We have assessed a range of high volume, low pressure (HVLP) cuffed tracheal tubes in a benchtop model, for leakage of fluid from above the cuff to the model trachea below, during various ventilatory modes. Rapid leakage occurred in the model during all modes of ventilation, unless tracheal pressure was greater than the height of fluid in the column above the cuff. This leakage occurred preferentially down longitudinal folds that occur in the HVLP cuff wall. This model suggests that, if a longitudinal fold within the cuff wall is patent, then the possibility exists of subglottic to tracheal leakage.
Summary
This guideline updates and replaces the 5th edition of the Standards of Monitoring published in 2015. The aim of this document is to provide guidance on the minimum standards for monitoring of any patient undergoing anaesthesia or sedation under the care of an anaesthetist. The recommendations are primarily aimed at anaesthetists practising in the UK and Ireland, but it is recognised that these guidelines may also be of use in other areas of the world. Minimum standards for monitoring patients during anaesthesia and in the recovery phase are included. There is also guidance on monitoring patients undergoing sedation and during transfer. There are new sections specifically discussing capnography, sedation and regional anaesthesia. In addition, the indications for processed electroencephalogram and neuromuscular monitoring have been updated.
The LVLP cuffed tracheal and tracheostomy tubes reduced pulmonary aspiration in the benchtop models and in anesthetized and critically ill patients. The single failure of the LVLP cuff in the anesthesia group was probably associated with accidental endobronchial intubation following tube movement.
Cuff lubrication with a water-soluble gel reduces pulmonary aspiration in anesthetized patients. In the critically ill patient with a tracheostomy the protective effect is lost after 24-120 h.
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