Endotracheal Intubation Following Trauma
Citation: J Trauma. 73(5):S333-S340, November 2012
Mayglothling, Julie MD; Duane, Therese M. MD; Gibbs, Michael MD; McCunn, Maureen MD, MIPP; Legome, Eric MD; Eastman, Alexander L. MD, MPH; Whelan, James MD; Shah, Kaushal H. MD
From the Virginia Commonwealth University Medical Center (J.M., T.M.D., J.W.), Richmond, Virginia; Carolinas Medical Center (M.G.), Charlotte, North Carolina; University of Pennsylvania (M.C.), Philadelphia, Pennsylvania; Kings County Medical Center (E.L.); and Mt Sinai Medical Center (K.H.S.), New York, New York; University of Texas Southwestern Medical Center (A.L.E.), Dallas, Texas.
Address for reprints: Julie Mayglothling MD, Virginia Commonwealth University Medical Center, Richmond, VA; email: email@example.com.
The first priority in the care of all trauma patients is the affirmation of a patent airway to ensure adequate oxygenation and ventilation. The ABCs of trauma resuscitation begin with the airway evaluation, and effective airway management is imperative in the care of a patient with critical injury. Patients may require emergency tracheal intubation (ETI) for various reasons following injury including hypoxia, hypoventilation, or failure to maintain or protect the airway owing to altered mental status. However, multiple factors may be present, which make the decision to intubate less straightforward. One of the most difficult aspects of airway management in trauma is the potential deterioration in clinical status, which may occur during the early phases of resuscitation. The decision to intubate may go well beyond a patient’s ability to oxygenate or ventilate.
It has long been established that any decrease in oxygen delivery to the injured brain, precipitated by hypoxia or hypotension, increases morbidity and mortality in the setting of severe traumatic brain injury.[1–6] Therefore, the decision is not only whether a patient needs intubation but also when and how to intubate. Delays in adequate airway management may have devastating consequences, and this is one of the more common causes of preventable death in both the prehospital and the emergency department setting. Even for patients that are initially stable, a delay in intubation is associated with increased mortality from 1.8% to 11.8% in one study. In addition, ETI has the potential to cause secondary injury if performed inadequately or unsuccessfully by creating or exacerbating hypoxia or hypotension.
In 2002, the Eastern Associated for the Surgery of Trauma (EAST) Practice Management Guidelines (PMGs) Committee work group on ETI formulated guidelines to assist clinicians with decisions regarding airway management for patients immediately following traumatic injury. The goals of the work group were to develop evidence-based guidelines to (1) characterize patients in need of ETI and (2) delineate the most appropriate procedure for patients undergoing ETI. The basis for these guidelines was an evidence-based review of patients who had sustained blunt trauma, penetrating trauma, or heat-related injury and had developed respiratory system insufficiency or required ETI in the immediate period after injury (first 2 hours after injury). The previous committee reviewed literature from 1970 to 2001 and formulated the guidelines published in 2003.
In creating the updated guidelines for ETI, committee members, with recognized expertise in trauma surgery, emergency medicine, and anesthesiology, formulated specific questions to be addressed during the assessment and revision process.
- Are the 2002 guidelines still valid, and is there any new evidence to change the level of the previous recommendations?
- Is direct laryngoscopy (DL) still the preferred method for ETI in trauma?
- What is the role of newly introduced airway adjuncts, such as blind insertion supraglottic devices and video laryngoscopy?
- Are there pharmacologic agents used for intubation that should be recommended for or against in the setting of acute injury?
- What is the role of prehospital ETI?
Studies appropriate for the ETI update were identified using MEDLINE. An initial database query was undertaken using the same search criteria that were used in the original PMG with citations published between January 2001 and December 2011. This included a combination of MESH headings and title words with limits to English-language, human, all ages, and all study types: hypercarbia, airway obstruction, hypoventilation, aspiration,psychomotor agitation, hypoxia, injury/injuries, trauma/traumatic, brain, head, intubation, endotracheal, tracheostomy, cricothyroidostomy,cricothyroidotomy, and cricothyrotomy. Given the specific questions posed by the work group, additional search terms were used: video-assisted laryngoscopy, videolaryngoscopy, laryngeal mask airway, King LT, Combi-tube, and cricoid pressure.
