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Conductive Keratoplasty for the Correction of Low to Moderate Hyperopia: U.S. Clinical Trial 12-Month Results
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U.S. Clinical Investigators Penny Asbell, MD Stephen Brint, MD William Culbertson, MD Jonathan Davidorf, MD Elizabeth Davis, MD Dan Durrie, MD R. Bruce Grene, MD Peter Hersh, MD David Hardten, MD Vera Kowal, MD Richard Lindstrom, MD Robert Maloney, MD Edward Manche, MD Roger Meyer, MD Thomas Samuleson, MD Timothy Schneider, MD Kaz Soong, MD Alan Sugar, MD Marguerite McDonald, MD – Medical Monitor
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Treats hyperopia, astigmatism, presbyopia and over/under LASIK corrections Induces permanent collagen shrinkage Creates a column of treatment Utilizes cornea’s conductive properties Conductive Keratoplasty Features
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ViewPoint ™ CK System
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The Keratoplast™ tip (90 µm wide, 450 µm long) with coated stop at the distal end (shown next to a 7-0 suture)
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Conductive Keratoplasty (CK)
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US FDA Phase III Study 400 Patients –Spherical hyperopia 0.75 D to 3.00 D –< 0.75 D of cylinder –No prior refractive surgery –No significant ocular/physical history 24 Month Follow-Up Study Objective
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Demographics Number of Patients Number of Eyes 233 401 Mean Age Range 55 +/- 5.4 years (40 to 74) Mean Preoperative MRSE Median MRSE +1.82 +/- 0.60 D +1.75 D Mean Preoperative CRSE+1.86 +/- 0.63 D
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Simple Procedure Instill topical anesthesia Insert lid speculum (return path for energy) Mark eye Apply treatment Total time less than 5 minutes
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Conductive Keratoplasty (CK)
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6 mm OZ Number, Location, and Sequence of Treatment Spots Sequence 2 6 4 7 3 5 1 8 8 mm OZ 7 mm OZ 32 spots (2.375 to 3.00 D) 24 spots (1.75 to 2.25 D) 16 spots (1.00 to 1.625 D) 8 spots (0.75 to 0.875 D)
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Slit Lamp Photo 1 Hour After CK Small leucoma Visible striae
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Postoperative UCVA Over Time
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Accuracy of Achieved Refraction
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MRSE Stability through 12 Months Patients with Consecutive Visits Mean Change 0.25 D (0.50) 0.11 D (0.41) 0.11 D (0.35) in MRSE Conf. Interval 0.19, 0.31 0.07, 0.15 0.07, 0.15
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Safety Variables 12 Months N=383 2 lines lost BSCVA 2% > 2 lines lost BSCVA 0.0% BSCVA Worse than 20/40 0.0% Increase >2.00 D Cylinder 0.3% Pre-Op 20/20, Post-op 20/25 0.0%
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Induced Cylinder >2.00 D CK vs. Non-Contact LTK Post-op MonthLTK 1 CK 2 1 Month3.4%3.0% 3 Months1.4%2.0% 6 Months0.9%1.0% 12 Months0.2%0.3% 1 Sunrise LTK FDA Clinical Study, 2 Conductive Keratoplasty 12-Month FDA Clinical Study Results.
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Summary Efficacy Variables FDA Guideline 6 Mos. (N = 352) 12 Mos. (N = 318) UCVA < 20/2050%45%56% UCVA < 20/25 Not Stipulated 64%75% UCVA < 20/4085%90%92% MRSE + 0.5050%61%63% MRSE + 1.0075%88%89% Data from patients with single treatment. No retreatments included.
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Conductive Keratoplasty: Case Study Preoperative –50 year old –Female –African American –Good health –No ocular history –6 mm pachymetry: 556 µm –IOP: 15 mm Hg Preoperative –UCVA D : 20/125 –UCVA N : J12 –Manifest RX: + 3.25 – 0.75 X 130 –Cycloplegic RX: + 3.25 – 0.25 X 130 –BSCVA D : 20/25
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Operative –Instilled three drops topical anesthesia –Inserted lid speculum –Applied 32 treatment spots –Removed lid speculum –Instilled NSAID and antibiotic –Immediate K-Readings: 51.75 @ 180 X 49.62 @90 Conductive Keratoplasty: Case Study
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1 Day Post-Operative –UCVA D : 20/32 –UCVA N : J7 –Manifest RX: + 1.50 – 0.50 X 120 –BSCVA D : 20/20 –BSCVA N : J2 –Slit Lamp: small epithelial defects Conductive Keratoplasty: Case Study
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1 Month Post-Operative –UCVA D : 20/20 –UCVA N : J2 –Manifest RX: - 0.25 – 0.75 X 125 –BSCVA D : 20/20 –BSCVA N : J1 –Slit Lamp Exam: WNL Conductive Keratoplasty: Case Study
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3 Month Post-Operative –UCVA D : 20/32 –UCVA N : J2 –Manifest RX: plano – 1.00 X 125 –BSCVA D : 20/16 –BSCVA N : J1 –Slit Lamp Exam: WNL Conductive Keratoplasty: Case Study
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6 Month Post-Operative –UCVA D : 20/30 –UCVA N : J2 –Manifest RX: + 0.25 – 0.75 X 125 –BSCVA D : 20/25 –BSCVA N : J1 –Slit Lamp Exam: WNL Conductive Keratoplasty: Case Study
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12 Month Post-Operative –UCVA D : 20/20 –UCVA N : J2 –Manifest RX: + 0.25 – 0.25 X 110 –BSCVA D : 20/16 –BSCVA N : J1 –Slit Lamp Exam: WNL Conductive Keratoplasty : Case Study
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Preoperative –50 year oldFemale –UCVA D : 20/125 –UCVA N : J12 –Manifest RX: + 3.25 – 0.75 X 130 –BSCVA D : 20/25 12 Months Post-op –UCVA D : 20/20 –UCVA N : J2 –Manifest RX: + 0.25 – 0.25 X 110 –BSCVA D : 20/16 No retreatment. Spherical correction only
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Corneal Topography: Case Study Preoperative 12 month Post-op
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Confocal View Of CK Folds Between Treatment Spots Sabry, McDonald, Klyce - 2001
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Confocal View Of CK Deep CK Treatment With Healthy Endothelium Sabry, McDonald & Klyce - 2001
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Cylindrical Footprint of CK
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Summary of Phase III Study Highly effectiveHighly effective – comparable to H-LASIK Stability at 6 monthsStability at 6 months Safe – low rate induced cylinderSafe – low rate induced cylinder Penetration depth confirmed by histology, confocal microscopyPenetration depth confirmed by histology, confocal microscopy
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Summary of Phase III Study Topography shows central corneal steepening with mid-peripheral flatteningTopography shows central corneal steepening with mid-peripheral flattening Visual axis sparedVisual axis spared Multicenter study continues for two yearsMulticenter study continues for two years
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