rolandic cortex or the pyramidal tract using IOM via direct cortical motor evoked potentials (MEPs). Postoperatively, MEP data were re-analyzed with respect to surgery-related paresis, residual tumor, and postoperative MRI with two different thresholds for MEP decline (50 and 80 % below baseline).
MEP monitoring was successful in 158 cases (92.4 %). MEPs were stable in 54.7 % of all metastases cases and in 65.2 % of all glioma cases (p < 0.0001). After metastases resection, 21.4 % of patients improved and 21.9 % deteriorated in motor function. Glioma patients improved in only 5.4 % and worsened in 31.3 % of cases (p < 0.05). Resection was stopped due to MEP decline in 8.0 % (metastases) and 34.8 % of cases (gliomas) (p < 0.0002).
There is significant difference between glioma and metastases resection. Post-hoc, metastases show more stable MEPs but a surprisingly high rate of surgery-related paresis and therefore a higher rate of false negative IOM.
For resection of gliomas within or adjacent to the motor system intraoperative neuromonitoring (IOM) is now widely used by many neurosurgeons [1–6]. Although surgery is currently limited to a subgroup of patients harboring brain metastases (BM), especially those symptomatic with a focal deficit are still considered for surgical resection in order to achieve early recovery from neurological deficits [7, 8]. Therefore, particularly metastases within or adjacent to the rolandic cortex or corticospinal tract (CST) are potentially treated by surgical resection. As current reports have shown the infiltrative nature of cerebral metastases, IOM of the motor systems might be helpful to reduce surgery-related motor deficits also in BM patiens and its use therefore increased recently [3, 9–12].
Studies on IOM by motor evoked potentials (MEP) for the resection of gliomas within the rolandic region or CST used various warning criteria with various predictive values even within a considerably homogeneous entity like gliomas [13–17].
The present study, therefore provides data on IOM of a large cohort of motor eloquently located tumors, but also provides a profound analysis of IOM data, which elucidates potential differences of IOM for surgery of supratentorial metastases compared to gliomas as also published earlier by our group. We especially focused on sensitivity, specificity, and predictive values of different warning criteria for each tumor type. Awareness has to be raised among neurosurgeons for these differences when performing surgery in motor eloquent cortex or fiber tracts for these tumor entities.
32 (61.0 %)
62 (59.1 %)
21 (39.0 %)
43 (40.9 %)
Type of primary cancer/WHO-grade
17 (30.0 %)
12 (21.0 %)
5 (9.0 %),
4 (7.0 %)
4 (7.0 %)
14 (26.0 %)
3 (2.7 %)
17 (15.2 %)
22 (19.6 %)
70 (62.5 %)
32 (57.0 %)
103 (100 %)
10 (18.0 %)
6 (11.0 %)
8 (14.0 %)
location of tumor
32 (57.0 %)
35 (31.3 %)
17 (30.0 %)
24 (21.4 %)
5 (9.0 %)
2 (4 %)
19 (17.0 %)
Intraoperative stable posthoc analysis >50 % amplitude loss
29 (54.7 %)
73 (65.2 %)
32 (60.0 %)
85 (80.1 %)
7 (13.0 %)
9 (8.6 %)
14 (27.0 %)
11 (10.3 %)
>80 % amplitude loss
30 (56.6 %)
24 (22.9 %)
20 (37.7 %)
3 (5.7 %)
11 (10.3 %)
5 (9.4 %)
19 (18.1 %)
7 (12.5 %)
14 (12.5 %)
Mean ± SD
2.9 ± 4.5
9.7 ± 10.5
The study is in accordance with ethical standards of the Declaration of Helsinki and was approved by the local institutional review board (IRB) of the Technical University Munich. The need for consent was waived by the IRB (registration number: 2826/10).
Standardized patient evaluation
Directly after anesthesia all patients were examined routinely and further assessments were performed from the first postoperative day until discharge. During follow-up, first at 6–8 weeks after surgery, and on a regular basis every 3–12 months this standardized protocol was conducted again. On basis of these data, temporary and permanent new surgery-related motor deficits were defined. A new permanent deficit was defined as a new or aggravated paresis due to resection that did not resolve to the preoperative status during follow-up (<6-8 weeks after surgery). A temporary deficit was defined as a new or aggravated postoperative paresis, which disappeared at least during the regular 8-week follow-up. Concerning postoperative imaging, all patients who presented with a new paresis immediately after surgery underwent a postoperative CT scan to exclude to secondary hemorrhage or ischemia. These events were regarded as secondary events, which could not be detected by IOM and therefore were excluded from subset analysis. Additionally, an MRI scan was performed within 48 h after surgery to assess the extent of tumor resection, potential diffusion impairment, increasing edema, or hemorrhage. These data were also reviewed during this study in order to find causes for potentially new postoperative deficits. During follow-up, MRI scans were also performed on a regular basis every 3–12 months depending on tumor entity and current adjuvant therapy. Follow-up MRI scans were reviewed for recurrent metastases and gliomas since the neurological status for this study was only considered during progression-free follow-up.
