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Wavelight ex500

Manufactured by Alcon
Sourced in United States

The WaveLight EX500 is a medical device used for refractive surgery procedures. It is designed to generate a laser beam for corneal reshaping, with the aim of correcting vision impairments.

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21 protocols using wavelight ex500

1

Bilateral PRK Randomization Study

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One hundred and thirty-seven subjects undergoing bilateral PRK at the Joint Warfighter Refractive Surgery center at Wilford Hall Ambulatory Surgical Center (WHASC) in San Antonio, Texas between June 2014 and May 2015 were studied. PRK was performed with either the VISX CustomVue STAR S4 IR (Abbott Medical Optics, Santa Ana, CA, USA) or WaveLight EX500 (Alcon Inc., Fort Worth, TX, USA) excimer laser machine at the surgeon’s discretion.
To be included in the study, patients needed to qualify for bilateral PRK and be at least 21 years old. Patients were excluded if they were pregnant, basic military trainees, prisoners, detainees, did not meet criteria for CRS, if they were receiving treatment on one eye, or if they were undergoing monovision PRK. Upon inclusion in the study cohort, patients were randomized to receive PRK in either the right or left eye first using the Research Randomizer tool (www.randomizer.org).
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2

Wavefront-Optimized LASIK Procedure

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All subjects underwent LASIK using a standard technique. All laser ablation treatments were performed using the wavefront-optimized Wavelight EX500 excimer laser (Alcon, USA). The procedure started with the creation of a 110-μm, 8.6-mm femtosecond laser (Wavelight FS200, Alcon, USA) flap. After flap creation, the excimer laser treatment was performed with up to 150 microns of ablated stromal tissue. Following the excimer laser treatment, the flap was carefully reapproximated and ensured to be in good position. A same-day flap check was performed in all patients. All patients were treated with a combination antibiotic-steroid drop for 4 weeks after the procedure.
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3

Wavefront-Guided LASIK Procedure

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Conventional bilateral LASIK was performed using a Wavelight FS200 (Alcon Laboratories, Inc.) for flap creation with thickness of 90 μm or 110 μm and a Wavelight EX500 excimer laser (Alcon Laboratories, Inc.) for refractive correction. All laser parameters and laser nomograms for LASIK were applied according to the clinic's typical LASIK protocol.
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4

Comparative Analysis of SMILE, FS-LASIK, and ICL

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Two surgeons performed all of the procedures (ZW and LX). Each surgeon had a similar experience with the operations. Levofloxacin 5 mg/mL was instilled into the eyes 4 times a day for 3 days before surgery. SMILE was performed on VisuMax femtosecond laser (Carl Zeiss Meditec AG, Jena, Germany). The cap thickness was 110 μm, the cap diameter was 7.5 mm and the incision was set at 135° with a width of 2.00 mm. The optical zone ranged from 6.0 to 6.5 mm. The flaps of FS-LASIK were created either on WaveLight FS200 (Alcon, Fort Worth, TX) or VisuMax femtosecond laser. Flap thickness ranged from 100 to 110 μm with a diameter from 8.1 to 8.5 mm. The flaps were roundly shaped with superior hinges. All the excimer laser treatments of FS-LASIK were done with the WaveLight EX500 (Alcon, Fort Worth, TX). During the ICL implantation procedure, a 2.8 mm temporal clear corneal incision was performed through which a loaded V4c ICL or TICL was injected and positioned to the posterior chamber with the footplates situated posterior to the iris plane. Emmetropia was the goal in all the investigated eyes. After all the procedures, steroids and antibiotics were administered 4 times daily for 7 days, and lubricating eye drops were used for 3 months.
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5

Wavefront-Optimized Ablation Profile Characterization

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As already mentioned, the algorithm for the computation of the ablation profile is proprietary of the manufacturing company and cannot be accessed. The user manual of the excimer laser Wavelight EX500 by Alcon describes the different ablation options, available to be used by the surgeon, by presenting multiple examples. The most used treatment is the wavefront-optimized or “standard” treatment for the calculation of the ablation map, where the user is required to insert the target refraction and the laser's software establishes the ablation profile. This kind of treatment is not patient specific: the software will propose the same ablation map for patients with the equal refraction, disregarding individual characteristics. As it can be seen in the treatment plan of a patient who received this treatment, the ablation map shows a pattern that follows an aspheric shape. The ablation profile shown in the treatment plan of the patient was reproduced by using a biconic (Equation 2) and by enforcing the same central ablation depth as the one of the real treatment. The standard or wavefront-optimized treatment must not be confused with the wavefront-guided treatment or customized treatment, which uses corneal wavefront aberrations to determine the customized ablation profile needed to correct patient's visual acuity in a personalized fashion.
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6

