[Treatment of Keratoconus with Corneal Cross-linking--Results and Complications in 2 Years Follow-up]. / Corneal cross-linking v liecbe keratokónusu--výsledky a komplikácie v dvojrocnom sledovaní.

OBJECTIVE: The objective of the study was to assessment of changes of monitored parameters after CXL. Incidence of complications were assessed in the whole group and in groups of patients divided according to the selected criteria. Evaluated parameters were also relations between them and in time. METHODS: The 86 eyes of patients with progressive keratoconus who underwent CXL according to the Dresden protocol in the years 2007-2009 at the Ophthalmic clinic FN Brno Bohunice were included in this study. RESULTS: There was observed significant increase of BCVA (letters--before CXL 42,30±10,35, 1st year after CXL (1Y) 44,68±10,04, p<0,01, 2nd year after CXL (2Y) 44,44±10,57, p<0,01) and SE (-5,95±3,98D, -5,27±3,84D, p<0,01, -4,94±3,68D, p<0,01), and decrease of maximum curvature of the cornea (MAX--before CXL 50,39±4,17D, 1Y 49,46±4,13D, p<0,01, 2Y 49,42±4,14D, p<0,01). Change of ultrasound CCT, polymegatisms, pleomorfisms and corneal endothelial cell density was not significant. The value of MAX is the most important parameter in estimating the effect of CXL. The highest incidence of corneal opacity after CXL was observed in the eyes of patients with III. stage of keratoconus over 40 years old, carrying hard contact lenses and with biomikroskopic symptom of keratoconus on the cornea. We found that corneal thickness measurement with Orbscan II and the mesurement of IOP with noncontact method is incorrect by patients after CXL. CONCLUSION: Corneal cross-linking of the cornea is safe and effective procedure of stopping the progression of keratoconus in 97% of eyes in the period up to 2 years after CXL.

[Trends in indications of perforating keratoplasty at the Department of Ophthalmology, Faculty Hospital, Brno, Czech Republic, E.U., during the period 2008-2012]. / Trendy v indikáciách k perforujúcej keratoplastike na Ocnej klinike FN Brno v rokoch 2008-2012.

INTRODUCTION: The aim of the study is retrospective analysis of perforating keratoplasty (PKP) indications at the Department of Ophthalmology, Faculty Hospital, Masaryk University, Brno, Czech Republic, E.U., during the period of 5 years, from January 1st, 2008 to December 31st, 2012. MATERIAL AND METHODS: We performed the PKP indications retrospective analysis at the Department of Ophthalmology, Faculty Hospital, Masaryk University, Brno, Czech Republic, E.U., during the period of 5 years, from January 1st, 2008 to December 31st, 2012, with complex evaluation of demographic and clinical data. The clinical diagnoses indicating the perforating keratoplasty were divided into 6 groups (keratoconus, bulous keratopathy, keratitis, corneal dystrophies, injuries, corneal transplant failure, and others) according to Cunningham et al. 2011 (2) and Boimer et al. 2012(1) methods. RESULTS: Our results correspond to data in the literature published abroad, where the majority of recently published papers refer significant increase of corneal transplant failure in the last years of follow-up.Key words: perforating keratoplasty, indications.

[Supracor, Laser Correction of Presbyopia: One-year Follow-up Outcomes]. / Supracor, laserová metoda korekce presbyopie: výsledky rocního sledování

PURPOSE: Evaluation of one-year postoperative results after Supracor laser procedure. METHODS: The study group consisted of 8 hyperopic patients (16 eyes) seeking alternatives to wearing glasses for both distance and near vision. These patients underwent Supracor refractive surgery in the Department of Ophthalmology of The University Hospital Brno in the time period from July 2012 to February 2013. The patient mean age at operation was 57,2 years (±4,6), mean binocular uncorrected near visual acuity was Jaeger No. 13, distance visual acuity 0,5 (±0,19). Average follow-up period was 15,5 months (±2,4). We evaluated binocular uncorrected and best corrected distance visual acuity (UDVA, BCDVA), near visual acuity (UNVA, BCNVA), and intermediate visual acuity (UIVA, BCIVA) 12 months after surgery, further the stability of visual acuity, objective refraction, mesopic contrast sensitivity, occurrence of complications, and patient satisfaction. RESULTS: In all 8 patients, binocular UDVA of at least 1,0 was achieved. The mean spherical equivalent was +0,25 D (±0,64). UNVA was Jaeger No. 3 or better in 7 patients (68,7 %), 5 of them could read Jaeger No. 1. UIVA Jaeger No. 1 was achieved in 5 patients (62,5 %), Jaeger No. 2 in 2 patients (25 %), and Jaeger No. 4 in 1 patient (12,5 %). In all eyes, preoperative mesopic contrast sensitivity was within the normal range for the given age. Postoperatively it remained within the normal range in 11 eyes (68,7 %). In 5 eyes (31,3 %) we found adecrease below the lower limit in higher spatial frequencies (12 and 18 cycles/degree) during the entire follow-up period. According to the patient questionnaire, 7 patients (87,5 %) were fully satisfied with the outcome of the surgery and they felt independent of wearing glasses, 1 patient was dissatisfied. 7 patients (87,5 %) did not report the presence of photic phenomena (halo, glare), 1 patient suffered from these problems. We did not encounter any intraoperative or postoperative complications.Conlusion: According to our first experience, good distance, near, and intermediate visual acuity and arather high patient satisfaction can be achieved with the use of the Supracor procedure. Supracor seems to be asuitable method of presbyopia correction in motivated, adaptable patients who meet strict indication criteria. With regard to the small number of patients in our study group, agreater number of patient evaluations will be required in the future, and long-term results will be of interest as well.Key words: Supracor, presbyopia, LASIK, refractive surgery.

