EDITOR:
We would like to report a potential critical incident resulting from an unauthorized unconventional modification of anaesthetic equipment. The ProSeal laryngeal mask airway (LMA) is a modification of the classic LMA [Reference Cook, Lee and Nolan1], designed to enable separate respiratory and gastrointestinal tracts. A gastric drain tube is incorporated, which can vent gas leakage during ventilation, thus preventing gastric insufflation. It also enables aspiration of gastric contents intraoperatively by insertion of an orogastric tube and has been used to detect malposition of the mask.
A ProSeal LMA was used to secure an airway after induction of general anaesthesia. After cuff inflation, the anaesthetic assistant picked up the anaesthetic breathing circuit to connect it to the ProSeal LMA, and encountered two possible connector choices at the distal end of the LMA. We then noticed that the drain tube of the LMA also had a 7 mm endotracheal tube connector securely attached to its distal end (Fig. 1). The breathing circuit was connected to the appropriate airway connector, avoiding the unintended oesophageal ventilation and insufflation. The unnecessary connector was removed from the drain tube to avoid future incident.
ProSeal LMA with two airway connectors, one at the distal end of reinforced LMA tube and the other unexpected connector attached to the drain tube. LMA: laryngeal mask airway.
Modification of anaesthetic equipment is well known and in the past has played an important part in the development of new equipment. Many modifications are widely accepted, used and even published in the journals [Reference Turkstra and Pellerin2]. The modification of the ProSeal LMA by connecting an endotracheal tube connector to the drain tube has been reported recently, when the lightwand was used in conjuction, to facilitate the insertion of the ProSeal LMA, as the endotracheal tube connector seats perfectly in the connector lock at the hilt of the lightwand. The author of this article stressed that the endotracheal tube connector must be removed immediately after the procedure to prevent inadvertent connection of the anaesthetic circuit to the drain tube [Reference Mutch3].
This ProSeal LMA is an essential item on our difficult airway trolley, as recommended in the Difficult Airway Society guidelines for unanticipated difficult intubation during rapid sequence induction in non-obstetric patient. In our case, the endotracheal tube connector was found to be firmly attached to the drain tube. The reason for this could not be determined: Either the ProSeal LMA was modified to be used with lightwand or an endotracheal tube connector was attached in error before sending for sterilization. All staff have been made aware of this, to prevent any future incident. This incident highlights the importance of a thorough check of all the equipment before sending for sterilization as well as before use in the theatre. Airway devices should be checked not only for its patency but also for any inadvertent modifications.
