SUMMARY The ultrasonic radiation utilised in phacoemulsification procedures for the removal of cataractous lenses results in the widespread production of discrete lesions in the corneal endothelium. The morphology of this induced damage has been examined in rabbit and man using both scanning and transmission electron microscopy. The illustrated results are related to both the duration of the ultrasonic exposure and to the mechanisms of damage.Phacoemulsification was introduced as a new technique for the surgical treatment of cataract by Kelman (1967). The principle of the technique is to fragment the lens nucleus by ultrasonic vibration, thereby allowing aspiration of the cataractous lens. The procedure is now used by many surgeons. The technique requires advanced microsurgical skills and there is a high incidence of complications during the period when a surgeon is inexperienced in the method (Cleasby et al., 1974;Hiles and Hurite, 1973). However, over a larger number of operations the complications are comparable to those with conventional cataract procedures (Kelman, 1973).Reports of the incidences of postoperative corneal oedema vary between zero (Kelman, 1974) and 18 % (Cleasby et al., 1974). Recently endothelial cell destruction has been shown to occur during the phacoemulsification procedure (Polack and Sugar, 1976;Binder et al., 1976). These lesions have been attributed to a number of mechanisms which include the effects of irrigation, lens manipulation, and lens fragments in the anterior chamber, instrument contact with the endothelium, and ultrasound. This paper investigates the effect of radiating ultrasound on corneal endothelium resulting from the application geometry and dosage commonly used during phacoemulsification.
Materials and methodsAdult Dutch rabbits weighing 2 to 3 kg were killed with intravenous pentobarbitone prior to enucleation. The pair of isolated eyes was transported to the Address for reprints: Mr Noel S. C. Rice, FRCS, Moorfields Eye Hospital, City Road, London ECIV 2PD. phacoemulsifier in a constant temperature container maintained at room temperature. An average journey time was 45 minutes. On arrival the eyes were placed in a holder and a 3 mm incision was made at the limbus with the aid of a surgical microscope. The tip of a Cavitron-Kelman phacoemulsifier (Model 7007) was inserted into the anterior chamber parallel to the iris and at a depth approaching the edge of the pupil. Care was taken to avoid either the endothelium or lens capsule. The tip direction and location were noted and recorded. To one eye of each pair irrigation, aspiration, and ultrasound were given continuously for times ranging from 10 seconds to 5 minutes. Fresh glutathionebicarbonate-Ringer (GBR) solution maintained at room temperature was used for irrigation in all procedures. The ultrasonic transducer of the phacoemulsifier was fully tuned with a power setting of 8. The other eye of each pair was used as a control and was therefore exposed only to irrigation and aspiration. In some control eyes air...