Intraoperative monitoring and resection procedure
All patients underwent surgical resection under total intravenous anesthesia (TIVA) by continuously administration of propofol and remifentanyl and volatile anesthetics were strictly avoided due to their interference with evoked potentials [16, 24, 25]. Neuromuscular blocking by rocuronium was used for intubation only and was avoided during surgery for the same reason. Continuous IOM by MEP monitoring was performed by a strip electrode with four to eight contacts (ADTech® strip electrode, AD Technic, City, WI, USA or Inomed Medizintechnik, Emmendingen, Germany), which was positioned onto the hand knob of the precentral gyrus. Subcortical stimulation was only used if needed in this particular surgical step. Somatosensory evoked potential phase reversal or preoperative mapping by navigated transcranial magnetic stimulation confirmed the location of the pre- and postcentral gyrus and the central sulcus [26–28]. For detection of compound muscle action potentials (CMAPs), 27-gauge disposable subdermal needle electrodes (AD-Tech needle electrode, AD-Tech, or Inomed needle electrode, Inomed Medizintechnik) were placed in a bipolar way with a distance of approximately 10 mm over relevant muscles of the contralateral side of the tumor in a standardized way: the thenar (abductor pollicis brevis), hypothenar (adductor digiti minimi), flexor carpi radialis, and brachial biceps for the upper extremity and the anterior tibial muscle for the lower extremity. Processing of the obtained data was achieved by the Axon EpocheXPe neuromonitoring system (Axon Systems, Hauppauge, New York) or the Inomed ISIS IOM system (Inomed Medizintechnik).
For stimulation, square-wave pulses with a duration of 200 to 300 microseconds, a frequency of 350 Hz, and a train of 5 pulses were applied. Stimulation intensity began with 6 mA and was increased continuously in steps of 1 mA until we were able to record a CMAP or until an upper limit of 30 mA was applied without eliciting a CMAP.
Every 2 to 60 s, sequential MEP monitoring was then performed by anodal direct cortical or subcortical stimulation of the rolandic cortex or CST until end of resection and before dural closure extensively described in earlier reports [2, 17, 29]. MEPs were continuously recorded and analyzed in real-time and monitored for amplitude and latency at least every 60 s by a technologist trained as a neurophysiologist or a neurosurgeon with certification in IOM. Depending on the status of the resection, intervals were shortened to 2 s to assure maximum safety during critical steps of resection. The MEP amplitude was evaluated by measuring peak-to-peak differences, whereas latency was defined as the span between the sequence start of the stimulation and the first assessable amplitude as also reported by other groups [17, 23, 29, 30]. During surgery, an amplitude decrease of 50 % or more of the baseline was considered a considerable decline and was immediately reported to the surgeon if not caused by technical issues. However, final consideration of the IOM data was left to the operating surgeon. He or she then reversed the supposed underlying surgical step, removed spatulas, or irrigated the exposed cortex and vasculature with warm Ringer’s solution. Moreover, when the resection was close to major blood vessels irrigation with nimodipine was performed to potentially reverse or avoid vasospasm. As soon as MEP amplitudes stabilized or recovered, tumor resection continued. Moreover, when MEP failed to recover, resection was stopped at this part of the resection cavity.
Post-hoc analysis of IOM data
Because a 50 % decline in amplitude was intraoperatively considered significant, all further data concerning surgical steps are related to this rule. A latency increase without simultaneous deterioration of amplitude was never seen in this series, so latency was excluded as a warning criteria. As all IOM data were routinely recorded and stored after every surgery, we were able to review these data post-hoc to determine the predictive value of different threshold values of substantial amplitude decline with respect to the patient’s postoperative status. Based on previous data of our and other groups, an amplitude decline of >50 and >80 % of baseline were therefore evaluated [2, 5, 6, 14, 31]. With regard to intraoperative data, incomplete reduction of compound muscle action potential (CMAP) was valued as deterioration rather than loss.
