Results of CO2 laser-assisted sclerotomy surgery (CLASS procedures) in eyes with primary open-angle glaucoma

Z. Nagy, M. Bausz, Kinga Kránitz, Huba J. M. Kiss
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Abstract

This study aimed to examine the effectiveness of CO2 laser-assisted sclerectomy surgery (CLASS) in eyes with primary open-angle glaucoma (POAG) showing progression in spite of maximal local antiglaucomatous therapy. Patients with progressive POAG received CLASS treatment. We performed CLASS on 15 eyes (eight males and seven females). The primary endpoint was the change in the intraocular pressure (IOP), and additionally best spectacle-corrected visual acuity (BSCVA), C/D ratio (cup-to-disc), as well as use of antiglaucomatous drops were also investigated. Following the preoperative assessment, measurements were performed at 6-month follow-up. The average preoperative IOP was 26.13 ± 6.79 mmHg that dropped to 9.57 ± 4.09 mmHg at 1 day. IOP was stable at 1 month, 3 months, and 6 months. The BSCVA decreased to the 1-day and 1-week follow-up but returned to its original value to the 1-month check-up. Preoperatively, all patients were on maximal antiglaucoma drop therapy, after CLASS none of the patients needed antiglaucomatous treatment at 1 month. However, at 3 months, one of them needed antiglaucoma drops. C/D ratio showed non-significant changes. CLASS procedure was found to be effective in decreasing IOP in POAG patients whose IOP was not compensated with maximal antiglaucomatous local therapy; patients needed significantly less local therapy following the CO2 laser surgery.
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CO2激光辅助巩膜切开术治疗原发性开角型青光眼的疗效观察
本研究旨在探讨CO2激光辅助巩膜切除术(CLASS)治疗原发性开角型青光眼(POAG)的有效性,尽管进行了最大限度的局部抗青光眼治疗,但仍有进展。进行性POAG患者接受CLASS治疗。我们对15只眼睛(8只雄性和7只雌性)进行了CLASS手术。主要终点是眼压(IOP)的变化,此外还调查了最佳眼镜矫正视力(BSCVA), C/D比(杯盘)以及抗青光眼滴剂的使用情况。术前评估后,随访6个月进行测量。术前平均IOP为26.13±6.79 mmHg, 1 d后降至9.57±4.09 mmHg。IOP在1个月、3个月和6个月时稳定。BSCVA在随访1天1周时有所下降,但在随访1个月时恢复到初始值。术前所有患者均给予最大剂量抗青光眼滴药治疗,CLASS术后1个月无患者需要抗青光眼治疗。然而,在3个月时,其中一人需要抗青光眼滴眼液。C/D比值变化不显著。发现CLASS手术可有效降低POAG患者的IOP,其IOP不能通过最大限度的抗青光眼局部治疗来补偿;患者在CO2激光手术后需要的局部治疗明显减少。
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15
审稿时长
34 weeks
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