Virtual Disaster Medicine

Training Center (VDMTC)

Module 14

Advanced Airway Techniques

Part 2 - New Generation Supraglottic Ventilatory Devices

Desirable Features and Optimal Methods for Testing

 

 

DESIRABLE FEATURES OF SUPRAGLOTTIC AIRWAYS

 

There are certain questions that influence the anesthesiologist’s choice of an airway for an individual patient.  For instance, does the anesthesiologist use a single-use device, a device that can be reused most often, the cheapest device, or the device that causes least trauma?  Do all devices maintain the airway reliably?  Do any of them protect the airway from regurgitation and pulmonary aspiration?  Which devices enable safe and effective positive pressure ventilation?  Will the device enable access to the airway if required?  Other questions relate to how well these devices function in large cohorts.  Are there differences in ease of insertion and airway seal pressure between the various devices?  How often are manipulations needed to maintain a clear airway during anesthesia?  Which devices are tolerated best during emergence?  What are the relative incidences of airway trauma and postoperative pharyngolaryngeal morbidity?  Unfortunately, in the majority of cases, remarkably few data are available.  The manner in which new medical devices are regulated contributes to this.

 

The desirable features of an ideal supraglottic device relate to efficacy, versatility, safety, reusability and cost.  Manufacturing a quality product is important.  The device should be made of good quality non-harmful materials.  A long shelf life is desirable.  Devices designed to be reusable should be robust enough to allow multiple uses without deterioration of performance.  Similarly, design should enable appropriate cleaning without damage or deterioration.  Most of these factors are overseen during the statutory evaluations.  Desirable features may be viewed from the patient’s or anesthesiologist’s perspective.

 

The anesthesiologist wants a device that is inserted reliably on the first attempt, producing a clear airway for both spontaneous and controlled ventilation.  It must enable the anesthesiologist to maintain hands-free anesthesia.  Emergence should be without complications.  The incidence of airway trauma and post-operative sore throat should be acceptably low.  Design features or clinical evidence of protection against aspiration is desirable, as is the ability to access the trachea through the device.  From the patient’s perspective, the ideal device should not cause intraoperative complications, device-associated trauma, or pharyngolaryngeal morbidity.  Let’s first consider the anesthesiologist’s requirements.

 

The device should enable insertion with minimal mouth opening (most require 2-3 cm mouth opening) and with a light depth of anesthesia (the dose range for different airways varies approximately two-fold).  Supraglottic devices requiring muscle relaxant for insertion are of limited use.

 

All supraglottic airway devices may cause airway obstruction from epiglottic downfolding.  This is reduced by ensuring correct insertion technique and by designing devices with a slim leading edge.  The slim profile of the deflated LT and the deflation device and tip flattener that are provided with the cLMA and pLMA are examples of such design.  The epiglottis may also cause obstruction by entering the orifice of the airway device and a variety of design features are aimed at avoiding this.  These include epiglottic bars (cLMA and FLMA), a large orifice too big to obstruct (pLMA), multiple holes (combitube, Laryngeal Tube™), and a hooded orifice with protective fins (PAx).

 

 

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