Yu Mengting, Tang Xianghua, Jiang Jinyun, Zhou Fengqi, Wang Lili, Xiang Chuqi, Hu Yin, Yang Xiao
State Key Laboratory of Ophthalmology Zhongshan Ophthalmic Center Sun Yat-sen University, Guangzhou, China.
Mayo Clinic College of Medicine and Science, Rochester, Minnesota, USA.
J Ophthalmol. 2024 Aug 10;2024:4133686. doi: 10.1155/2024/4133686. eCollection 2024.
To investigate the efficacy and safety of orthokeratology (ortho-k) and repeated low-level red-light (RLRL) therapy in treating poor responders of ortho-k in myopic children.
Study participants were 100 myopic children who completed two years of ortho-k treatment in a retrospective study. In the first year of ortho-k treatment (phase one), they experienced axial elongation of 0.30 mm or greater (defined as poor responders to ortho-k). Children were divided into two groups: the orthokeratology group (OK, = 45) continued to receive ortho-k monotherapy and the combination group (OK-RLRL, = 55) received RLRL in addition to ortho-k for the next year (phase two). Axial elongation over time between the groups was compared.
The mean age, male-to-female ratio, axial length (AL), and axial elongation in phase one were comparable between OK and OK-RLRL groups (all > 0.05). During phase two, significant AL shortening was observed in the OK-RLRL group compared with children in the OK group (-0.10 ± 0.16 mm vs 0.30 ± 0.19 mm, < 0.001). Among these 55 myopic children in the OK-RLRL group, 35 (63.6%), 25 (45.4%), 11 (20%), 6 (10.9%), and 3 (5.4%) of them had AL shortening over 0.05 mm/year, 0.10 mm/year, and 0.20 mm/year, 0.3 mm/year, and 0.4 mm/year, respectively. Older baseline age ( = -0.02), higher treatment compliance ( = -0.462), and AL change at 1 month ( = 1.263) were significantly associated with less AL elongation (all < 0.05).
For poor responders of orthokeratology, RLRL could slow axial elongation in addition to the ortho-k treatment effect. Those who respond poorly to ortho-k with elder age might benefit more from combined therapy.
探讨角膜塑形术(ortho-k)联合重复低强度红光(RLRL)疗法治疗近视儿童角膜塑形术反应不佳者的疗效和安全性。
在一项回顾性研究中,研究参与者为100名完成两年角膜塑形术治疗的近视儿童。在角膜塑形术治疗的第一年(第一阶段),他们的眼轴伸长0.30毫米或更多(定义为角膜塑形术反应不佳者)。儿童被分为两组:角膜塑形术组(OK,n = 45)继续接受角膜塑形术单一疗法,联合治疗组(OK-RLRL,n = 55)在接下来的一年(第二阶段)除角膜塑形术外还接受RLRL治疗。比较两组随时间的眼轴伸长情况。
OK组和OK-RLRL组在第一阶段的平均年龄、男女比例、眼轴长度(AL)和眼轴伸长情况相当(均P>0.05)。在第二阶段,与OK组儿童相比,OK-RLRL组观察到明显的眼轴缩短(-0.10±0.16毫米 vs 0.30±0.19毫米,P<0.001)。在OK-RLRL组的这55名近视儿童中,他们的眼轴每年缩短超过0.05毫米、0.10毫米、0.20毫米、0.3毫米和0.4毫米的人数分别为35名(63.6%)、25名(45.4%)、11名(20%)、6名(10.9%)和3名(5.4%)。基线年龄较大(P = -0.02)、治疗依从性较高(P = -0.462)和1个月时的眼轴变化(P = 1.263)与眼轴伸长较少显著相关(均P<0.05)。
对于角膜塑形术反应不佳者,除角膜塑形术的治疗效果外,RLRL还可减缓眼轴伸长。年龄较大且对角膜塑形术反应不佳者可能从联合治疗中获益更多。