Contact Lens Assisted Pharmacologically Induced Keratoshaping

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To retrospectively evaluate the effectiveness and describe the process of reducing hyperopia with a nonsteroidal antiinflammatory agent and a soft disposable contact lens in postoperative excimer laser patients with consecutive hyperopia.


Private practice.


This study includes a retrospective analysis of 14 eyes of 12 patients who underwent laser in situ keratomileusis or photorefractive keratectomy and experienced consecutive hyperopia. Patients were treated with a tightly fit, extended-wear contact lens in combination with the use of ketorolac tromethamine 0.5% (Acular) in an attempt to steepen the cornea. Uncorrected visual acuity, manifest refraction, and slitlamp examination were performed on a weekly basis until the desired outcome was achieved or until treatment was discontinued.


A total of 78.57% of eyes experienced a decrease in consecutive hyperopia (≥0.50 diopters [D]) (P = 0.002). The mean dioptric change was 1.05D. A total of 88.89% of eyes experienced an increase in uncorrected visual acuity (≥1 line) (P < 0.001). The mean increase was three lines of Snellen or Jaeger acuity. The mean number of weeks to see an effect was 1.71 weeks, and the mean number of weeks to achieve endpoint was 8.29 weeks (median, 6 weeks).


Contact lens–assisted pharmacologically induced keratoshaping is an effective treatment option for patients who experience consecutive hyperopia after laser in situ keratomileusis or photorefractive keratectomy.

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