Journal of Cataract & Refractive Surgery
Volume 34, Issue 1 , Pages 21-27, January 2008

Visual outcomes of wavefront-guided laser in situ keratomileusis in eyes with moderate or high myopia and compound myopic astigmatism

Department of Ophthalmology (Bababeygy, Zoumalan, Manche) and Howard Hughes Medical Institute (Bababeygy), Stanford University School of Medicine, Stanford, California, USA

Accepted 13 August 2007.

Article Outline

Purpose

To evaluate the safety, efficacy, and clinical outcomes of wavefront-guided laser in situ keratomileusis (LASIK) surgery for the treatment of moderate to high myopia and compound myopic astigmatism.

Setting

Stanford University School of Medicine, Department of Ophthalmology, Stanford, California, USA.

Methods

This retrospective study included patients with moderate (−6.0 to −8.0 diopters [D]) and high (greater than −8.00) myopia treated with wavefront-guided LASIK using the WaveScan linked to the CustomVue system (AMO USA, Inc.). Eyes were analyzed preoperatively and 1, 3, and 12 months postoperatively.

Results

The mean patient age was 38.4 years ± 7.14 (SD). Eighty-nine eyes of 45 patients were evaluated at 3 months and 50 eyes of 25 patients at 12 months. No eye was retreated during the study. The mean manifest refraction spherical equivalent was −8.10 ± 0.98 D (range −6.00 to −10.63 D) preoperatively and −0.33 ± 0.55 D (range −1.625 to 1.375 D) 12 months postoperatively. Ninety percent of the eyes were within ±1.00 D of the intended correction and 64.0%, within ±0.50 D. For all eyes, the safety index was 1.00 and the efficacy index, 1.18.

Conclusion

The data support the safety and efficacy of correcting moderate to high myopia and compound myopic astigmatism using wavefront-guided LASIK.

 

In recent years, wavefront-guided laser in situ keratomileusis (LASIK) has become the dominant procedure used in correcting refractive errors.1 This new technology is thought to have the potential to provide better postoperative quality of vision in patients, especially in contrast sensitive conditions such as scotopic and mesopic vision, than older conventional excimer laser technology.2 With the technological discovery of wavefront measurements, ophthalmologists were able to quantify and potentially treat ocular higher-order aberrations (HOAs) by excimer laser surgery.3 Hence, the concept of wavefront-guided ablation should improve the image and quality of the eye, improving patients' visual acuity, as can be observed with adaptive optics.4

Recent studies report excellent clinical outcomes, safety, and efficacy of various wavefront-guided and wavefront-optimized LASIK platforms (Visx Star S4, AMO; LADARVision 4000, Alcon Laboratories; WaveLight Allegretto, WaveLight; Zyoptix, Bausch & Lomb) in low to moderate myopia, although data in cases of high myopia are scarce.5, 6, 7, 8, 9, 10, 11 Unfortunately, LASIK has risks, especially in eyes with high myopia. Eyes with high myopia are at increased risk for ectasia, may have decreased visual and refractive outcomes, and have increased reoperation rates. In addition, wavefront-guided ablations consume greater amounts of corneal tissue than conventional lasers for a given refractive error. With proper preoperative screening and intraoperative pachymetry evaluations, such complications can be reduced.12

The purpose of this study was to evaluate the predictability, safety, efficacy, complications, and change in ocular aberrations after wavefront-guided LASIK in patients with moderate or high myopia and compound myopic astigmatism.

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Patients and methods 

Study Design 

This retrospective single-surgeon study examined 89 eyes of 45 healthy patients who were treated with wavefront-guided LASIK surgery using the Visx Star S4 excimer laser with software version 5.18 and the Visx WaveScan aberrometer with software version 3.67 (AMO USA, Inc.).

Enrollment Criteria 

A group of patients with moderate to high myopia was retrospectively selected from a large group of myopic eyes consecutively treated with the wavefront-guided platform. The inclusion criterion for patient selection was myopia of −6.0 diopters [D] or more. Patients with myopia less than −6.0 D were excluded. The patient population was further divided in 2 groups: moderate myopia (−6.0 to −8.0 D) and high myopia (greater than −8.0 D).

