Review

Acute Management of Spinal Cord Injury in Out-of-hospital and Emergency Department Settings

10.4274/eajem.galenos.2017.98698

  • Burak Katipoğlu
  • Arman Dağal
  • Semih Korkut
  • Abdullah Osman Koçak

Received Date: 23.02.2017 Accepted Date: 18.06.2017 Eurasian J Emerg Med 2020;19(2):55-62

Spinal cord injury (SCI) is a devastating neurological disorder that is estimated to affect approximately 1000 patients each year in the Republic of Turkey. With this review, we aim to update the recent evidence related to the acute management of patients with SCI in out-of-hospital and emergency department settings.

We performed a literature review of publications in the English language and indexed in PubMed, ScienceDirect and Scopus using the following search terms: “spinal cord injury” and “acute management”, “spinal cord injury” and “immobilisation”, “spinal cord injury” and “transfer”, “spinal cord injury” and “transport”, “spinal cord injury” and “airway management”, “spinal cord injury” and “haemodynamic management”, “spinal cord injury” and “steroid”. We also reviewed the recent international guidelines.

This review reports the immobilisation of patients with SCI and management strategies relevant to their transfer, airway management in cervical SCI, haemodynamic management and methylprednisolone use.

The patient’s spinal alignment should be maintained with appropriate techniques for sufficient immobilisation to ease safe extrication and transport. Patients with acute SCI should be promptly and carefully transported from the place of injury to the nearest specialist SCI facility.

Keywords: Spinal cord injury, haemodynamic management, airway, immobilisation

Introduction

Injuries contributed to the 6% of total deaths in Turkey (Table 1). Mostly young people affected by the injury related deaths (Figure 1). According to the data from the Turkish Statistical Institute, over one million traffic accidents occurred during the year 2014. 168,512 of the accidents resulted in fatality or injury. Seventy-five point one percent occurred in the populated areas, during the month of August at day hours. As a result of these accidents, 3,524 people died and 285,059 injured (Table 2). Among the people died in the accidents, 42.7% of them were drivers, 40.3% were travelers and 17% were people on foot. Concerning the sexual orientation breakdown of individuals died 76.8% of them were men and 23.2% were women; while for the general population harmed 70.2% of them were men and 29.8% were women (1).

There is no recent Turkish epidemiological study published in spinal cord injury (SCI) topic. According to a nation-wide retrospective study published by Karacan et al. (1) in 2000, 5,081 traumatic SCI cases were reported in 1992 (2). The estimated annual incidence of traumatic SCI was found 12.7 per million people. Male to female proportion was 2.5:1 and the normal age at harm was 35.5±15.1 (35.4±14.8 for guys and 35.9±16.0 for females). The most widely recognized reason for harm was engine vehicle mischances (48.8%) trailed by falls (36.5%), cut injuries (3.3%), shot wounds (1.9%) and wounds from jumping (1.2%). One hundred and eighty-seven patients (32.18%) were tetraplegic and 394 patients (67.8%) were paraplegic. The most well-known level of damage was C5 among tetraplegics and T12 among paraplegics. The most common related injury was head trauma took after by extremity fractures.

Acute phase of SCI management is critical for the minimization of the secondary injury, which directly affects the outcome quality and survival of the patient. Initial trauma results in an irreversible neuronal damage (Primary injury) and is only modifiable by prevention. Secondary injury starts within minutes and involves complex cascade of events including inflammation, oedema, ischemia, and excitotoxicity leading to further ischemia and progressive neurological deterioration in the following days. Carefully coordinated management strategies aim to limit/reverse this progression. Treatment and damage control starts at the seen and critical during the first 24 hours. Early clinical assessments, accurate spinal immobilisation, prompt transfer of injured patient to a SCI unit, and respiratory and haemodynamic support are recommended for the acute management of spinal cord injured patients (3).

It is important to recognize that 20-60% of SCI will also have a concurrent traumatic brain injury. Thoracic spine injuries may be accompanied by a major vascular injury pneumothorax, myocardial and/or pulmonary contusion. Lumbar spine fractures may be associated with bowel and solid organ injury (4-7).