In addition to the MEDLINE search, bibliography of reviews, letters to the editor, and meta-analyses were used to identify other relevant patient investigation articles. If an article investigated trauma and medical patients, the article was included if the trauma patient cohort was at least 50% or if the study included a subgroup analysis on the specific trauma population.
The initial search identified 2,688 citations. Letters to the editor, case reports, reviews, and articles dealing with airway training using simulation were excluded. The abstracts of the remaining citations were reviewed, and those articles that did not address the issues pertinent to the questions outlined previously were further excluded. In total, 93 citations met the inclusion criteria. These were distributed to members of the committee for review, and ultimately, 69 were included in the analysis. Citations were cross-referenced to the 2002 document to ensure that no articles included in the original database were repeated. The breakdown of the 69 articles was as follows:
- Population appropriate for intubation (11 articles),
- Prehospital care (36 articles),
- Pharmacologic agents (7 articles),
- Airway adjuncts and video-assisted laryngoscopy (9 articles), and
- Other (6 articles).
Articles and recommendations were classified as described in the EAST primer on using evidence-based outcome measures to develop PMGs:
Class I: Prospective randomized controlled trial (3 articles)
Class II: Prospective clinical trial or retrospective analysis based on reliable data (13 articles)
Class III: Retrospective case series or database review (53 articles)
Level 1: The recommendation is convincingly justifiable based on the available scientific information alone. This recommendation is usually based on Class I data; however, strong Class II evidence may form the basis for a Level 1 recommendation, especially if the issue does not lend itself to testing in a randomized format.
Level 2: The recommendation is reasonably justifiable by available scientific evidence and strongly supported by expert opinion. This recommendation is usually supported by Class II data or a preponderance of Class III evidence.
Level 3: The recommendation is supported by available data but adequate scientific evidence is lacking. This recommendation is generally supported by Class III data. This type of recommendation is useful for educational purposes and in guiding future clinical research.
There were no recommendations.
The recommendations are as follows:
- A careful airway assessment should be performed before initiating efforts to secure the airway. The goals of this assessment are to identify potential markers of difficulty with the following:
- Bag-valve mask ventilation,
- Laryngoscopy, and
- Surgical airway.
- The application of structured assessment tools (e.g., the LEMON law) is recommended.
- When significant difficulty is anticipated, neuromuscular blockade should be used with caution, and airway rescue devices, including surgical airway equipment, should be immediately available.
There were no recommendations.
The original PMGs did not include any recommendations for airway assessment. Although many emergency intubations are straightforward, as many as 0.3% to 2.7% result in “failed airways” in the setting of trauma. Recognition of specific attributes of the difficult airway allow for better preparation and potentially preventable adverse consequences. An assessment tool used in the current (eighth) version of advanced trauma life support is the LEMON mnemonic.
L: Look externally (facial trauma, large incisors, beard or moustache, large tongue);
E: Evaluate the 3-3-2 rule (incisor distance < 3 fingers, hyoid mental distance < 3 fingers, thyroid to mouth < 2 fingers);
M: Mallampati score;
O: Obstruction (presence of any condition that could cause obstruction); and
N: Neck mobility (all patients with blunt trauma require cervical in-line stabilization that makes visualization of the glottis more difficult).
The use of the LEMON score was able to successfully stratify the risk of intubation difficulty. Patients with a high airway assessment score were found to have a poor laryngoscopic view compared with those patients with a low airway assessment score.
Indications for ETI
- ETI is indicated in trauma patients with the following traits:
- Airway obstruction,
- Persistent hypoxemia (SaO2 ≤ 90%) despite supplemental oxygen,
- Severe cognitive impairment (Glasgow Coma Scale [GCS] score ≤ 8),
- Severe hemorrhagic shock, and
- Cardiac arrest.
- ETI is indicated for patients experiencing smoke inhalation with any of the following traits:
- Airway obstruction,
- Severe cognitive impairment (GCS score ≤ 8),
- Major cutaneous burn (≥40%),
- Major burns and/or smoke inhalation with an anticipated prolonged transport time to definitive care, and
- Impending airway obstruction as follows:
- Moderate-to-severe facial burn;
- Moderate-to-severe oropharyngeal burn, and
- Moderate-to-severe airway injury seen on endoscopy.
There were no recommendations.
