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1Department of Disaster and Emergency Medicine, Graduate School of Medicine, Kobe University, 650-0017 Kobe, Japan
2Department of Anesthesiology, Ohta General Hospital Foundation, Ohta Nishinouchi Hospital, 963-8558 Koriyama, Japan
3Futaba Medical Center, Fukushima Medical University, 960-1295 Fukushima, Japan
*Corresponding Author(s):windmill@people.kobe-u.ac.jp (Yuko Ono)
| History | Submitted: 28 November 2022 | Accepted: 24 February 2023 | Published: 08 September 2023 |
| Copyright: | ©2023 The Author(s). Published by MRE Press. |
The ongoing coronavirus 2019 (COVID-19) pandemic has increased the need for healthcare professionals to perform emergency endotracheal intubation (ETI) in patients with COVID-19-related respiratory failure outside of the operating room. Difficult airways and severe airway-related adverse events occur much more frequently in such settings due to limited time and resources as well as the patient’s reduced physiological reserve. The gum elastic bougie (GEB) intubation tube is an inexpensive, simple, and readily transportable aid to intubation, but its effectiveness in emergency airway management has not been comprehensively evaluated in recent years. Here, we performed a literature review and have updated the available evidence on the utility of GEB in emergency airway management. After a systematic MEDLINE search, we identified 36 relevant reports that compared GEB with alternative airway management approaches in a variety of real-world and simulated settings. In most studies, GEB increased the first-pass ETI success rate and decreased the force applied on the tongue and incisors during laryngoscopy. GEB also increased the speed, safety, and reliability of emergency cricothyrotomy. Conflicting results were obtained in studies examining GEB use for ETI during cardiopulmonary resuscitation, and other special circumstances such as selective lung ventilation, the presence of vomitus, and the use of personal protective equipment. These results suggest that GEB use could be expanded beyond difficult airways and rescue after failed ETI attempts, but further studies will be necessary to determine the utility of GEB under special conditions. Because fatal airway-related adverse events can in part be attributed to limited accessibility of proper airway management equipment, devices such as GEB may increase successful outcomes, especially under the overwhelmingly challenging conditions imposed by the COVID-19 pandemic.
Cite this article
Yuko Ono, Kazuaki Shinohara, Jiro Shimada, Shigeaki Inoue, Joji Kotani. Emergency airway management with the gum elastic bougie outside of the operating room: a narrative review. Signa Vitae. 2023; 19(5): 29-37. doi: 10.22514/sv.2023.074
The ongoing coronavirus 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has dramatically increased the need for healthcare professionals to perform emergency endotracheal intubation (ETI) in patients with respiratory failure outside of the operating room. Difficult airways and severe airway-related adverse events occur much more frequently in such settings due to a variety of factors, including limited time and resources, noisy and chaotic environments not conducive to successful ETI, and the reduced physiological reserve of the patients. For example, the rate of difficult ETIs ranges from 10.0% to 21.0% in intensive care units (ICUs) [1, 2, 3, 4, 5]; from 6.1% to 23.5% in emergency departments (EDs) [3, 6, 7, 8, 9, 10], from 6.0% to 17.7% in prehospital settings [11, 12, 13, 14], and from 0.5% to 8.5% in planned anesthesia settings [14, 15, 16, 17, 18, 19]. Life-threatening ETI-related complications, such as hypoxia, esophageal intubation, and aspiration, are more likely to occur outside of the operating room [20, 21, 22]; indeed, the incidence of death and brain damage is about 60-fold higher when major airway events occur in the ED or ICU than in the operative room [20, 21, 22].
Fatal airway-related adverse events can in part be attributed to limited access to proper difficult airway management (DAM) equipment resources [21, 22, 23, 24, 25]. There is thus an increasing need for such resources to be in place in every ED and ICU, especially in the era of COVID-19. The gum elastic bougie (GEB) tube is a valuable intubation aid that is also inexpensive, simple to use, and easy to transport. Sir Robert R. Macintosh first described the use of GEB as an adjunct for difficult ETI in 1949 [26], and it continues to be useful for emergency airway management 70 years later. However, the effectiveness of GEB under emergency airway management conditions outside of the operating room has not been comprehensively evaluated. In the present review, we performed a literature search to update and reappraise the utility of GEB in a variety of emergency airway management settings.
