PURPOSETo evaluate the efficacy, safety and stability of implantable contact lens (ICL) implantation for the correction of extreme myopia. METHODSThis prospective study included 137 eyes of 71 patients with a mean age of 31 years (18~44) from January 2004 to 2006.An implantable contact lens version 4(ICL V4,Staar Surgical Inc.) was inserted. Patients were prospectively followed preoperatively and at 1 day,l week,1,3,6,12 and 24 months include the unconnected visual acuity(UCVA) and best corrected visual acuity(BCVA), slitlamp examining, refraction,intraocular pressure and so on. The mean preoperative spherical equivalent is 18.24 ± 4.05D (-8.625D~-35.125D) diopters .Surgical implantation was performedthrough a 3mm clear corneal sutureless incision using paraocular anesthesia. The meanfollow-up was 19.6 months(range 6 to 24 months).RESULTSSuccessful implantation was achieved in all patients.Postoperatively,all eyes had a significant increase in uncorrected visual acuity.The mean spherical equivalent refraction at the last examination was -1.16D± 1. 49 (SD ) (+0.625D~-7.00D ) ,within ± 1.00D of the targeted refraction in 123 eyes (89.8%) and within ± 0.50D in 104 eyes(75.9%).In eyes in which the preoperative myopia was less than 20.00D (n=93),the achieved refraction was within ± 1.00D of the intended refraction in 91 eyes (97.8%) and within ± 0.50D in 80 eyes (86.0%).The refraction remained stable with a statistically insignificant change (P>0.05) at each interval during the follow-up.The best corrected visual acuity (BCVA) improved by 1 or more lines in 110 eyes (80.3%) at 1 year.1 eyes (0.730%) lost 1 line of BCVA.No pupillary block glaucoma and cataract requiring surgical intervention occurred during the follow-up. CONCLUSIONPosterior chamber phakic intraocular lens implantation appears to be a efficacy, safety and stability method for the correction of extreme myopia.
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