For testing the distribution of several attributes, a Chi-square or Fisher Exact test was performed. Differences between 2 groups were tested using the Mann–Whitney-Wilcoxon test for multiple comparisons on ranks for independent samples. Differences between groups were tested by the Kruskall-Wallis test for nonparametric one-way analysis of variance (ANOVA) followed by Dunn’s test as the post hoc test. All results are presented as mean ± standard deviation (SD). Median and range were also calculated (GraphPad Prism 5.0c, La Jolla, CA, USA); p < 0.05 was considered significant.
MEP monitoring was successful in 53 metastases (92.9 %) and 105 gliomas (90.5 %). Table 1 presents specific details of enrolled patients such as sex, age, type of primary cancer in metastases and number, location of tumor, preoperative status, MEP changes, and surgery-related deficits.
Correlation of tumor type and location to postoperative deficit
WHO grade of the tumor did not play a significant role for postoperative temporary or permanent impairment of motor function (p = 0.6013), but a trend towards a correlation of high grade tumors and degree of postoperative deficit is shown. None of the patients harboring WHO grade I tumors developed a new surgery-related deficits. In the WHO grade II group all new deficits were only temporary in 17.6 % of cases (n = 3). Regarding high-grade glioma (WHO grade III and IV) temporary deficits occurred in 22.7 (n = 5) and 18.6 % (n = 13) of cases. Permanent deficits were seen in 13.6 (n = 3) and 14.3 % (n = 10) in these patients. Tumor location and postoperative temporary and permanent impairment of motor function showed statistically significant differences only in the BM group (BM: p = 0.0209 vs. gliomas: p = 0.6013).
False positive and negative results
MEP decline >50 %
4/9 (44.4 %)
3 (33.3 %)
1 (11.1 %/1B)
0/7 (0.0 %)
19/85 (22.4 %)
14 (16.5 %)
5 (5.9 %/4B, 1I)
7/32 (21.8 %)
5 (17.2 %)
2 (6.9 %/1B,1 I)
2 (18.2 %)
8 (72.7 %)
3 (21.4 %)
MEP decline >80 %
5/24 (20.9 %)
4 (16.7 %)
4/30 (14.0 %)
2 (6.7 %)
2 (6.7 %/1B,1 I)
18/70 (25.7 %)
13 (18.6 %)
5 (7.1 %/4B, 1I)
4/20 (20.0 %)
3 (15 %)
1 (5.0 %/1B)
10/11 (90.9 %)
2 (18.2 %)
8 (72.7 %)
3/3 (100 %)
2 (66.7 %/1U)
Post-hoc analysis: MEP reduction >50 %
The post-hoc analysis of MEP recordings revealed stable MEP-amplitudes in only 7 BM cases (13.0 %) with unchanged neurological status in all of these cases.
Reversible decline >50 %
Out of 32 cases 25 BM patients (78.1 %) showed no new deficit. A new temporary motor deficit was found in 17.0 % (5 pts), and in 7.0 % (2 pts) motor function permanently deteriorated compared to the preoperative status. Both patients suffered from metastases within the precentral gyrus. In one case postoperative MRI revealed secondary postoperative hemorrhage and in the other patient an ischemic lesion was shown. Both presented with delayed paresis, which cannot always be detected by IOM. Thus, these events were considered to be secondary. Fig. 3c presents the data without those cases of secondary events. MEP amplitude reduction caused stop of resection in 6.0 % of these cases (2 patients). Postoperative MRI revealed residual tumor in one of these 2 cases.
In 85 glioma patients with reversible MEP decline 66 (77.6 %) remained their neurological status, while 19 patients developed transient (14 patients; 16.5 %) or permanent (5 patients; 5.9 %) new pareses. In these 5 patients suffering from permanent deficits MRI showed 4 secondary hemorrhages and one ischemia, which have to be seen as a secondary events and therefore not necessarily detectable by IOM (Fig. 3b).
Irreversible MEP decline >50 %
MEP recordings in BM cases showed an irreversible decline in 27.0 % (14 patients) of cases. No postoperative deterioration was observed in 11 patients, which represents false positive IOM. When investigating the time of continued IOM after amplitude decline, we found a range of IOM 2–27 min (median 4.7 min, mean 7.3 min) after >50 % decline. Maybe this period of IOM after MEP decline was too short to detect any MEP recovery. All but one patient harboring eloquently located gliomas and experiencing an intraoperative MEP decline of >50 % (n = 11) presented a new postoperative motor deficit. We found 2 temporary and 8 permanent pareses and had to deal with one false positive case (Table 2).
