Abstract
In the NERFACE study part I, the characteristics of muscle transcranial electrical stimulation motor evoked potentials (mTc-MEPs) recorded from the tibialis anterior (TA) muscles with surface and subcutaneous needle electrodes were compared. The aim of this study (NERFACE part II) was to investigate whether the use of surface electrodes was non-inferior to the use of subcutaneous needle electrodes in detecting mTc-MEP warnings during spinal cord monitoring. mTc-MEPs were simultaneously recorded from TA muscles with surface and subcutaneous needle electrodes. Monitoring outcomes (no warning, reversible warning, irreversible warning, complete loss of mTc-MEP amplitude) and neurological outcomes (no, transient, or permanent new motor deficits) were collected. The non-inferiority margin was 5%. In total, 210 (86.8%) out of 242 consecutive patients were included. There was a perfect agreement between both recording electrode types for the detection of mTc-MEP warnings. For both electrode types, the proportion of patients with a warning was 0.12 (25/210) (difference, 0.0% (one-sided 95% CI, 0.014)), indicating non-inferiority of the surface electrode. Moreover, reversible warnings for both electrode types were never followed by permanent new motor deficits, whereas among the 10 patients with irreversible warnings or complete loss of amplitude, more than half developed transient or permanent new motor deficits. In conclusion, the use of surface electrodes was non-inferior to the use of subcutaneous needle electrodes for the detection of mTc-MEP warnings recorded over the TA muscles.
Keywords: muscle-recorded transcranial electrical stimulation motor evoked potential, recording electrodes, warning criteria, neurological outcome
1. Introduction
Different stimulation settings, techniques and methods are used for intraoperative neuromonitoring (IONM) with muscle-recorded transcranial electrical stimulation motor evoked potentials (mTc-MEPs) [1]. The most commonly used method is the amplitude reduction method, which can be performed with either submaximal or supramaximal stimulation [1,2]. For submaximal stimulation, the voltage is usually 20–30% above the lowest stimulation intensity required to generate a motor threshold [2]. During supramaximal stimulation, the stimulation intensity is increased beyond the stimulation intensity necessary to evoke the maximum mTc-MEP amplitude [1,3].
IONM aims to prevent intraoperative neurological injury [4,5]. If signs of impending spinal cord injury are detected early, the operating theatre team can take measures to prevent the injury from becoming permanent. With the amplitude reduction method, the criterion for impending injury is a percentage decline from baseline in the mTc-MEP amplitude. Different relative amplitude decreases have been proposed as warning criteria for the amplitude reduction method [4,6,7], but there is no consensus on the optimal relative decline. Depending on the type of surgery, warning criteria of mTc-MEPs range from a 50% to 100% decrease in amplitude compared to the baseline. With supramaximal stimulation—which is associated with lower inter-trial variability—a warning criterion of ≥80% is associated with a positive predictive value of only 0.6 [1]. Therefore, a 50% warning criterion associated with an even lower positive predictive value and higher false positive rate might be too sensitive.
Different types of recording electrodes have been proposed for recording mTc-MEPs [4]. A distinction can be made between extramuscular recording electrodes, consisting of surface and subcutaneous needle electrodes, and intramuscular recording electrodes, consisting of needle and hookwire electrodes [4,8,9].
In part I of the NERFACE study, mTc-MEP monitoring characteristics were compared between subcutaneous needle and surface recording electrodes [10]. We concluded that both recording electrodes were acceptable for mTc-MEPs for spinal cord monitoring. It is however not known whether mTc-MEP recordings from surface electrodes are of equivalent utility to mTc-MEPs recorded from subcutaneous needles for detection of mTc-MEP warnings during spinal cord monitoring.
Therefore, this study aims to investigate if the use of surface recording electrodes is non-inferior to the use of subcutaneous needle recording electrodes for the detection of mTc-MEP warnings during spinal cord monitoring. Since Kim et al. reported that recordings from the TA were better predictors of new postoperative motor deficits than recordings from the abductor hallucis muscles, we recorded mTc-MEPs from the left and right TA muscles in this study [11].
2. Materials and Methods
2.1. Study Design
This was a prospective observational study. Since the data were collected during routine clinical care, the hospital ethical committee waived the requirement for full ethical committee review following the terms of the Dutch Act on Medical Research on Human Subjects (Wet Medisch-Wetenschappelijk Onderzoek, or “WMO”). The study was, however, registered and approved by a non-WMO study evaluation committee which deemed informed consent unnecessary.
2.2. Patients
Patients were included from March 2019 until January 2022. The inclusion criteria consisted of (1) ≥12 years old, (2) patients underwent spinal cord monitoring with mTc-MEPs, (3) ≥10 mTc-MEP measurements were performed, and (4) mTc-MEPs were elicitable in at least one TA muscle (left or right).
2.3. Objectives
The primary objective of this study was to investigate if the use of surface recording electrodes was non-inferior to the use of subcutaneous needle recording electrodes in detecting mTc-MEP warnings for the left and right TA muscles during spinal cord monitoring. The secondary objective was to investigate how well mTc-MEP warnings, recorded with either surface recording electrodes or subcutaneous needle recording electrodes, predict postoperative neurological injury of the left and right TA muscle during spinal cord monitoring.
2.4. Muscle-Recorded Transcranial Electrical Stimulation Motor Evoked Potentials
The mTc-MEP monitoring method and settings were described in the NERFACE study part I [10]. Surface and subcutaneous needle electrodes were placed at the TA muscles. A detailed description of the placement of recording electrodes has been described in the NERFACE study part I [10].
