Elsevier

Resuscitation

Volume 76, Issue 3, March 2008, Pages 364-368
Resuscitation

Clinical paper
Disposable laryngeal tube suction—A randomized comparison of two insertion techniques performed by novice users in anaesthetised patients

https://doi.org/10.1016/j.resuscitation.2007.08.018Get rights and content

Summary

Objective

Laryngeal tubes are supraglottic airway devices that can be used in alternative to a tracheal tube to provide ventilation during cardiopulmonary resuscitation. The product line has recently been expanded by the disposable laryngeal tube suction (LTS-D). We tested the hypothesis that, with a modified insertion technique (MIT), the rate of correct placement attempts within 45 s could be significantly increased compared to the standard insertion technique (SIT) recommended by the manufacturer.

Methods

Fifty-four adult patients undergoing trauma surgery under general anaesthesia had an LTS-D inserted by first-time users, randomly assigned to the SIT or a MIT. A brief manikin-based demonstration of the device and the assigned technique was given before insertion. In the MIT the tip of the LTS-D was rotated by 180° prior to insertion. Forced chin lift to create sufficient retropharyngeal space was performed with the other hand. Introduced to one-third of its length, the LTS-D was again rotated by 180° and pushed down the pharynx. The rate of successful tube placements within 45 s was the main outcome variable.

Results

Insertion took 73 ± 41 s (SIT) and 40 ± 8 s (MIT, P < 0.01). Insertion within 45 s was possible in n = 7/27 patients (26%, SIT) and in n = 20/27 patients (74%, MIT, P < 0.01). In one patient of the MIT group, placement failed. Non-anaesthesia personnel, such as nurses and emergency medical technicians (n = 27), performed comparably to board-certified anaesthesiologists or those in training (n = 27).

Conclusion

Applying a MIT significantly reduced the time for successful insertion of an LTS-D by first-time users. Insertion within 45 s was significantly more frequent with this technique. Further studies need to be conducted to determine if the LTS-D can be recommended as a first-line airway during cardiopulmonary resuscitation.

Introduction

Patients with unexpected difficult airway requiring ventilatory support still remain a challenge for anaesthesiologists, emergency physicians, and emergency medical technicians (EMT). If direct laryngoscopy fails, supraglottic airway devices, i.e. various types of laryngeal tubes, can be used to establish an artificial airway. The disposable laryngeal tube suction (LTS-D) is new, its value is unproven but its design makes it a potentially useful device for emergency use and for cardiopulmonary resuscitation. Other work on similar, but different laryngeal tubes1, 2 led us to consider whether novices might benefit from an alternative insertion techniques.

We tested the hypothesis that, with a modified introduction technique, novice users would be able to successfully place the new LTS-D within 45 s significantly more frequently than using the standard insertion technique recommended by the manufacturer.

Section snippets

Materials and methods

After approval of the study protocol by the institutional review board, 54 adult patients undergoing elective trauma and orthopaedic surgery under general anaesthesia were included in the study. Informed, written consent was obtained on the day before surgery. Sample size estimates suggested that 27 subjects per group would be needed to achieve 80% power to detect an absolute 40% reduction of LTS-D placement attempts lasting longer than 45 s (α = 5%) between standard and modified insertion

Results

No patient had predictors for a difficult airway, nor a history of difficult intubation. Also, no insertion attempt had to be aborted because of oxygen desaturation or exceeding the time limit of 180 s, and all 54 patients completed the study.

There were no clinically important differences between groups in terms of age, height, weight, and body mass index (Table 2).

All users were novices regarding clinical use of any type of laryngeal tubes regardless of the technique applied. LTS-D placement

Discussion

With a modified insertion technique using a reverse, “Guedel tube-like” approach and forced chin lift, inexperienced personnel was able to sufficiently place a LTS-D in anaesthetized patients significantly more frequently within a 45 s time frame than with the classic technique recommended by the manufacturer of the device. We could also find that non-anaesthesia personnel, such as EMT's, nurses, or medical students, performed comparably to board-approved anaesthesiologists or those in training.

Conflict of interest statement

The laryngeal tubes were provided free of charge by VBM Medizintechnik, Sulz, Germany. There were no other sources of funding. None of the authors has any conflict of interest with products and/or companies mentioned in the manuscript that could potentially bias their work.

References (9)

There are more references available in the full text version of this article.

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    The outstanding importance of continuous chest compressions and short no-flow intervals during cardiopulmonary resuscitation was emphasised in the 2005 ERC guidelines.2 Several manikin studies demonstrated that the use of a laryngeal tube significantly reduces such no-flow intervals.18,20–23 We could demonstrate that establishing an airway with the laryngeal tube required less than 45 s in most of the cases.

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    We used a modified insertion technique (Fig. 2). The main difference of this technique, compared to the manufacturer's instructions for use, is that a forced chin lift manoeuvre (“Esmarch grip”) was performed to create sufficient retropharyngeal space, thereby allowing the LTS II easier passage through the pharynx, resulting in a significantly higher rate of successful and fast placement attempts.20 This modified technique can be performed with both rescuer and patient being in almost any position.

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A Spanish translated version of the summary of this article appears as Appendix in the final online version at 10.1016/j.resuscitation.2007.08.018.

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