Guidelines For Choosing Your LASIK Surgeon
How do you find a LASIK surgeon? Friends and family are a great place to start. Also, ask your current optometrist or ophthalmologist. He or she knows your eyes and vision problems, and is likely to know which laser vision correction surgeons or centers in your area to recommend.
Once you've set up your initial appointment with a LASIK surgeon, you can start getting the answers you need to the important questions you're sure to have. (Learn more about what you should do before your LASIK surgery.) These guidelines will help you understand what questions to ask about the surgeon, his or her experience, and the vision correction procedure:
- Credentials
- Method of Practice
- Availability
- The Cost of LASIK Surgery
- Finding an OptiLASIK™ Treatment Specialist
Credentials
Most physicians are perfectly comfortable discussing their credentials. You can find out more information by calling local, state, or national ophthalmic associations, or by contacting the American Board of Ophthalmology or the Association of State Medical Board Executive Directors.
Questions to ask about credentials include:
- How long have you been performing laser vision corrections?
- How many laser eye procedures have you performed?
- What results can someone with my vision problem realistically expect from laser vision correction?
- What are the overall safety and risks associated with laser eye surgery?
LASIK surgeons should be licensed to practice ophthalmology and be trained in the use of laser equipment to perform this kind of vision correction. Medical licensing is in most cases done by local, state, or national medical boards.
Many laser vision correction surgeons are also qualified to perform any eye surgery, including other corrective procedures. Schools of ophthalmic medicine offer courses in these procedures. In addition, all physicians are required to participate in continuing educational opportunities each year by their state medical board. Refractive surgeons, who perform laser vision correction, typically receive training on the laser system they use as well.
Method of Practice
The outcome of laser eye surgery depends to a large degree on the skill of your LASIK surgeon and his or her level of experience with a particular procedure. How a surgeon handles his or her practice differs as well. Some questions to ask include:
- How many patients do you treat each hour? (The answer will help you gauge how much time you'll spend with the doctor.)
- What are your cumulative results? (Be sure to compare the post-LASIK visual acuity rates of physicians you are considering.)
Availability
Before your surgery, you should know exactly what is included in the price and how many interactions you will have with the LASIK surgeon. When planning your LASIK surgery, ask yourself:
- Will I be able to meet and interact with the LASIK surgeon until key questions are answered?
- Do I have a minimum of four follow-up visits included in the price? Follow-up visits are the doctor's chance to observe your progress.
- Will my surgeon be present at pre- and post-procedure testing and care?
The Cost of LASIK Surgery
LASIK surgery costs vary by the surgeon's experience, time dedicated to each patient and procedure, regional differences, and also by the quality of the laser system used: state-of-the-art technology costs more.
- How much is the total cost of the LASIK surgery per eye?
- Are the follow-up visits included in this cost? How many? (The average number of post-operative visits is four.) Is the doctor present at these visits?
- What financing programs does the doctor make available?
- What else is included in the cost? (The doctor could include pre-operative sedatives and treatments for side effects, such as prescription medicine drops or dark glasses.)
- Does my insurance cover all or part of the surgical cost? (This is unlikely, because LASIK is an elective surgery, but you should check in case your particular vision problem is covered.)
- Are the surgery's financial terms given to me in writing for my records?
Finding an OptiLASIK™ Treatment Specialist
Choosing the right LASIK surgeon can take a lot of time and research. To help get you started, we’ve created an online OptiLASIK™ Laser Vision Correction Surgeon Locator that allows you to quickly and easily find qualified OptiLASIK™ Treatment Specialists in your area. Each surgeon listed in the directory has been trained and certified to perform OptiLASIK™ Laser Vision Correction with the Allegretto Wave® Eye-Q Laser, so you can be sure you’re getting the most advanced LASIK technology available.
Alcon does not make physician recommendations and does not test the medical ability of surgeons using OptiLASIK™ Laser Vision Correction with the Allegretto Wave® Eye-Q Laser.
Glossary Entries
LASIK: An acronym for Laser In-Situ Keratomileusis. LASIK is a type of laser surgery in which the cornea is reshaped to improve vision. A device called a microkeratome is used to surgically create a thin, hinged flap of corneal tissue. The flap is folded back, the laser is directed to the corneal surface exposed beneath the flap and the flap is brought back into place.
optometrist: An eye care specialist who specializes in the examination, diagnosis, treatment, management and prevention of diseases and disorders of the eye and associated structures.
ophthalmologist: A medical doctor who specializes in the eye and is licensed to perform surgery on the eye. All LASIK surgeons are ophthalmologists.
ophthalmic: Pertaining to the eye.
ophthalmology: Pertaining to the eye, its function, and diseases.
visual acuity: Another phrase for visual clarity, a measure of the eye`s ability to distinguish the shape of objects. Visual acuity is measured with a traditional eye chart, with the goal traditionally being 20/20.
Glossary
Confused on LASIK jargon? Click on terms in bold to pull up the glossary tab.
