Photorefractive keratectomy for hyperopia using an erodible disc and axicon lens: 2-year results.

BACKGROUND: This paper presents the results over a 2-year follow-up of the first human trial of photorefractive keratectomy (PRK) for correction of hyperopia using an erodible disc excimer laser delivery system (Summit) coupled to an axicon lens. METHODS: We treated 25 eyes of 21 patients for a mean correction of +3.38 +/- 0.97 D (range, +1.00 to +4.00 D). The hyperopic correction was made using an erodible disc inserted on the laser optical pathway; an axicon lens was then used to create a blend transition zone. Eyes were evaluated at 1, 3, 6, and 12 months after surgery. For a smaller series of 11 eyes, we also present 24-month results. RESULTS: Mean refractive error 1 month after treatment (25 eyes) was -2.35 +/- 1.55 D (range, +1.00 to -6.50 D). Eight eyes (32%) had a spectacle-corrected visual acuity loss greater than 1 line. Twelve months after treatment, mean spherical equivalent refraction was -0.47 +/- 0.80 D (range, +1.25 to -2.25 D). Nineteen eyes showed an improvement (range, 3 to 8 lines) in uncorrected distance visual acuity and 23 showed improvement in uncorrected vision at reading distance (1 to 7 lines). CONCLUSION: This technique proved effective in reducing hyperopia, but predictability must be demonstrated in a larger treatment group. Safety was confirmed by the absence of delayed reepithelialization and the absence of spectacle-corrected visual acuity loss greater than 1 line at 1 year after surgery.

Hyperopia correction using an erodible mask excimer laser delivery system coupled to an axicon: preliminary results.

PURPOSE: This paper presents the results of the first human trial on the correction of hyperopia using an erodible mask excimer laser delivery system coupled to an axicon. METHODS: We treated 17 eyes of 17 patients (age range 34-62 years) for the correction of +3.21 +/- 1.04 D (range +1.00 to +4.00 D). The hyperopic correction was made using an erodible mask inserted on the laser optical pathway, to produce a circular ablation measuring 6.5 mm in diameter. An axicon was then used to create a blend transition zone from 6.5 mm up to 9.4 mm in diameter. Eyes were evaluated at one, three and six months after surgery. RESULTS: Reepithelization was always observed by the fifth postoperative day, despite the large area of deepithelization (diameter 9.5 mm). Mean refractive error one month after treatment was -2.44 +/- 1.59 D (range 0.00 to -6.50 D). Five eyes (29.4%) had a best corrected visual acuity loss more than two to three lines; all eyes showed mild annular haze not involving the central part of the cornea. Six months after treatment, mean refractive error was -0.88 +/- 0.99 D (range +0.50 to -3.00 D). Compared to preoperative status, 13 eyes (76.5%) showed an improvement in uncorrected distance visual acuity (1-8 lines), and 14 eyes (82.4%) showed an improvement in uncorrected vision at reading distance (3-7 lines). Two eyes (11.7%) showed a best corrected visual acuity loss of two of three lines. CONCLUSIONS: These preliminary results indicate this approach is effective in reducing hyperopia, while its predictability has still to be proved in a larger treatment group with longer follow-up. A cautious approach to this technique is still advisable, especially for higher hyperopic corrections, in view of the large best corrected visual acuity loss seen in two eyes at six months.

Compound myopic astigmatism correction using a mask in-the-rail excimer laser delivery system. Preliminary results.