Clinical Outcome Measures 

In addition to general medical and ophthalmic histories, preoperative measures included uncorrected visual acuity (UCVA), best corrected visual acuity (BCVA), manifest spherical refraction, cycloplegic refraction, ultrasonic pachymetry (Advent Pachymeter, Mentor O & O, Inc.), corneal topography (Orbscan, Bausch & Lomb), slitlamp examination of the anterior segment, and fundoscopy. Analysis of HOAs was performed using the Visx WaveScan aberrometer. The safety index was defined as the mean postoperative BCVA divided by the mean preoperative BCVA and the efficacy index, as the mean postoperative UCVA divided by the mean preoperative BCVA.13

Wavefront aberrations were measured with an undilated pupil (larger than 6.0 mm) in scotopic conditions at all preoperative and postoperative visits. To assess aberrometry readings, 3 readings of each eye were taken on each visit before and after surgery. The best acquisition of the 3 readings was determined by the clearest centroid image. The aberrometry image that closely matched the manifest refraction was selected. The best-acquired image was used as a standard study analysis for the aberrometry data before and after LASIK. The maximum allowed ablation depth was calculated as follows: [(total corneal thickness) − (planned flap thickness) − (minimum allowed residual bed thickness)]. The diameter treatment zone was set as wide as possible for the maximum allowed ablation depth in reference to corneal thickness and pupil diameter.

After topical anesthesia was administered, a flap of approximately 110 μm was created with a femtosecond laser (IntraLase, Inc.). The laser operated at a 15 kHz treatment rate. A superior hinge location with a flap diameter of 9.2 mm was used in all cases. Wavefront-based excimer laser treatment with the Visx WaveScan aberrometer was used (AMO USA Inc.). The WaveScan uses a Hartmann-Shack aberrometer for wavefront capture, in which light rays are projected into the eye and data are analyzed to measure aberrations. Data are then imported into the Visx Star S4 machine, and the corresponding laser ablation is performed by a variable size and shape beam (1.0 to 6.0 mm) using a 60 Hz eye tracker with a built-in iris registration platform. A minimum post-LASIK stromal bed of 300 μm was left in all cases, which was confirmed by intraoperative pachymetry testing. The flap and stromal bed were then irrigated with a balanced salt solution and dried for approximately 2 minutes.

Postoperatively, patients were instructed to instill gatifloxacin 4 times daily for 4 days and prednisolone acetate 1% 4 times daily for 7 days. Postoperative follow-up examinations were at 1 day, 1 week, and 1, 3, and 12 months. The 1-, 3-, and 12-month data are presented here.

Statistical Analysis 

Patient data were compiled in Microsoft Excel. Statistical significance was calculated using the Student t test (P<.05). Data are expressed as means ± standard deviation and ranges (minimum to maximum). For safety and efficacy, visual acuity was calculated using the logMAR scale for each individual eye and subsequently reconverted to the respective Snellen fraction.

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Results 

Demographics and Refractive Error 

The moderate myopia group comprised 44 eyes (49.4% of patient population) and the high myopia group, 45 eyes (50.6%). Eighty-nine eyes of 45 patients were followed for 3 months and 50 eyes of 25 patients, for 12 months. The mean age of patients was 38.4 ± 7.14 years (range 26 to 58 years). Table 1 shows the preoperative demographic and refractive data for all 89 eyes.

Table 1. Preoperative demographic and refractive information.
DemographicEyes at 3 Months (n = 89)Eyes at 12 Months (n = 50)
Sex, n (%)
Male19 (42.2)10 (40.0)
Female26 (57.8)15 (60.0)
Eye, n (%)
Right44 (49.4)25 (50.0)
Left45 (50.6)25 (50.0)
Age (y)
Mean ± SD38.4 ± 7.1439.6 ± 8.47
Range26–5826–58
Preoperative refractive data
Spherical correction (D)
Mean ± SD−8.48 ± 1.11−8.33 ± 0.97
Range−6.50 to −12.25−6.50 to −10.00
Cylinder (D)
Mean ± SD0.76 ± 0.710.75 ± 0.56
Range0.00 to 3.500.00 to 2.75
MRSE (D)
Mean ± SD−8.10 ± 0.98−7.95 ± 0.96
Range−6.00 to −10.63−6.00 to −9.85
Postoperative refractive data
Spherical correction (D)
Mean ± SD0.38 ± 0.54−0.51 ± 0.58
Range−2.00 to 1.75−1.75 to 1.00
Cylinder (D)
Mean ± SD0.34 ± 0.380.34 ± 0.38
Range0.00 to 1.25−0.25 to 2.25
MRSE (D)
Mean ± SD−0.24 ± 0.38−0.34 ± 0.55
Range−1.87 to 1.75−1.62 to 1.37

MRSE = mean refractive spherical equivalent

Table 2 shows the preoperative refractive error by sphere and cylinder. Preoperatively, the mean spherical correction in all 89 eyes was −8.48 ± 1.11 D (range −6.50 to −12.25 D), the mean cylinder was 0.76 ± 0.71 D (range 0.0 to 3.5 D), and the mean manifest refraction spherical equivalent (MRSE) was −8.10 ± 0.98 D (range −6.00 to −10.63 D).

