A Novel Intraocular Lens and Capsular Bag Complex Suspension Technique for Repositioning Late In-the-Bag Intraocular Lens Dislocation.

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2026-10-01 eCollection Date: 2026-01-01 DOI:10.2147/OPTH.S618477
Yingyan Ma, Baojiang Li
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Abstract

Purpose: To present a novel in situ scleral suspension surgical technique for the management of dislocated intraocular lens (IOL)-capsular bag complex and to evaluate its clinical efficacy.

Patients and methods: Patients who underwent the novel in situ scleral suspension technique for in-the-bag IOL dislocation at the Department of Ophthalmology, Shanghai General Hospital, between February 2024 and February 2025, were included. The technique involves performing a scleral puncture 3 mm posterior to the limbus, passing a single suspensory suture twice through the fibrotic capsular tissue of the dislocated IOL-capsular bag complex, and securing the suture to the sclera with a single knot. Preoperative and postoperative uncorrected distance visual acuity (UDVA) and best-corrected visual acuity (BCVA), as well as adverse events, were recorded.

Results: A total of 8 eyes from 8 patients were included. The median preoperative uncorrected distance visual acuity (UDVA), expressed as the logarithm of the minimum angle of resolution (logMAR), was 1.3 (range, 1.0-2.0), improving to 0.56 (range, 0-2.3) at the final follow-up. During the postoperative follow-up period (1 month to 1 year), transient ocular hypertension and uveitis occurred in one patient each, with no other significant adverse events observed, including IOL tilt, decentration, pupillary capture, suture exposure, or vision-threatening macular edema.

Conclusion: This novel in situ suspension technique for in-the-bag IOL dislocation demonstrates enhanced postoperative uncorrected distance visual acuity, a favourable short-term safety profile, simplified procedural steps with minimally tissue trauma, independence from the type of dislocated IOL, and no requirement for specialized instruments or bio-materials. Future studies with extended follow-up are warranted to validate its long-term efficacy and safety.

一种新型人工晶状体-囊袋复合悬浮技术治疗晚期袋内人工晶状体脱位。
目的:介绍一种原位巩膜悬吊术治疗脱位人工晶状体-囊袋复合体的新方法,并评价其临床疗效。患者和方法:纳入于2024年2月至2025年2月在上海总医院眼科接受新型原位巩膜悬吊技术治疗袋内人工晶状体脱位的患者。该技术包括在角膜缘后方3mm处进行巩膜穿刺,在脱位的人工晶状体-囊袋复合体的纤维化囊组织中两次使用单个悬吊缝线,并用单个结将缝线固定在巩膜上。记录术前、术后未矫正距离视力(UDVA)、最佳矫正视力(BCVA)及不良事件。结果:共纳入8例患者8只眼。术前未矫正距离视力(UDVA)中位数,以最小分辨角(logMAR)的对数表示,为1.3(范围1.0-2.0),在最终随访时改善至0.56(范围0-2.3)。术后随访1个月~ 1年,1例患者出现短暂性高眼压和葡萄膜炎,未见其他明显不良事件,包括IOL倾斜、脱位、瞳孔捕获、缝线暴露或威胁视力的黄斑水肿。结论:这种新颖的原位悬浮技术用于袋式人工晶状体脱位,可提高术后未矫正距离视力,具有良好的短期安全性,简化了手术步骤,组织损伤最小,与脱位的人工晶状体类型无关,不需要专门的器械或生物材料。未来的研究需要延长随访时间以验证其长期疗效和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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