Post-hoc analysis: Intraoperative MEP reduction >80 %
Regarding 80 % decline of initial MEP amplitude as considerable deterioration, we found stable results for IOM in 56.0 % (30 patients) of BM cases and in 22.9 % (24 patients) of glioma cases. In the BM group 86.0 % (26 patients) were neurologically unchanged in contrast to 7 % (2 patients) showing new temporary and 7 % (2 patients) new permanent deficit. One of the 2 patients with a new permanent paresis developed secondary hemorrhage postoperatively representing a case of false negative IOM at first glance. Out of the 24 glioma patients 19 (79.1 %) did not change postoperatively. Temporary deficit was seen in 4 cases and one patient developed permanent new deficit due to secondary ischemia in postoperative MRI, which might represent another case of false positive IOM. Figure 3c represents graph including secondary events.
Reversible MEP decline > 80 %
BM cases: In 20 cases (38.0 %) with reversible MEP reduction, 80.0 % (16 patients) kept their neurological status, 15.0 % (3 patients) showed new transient motor deficit, and 5 % (1 pt) worsened permanently. Glioma cases: in 70 (66.7 %) with reversible MEP reduction, the neurological status was unchanged in 74.3 % (52 patients), in 18.6 % (13 patients) temporary and in 7.1 % (5 patients) permanently worsened due to secondary hemorrhage in 4 cases and one case of ischemia.
Irreversible MEP decline >80 %
Receiver Operating Characteristics
negative predictive value
positive predictive value
Intraoperative MEP loss
Out of 171 enrolled patients, 3 cases (2 BM and 1 glioma case) had complete intraoperative MEP loss. Both BM patients showed permanently new paresis. During surgery we had to stop resection in one patient of the glioma group due to MEP loss. Nevertheless the existing preoperative high-grade paresis improved significantly after surgery, so this case has to be considered as a false positive case of IOM. No further explanation was found even after thorough analyses of anesthesia protocols.
Postoperative MRI scans
UR was defined as the difference of the surgeon’s intraoperative impression of GTR and real GTR on postoperative MRI. In the BM group GTR was expected in 92.5 % and in the glioma-group in 70.6 %. MRI revealed STR in 28.0 % of all BM cases and in 41.4 % in of all glioma cases. Concerning suspected GTR, MRI revealead an UR in 21.0 % (BM) and 12.0 % (glioma) of cases (p = 144). Fig. 4 represents the unexpected residual (UR) in all enrolled cases (p = 0.226).
Influence of IOM on the course of surgery
Extent of resection
In 54.7 % of all BM cases and in 65.2 % of all glioma cases, the neurophysiologist reported significant MEP deterioration of >50 % of baseline amplitude (Table 1). In cases of BM with stable MEP residual was found in 27.0 % on postoperative MRI, whereas STR was seen in 37.0 % in glioma cases (p < 0.05). Pausing of surgery due to MEP reduction or loss was caused in 34.8 % of all glioma-patients and in 8.0 % of BM patients (p = 0.0002). Resection had to be terminated in 15.2 % (17 patients) of glioma cases and 4.0 % (2 patients) of BM cases (p = 0.037). The incidence of new permanent motor deficit correlating with extent of resection was not statistically significant in both groups (STR: BM cases 25.0 %; glioma cases 11.4 % and GTR: BM cases 12.2 %; glioma cases 13.0 %).
False positive cases
In the BM group there were those 11 cases (22.0 %) in which irreversible MEP deterioration occurred during resection of the metastatic lesion without new surgery-related permanent deficit. In these cases postoperative MRI showed suspected residual tumor in 4 patients (36.4 %). In comparison, only 10 patients with STR out of the 50 remaining no false positive cases (20 %) were found (p = 0.0292). Regarding MEP decline >80 % we only had one false positive case without residual in postoperative MRI scan. Analysing the glioma data revealed different results. No matter whether 50 or 80 % MEP decline was used as cutoff, there was only one false positive case. This patient suffered from preoperative existing high-grade paresis due to left-sided postcentral GBM. Intraoperatively MEP loss caused stop of resection and motor deficit improved postoperatively. Postoperative MRI showed no residual tumor.
