Posterior chamber intraocular lens dislocations and malpositions

Decentration and malposition of posterior chamber intraocular lenses (PC IOL) accounts for one of the remaining and unresolved conditions associated with the implantation of these lenses. This condition assumes importance since in approximately 50% of cases where a PC IOL is removed there is an aspect of improper positioning. The common types of malpositions are: pupil capture; sunset syndrome; sunrise syndrome; horizontal decentration; and the windshield wiper syndrome. This paper will explore the causes and management of these conditions and discuss the virtues of capsular bag implantation.     

Stability of refraction during four years after radial keratotomy in the prospective evaluation of radial keratotomy study.

The Prospective Evaluation of Radial Keratotomy Study is a nine-center clinical trial of a standardized technique of radial keratotomy in 435 patients who had simple myopia with a preoperative refraction between -2.00 and -8.00 diopters. We studied the stability of the refractive error during four years after surgery for each of 341 eyes first operated on that had a single surgical procedure. Between baseline and two weeks after surgery, all eyes became less myopic; between two weeks and three months, 161 eyes (59%) lost 1.00 D or more of the initial effect; and between three and six months, 266 eyes (95%) had a stable refraction with less than 1.00 D change. The change from six months to four years was less than 1.00 D for 246 eyes (72%). There was 1.00 D or more decrease in surgical effect (increased minus power) for 13 eyes (4%), and 1.00 D or more increase in surgical effect (decreased minus power) for 82 eyes (24%). Eyes with larger amounts of preoperative myopia and smaller diameter of the clear zone were more likely to have an increasing effect of the surgery. The duration of this continued increasing effect of the surgery is unknown.     

Rationale for and design of the National Eye Institute Prospective Evaluation of Radial Keratotomy (PERK) Study

A five-year, multicenter, collaborative clinical trial of radial keratotomy for myopia is being carried out at nine clinical centers. The study, funded by the National Eye Institute, is recruiting approximately 500 patients aged 21 years or older with -2.00 to -8.00 diopters of physiologic myopia who also meet other clearly defined eligibility criteria. Surgeons use a diamond-bladed micrometer knife to make eight radial incisions in the anterior cornea. The diameter of the central clear zone is determined by the amount of myopia and the depth of the incisions by intraoperative ultrasonic pachymetry. Investigators other than the surgeon gather all pre- and post-operative data. Examinations include measurement of visual acuity with standardized charts, verification of refractions by a second observer, measurement of corneal curvature by keratometry and photokeratoscopy, quantitation of glare with a glare tester, and measurement of the size of individual endothelial cells from specular photomicrographs with a computerized digitizer. A formal psychometric questionnaire is used to evaluate the patients' subjective response. Physician monitors insure adherence to the protocol during site visits and members of the Data and Safety Monitoring Board oversee the progress of the study. Biostatisticians at the Coordinating Center insure complete data collection, process the data, and assist in the interpretation of results.