Delayed Intra-operative Spinal Cord Monitoring Events in Paediatric and Young Adult Spinal Deformity Patients

Tristan McMillan; Atul Vats; Enrique Garrido; Ciara Michaelson; ATHANASIOS I. TSIRIKOS

doi:10.20944/preprints202407.1948.v1

Submitted:

23 July 2024

Posted:

24 July 2024

You are already at the latest version

Abstract

Introduction Delayed intra-operative neuro-monitoring (IOM) events can be defined as loss of responses, after baseline traces were present upon completion of instrumentation and deformity correction. This study reports this subgroup of events, assesses their incidence and evaluates potential causative factors. Methods We reviewed 1881 consecutive patients who underwent spinal deformity correction between 2011 and 2021. Surgeries were performed using a standardised anaesthetic regimen and multimodal IOM protocol. Results 44 patients (2.4%) had an IOM event. 9 patients (6F:3M) had a true positive delayed event after posterior segmental pedicle screw instrumentation. Mean age was 12.5 (2-17) years with mean thoracic Cobb angle of 78° (51-94°). Mean estimated blood loss was 28%. Titanium beam shaped rods were utilised in 3 patients and 5.5mm titanium rods in 5 patients. Motor evoked potentials were lost on average 18 (10-30) minutes after completion of instrumentation. 7 patients had bilateral loss and 2 patients had unilateral loss of MEP traces. Sensory evoked potential amplitude was preserved in all cases. There was a transient latency shift in one patient. MEPs returned within 20 minutes of rod release. The rod was re-contoured to incorporate more scoliosis in 1 patient. 2 patients had beam rods exchanged to 5.5mm titanium rods. 6 patients had rod removal with retention of pedicle screws and staged completion of instrumentation at mean 5 (1-7) days later. No patients had a postoperative neurological deficit. Conclusion Delayed IOM loss represented 15% of all events. Increased cord tension and hypo-perfusion were considered likely mechanisms. Rod release restored MEPs in all cases. The timing of events emphasises the importance of continued monitoring for minimum 30 minutes after completion of spinal instrumentation or until wound closure.

Keywords:

Intraopeartive monitoring

;

spinal deformity

;

Spinal cord hypoperfusion

Subject:

Public Health and Healthcare - Health Policy and Services

Introduction

The incidence of neurological injury in paediatric and adolescent spinal deformity surgery varies within the literature but is thought to range from 1 to 2% [1,2]. Due to the significant variation within this large cohort, the incidence can vary depending on which subgroup of patients are analysed. Specifically, the type and severity of deformity, curve stiffness and curve correction, underlying medical conditions, surgical approach, intraoperative haemodynamic stability, and revision procedures are all thought to have an effect [1,2]. In most cases, injury to the spinal cord occurs due to direct trauma or secondary to ischemia. The utilisation of spinal cord monitoring can assist in alerting the operating team that the cord is at risk in the hope to reverse actions to prevent permanent neurological deficit. The method of assessing spinal cord function during deformity surgery has moved from the Stagnara wake-up test to intra-operative neuro-monitoring [3].

Intraoperative neurophysiological monitoring (IOM) helps assess the integrity of neural structures during surgical procedures. It includes both continuous monitoring of neural tissue, as well as the localization of vital neural structures. IOM methods have evolved from the use of only somatosensory evoked potentials (SSEPs) to the combined approach using SSEPs, motor evoked potentials (MEPs) and free running electromyography (EMG) [4,5]. SSEPs monitor the dorsal column–medial lemniscus pathway, which mediates tactile discrimination, vibration, and proprioception. MEPs monitor the motor pathways; transcranial electrical stimulation elicits excitation of corticospinal projections at multiple levels with the electrical potential recorded at the spinal cord or muscles. MEPs are generated and transported via the pyramidal tract. Electromyography (EMG) records myoelectric signals from peripheral musculature to monitor selective nerve root function.

