Airway topicalisation in morbidly obese patients using atomised lidocaine: 2% compared with 4%
- PMID: 17845648
- DOI: 10.1111/j.1365-2044.2007.05179.x
Airway topicalisation in morbidly obese patients using atomised lidocaine: 2% compared with 4%
Abstract
We evaluated the technique of airway anaesthesia using atomised lidocaine for awake oral fibreoptic intubation in morbidly obese patients using two doses of local anaesthetic. Morbidly obese patients were allocated to receive either 2% or 4% lidocaine (40 ml) for oral airway anaesthesia using an atomiser with high oxygen flow. Patients were carefully sedated using midazolam and fentanyl. Outcomes included patient tolerance to airway manipulation, haemodynamic parameters, and serial plasma lidocaine concentrations. In all, 27 patients were enrolled in the study (2% cohort n = 14, 4% cohort n = 13). Patient characteristics and time for topicalisation and airway management were similar. Haemodynamic parameters did not change significantly. Tolerance to insertion of the Ovassapian airway, bronchoscopy, and tracheal tube positioning was excellent (12 vs 12 patients, 12 vs 12 patients, and 8 vs 12 patients had no response, respectively, 2% vs 4%). Differences did not reach statistical significance. Peak plasma lidocaine concentration was significantly lower in the 2% group (2.8 (0.8) microg.ml(-1) compared with 6.5 (1.0) microg.ml(-1), p < 0.05). Airway anaesthesia using atomised lidocaine for awake fibreoptic intubation in the morbidly obese is efficacious, rapid, and safe. Compared with 4% lidocaine, the 2% dose provides acceptable intubating conditions in most cases and produces lower plasma lidocaine levels.
Comment in
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Lidocaine for airway topicalisation.Anaesthesia. 2008 Mar;63(3):316-7; author reply 317-8. doi: 10.1111/j.1365-2044.2008.05461_2.x. Anaesthesia. 2008. PMID: 18289241 No abstract available.
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Lidocaine for airway topicalisation.Anaesthesia. 2008 Mar;63(3):316; author reply 317-8. doi: 10.1111/j.1365-2044.2008.05461_1.x. Anaesthesia. 2008. PMID: 18289242 No abstract available.
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