State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.
Translational Research for Equitable Eye Care, Centre for Public Health, Royal Victoria Hospital, Queen's University, Belfast, United Kingdom.
JAMA Ophthalmol. 2021 Nov 1;139(11):1228-1234. doi: 10.1001/jamaophthalmol.2021.4148.
The conventional 2.2-mm clear corneal incision is relatively narrow compared with the sleeves of Phaco handpieces, resulting in friction at the incision site and increased risk of incision-related Descemet membrane detachment (DMD). The modified 2.2-mm incision only enlarged internal width to 3.0 mm, forming a trapezoid incision shape, which may reduce the friction of surgical instruments and decrease the risk of incisional DMD.
To compare the incidence of incision-related DMD between eyes undergoing modified vs conventional 2.2-mm incision phacoemulsification for hard nuclear age-related cataract.
DESIGN, SETTING, AND PARTICIPANTS: This double-masked, parallel randomized clinical trial was conducted from July 22, 2019, to January 22, 2020, at Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China. The study included patients with age-related cataract and nuclear opalescence grade of 4.0 or greater based on the Lens Opacities Classification System III. Patients were enrolled in this study according to the following inclusion criteria: (1) age between 65 to 90 years; (2) pupil size of 6 mm or greater after dilation; (3) Lens Opacities Classification System III nuclear opalescence grade of 4.0 or more; and (4) corneal endothelial cell density greater than 1500 cells/mm2.
Modified (enlarged internal width to 3.0 mm) or conventional 2.2-mm incision phacoemulsification with intraocular lens implantation.
Incidence of incision-related DMD at postoperative day 1.
A total of 130 eyes of 130 patients were randomized into the conventional group (n = 65) or the modified group (n = 65). The mean (SD) age of participants was 74.5 (5.9) years and 74.3 (6.0) years in the conventional and modified groups, respectively. A total of 26 participants in the conventional group (40%) and 27 in the modified group (42%) were men. Compared with eyes in the conventional group, the incidence of DMD in eyes in the modified group was significantly lower at postoperative day 1 (difference, 26.15; 95% CI, 9.60-42.71; P = .003). The difference at postoperative day 7 was 16.92 (95% CI, 2.91-30.94; P = .02). The length of DMD (postoperative day 1: difference, 0.188; 95% CI, 0.075-0.301; P = .002) and maximal corneal thickness at incision site (postoperative day 1: difference, 0.032; 95% CI, 0.006-0.057; P = .02; postoperative day 7: difference, 0.019; 95% CI, 0.003-0.035; P = .02) were lower in the modified group, while visual quality parameter modulation transfer function (postoperative day 1: difference, -0.033; 95% CI, -0.064 to -0.001; P = .04) was higher. No difference was observed between the 2 groups in best-corrected visual acuity, central corneal endothelium loss, or surgically induced astigmatism at any follow-up time. There were no intraoperative complications in the 2 groups.
These findings suggest that modified 2.2-mm trapezoid incision phacoemulsification reduces the incidence of DMD for hard nuclear age-related cataract at postoperative day 1 and might be considered in patients at high risk of incision-related DMD, although the clinical relevance cannot be determined with certainty from this trial.
ClinicalTrials.gov identifier: NCT04014699.
传统的 2.2 毫米透明角膜切口与超声乳化手柄的套管相比相对较窄,这会导致在切口部位产生摩擦,并增加与切口相关的后弹力层脱离(Descemet membrane detachment,DMD)的风险。改良的 2.2 毫米切口仅将内部宽度扩大到 3.0 毫米,形成一个梯形切口形状,这可能会减少手术器械的摩擦,并降低切口相关 DMD 的风险。
比较改良与传统 2.2 毫米切口白内障超声乳化术治疗硬核年龄相关性白内障的切口相关 DMD 发生率。
设计、设置和参与者:这项双盲、平行随机临床试验于 2019 年 7 月 22 日至 2020 年 1 月 22 日在中山大学中山眼科中心进行。该研究纳入了基于 Lens Opacities Classification System III 的核性白内障 4.0 级或更高级别的年龄相关性白内障患者。根据以下纳入标准招募了本研究的患者:(1)年龄 65 至 90 岁;(2)散瞳后瞳孔直径 6 毫米或以上;(3)Lens Opacities Classification System III 核性白内障 4.0 级或更高;(4)角膜内皮细胞密度大于 1500 个/平方毫米。
改良(内部宽度扩大到 3.0 毫米)或传统 2.2 毫米切口白内障超声乳化术联合人工晶状体植入术。
术后第 1 天切口相关 DMD 的发生率。
共有 130 名患者的 130 只眼被随机分为常规组(n=65)或改良组(n=65)。参与者的平均(标准差)年龄分别为 74.5(5.9)岁和 74.3(6.0)岁。常规组和改良组各有 26 名(40%)和 27 名(42%)男性参与者。与常规组相比,改良组术后第 1 天 DMD 的发生率显著降低(差异,26.15;95%置信区间,9.60-42.71;P=0.003)。术后第 7 天的差异为 16.92(95%置信区间,2.91-30.94;P=0.02)。DMD 长度(术后第 1 天:差异,0.188;95%置信区间,0.075-0.301;P=0.002)和切口处角膜最厚点(术后第 1 天:差异,0.032;95%置信区间,0.006-0.057;P=0.02;术后第 7 天:差异,0.019;95%置信区间,0.003-0.035;P=0.02)在改良组中较低,而视觉质量参数调制传递函数(术后第 1 天:差异,-0.033;95%置信区间,-0.064 至 -0.001;P=0.04)在改良组中较高。在任何随访时间点,2 组的最佳矫正视力、中央角膜内皮细胞丢失或手术诱导的散光均无差异。2 组术中均无并发症。
这些发现表明,改良的 2.2 毫米梯形切口白内障超声乳化术可降低术后第 1 天硬核年龄相关性白内障的 DMD 发生率,对于切口相关 DMD 风险较高的患者可考虑使用该方法,尽管无法从本试验确定其临床相关性。
ClinicalTrials.gov 标识符:NCT04014699。