iDesign - Advanced Custom Wavefront LASIK
iDesign - The Most Advanced CustomVue Wavefront System
LASIK Powered by iDesign LASIK is Similar to Technology used in NASA Telescopes!
The Orange County LASIK Institute has now upgraded our iLASIK and PRK technology to iDesign. This innovative custom and wavefront guided technology allows us to treat lower and higher order aberrations (imperfections) in the human visual system. This technology has been used by NASA! The development of the sensor technology within the iDESIGN System was the result of an earlier discovery by Abbott scientists. NASA used this technology to accurately measure and shape the mirrors in the James Webb Space Telescope to ensure it would transmit high resolution images of deep space back to earth. The James Webb Space Telescope launched in 2018.
What is iDesign Customized LASIK?
*The Orange County LASIK Institute's Actual iDesign Unit
The idesign is involved in the first step of your procedure. It is part of wave scan technology where a specialized sensor measures and maps your eye. This information is then used to deliver a completely custom iLASIK procedure. This wavefront guided technology is used to map your eye's lower and higher order aberrations and then treat them with the laser.
The idesign is able to get 5 different types of measurements in 3 seconds:
1. Wavefront Refraction (Your myopia and Astigmastism Measurements)
2. Wavefront Aberrometry (Higher Order Aberrations)
3. Corneal Topography (Corneal Shape)
4. Keratometry (Corneal Steepness)
5. Pupillometry (Pupil size in low and bright light conditions)
Key Advantages of iDesign Over Other LASIK Technologies
5X the Resolution!
- High definition Hartmann-Shack sensor with 5x the resolution versus the WaveScan system
- 1257 micro refractions over a 7 mm pupil
- Larger wavefront measurement, up to 8.5 mm
- This increased resolution allows us to capture more points to create a more detailed and customized map of your eyes.
- The measurements are up to 25X the resolution that is normally used when you get measured for glasses and contacts.
The image is comparing the wavescan of the sample key placed over the artificial eye. As you can see, the capture of more refractions (measurements) in the iDesign allows for a more accurate mapping of the key.
However, the iDesign is not approved for all prescriptions. Dr. Pham will be happy to discuss with you which technology (CustomVue or iDesign) is best and FDA approved for your prescription.
More LASIK Candidates - We Can Treat LARGER Prescriptions and MORE Astigmatism
iDesign Measures and Treats A Large Range of Patients:
IMPROVING QUALITY OF VISION FOR HIGH PATIENT SATISFACTION
REFERENCE: 1. Data on file: Myopia US IDE Study 110-IDMY. Additional Patient Reported Outcome Analyses. (N=170 patients)
iDesign 2.0 Upgrade
The Orange County LASIK Insitute is proud to offer OC's first idesign 2.0 upgrade. We were one of the first in the nation to offer this upgrade on proven technology. iDesign 2.0 improves upon previous custom guided technology. Learn more by clicking the link below.
iDesign 2.0 Video
- Combining full Gradiant topography to custom guided wavefront technology to treate more custom characteristics of the eye. This is the only system that combines these two technologies
- Increased range of monovision treatments for patients 45 years of age and beyond
- Improved capture sequences for more natural measurements
- Improved fixation targets for decreased accommodation
Indications and Important Safety Information
ATTENTION: Reference the Directions for Use for a complete listing of Indications and Important Safety Information.
INDICATIONS: The STAR S4 IR® Excimer Laser System and iDESIGN® Advanced WaveScan Studio System is indicated for wavefront‑guided laser assisted in situ keratomileusis (LASIK) in patients with myopia as measured iDESIGN® System up to -11.00 D spherical equivalent, with up to
-5.00 D cylinder; with agreement between manifest refraction (adjusted for optical infinity) and iDESIGN® System refraction of 1) spherical equivalent: magnitude of the difference is less than 0.625 D, and 2) cylinder: magnitude of the difference is less than or equal to 0.5 D; with patients 18 years of age or older, and with refractive stability (a change of ≤1.0 D in sphere or cylinder for a minimum of 12 months prior to surgery).
CONTRAINDICATIONS: Laser refractive surgery is contraindicated in patients with a) collagen vascular, autoimmune, or immunodeficiency diseases; b) pregnant or nursing women; c) keratoconus, abnormal corneal topography, epithelial basement membrane disease (EBMD) and degenerations of the structure of the cornea; d) symptoms of significant dry eyes; e) corneal thickness would cause anticipated treatment would violate the posterior 250 microns (μm) of corneal stroma; f) advanced glaucoma; and g) uncontrolled diabetes. If the patients have severely dry eyes, LASIK may increase the dryness. This may or may not go away. Severe eye dryness may delay healing of the flap or interfere with the surface of the eye after surgery. It may result in poor vision after LASIK.
WARNINGS AND PRECAUTIONS: LASIK is not recommended in patients who: a) have a history of Herpes simplex or Herpes zoster keratitis, b) have severe allergies or tendency rub their eyes often, c) are taking the medication Isotretinoin (Accutane), d) are taking antimetabolites for any medical conditions. The safety and effectiveness of this laser for LASIK correction have NOT been established in patients: a) with progressive refractive errors; previous corneal or intraocular surgery; or trauma in the ablation zone, b) who are taking the medication Sumatriptan (Imitrex) or Amiodarone hydrochloride (Cordarone), c) with corneal neovascularization within 1.0 mm of the ablation zone, d) over the long term (more than 1 year after surgery), e) for patients who engage in activities that could endanger or damage the LASIK flap, f) for patients who have a family history of degenerative corneal disease, g) history of inflammation of eye, h) for patients who have a history of crossed eyes (strabismus) or who have undergone strabismus surgery, i) prior LASIK or Refractive Surgery, j) with history of any eye diseases or abnormalities such as: corneal scars or active disease, k) whose BSCVA is worse than 20/20.
To reduce the risk of corneal ectasia, the posterior 250 microns (μm) of corneal stroma should not be violated. The treatment of highly myopic eyes necessitates the removal of significant amounts of corneal tissue. The iDESIGN® System calculates the estimated residual bed depth using the pachymetry and intended flap thickness entered by the user. Actual flap thicknesses may vary. If the estimated residual stromal bed is ≤ 320 microns, an in-the-bed pachymetric measurement should be performed.
ADVERSE EVENTS: Possible adverse events include loss of best spectacle corrected visual acuity (BSCVA), serious Transient Light Sensitivity Syndrome, serious primary open angle glaucoma, miscreated flap, melting of the flap, severe glare, and severe dry eyes. Complications can include corneal edema, epithelial ingrowth, diffuse lamellar keratitis, foreign body sensation, and pain.
CAUTION: U.S. Federal Law restricts this device to sale, distribution, and use by or on the order of a physician or other licensed eye care practitioner.
©2016 Abbott Medical Optics Inc. STAR S4 IR, iDESIGN, WaveScan, iLASIK, and iFS trademarks owned by or licensed to Abbott Laboratories, its subsidiaries or affiliates. PP2016RF0090
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The Orange County LASIK Institute
3500 Barranca Parkway Suite 150
Irvine , CA 92618
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