Bilateral Photorefractive Keratectomy Protocol

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All surgeries were performed by 2 surgeons (T.-Y.C. and D.H.L.) using standardized techniques. Eligible patients were scheduled to undergo bilateral PRK surgery using a WaveLight EX500 excimer laser (Alcon). The correction target was based on the manifest refraction adjusted using the Alcon nomogram, with emmetropia being the target in all patients. A few drops of 20% alcohol were instilled into an 8.0-mm well to create a round epithelial defect. After 25 seconds, the alcohol was removed, and a balanced salt solution was poured to irrigate the cornea. The epithelium was then removed smoothly using a spatula, and laser ablation was performed. The eyes were once again irrigated with a balanced salt solution. Sponges soaked in 0.05% mitomycin-C solution were placed on the eye for 20 seconds, followed by vigorous irrigation with a balanced salt solution. Finally, an AcuVue Oasys (Johnson and Johnson) bandage contact lens was placed on the eye. The same procedure was repeated in the other eye.
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7

Alcohol-Assisted Photorefractive Keratectomy

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Enhancement was performed via alcohol-assisted PRK. Epithelial debridement was performed with 18% alcohol for 25 seconds, followed by stromal ablation with a WaveLight EX500 excimer laser (Alcon Laboratories, Inc., Fort Worth, Texas, USA). Laser settings included an ablation zone of 6.5 mm and a transitional zone of up to 9.0 mm. Mitomycin C 0.02% was applied for 20 seconds whenever ablation depth exceeded 65 microns. After the procedure, a bandage contact lens was placed for one week. Post-operative regimen included topical moxifloxacin 0.5% four times daily for one week and prednisolone acetate 1% four times daily for one month. After one month, prednisolone acetate was replaced with fluorometholone 0.1% four times daily, which was then tapered until 12 weeks post-operative.
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8

Comparative Corneal Refractive Surgery

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All surgeries were performed by the same experienced surgeon (DS) under topical anesthesia. In LASIK surgeries, the FS200 femtosecond laser (Wavelight FS200, Alcon Laboratories Inc., Fort Worth, TX, USA) was first used to create a 9 mm diameter and 110 μm thickness corneal flap. Stromal ablations were performed over a 6.5 mm optical zone using the wavefront-optimized ablation profile, with the same excimer laser used in all eyes (Wavelight EX500, Alcon Laboratories Inc., Fort Worth, TX, USA). In all PRK procedures, mitomycin 0.02% solution was used for 30 s after stromal ablation. Then, a balanced salt solution was used for irrigation before a bandage contact lens was placed for one week. Following surgery, all patients were prescribed moxifloxacin 0.5% (q.i.d), dexamethasone 0.1% (b.i.d or q.i.d) for one week as well, and artificial tears (q.i.d) for as long as needed. Steroid treatment was extended and tapered for three months in all patients with PRK. Patients were routinely examined at one day, one week, one month and three months postoperatively, and more if necessary. The one and three months follow-up visits included slit-lamp examination, IOP check, uncorrected distance visual acuity (UCDVA), manifest refraction, corneal topography and retinal image quality using a double-pass aberrometer.
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9

Wavefront Optimized Laser Refractive Surgery

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All patients underwent wavefront optimized laser refractive surgery, PRK in 50 eyes and LASIK in 106 eyes, for correction of simple, myopic, hyperopic or mixed astigmatism, applying WaveLight EX500 (Alcon Laboratories; Ft Worth, TX, USA). All surgeries were performed by a single surgeon, the author. A superior hinge was applied in LASIK cases using Moria Evolution 3 Microkeratome (Moria, Antony, France) with a programmed planned flap thickness of 110 μm and a diameter of 8 mm. In PRK, the corneal epithelium was removed in a diameter of 8 mm in a centripetal fashion using a blunt hockey blade. UCVA and manifest refraction were evaluated at 1 month post-operatively. Postoperative refraction was assessed by a TOPCON RM-8900 Auto Refractometer (Topcon Medical Systems, Tokyo, Japan).
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10

Corneal Crosslinking with Femtosecond Laser and Excimer Laser

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Femtosecond laser (FS200, Alcon Laboratories, Inc., USA) was used to create a corneal flap of 110 μm thickness with an 8.00 mm diameter [1 (link)]. Excimer laser (WaveLight EX500, Alcon Laboratories, Inc., USA) was used for the myopic ablation, and the ablation zone diameter was 6.00 to 6.50. After the excimer laser ablation (with the flap folded on itself), Vibex Xtra riboflavin solution containing 0.25% riboflavin (Avedro Inc., USA) was placed on the exposed stromal bed for 90 seconds. Following stromal soaking, the stroma was washed with BBS and the flap was repositioned in place. The cornea was then irradiated with ultraviolet-A (UVA) light (KXL System, Avedro Inc.) with a wavelength of 365 nm and an irradiance of 30 mW/cm2 for 90 seconds (total energy 2.7 J/cm2). After irradiation, a bandage contact lens was placed on the corneal surface for pain relief. After surgery, 0.5% lavo-ofloxacin eye drops were applied four times per day for two weeks; 0.1% fluorometholone eye drops were used four times per day for the first week, and then reduced gradually; 0.1% sodium hyaluronate eye drops were used four times per day for four weeks. The bandage contact lens was removed when the corneal epithelium healed.
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