An mTc-MEP warning was defined as a reproducible significant deterioration or complete loss of mTc-MEP amplitude of the left or right TA muscles, with other possible causes of deterioration or loss (i.e., technical issues, low blood pressure, increased propofol concentration) ruled out. If a warning occurred, it was communicated to the surgeon. The warning criteria depended on the type of surgery (Table 1) and were at either ≥50% or ≥80% deterioration of mTc-MEP amplitude [7]. If an mTc-MEP warning occurred only at one type of recording electrode, the warning was communicated to the surgeon. Different measures were employed to reverse the amplitude decline if a warning occurred. Measures included (1) surgical pause, (2) decreased propofol target concentration, (3) increased blood pressure, (4) irrigation of the spinal cord, (5) removal of traction/screws/hooks/sheaths, (6) autologous blood transfusion (only in the presence of anaemia) using blood recovered with the Xtra Cell Saver device (LivaNova, London, United Kingdom).
Table 1.
Warning Criteria mTc-MEP Amplitude | |
---|---|
Scoliosis surgery Neurosurgical surgeries Vascular surgeries |
≥80% decrease in mTc-MEP amplitude ≥50% decrease in mTc-MEP amplitude ≥50% decrease in mTc-MEP amplitude |
mTc-MEP, muscle-recorded transcranial electrical stimulation motor evoked potential.
For the primary objective, mTc-MEP monitoring results were classified as “no warning” or “warning”. For the secondary objective, mTc-MEP monitoring results were classified as follows: (1) no warning, (2) reversible deterioration or loss, (3) irreversible deterioration, or (4) irreversible loss. Postoperative neurological outcomes were classified as: (1) no new postoperative motor deficits, (2) transient new postoperative deficits, or (3) permanent new motor deficits. Muscle strength was determined using the Medical Research Council (MRC) scale [12]. The MRC grades range from 0 (no visible contraction) to 5 (active movement against full resistance).
2.5. Anaesthesia
Anaesthetic management was described in NERFACE study part I [10]. In short, for general anaesthesia, total intravenous anaesthesia (TIVA) using propofol with either sufentanil or remifentanil was used during all surgeries. In 110 (52.4%) patients, esketamine was administered as an analgesic adjunct.
2.6. Data Collection
mTc-MEP warnings recorded at the left and right TA muscles were collected from the clinical neurophysiologist IONM reports. mTc-MEP signals were exported from the NIM-Eclipse E4 IONM system (Medtronic BV, the Netherlands) after which the mTc-MEP amplitudes were calculated and collected using software routines written in Python (version 3.7.1). The consecutive mTc-MEP amplitudes were plotted per patient, muscle and type of recording electrode for visual inspection to objectify the warnings from the clinical neurophysiologist IONM reports. Pre- and postoperative MRC grades from the left and right TA were collected retrospectively from the electronic patient records.
2.7. Sample Size Calculation
The sample size calculation was performed using PASS V.15 (NCSS, Kaysville, Utah, USA). The subcutaneous needle recording electrode was considered the gold standard for the sample size calculation. Based on an interim analysis of the first 53 patients, in which six patients had a warning detected by both surface and subcutaneous needle electrodes, we assumed a warning proportion of 0.113 (6/53). A sample size of 210 subjects achieved 97.4% power at a 5.0% significance level using a one-sided equivalence test of correlated proportions when the standard proportion, the proportion of the warnings detected by the subcutaneous needle electrodes was 0.113. Since there was a perfect agreement in the interim analysis between the recording electrode types for the detection of an mTc-MEP warning, the maximum allowable difference between the correlated proportions that still results in equivalence (the range of equivalence) was specified at 5.0% and the actual difference of the proportions was 0.0. The observed final warning proportion was 0.119 (25/210), which was remarkably similar to the proportion from our interim analysis (proportion = 0.113). Therefore, we considered the interim sample size calculation valid for our final analysis.
2.8. Statistical Analysis
All analyses were performed in R Software version 4.0.5. (The R Foundation for Statistical Computing). Normally distributed variables were summarized using their mean and SD, while non-normally distributed as the median and interquartile range (IQR). Non-inferiority of the primary outcome was tested with the exact McNemar (paired binary) test with difference in proportions (mcnemarExactDP function in R from the exact 2 × 2 package [13]) at a one-sided 95% CI with a non-inferiority margin of 5.0%. The fragility index—the minimum number of patients with a warning detected by the subcutaneous needle recording electrode whose status (warning or no warning) must change to convert a statistically significant result to non-significant—was also calculated as a measure of robustness [14].
For the secondary outcome, monitoring results and neurological outcome were reported as frequencies in a 4 by 3 table separately for both the left TA and right TA. The sensitivity, specificity, positive predictive value, and negative predictive value were calculated separately for the left and right TA. To be able to calculate the predictive values, irreversible deterioration and irreversible loss of the mTc-MEP amplitude were defined as a warning. Transient and permanent new postoperative motor deficits were defined as motor deficits. To classify reversible warnings, we applied the method proposed by Skinner et al. [15]. The predictive values were calculated separately, in which the reversible warnings were either (1) excluded from the analysis, (2) defined as true positives, (3) defined as false positives, or (4) defined as true or false positives after the application of Hill’s causality guidelines [16]. Regarding the 4th category, only mTc-MEP warnings that reversed after removal of traction/screws/hooks/sheaths, were considered true positive warnings, similar to method reported by Skinner et al. [15].
