2.1. Study Design
This study was conducted with the approval of Xinqiao Hospital’s Institutional Review Board. All patients included in this study signed the informed consent form. Here in, we retrospectively reviewed a series of consecutive PE-TLIF patients seen at a single spine center between June 2018 and April 2020. All surgeries were performed by trained full-time orthopedic surgeons using MIONM. Inclusion criteria included patients with lumbar spinal stenosis, spondylolisthesis, and degenerative lumbosacral spine diseases with instability, radiculopathy, or neurogenic claudication that did not respond to conservative treatments. Exclusion criteria included the presence of (1) serious underlying diseases or mental illnesses; (2) cauda equina syndrome or active infection;(3) previous lumbar surgical treatment, ozone intervention, or radiofrequency ablation; (4) bilateral canal decompression; (5) bleeding disorders, coagulation abnormalities, or pre-operative anaemia; (6) unwillingness or inability to participate in treatment and complete follow-up; or (7) a related electronic device implant.
2.2. Anaesthesia Protocol
General anaesthesia was induced with a bolus dose of propofol (1-2 mg/kg), midazolam (0.03-0.05 mg/kg)and fentanyl (0.25~0.5 μg/kg) combined with a short-acting muscle relaxant, cisatracurium (0.15-0.2 mg/kg), and an inhalation agent (sevoflurane). No muscle relaxants or inhalation agents were administered after induction and intubation. Subsequently, anaesthesia maintenance was propofol (3-6 mg/kg/h), based on haemodynamic response, and remifentanyl (0.15-0.3 μg/kg/min).The sedation depth monitoring index was observed using BIS/Narcotrend, and BIS values were maintained at 40-60. The train of four twitch test (TOF) was used to monitor metabolism and was maintained at values greater than 70%.
2.3. Surgical Technique
The setting of operation room is shown in Figure 1.After general anaesthesia, with the patient prone on the operating table, electrode wires for IONM were quickly connected. First, bilateral percutaneous pedicle screw fixation was performed via a posterolateral Wiltseapproach [3] at the responsibility levels. The skin entry point of the percutaneous endoscope enters at an angle of 50° to 60° from the horizontal and was fixed outside the spinous process. Second, we used an 18G needle to enter the skin and then replaced the needle with a 0.8-mm guide wire through the cannula. Traditional guide wire/rod replacement surgery was used to further expand the tissue. The plastic surgery of the upper extremity articular process (SAP) has been performed as a routine PELD operation [20].Intra-operative fluoroscopy confirmed that the pipeline was placed in the correct location (Fig. 2a). Nerve root decompression and discectomy were performed under endoscopic views (Fig. 2b).
Next, the TESSYS work tube was replaced with a tail-end expandable tubular dilator (PELIF®, Sanyou, Shanghai, China) [2], and the dilator was inserted into the intervertebral disc with a twisting movement through the caudal dilation tube using instruments, such as raspatories, pituitary rongeurs, and curettes, to prepare the endplate. Finally, under the close supervision of IONM, a cage (Halis®, PEEK material, Sanyou, Shanghai, China) was implanted (Fig. 2c). After the percutaneous posterior rod was fixed, the final pedicle screw was tightened and locked. Figure 2d showed the postoperative plain film of the patient.
2.4. Method and Principles of MIONM
Using a 16-channel multi-function monitor, continuous and uninterrupted joint monitoring of MEP, EMG, and SSEPs was performed in different time phases. IONM test selection for each case was based on the surgeon’s request with the guidance of a neurologist consult.
Motor-evoked potential (MEP) was elicited using subcutaneous needle electrodes stimulating at a constant voltage (400–500 V) and multiple trains of 5 to 7 pulses with a duration of 200 to 400 ms for each pulse. The interstimulus interval was 2.0 to 4.0 ms for each stimulation train. The recording electrode was placed on the muscle innervated by the corresponding nerve root, and the compound muscle action potential caused by the stimulation was recorded.
Somatosensory evoked potential (SSEP) involved the stimulation electrodes being placed at the posterior tibial nerve (PTN) at the ankle. The stimulation intensity ranged from 35 to 45mA with a stimulation rate of 2 Hz, and 160 to 300 trials were averaged for each trace. Responses were recorded in a referential fashion from multiple electrodes with fixed Cz and Fz(International 10-20 System).Primarily the P40 incubation period and amplitude of SSEP of both lower extremities were recorded.
Electromyography (EMG) monitoring is divided into triggered electromyography (Tr-EMG) and free electromyography (F-EMG).The former is discontinuous monitoring used to judge the integrity of the pedicle screw and identify adjacent nerve structures, while the latter continuously monitors EMG changes caused by nerve root traction, compression and manipulation stimulation, as well as pedicle screw placement damage.
2.5. Warning Criteria
MEP: The warning standard was that the waveform completely disappeared or the amplitude decreased by 80% from baseline [21].
SSEP: Continuous recording was compared to the baseline trajectory, and reductions in the amplitude by at least 50% or increases in the delay by 10% served as alarm criteria [22].
F-EMG: Explosive muscle contraction reaction occurs continuously, especially muscles dominated by nerve roots that might be damaged by surgery, serving as the warning standard. F-EMG activity was recorded using the same recording myotomes as for CM-EP responses. If one observed neurotonic discharges lasting longer than 5 seconds, this elicited a CM-EP trial [12].
2.6. Stagnara Wake-up Test
The Stagnara wake-up test was selectively used to confirm motor function after a loss or significant change in monitoring signals in some members of the study population.
2.7. Neurological Complication Definition
Nervous system examinations were performed before and after surgery, including assessment of changes in limb muscle strength and sensation. A neurological complication was defined as any new neurological symptom and/or sign or worsening of pre-existing symptom and/or sign occurring immediately after surgery and having either a transient or permanent nature. The final clinical evaluation was performed by the neurologist.
2.7. Data Analysis
True-positive (TP)
A change in evoked potential (EP) followed by a new neurological disorder being observed during the wake-up test or at the end of surgery.
True-Negative (TN)
During the entire operation, compared to baseline values, the evoked potential changed within normal ranges, and no neurological deterioration was observed after surgery.
False-Negative (FN)
Throughout the surgery, the evoked potentials remained consistent with baseline values, but post-operative neurological examination indicated new neurological defects.
False-Positive (FP)
The evoked potential (EP) changed, resulting in corresponding measures being taken that did not eliminate the alarm, but there were no new neurological defects observed during the wake-up test and no new defects at the end of surgery.
Indeterminate
There was an alarm, the surgeon adjusted the surgical method, the alarm was eliminated, and there were no new neurological defects after surgery. However, it was difficult to determine whether this was because of the alarm after taking measures to avoid post-operative neurological defects.
Sensitivity was defined as TP/(TP+ FN)*100%.
Specificity was defined as TN/(TN + FP)*100%.
Positive predictive value (PPV) was defined as TP/(TP+ FP)*100%.
Negative predictive value (NPV) was defined as TN/(TN + FN)*100%.