Intraoperative Neurophysiologic Monitoring - CAM 70158
Description
Intraoperative neurophysiologic monitoring describes a variety of procedures used to monitor the integrity of neural pathways during high-risk neurosurgical, orthopedic, and vascular surgeries. It involves the detection of electrical signals produced by the nervous system in response to sensory or electrical stimuli to provide information about the functional integrity of neuronal structures. This evidence review does not address established neurophysiologic monitoring (i.e., somatosensory-evoked potentials, motor-evoked potentials using transcranial electrical stimulation, brainstem auditory-evoked potentials, electromyography of cranial nerves, electroencephalography, electrocorticography), during spinal, intracranial, or vascular procedures.
Additional Information
2017 Clinical Input
Clinical input obtained in 2017 supports that the following indication provides a clinically meaningful improvement in net health outcome and is consistent with generally accepted medical practice:
- Use of intraoperative neurophysiologic monitoring of the recurrent laryngeal nerve for individuals undergoing cervical spine surgery with:
- prior anterior cervical surgery, particularly revision anterior cervical discectomy and fusion, revision surgery through a scarred surgical field, reoperation for pseudarthrosis, or revision for failed fusion;
- multilevel anterior cervical discectomy and fusion; and
- preexisting recurrent laryngeal nerve pathology, when there is residual function of the recurrent laryngeal nerve.
Thus, the above indication may be considered medically necessary considering the suggestive evidence and clinical input support.
2014 Clinical Input
Clinical input obtained in 2014 and professional society guidelines have supported the use of intraoperative neurophysiologic monitoring during spinal, intracranial, or vascular procedures. There was general agreement that intraoperative neurophysiologic monitoring of visual-evoked potentials and motor-evoked potentials using transcranial magnetic stimulation is investigational. It should be noted there is controversy about the utility of intraoperative neurophysiologic monitoring in some surgical procedures. Most of the published literature is from Europe, and, while many articles have reported the sensitivity and specificity of motor-evoked potentials for predicting postsurgical neurologic deficits, few have reported intraoperative interventions undertaken in response to information from monitoring.
Background
INTRAOPERATIVE NEUROPHYSIOLOGIC MONITORING
The principal goal of intraoperative neurophysiologic monitoring (IONM) is identification of nervous system impairment on the assumption that prompt intervention will prevent permanent deficits. Correctable factors at surgery include circulatory disturbance, excess compression from retraction, bony structures, hematomas, or mechanical stretching. The technology is continuously evolving with refinements in equipment and analytic techniques, including recording, with several patients monitored under the supervision of a physician who is outside the operating room.
The different methodologies of monitoring are described next.
Sensory-Evoked Potentials
Sensory-evoked potential (SEP) describes the responses of the sensory pathways to sensory or electrical stimuli. Intraoperative monitoring of SEPs is used to assess the functional integrity of central nervous system (CNS) pathways during surgeries that put the spinal cord or brain at risk for significant ischemia or traumatic injury. The basic principles of SEP monitoring involve identification of a neurologic region at risk, selection and stimulation of a nerve that carries a signal through the at-risk region, and recording and interpretation of the signal at certain standardized points along the pathway. Monitoring of SEPs is commonly used during the following procedures: carotid endarterectomy, brain surgery involving vasculature, surgery with distraction compression or ischemia of the spinal cord and brainstem, and acoustic neuroma surgery. SEPs can be further broken down into the following categories by type of simulation used.
Somatosensory-Evoked Potentials
Somatosensory-evoked potentials (SSEPs) are cortical responses elicited by peripheral nerve stimulations. Peripheral nerves, such as the median, ulnar, or tibial nerves, are typically stimulated, but, in some situations, the spinal cord may be stimulated directly. Recording is done either cortically or at the level of the spinal cord above the surgical procedure. Intraoperative monitoring of SSEPs is most commonly used during orthopedic or neurologic surgery to prompt intervention to reduce surgically induced morbidity and/or to monitor the level of anesthesia. One of the most common indications for SSEP monitoring is in patients undergoing corrective surgery for scoliosis. In this setting, SSEP monitors the status of the posterior column pathways and thus does not reflect ischemia in the anterior (motor) pathways. Several different techniques are commonly used, including stimulation of a relevant peripheral nerve with monitoring from the scalp, from interspinous ligament needle electrodes, or from catheter electrodes in the epidural space.
Brainstem Auditory-Evoked Potentials
Brainstem auditory-evoked potentials (BAEPs) are generated in response to auditory clicks and can define the functional status of the auditory nerve. Surgical resection of a cerebellopontine angle tumor, such as an acoustic neuroma, places the auditory nerves at risk, and BAEPs have been extensively used to monitor auditory function during these procedures.
Visual-Evoked Potentials
Visual-evoked potentials (VEPs) with light flashes are used to track visual signals from the retina to the occipital cortex. VEP monitoring has been used for surgery on lesions near the optic chiasm. However, VEPs are very difficult to interpret due to their sensitivity to anesthesia, temperature and blood pressure.
Motor-Evoked Potentials
Motor-evoked potentials (MEPs) are recorded from muscles following direct or transcranial electrical stimulation of motor cortex or by pulsed magnetic stimulation provided by a coil placed over the head. Peripheral motor responses (muscle activity) are recorded by electrodes placed on the skin at prescribed points along the motor pathways. MEPs, especially when induced by magnetic stimulation, can be affected by anesthesia. The Digitimer electrical cortical stimulator received U.S. Food and Drug Administration (FDA) premarket approval in 2002. Devices for transcranial magnetic stimulation have not been approved by FDA for this use.
Multimodal IONM, in which more than 1 technique is used, most commonly with SSEPs and MEPs, has also been described.
Electromyogram Monitoring and Nerve Conduction Velocity Measurements
Electromyography (EMG) monitoring and nerve conduction velocity measurements can be performed in the operating room and may be used to assess the status of the cranial or peripheral nerves (e.g., to identify the extent of nerve damage before nerve grafting or during resection of tumors). For procedures with a risk of vocal cord paralysis due to damage to the recurrent laryngeal nerve (i.e., during carotid artery, thyroid, parathyroid, goiter, or anterior cervical spine procedures), monitoring of the vocal cords or vocal cord muscles has been performed. These techniques may also be used during procedures proximal to the nerve roots and peripheral nerves to assess the presence of excessive traction or other impairment. Surgery in the region of cranial nerves can be monitored by electrically stimulating the proximal (brain) end of the nerve and recording via EMG activity in the facial or neck muscles. Thus, monitoring is done in the direction opposite that of SEPs, but the purpose is similar: to verify that the neural pathway is intact.
Electroencephalogram Monitoring
Spontaneous electroencephalography (EEG) monitoring can also be used during surgery and can be subdivided as follows:
- EEG monitoring has been widely used to monitor cerebral ischemia secondary to carotid cross-clamping during a carotid endarterectomy. EEG monitoring may identify those patients who would benefit from the use of a vascular shunt during the procedure to restore adequate cerebral perfusion. Conversely, shunts, which have an associated risk of iatrogenic complications, may be avoided in those patients with a normal EEG. Carotid endarterectomy may be done with the patient under local anesthesia so that monitoring of cortical function can be directly assessed.
- Electrocorticography (ECoG) is the recording of the EEG directly from a surgically exposed cerebral cortex. ECoG is typically used to define the sensory cortex and map the critical limits of a surgical resection. ECoG recordings have been most frequently used to identify epileptogenic regions for resection. In these applications, ECoG does not constitute monitoring, per se.
Intraoperative neurophysiologic monitoring, including SSEPs and MEPs using transcranial electrical stimulation, BAEPs, EMG of cranial nerves, EEG, and ECoG, has broad acceptance, particularly for spine surgery and open abdominal aorta aneurysm repairs. These indications have long been considered standard of care, as evidenced by numerous society guidelines, including those from the American Academy of Neurology, American Clinical Neurophysiology Society, American Association of Neurological Surgeons, Congress of Neurologic Surgeons, and American Association of Neuromuscular & Electrodiagnostic Medicine.1,2,3,4,5,6,7 Therefore, this evidence review focuses on monitoring of the recurrent laryngeal nerve during neck and esophageal surgeries and monitoring of peripheral nerves.
