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International Journal of Ophthalmology logoLink to International Journal of Ophthalmology
. 2015 Aug 18;8(4):777–783. doi: 10.3980/j.issn.2222-3959.2015.04.24

Effect of suction on macular thickness and retinal nerve fiber layer thickness during LASIK used femtosecond laser and Moria M2 microkeratome

Jing Zhang 1, Yue-Hua Zhou 1
PMCID: PMC4539638  PMID: 26309879

Abstract

AIM

To compare the effect of suction on the macular thickness and retinal nerve fiber layer (RNFL) thickness during laser in situ keratomileusis (LASIK) used Ziemer FEMTO LDV femtosecond laser (Ziemer group) and Moria M2 automated microkeratome (Moria group) for flap creation.

METHODS

Fourier-domain optical coherence tomography (FD-OCT) was used to measure macular thickness, ganglion cell complex thickness and (RNFL) thickness of 204 eyes of 102 patients with the Ziemer femtosecond laser (102 eyes) and the Moria M2 microkeratome (102 eyes) before surgery and 30min; 1, 3d; 1wk; 1, 3mo; 1y after surgery.

RESULTS

The average foveal thickness and parafoveal retinal thickness 30min after the surgery were statistically more than that before surgery (Ziemer P<0.001, P=0.003 and Moria P=0.001, P=0.006) and the effect was less in the Ziemer group than that in the Moria group (P all<0.05). The ganglion cell complex thickness was not significantly changed in both groups (P all>0.05). The RNFL thickness was statistically less 30min after surgery in both groups (P=0.014, P<0.001), but the influence was less in Ziemer group than that in Moria group (P=0.038). However, the RNFL thickness had recovered to the preoperative level only 1d after surgery.

CONCLUSION

The suction of femtosecond laser and mechanical microkeratome led to the increase in macular central fovea thickness and the decrease in RNFL thickness values at the early stage after LASIK. The effect of suction on macular and the RNFL thicknesses in Ziemer group is smaller than that in Moria group.

Keywords: laser in situ keratomileusis, femtosecond laser, macular, retinal nerve fiber layer, optical coherence tomography

INTRODUCTION

Femtosecond laser has a significant impact on refractive surgery by enabling nonmechanical creation of corneal flaps during laser in situ keratomileusis (LASIK). The femtosecond laser offers advatages over microkeratomes. These include increased precision, a reduced incidence of flap complications, and the ability to cut thinner flaps without the risk of buttonhole formation[1][6]. During LASIK flap creation, intraocular pressure (IOP) increases to levels exceeding 65 mm Hg. Femtosecond laser flap creation exerts less extreme IOP fluctuations but requires more procedural time than when a microkeratome is used[7][9]. The sudden spike in IOP, which can damage the eye, has been observed during LASIK[10],[11]. However, whether the sudden spike in IOP during femtosecond laser-assisted LASIK and automated microkeratome LASIK damages the retina requires further study. To our knowledge, there are no reports in the literature comparing the macular thickness and RNFL changes following the LASIK used femtosecond laser and mechanical microkeratome for flap creation.

The aim of this prospective study was to use Fourier-domain optical coherence tomography (OCT) (RTVue OCT-100, Optovue, Inc. Fremont, CA, USA) to evaluate and compare the effects of suction on the macular and the peripapillary retinal nerve fiber layer (RNFL) thickness during LASIK used Ziemer FEMTO LDV femtosecond laser (Ziemer group, Switzerland) and Moria M2 automated microkeratome (Moria group, Antony, France) for flap creation.

SUBJECTS AND METHODS

Subjects

Two hundred and four eyes of 102 patients who were consecutively scheduled for LASIK treatment from December 2009 to August 2010 in the Tongren Ophthalmic Center of Capital Medical University, were enrolled in this prospective study. All candidates had to be a minimum of 18y and were able to return to the center for one-year follow-up. The local ethics committee approved the study, and all patients informed consent.

All patients underwent a complete preoperative examination including uncorrected visual acuity (UCVA), best corrected visual acuity (BCVA), slitlamp examination, applanation tonometry, fundus biomicroscopy, manifest and cycloplegic refraction, keratometry, ultrasonic pachymetry, corneal topography and indirect ophthalmoscopy.

