Wavefront-optimized treatment for myopia using Allegretto Wave Eye-Q excimer laser
- Celeste P. Guzman, MD
Jessica Marie R. Abaño, MD
University of Santo Tomas Hospital
Manila, Philippines
THROUGH the years, ophthalmologists
have seen the evolution of
refractive surgery, from radial keratotomy
to modern-day laser in-situ
keratomileusis (LASIK). To date,
LASIK is one of the most commonly
performed surgical procedures to
correct errors of refraction particularly
myopia.1-2
Studies have shown that conventional
excimer corneal ablation
treatments have been safe and effective,
and most patients have excellent
uncorrected visual acuity and
best-corrected visual acuity.1,3-4 However,
unwanted postoperative visual
symptoms have been reported.1,4-7
Higher-order aberrations (HOAs)
have been reported in conventional
LASIK and were associated with
these symptoms. To minimize
postoperative visual aberrations,
advances in laser ablation profiles,
including increased ablation-zone
diameters, wavefront-guided and
wavefront-optimized platforms have
been introduced.
To create a more optically desired
outcome, wavefront-guided ablation
treatments measure corneal aberrations
and plan individual ablation
profiles. Wavefront-optimized laser
profiles adjust and optimize the
asphericity of the cornea based on
an ideal model.
A study by Stonecipher and
Kezirian compared the three-month
postoperative result of wavefrontoptimized
and wavefront-guided
LASIK for myopic astigmatism using
the Allegretto wave. They concluded
that in the majority of eyes, there
were no statistically significant differences
in visual acuity and refractive
outcomes between the treatment
groups.5
In 2007, the first Allegretto Wave
Eye-Q Excimer Laser was introduced
in the Philippines. Currently, there
are no local data on the safety profile
of this system. Thus, this paper
evaluated the efficacy, predictability,
and safety of LASIK surgery using
the Allegretto Wave Eye-Q excimer
laser in a tertiary hospital.
METHODOLOGY
A total of 154 consecutive eyes of
79 patients underwent myopic LASIK
treatment with the Allegretto Wave
Eye-Q excimer laser using the Magoulas’
revised Wellington Wavelight
Allegretto 400 treatment nomogram
performed by a single surgeon.
Chart review was performed
for all patients. Only those with
follow-up period of at least 3 months
postoperatively were included in this
retrospective study. Pre-operative
and postoperative data were tabulated
for each case using a specific
data sheet.
Patient demographics, manifest
and cycloplegic refraction, uncorrected
visual acuity (UCVA), and
best-corrected visual acuity (BCVA)
were noted for each case. Intraoperative
treatment parameters were,
likewise, established.
Postoperative UCVA and BCVA
were determined for each case.
Manifest refraction spherical equivalent
(MRSE) and complications were
also documented. Safety was defined
as maintenance or gain of Snellen
lines of BCVA postoperatively. Efficacy
and predictability were defined
as postoperative uncorrected visual
acuity ≥ 20/20 and within ± 0.50 diopters
of the target mean refractive
spherical equivalent respectively.
A full voluntary informed consent
was obtained from each patient after
a thorough discussion of the procedure
by the surgeon. All surgeries
were done under topical anesthesia
using Alcaine (Alcon, Fort Worth,
TX, USA).
Either a Moria Evolution 3 with
superior hinge or an Amadeus I with
nasal hinge microkeratome was used
for the creation of the flap. The flap
thickness varied from 120 to 140
microns. For patients with ≥ 1.5 D cylinder,
corneal markings were made
prior to the surgery. Treatment was
adjusted according to the Magoulas’
revised Wellington Wavelight Allegretto
400 treatment nomogram.
Postoperatively, patients were
given tobramycin/dexamethasone
(Tobradex, Alcon, Fort Worth, TX,
USA) 4 times a day for 10 days and
hypromellose (Genteal, Novartis,
Cambridge, Massachusetts, USA)
every 3 hours.
RESULTS
One hundred eight eyes of 56
patients, 21 (37.5%) males and 35
(62.5%) females, were included
in the study. The median age was
30 years (mean = 30.66 years). The
spherical error among the treated
eyes ranged between –1.75 D and
–10.25 D. The mean spherical error
corrected was –5.22 D (Table 1).
All eyes achieved UCVA of 20/30
or better, with 92.6% achieving ≥
20/20. Sixteen percent achieved
20/15 (Figure 1).
Table 1: Demographic profile of patients
who underwent myopic LASIK.


