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Randomized Controlled Trial Comparative Study
Performance of the PAxpress vs the ProSeal laryngeal mask airway during general anesthesia.
- Alexandre Lallo, Pierre Drolet, and Mélanie Lacroix.
- Department of Anesthesiology, University of Montreal, CHUM, Hôpital Notre-Dame, 1560, Sherbrooke East, Montreal, Quebec H2L 4M1, Canada. a.lallo@umontreal.ca
- Can J Anaesth. 2007 Jan 1;54(1):28-33.
PurposeThe PAxpress (PAx) is a relatively new pharyngeal airway device that is easily inserted and effective in routine airway management. A prospective, randomized study was undertaken to compare the PAx with the ProSeal laryngeal mask airway (PLMA) during anesthesia with positive pressure ventilation.MethodsOne hundred adult patients scheduled for elective surgery under general anesthesia were randomized to airway management with either the PAx (n=50) or the PLMA (n=50). All patients swallowed a methylene blue capsule before anesthesia. After insertion, leak and inspiratory pressures were measured. Fibrescopy was used to view the glottis. Devices were inspected for blood or methylene blue staining upon removal at the end of surgery. An interview was conducted postoperatively to evaluate the occurrence of sore throat, dysphagia and dysphonia.ResultsInsertion time was longer for the PAx than for the PLMA (52 +/- 44s vs 34 +/- 23 sec; P=0.003). Leak pressure was lower while peak inspiratory pressures, and EtCO2 values were higher (P=0.016; 0.027 and 0.04 respectively) with the PAx. Both devices provided comparable fibreoptic viewing of the glottis. There were no differences with respect to the incidence or pattern of blue stains upon removal. Blood was seen more often on the PAx (58% vs 19%) and dysphagia was also more frequent and severe with the PAx.ConclusionIn comparison with the PLMA, PAx insertion time is longer and the ventilatory characteristics of this new device may be marginally inferior. The PAx is also more traumatic and is associated with more postoperative discomfort compared to the PLMA.
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