Patients with ocular pathologies such as keratoconus, corneal scars, corneal dystrophies, previous ocular surgery, glaucoma, IOP>21 mm Hg, evidence of glaucomatous optic nerve damage, and cup-to-disc ratio>0.4, diabetes, or other systemic diseases known to affect the eye were excluded.

On the basis of the flap creation technique, 2 groups were formed. One group had femtosecond laser-assisted LASIK (Ziemer group) and the other, LASIK with microkeratome Moria M2 110 µm-head (Moria group).

Fourier-domain Optical Coherence Tomography Measurements

Macular and the peripapillary RNFL thickness measurements were performed by the same examiner (Zhang J) using the RTVue-100 OCT system (software version: 4.0.5.100), which is based Fourier-domain (FD) technology. The RTVue-100 has an axial resolution of 5 µm and acquires high-resolution images with 26 000 axial scans per second. The examinations were before surgery and 30min; 1, 3d; 1wk; 1, 3mo; 1y after surgery. The OCT measurements were performed without pupil dilation.

Macular thickness was measured using “MM6” mode, which is based on repeated A-scans arranged along 12 radial lines with a 6-mm scan length. Examinations were formed in the fovea, parafoveal and perifoveal zones according to the regions determined in ETDRS study (Early Treatment Diabetic Retinopathy Study Research Group 1985), and the average thickness is presented as numerical values or as a false color code for nine modified ETDRS areas (Figure 1). The thickness map represents the average thickness of fovea (1.0 mm diameter central circle area) and 3.0 mm parafoveal (ring area between 1 mm and 3 mm in diameter resulting in a 2.5 mm wide parafoveal ring) and 6.0 mm perifoveal (ring area between 3 mm and 6 mm in diameter resulting in a 3 mm wide perifoveal ring) regions divided into superior (S, 46°-135°), nasal (N, 136°-225°), inferior (I, 226°-315°) and temporal (T, 316°-45°) quadrants (Figure 1).

Figure 1. The nine macular areas defined by the Early Treatment Diabetic Retinopathy Study Research Group (1985).

Figure 1

The ganglion cell complex was measured using the scan protocol “GCC”. This protocol uses one horizontal line with a 7-mm scan length (467 axial scans per line, centered 1 mm temporal to the fovea) followed by 15 vertical lines with a 7-mm scan length (400 axial scans per line, 0.5-mm interval between two lines, centered in the middle of the horizontal scan line). The GCC thickness was measured from the internal limiting membrane to the inner plexiform layer boundary. The following GCC parameters were analyzed in this study: average thickness, thickness in the superior and inferior hemisphere.

The RNFL thickness was determined using the optic nerve head protocol. The protocol uses 13 concentric ring scans 1.3 to 4.9 mm in diameter (587 to 965 different axial scans per ring) centered in the optic disc. The RNFL thickness results were shown as thickness map of 16 regions (Figure 2).

Figure 2. The retinal nerve fiber layer thickness was measured in 16 regions. Data obtained were compared with the normative database provided with the OCT software, taking the patient age and size of the optic disc into account.

Figure 2

The Signal Strength Index (SSI) was used to control for image quality. Images with a SSI less than 50 were excluded, and scans with movement or decentration artifacts were repeated. The results from the comparison of macular, GCC and RNFL thicknesses to normative data were illustrated with a stoplight color scheme for each protocol. Thicknesses in the normal range were represented by green areas, those that were abnormal at the 5% level were represented by yellow areas, and those that were abnormal at the 1% level were represented by red areas.

Surgical Procedure

The same experienced surgeon (Zhou YH) performed all the LASIK procedures under topical anesthesia. The Ziemer femtosecond laser was programmed to a thickness of 110 µm and was used to create an 8.5 mm diameter corneal flap with the hinge placed superiorly. The laser energy was set at <10 nanojoule (nJ) pulse energy with a frequency higher than 5 MHz. The pulse duration was between 200 and 350 femtosecond. The line and spot separations were less than 2 µm.

