Comparative study between fibrin glue prepared from a single human donor and sutures for sealing induced corneal penetrating wounds on porcine eyes

@#<p style="text-align: justify;"><strong>OBJECTIVE:</strong> To determine the efficacy of fibrin glue derived from a single human donor for sealing induced penetrating corneal wounds on cadaveric porcine eyes compared to conventional suturing.</p> <p style="text-align: justify;"><strong>METHODS:</strong> Forty (40) porcine eyes were randomized into two groups. In the experimental group, the corneal incisions were sealed using fibrin glue prepared from a single human donor. Eyes in the control group were sealed using two interrupted nylon 10-0 sutures. Baseline intraocular pressures were obtained and an anterior chamber maintainer connected to the Centurion Vision System was inserted through a side port. A 3 mm metal keratome was used to create a uniform, central, full-thickness straight incision in all eyes. After making the incision, the presence or absence of leakage was determined using Seidel's test. The eyes were then sealed according to the group they were randomized in. The intraocular pressure (IOP) was gradually increased using the Centurion Vision System to determine the leakage pressure of all sealed eyes in both groups.</p> <p style="text-align: justify;"><strong>RESULTS:</strong> The mean baseline IOP was comparable between the two groups (control group = 21.15 + 1.66 mmHg; experimental group = 21.65 + 1.81, p value = 0.299). All eyes in the control group, showed no leakage immediately after sealing the corneal wounds with sutures. One out of twenty eyes in the experimental group was positive for leakage after application of the fibrin glue (p value = 0.5). The mean leakage pressure was significantly higher for the suture group at 90.25 + 14.9 mmHg compared to the fibrin glue group at 32.30 + 7.6 mmHg (p value = <0.001).</p> <p style="text-align: justify;"><strong>CONCLUSION:</strong> Fibrin glue prepared from a single donor is comparable to two nylon 10-0 sutures in sealing 3 mm corneal penetrating wounds at IOP of up to 32 mmHg. For higher IOP, nylon 10-0 suture is more effective than fibrin glue in sealing the corneal penetrating wounds in cadaveric porcine eyes. </p>

Comparison of Small Incision Lenticule Extraction (SMILE) and Femtosecond Laser In-Situ Keratomileusis (F-LASIK) for the correction of myopia and astigmatism: 1-year clinical outcome

@#<p style="text-align: justify;"><strong>OBJECTIVE:</strong> To compare the efficacy, refractive predictability, stability and safety of Small Incision Lenticule Extraction (SMILE) and Femtosecond Laser In-Situ Keratomileusis (F-LASIK) for the correction of myopia and astigmatism.</p> <p style="text-align: justify;"><strong>METHOD:</strong> This study was approved by the Institutional Review Committee of the St. Luke's Medical Center. A retrospective chart review was conducted at the Vision Laser Center of the St. Luke's Medical Center-Global City. All patients that underwent SMILE from January 2014 to July 2014, with adequate follow-up at 1 day, 1 week, 1 month, 3 months and 1 year, were included in the study. Age-matched and refraction-matched patients, who underwent F-LASIK from January 2012 to April 2014, were chosen as comparators. Uncorrected visual acuity (UCVA), best spectacle-corrected visual acuity (BSCVA), attempted refraction versus achieved refraction and adverse events at 1 day, 1 week, 1 month, 3 months and 1 year were compared postoperatively in both groups. Primary outcome measures were efficacy expressed as the percentage of eyes achieving UCVA of 20/25 or better during the postoperative follow-up, refractive predictability, safety and stability. </p> <p style="text-align: justify;"><strong>RESULTS:</strong> Thirty-five eyes of 18 patients who underwent SMILE and 38 eyes of 19 patients who underwent FLASIK were included in the study. The mean preoperative spherical equivalent of both groups had no statistical difference, with -3.84 ± 1.31 D and -4.07 ± 1.39 D for SMILE and F-LASIK, respectively (p=0.801). At 1 week postoperatively, 51% and 97% achieved UCVA of 20/25 or better in the SMILE and F-LASIK groups. At 3 months, 97% had 20/25 vision or better for the SMILE group, while 100% had 20/25 vision or better for the F-LASIK group. At 1 year, both groups achieved 100% 20/25 or better vision. Three percent lost one line of BCVA in both groups at 1 year. Mean spherical equivalent (SE) between groups at 1 year showed no statistically significant difference (p=0.21), with 0.05 ± 0.18 D in the SMILE group and -0.1 ± 0.15 D in the F-LASIK group. No significant change in mean SE was observed within groups from 1 day to 1 year post op, p=0.166 for SMILE and p=0.226 for F-LASIK. At 1 year, 100% of the SMILE and F-LASIK groups were within ± 0.5 D of target refraction. No adverse events were noted in either group. </p> <p style="text-align: justify;"><strong>CONCLUSION:</strong> SMILE was comparable to F-LASIK in terms of visual outcomes (efficacy, refractive predictability, stability) and safety for the treatment of myopia and astigmatism. However, a slight delay in visual improvement during the first week was observed in the SMILE group.</p>