Multimodal IOM has been established as standard method for early detection of an evolving or impending spinal cord deficit during surgical deformity correction of the spine, that will allow timely intervention before permanent neurologic injury occurs (SRS information statement 2019). This combined approach has increased sensitivity and specificity for detecting neurological damage during deformity correction [4,6,7]. Despite this there remains variability in individual practice during utilisation of IOM and in handling of neuro-monitoring alerts [8]. There is also discrepancy between surgeons with regard to when they discontinue monitoring. 12.7% of surgeons stop monitoring when the anaesthetic is discontinued, 29.2% continue monitoring for 60 minutes after deformity correction or until the wound is closed, and 45.4% continue for 30 minutes after correction or until the wound is closed. Alarmingly, 12.7% of surgeons stop monitoring when the final tightening of implants has been completed.

Continuation of IOM after completion of instrumentation is very important as there is a potential for loss of IOM signals in this period. There is paucity of literature regarding these events. Within our institution we would classify this as a delayed IOM event. We define delayed IOM events as ‘loss of responses, after baseline responses were present upon completion of instrumentation and deformity correction’. The aim of this study is to evaluate the IOM results within our service and specifically investigate this subgroup of delayed events with the aim to assess their incidence and determine the need for continuation of IOM after completion of instrumentation.

Methods

We performed a retrospective study of all paediatric and young adult patients who underwent spinal deformity surgery with instrumentation and intended multimodal IOM within our service between December 2011 and August 2021. Patients under the age of 25 years were included for analysis. Data was collected from the medical, surgical, and IOM records and documented postoperative complications. The primary objective was to identify and investigate those patients who had an IOM event.

IOM Technique

IOM was performed by 2 nationally certified senior clinical physiologists who were present throughout the entire procedure using a 10-channel Medelec© Synergy IOM constant voltage system (2009–2013) and a 24-channel Inomed ISIS IOM constant current system (2014–2021). We aimed for multimodal IOM in all patients, recording of cortical SSEPs, cervical SSEPs, and MEPs. Reference traces were obtained before skin incision.

Somatosensory Evoked Potentials

Sensory evoked potentials were recorded from the brain (cortical SSEP) and spinal cord (cervical SSEP). Responses were evoked by cathodal delivery of 0.2 ms duration, square-wave impulses at a range of 3.7–4.3 Hz to bilateral posterior tibial nerves using pairs of adhesive electrodes. The stimulation intensity was 45 mA. Upper limb SSEPs were introduced in a similar fashion with square wave impulses delivered to bilateral ulnar nerves at 25 mA. Cortical SSEPs were recorded from corkscrew electrodes placed in the scalp at Cz’ and referred to Fz (identified using the 10–20 international head measurement system). Cervical SSEPs were recorded from a needle electrode placed subcutaneously over Cv2 and referred to Fz.

Motor Evoked Potentials

MEPs were recorded bilaterally as compound muscle action potentials (CMAPs) from the tibialis anterior (TA) and abductor hallucis (AH) muscles in the lower extremities (the rectus femoris [RF] was added in 2013) and from the abductor digiti minimi (ADM) muscle in the upper extremities. Bilateral ADM responses were used as controls to differentiate between surgical and nonsurgical loss of limb responses and identify brachial plexus compromise due to patient positioning. MEPs were elicited periodically by delivering an anodal pulse train of 4–7 pulses of 0.5 ms duration and interstimulus interval of 2–4 ms at amplitudes of 200–500 V (fixed voltage system) or 150–220 mA (fixed current system) between two corkscrew electrodes positioned over the motor cortex at C1 and C2. The stimulus strength was optimised to elicit reproducible responses. In patients with grade IV and V spondylolisthesis included in this series we added MEP recording from the anal sphincter and the gastrocnemius to the multimodal technique in order to monitor the sacral nerve roots.

Alarm Criteria

Action was taken when:

Mode 1-cortical SSEPs: unilateral or bilateral responses dropped >50% in amplitude with or without a corresponding increase in latency >10% of reference traces.
Mode 2-cervical SSEPs: unilateral or bilateral responses dropped >50% in amplitude with or without corresponding increase in latency >10% of reference traces.
Mode 3-MEPs: MEP-evoked CMAP responses in any muscle were lost and remained absent. Any sudden drop in amplitude of MEP traces >80% of reference traces was reported and investigated.