The microkeratome Moria M2 110 µm-head (Moria M2) was used to created an 8.5 mm diameter corneal flap with a superior hinge. It was used to attempt a flap thickness of 110 µm based on previous experience.

After lifting the flap, ablations were performed using the Visx S4 excimer laser (VISX Inc., Santa Clara, USA) with a 6.0 mm optical zone and 0.5 mm transition zone. The corneal flap and stroma surface were irrigated with balanced normal saline solution, and the flap was repositioned. After the operation, patients were instructed to instill fluorometholone 0.1% four times per day for 3d, and then tapered over for two weeks, and levofloxacin and artificial tears four times per day for 2wk. All patients were asked to have regular follow-up visits, and postoperative examinations were performed at 30min; 1, 3d; 1wk; 1, 3, 6mo and 1y after surgery.

Statistical Analysis

Statistical analysis was performed using SPSS software (version 17.0, SPSS Inc. Chicago, IL, USA). The thickness was compared between groups using an independent-samples t test. One-way analysis of variance (ANOVA) was used to analyze thickness between follow-up visits. The Wilcoxon signed-rank test was applied to identify measurement data not conforming to normal distribution. A P value less than 0.05 was considered statistically significant.

RESULTS

Participants

Table 1 shows the preoperative characteristics of the patients. There were no statistically significant differences between Ziemer group and Moria group (P>0.05).

Table 1. Mean±standard deviation characteristics of subjects.

Characteristics Ziemer LDV Moria M2 P
No. of eyes 102 102 -
Age (a) 26.05±4.67 25.32±3.93 0.546
F 62 (60.8%) 65(63.7%) 0.789
Intraocular pressure (mm Hg) 15.64±3.87 14.89±3.58 0.753
Spherical equivalent (D) -6.43±2.24 -5.93±1.95 0.436
Central Corneal Thickness (µm) 553.26±22.56 556.72±23.78 0.348
Corneal curvature (D) 44.46±1.89 43.66±1.54 0.637

n (%)

Macular Thickness

Table 2 shows the macular thickness values before and after surgery. In Ziemer group, the average foveal and parafoveal retinal thicknesses 30min after the surgery (243.19±25.51 µm, 316.21±14.77 µm) were significantly thicker than that before surgery (238.62±26.58 µm, 311.67±15.23 µm; P<0.001, P=0.003, ANOVA), among that paratemporal and paranasal quadrants were changed significantly (P=0.002, P=0.011, ANOVA). However, the perifoveal retinal thickness was not changed significantly (P=0.586, ANOVA) 30min after surgery. One day, 3d; 1wk; 1, 3mo and 1y after surgery, the foveal, parafoveal and perifoveal retinal thicknesses were not changed significantly (P all >0.05, ANOVA; Table 2).

Table 2. Macular thickness values before and after surgery (µm).