- ETI may also be indicated in trauma patients with any of the following traits:
- Facial or neck injury with the potential for airway obstruction,
- Moderate cognitive impairment (GCS score > 9–12),
- Persistent combativeness refractory to pharmacologic agents,
- Respiratory distress (without hypoxia or hypoventilation),
- Preoperative management (i.e., patients with painful injuries or undergoing painful procedures before nonemergent operation), and
- Early ETI is indicated in cervical spinal cord injury with any evidence of respiratory insufficiency (complete cervical SCI or incomplete injuries C5 and above).
After publication of the original PMG guidelines on ETI, there was some debate about whether the criteria recommended for ETI after trauma (Number 1 in the previous enumeration) fully represented the trauma population that would benefit from ETI. The committee expanded the criteria that may indicate a need for ETI (Number 3 in the previous enumeration). These recommendations were based on several retrospective studies that identified the need for airway management for patients with these criteria. Sise et al. performed a retrospective review of 1,000 consecutive patients that were intubated after injury. The study evaluated indications for intubation and characterized them as either those indicated by the EAST Guidelines or other discretionary indications (DI). In the study population of 1,000 patients, 44% were intubated for reasons other than those stated in the EAST guidelines. These DI included altered mental status with GCS score of greater than 8 (24.8%), combativeness (12.7%), preoperative management (4.8%), facial or neck injury (1.5%), and respiratory distress without hypoxia (0.6%). Importantly, one in three DI patients was found to have significant head injury. Despite a 12.6% rate of head injury in those patients intubated for combativeness in this study, intubation in this setting is not without risk. A study by Muakkassa et al.demonstrated that patients intubated for combativeness as the only indication have longer stay, an increased incidence of pneumonia, and poorer discharge status when compared with matched controls. However, given the risk of significant head injury and the importance of being able to complete a thorough trauma evaluation, persistent combativeness that inhibits the ability to adequately evaluate potential injuries and that is refractory to safe pharmacologic management is included in the criteria for ETI.
Another patient population studied with regard to early tracheal intubation are those with cervical spinal cord injuries. Three retrospective studies with more than 400 patients support thorough evaluation of respiratory status, and those with complete SCI should be intubated early, especially with injury levels of C5 and above.[17–19] Those patients with incomplete SCI with any sign of respiratory insufficiency should also be intubated early.
Patients with penetrating neck trauma are also at risk for airway compromise and increased mortality when airway management is delayed or ineffective. In addition to the data of Sise et al., multiple other studies support early ETI for patients with neck injury.[20–23] Given the risk of airway injury and potential difficulty with airway management, three studies have attempted to delineate the best approach for airway control in this patient population.[21–23] Although none was able to make definitive recommendations for the best method of obtaining ETI, these studies support either DL or awake nasotracheal intubation. In these situations, there are no definitive recommendations as to where ETI should take place, whether in the trauma bay or in the operating room. This decision is made by the trauma surgeon in charge based on airway stability, anticipation of difficult airway management, and available personnel.
- Orotracheal intubation guided by DL is the ETI procedure of choice for trauma patients.
- Rapid sequence intubation (RSI) should be used to facilitate orotracheal intubation unless markers of significant difficulty with intubation are present. An RSI drug regimen should be given to achieve the following clinical objectives:
- Adequate sedation and neuromuscular blockade,
- Maintenance of hemodynamic stability and CNS perfusion,
- Maintenance of adequate oxygenation,
- Prevention of increases in intracranial hypertension, and
- Prevention of vomiting and aspiration.
There are no recommendations regarding the use of specific induction agents used for RSI in trauma. Succinylcholine is the recommended agent of choice for neuromuscular blockade, in the absence of any contraindications to its use.
- Enhancements for safe and effective ETI in trauma patients include the following:
- Availability of experienced personnel,
- Pulse-oximetry monitoring,
- Maintenance of cervical neutrality,
- Confirmation of tube placement using auscultation of bilateral breath sounds and end-tidal CO2 detection, and
- Continuous end-tidal CO2 monitoring for patients with severe traumatic brain injury.
- Cricothyroidostomy is appropriate when emergent/urgent tracheal intubation is needed and cannot be achieved rapidly with DL or with the use of alternative airway techniques and devices.
- When ETI cannot be achieved rapidly with DL, a number of airway rescue devices may be used as follows:
- Blind-insertion supraglottic devices (i.e., LMA, Combitube, and King Airway),
- Gum-elastic bougie,
- Video laryngoscopy, and
- Surgical cricothyroidostomy.