Decisions during surgery in response to IOM findings rested with the surgeon. Close collaboration with our anaesthetic and neurophysiology teams was mandatory to secure accurate interpretation of IOM changes, to initiate an immediate response, and prevent neurological damage. In all cases of IOM events, the routine initial check included mean arterial blood pressure that was raised to >80mm Hg and body temperature >36.5°C. Technical problems with the recording system or due to dislodgement of the electrodes were also excluded. Muscle relaxant (atracurium) given during soft tissue dissection had metabolised and another baseline IOM recording was obtained before placement of instrumentation.

IOM Diagnostic Criteria

IOM events were classified by time of onset and by type of event. Time of onset was split into immediate events that occurred immediately after a surgical action or delayed events that we defined as a loss of responses, after baseline traces were present upon completion of instrumentation and correction. Our diagnostic criteria for type of IOM monitoring events are presented in Table 1 [11].

Results

We identified 1881 patients (562 male:1319 female) with a mean age of 14.2 years (range 1-25 years). 59.1% (n = 1112) of patients had surgery to treat an Adolescent Idiopathic Scoliosis (AIS). A further breakdown of the primary diagnosis is listed in Table 2. In total, 1780 patients underwent posterior spinal instrumentation and fusion, 41 patients underwent anterior spinal instrumentation and fusion, and 36 patients underwent a combined anterior release and posterior instrumented fusion. 24 patients had insertion of growing rods. Multimodal monitoring was achieved in 93.9% (1767/1881) of patients. In 0.6% (11/1881) of patients reproducible monitoring responses were unachievable and so intraoperative neuromonitoring was abandoned. Unimodal monitoring was achieved in 2.3% (44/1881) and bimodal monitoring was achieved in 3.1% (59/1881) of patients. Of those patients that multimodal was not achieved, the predominant (75%, 85/114 patients) diagnosis was either neuromuscular or syndromic scoliosis.

Neuro-Monitoring Events

Of the 1870 patients that had intra-operative monitoring for the duration of their surgical procedure, 3% (61/1870) of patients (18 male:43 female) had a positive IOM event meeting the alarm criteria outlined in Table 3. 2.4% (44/1870) of patients had a true positive event, of which 43 events were transient. 35 patients had acute events and 9 patients had delayed events. 0.9% (17/1870) of patients had a false positive event. 97% (1809/1870) of patients had a true negative IOM. No patient had a false negative IOM. The sensitivity of intraoperative spinal cord monitoring with MEPs and SSEPs for our cohort was 1.0 and the specificity was 0.99. The positive predictive value was 0.73 and the negative predictive value was 1.0.

True Positive Acute Events (Table 2)

There was 1 true positive event and 34 transient true positive events. In the true positive event the change in monitoring was not attributable to a surgical step and failed to improve after reversal of surgical steps including removal of spinal instrumentation. No canal breach was identified and postoperative investigations supported a vascular event to the cord. The patient recovered to baseline neurological function within 3 months of surgery. The transient events were associated with surgical events, with the most common being rod reduction (11 patients, 41%) and screw insertion (10 patients, 37%). Other causes included pedicle hook insertion (3 patients, 11%), sublaminar wire insertion (2 patients, 7%), posterior facetectomy (2 patients, 7%), patient positioning (2 patients, 7%), rod distraction (1 patient, 4%), application of skeletal traction (1 patient, 4%), psoas retraction during an antero-lateral approach (1 patient, 4%) and 1 was undetermined.

True Positive Delayed Events

9 patients (3 male:6 female) had a true positive delayed event after posterior segmental pedicle screw instrumentation. Mean age was 12.5 (2-17) years. 6 patients had idiopathic scoliosis (4 AIS, 2 JIS), 1 patient congenital scoliosis, 1 neuromuscular scoliosis and 1 patient had thoracic kyphosis post-vertebral osteomyelitis. In those patients with scoliosis, the mean thoracic curve angle was 78° (51-94°). Mean estimated blood volume loss was 28%. Titanium beam shaped rods were utilised in 3 patients and 5.5 mm titanium rods in 6. MEPs were lost on average 18 (10-30) minutes after completion of instrumentation. All alarms were Mode 3 alarms; 7 patients had bilateral loss and 2 patients had unilateral loss of MEPs. Sensory evoked potential amplitude was temporarily reduced in 1 patient and was preserved in all other cases. There was a transient latency shift in one another patient. The MEPs returned within 20 minutes of rod release in all patients. The rod was re-contoured to incorporate more scoliosis in 1 patient. 2 patients had beam rods exchanged to 5.5 mm titanium rods. 6 patients had rod removal with retention of pedicle screws and staged completion of instrumentation at mean 5 (1-7) days later. No patients had a postoperative neurological deficit.