Macular thickness Pre-surgery 30min 1d 3d 1wk 1mo 3mo 1y
Ziemer LDV
 Fovea 238.62±26.58a 243.19±25.51ab 239.78±28.77 240.29±20.79 238.38±23.28 240.53±21.69 241.89±22.23 239.68±20.63
 Parafovea 311.67±15.23a 316.21±14.77ab 311.74±14.32 312.10±12.93 311.02±13.56 310.33±13.07 312.64±14.38 311.51±13.15
 Paratempo 307.39±15.41a 314.76±20.72a 309.46±16.42 307.46±14.58 306.82±14.18 306.49±14.18 306.98±13.33 307.63±13.15
 Parasuperior 315.97±13.88 316.16±15.05b 315.79±13.44 314.92±13.68 314.82±13.81 314.38±13.56 316.91±14.01 315.48±13.38
 Paranasal 310.17±19.81a 316.65±19.22ab 311.85±16.93 311.71±13.88 309.98±14.32 309.65±13.02 311.94±16.64 311.25±13.16
 Parainferior 313.14±16.06 314.27±15.42 313.89±15.65 314.33±13.82 313.47±14.97 313.79±13.54 314.57±17.25 313.28±14.87
 Perifovea 272.63±13.62 273.20±13.23 274.55±13.55 271.88±16.64 272.89±12.86 272.57±13.15 273.38±17.63 273.14±12.88
 Peritempo 273.48±15.29 272.75±20.19 274.76±15.68 271.88±16.64 272.89±12.86 274.04±13.98 274.53±21.01 273.64±13.26
 Perisuperior 269.79±16.26 271.39±16.49 271.61±16.09 269.48±15.67 270.14±15.84 269.99±15.35 270.89±16.43 269.12±14.46
 Perinasal 279.72±17.21 278.76±15.35 280.63±22.22 278.77±14.52 279.95±13.62 278.78±14.29 279.29±21.38 279.35±15.19
 Periinferior 267.53±16.96 269.91±17.37 269.19±17.09 268.33±15.35 268.23±14.85 269.11±15.11 270.81±15.22 268.43±14.92
Moria M2
 Fovea 241.96±17.09a 249.85±22.41ab 243.55±21.48 241.95±17.51 243.12±20.36 242.02±19.72 241.96±14.49 242.74±14.89
 Parafovea 314.71±15.86a 320.21±15.97ab 316.51±15.76 315.81±13.69 315.17±16.88 315.19±12.33 314.95±10.89 315.07±11.41
 Paratempo 310.51±18.62a 316.09±17.05a 315.94±17.02a 315.33±13.67a 311.31±17.28 310.84±17.71 310.93±11.75 310.09±12.17
 Parasuperior 319.21±18.82a 326.59±16.21ab 321.94±15.98 320.21±14.54 320.81±17.21 320.01±9.96 319.37±11.43 319.7111.43±
 Paranasal 314.43±18.66a 321.71±16.71ab 319.04±17.26a 318.76±14.43a 316.1±17.82 314.32±17.81 313.13±11.36 313.05±12.09
 Parainferior 314.73±12.94 314.71±15.71 314.84±15.19 313.92±14.13 314.39±17.04 314.61±10.71 315.39±11.29 315.41±12.37
 Perifovea 274.44±14.93 274.15±14.24 274.02±15.29 273.93±13.12 274.37±16.09 273.96±11.23 275.39±8.42 274.29±9.74
 Peritempo 274.37±18.75 274.07±16.89 275.71±16.08 274.05±13.24 274.41±17.31 274.81±14.59 274.97±9.16 275.72±10.98
 Perisuperior 273.39±20.98 272.12±16.72 272.08±16.29 272.75±15.61 271.11±17.52 272.36±12.09 273.21±11.94 272.36±12.46
 Perinasal 281.26±16.44 281.12±15.23 281.63±15.47 280.47±14.34 280.55±17.19 279.57±17.27 281.75±8.91 280.84±10.46
 Periinferior 268.86±16.02 270.44±15.07 270.58±14.68 269.31±14.69 269.08±16.47 270.12±11.17 269.65±11.32 269.25±12.65

aValue for comparing the thicknesses of different follow-up visits used ANOVA, P<0.05; bValue for comparing the thicknesses of Ziemer LDV and Moria M2 groups used independent samples t-test, P<0.05.

n=102

In Moria group, the average foveal and parafoveal retinal thickness 30min after the surgery was significant thicker than that before surgery (P=0.001, P=0.006, ANOVA), among that the thickness of paratemporal, parasuperior and paranasal quadrants was also significant thicker than that preoperatively (P=0.034, P=0.025, P=0.032, ANOVA). However, the perifoveal retinal thickness was not changed significantly (P=0.812, ANOVA) 30min after the surgery. One day, 3d; 1wk; 1, 3mo and 1y after surgery, the averages of foveal, parafoveal and perifoveal retinal thicknesses were not changed significantly (P all>0.05, ANOVA), but the paratemporal and paranasal quadrants were still significantly thicker 1d and 3d after surgery than that before surgery (P=0.019-0.038, ANOVA).

The average foveal and parafoveal retinal thickness and parasuperior, paranasal retinal thickness in Moria group were statistically more than that in Ziemer group 30min after surgery (P all<0.05, t test for independent samples). However, the difference of the perifoveal retinal thickness between two groups was not significant (P all>0.05, t-test for independent samples; Figures 35).

