To evaluate the efficacy and safety of Excimer Laser Photorefractive Keratectomy (PRK) on the correction of high myopia, we performed planned double-pass PRK procedure at the same session on 62 eyes of 55 patients with myopia ranging from -6.30D to -15.25D (mean, -9.94D). In the first pass, a myopic correction of -6.00D with a 4.5 millimeter ablation zone was performed, and immediately after, a second correction of remaining myopia with a 5.0 millimeter ablation zone was performed. Attempted correction ranged from -6.30D to -9.50D (mean, -8.70D). The eyes were divided into two groups which were -10.50D or less (group A), and higher than -10.50D (group B). All the eyes received topical corticosteroid therapy postoperatively. One year after double-pass PRK, uncorrected visual acuity in group A and B improved to 20/40 or better in 84.0%, and 73.3% of the eyes and to 20/30 or better in 75.0% and 33.3% of the eyes respectively. The mean refractive errors at 12 months after PRK were -0.3 +/- 1.6D in group A, and -1.5 +/- 2.1D in group B. The percent of achieved correction within +/- 1.0D were 70.8% in group A, and 46.7% in group B 12 months after surgery. The epithelium healed by three days and there were no corneal erosions. Corneal haze (Grade 2 or more) was seen in 9.0% in group A and 36.4% in group B at 12 months after PRK. A planned double-pass PRK is a promising approach to correct high myopia (up to -10.50D), but long-term follow up will be required.
Topical fibronectin, autologous and homologous, was used to treat nine patients (eleven eyes) with persistent corneal epithelial defects and corneal ulcers that failed to improve with standard therapy. The fibronectin was purified from autologous and homologous plasma by gelatin-Sepharose 4B affinity chromatography and administered topically, 500 micrograms/ml five times a day, for three weeks. Complete or nearly complete reepithelialization was achieved in all patients regardless of the source of fibronectin, autologous or homologous. But healing times varied. The average healing time was 41.7 +/- 14.7 days (35.7 +/- 12.4 days for autologous, 50.8 +/- 14.4 days for homologous). Ocular symptoms were relieved significantly, and no side effects were observed. Over an average follow-up period of 5.2 months, no recurrences were noted. The results showed that homologous, as well as autologous, fibronectin was effective in patients with persistent corneal epithelial defects and corneal ulcers.
The clinical efficacy was investigated of topical homologous fibronectin on persistent corneal epithelial defects of various etiologies. Fibronectin was purified from blood bank homologous plasma by gelatin-Sepharose 4B affinity chromatography. Twenty eight eyes of twenty five patients with persistent corneal epithelial defects and sterile corneal ulcers that failed to improve with standard therapy were treated by the instillation of homologous fibronectin eyedrops 5 times a day (500 micrograms/ml). Complete reepithelialization was achieved in all patients except two eyes due to uncontrolled glaucoma and the taking of steroids. The healing time tended to be different depending on the duration of persistent corneal epithelial defects and the severity of underlying diseases. The mean +/- standard deviation duration of epithelial defect was 68.18 +/- 77.80 days. Average healing time was 42.07 +/- 17.47 days. Ocular symptoms were relieved significantly and no side effects were observed. Over an average follow-up period of about 8 months, two cases of recurrences were noted. These results show that homologous fibronectin was also effective in patients with persistent corneal epithelial defects and corneal ulcers.
We studied the ultrastructural features of four consecutive subfoveal neovascular membranes (SFNM) associated with age-related macular degeneration. Cellular components of the membranes included retinal pigment epithelial (RPE) cells, endothelium-lined vascular channels, macrophages, myofibroblasts, fibrocytes, glial cells, erythrocytes, and lymphocytes. Extracellular interstitial constituents included collagen fibrils, basal laminar deposits, fibrin and young elastic fibrils. These findings show that SFNMs consist of various cells originating from surrounding tissues and vessels. Among these RPE cells and macrophages are the main cellular components and in conjunction with various extracellular matrix, especially collagen, may play an important role in the formation and maintenance of the membranes.
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