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Preserflo微分流器植入术后低眼压的危险因素及保护策略。

Risk factors and protective strategies for hypotony following preserflo microshunt implantation.

作者信息

Mieno Hiroki, Mori Kazuhiko, Yoshii Kengo, Okada Yo, Ikeda Yoko, Ueno Morio, Sotozono Chie

机构信息

Department of Ophthalmology, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Baptist Eye Institute, Nagaokakyo, Japan.

出版信息

Sci Rep. 2025 Mar 11;15(1):8344. doi: 10.1038/s41598-025-92879-9.

Abstract

The PreserFlo MicroShunt (PMS) is a minimally invasive surgical device for glaucoma management. However, postoperative hypotony remains a significant complication. This retrospective cohort study analyzed 471 eyes to evaluate the efficacy of PMS implantation in reducing intraocular pressure (IOP) and medication dependency, as well as to identify risk factors associated with hypotony. The median IOP decreased significantly from 19 mmHg preoperatively to 10 mmHg three months postoperatively, with the median medications score dropping to zero. Postoperative hypotony occurred in 18.7% of the cases. Multivariate analysis identified preoperative IOP ≥ 25 mmHg (odds ratio (OR): 2.01, 95% confidence interval (CI): 1.00-4.02, p = 0.049) and medication scores ≥ 5 (OR: 2.12, 95% CI: 1.13-3.96, p = 0.019) as significant risk factors for hypotony, while axial length ≥ 25.5 mm (OR: 0.19, 95% CI: 0.09-0.39, p < 0.001) and intraluminal suture stenting (OR: 0.08, 95% CI: 0.03-0.25, p < 0.001) were significantly protective. Importantly, intraluminal suture stenting mitigated the risk of hypotony without compromising the short-term surgical outcomes. These findings emphasize the need for careful patient selection and the potential of intraluminal suture stenting as an effective intraoperative strategy to improve the safety and outcomes of PMS implantation.

摘要

PreserFlo微型分流器(PMS)是一种用于青光眼治疗的微创手术器械。然而,术后低眼压仍然是一个严重的并发症。这项回顾性队列研究分析了471只眼睛,以评估PMS植入术在降低眼压(IOP)和减少药物依赖方面的疗效,并确定与低眼压相关的危险因素。眼压中位数从术前的19 mmHg显著降至术后三个月的10 mmHg,药物评分中位数降至零。18.7%的病例发生了术后低眼压。多变量分析确定术前眼压≥25 mmHg(比值比(OR):2.01,95%置信区间(CI):1.00 - 4.02,p = 0.049)和药物评分≥5(OR:2.12,95% CI:1.13 - 3.96,p = 0.019)是低眼压的显著危险因素,而眼轴长度≥25.5 mm(OR:0.19,95% CI:0.09 - 0.39,p < 0.001)和腔内缝线支架置入(OR:0.08,95% CI:0.03 - 0.25,p < 0.001)具有显著的保护作用。重要的是,腔内缝线支架置入在不影响短期手术效果的情况下降低了低眼压的风险。这些发现强调了谨慎选择患者的必要性,以及腔内缝线支架置入作为一种有效的术中策略改善PMS植入术安全性和效果的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf2e/11897240/37ee3aa6f2db/41598_2025_92879_Fig1_HTML.jpg

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