Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub
September 2009
Aims: To evaluate the incidence, patient risk factors, diagnosis and management of suprachoroidal hemorrhage (SCH) after glaucoma filtering surgery.
Methods: Retrospective case series study comprised 1553 eyes having glaucoma filtering surgery during the last 15 years (between January 1993 and December 2007) at our department. Observations included incidence, patient risk factors, peri and postoperative diagnosis, management, and outcomes of SCH after this procedure.
Purpose: To prospectively compare the degree of posterior capsule opacification (PCO) after AquaLase and NeoSoniX phacoemulsification methods during the 3-year follow-up period.
Design: Prospective, randomized clinical trial.
Methods: Setting at the Department of Ophthalmology, University Hospital in Hradec Králové.
Purpose: To evaluate and compare posterior capsule opacification (PCO) incidence and the best-corrected visual acuity (BCVA) in patients who underwent the implantation of intraocular lens (IOL) made of polymethylmethacrylate (PMMA), or hydrophobic acrylic material, or silicone material. All patients were examined 7 years after the surgery at the Department of Ophthalmology, University Hospital, Hradec Králové, Czech Republic, E.U.
View Article and Find Full Text PDFCesk Slov Oftalmol
September 2008
Purpose: To compare the degree of posterior capsule opacification (PCO) after cataract surgery in patients with type 2 diabetes mellitus (DM) and in nondiabetic patients.
Patients And Methods: All surgeries were done at Department of Ophthalmology, University Hospital in Hradec Králové and three-piece Alcon AcrySof intraocular lens (MA60BM or MA30BA) was implanted in all eyes. Seven years after surgery, examination of eyes was done including best corrected Snellen visual acuity (BCVA) measurement.
Cesk Slov Oftalmol
September 2008
Purpose: To compare the results of the microbiological examination of aqueous humor after implantation of the intraocular lens (IOL) CORNEAL using either injector or forceps.
Materials And Methods: In this prospective randomized clinical study 46 eyes (43 patients) were implanted with the hydrophylic acrylic IOL CORNEAL ACR6D SE. Injector was used in 23 eyes and folding and implantation forceps in 23 eyes.