The Royal United Hospital Bath NHS Trust, Bath, UK.
Acta Ophthalmol. 2020 Sep;98(6):e743-e746. doi: 10.1111/aos.14368. Epub 2020 Feb 3.
To determine whether horizontal orientation of the intraocular lens optic-haptic junctions has an effect on the incidence of pseudophakic negative dysphotopsia.
Single-centre prospective double-masked randomized controlled trial. 220 eyes of 201 participants undergoing routine cataract surgery were randomized to receive their intraocular lens either orientated with the optic-haptic junctions at 180° ('horizontal') or without manipulation following implantation (control). Patients were excluded according to age (<19 and > 99 years), coexisting eye disease affecting visual function and insufficient cognitive function to complete the study. In the fourth postoperative week, a telephone interview was conducted to determine rates of negative dysphotopsia. The data were analysed to provide the relative risk of negative dysphotopsia with horizontal orientation of the intraocular lens (IOL) optic-haptic junctions compared with standard treatment.
Orientating the IOL optic-haptic junctions horizontally halved the incidence of pseudophakic negative dysphotopsia in the fourth postoperative week (9/110 in the intervention group; 18/110 in the control group; RR: 0.50, 95% confidence interval: 0.235-1.064, p = 0.072). The overall incidence of negative dysphotopsia was 12.2% (27/220 participating eyes). No intraoperative adverse effects of intraocular lens rotation were reported.
The simple intraoperative manoeuvre of rotating the intraocular lens to orientate the optic-haptic junctions at 180° may be a safe and effective measure to reduce the risk of developing postoperative pseudophakic negative dysphotopsia in the first postoperative month. This is the first report that demonstrates the benefit of horizontal optic-haptic junction positioning to be sustained beyond the first postoperative day.
确定人工晶状体光学-机械连接部的水平方向是否会影响后发性负性像差的发生率。
单中心前瞻性双盲随机对照试验。201 名患者的 220 只眼接受常规白内障手术,随机分为将人工晶状体的光学-机械连接部定向为 180°(“水平”)或在植入后不进行操作(对照组)。根据年龄(<19 岁和>99 岁)、影响视觉功能的并存眼病和完成研究的认知功能不足,排除患者。术后第 4 周进行电话访谈以确定负性像差的发生率。对数据进行分析,以提供人工晶状体光学-机械连接部水平定向与标准治疗相比发生负性像差的相对风险。
在术后第 4 周,人工晶状体光学-机械连接部水平定向将后发性负性像差的发生率减半(干预组 9/110;对照组 18/110;RR:0.50,95%置信区间:0.235-1.064,p=0.072)。负性像差的总发生率为 12.2%(27/220 只参与眼)。未报告人工晶状体旋转的术中不良影响。
在术中简单地旋转人工晶状体以将光学-机械连接部定向为 180°可能是一种安全有效的措施,可以降低术后第一个月发生后发性负性像差的风险。这是第一项表明水平光学-机械连接部定位的益处可持续超过术后第 1 天的报告。