Title:
1Development of Unilateral Corneal Ectasia After
PRK with Ipsilateral Preoperative Forme Fruste
KeratoconusJacob Reznik, MD¹ James J. Salz,
MD² Alena Klimava, MS³.1. Wilmer
Ophthalmological Institute, Johns Hopkins
University, Baltimore, MD, USA2. Laser Vision
Medical Associates, Cedars Sinai Medical Center,
Los Angeles, CA, USA3. The Johns Hopkins
University School of Medicine, Baltimore, MD,
USACorresponding authorJacob Reznik,
MDWilmer Ophthalmological InstituteJohns
Hopkins University600 N. Wolfe Street, Wilmer
B27Baltimore, MD 21287E-mail
jreznik1_at_jhmi.eduPhone (410)955-5700Fax
(410)955-0046The authors have no proprietary
interest in the materials presented herein.
2Abstract Purpose To describe clinical and
topographic features of a prominent keratectasia
after photorefractive keratectomy (PRK) in a
patient with abnormal preoperative
topography. Methods A 25-year-old man underwent
bilateral uneventful PRK for moderate myopia of -
5.75 - 1.75 x 95 OD and - 7.50 -1.25 x 80 OS with
BSCVA 20/25 OU. Preoperative corneal pachymetry
was 500 µm OD and 460 µm OS. The total calculated
ablation depth was 70 µm in the right eye and 100
µm in the left eye. Preoperative corneal
topography revealed forme fruste keratoconus
(FFK) OD with I-S ratio of 4. Results 5 years
postoperatively, the patient developed unilateral
inferior keratectasia OD with refraction of
0.50 - 5.50 x 90 with BSCVA of 20/100 and central
pachymetry of 481 µm with inferior pachymetry of
374 µm. Conclusion This case reports adds to
the growing body of evidence in the ophthalmic
literature suggesting that patients with
preoperative FFK or early keratoconus may develop
clinically-significant progression of corneal
ectaisa after PRK.
3 Case reportA 25-year-old man was evaluated
for refractive surgery to correct moderate
myopia. The patient deniedprevious contact lens
wear and his ocular history was otherwise
unremarkable. No previous history ofchronic eye
rubbing, other trauma, or atopy was reported. No
family history of corneal ectasia wasreported.
No signs of clinical keratoconus were seen on
slit-lamp biomicroscopy. Dilated
funduscopicexamination was within normal limits.
BSCVA was 20/25 in both eyes with a refraction
of - 5.75 - 1.75 x 95 OD and - 7.50 - 1.25 x 80
OS. Preoperative central corneal pachymetry was
500 µm OD and 460 µm OS.Keratometry readings
were 42.50/42.25 x 90 OD and 43.25/44.00 x 90 OS
with no distortion of thekeratometer mires
OU.No clinical signs of keratoconus were
observed with slit-lamp biomicroscopy in both
eyes. Cornealtopography (Optikon 2000) was
normal OS and abnormal OD with obvious inferior
steepening and I-Sratio of 4. (Figure 1). The
abnormal topography was discussed with the
patient. He was informed that laser in situ
keratomileusis (LASIK) was absolutely
contraindicated secondary to abnormal
topographicfindings. He was informed that if he
agreed to PRK this might accelerate the
progression of keratectasiaand if this did in
fact happen, he would most likely require a hard
contact lens and possibly even apenetrating
keratoplasty.On 4/1/98, patient received -6.86
-0.75 X 180 excimer laser correction with the
Visx Star laser (VISXInc., Santa Clara,
California, USA) with ablation zone 6.0 x 5.7 mm
for ellipse and 5.5 mm for sphereOS 303 pulses
were administered. The fellow eye was similarly
treated on 5/27/98 with correction of -4.71
-2.33 X 90 ablation zone of 6.0 mm x 4.9 mm 435
pulses were administered. The total
calculatedablation depth was 70 µm in the right
eye and 100 µm in the left eye.