Related Policies
20190 Navigated Transcranial Magnetic Stimulation
Policy
Intraoperative neurophysiologic monitoring, which includes somatosensory-evoked potentials, motorevoked potentials using transcranial electrical stimulation, brainstem auditory-evoked potentials, electromyography (EMG) of cranial nerves, electroencephalography, and electrocorticography, may be considered MEDICALLY NECESSARY during spinal, intracranial, or vascular procedures.
Intraoperative neurophysiologic monitoring of the recurrent laryngeal nerve may be considered MEDICALLY NECESSARY in patients undergoing:
- high-risk thyroid or parathyroid surgery, including:
- total thyroidectomy
- repeat thyroid or parathyroid surgery
- surgery for cancer
- thyrotoxicosis
- retrosternal or giant goiter
- thyroiditis
- anterior cervical spine surgery associated with any of the following increased risk situations:
- prior anterior cervical surgery, particularly revision anterior cervical discectomy and fusion, revision surgery through a scarred surgical field, reoperation for pseudarthrosis or revision for failed fusion
- multilevel anterior cervical discectomy and fusion
- pre-existing recurrent laryngeal nerve pathology, when there is residual function of the recurrent laryngeal nerve.
Intraoperative neurophysiologic monitoring of the recurrent laryngeal nerve during anterior cervical spine surgery not meeting the criteria above or during esophageal surgeries is considered investigatonal and/or unproven and therefore considered NOT MEDICALLY NECESSARY.
NOTE: laryngeal nerve and facial nerve monitoring are not separately allowable if the provider rendering the service is part of the operating room team (including but not limited to surgeon, surgical assistant, scrub and circulating nurses and anesthesia).
Intraoperative monitoring of visual-evoked potentials is considered investigational and/or unproven and therefore considered NOT MEDICALLY NECESSARY.
Due to the lack of monitors approved by the U.S. Food and Drug Administration, intraoperative monitoring of motor-evoked potentials using transcranial magnetic stimulation is considered investigational and/or unproven and therefore considered NOT MEDICALLY NECESSARY.
Intraoperative EMG and nerve conduction velocity monitoring during surgery on the peripheral nerves is considered NOT MEDICALLY NECESSARY.
Note: These policy statements refer only to use of these techniques as part of intraoperative monitoring. Other clinical applications of these techniques, such as visual-evoked potentials and EMG, are not considered in this policy.
Train of Four (TOF) monitoring is considered an integral component of other services being rendered and is not available for separate reimbursement.
Policy Guidelines
Intraoperative neurophysiologic monitoring including somatosensory-evoked potentials and motor-evoked potentials using transcranial electrical stimulation, brainstem auditory-evoked potentials, electromyography of cranial nerves, electroencephalography, and electrocorticography has broad acceptance, particularly for spine surgery and open abdominal aorta aneurysm repairs. Therefore, this evidence review focuses on monitoring of the recurrent laryngeal nerve during neck surgeries and monitoring of peripheral nerves.
Constant communication between surgeon, neurophysiologist, and anesthetist are required for safe and effective intraoperative neurophysiologic monitoring.
CODING
Please see the Codes table for details.
Benefit Application
BlueCard/National Account Issues
Intraoperative monitoring is considered reimbursable as a separate service only when a licensed health care practitioner, other than the operating surgeon, interprets the monitoring. The monitoring is performed by a healthcare practitioner or technician who is in attendance in the operating room throughout the procedure.
Implementation of a local policy on this technology may also involve discussions about credentialing of those providing the intraoperative monitoring services, as well as on-site versus remote real-time review and interpretation.
Coding for intraoperative monitoring uses time-based codes; they are not based on the number (single vs. multiple) of modalities used.
Rationale
Early literature focused on intraoperative monitoring of cranial and spinal nerves. This evidence review focuses on more recently investigated techniques, including monitoring of the recurrent laryngeal nerve and peripheral nerves.
Evidence reviews assess the clinical evidence to determine whether the use of technology improves the net health outcome. Broadly defined, health outcomes are length of life, quality of life, and ability to function, including benefits and harms. Every clinical condition has specific outcomes that are important to patients and managing the course of that condition. Validated outcome measures are necessary to ascertain whether a condition improves or worsens; and whether the magnitude of that change is clinically significant. The net health outcome is a balance of benefits and harms.
To assess whether the evidence is sufficient to draw conclusions about the net health outcome of technology, 2 domains are examined: the relevance, and quality and credibility. To be relevant, studies must represent 1 or more intended clinical use of the technology in the intended population and compare an effective and appropriate alternative at a comparable intensity. For some conditions, the alternative will be supportive care or surveillance. The quality and credibility of the evidence depend on study design and conduct, minimizing bias and confounding that can generate incorrect findings. The randomized controlled trial (RCT) is preferred to assess efficacy; however, in some circumstances, nonrandomized studies may be adequate. Randomized controlled trials are rarely large enough or long enough to capture less common adverse events and long-term effects. Other types of studies can be used for these purposes and to assess generalizability to broader clinical populations and settings of clinical practice.
Recurrent Laryngeal Nerve Monitoring During Thyroid or Parathyroid Surgery
Clinical Context and Therapy Purpose
The purpose of intraoperative neurophysiologic monitoring is to provide a treatment option that is an alternative to or an improvement on existing therapies, such as surgery without neurophysiologic monitoring, in patients who are undergoing thyroid or parathyroid surgery and are at high risk of injury to the recurrent laryngeal nerve.
The question addressed in this evidence review is: Does recurrent laryngeal nerve monitoring improve the net health outcome in patients undergoing thyroid or parathyroid surgery and at high risk of injury to the recurrent laryngeal nerve?
The following PICO was used to select literature to inform this review.
Populations
The relevant population of interest is individuals who are undergoing thyroid or parathyroid surgery and at high risk of injury to the recurrent laryngeal nerve.
Interventions
The therapy being considered is intraoperative neurophysiologic monitoring.
Intraoperative neurophysiologic monitoring describes a variety of procedures used to monitor the integrity of neural pathways during high-risk neurosurgical, orthopedic, and vascular surgeries. It involves the detection of electrical signals produced by the nervous system in response to sensory or electrical stimuli to provide information about the functional integrity of neuronal structures.
Comparators
Comparators of interest include surgery without neurophysiologic monitoring.
Outcomes
The general outcomes of interest are morbid events, functional outcomes, and quality of life.
The existing literature evaluating intraoperative neurophysiologic monitoring as a treatment for patients who are undergoing thyroid or parathyroid surgery and at high risk of injury to the recurrent laryngeal nerve has varying lengths of follow-up. While studies described below all reported at least 1 outcome of interest, longer follow-up was necessary to fully observe outcomes.
Study Selection Criteria
Methodologically credible studies were selected using the following principles:
- To assess efficacy outcomes, comparative controlled prospective trials were sought, with a preference for RCTs.
- In the absence of such trials, comparative observational studies were sought, with a preference for prospective studies.
- To assess long-term outcomes and adverse events, single-arm studies that capture longer periods of follow-up and/or larger populations were sought.
- Studies with duplicative or overlapping populations were excluded.
Review of Evidence
Systematic Reviews
Henry et al. (2017) reported on a systematic review of meta-analyses published up to February 2017 that compared intraoperative neurophysiologic monitoring with direct recurrent laryngeal nerve visualization by assessing rates of vocal fold palsy.7 Reviewers included 8 meta-analyses of RCTs or observational studies (prospective or retrospective) and selected the best evidence based on the Jadad algorithm. The 8 meta-analyses differed significantly in the literature search methodology, databases included, the inclusion of quality assessment, and most did not include a study quality assessment. Pisanu et al. (2014) was found to be the highest-quality meta-analysis8; it showed no statistically significant reductions in recurrent laryngeal nerve injury between procedures using intraoperative neurophysiologic monitoring versus direct recurrent laryngeal nerve visualization. However, reviewers also noted that recent developments in intraoperative neurophysiologic monitoring technology such as continuous vagal intraoperative neurophysiologic monitoring and staged thyroidectomy might provide additional benefits, which were out of the scope of their systematic review and need to be further assessed in prospective multicenter trials.
Sun et al. (2017) reported on a meta-analysis of recurrent laryngeal nerve injury during thyroid surgery with or without intraoperative neurophysiologic monitoring.9 Included were 2 prospective cohort studies and 7 retrospective cohort studies. Results are summarized in Tables 1 and 2. Intraoperative neurophysiologic monitoring was associated with a reduction in overall and permanent recurrent laryngeal nerve palsy in thyroid reoperations. Limitations included small sample sizes and study heterogeneity.