Confidence intervals of the predictive values were calculated with the MedCacl diagnostic test evaluation calculator (MedCalc Software version 20.123, MedCalc Software Ltd., Ostend, Belgium).
3. Results
3.1. Patients
From the 242 consecutive patients, 32 (13.2%) were excluded from this study (Figure 1). Twenty-one patients had fewer than ten mTc-MEP measurements, in seven patients mTc-MEP data could not be exported, in three patients, neither the left and right TA were elicitable, and in one patient, the surface electrodes might have been incorrectly connected to the recording device. Therefore, 210 patients were included in the final analysis. Patient characteristics are shown in Table 2.
Table 2.
Patient Characteristics | Patients (n = 210) | |
---|---|---|
Median age at surgery in years (IQR) | 19 (15, 51) | |
Female N (%) | 135 (64.3) | |
Diagnosis N (%) | ||
Orthopaedic surgery | 123 (58.6) | |
Idiopathic scoliosis | 83 (39.5) | |
Congenital scoliosis | 3 (1.4) | |
Neuromuscular scoliosis | 19 (9.0) | |
Syndromic scoliosis | 15 (7.1) | |
Kyphosis | 3 (1.4) | |
Neurosurgical surgery | 67 (31.9) | |
Extradural spinal tumour | 2 (1.0) | |
Intradural extramedullary tumour | 22 (10.5) | |
Intradural intramedullary tumour | 15 (7.1) | |
Intradural cauda equina tumour | 9 (4.3) | |
Tethered spinal cord | 3 (1.4) | |
ATSCH | 4 (1.9) | |
Thoracic HNP | 6 (2.9) | |
Transdural approach | 3 (1.4) | |
Extradural approach | 3 (1.4) | |
Cervical HNP (extradural approach) | 1 (0.5) | |
Extradural spinal nerve root tumour | 3 (1.4) | |
Transdural approach | 2 (1.0) | |
Extradural approach | 1 (0.5) | |
Degenerative spine instability (extradural approach) | 1 (0.5) | |
Trauma thoracic spinal cord compression (extradural approach) | 1 (0.5) | |
Endovascular thoracic/abdominal aortic aneurysm repair | 20 (9.5) | |
Mean surgery time in minutes (SD) | 334 (111) | |
Elicitability N patients (%) | ||
TA subcutaneous needle left | 206 (98.1) | |
TA surface left | 206 (98.1) | |
TA subcutaneous needle right | 208 (99.0) | |
TA surface right | 208 (99.0) | |
Preoperative TA strength N (%) | Left | Right |
MRC 0 | 1 (0.5) | 0 (0.0) |
MRC 1 | 1 (0.5) | 0 (0.0) |
MRC 2 | 2 (1.0) | 2 (1.0) |
MRC 3 | 1 (0.5) | 4 (1.9) |
MRC 4 | 8 (3.8) | 6 (2.9) |
MRC 5 | 187 (89.0) | 187 (89.0) |
MRC < 5 * | 10 (4.8) | 11 (5.2) |
Postoperative TA strength N (%) ** | Left | Right |
MRC 0 | 2 (1.0) | 1 (0.5) |
MRC 1 | 1 (0.5) | 0 (0.0) |
MRC 2 | 1 (0.5) | 3 (1.4) |
MRC 3 | 3 (1.4) | 4 (1.9) |
MRC 4 | 11 (5.3) | 11 (5.3) |
MRC 5 | 183 (87.6) | 182 (87.1) |
MRC < 5 * | 8 (3.8) | 8 (3.8) |
* MRC grade was below five but not further specified in the medical reports. ** n = 209; in one patient, there was no postoperative neurological examination. ATSCH, anterior thoracic spinal cord herniation; HNP, hernia nucleus pulposus; MRC, medical research council scale; TA, tibialis anterior.
3.2. Primary Outcome
In 25 (11.9%) out of 210 patients, an mTc-MEP warning was detected from the left and/or right TA (Table 3). There was a perfect agreement between both recording electrode types for the detection of mTc-MEP warnings.
Table 3.
mTc-MEP Warnings Tibialis Anterior Muscles (n = 210) | |||
---|---|---|---|
Subcutaneous needle electrode | |||
+warning | −no warning | ||
Surface electrode | +warning | 25 | 0 |
−no warning | 0 | 185 |
mTc-MEP, muscle-recorded transcranial electrical stimulation motor evoked potential.
The proportion of patients with a warning detected by the subcutaneous needle electrode was 0.12 (25/210), which was equal to the proportion of patients with a warning detected by the surface recording electrode (difference, 0.0% (one-sided 95% CI, 0.014)). As the point estimate and CI of the difference were 5.0% and 3.6%, respectively, lower than the non-inferiority margin of 5.0%; the non-inferiority of the use of surface recording electrode in detecting warnings was demonstrated (Figure 2). The fragility index—the minimum number of patients with a warning detected by the use of a subcutaneous needle recording electrode whose status (warning or no warning) must change to convert a statistically significant result to non-significant—yielded six patients.
Warnings in both the left and right TA were detected in 16 patients out of 25 patients (64.0%). In five patients (20.0%), there was a warning detected in only the right TA, and in four patients (16.0%), there was a warning detected in only the left TA. Warnings always occurred simultaneously for both recording electrodes, i.e., a significant deterioration or complete loss of the mTc-MEP amplitude of the TA muscles never started earlier or later for one type of recording electrode.
