Laserite kasutamine silmakirurgias
at 1 year 1.2% of patients had lost 2 lines of vision
(e.g. vision decreased from a preoperative level from 20/20 to
20/40)
No patients lost more than 2 lines of best corrected vision
FDA results (II)
The following adverse events occurred in at least 1% of patients
within 6 months following treatment:
Night vision difficulty 1.0%
Elevation of intraocular pressure 1.8%
Corneal Haze (sarkesta uduvine) 2.3%
Overcorrection (became farsighted) 5.0%
Undercorrection (remained nearsighted) 5.6%
Halos around lights 9.7%
Glare (pimestav valgus) 10.0%
KCard
KCard (II)
Kui kallid need operatsioonid on ?
FemtoLasik 2500
EpiLasik 1980
Super Lasik 1790
Lasik 1640
FRK 880