Hydrogel intracorneal lenses in aphakic eyes

被引:25
|
作者
Steinert, RF
Storie, B
Smith, P
McDonald, MB
vanRij, G
Bores, LD
Colin, JP
Durrie, DS
Kelley, C
Price, F
Rostron, C
Waring, GO
Nordan, LT
机构
[1] HARVARD UNIV, SCH MED, CTR EYE RES, BOSTON, MA USA
[2] HARVARD UNIV, SCH MED, DEPT OPHTHALMOL, BOSTON, MA USA
[3] ALLERGAN MED OPT, IRVINE, CA USA
[4] LOUISIANA STATE UNIV, MED CTR, SCH MED, CTR EYE, NEW ORLEANS, LA 70112 USA
[5] UNIV GRONINGEN, DEPT OPHTHALMOL, GRONINGEN, NETHERLANDS
[6] UNIV HOSP, DEPT OPHTHALMOL, BREST, FRANCE
[7] OHIO STATE UNIV, COLUMBUS, OH 43210 USA
[8] CORNEA CONSULTANTS, INDIANAPOLIS, IN USA
[9] UNIV LONDON ST GEORGES HOSP, SCH MED, DEPT OPHTHALMOL, LONDON SW17 0RE, ENGLAND
[10] EMORY UNIV, CTR EYE, DEPT OPHTHALMOL, ATLANTA, GA 30322 USA
关键词
D O I
10.1001/archopht.1996.01100130129002
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background: The theoretical benefits of synthetic keratophakia over conventional corneal lamellar procedures are the elimination of donor concerns and superior refractive predictability Additionally, synthetic material can be inspected for optical quality and power, and it can be sterilized. Furthermore, visual recovery should be more rapid since epithelium is not removed from the central part of the cornea and the need for keratocyte repopulation is eliminated. Objective: To present results on patients who received an intracorneal implant (Kerato-Gel, Allergan Medical Optics, Irvine, Calif) that was made from lidofilcon A, a glucose-permeable hydrogel with an equilibrium water content of 68%. Methods: The intracorneal implants were implanted in 35 adult patients for correction of aphakia. Inclusion criteria excluded patients with aphakia who were candidates for intraocular lenses. Results: A total of 19 patients were followed up through 2 years postoperatively. For 16 patients with 2-year postoperative refractive data, the average spherical equivalent was -0.63 +/- 2.07 diopters (D). At 2 years, 88% of patients were within +/-3.00 D of plano and 50% were within +/-1.00 D. The mean change in Snellen's line for corrected visual acuity was -3.25 lines at 2 years for an patients and -2.0 lines for a subgroup of five patients who were free of vision-limiting preoperative disease. Conclusions: Results suggest that this intracorneal implant is well tolerated by the cornea and can provide predictable refractive results in patients with high-risk aphakia. Limitations of the procedure are uneven microkeratome resections, loss of best-corrected visual acuity, and irregular astigmatism in some patients. Although these data show good evidence of biocompatibility of the implant material, technical surgical progress is needed to advance this procedure into clinical therapeutic practice.
引用
收藏
页码:135 / 141
页数:7
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