Patient characteristics of the 25 patients with a warning are shown in Table 4.
Table 4.
Patient | Age | Sex | Diagnosis | mTc-MEP Warning: TAL, TAR or Both | Subsequent Action | Reversible | MRC TAL Pre-op |
MRC TAL Post-op |
MRC TAR Pre-op |
MRC TAR Post-op |
New Postoperative Deficits | D-Wave Measured |
D-Wave Warning |
D-Wave Reversible |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | 57 | F | Intradural Meningioma Th6 | Both | None | Yes | 5 | 5 | 5 | 5 | No | Yes | No | |
2 | 12 | F | Syndromic scoliosis: SMs | Both | Autologous blood transfusion, decrease of NE concentration * | Yes | 5 | 5 | 5 | 5 | No | No | ||
3 | 52 | M | HNP C6-7 (extradural) | Both | None (warning after small dura laceration, spontaneous recovery) | Yes | 5 | 5 | 5 | 5 | No | No | ||
4 | 85 | M | Endovascular aneurysm repair | Both | Removal femoral artery sheaths | Yes | 5 | 5 | 5 | 5 | No | No | ||
5 | 17 | F | Idiopathic scoliosis | Both | Increase BP, decrease propofol | Yes | 5 | 5 | 5 | 5 | No | No | ||
6 | 13 | F | Aneurysmal bone cyst C5-C6 | Both | None | No | 5 | 5 | 5 | 5 | No | No | ||
7 | 33 | M | NF1, kyphosis | Both | Increase BP, decrease propofol concentration | No | 5 | 5 | 5 | 5 | No | Yes | Yes | No |
8 | 29 | F | ATSCH | Both | None | No | 5 | 5 | 5 | 5 | No | Yes | No | |
9 | 40 | F | ATSCH | Both | None | No | 5 | 5 | 5 | 5 | No | Yes | Yes | No |
10 | 30 | F | ATSCH | TAL | None | Yes | 5 | 5 | 5 | 5 | No | Yes | No | |
11 | 68 | F | Endovascular aneurysm repair | TAL | Removal femoral artery sheath | Yes | 5 | 5 | 5 | 5 | No | No | ||
12 | 13 | M | Neuromuscular scoliosis: SMA | TAR | Removal hooks, decrease traction | Yes | <5 | <5 | <5 | <5 | No | No | ||
13 | 16 | M | Neuromuscular scoliosis: CP | TAR | Removal rod | Yes | <5 | <5 | <5 | <5 | No | No | ||
14 | 74 | M | Endovascular aneurysm repair | TAR | Removal femoral artery sheath | Yes | 5 | 5 | 5 | 5 | No | No | ||
15 | 72 | F | Endovascular aneurysm repair | TAR | Removal femoral artery sheath | Yes | 5 | 5 | 5 | 5 | No | No | ||
16 | 63 | M | Intramedullary lipoma Th1-4 | Both | None | TAL yes, TAR no | 5 | 5 | 5 | 4 | Transient | Yes *** | ||
17 | 73 | F | Spinal ependymoma C2-Th2 | Both | Increase BP | No | 5 | 3 | 5 | 0 | Transient | Yes **** | ||
18 | 50 | F | Ependymoma Th8-Th10 | Both | None | No | 5 | 4 | 5 | 4 | Transient | Yes | No | |
19 | 15 | F | Congenital scoliosis | TAL | None (warning after mechanical replacement of a nerve root) | Yes | 5 | 4 | 5 | 5 | Transient | No | ||
20 | 65 | F | HNP Th11-12 (extradural) | TAR (TAL not elicitable) | Increase BP | No | 5 | 5 | 5 | 4 | Transient | No | ||
21 | 20 | M | Congenital scoliosis | Both | Increase BP, removal temporary rod | No | 5 | 4 | 5 | 4 | Transient | No | ||
22 | 54 | F | HNP Th10-11 (transdural) | Both | Increase BP | No | 5 | 3 | 5 | 0 | TAL transient, TAR Permanent | No | ||
23 | 55 | M | Chondrosarcoma th7-9 | Both | None | No | 5 | 4 | 5 | 4 | Permanent | Yes | Yes | No |
24 | 48 | F | HNP Th8-9 (transdural) | TAL (TAR not elicitable) | Increase BP, irrigation spinal cord | No | 5 | 5 | 5 | 2 | TAL No, TAR Permanent | Yes | Yes | Yes |
25 | 12 | F | Neuromuscular scoliosis: SMA | Both | Decrease traction | TAL yes, TAR no | NA | 3 | NA | 3 | NA | No |
* Noradrenaline concentration was decreased to address possible ischemic effects due to vasoconstriction. *** D-wave amplitudes were too small and polyphasic for reliable D-wave monitoring. **** Muscle artifacts were considered too large for reliable D-wave monitoring. No muscle relaxants were administered due to the large asymmetry between the mTc-MEPs of the left and right lower limbs. mTc-MEP, muscle-recorded transcranial electrical stimulation motor evoked potential; TAL, left tibialis anterior muscle; TAR, right tibialis anterior muscle right; MRC, Medical Research Council Scale; ATSCH, anterior thoracic spinal cord herniation; NF1, neurofibromatosis type 1; HNP, herniated nucleus pulposus; CP, cerebral palsy; SMs, Smith Magenis syndrome; BP, blood pressure; NE, norepinephrine; NA, not available; SMA, spinal muscular atrophy.