Table 2. Preoperative refractive error stratified by sphere and cylinder, all eyes (N = 89).
Cylinder (D)
0.000.25 to 0.50.75 to 1.00>1.00 to ≤2.00>2 to ≤3.5
Sphere (D)n(%)n(%)n(%)n(%)n(%)
<−6.00 to ≥−7.004(4.5)3(3.4)2(2.2)2(2.2)0
<−7.00 to ≥−8.005(5.6)9(10.1)5(5.6)2(2.2)0
<−8.00 to ≥−9.006(6.7)11(12.4)9(10.1)7(7.9)1(1.1)
<−9.00 to ≥−10.001(1.1)6(6.7)8(9.0)4(4.5)1(1.1)
<−10.000 0 0 0 3(3.4)

Predictability 

Twelve months postoperatively, the mean spherical correction in 50 eyes was −0.51 ± 0.58 D (range −1.75 to 1.00 D) and the mean cylinder was 0.34 ± 0.38 D (range −0.25 to 2.25 D). The mean MRSE was −0.33 ± 0.55 D (range −1.625 to 1.375 D) (Figure 1).

Stability 

Figure 2 shows the stability outcomes. Between 1 month and 3 months, the change in MRSE from emmetropia was within ±1.00 D of the intended correction in 39 (88.6%) of the 44 eyes in the moderate myopia group and all 45 eyes in the high myopia group. Of all eyes at 3 months, 94.4% were within ±1.00 D of the intended correction and 74.2% were within ±0.50 D. Between 3 months and 12 months, the change in MRSE from emmetropia was within ±1.00 D of the intended correction in 20 (83.3%) of 24 eyes in the moderate myopia group and 25 (96.2%) of 26 in the high myopia group. Of all eyes at 12 months, 90% were within ±1.00 D of the intended correction and 64.0% were within ±0.50 D.

Safety 

Twelve months after surgery, 11 (45.8%) of 24 eyes in the moderate myopia group had improved BCVA and 13 (54.2%) had BCVA similar to the preoperative BCVA. No eye in the moderate myopia group lost 1 or more lines of visual acuity. Sixteen (61.5%) of 26 eyes in the high myopia group had improved BCVA, and 7 (26.9%) had BCVA similar to the preoperative BCVA (Figure 3 and Table 3). Three eyes (11.5%) in the high myopia group lost 1 line of acuity; no eye lost 2 or more lines. The safety index (ratio of postoperative and preoperative BCVA) in all eyes at 12 months was 1.00.

Table 3. Change in postoperative BCVA in the moderate and high myopia groups at 12 months.
Moderate Myopia (n = 24)High Myopia (n = 26)
Changen(%)n(%)
Lost >0 to ≤1 line0 3(11.5)
None13(52.0)7(26.9)
Gained >0 to ≤1 line4(16.7)10(38.5)
Gained >1 to ≤2 lines5(20.8)6(23.1)
Gained >2 lines2(8.3)0

Efficacy 

Figure 4 compares the UCVA preoperatively and 12 months postoperatively. At 12 months, 17 (70.8%) of 24 eyes in the moderate myopia group had a UCVA better than or equal to 20/20, and 24 eyes (100%) had a UCVA better than or equal to 20/40. In the high myopia group, 15 (57.7%) of 26 eyes had a UCVA better than or equal to 20/20 and all 26 eyes (100%) had a UCVA better than or equal to 20/40. Furthermore, 27 of the total 50 eyes (54.0%) had a postoperative UCVA that was equal to or better than the preoperative BCVA. The efficacy index (ratio of postoperative UCVA and preoperative BCVA) in all eyes at 3 months was 1.18.

