Radial keratotomy for residual myopia after photorefractive keratectomy
Transcript of Radial keratotomy for residual myopia after photorefractive keratectomy
Radial keratotomy for residual myopia after photorefractive keratectomy
Marvin L. Kwitko, MD, Sayed Jovkar, MD, Hua Yan, MD, Moustafa Atas, MD
ABSTRACT
Purpose: To evaluate the safety, efficacy. and complications of radial keratotomy (RK) after photorefractive keratectomy (PRK) for myopia.
Setting: Laser Ultravision Institute. Montreal. Canada.
Methods: Surgically induced refractive and visual acuity changes were retrospectively evaluated in 14 eyes of 10 patients treated with RK after PRK. All patients had simple myopia or compound myopic astigmatism. Minimum follow-up was 6 months.
Results: Three eyes (21 %) had one PRK. 7 (50%) had two treatments, and 4 (29%) had three. Eleven eyes (79%) required four-incision RK and 3 (21%), eight-incision RK. All patients had improved uncorrected visual acuity. Six months after the RK retreatment. there was a significant reduction in spherical equivalent of 2.93 diop-ters :!: 1.53 (SO) (P < .05). No intraoperative or postoperative complications occurred except overcorrection (two cases).
Conclusion: Radial keratotomy is an effective, safe method for treating undercorrected myopia after PRK. Further study and analysis of this series of patients are planned. J Cataract Refract Surg 1998; 24:315-319
P hotorefractive keratectomy (PRK) can ablate mi
croscopic layers of tissue to reduce the curvature of
the cornea. I- 3 Radial keratotomy (RK) involves making
radial incisions in the cornea with a calibrated diamond
knife. The incisions weaken the peripheral cornea,4
which then moves anteriorly under the influence of
intraocular pressure (lOP), causing a compensatory
posterior movement and flattening of the central cornea.
From the Department of Ophthalmology, McGill University, and St. Mary's Hospital and Jewish General Hospital, Montreal, Quebec, Canada (Kwitko, Jovkar), Department of Ophthalmology, Tianjin Medical University Hospital, People's Republic of China (Yan), and Department of Ophthalmology, University of Firat, Eiazig, Turkey (Atas).
The side effects of excimer laser refractive surgery include corneal haze, irregular astigmatism, decentration,
undercorrection or overcorrection, delayed epithelial
healing, contact lens intolerance, and visual symptoms
such as halos, glare, and monocular diplopia. 5.6 Al
though excimer laser PRK is effective, predictable, and
safe in treating myopia/-9 undercorrections can persist
in some highly myopic eyes, even after one or more
repeated procedures. These undercorrections are the
result of the technique's limitations and the unique
tissue response of each eye.10-14 The residual refraction
treated initially by PRK can be corrected by PRK or RK
in some patients.
Reprint requests to Marvin L. Kwitko, MD, 5591 Cote des Neiges, Montreal, Quebec H3 T 1 Y8, Canada.
Several studies have reported PRK re-treatment for
undercorrection resulting from the initial PRK treat
ment. 10-
14 However, to our knowledge, the re-treatment
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RK AFTER PRK FOR UNDERCORRECTION
of undercorrection by RK has not been reported. This Table 1. Nomogram for four-incision RK.
study assessed the safety, efficacy, and complications of RK to correct residual myopia after PRK.
Patients and Methods
This retrospective study analyzed the results of RK to treat undercorrected myopia after PRK in 14 eyes of 10 patients. Inclusion criteria for the initial PRK treatment were contact lens intolerance, dissatisfaction with spectacle correction, 21 years or older, stable myopia, and best corrected visual acuity (BCVA) of 20/40 or better. Exclusion criteria included previous corneal disease, uveitis, glaucoma, collagen vascular disease, and use of systemic corticosteroids. The inclusion criteria for RK after PRK were a refractive power greater than 1.50 diopters (D), persistent myopia after multiple previous PRK treatments, or patient request.
Preoperative examinations included manifest and cycloplegic refractions, slitlamp biomicroscopy, ultrasonic pachymetry, corneal sensitivity (Cochet-Bonnet anesthesiometer), keratometry, videokeratography (EyeSys) , and measurements of Snellen visual acuity, pupil size in dim and normal light, and lOP.
PRJ( Protocol
The patient was placed in a supine position beneath the operating microscope delivery system of the ExciMed UV200LA (Summit Technology) or Technolas Keracor 116 (Chi ron Vision Corp.) excimer laser. A drop of proparacaine 0.5% was applied to the eye as a topical anesthetic and a lid speculum used to expose the cornea. The corneal epithelium was then removed by mechanical scraping with a blunt spatula for an optical zone of 7.0 mm. With the patient fixating on the fixation light, corneal ablation was performed. At the
end of the procedure, a contact lens was placed and a drop of diclofenac sodium (Voltaren®) and oxyfloxacin (Ocuflox®) were instilled in the eye.