The literature search strategy was determined a priori by the survey team, which comprised emergency physicians (YO, SI and JK), an anesthesiologist (KS), and a librarian (MJ, see Acknowledgments). In March 2022, we performed a MEDLINE database search for articles without language or publication date restrictions using the following search terms: tube introducer AND emergency airway management, gum elastic bougie AND emergency airway management, bougie AND emergency airway management, gum elastic bougie AND emergency endotracheal intubation, tube introducer AND emergency endotracheal intubation, and bougie AND emergency endotracheal intubation. PubMed® (https://pubmed.ncbi.nlm.nih.gov/) was used to search the MEDLINE database. We also performed cross-referencing of the articles included in this review. A total of 532 articles were obtained from this screen (Table 1). We then excluded (1) redundant articles; (2) articles other than original research, such as case reports, comments, editorials, and reviews; (3) original articles that lacked a control group or clearly defined outcome measures; and (4) articles that had been retracted after publication.
| Number | Search terms | Hit number |
| #1 | gum elastic bougie AND emergency endotracheal intubation | 60 |
| #2 | tube introducer AND emergency endotracheal intubation | 46 |
| #3 | bougie AND emergency endotracheal intubation | 147 |
| #4 | tube introducer AND emergency airway management | 48 |
| #5 | gum elastic bougie AND emergency airway management | 63 |
| #6 | bougie AND emergency airway management | 168 |
A total of 498 articles were excluded and 2 articles were added after cross-referencing, resulting in a final selection of 36 reports for inclusion in this review (Fig. 1) [27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62].
The following data were extracted: study design, country, sample number, setting or simulation model, subject number, exposure (intervention) group, control group, primary outcome(s), and main finding(s). The Oxford Centre for Evidence-Based Medicine Level of Evidence was also scored for each study [63]. We referred to the Scale for the Assessment of Narrative Review Articles (SANRA) [64] and Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) Extension for Scoping Reviews checklist [65] when conducting this literature review.

Fig. 1.Flow diagram for literature review.
Supplementary Table 1 provides a summary of these studies and outcomes. We investigated the role of GEB with respect to the following nine categories: first-pass ETI success; forces on oral structures during laryngoscopy; DAM; combination with videolaryngoscopy; ETI during cardiopulmonary resuscitation (CPR); emergency cricothyrotomy; COVID-19 patients; pediatric patients; and other special circumstances. All of the articles were written in English. We also reviewed the availability of GEB outside of the operating room, such as in ICUs, EDs, and prehospital settings, with a view to the impact on “safety through redundancy”.
Emergency ETI-related adverse events include hypoxemia, esophageal intubation, cardiac arrest, regurgitation, aspiration, hypotension, dysrhythmia, bradycardia, mainstem bronchus intubation, dental/lip trauma, and airway trauma [5, 6, 7, 8, 9, 10]. These adverse events are most common when multiple laryngoscopies, especially more than three, are performed [6, 7]. Airway manipulations such as endotracheal intubation [66] are aerosol-generating procedures, and multiple attempts may increase the risk of transmission of acute respiratory infection such as SARS-CoV-2. Therefore, airway-opening techniques that are reliable and have the greatest chance of first-pass success should be used not only to reduce the chance of ETI-related adverse events but also to protect healthcare professionals from infection [23, 66].
In two observational studies performed in prehospital settings [27, 28], one RCT in EDs [29] and one observational study in EDs [30], bougie-assisted endotracheal intubation (BAETI) was associated with a significantly higher first-pass emergency ETI success rate than non-BAETI interventions. In contrast, a recent large multicenter RCT involving 1102 critically ill adults undergoing emergency ETI in seven EDs and eight ICUs in the US, there was no significant difference in the first-pass success of intubation by BAETI or endotracheal tube with stylet [31]. Thus, four of these five studies provided evidence in favor of GEB use on the initial attempt at emergency ETI.
Excess force on upper airway structures during laryngoscopy can increase the activity of the sympathetic nervous system and raise plasma catecholamine levels [67], leading to adverse hemodynamic changes such as hypertension, tachycardia, arrhythmia, and even cardiac arrest [5, 6, 7, 8, 9, 10]. Moreover, excess force on the maxillary incisors increases the risk of dental injury and upper airway trauma, which is the most common medico-legal claim against laryngoscopists [68]. Therefore, ETI should be performed with as little force on oral structures as necessary to prevent such consequences.