Pardal-Refoyo and Ochoa-Sangrador (2016) reported on a systematic review of recurrent laryngeal nerve injury during total thyroidectomy with or without intraoperative neurophysiologic monitoring.10 Included were 1 large (N = 1,000) and 1 small (N = 23) RCT and 52 case series that estimated the risk to the recurrent laryngeal nerve. Twenty-nine studies used recurrent laryngeal nerve monitoring and 25 did not. Results are summarized in Tables 1 and 2. The observed differences in the subgroup analysis were imprecise because the number of observed instances of paralysis was very low.
Table 1. Characteristics of Systematic Reviews
Study | Dates | Trials | Participants | N (Range) | Design | Duration |
Pardal-Refoyo and Ochoa-Sangrador (2016)10 | 1987 – 2013 |
|
Studies reporting incidence of RLN paralysis after single-stage total thyroidectomy through open cervicotomy | 30,922 (23 to 2546 patients) |
|
NR |
Sun et al. (2017)9 | Up to Aug 2016 | 9 | Studies reporting incidence of RLN complications after thyroid surgery | 2436 nerves at risk (1,109 with IONM, 1,327 without IONM) |
Prospective and retrospective cohort studies | NR |
Henry et al. (2017)7 | Up to Feb 2017 | 8 meta-analyses | Meta-analyses of RCTs and non-RCTs comparing IONM with direct visualization for RLNs during thyroidectomy | 8 meta-analyses (6 to 23 patients) | Meta-analyses | NR |
IONM: intraoperative neurophysiologic monitoring; NR: not reported; RCT: randomized controlled trial; RLN: recurrent laryngeal nerve.
Table 2. Results of Systematic Reviews
Study | Risk of Bilateral RLN Paralysis | Transient RLN Palsy | Permanent RLN Palsy |
Pardal-Refoyo and Ochoa-Sangrador (2016)10 | |||
ARR (95% CI) | 2.75% (NR)a | NR | NR |
NNT (95% CI) | 364 (NR)a | NR | NR |
I2 (p) | 8% (NR)a | NR | NR |
Overall RLN Palsy | |||
Sun et al. (2017)9 | |||
With IONM | 4.69% | 3.98%b | 1.26%b |
Without IONM | 9.27% | 6.63%b | 2.78%b |
RR (95% CI) | 0.434 (0.206 to 0.916) | 0.607 (0.270 to 1.366) | 0.426 (0.196 to 0.925) |
NNT (95% CI) | NR | NRb | NRb |
I2 (p) | 70.2% (.029) | 67.4%b (.227) | 13.7%b(.031) |
ARR: absolute risk reduction; CI: confidence interval; IONM: intraoperative neurophysiologic monitoring NNT: number needed to treat; NR: not reported; RLN: recurrent laryngeal nerve; RR: relative risk.
a Sample size of 11947 patients.
b Sample of 7 studies.
Randomized Controlled Trials
Barczynski et al. (2009) reported results of the largest RCT evaluating recurrent laryngeal nerve monitoring as summarized in Tables 3 and 4.11,Recurrent laryngeal nerve monitoring was performed with electrodes on the vocal muscles through the cricothyroid ligament, which may not be the method currently used in the United States in high-risk patients, defined as those undergoing surgery for cancer, thyrotoxicosis, retrosternal or giant goiter, or thyroiditis.The prevalence of transient recurrent laryngeal nerve paresis was 2.9% lower in patients who had recurrent laryngeal nerve monitoring (p = .011) compared with those who received visual identification only. In low-risk patients, there was no significant difference in recurrent laryngeal nerve injury rates between monitoring and no monitoring. Notably, high-risk patients with prior thyroid or parathyroid surgery were excluded from this trial. A benefit of recurrent laryngeal nerve monitoring was also shown in patients undergoing high-risk total thyroidectomy.12,
Table 3. Summary of Key RCT Characteristics
Study | Countries | Sites | Dates | Participants | Active | Comparator |
Barczynski et al. (2009)11 | Poland | 1 | 2006 – 2007 | Patients undergoing bilateral neck surgery | 500 | 500 |
RCT: randomized controlled trial
Table 4. Summary of Key RCT Results
Study | RLN Injury | RLN Paresis | Permanent RLN Palsy |
Barczynski et al. (2009)11 | |||
RLN visualization alone, n/N | 8/500 | NR | NR |
RLN visualization plus monitoring, n/N | NR | NR | NR |
ARR (95% CI) (p) | 2.3% (NR) (0.007) | 1.9% (NR) (0.011) | 0.4% (NR) (NS) |
ARR: absolute risk reduction; CI: confidence interval; NNT: number needed to treat; NR: not reported; NS: not significant; RCT: randomized controlled trial; RLN: recurrent laryngeal nerve.
Section Summary: Recurrent Laryngeal Nerve Monitoring During Thyroid or Parathyroid Surgery
The evidence on the use of intraoperative neurophysiologic monitoring in reducing recurrent laryngeal nerve injury includes a large RCT and systematic reviews assessing thyroid and parathyroid surgery. The strongest evidence derives from an RCT of 1,000 patients undergoing thyroid surgery. This RCT found a minimal effect of intraoperative neurophysiologic monitoring overall but a significant reduction in recurrent laryngeal nerve injury in patients at high-risk for injury. High-risk in this trial was defined as surgery for cancer, thyrotoxicosis, retrosternal or giant goiter, or thyroiditis. The high-risk category may also include patients with prior thyroid or parathyroid surgery or total thyroidectomy.
Recurrent Laryngeal Nerve Monitoring During Cervical Spine Surgery
Clinical Context and Therapy Purpose
The purpose of intraoperative neurophysiologic monitoring is to provide a treatment option that is an alternative to or an improvement on existing therapies, such as surgery without neurophysiologic monitoring, in patients who are undergoing anterior cervical spine surgery and are at high risk of injury to the recurrent laryngeal nerve.
The question addressed in this evidence review is: Does recurrent laryngeal nerve monitoring improve the net health outcome in patients undergoing anterior cervical spine surgery and at high risk of injury to the recurrent laryngeal nerve?
The following PICO was used to select literature to inform this review.
Populations
The relevant population of interest is individuals who are undergoing anterior cervical spine surgery and at high risk of injury to the recurrent laryngeal nerve.
Interventions
The therapy being considered is intraoperative neurophysiologic monitoring.
Intraoperative neurophysiologic monitoring describes a variety of procedures used to monitor the integrity of neural pathways during high-risk neurosurgical, orthopedic and vascular surgeries. It involves the detection of electrical signals produced by the nervous system in response to sensory or electrical stimuli to provide information about the functional integrity of neuronal structures.
Comparators
Comparators of interest include surgery without neurophysiologic monitoring.
Outcomes
The general outcomes of interest are morbid events, functional outcomes, and quality of life.
The existing literature evaluating intraoperative neurophysiologic monitoring as a treatment for patients who are undergoing anterior cervical spine surgery and at high risk of injury to the recurrent laryngeal nerve has varying lengths of follow-up. While studies described below all reported at least 1 outcome of interest, longer follow-up was necessary to fully observe outcomes.
Study Selection Criteria
Methodologically credible studies were selected using the following principles:
- To assess efficacy outcomes, comparative controlled prospective trials were sought, with a preference for RCTs.
- In the absence of such trials, comparative observational studies were sought, with a preference for prospective studies.
- To assess long-term outcomes and adverse events, single-arm studies that capture longer periods of follow-up and/or larger populations were sought.
- Studies with duplicative or overlapping populations were excluded.
Review of Evidence
Systematic Reviews
Ajiboye et al. (2017) reported on the results of a systematic review that included 10 studies (N = 26,357 ).13 All studies were of low methodologic quality but had a low risk of bias. Only studies that compared the risk of nerve injury using intraoperative neurophysiologic monitoring with no intraoperative neurophysiologic monitoring were included. Based on data from these 2 studies, there was no statistically significant difference in the risk of neurologic injury with or without intraoperative neurophysiologic monitoring (odds ratio [OR], 0.726; 95% confidence interval [CI], 0.287 to 1.833; p = .498) (Tables 5 and 6).
