Saxena Ruchi, Landesz Monika, Noordzij Bastiaantje, Luyten Gregorius P M
Department of Ophthalmology, Erasmus MC, Dr. Molenwaterplein 40, 3015 GD Rotterdam, The Netherlands.
Ophthalmology. 2003 Jul;110(7):1391-5. doi: 10.1016/S0161-6420(03)00405-6.
We report the postoperative results of the Artisan Hyperopia phakic intraocular lens (IOL; model 203W; Ophtec, Groningen, The Netherlands).
Prospective, nonrandomized trial.
Twenty-six eyes of 13 self-selected patients with refractive error ranging from +3.00 to +11.00 diopters (D).
Patients with hypermetropia were implanted with the Artisan Hyperopia phakic IOL. Mean follow-up was 22.4 months (range, 3-36 months).
Predictability, stability, efficacy, loss of best spectacle-corrected visual acuity, and complications.
At six months, 90.9% (20 of 22 eyes) were +/-1.00 D of intended correction and 81.8% (18 eyes) were +/-1.00 D of emmetropia. The mean spherical equivalent was stable within 0.25 D during the entire 3-year follow-up period. Twenty-four eyes (92.3%) had a postoperative best spectacle-corrected visual acuity of 0.50 or better at all of their individual follow-up examinations. No patient lost 2 or more lines after the procedure. There was a significant negative correlation between anterior chamber depth and endothelial cell loss. Two patients experienced posterior synechiae with pigment deposits in both eyes. One of these patients had convex irides and underwent implant removal within 2 years with a consequent clear lens extraction and posterior chamber lens implantation.
Implantation of the Artisan Hyperopic lens leads to accurate and stable refractive results with no significant loss of vision. More attention should be paid to convex irides and shallow anterior chambers during the preoperative screening to avoid unnecessary complications.
我们报告了Artisan远视有晶状体眼人工晶状体(IOL;型号203W;Ophtec,荷兰格罗宁根)的术后结果。
前瞻性、非随机试验。
13例自我选择的患者的26只眼,屈光不正范围为+3.00至+11.00屈光度(D)。
远视患者植入Artisan远视有晶状体眼IOL。平均随访时间为22.4个月(范围3 - 36个月)。
可预测性、稳定性、有效性、最佳矫正视力丧失情况及并发症。
6个月时,90.9%(22只眼中的20只)达到预期矫正±1.00 D,81.8%(18只眼)达到正视化±1.00 D。在整个3年随访期内,平均球镜等效度在0.25 D内保持稳定。24只眼(92.3%)在所有个体随访检查中术后最佳矫正视力为0.50或更好。术后无患者视力下降2行或更多。前房深度与内皮细胞丢失之间存在显著负相关。2例患者双眼出现后粘连伴色素沉着。其中1例患者有虹膜膨隆,在2年内取出植入物,随后进行了透明晶状体摘除和后房型人工晶状体植入。
植入Artisan远视晶状体可获得准确、稳定的屈光结果,且视力无明显丧失。术前筛查时应更多关注虹膜膨隆和前房浅,以避免不必要的并发症。