PURPOSE: The latest development in the erodible mask technology is an excimer laser containing the mask in the laser optical pathway. This paper reports the results of the first human series of consecutive treatments performed for the correction of compound myopic astigmatism. METHODS: We have treated 83 eyes. Spherical equivalent attempted correction ranged between -1.75 and -11.75 D (mean -7.07+/- 2.45 D), astigmatic attempted correction ranged between -1.00 and -5.00 D (mean -2.42+/- 1.02 D). The sphere correction was made by diaphragm using a multi-zone software with three ablation zones: 100% of the total attempted correction for the central 5.0 mm zone, 70% for the second 6.0 mm zone, 30% for the outer 6.5 mm zone. Cylinder correction was made sequentially after myopic correction using the appropriate mask. RESULTS: One month after treatment, mean refractive error was + 1.07 +/- 1.24 D (range + 4.50/-1.75 D) for spherical equivalent, and -0.49 +/- 0.57 D (range + 0.75/-2.00 D) for astigmatism. Forty-eight eyes (57.8%) had uncorrected visual acuity of 20/40 or better. At six months, mean refractive error was +0.42 +/- 0.97 D (range + 3.75/-1.00 D) for spherical equivalent, and -0.44 +/- 0.51 D (range +0.25/-3.00 D) for astigmatism. Vector analysis showed that 57 eyes (68.7%) had 5 or less degrees rotation. Seventy-two (86.7%) and 54 eyes (65.1%) had uncorrected visual acuity equal or better than 20/40 and 20/25 respectively. One eye (1.2%) showed a best corrected visual acuity loss of more than one line, but 8 eyes (9.6%) had a gain of more than one line. One-year results on a smaller series (33 eyes) overlap with the six-month results. CONCLUSIONS: The mask in-the-rail excimer laser delivery system appears to be effective and predictable in the correction of compound myopic astigmatism. We observed no significant regression of the astigmatic correction over time. Longer follow-up on larger series is necessary to draw final conclusions.

Photorefractive keratectomy for compound myopic astigmatism with an eye cup erodible mask delivery system.

BACKGROUND: The erodible mask is a new energy delivery system for the 193-nm argon fluoride excimer laser. It consists of a polymethyl-methacrylate button, whose profile is transferred by photoablation onto the corneal surface. We present the 6- and 12-month results of this technique in the correction of compound myopic astigmatism. METHODS: We performed the mask procedure on 21 eyes of 16 subjects (mean age, 30.7 years; range, 24 to 46) to correct combined myopia and astigmatism. Attempted myopic correction ranged between -1.50 diopters (D) and -10.00 D (mean, -7.07 D). Attempted astigmatic correction ranged between -1.50 D and -4.00 D (mean, -2.46 D). RESULTS: Mean procedure error was: sphere +0.74 D (range, -3.00/+5.00), cylinder -1.41 D (range, -3.50/0.00) at 1 month after surgery; sphere +0.18 D (range, -2.50/+ 3.50), cylinder -1.56 D (range, -4.00/0.00) at 6 months; and sphere -1.30 D (range, -3.00/0.00), cylinder was -1.25 D (range, -2.00/-0.50) at 12 months (10 eyes). During follow up, haze values were never higher than 1, except for one case of haze 2 that regressed to 0 during follow up. Postoperative uncorrected visual acuity improved in all eyes where emmetropia was envisaged; none of the eyes lost spectacle-corrected visual acuity lines 6 or 12 months after surgery. CONCLUSIONS: The erodible mask proved effective and fairly predictable mainly in the correction of the spherical component of refractive error, while the correction of astigmatism revealed greater unpredictability, with a constant trend to undercorrection.

Evaluation of three different approaches to perform excimer laser photorefractive keratectomy for myopia.

