5 results match your criteria: "Ophthalmic Health Center[Affiliation]"
J Refract Surg
December 2004
Ophthalmic Health Center, Department of Ophthalmology, Tel-Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Purpose: To compare corneal flap thickness created in laser in situ keratomileusis (LASIK) in primary (right) and fellow (left) eyes (same blade for both eyes) using three microkeratomes.
Methods: The corneal thickness of 132 eyes (66 patients) was measured preoperatively and intraoperatively after flap creation. Corneal flap thickness was calculated by subtracting stromal bed thickness from total corneal thickness.
J Refract Surg
January 2003
Ophthalmic Health Center, 40 Einstein St., Tel Aviv 46101, Israel.
J Refract Surg
December 2002
Ophthalmic Health Center, Tel Aviv, Israel.
Purpose: To compare the accuracy and consistency of corneal flap thickness in the right and left eye created by three different widely used microkeratomes during consecutive laser in situ keratomileusis (LASIK).
Methods: Corneal thickness of 132 eyes of 66 patients was measured preoperatively and intraoperatively. Corneal flap thickness was calculated by subtracting the corneal stromal thickness from the total corneal thickness.
J Cataract Refract Surg
February 2001
Ophthalmic Health Center (Lipshitz, Shemesh), Israel.
Purpose: To assess the safety and efficacy of excimer laser in situ keratomileusis (LASIK) to correct hyperopic shift following radial keratotomy (RK).
Setting: Ophthalmic Health Center, Tel Aviv, Israel.
Methods: The study comprised 15 eyes of 12 patients who had uneventful RK and subsequently developed a hyperopic shift.
J Refract Surg
June 1999
Ophthalmic Health Center, Ramat-Aviv, Tel-Aviv, Israel.
Objective: The aim of this study was to compare the results of excimer laser photorefractive keratectomy (PRK) and laser in situ keratomileusis (LASIK) in the same patient.
Methods: All consecutive patients who underwent PRK in one eye and LASIK in the second eye using the same excimer laser (Nidek EC-5000) and had at least 12 months of follow-up were included in this retrospective study (N = 23). Uncorrected and spectacle-corrected visual acuity, final spherical equivalent refraction, and degree of haze were compared.