Dichoptic Rescue for Spectacle-Flip Sabotage of Anisometropic Amblyopia Therapy

Robert W Arnold
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Abstract

Background: To be successful, amblyopia therapeutic techniques must respond when ingenious (shrewd) amblyopic children sabotage treatment effect by discovering ways(1) to alter those therapy aspects they find frustrating. Methods: Her guardian consented to IRB-approved study outside typical FDA enrollment guidelines for CureSight dichoptic therapy. Acuity (EVA) and stereopsis was by PEDIG protocols. Results: A 6-year-old rural Alaska native girl in foster care had previously been diagnosed with anisometropic amblyopia and treated with spectacles and patching but had poor compliance with BCVA 0.9–1.0 logMAR. She demonstrated exceptional creativity and hyperactivity but had no other medical issues. Atropine was prescribed in addition to her spectacles +5.50+1.00x90 and +0.50+1.00x90, but the patient discovered the rare “Spectacle Flip” method that sabotaged therapeutic impact. She had EVA enrollment acuities of logMAR 0.9 right and −0.1 left with stereo 400 seconds of arc. After just one month dichoptic therapy 1.5 hours 6 days per week, acuity improved to logMAR 0.7 and −0.1 with stereo up to 140 second of arc. Four months later acuity was 0.6 right and −0.2 left. Stereoacuity improved from 400 to 200 arc seconds. Conclusion: Even when conventional compliance methods fail, dichoptic therapy with eye-tracking has the novel and unique potential to improve amblyopia treatment compliance with real-time monitored fixation compliance and confirmation of correct spectacle wear. Clinical Trial Registration: NCT06165705. Plain Language Summary: Dichoptic therapy with eye-tracking improved compliance and achieved de novo acuity and stereo gains in a girl with severe refractory anisometropic amblyopia compounded by the rare complication of topical atropine therapy called “spectacle-flip sabotage”
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眼镜翻转破坏各向异性弱视治疗的二向异性挽救方法
背景:弱视治疗技术要想取得成功,就必须对聪明(精明)的弱视儿童破坏治疗效果的行为做出反应,他们会想方设法(1) 改变那些他们认为令人沮丧的治疗方面。方法:她的监护人同意在美国食品药品管理局(FDA)典型的 CureSight 二向疗法注册指南之外进行 IRB 批准的研究。视敏度(EVA)和立体视采用 PEDIG 方案。结果:一名寄养在阿拉斯加州农村的 6 岁女孩以前曾被诊断为各向异性弱视,并接受过眼镜和视力矫正治疗,但 BCVA 0.9-1.0 logMAR 的依从性很差。她表现出超常的创造力和多动症,但没有其他疾病。除了+5.50+1.00x90和+0.50+1.00x90的眼镜外,医生还给她开了阿托品,但患者发现了罕见的 "眼镜翻转 "方法,从而破坏了治疗效果。她的 EVA 注册视力为右 0.9 logMAR 和左 -0.1,立体 400 秒弧。仅一个月后,她接受了每周 6 天、每次 1.5 小时的二分法治疗,视力分别提高到 0.7 和-0.1,立体视弧度达到 140 秒。四个月后,右眼视力为 0.6,左眼视力为-0.2。立体清晰度从 400 弧秒提高到 200 弧秒。结论:即使传统的依从性方法失效,采用眼动跟踪技术的二分法疗法也具有新颖独特的潜力,可通过实时监测固定依从性和确认正确佩戴眼镜来提高弱视治疗的依从性。临床试验注册:NCT06165705。白皮书摘要:对于一名患有严重难治性各向异性弱视并伴有被称为 "眼镜翻转破坏 "的外用阿托品治疗罕见并发症的女孩,采用眼动跟踪的二分法疗法提高了其治疗依从性,并重新获得了视力和立体感。
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Effectiveness of Mp-3 Microperimetric Biofeedback Fixation Training For Low Vision Rehabilitation in Patients Treated With Corticosteroid Ivt in Retinal Vein Occlusions Corneal Characteristics of Myopic Malay School Children and Their Association with Axial Length Dichoptic Rescue for Spectacle-Flip Sabotage of Anisometropic Amblyopia Therapy Effect of Contact Lens Solutions in Stabilizing the Activity of Tear Lysozyme [Letter]
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