Harrisberg Brian P, Chua Alfred W, Chua Matthew J, Taher Amir
Department of Ophthalmology, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Department of Anesthetics, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Clin Ophthalmol. 2023 Jan 19;17:273-282. doi: 10.2147/OPTH.S396472. eCollection 2023.
To assess the safety and efficacy of primary duet intraocular lens (IOL) procedure using an in-The-bag monofocal IOL and a sulcus-based multifocal reversible platform for cataract surgery. The visual outcomes were compared with a single in-The-bag multifocal IOL.
Retrospective cohort study. Consecutive patients who underwent primary duet IOL procedures were compared with consecutive patients who underwent single multifocal IOL surgery. Primary outcomes were uncorrected distance and near visual acuities (UDVA and UNVA), refraction and spherical equivalent data. Secondary outcomes included surgical complications.
The study group consisted of 32 eyes (22 toric IOLs) whilst the control group had 57 eyes (29 toric IOLs). There were no statistically significant differences between the two groups on post-operative 1-month and 1-year UDVA (=0.1522 and 0.4926, respectively) and UNVA (=0.1248 and 0.2738, respectively). There were no statistically significant differences in the postoperative 1-month spherical equivalent within ± 0.5 diopter (=0.1891). Postoperative intraocular pressure spikes were observed on day-1 in both groups, with most returned to their baseline at 1-month and all were normal at 1-year post surgery. There were no statistically significant differences in intraocular pressure between the two groups on day-1, 1-month and 1-year after surgery (=0.6421). There were no statistically significant differences in the IOL axis deviation from the intended axis in the toric subgroup analysis (=0.5843).
Primary duet IOL procedure is equally effective and safe in correcting distance and near vision when compared with single multifocal IOL in the capsular bag.
评估在白内障手术中使用囊袋内单焦点人工晶状体(IOL)和基于睫状沟的多焦点可逆平台进行原发性双焦点人工晶状体手术的安全性和有效性。将视觉结果与单个囊袋内多焦点人工晶状体进行比较。
回顾性队列研究。将接受原发性双焦点人工晶状体手术的连续患者与接受单焦点多焦点人工晶状体手术的连续患者进行比较。主要结果是未矫正的远距离和近距离视力(UDVA和UNVA)、屈光和球镜等效数据。次要结果包括手术并发症。
研究组包括32只眼(22只散光人工晶状体),而对照组有57只眼(29只散光人工晶状体)。两组术后1个月和1年的UDVA(分别为=0.1522和0.4926)和UNVA(分别为=0.1248和0.2738)无统计学显著差异。术后1个月球镜等效度在±0.5屈光度内无统计学显著差异(=0.1891)。两组均在术后第1天观察到眼内压峰值,大多数在1个月时恢复到基线水平,术后1年时均正常。术后第1天、1个月和1年两组间眼内压无统计学显著差异(=0.6421)。在散光亚组分析中,人工晶状体轴与预期轴的偏差无统计学显著差异(=0.5843)。
与囊袋内单个多焦点人工晶状体相比,原发性双焦点人工晶状体手术在矫正远距离和近距离视力方面同样有效且安全。