Myopia:
a. Approval of the premarket approval application is for the WaveLight® ALLEGRETTO WAVE® / ALLEGRETTO WAVE® Eye-Q Excimer Laser System to perform LASIK treatments in patients 18 years of age or older for the reduction or elimination of myopic refractive errors up to -12.0 diopters (D) of sphere with and without astigmatic refractive errors up to -6.0 D; and in patients with documented evidence of a stable manifest refraction defined as less than or equal to 0.50 D of preoperative spherical equivalent shift over one year prior to surgery.
b. LASIK is an elective procedure with the alternatives including but not limited to eyeglasses, contact lenses, photorefractive keratectomy (PRK), and other refractive surgeries.
c. Approval of the application is based on clinical trials in the United States with 901 eyes treated, of which 813 of 866 eligible eyes were followed for 12 months. Accountability at 3 months was 93.8%, at 6 months was 91.9%, and at 12 months was 93.9%.
d. The studies found that of the 844 eyes eligible for the uncorrected visual acuity (UCVA) analysis of effectiveness at the 3-month stability time point, 98.0% were corrected to 20/40 or better, and 84.4% were corrected to 20/20 or better without spectacles or contact lenses.
e. The clinical trials showed that the following subjective patient adverse events were reported as “moderate to severe” at a level at least 1% higher than baseline of the subjects at 3 months posttreatment: visual fluctuations (12.8% at baseline versus 28.6% at 3 months).
f. Long-term risks of LASIK for myopia with and without astigmatism beyond 12 months have not been studied.
g. Note that the complete name for this ophthalmic laser is “WaveLight® ALLEGRETTO WAVE® / ALLEGRETTO WAVE® Eye-Q Excimer Laser System for laser assisted in-situ keratomileusis (LASIK) treatments of myopic refractive errors up to -12.0 diopters (D) of sphere with and without astigmatic refractive errors up to -6.0 D at the spectacle plane.”
Hyperopia:
a. Approval of the premarket approval application is for the WaveLight® ALLEGRETTO WAVE® / ALLEGRETTO WAVE® Eye-Q Excimer Laser System to perform LASIK treatments in patients 18 years of age or older for the reduction or elimination of hyperopic refractive errors up to +6.0 diopters (D) of sphere with and without astigmatic refractive errors up to 5.0 D at the spectacle plane, with a maximum manifest refraction spherical equivalent (MRSE) of +6.0 D; and in patients with documented evidence of a stable manifest refraction defined as less than or equal to 0.50 D of preoperative spherical equivalent shift over one year prior to surgery, exclusive of changes due to unmasking latent hyperopia.
b. LASIK is an elective procedure with the alternatives including but not limited to eyeglasses, contact lenses, photorefractive keratectomy (PRK), and other refractive surgeries.
c. Approval of the application is based on clinical trials in the United States with 290 eyes treated, of which 100 of 290 eligible eyes were followed for 12 months. Accountability at 3 months was 95.2%, at 6 months was 93.9%, and at 12 months was 69.9%.
d. The studies found that of the 212 eyes eligible for the uncorrected visual acuity (UCVA) analysis of effectiveness at the 6-month stability time point, 95.3% were corrected to 20/40 or better, and 67.5% were corrected to 20/20 or better without spectacles or contact lenses.
e. The study showed that the following subjective patient adverse events were reported as “much worse” by at least 1% of the subjects (in order of increasing frequency) at 6 months post final treatment: glare from bright lights (3.0%); night driving glare (4.2%) light sensitivity (4.9%); visual fluctuations (6.1%); and halos (6.4%).
f. Long term risks of LASIK for hyperopia with and without astigmatism beyond 12 months have not been studied.
g. Note that the complete name for this ophthalmic laser is “WaveLight® ALLEGRETTO WAVE® / ALLEGRETTO WAVE® Eye-Q Excimer Laser System for laser assisted in-situ keratomileusis (LASIK) treatments of hyperopic refractive errors up to +6.0 diopters (D) of sphere with and without astigmatic refractive errors up to 5.0 D with a maximum manifest refraction spherical equivalent (MRSE) of +6.0 D.”
Mixed Astigmatism:
a. Approval of the premarket approval application is for the WaveLight® ALLEGRETTO WAVE® / ALLEGRETTO WAVE® Eye-Q Excimer Laser System to perform LASIK treatments in patients 21 years of age or older for the reduction or elimination of naturally occurring mixed astigmatism of up to 6.00 D at the spectacle plane; and in patients with documentation of a stable manifest refraction defined as less than or equal to 0.50 D of preoperative spherical equivalent shift over one year prior to surgery.
b. LASIK is an elective procedure with the alternatives including but not limited to eyeglasses, contact lenses, photorefractive keratectomy (PRK), and other refractive surgeries.
c. Approval of the application is based on clinical trials in the United States with 162 eyes treated, of which 111 were eligible to be followed at 6 months. Accountability at 1 month was 99.4%, at 3 months was 96.0%, and at 6 months was 100.0%.