Decisions regarding the most appropriate rescue technique should be guided by the clinical scenario at hand, resource availability, and the skill and experience of the treating clinician.
- Video laryngoscopy may offer significant advantages over DL, including the following:
- Superior views of the glottis (Cormack-Lehane I/II);
- Higher intubation success rates for patients with anatomically difficult airways, in obese patients, and in those with the cervical spine held in-line; and
- Higher intubation success rates by inexperienced airway providers.
RSI is the preferred method of airway management for most of the injured trauma patients. RSI provides rapid unconsciousness (induction) and neuromuscular blockade (paralysis). This is especially important in trauma patients who likely are not fasted and are at much greater risk for vomiting and aspiration. This method has been proven safe and effective during the past several decades and is considered standard of care for emergency airway management. The choice of pharmacologic agents used for RSI, however, is less straightforward. Multiple factors, such as hemodynamic instability, the presence of traumatic brain injury, or comorbid conditions, may alter the use of specific pharmacologic agents.
After careful review of the literature, the committee decided not to make recommendations on the use of specific pharmacologic agents for induction during RSI. In many centers, etomidate is the drug of choice for induction because of its rapid onset, hemodynamic stability, and extensive experience with its use. The use of etomidate for induction has been the source of much controversy and has been studied specifically in trauma patients. Single-dose etomidate has been associated with adrenal insufficiency, as well as increased incidence of adult respiratory distress syndrome and multiple-organ dysfunction syndrome Despite these two retrospective reviews, the evidence is not strong enough to recommend against its use. Ketamine has long been avoided for induction in patients suspected of traumatic brain injury because of a theoretical increase in intracranial pressure (ICP). Multiple reviews and editorials have questioned this historical bias. In addition, several studies have assessed the use of ketamine as a sedative agent and its effect on ICP, some demonstrating actual decreases in ICP. There are no convincing studies evaluating the effects of ketamine on ICP when used as an induction agent. Ketamine may be a preferable agent for patients in shock because it may actually increase blood pressure in normotensive or hypotensive patients. A review of other possible induction agents used for intubation after trauma is available.
The use of a neuromuscular blocking agent (NMBA) is a fundamental part of RSI. Succinylcholine remains the agent of choice in trauma because of its consistently rapid onset and short duration of action. There is no evidence that the fasciculations caused by succinylcholine cause significant increases in ICP for patients with traumatic brain injury, and there is no support for giving defasciculating doses of nondepolarizing NMBAs. Suspected elevation of ICP is not a contraindication for the use of succinylcholine. For patients with a contraindication to succinylcholine, such as prolonged immobilization, chronic kidney disease, or skeletal muscle myopathies, high-dose rocuronium is the preferred alternative.
Although a standard of care in emergency intubations, the efficacy of cricoid pressure (CP) has recently been questioned. Its introduction into clinical practice followed a description of the technique and small case series and was never subject to rigorous evaluation. The technique is used in theory to reduce the risk of aspiration during the induction phase of anesthesia, although its application, timing, and technique are not standardized. Recent evidence suggests that CP impairs laryngoscopic view, reduces bag-valve mask ventilation efficiency, and does not prevent aspiration. In a prospective, observational study of 400 adult trauma patients intubated with CP, researchers compared the effect on laryngoscopic view of three maneuvers (release of CP, BURP, and laryngeal manipulation under direct vision). Removing CP facilitated intubation in most cases and was not associated with a worsening view of the glottis in any case. The authors reported only two cases of regurgitation associated with failed intubation, prolonged BVM, and the removal of CP. The current recommendation is that early removal of CP in cases of poor laryngeal view will likely facilitate intubation with minimal risk to the patient. Because of this controversy and lack of evidence base, the application of CP was removed as a Level 1 recommendation.
Since the 1980s, when the use of the LMA was first reported, the use of supraglottic airway devices has become increasingly popular. Currently, multiple versions of the LMA, the Combitube, and the King Airway (LT, LTS, and LTS-D) are available. Benefits of supraglottic devices are that they can be placed blindly, rapidly, and the performance of these devices is not affected by the patient characteristics that negatively affect mask ventilation, laryngoscopy and successful performance of cricothyroidotomy (obesity, limited neck movement, facial hair, etc.). In a large study of prehospital airway management, alternate airway insertions (primarily the Combitube) occurred in 96 of 100,000 patient care events with a success rate of 87.2%. Other studies using the Combitube as a rescue device for failed ETI show success rates of 95%. Studies with the King airway show success rates of 92% to 100%,[37–39] and 96% of participants in one study preferring the King to the Combitube.