Erwood et al. (2016) reported on the results of a meta-analysis that summarized the relative rate of recurrent laryngeal nerve injury following revision anterior cervical discectomy and fusion.14 The meta-analysis did not report recurrent laryngeal nerve injury rate with intraoperative neurophysiologic monitoring versus without intraoperative neurophysiologic monitoring. Based on pooled data from 3 prospective cohort studies and 5 retrospective series (N = 238), reviewers reported an overall recurrent laryngeal nerve injury rate of 14.1% (95% CI, 9.8% to 19.1%)(Tables 5 and 6).
Daniel et al. (2018) published a literature review and meta-analysis evaluating intraoperative neurophysiologic monitoring during spinal operative surgical procedures.15 Six retrospective studies, published between 2006 and 2016, with a total of 335,458 patients (range, 74 to 231,067) were included. Pooled OR for neurological events with and without intraoperative neurophysiologic monitoring was 0.72 (95% CI, 0.71 to 1.79; p = .4584), and sensitivity analysis, which included only 2 studies, had a pooled OR of 0.199 (95% CI, 0.038 to 1.035; p = .055). The review was limited by the lack of prospective studies, by only 3 of the included studies being considered to have high methodological quality assessment, and by many heterogeneous spinal procedures with different rates of neurological events and wide CIs being included.
Table 5. Characteristics of Systematic Reviews
Study | Dates | Trials | Participants | N (Range) | Design | Duration |
Ajiboye et al. (2017)13 | NR | 10 | Studies reporting IONM use for ACSS | 26,357 (16 to 22,768) | 9 retrospective, 1 prospective | NR |
Erwood et al. (2016)14 | 1998 – 2015 | 8 | Studies reporting reoperative ACSS for RLN | 238 (13 to 63) | 5 prospective, 3 retrospective | 2 wk to 24 mo |
Daniel et al. (2018)15 | 2006 – 2016 | 6 | Studies reporting IONM use for spinal surgical procedures | 335,458 (74 to 231,067) | 2 cohort, 4 retrospective | NR |
ACSS: anterior cervical spine surgery; IONM: intraoperative neurophysiologic monitoring; NR: not reported; RLN: recurrent laryngeal nerve.
Table 6. Results of Systematic Reviews
Study | Risk of Neurologic Injury |
Ajiboye et al. (2017)13 | |
ORa,b (95% CI) | 0.726 (0.287 to 1.833) |
I2 (p) | 0% (0.44) |
Erwood et al. (2016)14 | |
Estimatec (95% CI) | 0.14 (0.10 to 0.19) |
I2 (p) | 10.7% (NR) |
Daniel et al. (2018)15 | |
ORa (95% CI) | 0.72 (0.71 to 1.79) |
I2 (p) | NR (.4584) |
CI: confidence interval; NNT: number needed to treat; NR: not reported; OR: odds ratio.
a Risk of neurologic injury after spine surgery with or without intraoperative neurophysiologic monitoring.
b Included 2 studies.
c Overall rate of recurrent laryngeal nerve injury.
Section Summary: Recurrent Laryngeal Nerve Monitoring During Cervical Spine Surgery
The evidence on the use of intraoperative neurophysiologic monitoring in reducing recurrent laryngeal nerve injury during cervical spinal surgery includes 3 systematic reviews. Two of the 3 analyses compared the risk of nerve injury using intraoperative neurophysiologic monitoring with no intraoperative neurophysiologic monitoring and found no statisticallysignificant difference.
Recurrent Laryngeal Nerve Monitoring During Esophageal Surgery
Clinical Context and Therapy Purpose
The purpose of intraoperative neurophysiologic monitoring is to provide a treatment option that is an alternative to or an improvement on existing therapies, such as surgery without neurophysiologic monitoring, in patients who are undergoing esophageal surgery.
The question addressed in this evidence review is: Does recurrent laryngeal nerve monitoring improve the net health outcome in patients undergoing esophageal surgery during surgeries that could damage their recurrent laryngeal nerve?
The following PICO was used to select literature to inform this review.
Populations
The relevant population of interest is individuals who are undergoing esophageal surgery.
Interventions
The therapy being considered is intraoperative neurophysiologic monitoring.
Intraoperative neurophysiologic monitoring describes a variety of procedures used to monitor the integrity of neural pathways during high-risk neurosurgical, orthopedic, and vascular surgeries. It involves the detection of electrical signals produced by the nervous system in response to sensory or electrical stimuli to provide information about the functional integrity of neuronal structures.
Comparators
Comparators of interest include surgery without neurophysiologic monitoring.
Outcomes
The general outcomes of interest are morbid events, functional outcomes, and quality of life.
The existing literature evaluating intraoperative neurophysiologic monitoring as a treatment for patients who are undergoing esophageal surgery has varying lengths of follow-up. While studies described below all reported at least 1 outcome of interest, longer follow-up was necessary to fully observe outcomes.
Study Selection Criteria
Methodologically credible studies were selected using the following principles:
- To assess efficacy outcomes, comparative controlled prospective trials were sought, with a preference for RCTs.
- In the absence of such trials, comparative observational studies were sought, with a preference for prospective studies.
- To assess long-term outcomes and adverse events, single-arm studies that capture longer periods of follow-up and/or larger populations were sought.
- Studies with duplicative or overlapping populations were excluded.
Review of Evidence
Nonrandomized Comparative Study
Zhong et al. (2014) published a comparative study from Asia evaluating recurrent laryngeal nerve monitoring during surgery for esophageal cancer.16 One hundred fifteen patients with esophageal cancer were enrolled in this prospective study. In 54 patients, the left recurrent laryngeal nerve was found and underwent monitoring. In the remainder (n = 61), the recurrent laryngeal nerve was not located. No recurrent laryngeal nerve injury was reported during surgery in either group, but 6 (10%) of 61 patients who did not receive monitoring had notable recurrent laryngeal nerve injury identified postoperatively. It is unclear whether the difference in outcomes was due to monitoring or to the inability to identify the recurrent laryngeal nerve during surgery.
Section Summary: Recurrent Laryngeal Nerve Monitoring During Esophageal Surgery
One nonrandomized comparative study on surgery for esophageal cancer was identified. Interpretation of this study is confounded because only the patients who had visual identification of the nerve underwent intraoperative neurophysiologic monitoring. Current evidence does not support conclusions on whether intraoperative neurophysiologic monitoring reduces recurrent laryngeal nerve injury in patients undergoing surgery for esophageal cancer.
Monitoring Peripheral Nerves
Clinical Context and Therapy Purpose
The purpose of intraoperative neurophysiologic monitoring is to provide a treatment option that is an alternative to or an improvement on existing therapies, such as surgery without neurophysiologic monitoring, in patients who are undergoing surgery proximal to a peripheral nerve.
The question addressed in this evidence review is: Does neurophysiologic monitoring improve the net health outcome in patients during surgeries that could damage their peripheral nerves?
The following PICO was used to select literature to inform this review.
Populations
The relevant population of interest is individuals who are undergoing surgery proximal to a peripheral nerve.
Interventions
The therapy being considered is intraoperative neurophysiologic monitoring.
intraoperative neurophysiologic monitoring describes a variety of procedures used to monitor the integrity of neural pathways during high-risk neurosurgical, orthopedic, and vascular surgeries. It involves the detection of electrical signals produced by the nervous system in response to sensory or electrical stimuli to provide information about the functional integrity of neuronal structures.
Comparators
Comparators of interest include surgery without neurophysiologic monitoring.
Outcomes
The general outcomes of interest are morbid events, functional outcomes, and quality of life.
The existing literature evaluating intraoperative neurophysiologic monitoring as a treatment for patients who are undergoing surgery proximal to a peripheral nerve has varying lengths of follow up. While studies described below all reported at least 1 outcome of interest, longer follow-up was necessary to fully observe outcomes.
Study Selection Criteria
Methodologically credible studies were selected using the following principles:
- To assess efficacy outcomes, comparative controlled prospective trials were sought, with a preference for RCTs.
- In the absence of such trials, comparative observational studies were sought, with a preference for prospective studies.
- To assess long-term outcomes and adverse events, single-arm studies that capture longer periods of follow-up and/or larger populations were sought.
- Studies with duplicative or overlapping populations were excluded.