EDs play an important role in teaching airway management skills to novice physicians. In developed countries, approximately 33%–50% of ETI procedures in EDs are performed by junior residents [10, 69, 70], highlighting the need for effective training. Inexperienced laryngoscopists tend to apply more force to the incisors and tongue than do experienced laryngoscopists [71]; thus, senior physicians should employ effective airway adjuncts when supervising ETI performed by novices.
In one simulation study of medical students with normal airways, the maximum forces on tongue and incisors were significantly lower with BAETI compared with endotracheal tube with stylet during both direct and indirect laryngoscopy [32], suggesting a role for GEB beyond DAM in facilitating more gentle ETIs among inexperienced laryngoscopists.
The usefulness of the GEB as a rescue device after failed ETI attempts is well documented in the anesthesiology literature [11, 72]. However, of the four simulation studies reviewed that modeled DAM in emergency medicine settings [33, 34, 35, 36], only one reported a superior ETI success rate with BAETI compared with non-BAETI [35]. Likewise, there was no significant difference in mean time to successful ETI with BAETI compared with endotracheal tube and style in four previous studies with various DAM simulations [33, 34, 35, 37]. In fact, two studies reported that BAETI actually significantly increased the time to ETI compared with non-BAETI approaches [33, 34]. In a simulation study examining ETI through supraglottic airway devices, the fiberscope-guided technique was significantly more successful than blind attempts using GEB [38]. Two large observational studies conducted in the US compared first-pass ETI success rates using direct laryngoscopy augmented by laryngeal manipulation, ramped patient positioning, and GEB use with unaided video laryngoscopy [39, 40]. Both studies found a significantly higher success rate with video laryngoscopy compared with the augmented direct laryngoscopy groups [39, 40]. Collectively, these results suggest that video laryngoscopy is superior to GEB as an intubating device.
The combined use of GEB and videolaryngoscopy may further increase first-pass success. In a single-center RCT that included 757 adults undergoing emergency ETI in the ED, the use of GEB while performing videolaryngoscopy resulted in a higher overall first-pass success rate compared with videolaryngoscopy performed with a standard endotracheal tube and stylet [29]. The authors of that study claimed that the higher success rate when using GEB might be due to improved visibility. The smaller diameter of the GEB may render it less likely than an endotracheal tube and stylet to obscure the glottis view.
Special attention should be paid to airway management in patients with unstable cervical spine. In a planned anesthesia setting, the use of GEB with videolaryngoscope during ETI significantly reduced movement of the cervical spine compared with the use of videolaryngoscope alone [73]. Therefore, a combination of GEB and videolaryngoscopy may be useful in patients needing cervical spine protection, such as those with multiple injuries.
ETI during CPR plays an important role in protecting health care professionals from aerosol exposure, which is particularly pertinent to the current COVID-19 pandemic. Five simulation studies have examined the success rates of ETI with or without GEB during manual or mechanical chest compression [41, 42, 43, 44, 45]. Four of the five studies were relatively small and examined ETI success rate as the primary outcome [41, 42, 43, 44]; three of those studies reported significantly higher success rates in the BAETI group than in the non-BAETI group [41, 42, 43]. Three of the simulation studies [41, 42, 45] also compared the time to ETI completion between the BAETI and non-BAETI groups but conflicting results were reported: one study each reported similar times [41], shorter time in the BAETI group [42], and longer time in the BAETI group [45].
In the real-world clinical setting, CPR and ETI are frequently performed in a moving ambulance. In a simulation study, the mean time to ETI completion was significantly longer in the BAETI group compared with the non-BAETI group in both moving and stationary ambulances [46].
In contrast to the simulation studies, no significant difference in first-pass ETI success between BAETI and non-BAETI groups was detected in a large observational study of 3004 patients undergoing CPR after cardiac arrest in a prehospital setting [47].
Collectively, these results indicate that the utility of GEB in ETI during CPR remains controversial and further studies will be required to settle the issue.
