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Primary IOL implantation in children: a risk analysis of foldable acrylic v PMMA lenses

机译:儿童原发性人工晶状体植入:可折叠丙烯酸v PMMA镜片的风险分析

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摘要

>Background/aims: To compare the relative risks of poly (methylmethacrylate) (PMMA) and soft acrylic (AcrySof) primary intraocular lens (IOL) implantation in paediatric cataract surgery.>Methods: A retrospective analysis of clinical data was performed on eyes of 61 infants and children who underwent cataract surgery with primary IOL implantation. Age at operation ranged from 3 weeks to 15 years. Mean follow up duration was 24.5 months (range 0.5–68 months). Factors examined included type of IOL (PMMA, acrylic), performance of a primary posterior continuous curvilinear capsulorhexis (PCCC) or capsulotomy with limited anterior vitrectomy, perioperative complications, and subsequent intervention for posterior capsule opacification (PCO). Risk factors for perioperative complications were examined with 2×2 tables to give odds ratios (OR) as measures of association. A survival analysis was performed to assess risk of subsequent intervention for PCO with different IOL types. Relative risks (hazards) and confidence intervals (CI) were calculated with Cox regression to adjust for potential confounding.>Results: Compared to acrylic, PMMA IOLs were significantly associated with perioperative complications (OR 5.2, 95% CI 1.4 to 19, p = 0.01). However, IOL and type of section were highly correlated factors, and this finding may reflect risks associated with larger scleral wounds used for PMMA IOLs. No statistically significant difference in risk of subsequent intervention for PCO was found between different IOL types. Mean times till intervention for PMMA and acrylic IOLs were 30.1 months (95% CI 22 to 38) and 19.8 months (95% CI 12 to 27) respectively (log rank test statistic 1.53, one degree of freedom, p = 0.22). At 12 months post-implant surgery, 76% (95% CI 59 to 93) of PMMA cases and 54% (95% CI 35 to 72) of acrylic cases had not required intervention for PCO; these proportions fell to 55% (95% CI 35 to 75) and 38% (95% CI 14 to 61) for PMMA and acrylic cases respectively at 2 years post-surgery. After adjustment for age at surgery, primary posterior capsulorhexis, and perioperative complications relative risk of intervention after acrylic IOL implantation was 1.6 (95% CI 0.66 to 3.9, p = 0.29).>Conclusion: Primary implantation of foldable soft acrylic IOLs in paediatric eyes may allow fewer perioperative complications than rigid PMMA IOLs. Short term safety profiles of primary implantation in paediatric cataract surgery are otherwise comparable for PMMA and soft acrylic IOLs.
机译:>背景/目的:比较小儿白内障手术中聚甲基丙烯酸甲酯(PMMA)和丙烯酸软质(AcrySof)人工晶状体(IOL)植入的相对风险。>方法:对61例初次人工晶体植入白内障手术的婴儿和儿童的眼睛进行了临床资料的回顾性分析。手术年龄从3周到15岁不等。平均随访时间为24.5个月(范围0.5-68个月)。检查的因素包括人工晶体的类型(PMMA,丙烯酸树脂),原发性后路连续弯曲撕囊术(PCCC)或前房玻璃体切除术受限的囊切开术,围手术期并发症以及随后的后囊混浊干预(PCO)。用2×2表检查围手术期并发症的危险因素,以比值比(OR)作为关联的度量。进行了生存分析,以评估随后对不同IOL类型的PCO进行干预的风险。 >结果:与丙烯酸相比,PMMA IOL与围手术期并发症显着相关(OR 5.2,95%CI),采用Cox回归计算相对风险(危险)和置信区间(CI)。 1.4至19,p = 0.01)。但是,IOL和切片类型是高度相关的因素,这一发现可能反映出与用于PMMA IOL的较大巩膜伤口相关的风险。在不同的IOL类型之间,未发现PCO后续干预风险的统计学差异。直到进行干预,PMMA和丙烯酸类人工晶体的平均时间分别为30.1个月(95%CI为22至38)和19.8个月(95%CI为12至27)(对数秩检验统计量为1.53,一自由度,p = 0.22)。植入术后12个月,不需要进行PCO干预的PMMA病例为76%(95%CI为59至93)和54%(95%CI为35至72)。术后2年,PMMA和丙烯酸树脂病例的这些比例分别降至55%(95%CI 35至75)和38%(95%CI 14至61)。调整手术年龄,原发性后囊撕脱和围手术期并发症后,丙烯酸类人工晶体植入后的相对介入风险为1.6(95%CI 0.66至3.9,p = 0.29)。>结论:与刚性PMMA IOL相比,小儿眼中的丙烯酸软质IOL可能会减少围手术期并发症。小儿白内障手术中一次植入的短期安全性在其他方面与PMMA和丙烯酸软性IOL相当。

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