8,098 research outputs found
Epithelial ingrowth following laser in situ keratomileusis (LASIK): prevalence, risk factors, management and visual outcomes
The number of laser in situ keratomileusis (LASIK) procedures is continuing to rise. Since its first application for correcting simple refractive errors over 25 years ago, the role of LASIK has extended to treat other conditions, including postkeratoplasty astigmatism/ametropia, postcataract surgery refractive error and presbyopia, among others. The long-term effectiveness, predictability and safety have been well established by many large studies. However, due to the creation of a potential interface between the flap and the underlying stroma, interface complications such as infectious keratitis, diffuse lamellar keratitis and epithelial ingrowth may occur. Post-LASIK epithelial ingrowth (PLEI) is an uncommon complication that usually arises during the early postoperative period. The reported incidence of PLEI ranged from 0%–3.9% in primary treatment to 10%–20% in retreatment cases. It can cause a wide spectrum of clinical presentations, ranging from asymptomatic interface changes to severe visual impairment and flap melt requiring keratoplasty. PLEI can usually be treated with mechanical debridement of the affected interface; however, additional interventions, such as alcohol, mitomycin C, fibrin glue, ocular hydrogel sealant, neodymium:yttriumaluminum garnet laser and amniotic membrane graft, may be required for recurrent or refractory cases. The aims of this review are to determine the prevalence and risk factors of PLEI; to describe its pathogenesis and clinical features and to summarise the therapeutic armamentarium and the visual outcome of PLEI
Posterior corneal surface stability after femtosecond laser-assisted keratomileusis
The purpose of this study was to evaluate posterior corneal surface variation after femtosecond laser-assisted keratomileusis in patients with myopia and myopic astigmatism. Patients were evaluated by corneal tomography preoperatively and at 1, 6, and 12 months. We analyzed changes in the posterior corneal curvature, posterior corneal elevation, and anterior chamber depth. Moreover, we explored correlation between corneal ablation depth, residual corneal thickness, percentage of ablated corneal tissue, and preoperative corneal thickness. During follow-up, the posterior corneal surface did not have a significant forward corneal shift: no significant linear relationships emerged between the anterior displacement of the posterior corneal surface and corneal ablation depth, residual corneal thickness, or percentage of ablated corneal tissue
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Monovision LASIK in emmetropic presbyopic patients.
BackgroundTo evaluate the efficacy and patient satisfaction of laser in situ keratomileusis (LASIK) monovision correction in presbyopic emmetropic patients.MethodsA retrospective review of 294 patients who underwent LASIK for monovision was conducted. All patients had preoperative uncorrected distance visual acuity in each eye of 20/25 or better in both eyes and underwent primary LASIK treatment in one eye with a near target; 82 patients underwent surgery in the distant eye for hypermetropia. Patients completed a patient-reported-outcome questionnaire at their one-month postoperative visit. Analysis was performed on a per patient basis with a logistic regression model.ResultsPatients achieved a postoperative mean spherical equivalent of -0.05 diopters (D) in the distant eye and -1.92 D in the near eye. Prior to surgery, 64.7% (n=178) of patients reported they were satisfied or very satisfied with their vision; postoperatively, this increased to 85.4% (n=251). The greatest predictor of dissatisfaction after surgery was severe patient-reported visual phenomena (glare, halos, starbursts, ghosting) (odds ratio 1.18, P=0.001).ConclusionsLASIK monovision for presbyopic patients with low refractive error and good preoperative uncorrected distance visual acuity is both safe and effective with high patient satisfaction. Patients who were dissatisfied in the postoperative period tended to be those with postoperative visual symptoms
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Femtosecond Laser-Assisted In Situ Keratomileusis Treatment of Residual Refractive Error following Femtosecond Laser-Enabled Keratoplasty.
Purpose:To evaluate the safety and effectiveness of femtosecond laser-assisted in situ keratomileusis (LASIK) in the treatment of residual myopia and astigmatism following femtosecond laser-enabled keratoplasty (FLEK). Design:Retrospective case review. Methods:Chart review of all patients with prior FLEK who subsequently underwent femto-LASIK surgery after full suture removal was performed at the Gavin Herbert Eye Institute at the University of California, Irvine. A total of 14 eyes in 13 patients met this criterion, and their comprehensive examinations performed at standard intervals were reviewed. Main outcome measures include uncorrected distance visual acuity (UDVA) and corrected distance visual acuity (CDVA) expressed as the logarithm of the minimum angle of resolution (logMAR), manifest refractive astigmatism, and spherical equivalent. Results:From the preoperative visit to the 3 month visit, all 14 eyes significantly improved in UDVA (logMAR, 0.93 ± 0.23 to 0.44 ± 0.32, P = 0.002) with no loss of CDVA (logMAR, 0.26 ± 0.19 to 0.18 ± 0.23, P = 0.50). All 14 eyes showed significant improvement in manifest refractive astigmatism (4.71 ± 1.77 to 2.18 ± 1.45 diopters (D), P = 0.003) and spherical equivalent (-2.57 ± 2.45 to -0.48 ± 0.83 D, P = 0.0007). There were no flap or graft complications as a result of femto-LASIK. Conclusions:Our findings suggest that femto-LASIK on eyes with prior FLEK is safe and effective in improving visual acuity and reducing residual astigmatism
Analysis of best corrected visual acuity following corneal refractive surgery comparing low and standard predicted postoperative keratometry
BACKGROUND: It is a commonly held view in the ophthalmologic community that eyes with sufficiently low calculated postoperative corneal keratometry, less than 35 diopters, should not undergo corrective refractive laser surgery (CRLS) due to the increased risk of best corrected visual acuity (BCVA) loss. Typical CRLS include Laser In-Situ Keratomileusis (LASIK), Photorefractive Keratectomy (PRK), and Laser-Assisted Sub-Epithelial Keratectomy (LASEK). Evidence for this claim in currently available literature is sparse and inconsistent.