Higher-Order Wavefront Aberrations 

Table 4 shows the HOA parameters, including total HOA root mean square (RMS), coma, trefoil, spherical aberration, and axis of astigmatism in the moderate and high myopia groups preoperatively and 3 months postoperatively. Table 5 shows the same parameters preoperatively and at 12 months. Measurements were taken at the 6.0 mm optical zone without dilation. The mean preoperative total HOA RMS error in all eyes was 0.34 ± 0.17 μm. The error was increased by a factor of 1.55 to 0.53 ± 0.20 μm after 3 months (P<.001) and by a factor of 1.59 to 0.54 ± 0.25 μm after 12 months (P<.001). A small but significant increase in coma and spherical aberration was observed in the moderate myopia and high myopia groups at 3 months and 12 months (Table 4, Table 5, respectively). Trefoil and axis of astigmatism values decreased in both the moderate and high myopia groups at 3 months and 12 months.

Table 4. Root mean square parameters before and after surgery in the moderate myopia and high myopia groups at 3 months.
Changes in HOA (μm)
Moderate Myopia Group (n = 89)High Myopia Group (n = 45)
Mean ± SD (Range) Mean ± SD (Range)
ParameterPreoperativePostoperativeIncrease FactorP ValuePreoperativePostoperativeIncrease FactorP Value
Total HOA RMS0.31 ± 0.13 (0.14–0.63)0.49 ± 0.17 (0.19–0.77)1.58<.0010.36 ± 0.19 (0.11–1.07)0.56 ± 0.22 (0.19–1.1)1.56<.001
Coma0.18 ± 0.10 (0.015–0.418)0.32 ± 0.15 (0.052–0.623)1.78<.0010.21 ± 0.16 (0.41–0.751)0.35 ± 0.23 (0.028–0.896)1.67<.001
Trefoil0.14 ± 0.09 (0.022–0.456)0.13 ± 0.08 (0.038–0.358)0.93.770.15 ± 0.08 (0.055–0.361)0.13 ± 0.08 (0.034–0.333)0.87.19
Spherical aberrations0.13 ± 0.13 (0.008–0.456)0.22 ± 0.19 (0.005–0.607)1.69<.0010.16 ± 0.15 (0.003–0.662)0.27 ± 0.21 (0.007–0.784)1.69<.001
Axis of astigmatism0.79 ± 0.55 (0.07–1.963)0.33 ± 0.21 (0.041–0.818)0.42<.0010.83 ± 0.59 (0.129–2.58)0.40 ± 0.21 (0.05–0.937)0.48<.001

HOA = higher-order aberration; RMS = root mean square

Table 5. Root mean square parameters before and after surgery in the moderate myopia and high myopia groups at 12 months.
Changes in HOA (μm)
Moderate Myopia Group (n = 24)High Myopia Group (n = 26)
Mean ± SD (Range) Mean ± SD (Range)
ParameterPreoperativePostoperativeIncrease FactorP ValuePreoperativePostoperativeIncrease FactorP Value
Total HOA RMS0.31 ± 0.13 (0.14–0.63)0.45 ± 0.21 (0.14–0.83)1.45<.0020.36 ± 0.19 (0.11–1.07)0.61 ± 0.25 (0.26–1.20)1.69<.001
Coma0.18 ± 0.10 (0.015–0.418)0.26 ± 0.18 (0.05–0.617)1.44<.020.21 ± 0.16 (0.41–0.751)0.37 ± 0.24 (0.005–1.02)1.76<.001
Trefoil0.14 ± 0.09 (0.022–0.456)0.11 ± 0.08 (0.011–0.321)0.79.460.15 ± 0.08 (0.055–0.361)0.13 ± 0.09 (0.037–0.458)0.87.26
Spherical aberrations0.13 ± 0.13 (0.008–0.456)0.25 ± 0.18 (0.051–0.683)1.92<.0010.16 ± 0.15 (0.003–0.662)0.36 ± 0.20 (0.03–0.747)2.25<.001
Axis of astigmatism0.79 ± 0.55 (0.07–1.963)0.32 ± 0.23 (0.027–0.818)0.41<.0010.83 ± 0.59 (0.129–2.58)0.32 ± 0.14 (0.117–0.659)0.39<.001

HOA = higher-order aberration; RMS = root mean square

Complications 

No flap complications (epithelial defects, microstriae, or macrostriae) were observed. No eye developed epithelial ingrowth. There was no topographic evidence of ectasia.

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Discussion 

Our retrospective review of patients supports that the new commercially available wavefront-guided LASIK procedure is predictable, safe, and effective. At 12 months, more than 92% of eyes with moderate myopia and more than 81% with high myopia had similar or better postoperative BCVA than preoperatively. Furthermore, 18 (75.0%) of 24 eyes with moderate myopia and 25 (96.2%) of 26 with high myopia were within ±1.00 D of the intended correction at 12 months.