The incidence of emergency surgical airway after failed ETI is reported to be 0.005–0.025% [74] in the operating room, 0.72% [75] during emergency trauma surgery, and 0.26%–0.9% [76, 77, 78, 79] outside of the operating room. Ten original studies have been performed to clarify the relative benefits of bougie-assisted emergency surgical cricothyrotomy technique (BACT) and non-BACT in emergency surgical airway. Of the ten, nine were simulations with animal models and one was a high-fidelity normal airway simulation model [48, 49, 50, 51, 52, 53, 54, 55, 56, 57]. Eight studies examined time to completion of surgical airway as the primary endpoint [48, 49, 50, 51, 52, 53, 54, 55]: the time was found to be significantly shorter in the BACT group in five studies [48, 49, 50, 52, 53] and in the non-BACT group in the two studies [54, 55]. In the remaining one study, median time to completion of surgical airway was similar between two groups [51]. One of these studies also examined the surgical airway success rate and found that the BACT group had significantly higher success and a lower rate of iatrogenic posterior tracheal wall injury compared with the non-BACT group [56]. In an anesthetized porcine model [57], BACT was significantly more successful in achieving rescue oxygenation (maintenance of arterial oxygen saturation of >90% at 5 min after the beginning of oxygenation) than the cannula technique using a 14-gauge needle [57].
Taken together, these results show a clear advantage for BACT over non-BACT techniques in emergency cricothyroidotomy with respect to time to completion, success rate, complication rate, and successful rescue oxygenation. Recent consensus guidelines for managing the airway in patients with COVID-19 also recommend BACT as a reliable method of emergency surgical airway [23, 80].
The incidence of difficult airway may be increased in COVID-19 patients due to physiological issues. For example, COVID-19 patients are often critically ill and are at risk of respiratory and circulatory collapse during emergency ETI [80]. Thus, COVID-19 patients are often considered to be at risk of a physiologically difficult airway [80]. Recent consensus guidelines for managing the airway in patients with COVID-19 refer to the usefulness of GEB [23, 80] based on cumulative evidence in the operating room.
Personal protective equipment (PPE), which comprises surgical face masks, N95 face masks, eye protection, disposable medical gowns, and gloves, have become mandatory for health care professionals during the COVID-19 pandemic [23]. Wearing PPE adds both physiological and psychological burdens on the healthcare professional and may compromise DAM. Hendler et al. [81] and Castle et al. [82] reported that wearing PPE nearly doubled the time to perform ETI and hampered the laryngoscopic view.
One study evaluated the impact of PPE on emergency ETI parameters, which is of particular interest in the context of the current COVID-19 pandemic. This high-performance simulation study demonstrated that ETI took significantly longer and had a lower success rate in the BAETI group than the non-BAETI group when the practitioners were wearing PPE [58]. Further studies will be required to clarify the usefulness of GEB in airway management in patients with COVID-19.
In a simulated difficult airway model in infants, BAETI was associated with a higher success rate and shorter ETI time compared with non-BAETI [59]. Similar results were obtained in an infant Pierre Robin mannequin that mimicked congenital difficult airway [60]. Likewise, in an infant mannequin receiving chest compression, the use of GEB was associated with a higher success rate and shorter ETI time [42]. Collectively, these results suggest that GEB may also be useful in pediatric emergency airway management.
Healthcare professionals in EDs sometimes encounter patients who need differential lung ventilation, such as those with severe pulmonary contusion. In one simulation study, the time to successful selective lung ventilation was significantly longer for the BAETI group compared with the non-BAETI group [61]. A study of ETI in simulated normal and vomitus settings showed that the time to ETI success with both direct and indirect laryngoscopy was significantly shortened by GEB use in the vomitus setting but significantly lengthened by GEB use in the normal setting [62].
In summary, the usefulness of GEB when performing emergency ETI under special circumstances such as selective lung ventilation, and vomitus remains unclear and must await further studies.
Multiple backup options or “safety through redundancy” are routinely required in high-stakes situations where failure or accidents can result in fatalities [83]. In engineering, such redundancy is achieved by duplication of critical system components or functions, usually in the form of a backup or fail-safe mechanism such as multiple engines on aircraft and multi-threaded processing in computing. Safety through redundancy requires rigorous testing under normal conditions [83] and obviously cannot wait to be tested only when major incidents occur. Emergency airway management is another setting where safety redundancy is essential [84], and DAM devices should be used during normal airway management practice, not reserved for use only in patients with difficult airway. In this regard, GEB use should not be limited to aid ETI when laryngoscopic views are poor or after intubation attempts fail. This suggestion is supported by studies by Ångerman et al. [28] and Driver et al. [29, 30], which demonstrated the benefits of routine GEB use on the success of first-pass intubation in prehospital and ED settings.