3.3. Secondary Outcome
For the secondary objective, monitoring results were separately compared to the postoperative neurological outcome for the left and right TA (Table 5). Since there was a perfect agreement in monitoring results between surface recording electrodes and subcutaneous needle electrodes, no distinction was made between the recording electrodes for the secondary outcome.
Table 5.
Tibialis Anterior Left (n = 204) * | ||||
---|---|---|---|---|
New postoperative motor deficit | ||||
Permanent | Transient | None | ||
mTc-MEP result | Warning: complete loss | 1 | 2 | 1 |
Warning: irreversible deterioration | 0 | 2 | 4 | |
Reversible deterioration or loss | 0 | 1 | 8 | |
No warning | 0 | 0 | 185 | |
Tibialis Anterior Right (n = 206) ** | ||||
New postoperative motor deficit | ||||
Permanent | Transient | None | ||
mTc-MEP result | Warning: complete loss | 2 | 4 | 1 |
Warning: irreversible deterioration | 0 | 1 | 3 | |
Reversible deterioration or loss | 0 | 0 | 9 | |
No warning | 0 | 1 | 185 |
* In four patients, the tibialis anterior left was not elicitable. In one patient there was a warning; however, no preoperative neurological examination was performed. In one patient, there was no postoperative neurological examination. These six patients were excluded from this table. ** In two patients, the tibialis anterior right was not elicitable. In one patient, there was a warning; however no preoperative neurological examination was performed. In one patient, there was no postoperative neurological examination. These four patients were excluded from this table.
There were no false negatives for the left TA since all 185 patients (100.0%) without warning had no new postoperative motor deficits. For the right TA, one patient (0.5%) out of 186 patients without warning had transient new postoperative motor deficits. In this patient, the preoperative MRC of the right TA was 5 and the postoperative MRC was 4+. After three days, the MRC was 5 again.
Seven patients (58.3%) (patients 16-18, 20-23, Table 4) out of twelve patients with an irreversible deterioration or complete loss of the mTc-MEPs had either transient or permanent new postoperative motor deficits.
For the left TA, ten patients had an irreversible deterioration or complete loss of the mTc-MEP amplitude. One of them (10.0%) had permanent new postoperative motor deficits (patient 23, Table 4; follow-up: 301 days). Four patients (40.0%) had transient new postoperative motor deficits. Five patients (50.0%) had no new postoperative motor deficits of the left TA.
For the right TA, 11 patients had either an irreversible deterioration or complete loss of the mTc-MEP amplitude. Two patients (18.2%) had permanent new postoperative motor deficits (patient 22 and 23, Table 4; follow-up 77 and 301 days, respectively). Five patients (45.5%) had transient new postoperative motor deficits. Four patients (36.4%) had a false positive warning since they had no new postoperative motor deficits of the right TA muscle.
Nine patients had a reversible deterioration or loss of the left TA amplitude. Eight (88.9%) out of the nine patients did not have new postoperative motor deficits involving the left TA. One patient (11.1%) had a transient new postoperative motor deficit involving the left TA. All nine patients (100.0%) who had a reversible deterioration or loss of the right TA amplitude did not have new postoperative motor deficits. In Figure 3 a case example of a reversible warning is shown (patient 19, Table 4).
Predictive values were calculated for the left and right TA muscles and are shown in Table 6. The predictive values were calculated separately, in which the reversible warnings were either (1) excluded from the analysis, (2) defined as true positives, (3) defined as false positives or (4) defined as true or false positives after application of the Hill’s causality guidelines [16]. After application of the Hill’s causality guidelines, for the left TA, two (22.2%) out of the nine patients with a reversible warning were considered true positive (patients 4 and 11, Table 4). For the right TA, five (55.6%) out of the nine patients with a reversible warning were considered true positive (patient 4 and 12–15, Table 4).
Table 6.
Tibialis Anterior Left * | ||||
---|---|---|---|---|
Predictive values of mTc-MEP warnings for new postoperative motor deficits % (CI) | ||||
Without RW (n = 195) | RW as TP (n = 204) | RW as FP (n = 204) | RW after application of causality guidelines (n = 204) *** | |
Sensitivity | 100.0 (47.8–100.0) | 100.0 (76.8–100.0) | 100 (47.8–100.0) | 100 (59.0–100.0) |
Specificity | 97.4 (94.0–99.1) | 97.37 (94.0–99.1) | 93.0 (88.5–96.1) | 93.9 (89.6–96.8) |
Positive predictive value | 50.0 (29.6–70.4) | 73.7 (54.1–86.9) | 26.3 (17.7–37.2) | 36.8 (25.2–50.2) |
Negative predictive value | 100.0 (100.0–100.0) | 100.0 (100.0–100.0) | 100.0 (100.0–100.0) | 100.0 (100.0–100.0) |
Tibialis Anterior Right ** | ||||
Predictive values of mTc-MEP warnings for new postoperative motor deficits % (CI) | ||||
Without RW (n = 197) | RW as TP (n = 206) | RW as FP (n = 206) | RW after application of causality guidelines (n = 206) *** | |
Sensitivity | 87.5 (47.4–99.7) | 94.1 (71.3–99.9) | 87.5 (47.4–99.7) | 92.3 (64.0–99.8) |
Specificity | 97.9 (94.7–99.4) | 97.9 (94.7–99.4) | 93.4 (89.0–96.5) | 95.9 (92.0–98.2) |
Positive predictive value | 63.6 (39.1–82.7) | 80.0 (60.1–91.4) | 35.0 (23.0–49.2) | 60.0 (42.8–75.1) |
Negative predictive value | 99.5 (96.7–99.9) | 99.5 (96.5–99.2) | 99.5 (88.9–96.2) | 99.5 (91.9–98.0) |
* In four patients, the tibialis anterior left was not elicitable. In one patient there was a warning, however no preoperative neurological examination was performed. In one patient, there was no postoperative neurological examination. These six patients were excluded from this table. ** In two patients, the tibialis anterior left was not elicitable. In one patient there was a warning; however, no preoperative neurological examination was performed. In one patient, there was no postoperative neurological examination. These four patients were excluded from this table. *** For the left TA, two out of the nine patients with a reversible warning were considered true positive. For the right TA, five out of the nine patients with a reversible warning were considered true positive. RW, reversible warnings; TP, true positives; FP, false positives.