1. Transfer of Spinal Cord Injured Patient

SCI occurs in up to 2-5% of all major trauma cases and at least 14% of these cases have the potential to have an unstable spine. Emergency first responders therefore should exercise high index of suspicion for SCI in the major trauma settings. In a study performed to evaluate pre-hospital management of spinal cord injuries in New South Wales between 2004 and 2008, found that the median time from the scene to a SCI unit was 12 hours, with 60% of patients needed multiple transfers. The odds of reaching a SCI unit in 24 hours were 1.71 times greater for patients injured in a major city (95% CI: 1.00-2.90) than in the other areas. SCI patients with multiple traumas had more delays to reach a SCI unit (59%) than the isolated SCI patients (40%). Patients who reached a SCI unit after 24 hours were at 2.5 times greater risk to develop a secondary complication (95% CI: 1.51-4.17) (8).

The trauma patient triage scheme of the American College of Surgeons Committee on Trauma has 4-step evaluation process, first the assessment of vital signs and Glasgow Coma scale score, second the evaluation for critical injury patterns, third the assessment of high- energy impact mechanism, and, fourth, the assessment of special patient characteristics, like age, pregnancy, anticoagulation treatment, burns, and end-stage renal disease (9).

In a review of the cases with SCI after the 2005 Pakistan earthquake, reported that the lack of SCI evacuation protocols caused permanent neurological deficits in some patients because of missed stabilisation of spinal column. On the other hand, air transport of patients and on time transfers of the patients from the disaster zone to tertiary care hospitals had provided low mortality rates (10).

However, Oteir et al. (11) found that there is a lack of high-level evidence on the effect of pre-hospital cervical immobilisation on consequences in their systematic review of the literature to determine the efficacy of cervical immobilisation in patients with suspected cervical SCI. In their systematic review, which the eight studies included, cervical collar application in penetrating trauma was associated with increased mortality in two of the studies. In blunt trauma, one study indicated that stabilization might worsen the neurological consequences. In another study, investigators found that there are some adverse effects of pre-hospital immobilization, including increased aspiration risk, airway problems, delay in transfer, and patient discomfort (12).

In a recent systematic review of 47 studies about spinal immobilization in pre-hospital and emergency care settings from 1966 to 2015, authors found that there were 15 studies supportive of spinal immobilization, 13 studies neutral for spinal immobilization and also 19 studies opposing spinal immobilization. They said that; decisions to use spinal immobilisation should be based upon careful assessment of the risk-benefit ratio (13).

Burton et al. (14) found that, emergency medicine service providers were able to triage prehospital trauma patients with a four-step clinical assessment protocol and to accurately identify the patients likely to benefit from immobilization. Data from a statewide hospital registry included all patients treated for spine fracture during the 12-month period with 207,545 encounters, including 31,885 transports to an emergency department for acute trauma-related illness. The protocol sensitivity for immobilization of any acute spine fracture was found 87.0% (14). In a recent study conducted a retrospective analysis of penetrating trauma patients in the National Trauma Data Bank of United States, 45,284 penetrating trauma patients were concentrated; 4.3% of whom experienced spine immobilisation.

In a recent study, a retrospective analysis of penetrating trauma patients was performed in the National Trauma Data Bank of United States, 45,284 penetrating trauma patients were concentrated; 4.3% of whom experienced spine immobilization. General mortality was 8.1%. Unadjusted mortality was twice as high in spine-immobilized patients (14.7% vs 7.2%, p<0.001). The chances proportion of death for spine-immobilised patients was 2.06 (95% CI: 1.35-3.13) contrasted and non-immobilised patients. Prehospital spine immobilisation is related with higher mortality in penetrating trauma (15).

Various devices and methods were used for immobilization of the cervical spine in SCI patients. Before the immobilisation, spinal posture should be evaluated to prevent secondary injuries. The neutral spinal posture was defined as “the normal anatomic position of the head and torso that one assumes when standing and looking ahead” by Schriger (16). This posture corresponds to 12 degrees of cervical spinal extension on a lateral radiograph. Podolsky et al. (17) found that hard collars had better outcomes than soft collar.

The American College of Surgeons suggests the utilization of a hard backboard, an inflexible cervical neckline, horizontal bolster gadgets, and tape or straps to secure the patient’s head, the neckline, and the parallel bolster gadgets to the backboard. Pronged and wrong utilisation of unbending backboard can bring about patient dismalness and ought to be stayed away from. Backboard ought to be expelled when a complete assessment is refined as well as conclusive administration is started. Spinal immobilisation of injury patients with entering wounds is not prescribed.

