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Correspondence |
Rome, Italy
To the Editor:
The Laryngeal Tube® (LT; VBM, Medizintechnik, GmbH, Sulz, Germany) is a novel airway device consisting of a silicone airway tube and two cuffs. Once inserted, the proximal cuff lies in the hypopharynx and the distal cuff in the upper esophagus (Figure
). We conducted a pilot study to assess the efficacy of the LT13 throughout the surgical procedure and to determine whether the ability to obtain an effective airway with the LT is affected by the body mass index (BMI) of patients.
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Patients were divided in three groups, based on BMI: 1 < 20 kgm-2, 2 = 2024.9 kgm-2, and 3 = 2530 kgm-2. The LT size was chosen according to patient height: size 3 (< 155 cm), size 4 (155180 cm), size 5 (> 180 cm). The LT was inserted with the head in the sniffing position. Cuffs were inflated to a pressure of 60 cm H2O. To evaluate the airway, the following scoring system was used: 1 = easy (immediate effective ventilation); 2 = difficult (effective ventilation after adjustment of the position of the LT); 3 = impossible (ventilation not achieved, tracheal intubation performed). Data were compared using the Spearman correlation test (significant P < 0.05). Duration of anesthesia ranged between 20 and 90 min. The hemodynamic variables remained stable throughout the surgery. In 95.6% patients an effective ventilation was obtained: 72.5% could be ventilated immediately; 27.5% needed further maneuvers to obtain effective ventilation (the device was pulled up in 42/59 patients and it was pushed down in 17/59). In 4.4% of patients, ventilation was impossible and tracheal intubation had to be performed. Oxygen saturation remained above 98% in all patients. The patients presented neither regurgitation nor other respiratory problems. After removal, 1.0% patients coughed, 2.6% suffered from sore throat and 1.5% from pain on swallowing. No patient had any adverse event after 24 hr. The high rate (95.6%) of effective ventilation suggests that the LT may be a reliable device for airway management and we found that the effectiveness of the LT does not decrease over time.4
Mean BMI (± standard deviation) was 23.9 ± 2.4 kgm-2. There were 18 patients in Group I, 138 in Group II and 72 in Group III and adjustment of device position was required in three (17%), 29 (21%) and 27 (38%) respectively. A significant correlation between BMI and the airway scoring system was present (P < 0.001). Goodman et al.5 showed a correlation between increasing BMI and decreasing pharyngeal height. Furthermore, there is an inverse relationship between increasing BMI and pharyngeal area. Such observations reinforce our finding.
In conclusion, the LT provided effective ventilation during general anesthesia. Correct LT positioning may require more adjustments in patients with an increasing BMI.
References
1 Agrò F, Cataldo R, Alfano A, Gallì B. A new prototype for airway management in an emergency: the laryngeal tube. Resuscitation 1999; 41: 2846.[Medline]
2 Agrò F, Gallì B, Ravussin P. Preliminary results using the laryngeal tube for supraglottic ventilation. Am J Emerg Med 2002; 20: 578.[Medline]
3 Agrò F, Cataldo R, Alfano A, Gallì B, Ravussin P. A comparison of two new devices for emergency airway management: laryngeal tube and airway management device. Am J Emerg Med 2001; 19: 1634.[Medline]
4 Asai T, Murao K, Shingu K. Efficacy of the laryngeal tube during intermittent positive-pressure ventilation. Anaesthesia 2000; 55: 1099102.[Medline]
5 Goodman EJ, Eisenmann UB, Dumas SD. Correlation of pharyngeal size to body mass index in the adult. Anesth Analg 1997; 84: 584.
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