Mixed ciliary-capsular fixation of a three-piece IOL during phacoemulsification in patients with the lenticular ligamentous-capsular system's failure

B. Malyugin, E. N. Panteleev, L. L. Khapaeva, S.G. Savenkov
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Abstract

Purpose. To evaluate clinical results of mixed ciliary-capsular fixation of a three-piece IOL in combination with the intracapsular ring's implantation during phacoemulsification in patients' zonular weakness caused by pseudoexfoliative (PEX) syndrome. Material and methods. This study included 78 patients (86 eyes) with complicated cataract and PEX syndrome associated with zonular weakness and natural lens instability. The average age of the patients was 74.3±9.3 years. Phacoemulsification was performed in a standard technique and followed by ciliary-capsular fixation of a three- piece IOL in all cases. Preoperative and postoperative follow up period lasted from 1st day until 10 months postop. It included biomicroscopy, visual acuity measurement, keratometry, tonometry, ultrasonic biomicroscopy, optical coherence tomography of the posterior segment of the eye. Results. At the 2nd day postop (86 cases) UCVA and BCVA were 0.46±0.29 and 0.58±0.27 respectively, IOP was 16.48±2.81 mm Hg; at 10 months postop (38 cases) UCVA and BCVA – 0.54±0.31 and 0.79±0.28, IOP – 15.34±3.71 mm Hg. The average deviation of the predicted refraction at the 2 days after surgery was –0.29±0.77 D with no significant change after 10 months. Efficiency ratio at 10 months postop was 193, the safety factor was 285. This type of IOL fixation didn't lead to an increase in IOP, development of chronic inflammation such as iridocyclitis or any other comorbidity. All IOLs were stable position regardless of the status of the zonular fibers. Conclusion. As a result of a preliminary study, it was found that mixed ciliary-capsular fixation of a three-piece IOL provides its stable position, high clinical and functional results in the early and late postoperative period after phacoemulsification in patients with pseudoexfoliative syndrome and failure of the lenticular ligamentous-capsular system. Key words: pseudoexfoliative syndrome, zonular weakness, intraocular lens, ciliary-capsular fixation, lens subluxation, myopic shift
晶状体韧带-晶状体系统故障患者超声乳化术中睫状体-晶状体混合固定的应用
目的。目的探讨超声乳化术中睫状体带性剥脱(PEX)综合征患者睫状体带性虚弱时,睫状体-晶状体混合固定联合囊内环植入术的临床效果。材料和方法。本研究纳入了78例(86只眼)伴有睫状体虚弱和自然晶状体不稳定的复杂白内障和PEX综合征患者。患者平均年龄74.3±9.3岁。所有病例均采用标准的超声乳化术,并行三件套人工晶状体睫状囊内固定。术前、术后随访时间为术后第1天至术后10个月。它包括生物显微镜、视力测量、角膜测量、眼压测量、超声生物显微镜、眼后段光学相干断层扫描。结果。术后第2天(86例)UCVA和BCVA分别为0.46±0.29和0.58±0.27,IOP为16.48±2.81 mm Hg;术后10个月(38例)UCVA和BCVA分别为- 0.54±0.31和0.79±0.28,IOP为- 15.34±3.71 mm Hg,术后2天预测屈光平均偏差为- 0.29±0.77 D,术后10个月无明显变化。术后10个月效率比为193,安全系数为285。这种类型的人工晶状体固定不会导致IOP升高、虹膜睫状体炎等慢性炎症的发展或任何其他合并症。所有人工晶状体均处于稳定位置,与带状纤维状态无关。结论。初步研究发现,对于假剥脱综合征和晶状体韧带-晶状体系统失效的患者,采用睫状体-晶状体-晶状体混合固定三片式人工晶状体在超声乳化术术后早期和后期,其位置稳定,临床和功能效果高。关键词:假性剥脱综合征,睫状体无力,人工晶状体,睫状体-晶状体固定,晶状体半脱位,近视移位
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