Review of Evidence
Case-Control Study
Kneist et al. (2013) assessed monitoring peripheral nerves during surgery in a case-control study of 30 patients.17 In patients undergoing total mesorectal excision, impaired anorectal function was observed in 1 (7%) of 15 patients who had intraoperative neurophysiologic monitoring compared with 6 (40%) of 15 without monitoring. Kneist et al. (2013) also reported on erectile function following low anterior rectal resection in a pilot study with 17 patients.18 In this study, the combined intraoperative measurement of the bladder and internal anal sphincter innervation was a strong predictor of postoperative erectile function, with a sensitivity of 90%, specificity of 86%, positive predictive value of 90%, and negative predictive value of 86%. The possibility of intervention during surgery was not addressed.
Case Series
Clarkson et al. (2011) described the use of intraoperative nerve recording for suspected brachial plexus root avulsion.19 Included in this retrospective review were 25 consecutive patients who underwent intraoperative nerve recording during surgery for unilateral brachial plexus injury. Of 55 roots thought to be avulsed preoperatively, 14 (25%) were found to be intact using intraoperative nerve recording. Eleven of them were then used for reconstruction, of which 9 (82%) had a positive functional outcome.
Electrophysiologic monitoring has also been reported to guide selective rhizotomy for glossopharyngeal neuralgia in a series of 8 patients.20
Use of intraoperative neurophysiologic monitoring of peripheral nerves has also been reported in patients undergoing orthopedic procedures, including tibial/fibular osteotomies, hip arthroscopy for femoroacetabular impingement, and shoulder arthroplasty.21,22,23
Section Summary: Monitoring Peripheral Nerves
Surgical guidance with peripheral intraoperative neurophysiologic monitoring has been reported in case series and 1 case-control study. Other case series have reported on the predictive ability of monitoring of peripheral nerves. No prospective comparative studies identified have assessed whether outcomes are improved with neurophysiologic monitoring.
Summary of Evidence
For individuals who are undergoing thyroid or parathyroid surgery and are at high risk of injury to the recurrent laryngeal nerve who receive intraoperative neurophysiologic monitoring, the evidence includes a large RCT and systematic reviews. Relevant outcomes are morbid events, functional outcomes, and quality of life. The strongest evidence on neurophysiologic monitoring derives from a RCT of 1,000 patients undergoing thyroid surgery. This RCT found a significant reduction in recurrent laryngeal nerve injury in patients at high-risk for injury. High-risk in this trial was defined as surgery for cancer, thyrotoxicosis, retrosternal or giant goiter, or thyroiditis. The high-risk category may also include patients with prior thyroid or parathyroid surgery or total thyroidectomy. A low volume of surgeries might also contribute to a higher risk for recurrent laryngeal nerve injury. The evidence is sufficient to determine that the technology results in an improvement in the net health outcome.
For individuals who are undergoing anterior cervical spine surgery and are at high-risk of injury to the recurrent laryngeal nerve who receive intraoperative neurophysiologic monitoring, the evidence includes 3 systematic reviews of case series and cohort studies. Relevant outcomes are morbid events, functional outcomes, and quality of life. Two of the 3 analyses compared the risk of nerve injury using intraoperative neurophysiologic monitoring with no intraoperative neurophysiologic monitoring and found no statistically significant difference. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.
For individuals who are undergoing esophageal surgery who receive intraoperative neurophysiologic monitoring, the evidence includes a nonrandomized comparative study. Relevant outcomes are morbid events, functional outcomes, and quality of life. One nonrandomized comparative study on surgery for esophageal cancer was identified. Interpretation of this study is confounded because only those patients who had visual identification of the nerve underwent neurophysiologic monitoring. Current evidence is not sufficiently robust to determine whether neurophysiologic monitoring reduces recurrent laryngeal nerve injury in patients undergoing surgery for esophageal cancer. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.
For individuals who are undergoing surgery proximal to a peripheral nerve who receive intraoperative neurophysiologic monitoring, the evidence includes case series and a controlled cohort study. Relevant outcomes are morbid events, functional outcomes, and quality of life. Surgical guidance with peripheral intraoperative neurophysiologic monitoring and the predictive ability of monitoring of peripheral nerves have been reported. No prospective comparative studies were identified that assessed whether outcomes are improved with neurophysiologic monitoring. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.
The purpose of the following information is to provide reference material. Inclusion does not imply endorsement or alignment with the evidence review conclusions.
Clinical Input From Physician Specialty Societies and Academic Medical Centers
While the various physician specialty societies and academic medical centers may collaborate with and make recommendations during this process, through the provision of appropriate reviewers, input received does not represent an endorsement or position statement by the physician specialty societies or academic medical centers, unless otherwise noted.
2017 Input
Clinical input was sought to help determine whether the use of intraoperative neurophysiologic monitoring of the recurrent laryngeal nerve for individuals undergoing cervical spine surgery would provide a clinically meaningful improvement in net health outcome and whether the use is consistent with generally accepted medical practice. In response to requests, clinical input was received from 5 specialty society-level responses while this policy was under review in 2017.
For individuals undergoing cervical spine surgery who receive intraoperative neurophysiologic monitoring of the recurrent laryngeal nerve, clinical input supports this use provides a clinically meaningful improvement in net health outcome and indicates this use is consistent with generally accepted medical practice in a subgroup of appropriately selected patients. The following patient selection criteria are based on clinical expert opinion and information from clinical study populations:
- prior anterior cervical surgery, particularly revision anterior cervical discectomy and fusion, revision surgery through a scarred surgical field, reoperation for pseudarthrosis, or revision for failed fusion;
- multilevel anterior cervical discectomy and fusion; and
- preexisting recurrent laryngeal nerve pathology, when there is residual function of the recurrent laryngeal nerve.
2014 Input
In response to requests, input was received from 5 physician specialty societies (7 responses) and 2 academic medical centers while this policy was under review in 2014. Input agreed that intraoperative neurophysiologic monitoring with somatosensory-evoked potentials, motor-evoked potentials using transcranial electrical stimulation, brainstem auditory-evoked potentials, electromyography of cranial nerves, electroencephalography, or electrocorticography might be medically necessary during spinal, intracranial, or vascular procedures. There was general agreement that intraoperative neurophysiologic monitoring of visual-evoked potentials and motor-evoked potentials using transcranial magnetic stimulation is investigational. Input was mixed on whether intraoperative neurophysiologic monitoring of peripheral nerves would be considered medically necessary. Some reviewers recommended monitoring some peripheral nerves during spinal surgery (e.g., nerve roots, percutaneous pedicle screw placement, lateral transpsoas approach to the lumbar spine). Other reviewers suggested using intraoperative neurophysiologic monitoring during resection of peripheral nerve tumors or surgery around the brachial plexus or facial/cranial nerves.
Practice Guidelines and Position Statements
Guidelines or position statements will be considered for inclusion in Supplemental Information if they were issued by, or jointly by, a U.S. professional society, an international society with U.S. representation, or National Institute for Health and Care Excellence (NICE). Priority will be given to guidelines that are informed by a systematic review, include strength of evidence ratings, and include a description of management of conflict of interest.
American Academy of Neurology
In 1990 (updated in 2012), the American Academy of Neurology (AAN) published an assessment of intraoperative neurophysiologic monitoring, with an evidence-based guideline update by the AAN and ACNS in 2012 (guideline last reaffirmed on Oct. 17, 2020).1,2 The 1990 assessment indicated that monitoring requires a team approach with a well-trained physician-neurophysiologist to provide or supervise monitoring. Electroencephalogram (EEG) monitoring is used during carotid endarterectomy or for other similar situations in which cerebral blood flow is at high risk. Electrocorticography from surgically exposed cortex can help to define the optimal limits of surgical resection or identify regions of greatest impairment, while sensory cortex somatosensory-evoked potentials can help to localize the central fissure and motor cortex. Auditory-evoked potentials, along with cranial nerve monitoring can be used during posterior fossa neurosurgical procedures. Spinal cord somatosensory-evoked potentials are frequently used to monitor the spinal cord during orthopedic or neurosurgical procedures around the spinal cord, or cross-clamping of the thoracic aorta. Electromyographic monitoring during procedures near the roots and peripheral nerves can be used to warn of excessive traction or other impairment of motor nerves. At the time of the 1990 assessment, motor-evoked potentials were considered investigational by many neurophysiologists. The 2012 update, which was endorsed by the AANEM, concluded that the available evidence supported intraoperative neurophysiologic monitoring using somatosensory-evoked potentials or motor-evoked potentials when conducted under the supervision of a clinical neurophysiologist experienced with intraoperative neurophysiologic monitoring. Evidence was insufficient to evaluate intraoperative neurophysiologic monitoring when conducted by technicians alone or by an automated device.