Patients were followed daily until complete re
epithelialization. The contact lens was then removed, and fluorometholone (FML Forte®) drops were instilled four times daily for 1 month and then tapered to three times daily for 2 months. Follow-up examinations were performed at 1, 2, 3, and 6 weeks and 3 and 6 months.
Optical ZOne (mm)
ComIctIon (0) Age 20 Age 30 Age 40 Age &0, Age 60
1.50 4.00 4.50 4.75 5.00 5.50
2.00 3.50 4.00 4.50 4.75 5.25
2.25 3.25 3.50 4.00 4.25 4.75
2.50 3.25 3.50 4.00 4.25 4.75
2.75 3.00 3.25 3.75 4.00 4.50
3.00 3.00 3.25 3.75 4.00 4.50
3.50 3.50 3.75 4.25
4.00 3.00 3.50 4.00
4.50 3.25 3.75
5.00 3.00 3.50
6.00 3.00
Note: Age given in years
RJ( Protocol Corneal anesthesia was achieved with proparacaine
hydrochloride 0.5%. With the patient fixating on the operating microscope light, the center of the pupil was marked. The diamond knife was calibrated with a microscope. The blade was set at 110% of the thinnest eight paracentral intraoperative pachymetry measurements 1.5 mm from the optical center.
A back-cutting knife was set into the cornea at the optical zone and with steady guidance, an incision made to the limbus (one pass). The nomograms used are shown in Tables 1 and 2. At the end of the procedure, topical antibiotic drops were instilled on the cornea and an eyepatch was applied. Patients were examined at 1 day and 1 week, during which they took antibiotics, and at 1 month postoperatively. After reepithelialization, fluorometholone 0.1 % was instilled four times daily for 1 month and then tapered to three times daily for another month.
Results Minimum follow-up for all patients was 6 months.
Age of the 5 men and 5 women ranged from 26 to 68 years. The mean interval between PRK re-treatments was about 3.25 months (range 3 to 4 months) and between PRK and RK re-treatment, about 20 months (range 4 to 27 months). Three eyes (21 %) had one PRK, 7 (50%) had a second PRK, and 4 (29%) had a third PRK. Of the 14 treated eyes,
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Table 2. Nomogram for eight-incision RK.
Optical Zone (mm) (WomanlMan)
Correction (D) Age 20 Age 30 Age 40 Age 50 Age 60
1.50* 4.75/5.00 5.00 5.25 5.50 5.75
2.00* 4.50/4.75 4.75/5.00 5.50 5.25 5.75
2.50* 4.25/5.00 4.50/4.75 4.75 5.00 5.50
3.00* 400/4.25 4.25/4.50 4.75 5.00 5.25
3.50* 3.75/4.00 4.00 4.25 4.75 5.00
4.00* 3.50/3.75 3.75 4.00 4.50 4.75
4.50* 3.25/3.50 3.50 3.75 4.25 4.50
5.00 3.00/3.25 3.25 3.50 4.00 4.25
5.50 3.00 3.25 3.25 3.75 4.00
6.00 3.00 3.00 3.00 3.50 3.75
7.00 3.25 3.50
8.00 3.00 3.25
Note: Age given in years. If one value is given for optical zone size, it applies to both men and women. *Consider using a smaller optical zone and four-incision RK if recommended optical zone is larger than 4.0 mm
11 (79%) received four-incision RK and 3 (21%), eight-incision RK.
Visual Acuity Uncorrected visual acuity (UCVA) ranged from
20/300 to 20/400 preoperatively, 20/60 to 20/400 after PRK, and 20/20 to 20/80 6 months after RK. All patients had an improved UCVA after the RK retreatment. Nine patients (64%) had a UCVA of 20/40 or better.
Refraction Table 3 shows refraction over time. Preoperative
and postoperative refractions were manifest refractions. When the astigmatism was 0.750 or less, the spherical equivalent was used. In eyes with the RK treatment after PRK, the mean spherical equivalent was -7.95 0 ± 2.92 (SO) before PRK, - 3.50 ± 1.56 0 after PRK, and -0.61 ± 1.14 0 6 months after RK (Figure 1). There was a significant reduction in spherical equivalent of 2.93 ± 1.53 0 6 months after RK (P < .05).
Overcorrection Overcorrection was defined as a change in spherical
equivalent in excess of the original refraction. Six months after RK, two eyes were overcorrected. In one,
with a pre-RK refraction of -5.00 0, the overcorrec
tion was 1.75 O. In the other, with a pre-RK refraction of -2.50 0, the overcorrection was about 0.50 O. There were no other complications including corneal perforation, corneal edema, delayed epithelialization, and corneal ulcers.
The keratometry, computerized videokeratography, pupil measurements, and corneal sensitivity results will be published later.
PostRK 0
·2
rI.l a. -4 ~ ..... Q.