It is estimated that up to quarter of SCI occur following the initial trauma during the acute phase.  Expeditious and careful transport of patients with acute SCI is recommended from the site of injury by the most appropriate mode of transportation available to the nearest capable definitive care medical facility. Whenever it’s possible, patients should be transported to specialised acute spinal cord injury treatment centre.


2. Airway Management in Cervical Spine Injury

Inappropriate and/or insufficient airway management is a leading cause of preventable death following injury (18,19). In trauma endotracheal intubation frequently needs to be accomplished before the presence or location of an injury can be confirmed. As a result, cervical spine injury should be presumed in all trauma patients requiring intubation prior to complete physical and radiographic evaluation. If the level of injury is at or above C5, tracheal intubation and ventilation are often required (20).

Since the mid-eighties, manual in-line adjustment (MILS) is prescribed to help aviation route administration in patients with suspected SCI (21). The point of MILS is to keep any flexion; expansion or pivot of the cervical spine amid laryngoscopy is performed. In any case, use of MILS appeared to exacerbate the laryngoscopic see, draw out the intubation time or make disappointment secure the aviation route (22). One must adjust the advantages of MILS against the hazard for hypoxic harm if intubation and sufficient ventilation can’t be refined. In this way, MILS might be changed or ceased if its utilisation hinders tracheal intubation.

Direct laryngoscopy is more straightforward than fiberoptic or video assisted laryngoscopy and, in this way, favoured in pressing circumstances. It was established to be more sheltered, powerful, and quicker in ordinary aviation routes and in any event proportional in troublesome aviation routes. In immobilised patients, particularly for dire intubations, coordinate laryngoscopy with the utilisation of a gum flexible bougie is a phenomenal decision to rapidly and dependably secure the aviation route while limiting the compel to the cervical spine (23).

Alternative methods may include flexible scope intubation (FSI) and nasotracheal intubation; both have restricted application in the acute trauma management. Because of the nasotracheal intubation is contraindicated with particular craniofacial injuries, and may causes further trauma and bleeding in the upper airway (24). FSI provide little spinal motion, however, it is hard to perform for inexperienced providers, results in slower intubation compared to orotracheal intubation, and also is hindered by secretions and bleeding, needs continuous patient cooperation (25).

The blind-intubating laryngeal mask airway has been used successfully in trauma settings and uninjured but immobilised patients with rigid cervical collars (26,27). But this approach showed to cause low intubation success rate in inexperience staff (24). Video assisted laryngoscopes and other imaging approaches allow a better laryngeal view than traditional methods in immobilised SCI patients (28) Table 3 provides the pros and cons of commonly used airway management devices.

Muscle trismus or clenched jaw may cause failure in pre-hospital intubation (29,30). But these situations can be eliminated with the appropriate use of fast acting neuromuscular blocking agents (31). Regarding the choice of muscle relaxant, succinylcholine remains the gold standard for rapid sequence intubation in the early stages of SCI management. If these techniques fail to intubate the trachea of SCI patients, surgical methods like cricothyrotomy should be tried (32).

Each airway manoeuvre has its inherent weaknesses and advantages. There is no conclusive evidence that an optimal airway management strategy in patients with cervical instability affects outcome. The most suitable choice will often depend on the practitioner’s experience with a particular technique and the specifics of the clinical situation (33).

In the post-traumatic period, progressive neck swelling due to oedema and pre-vertebral haematoma expansion may further compromise the airway, even in the absence of positive examination findings in the early phase of the injury. Intubation should minimise cervical movement to prevent further neurological deterioration in a potential or actual SCI. Manual inline stabilization, gum elastic bougie and attention to detail required. Cricoid pressure (CP) ought to be connected amid acceptance and kept up through intubation until tube arrangement is confirmed; it might be connected through the front opening in cervical neckline before the neckline is briefly expelled. Both MILS and CP ought to be adjusted or expelled on the off chance that they hinder sufficient intubation or ventilation (34).


3. Haemodynamic Management of Spinal Cord Injury

7-10% of the SCI patients develop neurogenic circulatory shock and demonstrate hypotension with or without bradycardia (35,36). Besides to this condition, hypotension may be caused by trauma itself and may be difficult to differentiate in acute trauma (37). Kong et al. (38) found that 18.4% of the cervical SCI patients had 80 mmHg or below mean arterial pressure levels. Other possible major cardiovascular complications in the acute stage following SCI were heart rate abnormalities and venous thromboembolism. These heart rate abnormalities may lead to sinus bradycardia, repolarization changes, atrioventricular block, supraventricular tachycardia, ventricular tachycardia, and primary cardiac arrest (39,40).