In 2012, the AAN published a model policy on principles of coding for intraoperative neurophysiologic monitoring and testing.24 The background section of this document provides the following information on the value of intraoperative neurophysiologic monitoring in averting neural injuries during surgery:
"Value of EEG Monitoring in Carotid Surgery. Carotid occlusion, incident to carotid endarterectomies, poses a high-risk for cerebral hemispheric injury. Electroencephalogram (EEG) monitoring is capable of detecting cerebral ischemia, a serious prelude to injury. Studies of continuous monitoring established the ability of electroencephalogram EEG to correctly predict risks of postoperative deficits after a deliberate, but necessary, carotid occlusion as part of the surgical procedure. The surgeon can respond to adverse EEG events by raising blood pressure, implanting a shunt, adjusting a poorly functioning shunt, or performing other interventions.
Multicenter Data in Spinal Surgeries. An extensive multicenter study conducted in 1995 demonstrated that [intraoperative neurophysiologic monitoring] using [sensory-evoked potentials] reduced the risk of paraplegia by 60% in spinal surgeries. The incidence of false negative cases, wherein an operative complication occurred without having been detected by the monitoring procedure, was small: 0.06%.
Technology Assessment of Monitoring in Spinal Surgeries. A technology assessment by the McGill University Health Center ... reviewed 11 studies and concluded that spinal [intraoperative neurophysiologic monitoring] is capable of substantially reducing injury in surgeries that pose a risk to spinal cord integrity. It recommended combined sensory-evoked potentials/motor-evoked potential monitoring, under the presence or constant availability of a monitoring physician, for all cases of spinal surgery for which there is a risk of spinal cord injury.
Value of Combined Motor and Sensory Monitoring. Numerous studies of post-surgical paraparesis and quadriparesis have shown that both sensory-evoked potentials and motor-evoked potential monitoring had predicted adverse outcomes in a timely fashion. The timing of the predictions allowed the surgeons the opportunity to intervene and prevent adverse outcomes. The 2 different techniques (sensory-evoked potentials and motor-evoked potential) monitor different spinal cord tracts. Sometimes, one of the techniques cannot be used for practical purposes, for anesthetic reasons, or because of preoperative absence of signals in those pathways. Thus, the decision about which of these techniques to use needs to be tailored to the individual patient’s circumstances.
Protecting the Spinal Cord from Ischemia during Aortic Procedures. Studies have shown that [intraoperative neurophysiologic monitoring] accurately predicts risks for spinal cord ischemia associated with clamping the aorta or ligating segmental spinal arteries. [Intraoperative neurophysiologic monitoring] can assess whether the spinal cord is tolerating the degree of relative ischemia in these procedures. The surgeon can then respond by raising blood pressure, implanting a shunt, re-implanting segmental vessels, draining spinal fluid, or through other interventions...
Value of EMG [electromyogram] monitoring. Selective posterior rhizotomy in cerebral palsy significantly reduces spasticity, increases range of motion, and improves functional skills. Electromyography during this procedure can assist in selecting specific dorsal roots to transect. Electromyogram (EMG) can also be used in peripheral nerve procedures that pose a risk of injuries to nerves.
Value of Spinal Monitoring using somatosensory-evoked potentials and motor-evoked potentials. According to a recent review of spinal monitoring using somatosensory-evoked potential and motor-evoked potentials by the Therapeutics and Technology Assessment Subcommittee of AAN and ACNS, [intraoperative neurophysiologic monitoring] is established as effective to predict an increased risk of the adverse outcomes of paraparesis, paraplegia, and quadriplegia in spinal surgery (4 Class I and 7 Class II studies). Surgeons and other members of the operating team should be alerted to the increased risk of severe adverse neurologic outcomes in patients with important [intraoperative neurophysiologic monitoring] changes (Level A)."
The AAN model policy also offered guidance on personnel and monitoring standards for intraoperative neurophysiologic monitoring and somatosensory-evoked potential.
American Association of Neurological Surgeons and Congress of Neurological Surgeons
In 2018, the American Association of Neurological Surgeons (AANS) and Congress of Neurological Surgeons updated their position statement on intraoperative neurophysiologic monitoring during routine spinal surgery.25 They stated that intraoperative neurophysiologic monitoring, especially motor evoked potential, “is a reliable diagnostic tool for assessment of spinal cord integrity during surgery” (Level 1 evidence). Intraoperative motor evoked potentials may also “predict recovery in traumatic cervical spinal cord injury.” However, AANS and Congress of Neurological Surgeons found no evidence that such monitoring provides a therapeutic benefit. The statement also recommends that intraoperative neurophysiologic monitoring should be used when the operating surgeon believes it is warranted for diagnostic value, such as with “deformity correction, spinal instability, spinal cord compression, intradural spinal cord lesions, and when in proximity to peripheral nerves or roots.” In addition, they recommend spontaneous and evoked electromyography “for minimally invasive lateral retroperitoneal transpsoas approaches to the lumbar spine" and during pedicle screw insertion.
American Association of Neuromuscular & Electrodiagnostic Medicine
In 2019, the American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM) updated their position statement on electrodiagnostic medicine.5 The recommendations indicated that intraoperative sensory-evoked potentials have demonstrated usefulness for monitoring of spinal cord, brainstem, and brain sensory tracts. The AANEM stated that intraoperative somatosensory-evoked potential monitoring is indicated for select spine surgeries in which there is a risk of additional nerve root or spinal cord injury. Indications for somatosensory-evoked potential monitoring may include, but are not limited to, complex, extensive, or lengthy procedures, and when mandated by hospital policy. However, intraoperative somatosensory-evoked potential monitoring may not be indicated for routine lumbar or cervical root decompression.
American Clinical Neurophysiology Society
In 2009, the American Clinical Neurophysiology Society (ACNS) recommended standards for intraoperative neurophysiologic monitoring.4 Guideline 11A included the following statement:26
“The monitoring team should be under the direct supervision of a physician with training and experience in neurophysiologic intraoperative monitoring. The monitoring physician should be licensed in the state and privileged to interpret neurophysiologic testing in the hospital in which the surgery is being performed. He/she is responsible for real-time interpretation of neurophysiologic intraoperative monitoring data. The monitoring physician should be present in the operating room or have access to intraoperative neurophysiologic monitoring data in real-time from a remote location and be in communication with the staff in the operating room. There are many methods of remote monitoring, however any method used must conform to local and national protected health information guidelines. The specifics of this availability (i.e., types of surgeries) should be decided by the hospital credentialing committee. In order to devote the needed attention, it is recommended that the monitoring physician interpret no more than three cases concurrently.”
American Society of Neurophysiological Monitoring
In 2018, the American Society of Neurophysiological Monitoring (ASNM) published practice guidelines for the supervising professional on intraoperative neurophysiologic monitoring.15 The ASNM (2013) position statement on intraoperative motor-evoked potential monitoring indicated that motor-evoked potentials are an established practice option for cortical and subcortical mapping and monitoring during surgeries risking motor injury in the brain, brainstem, spinal cord, or facial nerve.27
National Institute for Health and Care Excellence
In 2008, a guidance from the National Institute for Health and Care Excellence on intraoperative neurophysiologic monitoring during thyroid surgery found no major safety concerns.28 Regarding efficacy, intraoperative neurophysiologic monitoring was indicated as helpful “in performing more complex operations such as reoperative surgery and operations on large thyroid glands.”
U.S. Preventive Services Task Force Recommendations
Not applicable
Ongoing and Unpublished Clinical Trials
Some currently unpublished trials that might influence this review are listed in Table 7.
Table 7. Summary of Key Trials
NCT No. | Trial Name | Planned Enrollment | Completion Date |
Ongoing | |||
NCT01630785 | Retrospective Data Analysis of Neurophysiological Data for Intraoperative or Epilepsy Monitoring | 5000 | Dec 2025 |
Unpublished | |||
NCT01585727 | Continuous Intraoperative Monitoring of the Pelvic Autonomic Nerves During Total Mesorectal Excision (TME) for the Prevention of Urogenital and Anorectal Dysfunction in Patients With Rectal Cancer (NEUROS) | 188 | Dec 2018 (updated 02/27/19) |
Terminated | |||
NCT03773120 | Effectiveness of Intraoperative Neuromonitoring of the External Branch of the Superior Laryngeal Nerve During Thyroid Surgery | 126 | Jan 2022 |
NCT: national clinical trial.