Analysis of IOM characteristics
When analyzing MEP amplitude characteristics post-hoc, we also examined any amplitude reduction of more than 25 % as well as any latency prolongation of more than 10 %. Interestingly, there were differences between both groups. Regarding mean MEP reduction no statistical difference was found in both groups, whereas the mean time of reduced MEP only in the glioma group showed a significant difference between permanent and no new postoperative deficit (new permanent deficit: 445.1 ± 313.4 s [median 180.1 s; range 60.0 - 1800.0 s]; new temporary deficit: 100.1 ± 141.1 s [median 100.0 s; range 0.0 - 803.7 s]; no new deficit: 88.6 ± 64.3 s [median 80.6 s; range 0.0 - 421.3 s]; p = 0.001). Total MEP decline per recorded electrode did not reach statistical significance. But again, only in the glioma group mean time of MEP latency prolongation showed a significant difference between postoperative temporary or permanent motor deficit despite severe standard deviation (new permanent deficit: 142.1 ± 201.4 s [median 113.6 s; range 0.0 - 780.0 s]; new temporary deficit: 93.0 ± 186.3 s [median 40.0 s; range 0.0 - 816.3 s]; no new deficit: 43.2 ± 67 s [median 0.0 s; range 0.0 - 280.0 s]; p = 0.05).
In our study, both groups developed a new permanent motor deficit (BM 9.4 % vs. 12.5 % glioma), whereas the number of improved neurological status was much higher in the BM group (21.0 % vs. 5.4 %). These findings are in accordance to recent studies that reported similar results of motor function after resection of eloquently located lesions [2, 14, 17, 32]. We found a high number of UR with a trend towards a higher rate of UR in the BM group (21.0 % vs. 12.0 %; p = 0.144) without reaching statistical significance. Recently published studies could show a more infiltrative growth pattern of BM as expected in the past [1, 7]. The number of cases with estimated complete resection revealed a significant difference (p = 0.0013): In 93.0 % of BM cases GTR was expected by the surgeon in contrast to 72.0 % of GTR on postoperative MRI, which reflects the underestimation of real extent of BM.
Correlation of tumor type, location, and postoperative pareses
In the glioma group we found no significant difference between WHO grade and surgery-related pareses, but a trend towards high grade tumors and degree of postoperative new paresis was shown, which can be related to a more aggressive resection of high-grade gliomas. In terms of tumor location only the BM group showed statistically significant differences (p = 0.0209), which seems not plausible at first glance. Regarding our patient cohort and its preoperative status (preoperative paresis in 57.0 % of BM vs. 31.3 % in glioma patients), pre-existing deficit is known to be a risk-factor for postoperatively aggravated paresis.
The MEP evaluated by the neurophysiologist was more stable in glioma cases (65.2 % vs. 54.7 %). Based on different thresholds of MEP reduction we compared our results of BM cases with glioma cases in a post-hoc analysis. Contrary to the postoperative analysis of MEP recordings, the intraoperatively graded findings of the neurophysiologist show less stable MEP amplitudes during BM resection (Table 1). However, in the post-hoc analysis, MEPs were more stable in BM cases no matter what extent of MEP decline was taken. At a threshold of 80 % MEP decline we only had one false positive case instead of 11 cases at a MEP decline of 50 % (Table 2). As some other authors already stated, one reason could be the progressive depression of MEPs during general anesthesia .
As mentioned above, the median time frame of 7.5 min further recording after MEP decline could be a conceivable reason for missing a supposed MEP recovery. In the glioma group there was only one false positive case no matter what MEP decline was chosen to be considered. The other 10 of 11 cases with irreversible MEP decline all harbored high-grade gliomas and developed permanent (n = 8) and temporary (n = 2) pareses.
False negative cases
In both groups we found patients with suspected false negative IOM. All these cases could be explained by secondary events as revealed by postoperative MRI and no real false negative case was seen. Previous reports on false negative IOM are rare. Kombos et al. 2001 reported some false negative cases and Neuloh et al. described 2 patients with stable MEP recordings and new postoperative temporary mild facial palsy [32, 34]. Krieg et al. 2012 found no real false negative case in their study of predictive value of IOM in glioma surgery and all cases of motor deficits not detected by IOM could be explained by secondary events . The result of no real false negative case of IOM is a very important information for the surgeon to believe in IOM.
False positive cases
Unfortunately we had to face 11 BM cases and one glioma case that had to be categorized as false positive cases when using MEP decline >50 % to be considered. Thus, the positive predictive value (PPV) of both groups differed considerably (Table 3). When using a MEP decline >80 % as threshold level, the PPV for BM approximated to the PPV of glioma cases, which shows that IOM is not the same in both groups and is more reliable in glioma cases, respectively. Comparing false positive cases with other BM cases we were most concerned about the significantly higher rate of STR in false positive BM cases. One explanation for this high rate of false positive IOM cases in BM patients could be that BM are moved within the brain parenchyma during resection and therefore causing some kind of mass effects in vasculature with transient subcortical hypoperfusion while gliomas are resected without moving the tumor and therefore causing less pressure on surrounding brain tissue. Another explanation may be the high rate of already existing preoperative pareses in BM patients. However, we have to keep in mind that only half of these 11 patients suffered from preoperative pareses. Worth mentioning that no matter which threshold was used for MEP decline, there was no difference of PPV for glioma patients. Yet, we could not find any reason for the one false positive glioma case in this retrospective setup.