Vale et al. (41) applied resuscitation standards of volume development and circulatory strain upkeep to 77 patients who had intense neurological deficiencies taking after SCI happening from C-1 through T-12 with an end goal to keep up spinal line blood stream and avert optional harm. They performed surgical strategies for decompression and adjustment, and combination in chose cases. Sixty-four of the patients have been taken after no less than 12 months post-harm by methods for point by point neurological appraisals and useful assessments. After the 12-month follow-up period, 92% of patients exhibited clinical change subsequent to managing inadequate cervical spinal line wounds contrasted with their underlying neurological status. Ninety-two percent recaptured the capacity to walk and 88% recovered bladder work.

Levi et al. (42) studied the acute phase of SCI. Management protocol included invasive haemodynamic monitoring and cardiovascular support with dopamine and/or dobutamine, titrated to maintain a haemodynamic profile with adequate cardiac output and a mean arterial pressure of >90 mmHg.

Stevens et al. (43) reported that the neurogenic circulatory shock should be treated with fluid resuscitation until intravascular volume is restored and, afterwards, use of vasopressors (eg. dopamine, norepinephrine, and phenylephrine) should be considered. Zäch et al. (44) given an account of a planned medical administration worldview in the treatment of 117 back to back intense SCI patients in the Swiss Paraplegic Centre of Basel, Switzerland in 1976. The creators reasoned that early exchange and “prompt medicinal particular treatment of the spinal damage” with consideration regarding upkeep of adequate circulatory strain seemed to enhance neurological recuperation. Another systematic review of intensive cardiopulmonary management following acute SCI, stated that there is weak evidence supporting the maintenance of MAP higher than 85 mm Hg for a period extending up to one week following acute SCI (45).


4. Steroids in Spinal Cord Injury

Bracken et al. (46) first reported the effectiveness of methylprednisolone treatment in SCI patients. After this study the use of intravenous high-dose methylprednisolone became a standard approach in acute management SCI patients (47). On the other hand, two other studies reported that high-dose methylprednisolone can be associated increased complication rates (48,49).

The role of the steroids in treatment of SCI patients is debatable. The possible mechanisms for proposed benefits include the inhibition of lipid peroxidation and inflammatory cytokines, modulation of the inflammatory/immune cells, improved vascular perfusion and prevention of calcium influx and accumulation (50).

The current use of methylprednisolone therapy based upon three prospective randomised multi-centre trials named National Acute Spinal Cord Injury Studies (NASCIS) I, II and III (46,51-53).

In NASCIS I, 330 patients treated first 48 hours of SCI, in one group with methylprednisolone with dose of 100 mg bolus, then 25 mg every 6 hours for 10 days, in other group with methylprednisolone with dose of 1,000 mg bolus, then 250 mg every 6 hours for 10 days. No significant difference in neurologic recovery between the two groups with different dose regiments at six-month follow-up period was detected (51).

In NASCIS II, 487 patients treated first 12 hours of SCI, in the first group with methylprednisolone with dose of 30 mg bolus, then 5.4 mg/kg/hour x 23 hours, in the second group with naloxone with dose of 5.4 mg/kg bolus, then 4.0 mg/kg/hourx 23 hours. The third group was placebo group. In patients treated with methylprednisolone within 8 hours of SCI, significant motor and sensory improvement was observed at 6 months and 12 months after both complete and incomplete injury groups (46,52,53).

NASCIS III was performed with 499 patients treated within first 8 hours of SCI, in the first group with methylprednisolone with dose of 30 mg bolus, then 5.4 mg/kg/hour×23 hours, in the second group with methylprednisolone with dose of 30 mg bolus, then 5.4 mg/kg/hour×47 hours, in the third group with tirilazad mesylate with dose of 2.5 mg/kg every 6 hours for 48 hours. It was found that there was no significant difference in neurologic recovery between the three groups at 6 or 12 months follow-up period. If the treatment was started 3 to 8 hours after SCI, 48-hour methylprednisolone group had significantly better improvement than 24-hour methylprednisolone group at 6 months and 12 months follow-up period but had more severe sepsis and severe pneumonia (53-55).

