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Solid-state laser PRK yields favourable
results for myopia
By
Cheryl Guttman
PHILADELPHIA - Photorefractive keratectomy (PRK) with a 213 nm solid-state
laser (Eye:Q) is safe and effective for treating low levels of myopia
but larger studies are needed to assess its value in the treatment
of hyperopia.
Robert Paul MBBS, FRANZCO and Ian Constable FRACO, FRACS conducted
a single-centre study at the Lions Eye Institute/Sir Charles Gairdner
Hospital, Perth, Australia. Dr Paul presented two-year follow-up
results at the annual ASCRS Symposium on Cataract, IOL and Refractive
Surgery.
He was a senior training registrar when the patients were treated
and currently practises as a corneal/external eye disease and refractive
surgeon at Fremantle Hospital, Perth.
The study's participants included 12 myopes and five hyperopes who
had preoperative errors ranging from -5.75 D to +5.75 D and less
than 3.0 D of astigmatism. Baseline UCVA was 20/200 or worse in
67% of eyes, with BCVA of 20/20 or better in 80%.
Excluding data from three eyes which underwent LASIK re-treatment
with an excimer laser, the results were within 1.0 D of intended
in 82% of eyes and within 0.5 D in 63%.
A total of 90% of eyes achieved a UCVA of 20/40 or better. No eye
lost more than one line of BCVA, while 50% gained one or more lines.
BCVA values remained unchanged in 40% of cases.
There were no cases of induced astigmatism or significant haze during
follow-up. Trace amounts of haze were present in 57% of eyes at
three months. This declined to 44% after two years.
"Our outcomes compare favourably with results achieved with
excimer laser PRK, especially in terms of the uncorrected vision
that is most important to the patients," Dr Paul said.
Evaluating the myopes and hyperopes separately, he noted the results
were best for the low myopes. Among those treated for less than
3.0 D of myopia, all had UCVA of 20/40 or better and 50% saw 20/20
or better. For those with 3.0 D to 6.0 D of myopia, 83.3% achieved
UCVA of better than 20/40.
Follow-up of refraction over time showed the myopes as a group were
initially over-corrected, experienced regression and were close
to emmetropia at two years.
In contrast, the hyperopes fared worse in terms of UCVA outcomes
and exhibited greater variability in refraction during the postoperative
course, Dr Paul reported.
"Given the very small number of hyperopic eyes treated, it
is not possible to interpret the results to reach any conclusions
about PRK treatment of hyperopia with this solid-state laser,"
he said.
LASIK re-treatment with an excimer laser was performed safely in
two myopes and one hyperope after stable refraction was demonstrated.
Both myopes were treated initially for more than 5.0 D of error.
One had regressed and the other was under-treated and regressed.
Both maintained BCVA of 20/20 at one year after the re-treatment.
The hyperope regressed +2.0 D and was re-treated twice at 10 and
13 months with the excimer laser. After one year, there was a single
line loss of BCVA to a level of 20/25.
Regression in two other patients was not re-treated. One individual
refused treatment and the other was a hyperope with vitelliform
dystrophy.
The solid-state laser is a quintupled Nd:YAG device that emits a
wavelength one fifth that of a standard Nd:YAG laser because the
initially produced infrared beam passes through a crystal system
where it is converted to 213 nm.
Compared to gas-based excimer lasers, the solid-state laser has
the benefit of being much more compact as well as easier and less
costly to maintain, Dr Paul said.
"Another potential benefit is that the 213 nm wavelength penetrates
better through the balanced salt solution (BSS) compared to the
193 nm excimer laser beam, and thus the solid-state device offers
the possibility of performing wet-field surgery," he added.
The solid-state laser features an infrared, video-based 200 Hz eyetracker
and a variable size (0.5 mm to 4.0 mm) flying spot. It has a beam
fluence of 170 mJ/cm2, operates at an ablation rate of up to 20
Hz and removes 0.25 microns of tissue per pulse.
The ablation zone measures 6.2 mm for myopic corrections and 6.0
mm to 9.5 mm for treatment of hyperopia.
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