[A comparative study of rigid gas permeable corneal contact lenses versus frame glasses for refractive correction of postoperative aphakic eyes after congenital cataract surgery in infants and children].

S R Lin, Y H Jiao, J J Cheng, L Z Liu, J P Hu
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Abstract

Objective: The aim of this paper is to compare the refractive correction effects of rigid gas permeable contact lenses (RGPCL) and spectacle correction in children with aphakia after congenital cataract surgery. Methods: This was a prospective non-randomized controlled trial. Children with aphakic eyes after congenital cataract surgery, who underwent vision correction in the Strabismus and Pediatric Ophthalmology Clinic of Beijing Tongren Hospital affiliated with Capital Medical University from April 2012 to November 2019, were continuously collected. Those who voluntarily chose to wear RGPCL for refractive correction were included in the experimental group. Patients with monocular disease were in trial group 1, and patients with binocular disease were in trial group 2. Patients who chose to wear frame glasses for refractive correction were included in the control group. Patients with monocular disease were in control group 1, and patients with binocular disease were in control group 2. Regional origin, medical history, and family information were collected at the first diagnosis. During the follow-up, adverse reactions occurring during the process of wearing glasses were recorded. The Teller acuity card was used for visual examination to obtain the best-corrected visual acuity and convert it into the logarithm of the minimum resolution angle. The degree of nystagmus was determined according to the amplitude and frequency of nystagmus. Treatment cost, treatment compliance, and the reasons for adopting or not adopting RGPCL were analyzed through a questionnaire completed by the parents of children with RGPCL. Results: A total of 203 children (344 eyes) who underwent congenital cataract surgery were included, including 124 males (210 eyes) and 79 females (134 eyes). The age range was 3 to 36 months. There were 28 cases in the experimental group, including 19 cases in trial group 1 and 9 cases in trial group 2. There were 175 cases in the control group, including 43 cases in control group 1 and 132 cases in control group 2. Except for 6 months of age, the visual acuity of the experimental group was better than that of the control group, and the differences were statistically significant (P<0.05). The visual acuity of children in trial group 1 was better than that of children in control group 1 at the same age. Among them, at 12 months of age [1.54 (1.27, 1.97), 1.84 (0.97, 2.12)], 18 months of age [1.27 (0.97, 1.84), 1.84 (0.97, 2.12)], 24 months of age [1.54 (1.27, 1.84), 1.84 (0.97, 2.12)], and 30 months old [0.97 (0.66, 1.27), 1.54 (0.66, 2.12)], the difference was statistically significant (P<0.001). The visual acuity of children in trial group 2 was better than that in control group 2 at the same age. Among them, at 18 months old [1.27 (0.97, 1.54), 1.27 (0.66, 2.12)], 24 months old [0.97 (0.66, 1.27), 1.27 (0.66, 2.12)], and 30 months old [1.27 (0.66, 2.12)], the difference was statistically significant (P<0.05). The remission rate of nystagmus in the experimental group was 8/9 (8 cases), the remission rate of nystagmus in the control group was 34.40% (32 cases), and the exacerbation rate was 29.03% (27 cases). The average annual cost of the experimental group was 25 125 yuan, and that of the control group was 2 511 yuan. Conclusions: RGPCL is a well-tolerated, safe, and effective treatment for infants and young children. The visual acuity and degree of nystagmus were significantly improved in children who wore RGPCL for aphakia refractive correction after congenital cataract surgery compared with spectacle correction.

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[硬性透气角膜接触镜与框架眼镜对婴幼儿先天性白内障术后无晶体眼屈光矫正的比较研究]。
目的:本文旨在比较硬性透气接触镜(RGPCL)和眼镜矫正对先天性白内障术后无晶体眼儿童的屈光矫正效果。方法:这是一项前瞻性非随机对照试验。连续收集2012年4月至2019年11月在首都医科大学附属北京同仁医院斜弱视与小儿眼科门诊接受视力矫正的先天性白内障术后无晶体眼患儿。自愿选择佩戴RGPCL进行屈光矫正的患者被纳入实验组。单眼患者为试验 1 组,双眼患者为试验 2 组。选择佩戴框架眼镜进行屈光矫正的患者被纳入对照组。单眼疾病患者为对照组 1,双眼疾病患者为对照组 2。首次诊断时收集了患者的籍贯、病史和家庭信息。随访期间,记录配戴眼镜过程中出现的不良反应。使用泰勒视力表进行视力检查,以获得最佳矫正视力,并将其转换为最小分辨角的对数。根据眼球震颤的幅度和频率确定眼球震颤的程度。通过 RGPCL 患儿家长填写的调查问卷,对治疗费用、治疗依从性以及采用或不采用 RGPCL 的原因进行了分析。结果:共有 203 名儿童(344 只眼)接受了先天性白内障手术,其中男性 124 名(210 只眼),女性 79 名(134 只眼)。年龄范围为 3 至 36 个月。试验组 28 例,其中试验 1 组 19 例,试验 2 组 9 例;对照组 175 例,其中对照 1 组 43 例,对照 2 组 132 例。除 6 个月的年龄外,试验组的视力均优于对照组,差异有统计学意义(PPP结论:RGPCL 对婴幼儿来说是一种耐受性良好、安全有效的治疗方法。与佩戴眼镜矫正相比,佩戴 RGPCL 矫正先天性白内障术后无晶体眼屈光的儿童的视力和眼球震颤程度均有明显改善。
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来源期刊
中华眼科杂志
中华眼科杂志 Medicine-Ophthalmology
CiteScore
0.80
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0.00%
发文量
12700
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