d. The studies found that of the 142 eyes eligible for the uncorrected visual acuity (UCVA) analysis of effectiveness at the 3-month stability time point, 95.8% achieved acuity of 20/40 or better, and 67.6% achieved acuity of 20/20 or better without spectacles or contact lenses.
e. The clinical trials showed that the following subjective patient adverse events were reported as “moderate to severe” at a level at least 1% higher than baseline of the subjects at 3 months post-treatment: sensitivity to light (43.3% at baseline versus 52.9% at 3 months); visual fluctuations (32.1% at baseline versus 43.0% at 3 months); and halos (37.0% at baseline versus 42.3% at 3 months).
f. Long term risks of LASIK for mixed astigmatism beyond 6 months have not been studied.
g. The safety and effectiveness of LASIK surgery has ONLY been established with an optical zone of 6.0 - 7.0 mm and an ablation zone of 9.0 mm.
h. Note that the complete name for this ophthalmic laser is “WaveLight® ALLEGRETTO WAVE® / ALLEGRETTO WAVE® Eye-Q Excimer Laser System for laser assisted in-situ keratomileusis (LASIK) treatments of naturally occurring mixed astigmatism of up to 6.00 D at the spectacle plane.”
Wavefront-Guided Treatment of Myopia:
a. Approval of the premarket approval application is for the WaveLight® ALLEGRETTO WAVE® / ALLEGRETTO WAVE® Eye-Q Excimer Laser System used in conjunction with the WaveLight® ALLEGRO Analyzer® device. The device uses a 6.5 mm optical zone, a 9.0 mm ablation/treatment zone, and is indicated for wavefront-guided (WFG) laser assisted in-situ keratomileusis (LASIK): 1) for the reduction or elimination of up to -7.00 diopters (D) of spherical equivalent myopia or myopia with astigmatism, with up to -7.00 D of spherical component and up to 3.00 D of astigmatic component at the spectacle plane; 2) in patients who are 18 years of age or older; and 3) in patients with documentation of a stable manifest refraction defined as ≤0.50 D of preoperative spherical equivalent shift over one year prior to surgery.
b. LASIK is an elective procedure with the alternatives including but not limited to eyeglasses, contact lenses, photorefractive keratectomy (PRK), traditional LASIK and other refractive surgeries.
c. Approval of the application is based on a randomized clinical trial in the United States with 374 eyes treated; 188 with wavefront-guided LASIK (Study Cohort) and 186 with Wavefront Optimized® LASIK (Control Cohort). 178 of the Study Cohort and 180 of the Control Cohort were eligible to be followed at 6 months. In the Study Cohort, accountability at 1 month was 96.8%, at 3 months was 96.8%, and at 6 months was 93.3%. In the Control Cohort, accountability at 1 month was 94.6%, at 3 months was 94.6%, and at 6 months was 92.2%.
d. The studies found that of the 180 eyes eligible for the uncorrected visual acuity (UCVA) analysis of effectiveness at the 6-month stability time point in the Study Cohort, 99.4% were corrected to 20/40 or better, and 93.4% were corrected to 20/20 or better without spectacles or contact lenses. In the Control Cohort, of the 176 eyes eligible for the uncorrected visual acuity (UCVA) analysis of effectiveness at the 6-month stability time point, 99.4% were corrected to 20/40 or better, and 92.8% were corrected to 20/20 or better without spectacles or contact lenses.
e. The clinical trials showed that the following subjective patient adverse events were reported as “moderate to severe” at a level at least 1% higher than baseline of the subjects at 3 months post-treatment in the Study Cohort, light sensitivity (37.2% at baseline versus 47.8% at 3 months) and visual fluctuations (13.8% at baseline versus 20.0% at 3 months). In the Control Cohort, halos (36.6% at baseline versus 45.4% at 3 months) and visual fluctuations (18.3% at baseline versus 21.9% at 3 months).
f. Long term risks of wavefront-guided LASIK for myopia with and without astigmatism beyond 6 months have not been studied.
g. Note that the complete name for this ophthalmic laser is “WaveLight® ALLEGRETTO WAVE® / ALLEGRETTO WAVE® Eye-Q Excimer Laser System used in conjunction with the WaveLight® ALLEGRO Analyzer® device. The device uses a 6.5 mm optical zone, a 9.0 mm ablation/treatment zone, and is indicated for wavefront-guided (WFG) laser-assisted in-situ keratomileusis (LASIK): 1) for the reduction or elimination of up to -7.00 diopters (D) of spherical equivalent myopia or myopia with astigmatism, with up to -7.00 D of spherical component and up to 3.00 D of astigmatic component at the spectacle plane; 2) in patients who are 18 years of age or older; and 3) in patients with documentation of a stable manifest refraction defined as ≤0.50 D of preoperative spherical equivalent shift over one year prior to surgery.”