Influence of IOM on the course of surgery
Analysis of IOM characteristics
We had to face a low rate of stable MEPs in both groups with a trend to more stable MEP recordings in gliomas as graded by the neurophysiologist. Yet, small changes of MEPs did not correlate with development of postoperative new paresis, which was stated by several studies previously [2, 16, 30, 34]. Furthermore a problem was the high rate of presumably false positive IOM cases of BM, if a threshold for MEP-decline >50 % was used. This indicates that different thresholds of MEP reduction have to be adapted to the patient’s lesion [14, 32, 34]. No matter what kind of lesion we were dealing with, IOM should be combined by diffusion tensor imaging fiber tracking, subcortical stimulation and navigated transcranial magnetic stimulation (nTMS). Furthermore monitoring of somatosensory evoked potentials can help us to estimate proximity of the CST, detect changes despite stable MEPs and increase the safety of resection [16, 27, 35, 36].
Potential changes and postoperative outcome
IOM-related complications were very rare in this series, again pointing to the safety of IOM itself and the algorithms used in this considerably large series. All presumed false negative results in IOM can be explained by secondary hemorrhage or ischemia (Table 2). As some previous studies reported, if postoperative MRI scan showed no pathology, new postoperative motor deficit was always transient [2, 3]. We have to keep in mind that the shorter duration of follow-up in BM cases (0.7 months vs 6.1. months in glioma cases) maybe could not detect a recovery from permanent deficit. Apart from motor function, we still have to face the problem that we are unable to detect visual impairment or distinctive neuropsychological changes by only using cortical MEPs. Concerning the observed differences between IOM in metastases and gliomas the physiological or technical reasons are still not clear. Yet, this important issue has to undergo further investigation by a broad neurophysiological community.
In none of our cases intraoperative electrocorticography was used to detect intraoperative seizures as a confounding factor of the acquired IOM data. Senft et al. used multimodality such as intraoperative MRI combined with IOM to extend resection .
In BM cases stimulation of up to 20 mA and in one glioma case an intensity up to 30 mA was applied and therefore especially subcortical axons could be activated. In all these cases MEPs were stable and the patients developed no deterioration postoperatively. Routinely we used stimulation intensity of 6–12 mA.
We are aware of the fact that our median follow-up in BM group (0.7 months) does not allow defining a permanent deficit.
Most importantly, we also have to mention that the retrospective review of the patients’ outcome data might also have affected the results. Yet, due to the standardized neurological evaluation and follow-up of our patients, the loss of clinical information seems rather small. The short time of ongoing IOM after MEP decline or loss has to be considered, as maybe the rate of irreversible decline of MEP would have been lower.
Another major limitation of this study is that both groups differ in the number of lesions per patient, tumor location, follow-up, age, and baseline motor status (Table 1). However, due to the generally followed guidelines for indication of metastases resection, there is no option to provide two homogeneous groups to compare. Nonetheless, the differing baseline motor status might indeed be the reason for a significantly higher number of improved pareses in the BM group.
By analyzing the results of MEP monitoring, we found a difference between glioma and metastases resection. MEPs in BM patients were more stable than in glioma patients in the post-hoc analysis. Moreover, the threshold for considerable MEP decline has to be chosen differently in glioma and BM surgery to reach the same level of reliability. Due to a surprisingly high rate of surgery-related new paresis in BM patients and therefore a remarkably higher rate of false negative IOM, an amplitude decline >80 % can be recommended for BM surgery, whereas this issue does no make any difference in glioma cases.
Right now, we do not know the reason for the observed differences. Thus, this report should motivate the IOM community to clarify this issue in order to provide improved care for our patients.
The study was completely financed by institutional grants from the Department of Neurosurgery.