In a case report of a 37-year-old woman with whiplash injury after a motor vehicle collision, who had treated with intravenous high-dose methylprednisolone with a bolus dose of 30 mg/kg over 15 min followed by maintenance infusion of 5.4 mg/kg per hour for 23 hours, the patient became unresponsive; electrocardiography showed ventricular fibrillation, necessitating prompt cardiac defibrillation and renal failure after the infusion. The evaluation of the patient showed that, the patient had diffused large B-cell lymphoma and methylprednisolone induced acute tumour lysis syndrome causing ventricular fibrillation and renal failure. The authors said that, the physicians be aware of this clinical entity, and the importance of monitoring patients very close when prescribing corticosteroids, even in those with only mild anaemia (56).

In a cohort study, all patients with cervical cord injury were treated with methylprednisolone sodium succinate within 8 hours of their injuries (MPSS group) versus no treatment group (non-MPSS) and both groups followed up for two years. Early spinal decompression and stabilization was performed as early as possible after injury in both groups. The authors found that there was no evidence to support that high-dose methylprednisolone administration facilitates neurologic improvement in patients with SCI. They said that, methylprednisolone ought to be utilised under constrained conditions due to the high occurrence of pulmonary complications (57).


Summary

Spinal immobilisation can diminish improvement of the cervical spine and can decrease the probability of helper neurological injuries in patients with problematic cervical spinal breaks after harm. Immobilisation of the entire spinal section is crucial in these patients until a spinal string harm (or various injuries) is disallowed or until fitting treatment is begun. Regardless, not all damage patients must be treated with spinal immobilisation in the midst of prehospital restoration and transport. Various patients do not have spinal injuries and along these lines don’t require such mediation.

There is an absence of authoritative proof to suggest a uniform gadget for spinal immobilisation and system. It gives the idea that a mix of an inflexible cervical neckline with steady pieces on an unbending backboard with straps and tape to immobilise the whole body is powerful at accomplishing protected, successful spinal immobilisation for transport. Spinal immobilisation gadgets ought to be utilised to accomplish the objectives of spinal strength for safe removal and transport. Spinal immobilization of injury patients with entering wounds is not prescribed.

Tolerant with an intense cervical spinal damage ought to be quickly and precisely transported from the site of harm to the closest office with SCI unit. The method of transportation picked ought to be founded on the clinical conditions, separation, and geology to be voyage and ought to be the quickest means accessible. Cervical SCI patients have a high occurrence of aviation route trade off and pneumonic brokenness; along these lines, respiratory bolster measures ought to be accessible amid transport.

In spite of beginning stable heart and pneumonic capacity it is normal to watch hypotension, hypoxemia, aspiratory brokenness, and cardiovascular insecurity in patients with intense cervical SCI. Patients with the most extreme neurological wounds seem to have the most serious danger of these life-undermining occasions. Administration in an ICU or other checked setting seems to favourably affect neurological result after intense cervical SCI. Keeping up MAP between 85-90 mm Hg for the initial seven days taking after intense SCI to enhance spinal string perfusion is the present proposal of the American Association of Neurological Surgeons and Congress of Neurological Surgeons (58).


Conclusion

Both noteworthy methodological mistakes and conflicting neurological results in the reviews distributed to date with respect to the gainful impacts of methylprednisolone can as effectively be devoted to irregular shot as to any genuine restorative impact. Abnormal state of proof exists with respect to the hurtful symptoms of methylprednisolone organization in the setting of intense SCI including wound contamination, pneumonia, hyperglycaemia requiring insulin organization, GI discharge and demise. Methylprednisolone ought not be routinely utilized as a part of the treatment of patients with intense SCI (59).


Ethics

Peer-review: Externally peer-reviewed.

Authorship Contributions

Concept: A.D., Design: A.D., Data Collection or Processing: B.K., Analysis or Interpretation: B.K., Literature Search: B.K., Writing: B.K., A.D., S.K., A.O.K.

Conflict of Interest: No conflict of interest was declared by the authors.

Financial Disclosure: The authors declared that this study received no financial support.