Our postoperative results are consistent with the U.S. Food and Drug Administration's (FDA) summary of safety and effectiveness data for the Visx ophthalmic excimer laser system (http://www.fda.gov/cdrh/pdf/P930016s021b.pdf. Accessed October 3, 2007). In that report, 184 eyes had a preoperative MRSE ranging between −5.0 D and −12.0 D. Twelve months postoperatively, 95.3% of eyes (102 of 107) in the FDA report were within ±1.0 D of the intended spherical correction compared with 90.0% (45 of 50) in our study. Furthermore, 12 months postoperatively, the FDA report showed that 86.0% of all eyes had a UCVA better than or equal to 20/20 and all had a UCVA better than or equal to 20/40, compared with 64.0% and 100% of total eyes, respectively, in our study. These comparisons show that the wavefront-guided LASIK procedure is predictable and effective in cases of moderate to high myopia.

Wavefront-guided LASIK ablations may yield superior results compared with the results of conventional LASIK ablations.6, 14, 15, 16 However, confounding variables prevent a true side-by-side comparison of the 2 technologies. One issue is the optical zone treatment diameter. Most conventional LASIK ablations use smaller ablation diameters than used in wavefront LASIK ablations. A larger ablation diameter can independently influence the effect of LASIK on HOAs. In addition, most conventional LASIK ablations do not use blend zones. The blend zones used in wavefront-guided ablations can also influence outcomes. A true comparison between wavefront-guided LASIK and conventional LASIK would have to control for these important variables.

Changes in HOAs, notably spherical aberrations, are observed postoperatively with conventional LASIK and photorefractive keratectomy (PRK).17, 18 Customized ablation such as wavefront-guided LASIK was designed to help minimize postoperative HOAs. Despite limited evidence that wavefront-guided laser ablation has notably better outcomes than conventional treatment,19 it is evident that wavefront-guided laser procedures induce fewer aberrations than conventional treatments, suggesting improved vision quality.20, 21 Recent studies show that wavefront-guided LASIK induces increases in HOAs, especially spherical aberration, although the increases are minimal.22, 23 Furthermore, increases in HOAs have been documented with various wavefront-guided or optimized LASIK platforms such as the Visx Star S4, LADARVision 4000, WaveLight Allegretto, and Zyoptix.8, 9, 10, 11 It is also important to note that creating a LASIK flap has been shown to increase HOAs in previous studies,24, 25, 26, 27 but it is still unclear whether this translates into a good measure of visual performance.23 Our study is consistent with the literature in that we reveal an increase in total HOA RMS, coma, and spherical aberration at 12 months postoperatively in both moderate and high myopia groups. Although the postoperative trefoil and axis of astigmatism values decreased in both the moderate and high myopia groups, the overall total HOA RMS increased.

A limitation to our HOA analysis is that we did not control for pupil size in preoperative and postoperative measurements. Spherical-like aberrations have been shown to increase significantly with increasing pupil size in unoperated corneas.28 In our study, all eyes had pupils of at least 6.0 mm in diameter preoperatively and postoperatively, and the lighting conditions for aberrometry images were identical for all preoperative and postoperative measurements (3 lux). Based on the minimum pupil size and standardized lighting conditions, we believe our data are worth reporting in this study.

Our retrospective review supports the use of wavefront-guided LASIK procedures in selected patients with high myopia. However, not all patients, especially those with high myopia, are candidates for wavefront-guided LASIK. In these cases, surgeons can offer alternative procedures that may be suitable, such as wavefront-guided PRK, conventional LASIK or PRK, phakic intraocular lenses, or clear lens extraction. Surgeons should be aware of such alternatives to wavefront-guided LASIK, although further discussion of these procedures and their benefits to wavefront-guided LASIK in selected cases is outside the scope of our study.

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References 

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biography

First author:

Simon R. Bababeygy

Department of Ophthalmology, Stanford University School of Medicine, Stanford, California, USA

 No author has a financial or proprietary interest in any material or method mentioned.

 Presented in part as a poster at the annual meeting of the ASCRS Symposium on Cataract and Refractive Surgery, San Diego, California, USA, April 2007.

PII: S0886-3350(07)01769-5

doi:10.1016/j.jcrs.2007.08.032

Journal of Cataract & Refractive Surgery
Volume 34, Issue 1 , Pages 21-27, January 2008