American journal of ophthalmology · 2008
Correction of residual hyperopia after cataract surgery using the light adjustable intraocular lens technology.
Клиническое исследованиеСтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Chayet Arturo, Sandstedt Christian A, Chang Shiao H, Rhee Paul, Tsuchiyama Barbara, Schwartz Daniel
Аннотация
PURPOSE: To determine whether residual hyperopia could be corrected postoperatively using the light adjustable lens technology in patients undergoing cataract surgery and light adjustable lens implantation.
DESIGN: Prospective, nonrandomized clinical trial.
METHODS: Fourteen eyes of 14 patients were studied. The manifest refraction, uncorrected visual acuity (UCVA), and best-corrected visual acuity (BCVA) were determined with follow-up time to determine the achieved refractive corrections and their stability.
RESULTS: Of 14 eyes, 13 eyes (92.9%) achieved +/- 0.25 diopters (D) of the target refraction at one day post lock-in, with 100% of the eyes achieving the targeted refractive adjustment within 0.5 D or better up to six months postoperative follow-up. All eyes treated show no change in manifest spherical refraction >0.25 D between one day post lock-in, and three and six months postoperative visits. The data demonstrate the stability of the achieved refractive change after the adjustment and lock-in procedures. The mean rate of change was 0.006 D per month, which is six times more stable than that of refractive procedures.
CONCLUSIONS: Residual hyperopia errors in the range of +0.25 to +2.0 D were successfully corrected with precision and significant improvement in UCVA and without compromising BCVA using the light adjustable intraocular lens technology.
DESIGN: Prospective, nonrandomized clinical trial.
METHODS: Fourteen eyes of 14 patients were studied. The manifest refraction, uncorrected visual acuity (UCVA), and best-corrected visual acuity (BCVA) were determined with follow-up time to determine the achieved refractive corrections and their stability.
RESULTS: Of 14 eyes, 13 eyes (92.9%) achieved +/- 0.25 diopters (D) of the target refraction at one day post lock-in, with 100% of the eyes achieving the targeted refractive adjustment within 0.5 D or better up to six months postoperative follow-up. All eyes treated show no change in manifest spherical refraction >0.25 D between one day post lock-in, and three and six months postoperative visits. The data demonstrate the stability of the achieved refractive change after the adjustment and lock-in procedures. The mean rate of change was 0.006 D per month, which is six times more stable than that of refractive procedures.
CONCLUSIONS: Residual hyperopia errors in the range of +0.25 to +2.0 D were successfully corrected with precision and significant improvement in UCVA and without compromising BCVA using the light adjustable intraocular lens technology.