Femtosecond thin-flap laser assisted in situ keratomileusis for correction of post-penetrating keratoplasty ametropia: long-term outcome.

PURPOSE: To evaluate the long-term clinical outcomes of femtosecond thin-flap LASIK (femto-LASIK) for correction of refractive error after penetrating keratoplasty in keratoconus-affected eyes. SETTING: a private ophthalmology clinic. DESIGN: Prospective interventional case series. METHODS: This prospective interventional case series enrolled 22 eyes of 22 patients who underwent femto-LASIK for the management of post-penetrating keratoplasty ametropia. The refractive error, uncorrected (UDVA), and corrected (CDVA) distance visual acuities and vector analysis were reported in short-term and long-term period after surgery. RESULTS: The mean age was 32.7 ± 7.5 years (range, 23 to 47 years) at the surgery time. The average time between PK and femto-LASIK was 42.5 ± 31.7 months. The average follow-up duration after femto-LASIK was 81.2 ± 18.6 months. The mean preoperative UDVA significantly improved from 0.47 ± 0.15 logMAR to 0.35 ± 0.14 logMAR at 12 months (P = 0.048) and 0.4 ± 0.17 at final follow-up exam (P = 0.007). CDVA was 0.22 ± 0.1 at baseline which improved to 0.18 ± 0.15 and 0.15 ± 0.1 logMAR at 12 and 81 months, respectively. (Ps = 0.027, 0.014). The mean cylinder before surgery was - 5.04 ± 1.4D which significantly decreased to -1.5 ± 0.8 D at 12 months postoperatively. (P < 0.001). There was a significant increase in refractive astigmatism from 12 months to 81 months postoperatively (-3.1 ± 2.0, P = 0.002). At the final visit, the efficacy index was 0.83, and the safety index was 1.16. CONCLUSIONS: Despite the short-term outcome indicated that femo-LASIK was effective for correction of post-keratoplasty ametropia during short-term period, a notable regression in its effect was observed in the long-term follow-up. Therefore, the predictability of this technique might decrease in the long-term.

Femtosecond laser implantation of a 340-degree intrastromal corneal ring segment in keratoconus: Short-term outcomes.

PURPOSE: To evaluate the short-term outcomes of femtosecond laser-assisted implantation of a 340-degree intracorneal ring (ICR) (Keraring) in patients with keratoconus. SETTING: Four centers in Iran. DESIGN: Prospective case series. METHODS: All cases had implantation of the 340-degree ICR after tunnel creation with a femtosecond laser. The uncorrected (UDVA) and corrected (CDVA) distance visual acuities, sphere, cylinder, manifest refraction spherical equivalent (MRSE), mean keratometry (K), steep K, and flat K were evaluated preoperatively and 1, 3, and 6 months postoperatively. RESULTS: Eighteen eyes of 17 patients were included. The mean follow-up was 4.33 months (range 1 to 6 months). The mean UDVA improved from 0.95 logarithm of the minimum angle of resolution (logMAR) ± 0.33 (SD) to 0.53 ± 0.35 logMAR (P = .001) and the mean CDVA from 0.39 ± 0.22 logMAR to 0.26 ± 0.21 logMAR (P = .09). The mean sphere decreased from -5.08 ± 3.74 diopters (D) to -1.67 ± 2.59 D, the mean cylinder from -5.83 ± 2.02 D to -2.72 ± 1.81 D, and the mean MRSE from -8.03 ± 3.88 D to -3.01 ± 2.82 D (P < .001). The mean K decreased from 51.43 ± 3.59 D to 47.42 ± 3.59 D (P < .001). All patients with a preoperative mean K greater than 55.0 D had worse CDVA. CONCLUSIONS: Implantation of a 340-degree ICR using femtosecond laser improved the visual, refractive, and topographic parameters in keratoconic patients. The findings indicate that patients with severe keratoconus (mean K >55.0 D) are not good candidates for this type of ICR.

Clinical Evidence of Decreased Iris Resistance in Patients With Keratoconus.

PURPOSE: To compare the total energy required for producing patent neodymium:yttrium-aluminum-garnet laser peripheral iridotomy in patients with or without keratoconus (KC). METHODS: In this case-control study, 36 eyes from 36 patients with KC and 24 eyes from 24 patients with myopia with or without astigmatism (as control group) who were scheduled for phakic intraocular lens implantation underwent neodymium:yttrium-aluminum-garnet laser peripheral iridotomy 1 week before surgery. The total laser energy was recorded and compared between the 2 groups. RESULTS: Mean total laser energy was significantly lower in patients with KC compared with the control group (114.7 ± 41.0 mJ and 263.9 ± 79.6 mJ, respectively, P < 0.01). Total laser energy was not correlated with patients' age, sex, race, refraction, maximum keratometry, or corneal thickness. CONCLUSIONS: Lower tissue resistance may be present in other ocular structures, such as iris, in patients with KC. Our findings supported a generalized abnormality in patients with KC rather than a localized corneal disease, at least in some cases.

Measurement of Central Corneal Thickness Using Ultrasound Pachymetry and Orbscan II in Normal Eyes.

PURPOSE: To compare ultrasound pachymetry and Orbscan II for measurement of central corneal thickness (CCT) in normal eyes. METHODS: The current study was performed at Labbafinejad Medical Center (LMC), Tehran, Iran. Three hundred eyes from 150 healthy individuals referred for keratorefractive surgery were assessed first by Orbscan II and then by ultrasound pachymetry, and CCT values were recorded and compared. RESULTS: Overall, Orbscan II overestimated CCT as compared to ultrasound pachymetry by about 2.4% (mean values 547.6 ± 34.7 versus 534.8 ± 34.7, respectively, P < 0.001). The difference was more significant when CCT was less than 500 microns (mean values 493.2 ± 16.9 versus 479.9 ± 15.6, mean overestimation: 2.6%, P < 0.001). There was good linear correlation between the two methods (Pearson's correlation r = 0.968, P < 0.0001). CONCLUSION: Orbscan II has good correlation with ultrasound pachymetry for measurement of CCT in normal eyes; however Orbscan II should not be used to evaluate corneal thickness before keratorefractive surgeries, as it tends to overestimate corneal thickness and may result in undesirable, low residual stromal thickness.