Anaesthesia
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Clinical Trial Controlled Clinical Trial
Use of the oesophageal detector device in children under one year of age.
The efficacy of a modified oesophageal detector device was evaluated in a single-blind study of 20 healthy infants. It was found to be unreliable as a method to discriminate oesophageal from tracheal intubation in this age group.
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Comparative Study
Pressure generated during insertion of lumbar epidurals. A comparison with the Portex epidural injection simulator.
The aim of this study was to measure pressures exerted during insertion of lumbar epidurals in obstetric patients. The pressures were compared with those obtained when the Portex epidural injection simulator was used, and were significantly greater when a saline technique was used compared to those when air was used (p less than 0.05). There were no differences between the pressures obtained with the simulator and those measured in vivo.
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The laryngoscopic conditions of 62 diabetic patients who underwent renal transplantation or vitrectomy were studied. Anaesthesia was induced with fentanyl and a sleep dose of thiopentone. Conditions for direct laryngoscopy after 0.1 mg/kg vecuronium were scored from 0 to 3 (easy-very difficult). ⋯ The correlation coefficient between these two factors was r = 0.6 (p less than 0.001). Our study shows that joint rigidity possibly caused by tissue glycosylation may also involve laryngeal and cervical areas resulting in a strenuous laryngoscopy. A defective palm print is a warning sign for difficult laryngoscopy.
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The three currently available paper radioallergosorbent tests ('suxamethonium', alcuronium and thiopentone) were evaluated. 'Suxamethonium' radioallergosorbent test (which employs choline conjugated to paper discs) proved to be reliable in the detection of allergy to neuromuscular blockers, which were confirmed as the most common cause of anaphylactic reaction during general anaesthesia. Thiopentone radioallergosorbent test may also be useful, and is recommended in conjunction with 'suxamethonium' radioallergosorbent test in the preliminary investigation of reactions. Patients with positive 'suxamethonium' radioallergosorbent test usually require further testing, including alcuronium radioallergosorbent test, skin testing with a wide range of drug concentrations or leucocyte histamine release test.