Efficacy and safety of ultrasound cycloplasty as the first treatment in glaucoma for eyes with functional vision: A 1-year prospective study

IF 4.5
Dingqiao Wang , Zhihong Huang , Yanlin Li , Shaoyang Zheng , Ni Guo , Huanyang Shi , Lin Jin , Yixiu Lin , Jian Ge , Mingkai Lin , Chengguo Zuo
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Abstract

Objective

Ultrasound cycloplasty (UCP) is a non-invasive treatment traditionally used for advanced glaucoma. However, its potential as the first surgical option for moderate glaucoma with functional vision has not been thoroughly investigated. This study aimed to assess the effectiveness and safety of UCP as the initial surgery for glaucoma with residual visual function.

Methods

This prospective study included 117 glaucoma patients (63 males, 54 females; mean age 48.3 ​± ​17.2 years) with various glaucoma subtypes and best-corrected visual acuity (BCVA) better than 1.30 logMAR who underwent UCP as their first treatment. The primary outcomes were the surgical success rates at 12 months for both qualified and complete success. Qualified success was defined as a ≥20% reduction in intraocular pressure (IOP) from baseline, IOP between 6 and 21 mmHg, and no additional glaucoma surgery, achieved with or without anti-glaucoma medication. Complete success was defined by the same criteria, but achieved without any anti-glaucoma medications. Secondary outcomes included mean IOP, BCVA, and postoperative complications.

Results

The qualified success rate of UCP as the first treatment was 71.8% at 12 months, with a complete success rate (medication-free) of 27.4%. Subgroup analysis revealed that PACG had the highest qualified success rate (84.8%), followed by POAG (73.0%) and NVG (66.7%). Patients with ≤0.30 logMAR achieved the highest rate (80.0%), followed by those with 0.30-0.50 logMAR (75.0%), 0.50-1.00 logMAR (66.7%), and 1.00-1.30 logMAR (63.6%). The overall mean BCVA showed minimal change from 0.62 ​± ​0.42 logMAR at baseline to 0.63 ​± ​0.43 logMAR at 1 year. Patients experienced initial visual acuity decline in the early postoperative period, which gradually recovered after 1 week. Only 2.6% (3/117) of patients experienced a clinically significant visual decline of more than 2 lines at 12-month follow-up. No severe complications were observed.

Conclusions

UCP can be an effective and safe option as the first surgical treatment for glaucoma patients with visual function. UCP significantly reduces IOP over 12 months without causing significant visual acuity decline or severe complications.
超声睫状体成形术作为功能性视力青光眼的首选治疗方法的有效性和安全性:一项为期1年的前瞻性研究
目的超声青光眼成形术(UCP)是治疗晚期青光眼的一种非侵入性治疗方法。然而,其作为具有功能视力的中度青光眼的第一手术选择的潜力尚未得到充分的研究。本研究旨在评估UCP作为青光眼残视初始手术的有效性和安全性。方法前瞻性研究纳入117例青光眼患者,其中男性63例,女性54例,平均年龄48.3±17.2岁,不同青光眼亚型,最佳矫正视力(BCVA)优于1.30 logMAR,首次行UCP治疗。主要结果是12个月的手术成功率,合格和完全成功。合格的成功定义为眼内压(IOP)较基线降低≥20%,IOP在6 - 21 mmHg之间,没有额外的青光眼手术,使用或不使用抗青光眼药物。完全成功的定义是相同的标准,但没有任何抗青光眼药物。次要结局包括平均IOP、BCVA和术后并发症。结果首次应用UCP治疗12个月的成功率为71.8%,完全成功率(无药)为27.4%。亚组分析显示PACG组的成功率最高(84.8%),其次是POAG(73.0%)和NVG(66.7%)。logMAR≤0.30的患者发生率最高(80.0%),其次为0.30 ~ 0.50 logMAR(75.0%)、0.50 ~ 1.00 logMAR(66.7%)和1.00 ~ 1.30 logMAR(63.6%)。总体平均BCVA从基线时的0.62±0.42 logMAR到1年后的0.63±0.43 logMAR变化最小。患者术后早期出现初期视力下降,术后1周后逐渐恢复。在12个月的随访中,只有2.6%(3/117)的患者出现了超过2线的临床显著视力下降。无严重并发症。结论视功能青光眼的首选手术治疗是一种安全有效的选择。UCP可在12个月内显著降低IOP,而不会引起明显的视力下降或严重的并发症。
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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来源期刊
CiteScore
1.70
自引率
0.00%
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审稿时长
66 days
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