We have evaluated the Airway Management Device (AMD (TM)) in 105 anaestheti
sed patients. We were successful in establishing a clear airway on the firs
t attempt on 69 occasions and unable to establish a patent airway at all in
10 patients. Airway obstruction requiring removal of the device occurred d
uring maintenance of anaesthesia in a further two cases and during emergenc
e in three. Loss of the airway during anaesthesia occurred in eight of 95 p
atients and could be reversed by manipulation of the airway in six cases. O
verall, a mean of 0.56 manipulations per patient were required to establish
an airway and a further 0.42 per patient were required during maintenance
of anaesthesia. In the 95 patients in whom an airway was established, assis
ted ventilation was satisfactory in 93, with a leak pressure above 20 cmH(2
)O in 65. Intracuff pressure was measured in 12 cases and was above 100 cmH
(2)O in eight. Minor complications occurred in 12 patients. Blood was visib
le on removal of the device in six cases.