False Positive Events

0.9% (17/1870) of patients had a false positive event. 14 of these were acute and 3 were delayed events experienced after completion of instrumentation. 53% (9/17) of false positive events were associated with a reduction in patient blood pressure and resolved with an increase in mean arterial pressure to 85-90 mm Hg. In one patient this hypotension was secondary to intra-operative administration of Clonidine for analgesia. In 1 patient, responses dropped during exposure and recovered before placement of instrumentation. This was attributed to be an acute drop in patient temperature, normalising with patient warming. In 1 patient MEP loss recovered to reproducible baseline after adjustment of stimulus. 1 patient had IOM loss attributed to a technical fault with the monitoring software and confirmed with a normal wake up test. 2 patients had return of baseline monitoring without surgical intervention or identified haemodynamic adjustment. In 2 patients with AIS, removal of instrumentation was done with no change in monitoring. Despite monitoring change, both patients woke with no neurological deficit and normal postoperative imaging. Re-instrumentation and definitive fusion were successfully re-attempted and completed within two weeks of initial surgery.

Discussion

IOM is recommended in procedures where there is risk of neurological injury including scoliosis surgery [6,10]. Fehlings et al. [11], in their systematic review of 32 studies determined that strong evidence exists that multimodal IOM is sensitive and specific for detecting intra-operative neurological injury and recommended the use of such monitoring for spinal deformity correction. Our series shows that multimodal IOM is achievable in 94% of paediatric and adolescent spinal deformity procedures while reproducible neuro-monitoring was not achievable in less than 1% of patients. Furthermore, when used in conjunction with a standardised management algorithm, IOM is highly sensitive (100%) and specific (99%) in the detection of acute intra-operative neurological dysfunction [9].

Thuet et al. [6] reported a false negative rate of 0.2% in their 23-year retrospective series of 3436 pediatric patients undergoing spinal surgery using varying IOM methods. This is in contrast to our study where we had 0% false negative IOM events. We feel that this reflects the advancement of monitoring techniques and further development of the skills of the specialised neuro-physiology teams. Fortunately, the incidence of true positive events is low with only 1 patient having sustained IOM loss together with a postoperative deficit that later recovered. The remainder of the acute true positive events were transient with recovery to baseline following surgical intervention. Lee et al. [12] identified greater preoperative Cobb angle of the major structural curve, number of levels fused, operative time and estimated blood loss as risk factors for spinal cord injury during deformity correction which can cause IOM loss. In our cohort, the most common cause of a transient true positive event was during placement of instrumentation of the spine, accounting for 44% (15/34) of events (29% screw insertion, 9% pedicle hook insertion and 6% sublaminar wire insertion). The second most common cause of transient true positive events was during reduction manoeuvres including rod distraction (35%, 11/34).

In our series, the highest risk of true positive IOM event was seen in syndromic scoliosis (5.5%). The next highest within our cohort was seen in spondylolisthesis (3.7%). However, this only represented a single event in a small sample size (1/27). The next highest was seen in juvenile idiopathic scoliosis and adolescent idiopathic scoliosis. Neuromuscular scoliosis and Scheuermann kyphosis had similar rate of true positive IOM events (Table 2). This is different from the rate of true positive events reported in the literature [10,13,14,15]. We found a difference between Scheuermann kyphosis and AIS on the risk of true positive events with event incidence of 2/111 patients (1.8%) in Scheuermann kyphosis versus 23/1112 patients (2.1%) in AIS. Previous studies suggested greater risk of neurological complications in patients with thoracic hyper-kyphosis and those requiring corrective osteotomies [10,16,17]. Although there are differences in sample size, this was not demonstrated in our cohort. The increased rate of events in early onset idiopathic scoliosis is likely representative of curve severity and curve stiffness within this subgroup.

