激光或抗血管内皮生长因子单药治疗早产儿视网膜病变屈光不正

Tayyebeh Davabi, Afsar Farahani, Mohamad Ghasemi Broumand, Elham Ashrafi, Mehdi Yaseri
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引用次数: 0

摘要

背景:早产儿视网膜病变(ROP)治疗的婴儿可能出现明显的屈光不正。在这项研究中,我们报告了使用激光或抗vegf单药治疗需要治疗的ROP的早产儿的治疗前屈光不正,并比较了两个治疗组在不同随访时间点的治疗后屈光不正值的组成。 方法:在这项回顾性队列研究中,我们分析了2020年3月至2021年4月在伊朗德黑兰法拉比眼科医院转诊的181名需要治疗的ROP早产儿的360只眼睛。360只眼中,195只接受激光单药治疗(激光治疗组),165只接受玻璃体内抗vegf注射(抗vegf治疗组)。所有纳入的眼睛在治疗前和治疗后都进行了单眼麻痹性屈光。通过在每只眼睛内灌注含有1%托品酰胺、2.5%苯肾上腺素和0.5%丁卡因(等体积)的混合滴眼液三次,每隔5分钟引起每个婴儿的单眼麻痹。第三次滴注后30分钟进行睫状体麻痹屈光检查。 结果:新生儿平均胎龄(GA)为29.0(2.0)周,出生体重(BW)为1241.0 (403.0)g。整个研究队列的男女比例为107(59.1%)/ 74(40.9%),而抗vegf治疗组和激光治疗组的男女比例分别为47(56.6%)/ 36(43.4%)和60(61.2%)/ 38(38.8%)。治疗前评估显示远视218只(60.6%),近视眼112只(31.1%),远视30只(8.3%)。抗vegf治疗组远视87只(52.7%)眼,近视63只(38.2%)眼,远视15只(9.1%)眼。激光治疗组远视131只(67.2%),近视眼49只(25.1%),远视15只(7.7%)。1周、1个月、1 gt时的平均球面屈光不正(SD)和球面等效屈光不正(SEQ);治疗后6个月随访时间点;治疗后3个月时间点的平均柱形屈光不正;两组间ROP回归时SEQ均值差异均有统计学意义(P <0.05)。在治疗后6个月的随访时间点,屈光参差率从基线时的3.4%显著增加到9.2% (P <0.05)强生# x0D;结论:在本研究中,所有纳入治疗所需ROP的眼和各治疗组中最常见的治疗前屈光状态是远视,其次是近视和远视。在治疗后6个多月的随访中,睫状体麻痹性屈光显示激光治疗的眼睛明显比抗vegf治疗的眼睛远视,这一发现与治疗前的屈光结果相似。需要对同一队列进行更长的随访期和对照组的进一步研究,以确定每种治疗方式对治疗ROP的儿童屈光状态的实际影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Refractive errors in infants with retinopathy of prematurity treated using laser or anti-vascular endothelial growth factor monotherapy
Background: Infants treated for retinopathy of prematurity (ROP) could develop visually significant refractive errors. In this study, we report pre-treatment refractive errors in premature infants with treatment-requiring ROP treated using laser or anti-VEGF monotherapy and compare the components of post-treatment refractive error values between the two treatment groups at different follow-up timepoints. Methods: In this retrospective cohort study, we analyzed 360 eyes of 181 premature infants with treatment-requiring ROP who were referred to Farabi Eye Hospital, Tehran, Iran between March 2020 and April 2021. Of the 360 eyes, 195 received laser monotherapy (laser treatment group) and 165 received an intravitreal anti-VEGF injection (anti-VEGF therapy group). All included eyes underwent pre- and post-treatment cycloplegic refraction. Cycloplegia was induced for each infant by instilling a mixed eye drop containing 1% tropicamide, 2.5% phenylephrine, and 0.5% tetracaine (in equal volumes) in each eye three times at five-minute intervals. Cycloplegic refraction was performed 30 minutes after the third instillation. Results: The mean (standard deviation [SD]) gestational age (GA) and birth weight (BW) of the infants were 29.0 (2.0) weeks and 1241.0 (403.0) g, respectively. The male-to-female ratio in the entire study cohort was 107 (59.1%) / 74 (40.9%), whereas the ratios in the anti-VEGF therapy group and laser treatment group were 47 (56.6%) / 36 (43.4%) and 60 (61.2%) / 38 (38.8%), respectively. The pre-treatment assessment revealed that 218 (60.6%) eyes were hyperopic, 112 (31.1%) were myopic, and 30 (8.3%) were emmetropic. In the anti-VEGF therapy group, 87 (52.7%) eyes were hyperopic, 63 (38.2%) were myopic, and 15 (9.1%) were emmetropic. In the laser treatment group, 131 (67.2%) eyes were hyperopic, 49 (25.1%) were myopic, and 15 (7.7%) were emmetropic. The mean (SD) spherical refractive error and spherical equivalent of refractive error (SEQ) at the 1-week, 1-month, and > 6-month post-treatment follow-up timepoints; the mean cylindrical refractive error at the 3-month post-treatment timepoint; and the mean SEQ at the time of ROP regression were significantly different between the treatment groups (all P < 0.05). The rate of anisometropia increased significantly from 3.4% at baseline to 9.2% at the 6-month post-treatment follow-up timepoint (P < 0.05). Conclusions: In this study, the most common pre-treatment refractive status of all included eyes with treatment-requiring ROP and eyes in each treatment group was hyperopia, followed by myopia and emmetropia. At the more than 6-month post-treatment follow-up, cycloplegic refraction revealed that the laser-treated eyes were significantly more hyperopic than the anti-VEGF-treated eyes, a finding similar to the pre-treatment refraction results. Further studies of same cohort with a longer follow-up period and a control group are needed to determine the real-world effect of each treatment modality on the refractive statuses of children treated for ROP.
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