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- Duffau H, Lopes M, Arthuis F, Bitar A, Sichez JP, Van Effenterre R, et al. Contribution of intraoperative electrical stimulations in surgery of low grade gliomas: a comparative study between two series without (1985–96) and with (1996–2003) functional mapping in the same institution. J Neurol Neurosurg Psychiatry. 2005;76(6):845–51.PubMedPubMed CentralGoogle Scholar
- Krieg SM, Shiban E, Droese D, Gempt J, Buchmann N, Pape H, et al. Predictive value and safety of intraoperative neurophysiological monitoring with motor evoked potentials in glioma surgery. Neurosurgery. 2012;70(5):1060–71.PubMedGoogle Scholar
- Krieg SM, Schaffner M, Shiban E, Droese D, Obermuller T, Gempt J, et al. Reliability of intraoperative neurophysiological monitoring using motor evoked potentials during resection of metastases in motor-eloquent brain regions. J Neurosurg JUn. 2013;118(6):1269–78.Google Scholar
- Neuloh G, Bien CG, Clusmann H, Von LM, Schramm J. Continuous motor monitoring enhances functional preservation and seizure-free outcome in surgery for intractable focal epilepsy. Acta Neurochir(Wien). 2010;152(8):1307–14.Google Scholar
- Sanai N, Berger MS. Mapping the horizon: techniques to optimize tumor resection before and during surgery. Clin Neurosurg. 2008;55:14–9.PubMedGoogle Scholar
- Sanai N, Berger MS. Intraoperative stimulation techniques for functional pathway preservation and glioma resection. Neurosurg Focus. 2010;28(2), E1.PubMedGoogle Scholar
- Rades D, Kueter JD, Meyners T, Pluemer A, Veninga T, Gliemroth J, et al. Single brain metastasis: resection followed by whole-brain irradiation and a boost to the metastatic site compared to whole-brain irradiation plus radiosurgery. Clin Neurol Neurosurg. 2012;114(4):326–30.PubMedGoogle Scholar
- Rades D, Veninga T, Hornung D, Wittkugel O, Schild SE, Gliemroth J. Single brain metastasis: whole-brain irradiation plus either radiosurgery or neurosurgical resection. Cancer. 2012;118(4):1138–44.PubMedGoogle Scholar
- Kamp MA, Dibue M, Santacroce A, Zella SM, Niemann L, Steiger HJ, et al. The tumour is not enough or is it? Problems and new concepts in the surgery of cerebral metastases. Ecancermedicalscience. 2013;7:306.PubMedPubMed CentralGoogle Scholar
- Rowed DW, Houlden DA, Basavakumar DG. Somatosensory evoked potential identification of sensorimotor cortex in removal of intracranial neoplasms. Can J Neurol Sci. 1997;24(2):116–20.PubMedGoogle Scholar
- Yoo H, Kim YZ, Nam BH, Shin SH, Yang HS, Lee JS, et al. Reduced local recurrence of a single brain metastasis through microscopic total resection. J Neurosurg Apr. 2009;110(4):730–6.Google Scholar
- Baumert BG, Rutten I, Dehing-Oberije C, Twijnstra A, Dirx MJ, Debougnoux-Huppertz RM, et al. A pathology-based substrate for target definition in radiosurgery of brain metastases. Int J Radiat Oncol Biol Phys. 2006;66(1):187–94.PubMedGoogle Scholar
- Deletis V. Intraoperative monitoring of the functional integrity of the motor pathways. Adv Neurol. 1993;63:201–14.PubMedGoogle Scholar
- Kombos T, Picht T, Derdilopoulos A, Suess O. Impact of intraoperative neurophysiological monitoring on surgery of high-grade gliomas. J Clin Neurophysiol. 2009;26(6):422–5.PubMedGoogle Scholar
- Krammer MJ, Wolf S, Schul DB, Gerstner W, Lumenta CB. Significance of intraoperative motor function monitoring using transcranial electrical motor evoked potentials (MEP) in patients with spinal and cranial lesions near the motor pathways. Br J Neurosurg. 2009;23(1):48–55.PubMedGoogle Scholar
- Neuloh G, Pechstein U, Cedzich C, Schramm J. Motor evoked potential monitoring with supratentorial surgery. Neurosurgery. 2004;54(5):1061–70.PubMedGoogle Scholar
- Neuloh G, Pechstein U, Schramm J. Motor tract monitoring during insular glioma surgery. J Neurosurg. 2007;106(4):582–92.PubMedGoogle Scholar
- Krieg SM, Schnurbus L, Shiban E, Droese D, Obermueller T, Buchmann N, et al. Surgery of highly eloquent gliomas primarily assessed as non-resectable: risks and benefits in a cohort study. BMC Cancer. 2013;13(1):51.PubMedPubMed CentralGoogle Scholar