PreRK
I I
= -6 ... ~
-8
-10 -'--
Figure 1. (Kwitko) Change in spherical equivalent. The black squares denote the mean and the bars, the standard deviation.
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Table 3. Summary of refractive data.
Pa· Age tlent Sex, f(em) 'Eye UCVA BCVA
Retractfon (D)
RK
Clear zone fnd. (10m) sIons UCVA BCVA
ReI't'ac>, ,I!on(O}
RK-Induced RJfractive
" Change
M
2 M
3 F
4 M
5 F
6 F
7 F
54
26
34
51
30
41
42
L 20/400 20/50 -12.00 -1.25 x 170 3
R 20/400 20/20 -7.00
R 20/400 20/20 -4.50 2
L 20/400 20/20 -5.50 2
R 20/400 20/20 -5.50 -0.75 x 90 3
R 20/400 20/20 -6.00
L 20/400 20/20 -6.00
R 20/400 20/40 -10.25 -3.00 x 14 3
R 20/300 20/20 -5.25 2
20/300 20/50
20/80 20/20
20/80 20/20
20/100 20/20
20/60 20/20
20/80 20/20
20/100 20/20
20/400 20/40
20/100 20/20
-5.00
-1.75
-3.25
-4.00
-2.50
-2.00
-2.75
-5.00
-2.25
3.00
3.75
3.25
3.00
4.25
4.00
3.25
3.50
4.00
8
4
4
4
4
4
4
8
4
20/60 20/50
20/20 20/20
20/25 20/20
20/20 20/20
20/30 20/20
20/30 20/20
20/30 20/20
20/50 20/40
20/20 20/20
-1.25
o -0.75
-0.50
-100
-100
-0.75
+1.75
o
-3.75
-1.75
-2.50
-3.50
-150
-100
-2.00
-6.75
-2.25
L 20/300 20/20 - 5.25 2 20/100 20/20 -1.50 4.50 4 20/20 20/20 o -1.50
8 F 38 R 20/400 20/40 -9.25 -100 x 20 2 20/200 20/40 -4.50 4.00 4 20/50 20/40 plano -100 x 20 -4.50
L 20/400 20/40 -12.00 3 20/100 20/40 -2.50 4.00 4 20/40 20/40 +0.50 -3.00
9 M 59 L 20/400 20/40 -8.50 -0.50 x 180 2 20/200 20/40 -6.00 3.25 8 20/80 20/40 -3.25 - 2. 75
10 M 68 R 20/400 20/25 -11.00 2 20/300 20/25 -6.00 3.00 4 20/60 20/25 -175 -4.25
Note: The postoperative refractions are spherical equivalents. The complete refraction is listed only if astigmatism was 1.00 D or greater.
Discussion
Changing the shape of the cornea with the excimer laser is a more recently developed technique than RK. Photo refractive keratectomy is safe, predictable, and effective in treating myopia. However, undercorrection after PRK still occurs in eyes with high myopia because of individual corneal tissue response. 10-14
There are several approaches to treating undercorrection after PRK. Snibson et al. 13 found that retreatment with PRK appeared to enhance the results of previous PRK, although it was less successful than the initial procedure. In a study by Epstein and coauthors, 14
the majority of PRK regressions were successfully retreated with PRK. Seiler and coauthors l5 reported that repeated photoablation seemed to be valuable for treat
ing undercorrection after PRK. Another technique to treat undercorrection after
PRK is RK. We evaluated the safety of RK treatment
after PRK. There was no loss of BCVA, and all patients had improved UCVA. No intraoperative or postoperative complications occurred except overcorrection (two cases). Uncorrected visual acuity remained stable from 1 to 6 months after RK.
Table 4 compares our results using RK with previous reports using PRK to re-treat residual myopia. The
Table 4. Summary of results of PRK and RK re-treatments for residual myopia after PRK.
Matta 'O 22
Sutton" 18
POp'2 56
Snibson '3 48
Epstein14
Present
17
14
Results at (Months)
12
6
12
12
6
6
UCVA = uncorrected visual acuity 'Only first author listed tOf intended correction
Percentage Of Patients
UCVA 20140 Within or Better :::!: 1.00 ot
77 82
50 50
76' 50'
64 69
65
64
59
71
'Authors divided patients into two subgroups: no haze and
previous haze; percentages represent the subgroup with previous haze
percentage of eyes achieving a UCVA of20/40 or better and of eyes within ± 1.00 D of intended correction were similar for both RK and PRK re-treatment. Thus,
both PRK and RK were effective in treating undercorrection after PRK.
In our study, there was a significant reduction in mean spherical equivalent from post-PRK (-3.50 +
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RK AFTER PRK FOR UNDERCORRECTION
1.56 D) to post-RK (-0.61 ± 1.14 D). Although the
number of eyes and follow-up were limited, the treat
ment of RK after PRK for residual myopia appears to
be effective. We will follow these patients and study the
long-term effects of RK for undercorrection after PRK.
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