Efficacy and safety of first-line or second-line selective laser trabeculoplasty for normal-tension glaucoma: a multicentre cohort study

IF 2 Q2 OPHTHALMOLOGY
Koji Nitta, Kae Sugihara, Akiko Narita, Tomoko Naito, Takako Miki, Maki Katai, Shiro Mizoue, Keiji Yoshikawa, Masaki Tanito, Kazuhisa Sugiyama
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Abstract

Background/aims This study aimed to investigate and compare the efficacy and safety of first-line and second-line selective laser trabeculoplasty (SLT) in Japanese patients with normal-tension glaucoma (NTG). Methods 100 patients with NTG were enrolled in this study. Patients were treated with SLT as a first-line or second-line treatment for NTG. Main outcome measures were intraocular pressure (IOP) reduction rate, outflow pressure improvement rate (ΔOP), success rate at 1 year and complications. Success was defined as ΔOP≥20% (criterion A) or an IOP reduction ≥20% (criterion B) without additional IOP-lowering eye-drops, repeat SLT or additional glaucoma surgeries. The incidence of transient IOP spike (>5 mm Hg from the pretreatment IOP), conjunctival hyperaemia, inflammation in the anterior chamber and visual impairment due to SLT were assessed. Results A total of 99 patients (99 eyes) were initially enrolled in this study, including 74 eyes assigned to the first-line SLT group and 25 eyes to the second-line SLT group. The mean IOP of 16.3±2.1 mm Hg before SLT decreased by 17.1%±9.5% to 13.4±1.9 mm Hg at 12 months after SLT in the first-line group (p<0.001), and the mean IOP of 15.4±1.5 mm Hg before SLT decreased by 12.7%±9.7% to 13.2±2.0 mm Hg at 12 months after SLT (p=0.005) in the second-line group. Both groups showed significant reductions in IOP. Higher pre-SLT IOP and thinner central corneal thickness were associated with greater IOP reduction. The success rate at 1 year was higher in the first-line compared with the second-line group, with lower pretreatment IOP and the use of IOP-lowering medication before SLT being associated with treatment failure. Most post-treatment complications were minor and transient. Conclusions SLT may be an effective and safe treatment option for NTG, as either a first-line or second-line treatment. Trial registration number The study was registered in the UMIN-CTR (UMIN Test ID: UMIN R000044059). Data are available on reasonable request.
一线或二线选择性激光小梁成形术治疗正常张力青光眼的疗效和安全性:一项多中心队列研究
背景/目的 本研究旨在调查和比较日本正常张力青光眼(NTG)患者一线和二线选择性激光小梁成形术(SLT)的疗效和安全性。方法 100 名 NTG 患者参加了这项研究。作为 NTG 的一线或二线治疗方法,患者接受了 SLT 治疗。主要结果指标包括眼压降低率、流出压改善率(ΔOP)、1 年成功率和并发症。成功定义为ΔOP≥20%(标准 A)或眼压降低≥20%(标准 B),且无需额外使用降眼压眼药水、重复 SLT 或进行额外的青光眼手术。对一过性眼压飙升(与治疗前眼压相比>5 毫米汞柱)、结膜高血症、前房炎症和 SLT 引起的视力损害的发生率进行了评估。结果 共有 99 名患者(99 只眼)参与了这项研究,其中 74 只眼被分配到一线 SLT 组,25 只眼被分配到二线 SLT 组。一线组在 SLT 前的平均眼压为 16.3±2.1 mm Hg,SLT 12 个月后下降了 17.1%±9.5%,降至 13.4±1.9 mm Hg(p<0.001);二线组在 SLT 前的平均眼压为 15.4±1.5 mm Hg,SLT 12 个月后下降了 12.7%±9.7%,降至 13.2±2.0 mm Hg(p=0.005)。两组患者的眼压均有明显下降。SLT前眼压较高和角膜中央厚度较薄与眼压降低幅度较大有关。与二线组相比,一线组 1 年后的成功率更高,治疗前眼压较低和 SLT 前使用降眼压药物与治疗失败有关。大多数治疗后并发症都是轻微和短暂的。结论 SLT 可作为 NTG 的一线或二线治疗方案,是一种有效而安全的治疗方法。试验注册号 该研究已在 UMIN-CTR 注册(UMIN 试验 ID:UMIN R000044059)。如有合理要求,可提供相关数据。
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
BMJ Open Ophthalmology
BMJ Open Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
4.20%
发文量
104
审稿时长
20 weeks
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