Güell Jose Luis, Morral Merce, Gris Oscar, Gaytan Javier, Sisquella Maite, Manero Felicidad
Instituto de Microcirugia Ocular, Barcelona, Spain.; Autonoma University of Barcelona, Barcelona, Spain.
Ophthalmology. 2008 Jun;115(6):1002-12. doi: 10.1016/j.ophtha.2007.08.022. Epub 2007 Nov 5.
To report long-term results of Artisan-Verisyse phakic intraocular lenses (PIOLs) to correct myopia, hyperopia, and/or astigmatism and the percentage of additional keratorefractive surgery to eliminate residual refractive errors.
Retrospective, nonrandomized, interventional case series.
From January 1996 to January 2003, 399 Artisan-Verisyse PIOLs were consecutively implanted. To correct myopia, 101 5-mm optic Verisyse PIOLs (group 1) and 173 6-mm optic Verisyse PIOLs (group 2) were implanted. Forty-one were PIOLs for hyperopia (group 3), and 84 were toric (group 4).
Manifest refraction, uncorrected visual acuity (UCVA), best spectacle-corrected visual acuity (BSCVA), biomicroscopy, tonometry, funduscopy, and central endothelial cell count (ECC) were determined before surgery, at 3 months, and at yearly intervals up to 5 years.
Refraction, UCVA, BSCVA, efficacy and safety indexes, enhancements' rate with keratorefractive surgery, central ECC, and complications.
Mean follow-up was 4.05 years. Mean preoperative spherical equivalent (SE) and that at last follow-up were, respectively, -19.8+/-3.23 and -0.5 +/- 0.89 diopters (D) (group 1), -11.27+/-3.11 and -0.64+/-0.8 D (group 2), +4.92+/-1.7 and +0.02+/-0.51 D (group 3), and -6.82+/-8.69 and -0.09+/-0.64 D (group 4). Group 4 had a mean preoperative cylinder of -3.24+/-1.02 D, which decreased to -0.83+/-0.74 D postoperatively. Additional keratorefractive surgery was performed in 60.39% of eyes (group 1), 19.6% (group 2), 41.4% (group 3), and 5.95% (group 4). Mean preoperative central ECC and that at last follow-up were, respectively, 2836+/-398 and 2514+/-529 cells/mm(2) (group 1), 2755+/-362 and 2454+/-588 cells/mm(2) (group 2), 2735+/-355 and 2560+/-335 cells/mm(2) (group 3), and 2632+/-543 and 2537+/-615 cells/mm(2) (group 4). Main complications were 3 explantations due to an unacceptable drop in ECC, 3 lenses' repositioning (2 ocular trauma and 1 unappropriate iris capture), 3 lenses' exchange due to refractive errors, 1 macular hemorrhage, 1 retinal detachment, and 2 cataracts.
According to our experience, implantation of iris-claw PIOLs is a reversible, effective, stable, safe procedure in the first 5 years of follow-up.
报告Artisan-Verisyse有晶状体眼人工晶状体(PIOL)矫正近视、远视和/或散光的长期结果,以及通过额外的角膜屈光手术消除残余屈光不正的百分比。
回顾性、非随机、干预性病例系列。
1996年1月至2003年1月,连续植入399枚Artisan-Verisyse PIOL。为矫正近视,植入了101枚5毫米光学区的Verisyse PIOL(第1组)和173枚6毫米光学区的Verisyse PIOL(第2组)。41枚为远视PIOL(第3组),84枚为散光PIOL(第4组)。
在手术前、术后3个月以及直至5年的每年间隔时间,测定显验光、未矫正视力(UCVA)、最佳眼镜矫正视力(BSCVA)、生物显微镜检查、眼压测量、眼底检查和中央内皮细胞计数(ECC)。
屈光、UCVA、BSCVA、疗效和安全性指标、角膜屈光手术的增效率、中央ECC和并发症。
平均随访4.05年。第1组术前平均等效球镜度(SE)和最后随访时分别为-19.8±3.23和-0.5±0.89屈光度(D),第2组为-11.27±3.11和-0.64±0.8 D,第3组为+4.92±1.7和+0.02±0.51 D,第4组为-6.82±8.69和-0.09±0.64 D。第4组术前平均柱镜度为-3.24±1.02 D,术后降至-0.83±0.74 D。60.39%的眼(第1组)、19.6%(第2组)、41.4%(第3组)和5.95%(第4组)接受了额外的角膜屈光手术。术前平均中央ECC和最后随访时分别为2836±398和2514±529个细胞/mm²(第1组),2755±362和2454±588个细胞/mm²(第2组),2735±355和2560±335个细胞/mm²(第3组),以及2632±543和2537±615个细胞/mm²(第4组)。主要并发症包括3例因ECC不可接受的下降而取出人工晶状体,3例人工晶状体重新定位(2例眼外伤和1例不适当的虹膜捕获),3例因屈光不正而更换人工晶状体,1例黄斑出血,1例视网膜脱离和2例白内障。
根据我们的经验,在随访的前5年中,植入虹膜爪型PIOL是一种可逆、有效、稳定、安全的手术。