首页> 外文期刊>Ophthalmology >Therapeutic benefits of infrared (810-nm) diode laser macular grid photocoagulation in prophylactic treatment of nonexudative age-related macular degeneration: two-year results of a randomized pilot study.
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Therapeutic benefits of infrared (810-nm) diode laser macular grid photocoagulation in prophylactic treatment of nonexudative age-related macular degeneration: two-year results of a randomized pilot study.

机译:红外(810-nm)二极管激光黄斑栅格光凝术在预防与年龄相关的非渗出性黄斑变性中的治疗作用:一项随机试验研究的两年结果。

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OBJECTIVE: This pilot study collected preliminary information on the effectiveness and safety of infrared (810-nm) diode laser macular grid photocoagulation in patients with nonexudative age-related macular degeneration (AMD). Results from this pilot study were used in designing a larger, multicenter, randomized clinical trial. DESIGN: A multicenter, randomized, controlled, clinical trial. PARTICIPANTS: A total of 229 eyes of 152 patients with AMD were enrolled in the pilot study. Seventy-five patients with 1 eye eligible (75 eyes) were enrolled in the unilateral arm of the study; 77 patients with both eyes eligible (154 eyes) were enrolled in the bilateral arm of the study. In the unilateral study arm, 32 eyes were randomized to the observation group, 27 eyes were treated with visible endpoint burns, and 16 eyes were treated with invisible endpoint (subthreshold) lesions. In the bilateral study arm, 77 eyes were in the observation group, 36 eyes were treated with visible burns, and 41 eyes were treated with subthreshold (invisible) lesions. INTERVENTION: Eyes were treated with infrared (810-nm) diode laser macular grid photocoagulation using either visible burns or subthreshold (invisible) lesions and compared to eyes receiving no treatment. MAIN OUTCOME MEASURES: Reduction of drusen, change in visual acuity, and rate of choroidal neovascularization (CNV) membrane formation. RESULTS: At 12 months after treatment, 62% of eyes treated with visible burns had a clinically significant reduction in drusen, whereas this proportion (65%) was reached in 18 months for eyes treated with subthreshold lesions. At 24 months' follow-up, treated eyes had a significant reduction in drusen compared to observation eyes (P < 0.0001). Visual acuity was significantly improved in treated eyes at 12, 18, and 24 months compared to observation eyes (P < 0.001). Choroidal neovascularization formation was similar in treated and observation eyes through 24 months' follow-up. Complications included CNV associated with six eyes treated with visible burns and a juxtafoveal laser scar in one eye treated with visible burns. CONCLUSIONS: Infrared (810-nm) diode laser macular grid photocoagulation in patients with nonexudative AMD significantly reduces drusen levels (P < 0.0001) and significantly improves visual acuity (P < 0.001) when either visible endpoint burns or subthreshold endpoint lesions are used. Complications were fewer using subthreshold endpoint lesions. A larger, multicenter, prospective clinical trial with longer follow-up is needed to determine the efficacy of treatment in reducing the rate of CNV formation. Data from this clinical pilot study have been used to design the Prophylactic Treatment of AMD Trial (PTAMD), a multicenter, randomized, prospective clinical trial currently in progress comparing subthreshold (invisible) treatment to observation in eyes with nonexudative AMD.
机译:目的:这项初步研究收集了有关红外(810 nm)二极管激光黄斑栅格光凝治疗非渗出性年龄相关性黄斑变性(AMD)患者的有效性和安全性的初步信息。该初步研究的结果用于设计更大的多中心随机临床试验。设计:一项多中心,随机,对照的临床试验。参与者:152名AMD患者中的229只眼共纳入了该初步研究。该研究的单侧臂纳入了75只1眼合格(75眼)的患者。该研究的双侧臂入选了77例双眼合格的患者(154眼)。在单侧研究组中,将32眼随机分为观察组,对27眼进行了可见的终点烧伤治疗,对16眼进行了对不可见的终点(阈下)病变的治疗。在双边研究组中,观察组有77眼,有可见烧伤的有36眼,有阈下(不可见)病变的有41眼。干预措施:使用可见光灼伤或亚阈值(不可见)病变,使用红外(810-nm)二极管激光黄斑栅格光凝治疗眼睛,并与未接受治疗的眼睛进行比较。主要观察指标:减少玻璃疣,视力改变和脉络膜新血管形成(CNV)膜形成率。结果:在治疗后12个月,有62%的可见烧伤治疗的眼睛的玻璃膜疣临床上显着减少,而在亚阈值病变治疗的眼中,在18个月内达到了这一比例(65%)。在24个月的随访中,与观察眼相比,治疗眼的玻璃膜疣明显减少(P <0.0001)。与观察眼相比,经治疗的眼在第12、18和24个月时的视力显着改善(P <0.001)。经过24个月的随访,治疗眼和观察眼的脉络膜新生血管形成相似。并发症包括与六眼经可见烧伤治疗的眼睛相关的CNV,以及在一眼经可见烧伤治疗的眼睛的近凹凹痕。结论:对于非渗出性AMD患者,红外(810-nm)二极管激光黄斑栅格光凝术可显着降低玻璃疣水平(P <0.0001),并显着改善视敏度(P <0.001),无论是使用可见终点灼伤还是低于阈下终点的病灶。使用亚阈值以下终点病变的并发症更少。需要更大的,多中心的,具有更长随访时间的前瞻性临床试验,以确定治疗在降低CNV形成率方面的功效。来自该临床试验研究的数据已用于设计AMD预防性治疗试验(PTAMD),这是一项正在进行的多中心,随机,前瞻性临床试验,目前正在比较阈下(无形)治疗与非渗出性AMD眼睛的观察。

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