From the Department of Ophthalmology, Saarland University Medical Center, Homburg/Saar, Germany (Sabau, Daas, Flockerzi, Seitz); Medical Biometrics, Epidemiology and Health Informatics Institute, Homburg/Saar, Germany (Behkit, Wagenpfeil); Institute of Experimental Ophthalmology, Saarland University, Homburg/Saar, Germany (Langenbucher); Department of Ophthalmology, Medical University of Graz, Graz, Austria (Ardjomand).
J Cataract Refract Surg. 2021 May 1;47(5):634-640. doi: 10.1097/j.jcrs.0000000000000487.
To evaluate the efficacy, safety, and predictability of transepithelial photorefractive keratectomy (TransPRK) for correcting myopia, astigmatism, and hyperopia.
Department of Ophthalmology, Saarland University Medical Center, Homburg/Saar, Germany.
Meta-analysis of retrospective or prospective studies.
Relevant studies were collected from Medline and included when meeting the following predefined criteria: randomized controlled trials, at least 1 of the main outcome measures as efficacy, safety, or predictability, and 1 common TransPRK laser (Schwind Amaris). The parameters estimates and 95% CI were derived from random-effects meta-analysis to account for possible heterogeneity.
Because hyperopia studies did not meet the inclusion criteria, the results are centered on myopia and astigmatism. Sixteen studies with a total of 1924 treated eyes were included in the meta-analysis. The mean efficacy, safety, and predictability had a probability of 94% (CI, 0.86-0.97), 0% (CI, 0.00-0.03), and 89% (CI, 0.82-0.93), respectively. The mean correction index, difference vector, and index of success had a value of 1.01 (CI, 1.01-1.02), 0.20 (CI, 0.06-0.34), and 0.12 (CI, 0.07-0.18), respectively.
This summary estimate showed that TransPRK was highly effective, safe, and predictable in correcting myopia and/or astigmatism.
评估经上皮准分子激光角膜切削术(TransPRK)矫正近视、散光和远视的疗效、安全性和可预测性。
德国萨尔兰大学医学中心眼科。
回顾性或前瞻性研究的荟萃分析。
从 Medline 收集相关研究,并在符合以下预设标准的情况下纳入:随机对照试验,主要结局指标至少有 1 个为疗效、安全性或可预测性,且使用 1 种常见的 TransPRK 激光(Schwind Amaris)。参数估计值和 95%置信区间采用随机效应荟萃分析得出,以考虑可能的异质性。
由于远视研究不符合纳入标准,因此结果主要集中在近视和散光上。荟萃分析共纳入 16 项研究,共计 1924 只治疗眼。平均疗效、安全性和可预测性的概率分别为 94%(CI,0.86-0.97)、0%(CI,0.00-0.03)和 89%(CI,0.82-0.93)。平均矫正指数、差异向量和成功率指数分别为 1.01(CI,1.01-1.02)、0.20(CI,0.06-0.34)和 0.12(CI,0.07-0.18)。
该汇总估计表明,TransPRK 治疗近视和/或散光高度有效、安全且可预测。