Figure 3. The average foveal retinal thickness values before and after surgery.

Figure 3

Figure 5. The perifoveal retinal thickness values before and after surgery.

Figure 5

Figure 4. The average parafoveal retinal thickness values before and after surgery.

Figure 4

Perimacular Ganglion Cell Complex

In both groups, the ganglion cell complex thickness, including average thickness, thickness in the superior and inferior hemisphere, was not significantly changed 30min; 1, 3d; 1wk; 1, 3mo and 1y compared with that preoperatively (P all>0.05, ANOVA). The difference in the gaglion cell complex thickness between Ziemer group and Moria group was not statistically significant at any follow-up visits (P all>0.05, ANOVA; Table 3).

Table 3. Perimacular ganglion cell complex parameters (µm).

Time Ziemer LDV
Moria M2
Average Superior Inferior Average Superior Inferior
Pre-surgery 93.59±6.26 93.79±6.86 93.44±6.19 94.39±7.19 93.96±7.64 94.91±7.46
30min 94.39±8.13 94.46±8.43 94.38±8.81 94.86±6.64 94.78±7.57 95.12±6.63
1d 93.89±6.67 93.60±6.36 93.78±7.79 94.74±7.25 94.34±7.77 95.06±7.45
3d 93.99±6.45 93.82±7.04 93.54±7.27 94.69±6.71 93.95±7.12 94.62±6.91
1wk 93.68±6.73 93.69±6.90 93.62±7.63 93.91±6.89 93.59±7.35 94.24±7.02
1mo 93.12±6.97 93.31±6.03 93.01±8.67 93.38±4.52 93.89±5.24 94.94±4.84
3mo 94.03±8.21 94.19±7.44 93.97±8.75 93.71±4.86 94.40±5.92 93.15±4.92
1y 93.54±7.45 93.79±7.14 93.33±8.49 93.81±6.05 93.95±6.50 93.71±6.35

n=102

Peripapillary Retinal Nerve Fiber Layer Thickness

In Ziemer group, the RNFL thickness, including the average thickness, and SN1, SN2 and TL2 RNFL thickness 30min after surgery and the superior, SN1, SN2 and TL2 RNFL thickness 1d after surgery, was statistically less than that before surgery (P all<0.05, ANOVA). The difference in the RNFL thickness was not statistically significant at 3d; 1wk; 1, 3mo and 1y after surgery (P all>0.05, ANOVA; Table 4).

Table 4. Peripapillary retinal nerve fibre layer thickness (µm).