4- The early postoperative course was uneventful. 6
weeks after the procedure, UCVA was 20/20 OU, and - BSCVA OD was 20/15 (plano -0.25 X 35). Slit-lamp
biomicroscopy was normal OU. - At 5 years follow up UCVA was CF at 6 feet OD and
20/40 OS. BSCVA was 20/25 OD with refraction - of 0.50 -5.50 x 90 and 20/20 with refraction of
-1.00 sphere OS. Corneal pachymetry OD was 481 µm - centrally and 374 µm inferiorly. With
preoperative pachymetry of 500 µm OD, we thought
the - postoperative values might have been related to a
combination of corneal epithelial hyperplasia and
new - collagen deposition. Pachymetry of the fellow eye
was 450 µm centrally and 450 µm inferiorly. - Corneal topography (Zeiss Hymphrey Systems)
showed marked inferior steepening OD and was
normal - topography in the fellow eye. (Figure 2) The
patient underwent Intacs (Addition Technology,
Inc.) - insertion with IntraLase femtosecond laser
(IntraLase Corp.) channels OD in 01/2005. - Most recent follow up in 04/06 revealed UCVA CF
at 6 feet OD. BSCVA was 20/70 with - 3.50 - 2.25
x 105. - The fellow eye remained stable both
topographically and clinically. (Figure 2) - Patient was referred for SynergEyes (SynergEyes
Inc., Carlsbad, CA) contact lens fit. (Figure 3)
SynergEyes is a - hybrid contact lens made of a rigid gas permeable
(RGP) center fused to a soft, hydrophilic outer
skirt. This - design is thought to provide vision correction
through the central RGP portion of the lens
combined with a
5- Discussion
- Keratectasia is a known major complication of
LASIK. To date, over 100 cases have been reported
in - refractive surgery literature (1). Several
preoperative risk factors have been proposed for
keratectasia after - LASIK, such as high myopia, forme fruste
keratoconus (FFK), and low residual stromal bed,
but cases - with mild myopia, normal topography, and residual
stromal bed gt300 µm also may develop ectasia.
(2,3) - Keratectasia is also one of the most difficult
post-LASIK complications to manage current
options - include RGP contact lenses, intracorneal rings,
phakic toric IOLs and lamellar or penetrating
keratoplasty - (4,5,6).
- Even though the upper limit of myopia suitable
for treatment by LASIK has been arbitrarily set
as -12.0, - keratectasia cases after LASIK was noted in cases
treated for much lower degrees of myopia, from
4.0 - to 7.0 D (7). Inferior corneal steepening was
noted in some of these cases pre-operatively. In
the - absence of refractive instability or
biomicroscopic features of keratoconus these
corneal changes have - been termed forme fruste keratoconus (FFK) (8).
There are a few case reports indicating good
long-term - refractive outcomes and corneal stability after
PRK in such cases as compared to LASIK (9,10).
One - study of a corneal forward shift after PRK using
a scanning-slit corneal topography found that
these - changes usually stabilize 6 months after surgery
(11). A more recent case report described a
patient with - thin central corneas (485 microns in the right
eye and 500 microns in the left eye) and corneal
topography
6- Discussion (continued)
- Our patient had a clear preoperative FFK in the
right eye and normal topography in the left eye.
His other - risk factors included BSCVA of less than 20/20
and relatively thin corneas. He elected to
proceed with - bilateral PRK and had developed progressive
corneal changes consistent with clinical
keratoconus in the - right eye. The left eye has remained stable over
the period of 7 years in regards to visual
acuity, corneal - topography and biomicroscopic findings. The
question to ask here is would this patient have
developed - progression of FFK in the right eye without PRK?
Previous studies have clearly demonstrated - spontaneous progression of FFK into clinical
keratoconus (13). Our patient has developed
progressive - unilateral corneal changes after PRK. His
refraction has been stable in that eye for
several years preoperatively. - It is not unreasonable to suggest that post-PRK
biomechanical corneal weakening had - accelerated progression of unilateral FFK to
clinical keratoconus. A recent longitudinal study
of - keratoconus patients concluded that around 50 of
clinically normal fellow eyes will progress to - keratoconus in 16 years. (14) It is also not
unreasonable to theorize that out patient may
still develop - clinical keratoconus in the fellow eye in the
future.
7 Discussion (continued) We conclude
that the issue of PRK safety over LASIK for
patients with FFK and thin, irregular
corneas needs to be studied further before any
recommendations of its preference is universally
accepted. In addition, a careful preoperative
discussion, clinical evaluation and informed
consent are of a paramount importance for
patients with preoperative risk factors who
desire refractive surgery, either LASIK or PRK.
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10Figure 3
11Figure 4
Figure 5
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