4. Discussion
This study investigated whether the use of surface recording electrodes was non-inferior to the use of subcutaneous needle electrodes for the detection of mTc-MEP warnings recorded over the TA muscles during spinal cord monitoring. There was a perfect agreement between both recording electrodes for the detection of mTc-MEP warnings. The use of surface electrodes was non-inferior to the use of subcutaneous needle electrodes for the detection of mTc-MEP warnings recorded over the TA muscles. Moreover, reversible warnings were never associated with permanent new motor deficits involving the left and right TA muscles. Among patients with irreversible warnings, transient or permanent new postoperative motor deficits were found in 5 (50.0%) out of 10 patients in the left TA and in 7 (63.6%) out of 11 patients (63.6%) in the right TA.
This is the first study that compares the frequencies and outcomes of mTc-MEP warnings recorded from the surface and subcutaneous needle electrodes over the TA muscles. All warnings were simultaneously detectable in the mTc-MEPs from both the surface and subcutaneous needle electrodes. The use of surface electrodes was non-inferior to the use of subcutaneous needle electrodes for detecting mTc-MEP warnings recorded over the TA muscles. Therefore, recording mTc-MEP amplitudes from the TA muscles with surface electrodes is as reliable as recording mTc-MEP amplitudes with subcutaneous needle electrodes for detecting mTc-MEP warnings during spinal cord monitoring of the TA muscles. To assess the robustness of our results, the fragility index was calculated. The minimum number of patients with a warning detected by the subcutaneous needle electrode whose status statistically changed our significant result to a non-significant result was n = 6. Since the higher the fragility index, the more robust the results, and in a systematic review of 40 surgical spine trials, the median fragility index was n = 2 (IQR 1, 3), we consider the fragility index of n = 6 to support the robustness of our results [17].
All patients who had a reversible warning, did not have permanent new postoperative motor deficits. Four (44.4%) out of the nine patients with reversible warnings underwent an endovascular aneurysm repair. Although, these warnings were due to the deployment of sheaths in the femoral arteries, and therefore caused ischemia of the peripheral nerves, there still was a perfect agreement between both recording electrodes. Reversible mTc-MEP warnings have proven challenging to classify as either true positive or false positive warnings, since the neurological status at the time of the warning is unknown [4]. Therefore, in this study, we applied the method proposed by Skinner et al., in which Hill’s causality guidelines were used [15,16]. Only mTc-MEP warnings that reversed after removal of traction/screws/hooks/sheaths, were considered true positive warnings, similar to the method reported by Skinner et al. This might be an underestimation of true positive mTc-MEP warnings, since one could argue that increasing blood pressure or administering autologous blood transfusion may have prevented neurological deficits caused by ischemia. Therefore, the classification of reversible mTc-MEP warnings remains challenging.
Monitoring mTc-MEPs from the TA muscles, using the amplitude reduction method, resulted in a high sensitivity and specificity regarding the neurological outcome. There was one false negative mTc-MEP outcome for the right TA. However, the difference in motor strength was small (preoperative MRC 5, postoperative MRC 4+), and different physicians performed the neurological examination. Therefore, it is possible that this difference could have been the result of inter-observer variability, and not a true false negative.
Five patients had an irreversible warning without new postoperative motor deficits (patients 6–9 and 24, Table 4). D-waves were measured in four out of these five patients (patients 7–9 and 24, Table 4). In one patient (patient 8, Table 4) there was no D-wave warning and in one patient (patient 24, Table 4) there was a reversible D-wave warning. It has been reported that patients can have significant mTc-MEP deteriorations while D-wave amplitudes remain stable [4]. Studies showed that in these cases, no long-term motor deficits should be expected [4,8,18,19]. This might be why the two patients without the D-wave warning, or reversible D-wave warning, did not have new postoperative motor deficits. In two patients, there was an irreversible D-wave warning (patients 7 and 9, Table 4). In patient 7 from Table 4, D-waves were recorded during a kyphosis correction. However, D-wave recordings during scoliosis surgery appeared to produce false positive warnings and might therefore not be reliable for monitoring scoliosis patients [20]. In a more recent study, the authors reported that there might be added value in performing D-waves in patients undergoing thoracic spinal osteotomy or scoliosis correction, since it lowered the number of false positive outcomes of the mTc-MEPs [21]. However, they still reported false positive warnings of the D-wave monitoring. In patient 9 from Table 4, there was an irreversible mTc-MEP and D-wave warning. Although we do not completely understand the underlying physiology of why the D-wave deteriorated, the surgery lasted very long (10 h and 16 min) and the D-wave declined gradually over time. The final patient (patient 6, Table 4) with an irreversible mTc-MEP warning without new postoperative motor deficits, had what we consider a false positive warning.