The exact role for supraglottic devices compared with prehospital DL is unclear. A review of five controlled clinical trials with more than 1,500 patients comparing ETI with alternative airway techniques was unable to show a difference in outcome. The high variability in prehospital provider competence and experience make recommendations for a specific rescue device a challenge. Based on the available data, it seems that supraglottic airway devices show an acceptable success rate as primary and rescue airway adjuncts.
DL by trained physicians, with the use of in-line stabilization for cervical spine protection, has been shown to be a safe and effective means of intubation after trauma.[41–45] Despite good success rates with DL, the use of video laryngoscopy and the studies evaluating its use have been increasing. So far, there is inconclusive evidence indicating that video laryngoscopy should replace DL in trauma patients requiring ETI. Several studies in nontrauma patients have investigated various types of video laryngoscopes (i.e., Glidescope, Bullard, Airtraq, and Pentax AWS). The specific features and characteristics of the video laryngoscopes vary, but they each provide an indirect view of the upper airway and a theoretical advantage in minimizing cervical spine motion during intubation. Studies have supported that the Cormack-Lehane grade is improved,[46–48] cervical spine motion is lessened,[49–52] force and pressures exerted on the airway are decreased, hemodynamic responses are minimized, and time to intubation is similar with video as compared with DL. One study specifically looking at patients intubated with cervical spine immobilization by a semirigid collar showed improved views with the Glidescope over a Macintosh blade. However, improved laryngeal views are not always matched with higher intubation success rate. Despite the good visualization of the glottis, the insertion and advancement of the endotracheal tube may occasionally fail, and despite the growing evidence that video laryngoscopy may be superior to DL in some cases, many of these studies are performed in cadaver models, simulation scenarios, and elective nontrauma patients and performed by personnel well trained with the use of the devices. One retrospective study of 822 emergency department intubations (of which, >60% were trauma patients) showed that overall success rates for video laryngoscopy were similar to DL, but first-attempt success rates were higher using the Glidescope. Another emergency department–based review also showed similar overall success rates but an increased time to completion when the Glidescope was used compared with DL.
Video-assisted devices may have a greater role for patients with potentially difficult airways. Studies performed in patients with easy laryngoscopy (Cormack-Lehane grade I or II) demonstrate similar success rates as DL but increased time to intubation. The benefit is more measurable for patients with difficult airways, where DL may not provide good visualization. Further studies, looking specifically at trauma patients, need to be performed before further recommendations may be made regarding the use of video laryngoscopy for ETI.
Areas for Future Investigation
The subject with the most literature and the most Level 1 and Level 2 data is regarding the role of prehospital intubation in trauma. Of the 69 articles reviewed for this PMG, 31 involved this perplexing question. Many studies support improved functional outcomes for those receiving ETI in the field,[64–71] but as many demonstrate delays in transport to definitive care and similar or worse outcome.[72–84] More specifically, some studies evaluated the benefit of RSI versus intubation without RSI[85–90] However, despite the plethora of data, literature reviews,[91–93] as well as expert panels formed to attack this particular question, no conclusion could be reached regarding prehospital intubation for patients with traumatic brain injury, with or without RSI. Diversity of patient population, differing airway algorithms, various experience among emergency medical service personnel in ETI, and differing reporting make consensus difficult. Until further multicenter prospective studies are performed, local emergency medical service directors must evaluate local factors to ensure optimal outcome for patients meeting this criteria.
This review also did not take into consideration specific pediatric trauma airway considerations. The committee thought as though the scope of experience as well as the lack of significant data made recommendations in this area beyond this committee’s expertise.
- The decision to intubate a patient following traumatic injury is based on multiple factors including not only the need for oxygenation and ventilation but also mechanism of injury, predicted operative need, or progression of disease (i.e., burns, spinal cord injury).
- ETI is best achieved by an RSI technique with DL.
- There is no pharmacologic induction agent of choice for ETI.
- Succinylcholine is the NMBA of choice for paralysis for ETI.
- The use of CP is no longer a Level 1 recommendation.
- Airway adjuncts may be useful in facilitating successful ETI.
The authors declare no conflicts of interest.
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