RNFL Pre-surgery 30min 1d 3d 1wk 1mo 3mo 1y
Ziemer LDV
 Average 106.06±9.70a 104.17±9.31a 105.80±9.67 106.25±9.94 105.96±9.29 105.68±12.74 105.83±15.98 105.49±10.09
 Tempo 89.08±14.94 89.81±14.04b 88.84±13.43 89.01±15.73 89.01±14.06 88.99±21.84 89.13±20.77 89.35±17.11
 Superior 128.97±17.73a 127.79±17.73 126.88±18.82a 128.29±19.48 128.92±19.16 128.29±20.78 128.88±19.71 127.62±20.09
 Nasal 71.12±16.73 70.67±16.92 71.86±16.34 71.52±17.09 71.38±16.01 71.67±14.39 71.09±17.42 71.87±12.27
 Inferior 135.06±14.52 134.39±15.56 135.99±15.76 135.29±14.27 135.08±16.22 135.15±21.83 135.41±22.75 135.19±16.21
 TU1 78.59±16.27 79.82±15.93 79.47±15.21 79.24±15.85 78.50±13.81 78.54±22.57 78.93±24.95 78.26±16.69
 TU2 107.78±19.95 107.23±19.57 108.31±19.33 108.68±22.85 107.95±20.03 108.76±26.11 108.05±23.17 107.31±23.64
 ST2 140.99±20.95 141.49±22.36 139.40±22.29 139.09±24.51 142.39±22.40 140.04±21.61 139.98±27.50 140.13±22.16
 ST1 131.72±27.10 132.21±27.69 129.68±27.69 132.86±28.41 134.19±28.57 131.68±28.13 131.40±28.46 131.93±28.15
 SN1 122.65±24.79a 119.72±23.19a 120.32±25.93a 121.13±27.13 124.16±27.27 122.48±28.41 122.34±24.90 122.35±27.99
 SN2 120.61±23.38a 117.86±22.08a 118.21±22.42a 120.14±24.52 119.06±22.76 119.07±23.58 120.34±20.55 119.74±23.76
 NU2 89.19±22.47 87.21±23.05 89.40±23.37 90.52±23.14 89.15±24.54 89.86±19.43 89.44±23.32 89.40±18.84
 NU1 61.03±15.23 61.72±16.68 62.37±14.71 62.54±15.51 61.02±15.23 61.95±12.59 61.42±17.78 61.87±11.79
 NL1 57.61±13.74 58.16±15.80 58.80±14.99 58.82±14.02 58.01±14.68 57.45±11.02 57.13±14.37 57.19±11.06
 NL2 76.71±20.08 75.67±20.42 76.92±20.74 78.30±20.49 76.84±17.94 76.45±20.28 76.46±18.25 76.67±15.89
 IN2 108.84±19.59 108.59±20.58 111.12±22.81 109.98±19.63 108.73±19.76 109.62±24.51 108.81±20.15 108.39±18.13
 IN1 128.92±23.24 128.63±24.64 130.82±27.45 129.44±24.58 128.70±25.48 128.20±30.61 129.41±27.48 128.71±23.56
 IT1 153.36±22.35 153.78±24.66 155.29±23.18 154.22±23.63 152.51±26.73 153.15±32.32 152.48±35.94 152.65±27.35
 IT2 148.99±24.48 146.44±23.70 146.65±23.58 147.42±24.44 148.08±24.27 148.16±34.35 148.74±30.37 148.91±26.09
 TL2 98.89±21.55a 94.85±19.56a 95.16±19.34a 99.62±22.27 98.89±21.59 98.82±29.19 98.12±22.02 98.19±23.09
 TL1 71.04±12.61 69.32±12.68 70.96±11.22 72.38±13.64 71.68±12.09 71.21±12.89 71.08±15.78 71.62±14.25
Moria M2
 Average 107.10±10.68a 105.07±9.78a 107.41±10.13 107.54±9.72 107.19±9.62 106.95±8.13 107.15±7.22 107.41±9.13
 Tempo 87.83±14.98a 84.45±13.24ab 87.24±15.38 88.01±14.47 87.63±15.10 87.72±14.64 87.03±12.00 87.13±13.28
 Superior 128.11±13.84a 124.78±14.12a 128.38±15.76 128.35±15.79 128.12±16.56 127.80±17.65 129.03±15.31 129.24±18.19
 Nasal 72.69±13.97 71.83±11.83 73.09±14.21 72.99±12.48 72.87±12.44 72.58±14.69 72.44±12.18 72.09±12.00
 Inferior 139.78±21.62 138.23±19.44 139.54±19.34 140.16±19.96 140.05±18.37 138.93±17.22 140.01±16.35 139.47±20.64
 TU1 77.62±13.08 75.76±15.69 77.46±15.35 78.48±12.94 78.68±12.82 78.77±14.31 77.82±14.67 77.49±14.02
 TU2 106.97±21.71a 102.40±19.69a 106.54±22.83 107.09±23.38 108.35±23.68 108.39±20.84 106.52±20.71 108.28±19.54
 ST2 142.73±25.67a 137.23±22.46a 140.97±21.96 141.88±21.87 141.49±22.78 141.75±21.18 143.94±17.60 141.85±22.97
 ST1 135.32±26.75 133.57±27.56 135.16±25.93 136.66±25.56 135.15±25.63 135.22±28.51 135.46±24.87 134.54±26.59
 SN1 118.67±21.64 116.42±20.50 119.25±20.65 118.74±21.76 119.20±22.92 118.43±21.97 118.12±19.27 118.73±21.49
 SN2 115.76±17.67 115.95±16.44 118.20±20.84 117.12±17.16 116.73±17.14 117.13±19.62 117.50±19.27 117.23±19.37
 NU2 89.38±18.53 88.41±17.09 90.68±24.22 88.67±16.68 88.06±16.97 89.87±19.12 88.72±17.69 88.88±16.89
 NU1 62.60±13.46 61.40±10.95 62.67±13.34 62.64±11.67 62.08±12.34 63.62±15.14 62.88±12.11 61.92±12.25
 NL1 59.20±12.96 58.15±9.84 60.09±10.98 59.80±10.84 58.75±10.34 59.45±12.86 58.51±10.71 59.27±10.64
 NL2 79.65±17.59 79.42±15.36 80.59±15.74 80.93±15.94 78.35±16.21 79.44±16.75 79.72±13.26 79.51±14.57
 IN2 114.77±26.04 114.21±20.49 115.34±20.96 115.41±22.04 113.55±19.91 114.84±21.13 114.31±19.01 113.95±19.91
 IN1 135.86±31.58 135.73±26.15 135.31±30.29 136.56±27.19 136.05±25.04 135.11±28.34 135.80±27.29 135.33±30.32
 IT1 161.19±30.29 160.42±29.22 162.31±29.34 161.70±28.18 161.96±26.83 160.87±26.15 160.39±23.48 160.74±31.82
 IT2 147.26±24.31a 142.54±23.43a 147.57±24.30 148.51±24.63 148.95±25.34 148.84±25.32 149.39±23.48 148.62±25.78
 TL2 95.70±20.54a 90.41±16.41a 95.23±19.12 95.63±19.22 96.28±20.84 95.59±20.43 95.58±14.21 96.44±18.59
 TL1 70.99±12.10a 69.17±11.62a 69.71±11.96 70.79±10.03 71.17±10.79 70.25±10.88 70.13±7.68 70.30±10.86