Limitations
Although this is the first extensive study investigating the reliability of two recording electrode types for detecting mTc-MEP warnings, it has its limitations. Even though this was a prospective study, for the secondary objective, the neurological outcomes of the patients were collected retrospectively. Because of this, not all MRC grades were reported, specifically in patients who underwent orthopaedic surgery or vascular surgery. However, it was not stated if there were new postoperative deficits or not. Moreover, pre- and postoperative neurological examinations were not always performed by the same physician. Secondly, the study’s results apply only to the specific surface and subcutaneous needle electrodes used in this study. Moreover, whether the use of surface electrodes is non-inferior to the use of subcutaneous needle electrodes for detecting mTc-MEP warnings in other muscles besides the TA muscles has yet to be investigated. Lastly, for lower motor neuron monitoring, it is probably advisable to record mTc-MEPs with intramuscular needles to be able to detect myotonic discharges.
5. Conclusions
The use of surface electrodes was non-inferior to the use of subcutaneous needle electrodes for detecting mTc-MEP warnings over the TA muscles during spinal cord monitoring. Moreover, reversible warnings never resulted in permanent new motor deficits of the left and right TA. Irreversible warnings resulted in a range from 50.0% (TA left) to 63.6% (TA right) in transient or permanent new postoperative motor deficits.
Author Contributions
Conceptualization, S.E.D., G.D.; methodology, S.E.D., M.C.G., G.D., K.T., F.L. and S.U.; formal analysis, S.E.D., M.C.G., G.D. and K.T.; investigation, S.E.D., M.C.G., G.D., C.H.M.S.-H. and F.L.; writing—original draft preparation, S.E.D., M.C.G. and G.D.; writing—review and editing, all authors; visualization, S.E.D. and M.C.G.; supervision, G.D., F.L., A.R.A., M.M.S., R.J.M.G. and S.U. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
The hospital ethical committee waived the requirement for full ethical committee review following the terms of the Dutch Act on Medical Research on Human Subjects (Wet Medisch-Wetenschappelijk Onderzoek, or ‘WMO’) since the data were collected during routine clinical care.
Informed Consent Statement
The study was registered and approved by a non-WMO study evaluation committee who deemed informed consent unnecessary/patients provided informed consent for the use of their data.
Data Availability Statement
The data may be available at a reasonable request.
Conflicts of Interest
ARA reports receipt of unrestricted research funding and/or reimbursement for consultancy for The Medicines Company, Janssen Pharma, Carefusion/BD, Orion Pharma, Ever Pharma, Terumo, PAION and Philips (all for work unrelated to the current study; all payments to institution). G. Drost is the guest editor of the special issue “Intraoperative Neurophysiology: Optimizing Current and Developing New Techniques”. The other authors report no competing interests.
Funding Statement
No funding was received for this study.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
References
- 1.Langeloo D.-D., Journée H.-L., de Kleuver M., Grotenhuis J.A. Criteria for Transcranial Electrical Motor Evoked Potential Monitoring during Spinal Deformity Surgery. Clin. Neurophysiol. 2007;37:431–439. doi: 10.1016/j.neucli.2007.07.007. [DOI] [PubMed] [Google Scholar]
- 2.Hausmann O.N., Min K., Boos N., Ruetsch Y.A., Erni T., Curt A. Transcranial Electrical Stimulation: Significance of Fast versus Slow Charge Delivery for Intra-Operative Monitoring. Clin. Neurophysiol. 2002;113:1532–1535. doi: 10.1016/S1388-2457(02)00213-4. [DOI] [PubMed] [Google Scholar]
- 3.van Hal C., Hoebink E., Polak H.E., Racz I., de Kleuver M., Journee H.L. Optimum Interpulse Interval for Transcranial Electrical Train Stimulation to Elicit Motor Evoked Potentials of Maximal Amplitude in Both Upper and Lower Extremity Target Muscles. Clin. Neurophysiol. 2013;124:2054–2059. doi: 10.1016/j.clinph.2013.04.011. [DOI] [PubMed] [Google Scholar]
- 4.MacDonald D.B., Skinner S., Shils J., Yingling C. Intraoperative Motor Evoked Potential Monitoring—A Position Statement by the American Society of Neurophysiological Monitoring. Clin. Neurophysiol. 2013;124:2291–2316. doi: 10.1016/j.clinph.2013.07.025. [DOI] [PubMed] [Google Scholar]
- 5.Fehlings M.G., Brodke D.S., Norvell D.C., Dettori J.R. The Evidence for Intraoperative Neurophysiological Monitoring in Spine Surgery. Spine. 2010;35:S37–S46. doi: 10.1097/BRS.0b013e3181d8338e. [DOI] [PubMed] [Google Scholar]
