Cinhüseyinoglu Necdet, Celik Lider, Yaman Aylin, Arikan Gül, Kaynak Tülin, Kaynak Süleyman
Ophthalmology Clinic, SSK Okmeydani Hospital, Istanbul, Turkey.
Graefes Arch Clin Exp Ophthalmol. 2006 Jul;244(7):802-7. doi: 10.1007/s00417-005-0158-5. Epub 2005 Nov 29.
Microincisional cataract surgery is a safe procedure with a very short learning period for an experienced cataract surgeon and rollable ultrathin intraocular lenses eliminate the need for enlargement of corneal incision. The purpose of the study was to evaluate the safety and efficacy of cataract surgery through a corneal microincision and implantation of rollable ultrathin intraocular lenses. The setting was Dokuz Eylul University Medical Faculty, Ophthalmology Department, Izmir, Turkey and SSK Okmeydani Hospital, Ophthalmology Clinic, Istanbul, Turkey.
Ninety eyes in 85 patients were operated on through clear corneal microincisions with sleeveless phacoemulsification and rollable intraocular lenses were implanted. Forty-six of the patients were men and 39 were women between the ages of 27 and 83, with a mean of 51 years. Two eyes had atrophic senile macular degeneration, 4 eyes had nonspecific retinal pigment epithelial changes with chorioretinal atrophy, and 4 patients had diabetes mellitus without retinopathy. Three eyes had posterior capsular opacifications of unknown etiology. Two eyes had primary open angle glaucoma (PAAG) with cup to disc ratios of about 0.5. Three eyes had dense nuclear sclerosis of grade 4 with very low visibility of retinal structures. Other patients had no ocular or systemic pathology other than nuclear/corticonuclear cataract of grade 2-3. Uncorrected and best spectacle-corrected distance and near visual acuities, keratometric values, and refractive status were noted preoperatively and 1 week, 1 month, and 6 months postoperatively. Statistical analysis of keratometric changes between preoperative and postoperative findings was performed using the paired samples t test.
At 6 months postoperatively, 1 patient had a best spectacle-corrected visual acuity (BSCVA) of 0.2, the patient with atrophic senile macular degeneration. The rest of the eyes achieved a BSCVA of 0.63 or better. At 6 months postoperatively, 55 (61.11%) eyes had uncorrected visual acuities (UCVA) equal to or better than 0.8 and 83 (92.22%) eyes had BSCVA equal to or better than 0.8 according to the Snellen chart. The mean postoperative corneal astigmatisms at 1 week, 1 month, and 6 months were 0.69+/-0.43 D, 0.66+/-0.46 D and 0.65+/-0.48 D respectively. Statistical analysis revealed a significant change in corneal astigmatisms at the 1st week visit (p<0.05), but not at the 1st and 6th month visits (p>0.05) compared with preoperative findings.
Based on the limited data in the literature and in this study, it is not possible to make concrete decisions about the benefits and disadvantages of the ThinOptx IOL for longer durations. Intraoperatively, this IOL apparently eliminates the need for enlargement of the corneal incision during implantation. However, the statistical insignificance of induced astigmatisms after microincisions and classical phacoincisions should also be taken into consideration. We conclude that ThinOptx IOL is a pioneering intraocular lens implant that will contribute to the exciting future of cataract refractive surgical procedures. However, both clinical and laboratory investigations are needed to clearly describe the long-term effectiveness of this new rollable IOL.
对于经验丰富的白内障手术医生而言,微小切口白内障手术是一种安全的手术方式,学习周期非常短,可卷曲超薄人工晶状体消除了扩大角膜切口的必要性。本研究的目的是评估通过角膜微小切口进行白内障手术并植入可卷曲超薄人工晶状体的安全性和有效性。研究地点为土耳其伊兹密尔的多库兹艾吕尔大学医学院眼科以及土耳其伊斯坦布尔的SSK奥克梅达尼医院眼科诊所。
对85例患者的90只眼进行了透明角膜微小切口无袖套超声乳化手术,并植入了可卷曲人工晶状体。患者年龄在27至83岁之间,平均51岁,其中46例为男性,39例为女性。2只眼患有萎缩性老年性黄斑变性,4只眼有非特异性视网膜色素上皮改变伴脉络膜视网膜萎缩,4例患者患有糖尿病但无视网膜病变。3只眼有病因不明的后囊膜混浊。2只眼患有原发性开角型青光眼(PAAG),杯盘比约为0.5。3只眼有4级致密核硬化,视网膜结构能见度极低。其他患者除2 - 3级核性/皮质核性白内障外无眼部或全身病变。术前及术后1周、1个月和6个月记录未矫正及最佳眼镜矫正远、近视力、角膜曲率值和屈光状态。使用配对样本t检验对术前和术后角膜曲率变化进行统计分析。
术后6个月,1例患有萎缩性老年性黄斑变性的患者最佳眼镜矫正视力(BSCVA)为0.2。其余眼睛的BSCVA达到0.63或更好。根据斯内伦视力表,术后6个月,55只眼(61.11%)的未矫正视力(UCVA)等于或优于0.8,83只眼(92.22%)的BSCVA等于或优于0.8。术后1周、1个月和6个月的平均角膜散光分别为0.69±0.43 D、0.66±0.46 D和0.65±0.48 D。统计分析显示,与术前结果相比,术后第1周角膜散光有显著变化(p<0.05),但在第1个月和第6个月时无显著变化(p>0.05)。
基于文献和本研究中的有限数据,无法就ThinOptx人工晶状体在更长时间内的利弊做出具体决策。在手术中,这种人工晶状体显然消除了植入过程中扩大角膜切口的必要性。然而,也应考虑微小切口和传统超声乳化切口后诱导散光的统计学无显著性差异。我们得出结论,ThinOptx人工晶状体是一种开创性的人工晶状体植入物,将为白内障屈光手术令人兴奋的未来做出贡献。然而,需要临床和实验室研究来清楚地描述这种新型可卷曲人工晶状体的长期有效性。