aValue for comparing the thicknesses of different follow-up visits used ANOVA, P<0.05; bValue for comparing the thicknesses of Ziemer LDV and Moria M2 groups used independent samples t-test, P<0.05.

n=102

In Moria group, the RNFL thickness, including the average, temporal, superior and TU2, ST2, IT2, TL2, TL1 RNFL thickness 30min after surgery was significantly less than that preoperatively (P all<0.05, ANOVA). The difference in the RNFL thickness was not statistically significant at 1, 3d; 1wk; 1, 3mo and 1y after surgery (P all>0.05, ANOVA; Table 4).

The temporal RNFL thickness in Moria group was significantly less than that in Ziemer group 30min after surgery (P=0.038, t-test for independent samples). The difference in the RNFL thickness was not statistically significant between 2 groups preoperatively and at 1, 3d; 1wk; 1, 3mo and 1y after surgery (P all>0.05, t-test for independent samples; Table 4).

DISCUSSION

During LASIK, a suction ring applied to the anterior segment of the eye elevates the IOP to levels exceeding 65 mm Hg or more pressure during the application of suction. After stopping the vacuum suction, IOP drops to normal, even more 5 mm Hg lower than before suction. The US Food and Drug Administration reports a complication rate of 1% to 5% after LASIK[12]. Rare but devastating complications of LASIK surgery involve the occurrence of posterior segment damage during the LASIK procedure, relating to the sudden strike in IOP during the flap creation causing rhegmatogenous events or damage to retinal ganglion cells, resulting in visual field defects[13][16]. Recently, researchers reported that the maximum IOP levels were lower in the femtosecond laser group, while the duration of the suction phase was longer than that in the microkeratome group[17][20]. Compared to microkeratome, the effect of femtosecond laser on optic nerve and RNFL thickness caused the ophthalmologists' widespread concern. Increased IOP is considered one of the major risk factors for the development, progression, and evaluation of glaucoma. The potential long term damage to the eye caused by the sudden spike in IOP observed during surgery[21][23] is necessitated further investigation.

Thus, we performed this prospective clinical study of patients treated for myopia or myopic astigmatism. We used RTVue-100 OCT system to compare the effect of suction on the macular thickness, ganglion cell complex, and the peripapillary RNFL during femtosecond laser-assisted LASIK and LASIK with microkeratome. To our knowledge, this appears to be the first published study with long follow-up (1y) to use Fourier-domain OCT to compare the effect of suction on the retina during LASIK using the two major forms of flap creation, a microkeratome or a femtosecond laser.