False positive events do continue to occur, however these can only be classified after systematically excluding a direct cause for the event. This is best achieved by following a structured algorithm or cord-at-risk protocol, such as that illustrated in Figure 1 [9]. This requires effective working within the multi-disciplinary theatre team and good communication with the anaesthetic team to ensure drug administration, haemodynamic stability and temperature are all appropriate.

Delayed Event

A delayed IOM event is defined as change in IOM after completion of instrumentation. There is lack of information in the literature as far as delayed loss of IOM signals after spinal deformity surgery is concerned. Stöckl et al. [18] reported 2 cases of delayed motor deficit after posterior scoliosis correction. Both patients improved after removal of instrumentation. Lovi et al. [19] reported a case of delayed postoperative neurological deficit far from the surgical site in a patient with syndromic scoliosis. The authors concluded that delayed postoperative neurological deficit far from the surgical site can be considered a specific subgroup of these rare complication that can occur several hours after spine surgery, regardless of intraoperative complication. Removal of instrumentation was sufficient to regain full motor recovery caudal to the level of instrumentation.

In our study, there were 9 delayed true positive IOM events. These represented 16% of all true positive IOM events and an overall incidence of 1 in 200 procedures. This emphasises the importance of continuation of monitoring after deformity correction and completion of spinal instrumentation. In our cohort, patients’ MEPs were lost on average 18 minutes after completion of instrumentation with a range of 10-30 minutes. We, therefore, recommend continuing neuro-monitoring for at least 30 minutes after placement of instrumentation or until skin closure; thereby, minimising the period between discontinuing monitoring and the patient being awake to perform a formal neurological evaluation.

We would hypothesise that these delayed events are due to spinal cord ischaemia secondary to segmental artery hypo-perfusion as a result of vessel tension. Meylaerts et al. [20] showed recovery of MEPs by restoration of spinal cord perfusion during thoraco-abdominal aortic aneurysm repair. Sandhu et al. [21] also described fluctuations in spinal cord perfusion pressure as cause of delayed paraplegia after thoraco-abdominal aortic repair.

The pathophysiology of intra-operative spinal cord injury during deformity correction was studied by Turner et al. [22] combining spinal cord perfusion (SCP) with intrathecal pressure and neurological monitoring (MEP). The authors depicted a direct relation between SCP fluctuation and MEPs reduction. As we know hypotension correction is one of the most widely performed general measure following an intra-operative alert, since there is good evidence that even a mild drop in systemic systolic blood pressure can affect the motor potentials profile [11,22]. Releasing rods reduces cord/vascular tension and aids cord re-perfusion. MEPs returned within 20 minutes of rod release in all patients.

The stiffness of the rod could be influential in the incidence of delayed events. Within our institution the beam shape rods are utilised in a small percentage of patients, yet these were associated with 33% of the delayed IOM events. Due to the difference in Young’s modulus of elasticity, beam shape rods are stiffer than standard titanium cylindrical rods and, therefore, have reduced capacity to undergo plastic/elastic deformation, thereby potentially leading to increased cord/vascular tension. On review of patient risk factors for delayed events, we identified no significant difference within this subgroup when we looked at age, diagnosis, curve angle and estimated blood loss.

We have proposed an algorithm to allow the surgical team to decide appropriate actions in response to MEP loss (Figure 1) [9]. There are existing guidelines, checklists, and algorithms for the prevention, identification, and management of neurological complications in spine surgery [23,24,25,26]. We advocate the need for close cooperation and continuous communication of the surgical/anaesthetic/neurophysiology teams before, during, and after surgery. In our experience, this coordinated approach has allowed appropriate response to IOM changes and ensured that no patient in this series developed neurological deficits contrary to previous studies which reported risk of permanent neurological injury of 0.1–0.2% [13,17]. In the patient consent, we recommend a detailed discussion on IOM and the possible need to abandon surgery depending on IOM findings and complete it in a staged manner at a later date.