[The effectiveness of corneal cross-linking in stopping the progression of keratoconus]. / Efektivita corneal cross-linkingu v zastavení progresie keratokónusu.

OBJECTIVE: Objective of the study was to prove the efficiency of corneal cross-linking (CXL) in stopping the progression of keratoconus. METHODS: In this study were included 58 eyes of patients with progressive keratoconus who underwent CXL according to the Dresden protocol in the years 2007-2009 at the Ophthalmic clinic FN Brno Bohunice. The eyes of patients were divided into four groups according to the change of maximum curvature of the cornea two years after CXL. RESULTS: Stabilization of maximum curvature of the cornea have been reported in 40 % of eyes, regression in 57 % of eyes by an average of 1,92D and disease progression in 3 % of eyes 2 years after CXL. The eyes with regression over 2D had significantly higher best-corrected visual acuity before and after the procedure compared to the group with stabilization. Spherical equivalent increased significantly in all groups, on average, in the group with stabilization of 0,54D, in the group with mild regression of 0,71D and in the group with a large regression of 2,09D. In the group with a large regression 100 % of eyes had stabilization or increase in SE. Our observations showed that, when a decrease in the patient keratometric values of cornea is present after CXL, it is comprehensive and applies to all parameters. CONCLUSION: We have confirmed that corneal cross-linking stops the progression of the disease in 97 % of eyes two years after the procedure.

[The use of confocal corneal microscopy in the Cogan microcystic dystrophy diagnosis and follow-up of the ultrastructural changes after phototherapeutic keratectomy]. / Vyuzití konfokální mikroskopie rohovky v diagnostice Coganovy mikrocystické dystrofie a sledování ultrastrukturálních zmen po fototerapeutické keratektomii.

UNLABELLED: Confocal microscopy represents modern, non-invasive, semi-contact examination method making possible to visualize separate corneal layers (from the endothel to the epithel) in high resolution. Phototherapeutic keratectomy (PTK) is a method using argon-fluoride laser with 193 nm wavelength to treat corneal surface diseases. AIM: To evaluate the use of confocal microscopy for epithelial basal membrane dystrophy diagnosis (Cogan microcystic dystrophy) and following corneal ultra-structural changes in vivo after PTK. MATERIAL AND METHODS: The group consisted of 14 eyes of 9 patients (6 men and 3 women) of average age 45.8 +/- 14.4 years who underwent in the department in last two years phototherapeutic keratectomy for recurrent erosion in Cogan microcystic corneal dystrophy. For the diagnosis of this disease, the confocal corneal microscope (Confoscan 4, Nidek, probe x 40) was used. Computer controlled laser photoablation was in all patients performed; the average depth was 14.8 +/- 3.3 microm (Technolas 217, Bausch & Lomb). The follow-up visits were scheduled always day 5 and 12, and month 1, 3, 6, and 12 after the PTK. The reactive processes in all corneal layers, the subepithelial inervation restoration velocity and recurrence of the primary disease detectable by means of the confocal corneal microscope were followed-up. RESULTS: Cogan microcystic dystrophy was diagnosed in all followed-up patients by means of confocal microscope according to the findings of the area thickening and corneal epithelium basal membrane irregularities. These patients were indicated to the PTK. After the treatment, the healing of the epithelial layer was finished as early as the fifth day. The subepithelial nervous plexus average regeneration period was 6.2 +/- 2.8 months. In all patients, the edema of the anterior stroma was found at the day 5. The beginning of the re-popularization of the anterior stroma by keratocytes from deeper layers we diagnosed, on average, at the day 11.5 +/- 1.9 after the treatment and the following reduction after 5.1 +/- 1.4 months. In the posterior stroma and in the endothel, no changes were found. During the follow-up period, in none of the followed-up patients, the recurrence of the primary disease was found. CONCLUSION: The confocal microscopy may be recommended for superficial corneal dystrophies quality and accurate diagnosis and to follow up changes after phototherapeutic keratectomy as suitable treatment method of these diseases.