- 6.Journée H.L., Berends H.I., Kruyt M.C. The Percentage of Amplitude Decrease Warning Criteria for Transcranial MEP Monitoring. J. Clin. Neurophysiol. 2017;34:22–31. doi: 10.1097/WNP.0000000000000338. [DOI] [PubMed] [Google Scholar]
- 7.MacDonald D.B. Overview on Criteria for MEP Monitoring. J. Clin. Neurophysiol. 2017;34:4–11. doi: 10.1097/WNP.0000000000000302. [DOI] [PubMed] [Google Scholar]
- 8.Deletis V. Neurophysiology in Neurosurgery. Academic Press; Cambridge, MA, USA: 2002. Intraoperative Neurophysiology and Methodologies Used to Monitor the Functional Integrity of the Motor System; pp. 25–51. [Google Scholar]
- 9.Langeloo D.D., Lelivelt A., Louis Journée H., Slappendel R., de Kleuver M. Transcranial Electrical Motor-Evoked Potential Monitoring During Surgery for Spinal Deformity. Spine. 2003;28:1043–1050. doi: 10.1097/01.BRS.0000061995.75709.78. [DOI] [PubMed] [Google Scholar]
- 10.Gadella M.C., Dulfer S.E., Absalom A.R., Lange F., Scholtens-Henzen C.H.M., Groen R.J.M., Wapstra F.H., Faber C., Tamási K., Sahinovic M.M., et al. Comparing Motor-Evoked Potential Characteristics of NEedle versus SuRFACE Recording Electrodes during Spinal Cord Monitoring; The NERFACE Study Part I. J. Clin. Med. 2023;12:1404. doi: 10.3390/jcm12041404. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Kim S.-M., Yang H., Park S.-B., Han S.G., Park K.-W., Yoon S.H., Hyun S.-J., Kim H.-J., Park K.S., Lee K.-W. Pattern-Specific Changes and Discordant Prognostic Values of Individual Leg-Muscle Motor Evoked Potentials during Spinal Surgery. Clin. Neurophysiol. 2012;123:1465–1470. doi: 10.1016/j.clinph.2011.11.035. [DOI] [PubMed] [Google Scholar]
- 12.Compston A. Aids to the Investigation of Peripheral Nerve Injuries. Medical Research Council: Nerve Injuries Research Committee. His Majesty’s Stationery Office: 1942; pp. 48 (iii) and 74 Figures and 7 Diagrams; with Aids to the Examination of the Peripheral Nervous System. By Michael O’Brien for the Guarantors of Brain. Saunders Elsevier: 2010; pp. [8] 64 and 94 Figures. Brain. 2010;133:2838–2844. doi: 10.1093/brain/awq270. [DOI] [PubMed] [Google Scholar]
- 13.Fay M.P. Confidence Intervals That Match Fisher’s Exact or Blaker’s Exact Tests. Biostatistics. 2010;11:373. doi: 10.1093/biostatistics/kxp050. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Walsh M., Srinathan S.K., McAuley D.F., Mrkobrada M., Levine O., Ribic C., Molnar A.O., Dattani N.D., Burke A., Guyatt G., et al. The Statistical Significance of Randomized Controlled Trial Results Is Frequently Fragile: A Case for a Fragility Index. J. Clin. Epidemiol. 2014;67:622–628. doi: 10.1016/j.jclinepi.2013.10.019. [DOI] [PubMed] [Google Scholar]
- 15.Skinner S.A., Holdefer R.N. Intraoperative Neuromonitoring Alerts That Reverse with Intervention: Treatment Paradox and What to Do about It. J. Clin. Neurophysiol. 2014;31:118–126. doi: 10.1097/WNP.0000000000000030. [DOI] [PubMed] [Google Scholar]
- 16.Hill A.B. The Environment and Disease: Association or Causation? J. R. Soc. Med. 1965;58:295–300. doi: 10.1177/003591576505800503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Tignanelli C.J., Napolitano L.M. The Fragility Index in Randomized Clinical Trials as a Means of Optimizing Patient Care. JAMA Surg. 2019;154:74–79. doi: 10.1001/jamasurg.2018.4318. [DOI] [PubMed] [Google Scholar]
- 18.Sala F., Palandri G., Basso E., Lanteri P., Deletis V., Faccioli F., Bricolo A. Motor Evoked Potential Monitoring Improves Outcome after Surgery for Intramedullary Spinal Cord Tumors: A Historical Control Study. Neurosurgery. 2006;58:1129–1143. doi: 10.1227/01.NEU.0000215948.97195.58. [DOI] [PubMed] [Google Scholar]
- 19.Kothbauer K.F. Motor Evoked Potential Monitoring for Intramedullary Spinal Cord Tumor Surgery. In: Deletis V., Shills J.L., editors. Neurophysiology in Neurosurgery: A Modern Intraoperative Approach. Academic Press; San Diego, CA, USA: 2002. pp. 73–92. [Google Scholar]
- 20.Ulkatan S., Neuwirth M., Bitan F., Minardi C., Kokoszka A., Deletis V. Monitoring of Scoliosis Surgery with Epidurally Recorded Motor Evoked Potentials (D Wave) Revealed False Results. Clin. Neurophysiol. 2006;117:2093–2101. doi: 10.1016/j.clinph.2006.05.021. [DOI] [PubMed] [Google Scholar]
- 21.Chen J., Deng Y.L., Sui W.Y., Yang J.F., Xu J., Huang Z.F., Yang J.L. Intraoperative Neuromonitoring Auxiliary Significance of DNEP for MEP-Positive Event During Severe Spinal Deformity Surgery. Clin. Spine Surg. 2022;35:E167–E174. doi: 10.1097/BSD.0000000000001190. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data may be available at a reasonable request.