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XEN凝胶支架植入术或联合白内障超声乳化吸除及人工晶状体植入术治疗青光眼的临床疗效

[Clinical effect of XEN gel stent implantation or combined with phacoemusification and intraocular lens implantation on glaucoma].

作者信息

Zhang B, Shen X L, Wang X P, Gong D, Guo J H, Wang J T

机构信息

Shenzhen Eye Hospital, Shenzhen Eye Institute, Shenzhen Eye Hospital affiliated to Jinan University, School of Optometry, Shenzhen University, Shenzhen 518040, China.

出版信息

Zhonghua Yan Ke Za Zhi. 2024 Sep 11;60(9):746-756. doi: 10.3760/cma.j.cn112142-20231223-00304.

Abstract

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. 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- test, and rank sum test were used for statistical analysis. 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; <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; <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 (<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. 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.

摘要

评估内植XEN凝胶支架植入术或联合超声乳化白内障吸除及人工晶状体(IOL)植入术治疗青光眼的疗效和安全性。这是一项回顾性病例系列研究。纳入了2021年12月至2023年6月在深圳眼科医院接受不同类型青光眼治疗的45例患者(28例男性和17例女性;52只眼)。对这些患者实施了XEN凝胶支架植入术(XEN组)或XEN植入联合超声乳化白内障吸除及IOL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(记录为最小分辨角的对数)、眼压(IOP)、XEN植入象限、降低眼压药物的数量、角膜内皮细胞计数、手术成功率和手术并发症。采用单向重复测量方差分析、LSD检验和秩和检验进行统计学分析。XEN组有28例患者(33只眼),联合组有17例患者(19只眼)。XEN组术后最佳矫正视力无显著变化,但联合组与术前值相比有显著改善(6个月时为0.21±0.30;<0.05)。两组术后18个月时的眼压[(12.2±3.1)和(11.9±3.9)mmHg(1 mmHg = 0.133 kPa)]显著低于术前[(22.1±8.5)和(19.4±10.2)mmHg;<0.05]。所有患者术前降低眼压药物的平均数量为3(2,3),术后18个月时为0(0,0)。差异有统计学意义(<0.05)。XEN组术前角膜内皮细胞计数为(2387.37±478.2)个/mm²,12个月时为(2193.89±311.96)个/mm²。减少无统计学意义。8只眼(15.4%)的XEN凝胶支架植入于鼻上象限,36只眼(69.2%)植入于鼻下象限,8只眼(15.4%)植入于颞下象限。手术成功率[完全成功率,86.5%(45/52);条件成功率,9.6%(5/52)]为96.2%(50/52)。9.6%(5/52)的眼出现滤过泡瘢痕形成。分别有7.7%(4/52)的眼出现少量前房积血、术后浅前房、短暂性高血压和术中引流管破裂。5.8%(3/52)的眼观察到少量结膜下出血。5.8%(3/52)的眼进行了XEN凝胶支架再植入。分别有1.9%(1/52)的眼观察到术中结膜组织破裂、低眼压性黄斑水肿和引流管暴露。XEN凝胶支架植入术或联合超声乳化白内障吸除及IOL植入术治疗不同类型青光眼有效且安全,但其长期临床疗效需要多中心、大规模研究的进一步随访观察。

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