Eye Center, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Eye Center, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany; Department of Pediatric Surgery, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Ophthalmology. 2022 Sep;129(9):997-1003. doi: 10.1016/j.ophtha.2022.05.007. Epub 2022 May 17.
To assess the time course of secondary visual axis opacification (VAO) leading to additional surgery after primary intraocular lens (IOL) implantation in children and to describe further surgical outcomes. Comparison of lens types.
Single-center, retrospective analysis of children aged 1 to 14 years who underwent cataract surgery with primary IOL implantation. The surgical technique was either in-bag IOL placement with primary posterior capsulotomy and anterior vitrectomy or bag-in-lens IOL placement. We excluded eyes with visually significant ocular comorbidities.
Total of 135 eyes of 95 children. Of these, 64 had received an acrylic 3-piece IOL, 51 had an acrylic single-piece IOL, and 20 had an acrylic single-piece bag-in-lens IOL. The median ages at surgery were 53 months (interquartile range [IQR], 35-75), 52 months (27-65), and 60 months (40-84) in the 3-piece, 1-piece, and bag-in-lens groups, respectively.
Analysis of medical records. We used the Kaplan-Meier method and a Cox proportional hazards model with predefined adjustments for age at surgery, year of surgery, and the German Index of Socioeconomic Deprivation (score by postal code) to analyze VAO-free survival by lens type. Patients were invited to attend a clinical visit to achieve longer follow-ups.
The rate of survival without VAO that required clearing of the visual axis after cataract surgery with primary IOL implantation. Any other surgical complications.
The overall median follow-up was 19 months (IQR, 3-58). There were 13 cases of VAO, occurring at a median of 10 months (IQR, 10-12) after surgery. Of these, 1 eye had a 3-piece in-bag IOL, 10 eyes had 1-piece in-bag IOLs, and 2 eyes had bag-in-lens IOLs. The adjusted hazard ratio was 32.8 (95% confidence interval [CI], 3.3-327, P = 0.003) for 1-piece acrylic IOLs and 19.6 (CI, 1.22-316, P = 0.036) for bag-in-lens IOLs, compared with 3-piece acrylic in-bag IOLs. Two eyes with bag-in-lens surgery (10%) had an iris capture. There was 1 case of endophthalmitis. We found no cases of postoperative retinal detachment or new glaucoma.
Children with secondary VAO who required a procedure to clear the visual axis generally presented within 15 months. Opacification rates were lowest when a 3-piece acrylic IOL was used.
评估儿童原发性人工晶状体(IOL)植入术后继发性第二视觉轴混浊(VAO)导致额外手术的时间过程,并描述进一步的手术结果。晶状体类型的比较。
对在 1 至 14 岁儿童中进行白内障手术并植入原发性 IOL 的患者进行单中心回顾性分析。手术技术为袋内 IOL 放置联合原发性后囊切开术和前段玻璃体切除术,或袋内晶状体 IOL 放置。我们排除了存在明显眼部合并症的眼睛。
共 95 名儿童的 135 只眼。其中,64 只眼接受了丙烯酸 3 件式 IOL,51 只眼接受了丙烯酸单件式 IOL,20 只眼接受了丙烯酸单件式袋内晶状体 IOL。3 件式、1 件式和袋内晶状体组的手术年龄中位数分别为 53 个月(四分位距 [IQR],35-75)、52 个月(27-65)和 60 个月(40-84)。
分析病历。我们使用 Kaplan-Meier 方法和 Cox 比例风险模型,根据手术时的年龄、手术年份和德国社会经济剥夺指数(按邮政编码评分)进行了预设调整,按晶状体类型分析 VAO 无生存情况。邀请患者参加临床就诊以实现更长的随访。
原发性 IOL 植入术后白内障手术无 VAO 清除要求的生存率。任何其他手术并发症。
总体中位随访时间为 19 个月(IQR,3-58)。有 13 例 VAO,术后中位数为 10 个月(IQR,10-12)发生。其中,1 只眼为 3 件式袋内 IOL,10 只眼为 1 件式袋内 IOL,2 只眼为袋内晶状体 IOL。调整后的风险比为 32.8(95%置信区间 [CI],3.3-327,P=0.003),用于 1 件式丙烯酸 IOL,19.6(CI,1.22-316,P=0.036),用于袋内晶状体 IOL,与 3 件式丙烯酸袋内 IOL相比。接受袋内晶状体手术的 2 只眼(10%)发生虹膜嵌顿。有 1 例眼内炎。我们没有发现术后视网膜脱离或新发生青光眼的病例。
需要清除视觉轴的继发性 VAO 儿童通常在 15 个月内出现。使用 3 件式丙烯酸 IOL 时混浊率最低。