Images

  1. Karacan I, Koyuncu H, Pekel O, Sumbuloglu G, Kirnap M, Dursun H, et al. Traumatic spinal cord injuries in Turkey: a nation-wide epidemiological study. Spinal cord. 2000;38:697-701.
  2. Road Traffic Accident Statistics, 2014: Turkish Statistical Institute; 2015 [12.05.2016]. Available from: http://www.turkstat.gov.tr/PreHaberBultenleri.do?id=18760.
  3. Early Acute Management in Adults with Spinal Cord Injury: A Clinical Practice Guideline for Health-Care Professionals. The Journal of Spinal Cord Medicine. 2008;31:403-79.
  4. Saboe LA, Reid DC, Davis LA, Warren SA, Grace MG. Spine trauma and associated injuries. The Journal of Trauma. 1991;31:43-8.
  5. Holly LT, Kelly DF, Counelis GJ, Blinman T, McArthur DL, Cryer HG. Cervical spine trauma associated with moderate and severe head injury: incidence, risk factors, and injury characteristics. Journal of Neurosurgery. 2002;96(3 Suppl):285-91.
  6. Hackl W, Hausberger K, Sailer R, Ulmer H, Gassner R. Prevalence of cervical spine injuries in patients with facial trauma. Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics. 2001;92:370-6.
  7. Rabinovici R, Ovadia P, Mathiak G, Abdullah F. Abdominal injuries associated with lumbar spine fractures in blunt trauma. Injury. 1999;30:471-4.
  8. Middleton PM, Davies SR, Anand S, Reinten-Reynolds T, Marial O, Middleton JW. The pre-hospital epidemiology and management of spinal cord injuries in New South Wales: 2004-2008. Injury. 2012;43:480-5.
  9. Bulger EM, Maier RV. Prehospital care of the injured: what’s new. The Surgical clinics of North America. 2007;87:37-53.
  10. Rathore FA, Farooq F, Muzammil S, New PW, Ahmad N, Haig AJ. Spinal cord injury management and rehabilitation: highlights and shortcomings from the 2005 earthquake in Pakistan. Archives of physical medicine and rehabilitation. 2008;89:579-85.
  11. Oteir AO, Jennings PA, Smith K, Stoelwinder J. Should suspected cervical spinal cord injuries be immobilised? A systematic review protocol. Injury prevention: journal of the International Society for Child and Adolescent Injury Prevention. 2014;20:e5.
  12. Brouhard R. To immobilize or not immobilize: that is the question. Emergency medical services. 2006;35:81-2.
  13. Hood N, Considine J. Spinal immobilisaton in pre-hospital and emergency care: A systematic review of the literature. Australasian emergency nursing journal: AENJ. 2015;18:118-37.
  14. Burton JH, Dunn MG, Harmon NR, Hermanson TA, Bradshaw JR. A statewide, prehospital emergency medical service selective patient spine immobilization protocol. The Journal of trauma. 2006;61:161-7.
  15. Haut ER, Kalish BT, Efron DT, Haider AH, Stevens KA, Kieninger AN, et al. Spine immobilization in penetrating trauma: more harm than good? The Journal of trauma. 2010;68:115-20.
  16. Schriger DL. Immobilizing the cervical spine in trauma: should we seek an optimal position or an adequate one? Annals of emergency medicine. 1996;28:351-3.
  17. Podolsky S, Baraff LJ, Simon RR, Hoffman JR, Larmon B, Ablon W. Efficacy of cervical spine immobilization methods. The Journal of trauma. 1983;23:461-5.
  18. Esposito TJ, Sanddal ND, Dean JM, Hansen JD, Reynolds SA, Battan K. Analysis of preventable pediatric trauma deaths and inappropriate trauma care in Montana. The Journal of trauma. 1999;47:243-51.
  19. Esposito TJ, Sanddal ND, Hansen JD, Reynolds S. Analysis of preventable trauma deaths and inappropriate trauma care in a rural state. The Journal of trauma. 1995;39:955-62.
  20. Dagal A, Acute care of traumatic spinal cord injury. The IARS 2014 Annual Meeting and International Science Symposium 2014 May 17-20, 2014; Montreal, Quebec.
  21. Grande CM, Barton CR, Stene JK. Appropriate techniques for airway management of emergency patients with suspected spinal cord injury. Anesthesia and analgesia. 1988;67:714-5.
