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首页> 外文期刊>Journal of cataract and refractive surgery >Single-piece AcrySof intraocular lens implantation in children with congenital and developmental cataract.
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Single-piece AcrySof intraocular lens implantation in children with congenital and developmental cataract.

机译:先天性和发育性白内障患儿的单片AcrySof人工晶状体植入术。

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PURPOSE: To evaluate surgical outcomes of 1-piece AcrySof SA30AL intraocular lens (IOL) (Alcon Laboratories) implantation in children having surgery for congenital and developmental cataracts. SETTING: Iladevi Cataract & IOL Research Centre, Raghudeep Eye Clinic, Ahmedabad, India. METHODS: This prospective observational study comprised 134 consecutive eyes of 84 children from 2 to 15 years old who had surgery for congenital and developmental cataract. Two groups were formed depending on the age of the child at surgery. Primary posterior continuous curvilinear capsulorhexis (PCCC) was performed in children younger than 6 years (Group 1, 66 eyes), and no PCCC was performed in children older than 6 years (Group 2, 68 eyes). Vitrectomy was not performed. An AcrySof IOL was implanted in the bag in all eyes except 1 in Group 1, which received a sulcus-fixated IOL. The study's primary outcome measures were the incidence of visual axis obscuration and the need for a secondary procedure to clear the axis. Secondary observations included the incidence of posterior synechias, cell deposits, and haptic compression. A test of proportion was applied to determine whether age was a risk factor for the development of visual axis obscuration. RESULTS: The mean age at surgery was 6.0 years +/- 3.2 (SD). The mean follow-up was 2.6 +/- 0.6 years. In Group 1, 20 eyes (30.3%) developed visual axis obscuration but only 6 (9.1%) required a secondary procedure. In Group 2, 20 eyes (29.4%) developed visual axis obscuration and 10 (14.7%) required secondary procedures. Posterior synechias were observed in 2 eyes (3.0%) in Group 1 and none in Group 2. Cell deposits were seen in 8 eyes (12.1%) in Group 1 and 8 eyes (11.8%) in Group 2. Haptic compression was noted in 1 eye in Group 2. Mild IOL decentration was observed in the 1 eye with a sulcus-fixated IOL. CONCLUSION: The 1-piece AcrySof IOL provided satisfactory visual axis clarity, produced an acceptable inflammatory response, and maintained centration in pediatric eyes.
机译:目的:评估接受先天性和发育性白内障手术的儿童单件AcrySof SA30AL人工晶状体(IOL)(Alcon Laboratories)植入的手术效果。地点:印度艾哈迈达巴德Raghudeep眼科诊所Iladevi白内障和IOL研究中心。方法:这项前瞻性观察性研究包括84例2至15岁的先天性和发育性白内障手术患儿的134眼。根据手术时孩子的年龄分为两组。 6岁以下儿童(第1组,共66眼)进行了原发性后路连续曲线撕囊术(PCCC),而6岁以上儿童(第2组,共68眼)未进行过PCCC。未进行玻璃体切除术。将AcrySof IOL植入除第1组中的1只接受眼沟固定IOL之外的所有眼睛的袋中。这项研究的主要结局指标是视轴模糊的发生率以及是否需要进行第二次手术来清除视轴。次要观察包括后粘连,细胞沉积和触觉受压的发生率。应用比例测试来确定年龄是否是视轴模糊发展的危险因素。结果:手术的平均年龄为6.0岁+/- 3.2(SD)。平均随访时间为2.6 +/- 0.6年。在第1组中,有20只眼(30.3%)发展为视轴模糊,但仅6只(9.1%)需要进行二次手术。在第2组中,有20眼(29.4%)发生了视轴模糊,而10眼(14.7%)需要进行二次手术。在第1组中有2只眼(3.0%)观察到后粘连,在第2组中没有观察到后粘连。在第1组中有8只眼(12.1%)和在第2组中有8只眼(11.8%)观察到了细胞沉积。第2组中有1只眼。在有沟固定IOL的1只眼中观察到IOL偏低。结论:1片AcrySof IOL可提供令人满意的视轴清晰度,产生可接受的炎症反应,并保持小儿眼睛的集中。

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