Güell Jose L, Verdaguer Paula, Elies Daniel, Gris Oscar, Manero Felicidad, Mateu-Figueras Gloria, Morral Merce
Department of Cornea and Refractive Surgery, Instituto Microcirugia Ocular, , Barcelona, Spain.
Br J Ophthalmol. 2014 May;98(5):658-63. doi: 10.1136/bjophthalmol-2013-304035. Epub 2014 Jan 31.
BACKGROUND/AIMS: To evaluate the efficacy, predictability, safety and complications of secondary iris-claw intraocular lens (IOL) implantation in aphakic eyes without capsular support.
Retrospective, non-comparative, interventional case series of 128 aphakic eyes, which consecutively underwent secondary iris-claw Artisan IOL (Ophtec BV) implantation, were included. Manifest refraction, uncorrected visual acuity, best-spectacle corrected visual acuity, biomicroscopy, tonometry, funduscopy and central endothelial cell count (cECC) were evaluated before surgery, and at yearly intervals up to 5 years. Minimum follow-up time was 1 year.
One hundred twenty-eight eyes were treated. Mean age was 54.55 years (range, 1-98 years). Mean follow-up was 41.8 months (SD 23.63). Mean preoperative logarithm of the minimum angle of resolution BSCVA and spherical equivalent (SE) were 0.67 ((SD) 0.53) and 9.63 D (SD 5.50), respectively. One year postoperatively, mean logarithm of the minimum angle of resolution best-spectacle corrected visual acuity improved to 0.52 (SD 0.46) (p<0.05), and remained stable up to 5 years. One year postoperatively, mean SE was -0.52 (SD 2.21) (p<0.05). Mean SE progressively decreased during the 1st year, and remained stable thereafter (p<0.05). Mean preoperative cECC was 2237.47 (SD 793.33) cells/mm(2). cECC showed a slight, though statistically significant, decrease over the years (p=0.05). Main complications were: 2 pupillary block; 3 transient increase in intraocular pressure; 1 IOL replacement; 2 penetrating keratoplasty and 4 cystoid macular oedema.
Iris-claw IOL implantation in aphakic eyes is an effective, predictable and safe procedure in the first 5 years of follow-up. However, a longer follow-up is required to demonstrate its long-term safety.
背景/目的:评估无晶状体囊支持的无晶状体眼中二期虹膜爪型人工晶状体(IOL)植入术的疗效、可预测性、安全性及并发症。
纳入128例连续接受二期虹膜爪型Artisan人工晶状体(Ophtec BV)植入术的无晶状体眼的回顾性、非对照、干预性病例系列。在手术前及术后每年直至5年,评估明显验光、未矫正视力、最佳眼镜矫正视力、生物显微镜检查、眼压测量、眼底检查及中央内皮细胞计数(cECC)。最短随访时间为1年。
共治疗128只眼。平均年龄54.55岁(范围1 - 98岁)。平均随访41.8个月(标准差23.63)。术前最小分辨角最佳眼镜矫正视力的平均对数和球镜等效度(SE)分别为0.67(标准差0.53)和9.63 D(标准差5.50)。术后1年,最小分辨角最佳眼镜矫正视力的平均对数提高至0.52(标准差0.46)(p<0.05),并在5年内保持稳定。术后1年,平均SE为 - 0.52(标准差2.21)(p<0.05)。平均SE在第1年逐渐下降,此后保持稳定(p<0.05)。术前平均cECC为2237.47(标准差793.33)个细胞/mm²。多年来cECC呈轻微但有统计学意义的下降(p = 0.05)。主要并发症包括:2例瞳孔阻滞;3例眼压短暂升高;1例人工晶状体置换;2例穿透性角膜移植术和4例黄斑囊样水肿。
在随访的前5年,无晶状体眼中虹膜爪型人工晶状体植入术是一种有效、可预测且安全的手术。然而,需要更长时间的随访来证明其长期安全性。