BACKGROUND AND OBJECTIVE: The aim of this study was to evaluate the results of myopic excimer laser photorefractive keratectomy (PRK) performed using three different ablation approaches. PATIENTS AND METHODS: Using the Apex excimer laser (Summit Technology, Inc., Waltham MA), we have treated 75 eyes. Twenty-five of them were treated by a single ablation zone (SA, 6.5 mm diameter) to correct myopia of -4.50 +/- 2.10 D (mean +/- SD); 25 eyes underwent PRK for the correction of myopia of -4.98 +/- 2.17 D using a multipass multizone technique (MP, 3 zones); and 25 eyes were corrected for myopia of -5.03 +/- 1.98 D using new software which enables the creation of three ablation zones in a single-pass fashion (MZ). RESULTS: Mean refractive error (+/-SD) at the first post-operative month was +1.34 +/- 1.00 D for SA, +1.78 +/- 1.49 D for MP, and +0.90 +/- 0.75 D for MZ. Eyes treated by MZ had significantly better uncorrected visual acuity than those treated by SA (P=0.04). Corneal topography revealed a central island in 14 eyes (56%) of those treated by SA and 2 eyes (8%) of those treated by MZ, but in no eyes treated by MP. Six months after treatment, mean refractive error was +0.28 +/- 0.75 D for SA, +0.36 +/- 0.92 D for MP, and - 0.07 +/- 0.77 D for MZ. CONCLUSION: MZ ablation induced less hyperopic shift at 1 month, thus leading to a faster visual recovery and better uncorrected visual acuity. MP and MZ ablations proved effective in preventing central island formation, thus inducing less visual disturbances than SA ablations. These results suggest that MZ ablation may be preferable to the other techniques in performing myopic PRK.

Automatic eye tracker for excimer laser photorefractive keratectomy.

Acute overlapping of successive laser pulses onto the cornea during photorefractive keratectomy (PRK) is important to avoid refractive distortions. Most excimer laser systems performing corneal ablation lack control of the patient's eye movements and they cannot track the target corneal zone. We developed an eye-tracker based on television monitoring of the pupil and on automatic electro-mechanical deflection of the laser turning mirror, and we applied it to the ExciMed UV200 ArF work station (Summit Technology, Inc., Waltham, Mass.). Basic components are a black and white CCD camera and two fast stepping motors. The circuitry for target discrimination and tracking, and the optical imaging system are designed specifically. The tracker assembly does not interfere with the laser beam path nor with the operator's observation. Tracking of the pupil has been successfully achieved on different color irides, with an accuracy better than 0.1 mm in a 6 x 6 mm2 tracking field. Response time is less than 100 ms. Recordings of eye movements during PRK are presented. Tracking ablations have been performed on moving test eye-balls with plastic corneas. The proposed automatic system appears to be a reliable and effective method for the compensation of patient eye movements appears to be a reliable and effective method during PRK procedures.

The corneal endothelium after myopic excimer laser photorefractive keratectomy.

OBJECTIVE: To investigate whether 193-nm excimer laser photorefractive keratectomy for the correction of myopia can determine in vivo changes in the human corneal endothelium 3 and 12 months after surgery. METHODS: Contact wide-field specular biomicroscopy of the central corneal endothelium was performed on 76 eyes of 61 patients (aged 20 to 49 years; mean, 29.7 years) who underwent photorefractive keratectomy for the correction of myopia ranging between -1.75 and -13.50 diopters (mean, -6.60 D). The maximum estimated central depth of the photoablation was 113 microns. Photomicrographs of the endothelium taken before surgery were processed by means of computer-assisted morphometric analysis and compared with those obtained 3 and 12 months after surgery. RESULTS: The mean (+/- SD) cell density was 2657 +/- 298 cells/mm2 preoperatively, 2672 +/- 286 cells/mm2 after 3 months (P = .670), and 2656 +/- 289 cells/mm2 after 1 year (P = .982). The mean (+/- SD) coefficient of cell area variation was 30.27% +/- 5.99% preoperatively, 28.25% +/- 5.21% after 3 months (P = .032), and 26.35% +/- 5.29% after 1 year (P = .001). The mean (+/- SD) percentage of hexagonal cells was 63.82% +/- 9.94% preoperatively, 64.02% +/- 10.53% after 3 months (P = .806), and 67.19% +/- 9.14% after 1 year (P = .025). CONCLUSIONS: Photorefractive keratectomy caused no damage to the corneal endothelium. Postoperative improvements of the coefficient cell area variation and the percentage of hexagonal cell values may be related to corneal metabolic modifications or discontinuance of contact lens use after surgery.