  22. Santoni BG, Hindman BJ, Puttlitz CM, Weeks JB, Johnson N, Maktabi MA, et al. Manual in-line stabilization increases pressures applied by the laryngoscope blade during direct laryngoscopy and orotracheal intubation. Anesthesiology. 2009;110:24-31.
  23. Austin N, Krishnamoorthy V, Dagal A. Airway management in cervical spine injury. International journal of critical illness and injury science. 2014;4:50-6.
  24. Levitan RM. Myths and Realities: The “Difficult Airway”and Alternative Airway Devices in the Emergency Setting. Academic Emergency Medicine. 2001;8:829-32.
  25. Brimacombe J, Keller C, Kunzel KH, Gaber O, Boehler M, Puhringer F. Cervical spine motion during airway management: a cinefluoroscopic study of the posteriorly destabilized third cervical vertebrae in human cadavers. Anesthesia and analgesia. 2000;91:1274-8.
  26. Martel M, Reardon RF, Cochrane J. Initial experience of emergency physicians using the intubating laryngeal mask airway: a case series. Academic emergency medicine: official journal of the Society for Academic Emergency Medicine. 2001;8:815-22.
  27. Komatsu R, Nagata O, Kamata K, Yamagata K, Sessler DI, Ozaki M. The Intubating Laryngeal Mask Airway Allows Tracheal Intubation When the Cervical Spine Is Immobilized by a Rigid Collar. British journal of anaesthesia. 2004;93:655-9.
  28. Kihara S, Yaguchi Y, Taguchi N, Brimacombe JR, Watanabe S. The StyletScope is a better intubation tool than a conventional stylet during simulated cervical spine immobilization. Canadian journal of anaesthesia = Journal canadien d’anesthesie. 2005;52:105-10.
  29. Wang HE, Kupas DF, Paris PM, Bates RR, Costantino JP, Yealy DM. Multivariate predictors of failed prehospital endotracheal intubation. Academic emergency medicine: official journal of the Society for Academic Emergency Medicine. 2003;10:717-24.
  30. Alanazi A. Intubations and airway management: An overview of Hassles through third millennium. Journal of Emergencies, Trauma, and Shock. 2015;8:99-107.
  31. Davis DP, Ochs M, Hoyt DB, Bailey D, Marshall LK, Rosen P. Paramedic-administered neuromuscular blockade improves prehospital intubation success in severely head-injured patients. The Journal of trauma. 2003;55:713-9.
  32. Robinson KJ, Katz R, Jacobs LM. A 12-year experience with prehospital cricothyrotomies. Air medical journal. 2001;20:27-30.
  33. DiGiacomo C, Neshat KK, Angus LD, Penna K, Sadoff RS, Shaftan GW. Emergency cricothyrotomy. Military medicine. 2003;168:541-4.
  34. Hagberg CA and O Kaslow, Difficult Airway Management Algorithm in Trauma Updated by COTEP. ASA Monitor, 2014;78:56-60.
  35. Mallek JT, Inaba K, Branco BC, Ives C, Lam L, Talving P, et al. The incidence of neurogenic shock after spinal cord injury in patients admitted to a high-volume level I trauma center. The American surgeon. 2012;78:623-6.
  36. Fox AD. Spinal shock. Assessment & treatment of spinal cord injuries & neurogenic shock. JEMS : a journal of emergency medical services. 2014;39:64-7.
  37. Blood Pressure Management after Acute Spinal Cord Injury. Neurosurgery. 2002;50:S58-S62.
  38. Kong CY, Hosseini AM, Belanger LM, Ronco JJ, Paquette SJ, Boyd MC, et al. A prospective evaluation of hemodynamic management in acute spinal cord injury patients. Spinal cord. 2013;51:466-71.
  39. Furlan JC, Fehlings MG. Cardiovascular complications after acute spinal cord injury: pathophysiology, diagnosis, and management. Neurosurgical focus. 2008;25:E13.
  40. Lehmann KG, Lane JG, Piepmeier JM, Batsford WP. Cardiovascular abnormalities accompanying acute spinal cord injury in humans: incidence, time course and severity. Journal of the American College of Cardiology. 1987;10:46-52.
  41. Vale FL, Burns J, Jackson AB, Hadley MN. Combined medical and surgical treatment after acute spinal cord injury: results of a prospective pilot study to assess the merits of aggressive medical resuscitation and blood pressure management. Journal of neurosurgery. 1997;87:239-46.
