Use of a digital infrared pupillometer to assess patient suitability for refractive surgery.

PURPOSE: To assess the role of binocular infrared dynamic pupillometry in measuring and recording the pupil size in scotopic, low mesopic, and high mesopic illumination prior to refractive surgery. SETTING: The Rosen Eye Surgery Centre, Alexandra Hospital Victoria Park, Manchester, United Kingdom. METHODS: In this prospective study, the pupil sizes of 58 patients (mean age 46 years +/- 11.7 [SD]) presenting for refractive surgery assessment were evaluated using the P2000 SA pupillometer (Procyon Instruments Ltd.). Each patient was measured at 3 illumination levels: 0.02 lux (scotopic), 0.15 lux (low mesopic), and 10.6 lux (high mesopic). At each level, 10 images were acquired by the system at 5 images per second. Both eyes were imaged at the same time, with a spatial accuracy of 0.03 mm per pixel. RESULTS: Pupillary unrest (PU) occurred at all levels of illumination. Some degree of PU amplitude was observed in both eyes of all patients. The median PU was 0.12 mm (95% confidence limits [CLs], 0.11, 0.14) in the scotopic range, 0.34 mm (95% CLs, 0.28, 0.38) in the low mesopic range, and 0.28 mm (95% CLs, 0.23, 0.30) in the high mesopic range. The degree of anisocoria varied among individuals. The median value was 0.28 mm (95% CLs, 0.21, 0.39) in the scotopic range, 0.32 mm (95% CLs, 0.26, 0.37) in the low mesopic range, and 0.16 mm (95% CLs, 0.12, 0.19) in the high mesopic range. Because of PU and anisocoria, single versus multiple binocular measurements demonstrated the possibility of errors greater than 1.0 mm in some patients. CONCLUSIONS: Patients showed an appreciable degree of pupillary motion during measurement at all levels of illumination; the motion was largest under low mesopic illumination. The 2 pupils were rarely identical. Multiple-measurement binocular pupillometry is better than single monocular measurement to gain a precise description of pupil behavior before refractive surgery.

Tracker-assisted laser in situ keratomileusis for myopia using the autonomous scanning and tracking laser: 12-month results.

OBJECTIVE: To determine the safety, efficacy, and predictability of the Autonomous scanning and tracking laser for the correction of myopia and myopic astigmatism with laser in situ keratomileusis (LASIK) procedure. DESIGN: Retrospective, noncomparative case series. PARTICIPANTS: The first 129 consecutive eyes with up to -13.00 diopters (D) of myopia and -5.00 D of astigmatism. INTERVENTION: Myopic tracker-assisted LASIK (T-LASIK) using the Autonomous Laser (Alcon Summit Autonomous, Waltham, MA) and Hansatome microkeratome (Bausch & Lomb Surgical, Bracknell, England). MAIN OUTCOME MEASURES: Uncorrected visual acuity (UCVA), manifest spherical equivalent (MSE), best spectacle-corrected visual acuity (BSCVA), and complications were studied. RESULTS: At 12 months, the mean MSE was -0.02 +/- 1.01 D, with 79.1% of eyes within 0.5 D and 89.9% of eyes within 1 D of the intended correction. UCVA was 20/20 or better in 71.4%, 20/25 or better in 78.5%, and 20/40 or better in 92.8% of eyes. Two eyes (1.6%) lost 2 lines and five eyes (3.8%) gained 2 lines of BSCVA. Sixteen eyes (12.4%) required retreatment to correct residual myopia or astigmatism. After retreatment, 14 of 16 eyes were within 0.5 D of emmetropia. Nine eyes (6.9%) had minor flap complications; two eyes (1.6%) had grade 2 diffuse lamellar keratitis, of which one eye had associated peripheral flap melt. One eye showed slight decentration; this eye was rolling throughout the procedure. All eyes had some dryness, with 10% severe enough to require temporary punctual occlusion with plugs. CONCLUSIONS: T-LASIK for myopic astigmatism with the Autonomous Laser is relatively safe, effective, and predictable. The tracker seems to be effective, and the complications are relatively few. Retreatment rates are acceptable and can be performed safely and effectively to improve visual outcome. The outcomes are comparable with other published data.

Correction of pseudophakic anisometropia with the Staar Collamer implantable contact lens.

PURPOSE: To assess the role of the Staar Surgical implantable contact lens (ICL) for the correction of pseudophakic anisometropia. SETTING: Oxford Eye Hospital, Oxford, and Rosen Eye Center, Alexandra Hospital, Manchester, United Kingdom. METHODS: Six patients with pseudophakic anisometropia ranging from 2.0 to 7.9 diopters (D) (mean 4.4 D) had ICL implantation as an alternative to intraocular lens (IOL) exchange or conventional piggyback IOLs. RESULTS: All patients had a reduction in anisometropia to asymptomatic levels. The mean reduction was 3.15 D. No patient experienced adverse effects. CONCLUSIONS: The implantable contact lens offers an alternative approach to the management of pseudophakic anisometropia that avoids some of the risks associated with IOL exchange, corneal refractive surgery, and conventional piggyback IOLs.