[XEN凝胶支架植入术或联合超声乳化术和眼内晶体植入术对青光眼的临床疗效]。

Q3 Medicine
B Zhang, X L Shen, X P Wang, D Gong, J H Guo, J T Wang
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引用次数: 0

摘要

目的评估内 XEN 凝胶支架植入术或联合超声乳化术和人工晶体植入术治疗青光眼的有效性和安全性。研究方法这是一项回顾性病例系列研究。研究纳入了自2021年12月至2023年6月在深圳眼科医院接受治疗的45例不同类型青光眼患者(男28例,女17例;52眼)。这些患者均接受了XEN凝胶支架植入术(XEN组)或XEN植入术联合超声乳化术和人工晶体植入术(联合组)。术后随访 18 个月。观察指标包括最佳矫正视力(以最小分辨角的对数记录)、眼压(IOP)、XEN植入象限、降眼压药物次数、角膜内皮细胞计数、手术成功率和手术并发症。统计分析采用单因素重复方差分析、LSD-t 检验和秩和检验。结果XEN 组有 28 名患者(33 只眼),联合组有 17 名患者(19 只眼)。XEN 组的术后最佳矫正视力无明显变化,但在 6 个月时有明显改善(0.21±0.30;PPPC 结论:XEN 凝胶支架植入术是一种有效的治疗方法:XEN凝胶支架植入术或联合超声乳化术和人工晶体植入术治疗不同类型的青光眼有效且安全,但其长期临床疗效还需要多中心、大规模研究的进一步跟踪观察。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinical effect of XEN gel stent implantation or combined with phacoemusification and intraocular lens implantation on glaucoma].

Objective: To evaluate the efficacy and safety of internal XEN gel stent implantation or combined with phacoemusification and intraocular lens (IOL) implantation in the treatment of glaucoma. Methods: It was a retrospective case series study. Forty-five patients (28 males and 17 females; 52 eyes) who had different types of glaucoma treated at the Shenzhen Eye Hospital from December 2021 to June 2023 were included. XEN gel stent implantation (the XEN group) or XEN implantation combined with phacoemusification and IOL implantation (the combined group) were performed in these patients. The postoperative follow-up was 18 months. The observational indexes included the best corrected visual acuity (recorded as the logarithm of the minimum angle of resolution), intraocular pressure (IOP), XEN implantation quadrant, number of IOP-lowering medications, corneal endothelial cell count, operation success rate and surgical complications. The one-way repeated measures of variance, LSD-t test, and rank sum test were used for statistical analysis. Results: There were 28 patients (33 eyes) in the XEN group and 17 patients (19 eyes) in the combined group. The postoperative best corrected visual acuity had no significant change in the XEN group, but improved significantly (0.21±0.30 at 6 months; P<0.05) in the combined group, compared with the preoperative value. The IOP of the two groups at 18 months after surgery [(12.2±3.1) and (11.9±3.9) mmHg (1 mmHg=0.133 kPa)] was significantly lower than that before surgery [(22.1±8.5) and (19.4±10.2) mmHg; P<0.05]. The average number of IOP-lowering medications in all patients was 3 (2, 3) before surgery and 0 (0, 0) at 18 months after surgery. The difference was statistically significant (P<0.05). In the XEN group, the corneal endothelial cell count was (2 387.37±478.22) cells/mm² preoperatively and (2 193.89±311.96) cells/mm² at 12 months. The decrease showed no statistical significance. The XEN gel stent was implanted in the supranasal quadrant in 8 eyes (15.4%), in the inferonasal quadrant in 36 eyes (69.2%), and in the infratemporal quadrant in 8 eyes (15.4%). The operation success rate [complete success rate, 86.5% (45/52); conditional success rate, 9.6% (5/52)] was 96.2% (50/52). The filtering bleb scarring occurred in 9.6% (5/52) of eyes. A small amount of hyphema, postoperative shallow anterior chamber, transient hypertension, and intraoperative drain breakage were found in 7.7% (4/52) of eyes, respectively. A small amount of subconjunctival bleeding was observed in 5.8%(3/52) of eyes. Re-implantation of an XEN gel stent was performed in 5.8% (3/52) of eyes. The intraoperative conjunctival tissue rupture, hypotony macular edema, and drain exposure were observed in 1.9% (1/52) of eyes, respectively. Conclusion: The XEN gel stent implantation or combined with phacoemusification and IOL implantation was effective and safe in treating different types of glaucoma, but its long-term clinical efficacy needs further follow-up observations in multi-center, larger-scale research.

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来源期刊
中华眼科杂志
中华眼科杂志 Medicine-Ophthalmology
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