PURPOSE: To further elucidate the relationship between calculated “flat” postoperative corneal keratometry and loss of BCVA. Additionally, to investigate the role of procedure type (LASIK, ASA, or LASEK) and degree of calculated postoperative corneal flatness on visual outcomes following CRLS.
METHODS: 222 eyes (111 candidates and 111 controls) were retrospectively analyzed and matched based on calculated postoperative keratometry compared to control subgroups with calculated postoperative keratometries ≥38 D and further stratified into subgroups 1b (K=38-38.99 D), 2b (K=39-39.99 D), 3b (K=40-40.9 9D), and 4b (K≥41 D). All of the eyes had undergone LASIK, PRK, or LASEK between December 2008 and November 2016 at Boston Eye Group/Boston Laser in Brookline, MA.
RESULTS: Statistical analyses showed no significant differences between candidates and controls in preoperative BCVA (p=0.650) and postoperative BCVA (p=0.081). Subgroup matching showed no significant differences in the amount of tissue ablated in 1a & 1b (p=0.946), 2a & 2b (p=0.694), 3a & 3b (p=0.989), and 4a & 4b (p=0.986). There was also no significant change between preoperative and postoperative BCVA in subgroups 1a (p=0.367), 2a (p=0.297), 3a (p=0.576), 4a (p=0.669), 1b (p=0.458), 2b (p=0.227), 3b (p=0.071), or 4b (p=0.703). 3 of 111 (2.70%) candidate eyes and 1 (0.90%) control eye lost 1+ lines of BCVA following surgery. There was no statistical difference in 1+ lines of BCVA lost between these groups (p=0.313). Similarly, the type of CRLS undergone did not affect the rate of BCVA line loss (p=0.793).
CONCLUSION: Our evidence suggests that in a matched comparison of flat and normal mathematically predicted postoperative keratometries, there was no increase in BCVA lost due to flat keratometry
Fifteen years follow-up of photorefractive keratectomy up to 10 D of myopia: outcomes and analysis of the refractive regression
PURPOSE:
To evaluate outcomes of photorefractive keratectomy up to -10.00 D of myopia and -4.50 of astigmatism and to develop a predictive model for the refractive changes in the long term.
SETTING:
Vissum Corporation and Miguel Hernandez University (Alicante, Spain).
DESIGN:
Retrospective-prospective observational series of cases.
METHODS:
This study included 33 eyes of 33 patients aged 46.79±7.04 years (range 40-57) operated with the VISX 20/20 excimer laser with optical zones of 6 mm. No mitomycin C was used in any of these cases. The minimum follow-up was 15 years. The main outcome measures were: uncorrected and corrected distance visual acuity, manifest refraction and corneal topography. Linear regression models were developed from the observed refractive changes over time.
RESULTS:
Safety and efficacy indexes at 15 years were 1.18 and 0.83, respectively. No statistically significant differences were detected for any keratometric variable during the follow-up (p≥0.103). 15 years after the surgery 54.55% of the eyes were within ±1.00 D of spherical equivalent and 84.85% within ±2.00 D. The uncorrected distance visual acuity at 15 years was 20/25 or better in 60.6% of the eyes and 20/40 or better in 72.73% of the eyes. The correlation between the attempted and the achieved refractions was r=0.948 (p<0.001) at 1 year, and r=0.821 (p<0.001) at 15 years. No corneal ectasia was detected in any case during the follow-up.
CONCLUSIONS:
Photorefractive keratectomy is a safe refractive procedure in the long term within the range of myopia currently considered suitable for its use, although its efficacy decreases with time, especially, in high myopia. The model developed predicts a myopic regression of 2.00 D at 15 years for an ablation depth of 130 µm
Contrast Sensitivity after Zyoptix Tissue Saving LASIK and Standard LASIK for Myopia with 6-Month Followup
This control-matched comparative study evaluated changes in contrast sensitivity after Zyoptix tissue-saving (TS) LASIK and Planoscan standard LASIK (Technolas 217z, Bausch & Lomb) for myopia 6 months postoperatively. 102 TS LASIK-treated eyes were matched with 102 standard LASIK-treated eyes (divided into low, moderate, and high groups). There were no significant differences in refraction outcomes between the groups postoperatively. In high group, a significant reduction in contrast sensitivity after TS LASIK was found at high spatial frequencies (P < .05) under photopic conditions and at middle to high spatial frequencies (P < .05) under mesopic conditions. And significant reduction was also found in standard LASIK at high spatial frequency (P < .05) under mesopic conditions. The reduction was significantly lower in TS LASIK than that in standard LASIK at high spatial frequencies (P < .05) under mesopic conditions. TS LASIK was prone to reduce mesopic contrast sensitivity of high myopia at high spatial frequencies
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