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METHOD FOR TREATMENT OF PROGRESSIVE MYOPIA AND LENS FOR TREATMENT OF PROGRESSIVE MYOPIA

机译:进行性近视的治疗方法和进行性近视的镜片

摘要

FIELD: medicine.;SUBSTANCE: group of inventions relates to medicine, namely to ophthalmology, and can be used to treat progressive myopia. Determine the patient's various parameters of his eyes. Also various parameters of the lens are determined by the parameters of the patient's eye. According to the parameters of this lens, a lens is manufactured which comprises at least two smoothly transferring central and annular regions on the outer surface. Central region of the lens has a circular shape with a diameter of about 2,000 mcm to about 4,000 mcm and a Y value of the optical power additive at the measurement points. Annular region of the lens, concentric to the central region, has values for the additive to the optical force at the measurement points. Values of Y and y additives are determined by different formulas. Next the lens is put on the patient's eye, combining its central area with the pupil of the patient. Measure the visual acuity of the patient in the lens. After this patient wears a lens during treatment period, lasting from about two months to about six months, during at least his wakefulness. Determine after the end of treatment period, the patient again has the parameters of his eye and the need to continue treatment.;EFFECT: method is effective of treating progressive myopia and the manufacture of an individual lens, which allow creation of a controlled peripheral myopic defocus on the retina of the patient's eye during the entire period of his wakefulness, regardless of the resistance of his cornea, and also to minimize the effect of catarrhal and/or inflammatory diseases on the effectiveness of treatment by obtaining an array of optical power values for each point of the lens optical zone and the parameters of the patient's eye.;4 cl, 1 ex, 1 tbl, 2 dwg
机译:技术领域:一组发明涉及医学,即眼科,并且可以用于治疗进行性近视。确定患者眼睛的各种参数。镜片的各种参数也由患者眼睛的参数确定。根据该镜片的参数,制造出一种镜片,该镜片在外表面上包括至少两个平滑传递的中央和环形区域。透镜的中心区域具有圆形形状,其直径为约2,000mcm至约4,000mcm,并且在测量点处的光焦度添加剂的Y值。与中心区域同心的透镜环形区域在测量点具有与光学力相加的值。 Y和y添加剂的值由不同的公式确定。接下来,将镜片戴在患者的眼睛上,将其中心区域与患者的瞳孔结合在一起。测量患者在镜片中的视敏度。在至少清醒期间,该患者在治疗期间(大约两个月至大约六个月)配戴了晶状体后。确定在治疗期结束后,患者再次具有其眼睛的参数和需要继续治疗的必要条件。效果:该方法可有效治疗进行性近视并制造单个晶状体,从而可产生可控的周边近视不论患者角膜有何抵抗力,在其整个觉醒期间都将焦点转移到患者眼睛的视网膜上,并通过获取一系列屈光度值来最大程度地减少卡他性和/或炎症性疾病对治疗效果的影响对于镜片光学区域的每个点和患者眼睛的参数。; 4 cl,1 ex,1 tbl,2 dwg

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