References:
- Assessment: intraoperative neurophysiology. Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. Nov 1990; 40(11): 1644-6. PMID 2234418
- Nuwer MR, Emerson RG, Galloway G, et al. Evidence-based guideline update: intraoperative spinal monitoring with somatosensory and transcranial electrical motor evoked potentials: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology and the American Clinical Neurophysiology Society. Neurology. Feb 21 2012; 78(8): 585-9. PMID 22351796
- Skinner SA, Cohen BA, Morledge DE, et al. Practice guidelines for the supervising professional: intraoperative neurophysiological monitoring. J Clin Monit Comput. Apr 2014; 28(2): 103-11. PMID 24022172
- American Clinical Neurophysiology Society. ACNS Guidelines and Consensus Statements. Updated January 18, 2022. http://www.acns.org/practice/guidelines. Accessed March 2, 2022.
- American Association of Neuromuscular & Electrodiagnostic Medicine. Position Statement: Recommended Policy for Electrodiagnostic Medicine. 2019; https://www.aanem.org/Advocacy/Position-Statements/Recommended-Policy-for-Electrodiagnostic-Medicine. Accessed March 3, 2022.
- Resnick DK, Choudhri TF, Dailey AT, et al. Guidelines for the performance of fusion procedures for degenerative disease of the lumbar spine. Part 15: electrophysiological monitoring and lumbar fusion. J Neurosurg Spine. Jun 2005; 2(6): 725-32. PMID 16028743
- Henry BM, Graves MJ, Vikse J, et al. The current state of intermittent intraoperative neural monitoring for prevention of recurrent laryngeal nerve injury during thyroidectomy: a PRISMA-compliant systematic review of overlapping meta-analyses. Langenbecks Arch Surg. Jun 2017; 402(4): 663-673. PMID 28378238
- Pisanu A, Porceddu G, Podda M, et al. Systematic review with meta-analysis of studies comparing intraoperative neuromonitoring of recurrent laryngeal nerves versus visualization alone during thyroidectomy. J Surg Res. May 01 2014; 188(1): 152-61. PMID 24433869
- Sun W, Liu J, Zhang H, et al. A meta-analysis of intraoperative neuromonitoring of recurrent laryngeal nerve palsy during thyroid reoperations. Clin Endocrinol (Oxf). Nov 2017; 87(5): 572-580. PMID 28585717
- Pardal-Refoyo JL, Ochoa-Sangrador C. Bilateral recurrent laryngeal nerve injury in total thyroidectomy with or without intraoperative neuromonitoring. Systematic review and meta-analysis. Acta Otorrinolaringol Esp. Mar-Apr 2016; 67(2): 66-74. PMID 26025358
- Barczynski M, Konturek A, Cichon S. Randomized clinical trial of visualization versus neuromonitoring of recurrent laryngeal nerves during thyroidectomy. Br J Surg. Mar 2009; 96(3): 240-6. PMID 19177420
- Vasileiadis I, Karatzas T, Charitoudis G, et al. Association of Intraoperative Neuromonitoring With Reduced Recurrent Laryngeal Nerve Injury in Patients Undergoing Total Thyroidectomy. JAMA Otolaryngol Head Neck Surg. Oct 01 2016; 142(10): 994-1001. PMID 27490310
- Ajiboye RM, Zoller SD, Sharma A, et al. Intraoperative Neuromonitoring for Anterior Cervical Spine Surgery: What Is the Evidence?. Spine (Phila Pa 1976). Mar 15 2017; 42(6): 385-393. PMID 27390917
- Erwood MS, Hadley MN, Gordon AS, et al. Recurrent laryngeal nerve injury following reoperative anterior cervical discectomy and fusion: a meta-analysis. J Neurosurg Spine. Aug 2016; 25(2): 198-204. PMID 27015129
- Daniel JW, Botelho RV, Milano JB, et al. Intraoperative Neurophysiological Monitoring in Spine Surgery: A Systematic Review and Meta-Analysis. Spine (Phila Pa 1976). Aug 2018; 43(16): 1154-1160. PMID 30063222
- Zhong D, Zhou Y, Li Y, et al. Intraoperative recurrent laryngeal nerve monitoring: a useful method for patients with esophageal cancer. Dis Esophagus. Jul 2014; 27(5): 444-51. PMID 23020300
- Kneist W, Kauff DW, Juhre V, et al. Is intraoperative neuromonitoring associated with better functional outcome in patients undergoing open TME? Results of a case-control study. Eur J Surg Oncol. Sep 2013; 39(9): 994-9. PMID 23810330
- Kneist W, Kauff DW, Rubenwolf P, et al. Intraoperative monitoring of bladder and internal anal sphincter innervation: a predictor of erectile function following low anterior rectal resection for rectal cancer? Results of a prospective clinical study. Dig Surg. 2013; 30(4-6): 459-65. PMID 24481247
- Clarkson JHW, Ozyurekoglu T, Mujadzic M, et al. An evaluation of the information gained from the use of intraoperative nerve recording in the management of suspected brachial plexus root avulsion. Plast Reconstr Surg. Mar 2011; 127(3): 1237-1243. PMID 21364425
- Zhang W, Chen M, Zhang W, et al. Use of electrophysiological monitoring in selective rhizotomy treating glossopharyngeal neuralgia. J Craniomaxillofac Surg. Jul 2014; 42(5): e182-5. PMID 24095216
- Ochs BC, Herzka A, Yaylali I. Intraoperative neurophysiological monitoring of somatosensory evoked potentials during hip arthroscopy surgery. Neurodiagn J. Dec 2012; 52(4): 312-9. PMID 23301281
- Jahangiri FR. Multimodality neurophysiological monitoring during tibial/fibular osteotomies for preventing peripheral nerve injuries. Neurodiagn J. Jun 2013; 53(2): 153-68. PMID 23833842
- Nagda SH, Rogers KJ, Sestokas AK, et al. Neer Award 2005: Peripheral nerve function during shoulder arthroplasty using intraoperative nerve monitoring. J Shoulder Elbow Surg. May-Jun 2007; 16(3 Suppl): S2-8. PMID 17493556
- American Academy of Neurology. Model Coverage Policy: Principles of Coding for Intraoperative Neurophysiologic Monitoring (IOM) and Testing. 2012; https://www.aan.com/siteassets/home-page/tools-and- resources/practicing-neurologist--administrators/billing-and-coding/model-coverage- policies/16iommodelpolicy_tr.pdf. Accessed March 3, 2022.
- American Association of Neurological Surgeons (AANS)/Congress of Neurological Surgeons (CNS). Joint Section on Disorders of the Spine and Peripheral Nerves updated position statement: intraoperative electrophysiological monitoring. January 2018. https://www.spinesection.org/statement-detail/intraoperative-electrophysiological-monitoring. Accessed March 3, 2022.
- American Clinical Neurophysiology Society. Guideline 11A: Recommended Standards for Neurophysiologic Intraoperative Monitoring Principles. 2009; https://www.acns.org/pdf/guidelines/Guideline-11A.pdf. Accessed March 3, 2022.
- Macdonald DB, Skinner S, Shils J, et al. Intraoperative motor evoked potential monitoring - a position statement by the American Society of Neurophysiological Monitoring. Clin Neurophysiol. Dec 2013; 124(12): 2291-316. PMID 24055297
- National Institute for Health and Care Excellence (NICE). Intraoperative nerve monitoring during thyroid surgery [IPG255]. 2008; https://www.nice.org.uk/guidance/ipg255/chapter/1-guidance. Accessed March 3, 2022.
- Centers for Medicare & Medicaid Services. National Coverage Determination (NCD) for Electroencephalographic Monitoring During Surgical Procedures Involving the Cerebral Vasculature (160.8). 2006; https://www.cms.gov/medicare-coverage-database/details/ncd- details.aspx?NCDId = 77&ncdver = 2&CoverageSelection = National&KeyWord = monitoring&KeyWordLookUp = Title &KeyWordLookUp = Title&KeyWordLookUp = Title&KeyWordSearchType = And&KeyWordSearchType = And&KeyW ordSearchType = And&bc = gAAAACAAAAAA&. Accessed March 3, 2022.