Limitations

While we have addressed some of the risk factors for neurological injury/IOM event, further analysis could have been performed looking at curve stiffness and it would also be useful to assess percentage curve correction at the time of IOM event but this is not possible with the patients lying in the supine position and the limited information provided by intra-operative imaging. Additionally, the literature reports the use of pre-operative MRI to assess the risk of intra-operative neuromonitoring data loss and it may have been beneficial utilise this classification in our patients and to correlate this with our findings [27]. Unfortunately, as we run a tertiary centre, many of the MRI scans are performed at the point of referral, and not at the point of surgery, therefore we did not feel they would accurately represent the curve characteristics at the time of intervention

Conclusions

We present one of the largest cohorts of spinal cord monitoring outcomes in spinal deformity. This provides further support that multimodal IOM is the gold standard of neuro-monitoring during deformity correction with excellent sensitivity and specificity. We feel that this study will aid the surgeons in standardisation of practice and will also facilitate in educating and consenting patients on the risks of monitoring events and neurological injury during spinal deformity surgery. Delayed IOM loss represented 16% of all events with the likely mechanism of increased cord tension and hypo-perfusion. The timing of events emphasises the importance of continued monitoring for at least 30 minutes after completion of instrumentation or until wound closure. Surgeons should be particularly vigilant for delayed events when using stiffer rod constructs.

Author Contributions

Tristan McMillan: writing original draft and review. Atul Vats: writing and editing. Enrique Garrido: review. Ciara Michaelson: review, Athanasios I. Tsirikos: Conceptualization (lead) and review.

Funding

Nothing to declare.

Consent and Institutional Review Board statement

As this is a retrospective analysis of practice and doesn’t involve any clinical encounter, no consent or institutional board approval was needed.

Data availability

Data that supports the study are available from the corresponding author(TM) on request.

Disclosure Statement

The authors did not receive grants or outside funding in support of their research or preparation of this manuscript. They did not receive payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. No commercial entity paid or directed, or agreed to pay or debit, any benefits to any research fund, foundation, educational institution, or other charitable or non-profit organisation with which the authors are affiliated or associated.

Conflicts of Interest

None.

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Figure 1. Algorithm to be followed by surgical team in the event of MEP loss [9].

Table 1. Description of our diagnostic criteria for IOM events [9].

Diagnostic performance characteristic	Criteria
True positive	Lost IOM responses Linked to patient positioning on the surgical table or a surgical event (occurring after instrumentation placement, spinal osteotomies, deformity correction manoeuvres) Responses do not return despite appropriate change in patient position or surgical action Potential postoperative neurological deficit
Transient true positive	Lost IOM responses Linked to patient positioning on the surgical table or a surgical event (occurring after instrumentation placement, spinal osteotomies, deformity correction manoeuvres) Responses return following appropriate change in patient position or surgical action No postoperative neurological deficit
Transient false positive	Lost IOM responses Not linked to a clear surgical event (possibly associated with an anaesthetic, metabolic, technical, or unknown cause) Responses return following appropriate action (for example increase in blood pressure, reversal of muscle relaxation, change in anaesthetic agents) No postoperative neurological deficit
True negative	IOM responses remain unchanged throughout No postoperative neurological deficit
False negative	IOM responses remain unchanged throughout Postoperative neurological deficit

Table 2. Primary diagnosis within our patient cohort and rate of true positive (TP) IOM events according to diagnosis.

Diagnosis	Number of Patients	Rate of TP IOM Events
Infantile Idiopathic Scoliosis	40	0% (n = 0)
Juvenile Idiopathic Scoliosis	85	3.5% (n = 3)
Adolescent Idiopathic Scoliosis	1112	2.1% (n = 23)
Adult Idiopathic Scoliosis	23	0% (n = 0)
Congenital Scoliosis	154	1.3% (n = 2)
Syndromic Scoliosis	181	5.5% (n = 10)
Neuromuscular Scoliosis	109	1.8% (n = 2)
Spondylolisthesis	27	3.7% (n = 1)
Scheuermann Kyphosis	111	1.8% (n = 2)
Other	39	2.6% (n = 1)

Table 3. Classification of IOM events.

Event Type	Event Timing
Event Type	Acute	Delayed	Total
True positive	1	0	1
Transient true positive	34	9	43
Transient false positive	14	3	17
True negative	-	-	1809
False negative	-	-	0

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