The crucial nature of emergency airway management means that physicians should employ laryngoscopy and intubation techniques that maximize the chance of first-pass ETI success [84]. Previous studies found that GEB is available in 21.0%–64.2% of prehospital settings [85, 86, 87, 88], 36%–100% of EDs [89, 90, 91, 92, 93, 94], and 50.0%–60.7% of ICUs [95, 96, 97] in various countries (Fig. 2).
These results suggest that safety redundancy outside of the operating room is, in general, insufficient. Several studies by professional anesthesiology societies [22, 24, 25] have strongly recommended that DAM resources available outside of the operating room should be consistent with those specified for hospital operating rooms. The professional anesthesiology society guidelines [98, 99, 100] and recent consensus guidelines for managing the airway in patients with COVID-19 [23, 81] both cite the usefulness of GEB. Because fatal airway-related adverse events can in part be attributed to the limited accessibility of proper DAM equipment resources [21, 22, 24, 25], it is important that every ED and ICU has appropriate DAM resources, including GEB.

Fig. 2.Comparison of the availability of gum elastic bougie in (A) prehospital settings, (B) emergency departments, and (C) intensive care units in various countries.
One major limitation of this literature review was that we searched for published articles in a single database (MEDLINE) using a single search engine (PubMed®). Some peer-reviewed articles may therefore have been overlooked. However, we believe that our search strategy was appropriate and clinically relevant because most biomedical researchers use MEDLINE as the first and most reliable source of medical information. It is also unlikely that the results would have substantially differed if other databases (e.g., Embase® and Google Scholar®) had been included. For example, Berry et al. [101] found that their MEDLINE search for articles included in systematic reviews of medical imaging successfully identified 94% of the target references. Despite these limitations, to the best of our knowledge, this is the first literature review to evaluate the effectiveness of GEB under emergency airway management conditions outside of the operating room.
The COVID-19 pandemic has increased the need for healthcare professionals to perform emergency ETI outside of the operating room. Difficult airways and severe airway-related adverse events occur much more commonly in such settings. The studies reviewed here suggest that, compared with alternative intubation techniques, GEB may increase the first-pass ETI success rate, decrease the force applied to oral structures during laryngoscopy, and aid in gentler ETI, and facilitate safer, faster, and more definitive cricothyrotomy. Moreover, combination GEB and video laryngoscopy may act additively to increase first-pass intubation success and decrease cervical spine movement during laryngoscopy. In high-stake potentially life-saving settings such as emergency airway management, a “safety through redundancy” approach with multiple backup systems is required. Immediate access to and proper implementation of DAM devices, including the GEB, is essential for the patient’s safety. As evident from this review, GEB represents an old but still helpful friend in overcoming the vast challenges associated with emergency airway management.
BACT, bougie-assisted emergency surgical cricothyrotomy technique; BAETI, bougie-assisted endotracheal intubation; CPR: cardiopulmonary resuscitation; COVID-19, coronavirus 2019; ED, emergency department; DAM, difficult airway management; ETI, endotracheal intubation; GEB, gum elastic bougie; ICU, intensive care units; LOE, level of evidence; PPE, personal protective equipment; RCT, randomized controlled trial; SARS-CoV, severe acute respiratory syndrome coronavirus.
All relevant data are contained within this article.
YO—conceived the study design, obtained the research funding, drafted the manuscript, and takes primary responsibility for the manuscript. KS and JS—validated the collected literature, critically reviewed the manuscript, and participated in editing. SI and JK—supervised the study and participated in discussing, revising, and editing the manuscript. All authors read and approved the final manuscript.
Not applicable.
The authors thank Mariko Jyukei (librarian, Library for Medical Sciences, School of Medicine, Kobe University) for advice in the PubMed® search strategy; Nozomi Ono, (Department of Psychiatry, Hoshigaoka Hospital, Koriyama, Japan) for manuscript review, and Anne M. O’Rourke, from Edanz (https://jp.edanz.com/ac) for editing a draft of this manuscript.
This work was partially supported by grants from the Public Trust Foundation of Marumo ER Medicine & Research Institute (2021 grant to YO). The funders had no role in the study design, data collection and analysis, or preparation of the manuscript.
The authors declare no conflict of interest.
Supplementary material associated with this article can be found, in the online version, at https://oss.signavitae.com/mre-signavitae/article/1688467581027926016/attachment/Supplementary%20material.docx.