Figure 1. Percentages of eyes and postoperative uncorrected visual
acuity (UCVA).

Figure 2. Percentages of eyes with change in best corrected visual acuity
(BCVA) lines.

Figure 3. Percentages of eyes and postoperative manifest refraction spherical
equivalent (MRSE).
Nearly 94% of eyes maintained or
gained 1 to 2 Snellen lines of BCVA
postoperatively. Sixty-three percent
had no change in BCVA, while 30%
gained 1 to 2 Snellen lines of BCVA
(14.8% gained 1 line, 15.7% gained
2 lines). One patient (0.9%) lost 2
Snellen lines of BCVA (Figure 2).
The mean postoperative MRSE was
–0.04 ± 0.26 D. The general refractive predictability was 93.52% within ± 0.5 D from the target
refraction, while 76% of all patients had a postoperative
MRSE of within ± 0.25 of the target (Figure 3).
One patient had bilateral epithelial slide intraoperatively
and was placed on bandage contact lens postoperatively
until the epithelium had fully healed. Three patients
had grade 1 to 2 diffuse anterior lamellar keratitis, which
eventually resolved on follow-up. No retreatment was
necessary for any case.
DISCUSSION
LASIK is the most common refractive surgery procedure
done today, as the safety, efficacy, and predictability
profiles have improved over the years. In the Philippines,
refractive-surgery procedures have been gaining wide
acceptance. There are several local refractive centers
equipped with different excimer lasers and variable treatment
profiles.
To the best of our knowledge, this is the first local study
on the wavefront-optimized treatment of myopia with the
Allegretto Wave Eye-Q excimer laser.
The efficacy and safety results of our study were comparable
to those conducted by the US Food and Drug
Administration (FDA) and other large studies for myopic
LASIK. Our efficacy profile showed that 92.6% of eyes
had UCVA of 20/20 or better, comparable to the 93%
achieved in the FDA study.5 All patients in our study
achieved 20/30 or better UCVA, also comparable to the
20/40 or better vision achieved in the FDA trial.
Yuen et al. presented a large-scale study showing
72.8% and 90% of patients achieved UCVA of 20/20 or
better and 20/40 or better respectively.8 Their results
were slightly lower and may be reflective of the longerterm
follow up and that not all their treatment profiles
were wavefront-optimized. Padmanabhan and coworkers
noted that 85% in wavefront-optimized patients had
uncorrected visual acuity of 20/20 or better,6 similar to
our results.
Our study also showed that 93.5% of patients maintained
or gained BCVA after surgery. This is similar to
the 97% seen in the FDA study. The mean percentage of
losing 2 or more lines of BCVA was 0.61% in the FDA trial
and 0.6% in the Yuen study, comparable with our results
of 0.93%.5, 8
The predictability profile in our study showed that 94%
of patients were within ± 0.50 D of the target refraction.
This was better than the Padmanabhan’s study at 89%.
For the past decades, conventional LASIK treatment
has been well tolerated and efficient for the treatment
of myopia. However, a decrease in visual performance,
particularly contrast sensitivity, and night vision problems
postoperatively have been reported in literature.
Thus, wavefront-guided profiles have been introduced
to achieve reduction and lessen induction of higherorder
aberrations in the treatment of refractive errors.4
More recently, wavefront-optimized treatment has been
developed to address some unexpected ablation results
in conventional LASIK. Results of studies comparing
wavefront-guided and wavefront-optimized treatment
have been promising, with 1 study concluding that the
efficacy, predictability, and safety were not statistically
different, and both groups have good outcomes.6 Others
have proposed using wavefront-optimized profiles
as default treatment due to its good results and reserve
wavefront-guided ablations for patients with large amount
of higher-order aberrations.
Using wavefront-optimized treatment in our study may
be one reason why some of the predictability and efficacy
profiles were better than those that received conventional
LASIK. The use of the accompanying nomogram further
helped in obtaining a more predictable outcome.
In conclusion, our study showed that myopic LASIK
performed in the local setting using the Allegretto Wave
Eye-Q excimer laser is safe and efficacious, with high
refractive predictability.