  42. Levi L, Wolf A, Belzberg H. Hemodynamic parameters in patients with acute cervical cord trauma: description, intervention, and prediction of outcome. Neurosurgery. 1993;33:1007-16.
  43. Stevens RD, Bhardwaj A, Kirsch JR, Mirski MA. Critical care and perioperative management in traumatic spinal cord injury. Journal of neurosurgical anesthesiology. 2003;15:215-29.
  44. Zach GA, Seiler W, Dollfus P. Treatment results of spinal cord injuries in the Swiss Parplegic Centre of Basle. Paraplegia. 1976;14:58-65.
  45. Casha S, Christie S. A systematic review of intensive cardiopulmonary management after spinal cord injury. Journal of neurotrauma. 2011;28:1479-95.
  46. Bracken MB, Shepard MJ, Collins WF, Holford TR, Young W, Baskin DS, et al. A Randomized, Controlled Trial of Methylprednisolone or Naloxone in the Treatment of Acute Spinal-Cord Injury. New England Journal of Medicine. 1990;322:1405-11.
  47. Suberviola B, Gonzalez-Castro A, Llorca J, Ortiz-Melon F, Minambres E. Early complications of high-dose methylprednisolone in acute spinal cord injury patients. Injury. 2008;39:748-52.
  48. Matsumoto T, Tamaki T, Kawakami M, Yoshida M, Ando M, Yamada H. Early complications of high-dose methylprednisolone sodium succinate treatment in the follow-up of acute cervical spinal cord injury. Spine. 2001;26:426-30.
  49. Qian T, Guo X, Levi AD, Vanni S, Shebert RT, Sipski ML. High-dose methylprednisolone may cause myopathy in acute spinal cord injury patients. Spinal cord. 2005;43:199-203.
  50. Young W. Molecular and cellular mechanisms of spinal cord injury therapies. In: Kalb RG, Strittmatter SM, editors. Neurobiology of spinal cord injury. Totowa: Humana Press; 2000.p.241-76.
  51. Bracken MB, Collins WF, Freeman DF, Shepard MJ, Wagner FW, Silten RM, et al. Efficacy of methylprednisolone in acute spinal cord injury. Jama. 1984;251:45-52.
  52. Bracken MB, Shepard MJ, Collins WF, Jr., Holford TR, Baskin DS, Eisenberg HM, et al. Methylprednisolone or naloxone treatment after acute spinal cord injury: 1-year follow-up data. Results of the second National Acute Spinal Cord Injury Study. Journal of neurosurgery. 1992;76:23-31.
  53. Bracken MB, Holford TR. Effects of timing of methylprednisolone or naloxone administration on recovery of segmental and long-tract neurological function in NASCIS 2. Journal of neurosurgery. 1993;79:500-7.
  54. Bracken MB, Shepard MJ, Holford TR, Leo-Summers L, Aldrich EF, Fazl M, et al. Administration of methylprednisolone for 24 or 48 hours or tirilazad mesylate for 48 hours in the treatment of acute spinal cord injury. Results of the Third National Acute Spinal Cord Injury Randomized Controlled Trial. National Acute Spinal Cord Injury Study. Jama. 1997;277:1597-604.
  55. Bracken MB, Shepard MJ, Holford TR, Leo-Summers L, Aldrich EF, Fazl M, et al. Methylprednisolone or tirilazad mesylate administration after acute spinal cord injury: 1- year follow up. Results of the third National Acute Spinal Cord Injury randomized controlled trial. Journal of neurosurgery. 1998;89:699-706.
  56. Tsao Y-T, Chen W-L, Tsai W-C. Steroids for acute spinal cord injury: revealing silent pathology. The Lancet. 2009;374:500.
  57. Ito Y, Sugimoto Y, Tomioka M, Kai N, Tanaka M. Does high dose methylprednisolone sodium succinate really improve neurological status in patient with acute cervical cord injury?: a prospective study about neurological recovery and early complications. Spine. 2009;34:2121-4.
  58. Ryken TC, Hurlbert RJ, Hadley MN, Aarabi B, Dhall SS, Gelb DE, et al., The acute cardiopulmonary management of patients with cervical spinal cord injuries. Neurosurgery. 2013;72(Suppl 2): 84-92.
  59. Hurlbert RJ, Hadley MN, Walters BC, Aarabi B, Dhall SS, Gelb DE, et al., Pharmacological therapy for acute spinal cord injury. Neurosurgery. 2015;76(Suppl 1):S71-83.