- Kalkanis SN, Kondziolka D, Gaspar LE, Burri SH, Asher AL, Cobbs CS, et al. The role of surgical resection in the management of newly diagnosed brain metastases: a systematic review and evidence-based clinical practice guideline. J Neurooncol Jan. 2010;96(1):33–43.Google Scholar
- Narita Y, Shibui S. Strategy of surgery and radiation therapy for brain metastases. Int J Clin Oncol. 2009;14(4):275–80.PubMedGoogle Scholar
- Sanai N, Chang S, Berger MS. Low-grade gliomas in adults. J Neurosurg Nov. 2011;115(5):948–65.Google Scholar
- Soffietti R, Baumert BG, Bello L, von Deimling A, Duffau H, Frenay M, et al. Guidelines on management of low-grade gliomas: report of an EFNS-EANO Task Force. Eur J Neurol. 2010;17(9):1124–33.PubMedGoogle Scholar
- Stummer W, Reulen HJ, Meinel T, Pichlmeier U, Schumacher W, Tonn JC, et al. Extent of resection and survival in glioblastoma multiforme: identification of and adjustment for bias. Neurosurgery. 2008;62(3):564–76.PubMedGoogle Scholar
- Neuloh G, Schramm J. Monitoring of motor evoked potentials compared with somatosensory evoked potentials and microvascular Doppler ultrasonography in cerebral aneurysm surgery. J Neurosurg. 2004;100(3):389–99.PubMedGoogle Scholar
- Scheufler KM, Zentner J. Total intravenous anesthesia for intraoperative monitoring of the motor pathways: an integral view combining clinical and experimental data. J Neurosurg. 2002;96(3):571–9.PubMedGoogle Scholar
- Cedzich C, Taniguchi M, Schafer S, Schramm J. Somatosensory evoked potential phase reversal and direct motor cortex stimulation during surgery in and around the central region. Neurosurgery. 1996;38(5):962–70.PubMedGoogle Scholar
- Krieg SM, Shiban E, Buchmann N, Gempt J, Foerschler A, Meyer B, et al. Utility of presurgical navigated transcranial magnetic brain stimulation for the resection of tumors in eloquent motor areas. J Neurosurg May. 2012;116(5):994–1001.Google Scholar
- Krieg SM, Shiban E, Buchmann N, Meyer B, Ringel F. Presurgical navigated transcranial magnetic brain stimulation for recurrent gliomas in motor eloquent areas. Clin Neurophysiol. 2013;124(3):522–7.PubMedGoogle Scholar
- Taniguchi M, Cedzich C, Schramm J. Modification of cortical stimulation for motor evoked potentials under general anesthesia: technical description. Neurosurgery. 1993;32(2):219–26.PubMedGoogle Scholar
- Suess O, Suess S, Brock M, Kombos T. Intraoperative electrocortical stimulation of Brodman area 4: a 10-year analysis of 255 cases. Head Face Med. 2006;2:20.PubMedPubMed CentralGoogle Scholar
- Kombos T, Suess O, Funk T, Kern BC, Brock M. Intra-operative mapping of the motor cortex during surgery in and around the motor cortex. Acta Neurochir(Wien). 2000;142(3):263–8.Google Scholar
- Neuloh G, Pechstein U, Cedzich C, Schramm J. Motor evoked potential monitoring with supratentorial surgery. Neurosurgery. 2007;61(1):337–46.PubMedGoogle Scholar
- Lyon R, Feiner J, Lieberman JA. Progressive suppression of motor evoked potentials during general anesthesia: the phenomenon of "anesthetic fade". J Neurosurg Anesthesiol. 2005;17(1):13–9.PubMedGoogle Scholar
- Kombos T, Suess O, Ciklatekerlio O, Brock M. Monitoring of intraoperative motor evoked potentials to increase the safety of surgery in and around the motor cortex. J Neurosurg. 2001;95(4):608–14.PubMedGoogle Scholar
- Buchmann N, Gempt J, Stoffel M, Foerschler A, Meyer B, Ringel F. Utility of diffusion tensor-imaged (DTI) motor fiber tracking for the resection of intracranial tumors near the corticospinal tract. Acta Neurochir (Wien). 2011;153(1):68–74. discussion 74.Google Scholar
- Krieg SM, Buchmann NH, Gempt J, Shiban E, Meyer B, Ringel F. Diffusion tensor imaging fiber tracking using navigated brain stimulation--a feasibility study. Acta Neurochir (Wien). 2012;154(3):555–63.Google Scholar
- Senft C, Forster MT, Bink A, Mittelbronn M, Franz K, Seifert V, et al. Optimizing the extent of resection in eloquently located gliomas by combining intraoperative MRI guidance with intraoperative neurophysiological monitoring. J Neurooncol Aug. 2012;109(1):81–90.Google Scholar