Because LASIK alters corneal curvature and thickness, the normative parameters of conventional glaucoma screening tools are being questioned[24]. The ability of OCT to assess retinal damage with measurements of the optic nerve head, the RNFL, and macular thickness has been demonstrated[25],[26]. Macular ganglion cell complex thickness measure by Fourier-domain OCT may be a good alternative or complementary to RNFL thickness and macular thickness assessment for detecting retinal damage in patients after LASIK[27].

In this study, the average foveal and parafoveal retinal thicknesses statistically increased 30min after the surgery, while the perifoveal retinal thickness was not changed significantly in the both groups. The average foveal and parafoveal retinal thickness and parasuperior, paranasal retinal thickness in the Moria group were significantly thicker than that in Ziemer group 30min after surgery. The foveal, parafoveal and perifoveal retinal thicknesses were not changed significantly both in two groups 1, 3d; 1wk; 1, 3mo and 1y after surgery. We speculate that the suction during femtosecond laser-assited LASIK and LASIK used microkeratome might have caused slight localized edema of the macula early after surgery, mainly in the foveal, parafoveal retinal regions, while the perifoveal retina was not affected. The effect on the macular thickness was slighter in femtosecond laser than microkeratome. One day after LASIK, the macular edema caused by the suction in LASIK used femtosecond laser and microkeratome had been recovered to the preoperative level.

The ganglion cell complex thickness did not significantly change in either groups. We hypothesize that the slight localized edema of the macula did not spread to the inner retina, which extends from the internal limiting membrane to the inner nuclear layer and includes the ganglion cell layer.

The effect of LASIK on RNFL thickness remains a matter of debates[10],[11],[28][30]. Some studies reported LASIK did not significantly affect the RNFL parameters postoperatively[10],[11],[28] while few studies found that RNFL thickness might decrease during uncomplicated LASIK[29],[30]. In our study, the RNFL thickness 30min after surgery was less than before surgery in both groups, and changes were less in the femtosecond laser group than in the microkeratome group. But this might not be of significance and is unlikely to have clinical consequences, because the corneal edema may affect the image quality of examination results 30min after surgery. Moreover, the RNFL thickness had recovered to the preoperative level only 1d after surgery. One of the interpretations about these results is that our study first proposed to measure the RNFL thickness 30min after surgery. Second, we used Fourier-domain OCT, which acquires high-resolution images with 26 000 axial scans per second and can detect changes of 5 µm magnitude. Other reasons were as follows: 1) The suction during surgery effects on retinal microcirculation. Research shows that whenever the IOP rise 10 mm Hg, the surrounding blood flow of optical disc decreases 7.4%-8.4%. Instantaneous changes of suction may cause ischemia-reperfusion injury. 2) The suction during surgery caused mechanical stretch to the retina. Sudden changes of IOP may cause mechanical stretch to vitreous base, and then cause posterior vitreous detachment, even retinal detachment. 3) The suction during surgery may cause disorder of optic nerve axoplasm, axon flow. High IOP can cause retinal ischemia, and axoplasm flow transport blocked in the sieve, malnutrition of retinal ganglion cells, so the RNFL thickness was thinning and defected. While the effect was transient and reversible, so the RNFL thickness thinning reverted to regain pre-operative thickness at day 1 after surgery.

In conclusion, slight localized edema of macula and reduction of the RNFL thickness were caused by LASIK using the two major forms of flap creation, namely a microkeratome or a femtosecond laser. While the changes were less in femtosecond laser group than those in the microkeratome group. Meanwhile, this effect was transient and reversible, because the macular thickness and the RNFL thickness recovered to the preoperative level only 1d after surgery. So the surgery of LASIK is safe and efficient, but surgeons should choose effective and safe suction mode, shorten the suction time and exclude potential retinopathy and preexisting glucoma before surgery to improve the safety and efficacy of LASIK.

Acknowledgments

Conflicts of Interest: Zhang J, None; Zhou YH, None.

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