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2.
Can J Anaesth ; 50(5): 495-500, 2003 May.
Article in English, French | MEDLINE | ID: mdl-12734160

ABSTRACT

PURPOSE: The PAxpress is a new, single-use, extraglottic airway device. We evaluate: 1) insertion success rates; 2) airway sealing pressure, ventilatory capability and calculated mucosal pressures (in vitro minus in vivo intracuff pressure) at 30-60 mL cuff inflation volume; 3) the feasibility of lightwand-guided tracheal intubation; and 4) the incidence of mucosal trauma. METHODS: Ninety anesthetized, paralyzed adults were studied. Airway management was by senior anesthesiologists with no prior experience with the PAX, but considerable experience with extraglottic airway devices and the flexible-lightwand. RESULTS: Insertion was successful at the first attempt in 95.5% (86/90) and at the second attempt in 4.5% (4/90). Mean +/- SD airway sealing pressure at 30, 40, 50 and 60 mL cuff inflation volume was 27 +/- 8, 29 +/- 9, 32 +/- 9 and 35 +/- 7 cm H(2)O respectively; expired tidal volume at airway sealing pressure was 16 +/- 6, 18 +/- 6, 19 +/- 5 and 19 +/- 6 mL.kg(-1); and calculated mucosal pressure was 38 +/- 14, 55 +/- 20, 56 +/- 19 and 57 +/- 20 cm H(2)O. Airway sealing pressure, expired tidal volume at airway sealing pressure and calculated mucosal pressures increased with cuff inflation volume (all: P < or = 0.0002). Esophageal leak was detected in 9% (8/90), but only at peak pressures > or = 35 cm H(2)O and cuff inflation volumes > or = 40 mL. Lightwand-guided intubation was successful in 82% (74/90) of patients. Mild, moderate and severe blood staining was detected in 40% (36/90), 15% (13/90) and 1% (1/90) respectively. Blood staining was more frequent after adjusting maneuvers (22/54 vs 32/36, P = 0.002). CONCLUSION: The PAX has a high insertion success rate and is an effective ventilatory device with a low risk of gastric insufflation, but has a moderately high failure rate for lightwand-guided intubation and is associated with a relatively high incidence of mucosal trauma. Mucosal pressures may exceed pharyngeal perfusion pressure.


Subject(s)
Anesthesia , Intubation, Intratracheal/instrumentation , Laryngeal Masks , Neuromuscular Blockade , Respiration, Artificial/instrumentation , Equipment Failure , Female , Humans , Male , Middle Aged , Pressure , Tidal Volume/physiology
3.
Anesthesiology ; 96(2): 296-9, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11818759

ABSTRACT

BACKGROUND: The authors determined the efficacy of using the intubating laryngeal mask airway Fastrach (ILM) as a ventilatory device and aid to flexible lightwand-guided tracheal intubation in patients with unpredicted failed laryngoscope-guided tracheal intubation when managed by experienced anesthetists. METHODS: During a 27-month period, 16 experienced anesthetists agreed to use the ILM as an airway device and airway intubator in patients (aged > 18 yr) with predicted normal airways who were subsequently found to be difficult to intubate (three failed attempts at laryngoscopy). Intubation via the ILM was performed with a flexible lightwand. The number of attempts at ILM placement, the number of adjusting maneuvers, the number of attempts at tracheal intubation via the ILM,and any episodes of hypoxia (oxygen saturation < 90%) were recorded. RESULTS: Forty-four of 11,621 patients (0.4%) met the inclusion criteria. ILM insertion and ventilation was successful at the first attempt in 40 of 44 patients (91%) and at the second attempt in 4 of 44 (9%). Flexible lightwand-guided tracheal intubation via the ILM was successful in 38 of 44 patients (86%) at the first attempt, 3 of 44 (7%) at the second attempt, 2 of 44 (5%) at the third to fifth attempts, and failed in 1 of 44 (2%). The median number of adjusting maneuvers before successful intubation was 1 (range, 0-4). Hypoxia occurred in 5 patients before ILM insertion (range, 52-82%), but none after ILM insertion. No patient developed hypoxia during or after intubation via the ILM. CONCLUSION: The ILM is an effective ventilatory device and aid to flexible lightwand-guided tracheal intubation in adult patients with predicted normal airways in whom laryngoscope-guided tracheal intubation subsequently fails when managed by experienced anesthetists.


Subject(s)
Intubation, Intratracheal , Laryngeal Masks , Adult , Aged , Female , Fiber Optic Technology , Humans , Intraoperative Complications/epidemiology , Laryngeal Masks/adverse effects , Laryngoscopy , Male , Middle Aged , Prospective Studies
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