- Centers for Medicare & Medicaid Services. Billing Medicare for Remote Intraoperative Neurophysiology Monitoring in CY 2013. Updated September 2020; https://www.cms.gov/Medicare/Medicare-Fee-for-Service- Payment/PhysicianFeeSched/Downloads/FAQ-Remote-IONM.pdf. Accessed March 3, 2022.
Coding Section
Codes | Number | Description |
---|---|---|
CPT | 95829 | Electrocardiogram at surgery (separate procedure) |
95865 | Needle electromyography; larynx | |
95867-95868 | Needle electromyography of cranial nerve supplied muscle(s) code range | |
95907-95913 | Nerve conduction study code range | |
95940 | Continuous intraoperative neurophysiology monitoring in the operating room, one on one monitoring requiring personal attendance, each 15 minutes (List separately in addition to code for primary procedure) | |
95941 | Continuous intraoperative neurophysiology monitoring, from outside the operating room (remote or nearby) or for monitoring of more than one case while in the operating room, per hour (List separately in addition to code for primary procedure) | |
95925-95927; 95938 | Somatosensory-evoked potential study code range | |
95928-95929; 95939 | Central motor evoked potential study (transcranial motor stimulation) code range | |
95930 | Visual evoked potential (VEP) checkerboard or flash testing, central nervous system except glaucoma, with interpretation and report | |
95955 | Electroencephalogram (EEG) during non-intracranial surgery (e.g., carotid surgery) | |
HCPCS | G0453 | Continuous intraoperative neurophysiology monitoring, from outside the operating room (remote or nearby), per patient, (attention directed exclusively to one patient) each 15 minutes (list in addition to primary procedure) |
ICD-10-CM | C41.2 | Malignant neoplasm of vertebral column |
C71.0-C71.9 | Malignant neoplasm of brain; code range | |
C72.0 | Malignant neoplasm of spinal cord | |
C73 | Malignant neoplasm of thyroid gland | |
C75.0 | Malignant neoplasm of parathyroid gland | |
C79.31-C79.32 | Secondary malignant neoplasm of brain and cerebral meninges; code range | |
D33.0-D33.9 | Benign neoplasm of brain and other parts of central nervous system; code range | |
D34 | Benign neoplasm of thyroid gland | |
D35.1 | Benign neoplasm of parathyroid gland | |
D43.0-D43.9 | Neoplasm of uncertain behavior of brain and central nervous system; code range | |
D44.0 | Neoplasm of uncertain behavior of thyroid gland | |
D44.2 | Neoplasm of uncertain behavior of parathyroid gland | |
D49.6 | Neoplasm of unspecified behavior of brain | |
E04.0-E04.9 | Other nontoxic goiter code range | |
E05.00-E05.91 | Thyrotoxicosis code range | |
E06.0-E06.9 | Thyroiditis code range | |
E21.0-E21.5 | Hyperparathyroidism code range (E21.0 is primary hyperparathyroidism) | |
I71.00-I71.9 | Aortic aneurysm and dissection; code range (Deleted I71.3 I71.4, I71.5, I71.6, Added I71.30-I71.33, I71.40-I17.43, I71.50-I71.53, I71.60-I71.63 eff 10/01/2022) | |
M50.00-M50.93 | Cervical disc disorders; code range | |
M48.00-M48.08 | Spinal stenosis; code range | |
M40.00-M40.57 | Kyphosis and lordosis; code range | |
M41.00-M41.9 | Scoliosis; code range | |
I65.01-I65.9 | Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction; code range | |
ICD-10-PCS | 4A0002Z | Measurement of Central Nervous Conductivity, Open Approach |
4A0004Z | Measurement of Central Nervous Electrical Activity, Open Approach | |
4A000BZ | Measurement of Central Nervous Pressure, Open Approach | |
4A00X2Z | Measurement of Central Nervous Conductivity, External Approach | |
4A00X4Z | Measurement of Central Nervous Electrical Activity, External Approach | |
4A01029 | Measurement of Peripheral Nervous Conductivity, Sensory, Open Approach | |
4A0102B | Measurement of Peripheral Nervous Conductivity, Motor, Open Approach | |
4A01329 | Measurement of Peripheral Nervous Conductivity, Sensory, Percutaneous Approach | |
4A0132B | Measurement of Peripheral Nervous Conductivity, Motor, Percutaneous Approach | |
4A01X29 | Measurement of Peripheral Nervous Conductivity, Sensory, External Approach | |
4A01X2B | Measurement of Peripheral Nervous Conductivity, Motor, External Approach | |
4A1002Z | Monitoring of Central Nervous Conductivity, Open Approach | |
4A1004Z | Monitoring of Central Nervous Electrical Activity, Open Approach | |
4A100BZ | Monitoring of Central Nervous Pressure, Open Approach | |
4A10X2Z | Monitoring of Central Nervous Conductivity, External Approach | |
4A10X4Z | Monitoring of Central Nervous Electrical Activity, External Approach | |
4A11029 | Monitoring of Peripheral Nervous Conductivity, Sensory, Open Approach | |
4A1102B | Monitoring of Peripheral Nervous Conductivity, Motor, Open Approach | |
4A11329 | Monitoring of Peripheral Nervous Conductivity, Sensory, Percutaneous Approach | |
4A1132B | Monitoring of Peripheral Nervous Conductivity, Motor, Percutaneous Approach | |
4A11X29 | Monitoring of Peripheral Nervous Conductivity, Sensory, External Approach | |
4A11X2B | Monitoring of Peripheral Nervous Conductivity, Motor, External Approach | |
4B00XVZ | Measurement of Central Nervous Stimulator, External Approach | |
4B01XVZ | Measurement of Peripheral Nervous Stimulator, External Approach | |
4B0FXVZ | Measurement of Musculoskeletal Stimulator, External Approach | |
F01Z77Z | Facial Nerve Function Assessment using Electrophysiologic Equipment | |
F01Z87Z | Neurophysiologic Intraoperative Assessment using Electrophysiologic Equipment | |
F01Z8JZ | Neurophysiologic Intraoperative Assessment using Somatosensory Equipment | |
F01Z9JZ | Somatosensory Evoked Potentials Assessment using Somatosensory Equipment | |
Type of service | Surgery | |
Place of service | Inpatient |
Procedure and diagnosis codes on Medical Policy documents are included only as a general reference tool for each policy. They may not be all-inclusive.
This medical policy was developed through consideration of peer-reviewed medical literature generally recognized by the relevant medical community, U.S. FDA approval status, nationally accepted standards of medical practice and accepted standards of medical practice in this community, Blue Cross Blue Shield Association technology assessment program (TEC) and other nonaffiliated technology evaluation centers, reference to federal regulations, other plan medical policies and accredited national guidelines.
"Current Procedural Terminology © American Medical Association. All Rights Reserved"
History From 2013 Forward
01/12/2023 | Annual review, no change to policy intent. Updating coding, rationale and references. Removing appendixes as they are no longer relevant |
01/03/2022 |
Annual review, no change to policy intent. Updating description, rationale and references. |
01/05/2021 |
Annual review, no change to policy intent. Updating rationale, references, guidelines and coding. |
07/08/2020 |
Interim review to add policy statement regarding train of four (TOF). No other changes. |
01/21/2020 |
Annual review, no change to policy intent. Updating rationale, references and description. |
05/21/2019 |
Corrected last review date. No other changes made. |
01/30/2019 |
Annual review, updating rationale and references. |
11/14/2018 |
Interim review updating note section to include facial nerve monitoring and adding specificity to the providers included in the note. No other changes made. |
09/11/2018 |
Interim review, updating coding. No other changes made. |
02/15/2018 |
Annual review, adding policy verbiage regarding the medical necessity of laryngeal nerve monitoring. Also updating title, background, description, guidelines, rationale and references. |
01/04/2017 |
Annual review, no change to policy intent. |
01/13/2016 |
Annual review, no change to policy intent. Updating background, description, rationale and references. |
01/29/2015 |
Annual review, no change to policy intent. Added coding & related policy. Updated guidelines, rationale and references. |
01/14/2014 |
Annual review. Updated rationale and references. Added benefit applications. No change to policy intent. |