首页> 外文期刊>Journal of cataract and refractive surgery >Canaloplasty: Three-year results of circumferential viscodilation and tensioning of Schlemm canal using a microcatheter to treat open-angle glaucoma.
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Canaloplasty: Three-year results of circumferential viscodilation and tensioning of Schlemm canal using a microcatheter to treat open-angle glaucoma.

机译:眼管成形术:使用微导管治疗开角型青光眼的Schlemm管周向粘连扩张和张紧的三年结果。

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摘要

PURPOSE: To report 3-year results of the safety and efficacy of canaloplasty, a procedure involving circumferential viscodilation and tensioning of the inner wall of Schlemm canal to treat open-angle glaucoma. SETTING: Multicenter surgical sites. DESIGN: Nonrandomized multicenter clinical trial. METHODS: This study comprised adult open-angle glaucoma patients having canaloplasty or combined cataract-canaloplasty surgery. Qualifying preoperative intraocular pressures (IOPs) were at least 16 mm Hg with historical IOPs of at least 21 mm Hg. A flexible microcatheter was used to viscodilate the full circumference of the canal and to place a trabecular tensioning suture. Primary outcome measures included IOP, glaucoma medication use, and adverse events. RESULTS: Three years postoperatively, all study eyes (n = 157) had a mean IOP of 15.2 mm Hg +/- 3.5 (SD) and mean glaucoma medication use of 0.8 +/- 0.9 compared with a baseline IOP of 23.8 +/- 5.0 mm Hg on 1.8 +/- 0.9 medications. Eyes with combined cataract-canaloplasty surgery had a mean IOP of 13.6 +/- 3.6 mm Hg on 0.3 +/- 0.5 medications compared with a baseline IOP of 23.5 +/- 5.2 mm Hg on 1.5 +/- 1.0 medications. Intraocular pressure and medication use results in all eyes were significantly decreased from baseline at every time point (P<.001). Late postoperative complications included cataract (12.7%), transient IOP elevation (6.4%), and partial suture extrusion through the trabecular meshwork (0.6%). CONCLUSION: Canaloplasty led to a significant and sustained IOP reduction in adult patients with open-angle glaucoma and had an excellent short- and long-term postoperative safety profile. FINANCIAL DISCLOSURE: No author has a financial or proprietary interest in any material or method mentioned. Additional disclosures are found in the footnotes.
机译:目的:报告3年管腔成形术的安全性和有效性的结果,该过程涉及周向粘膜扩张和张拉施莱姆管内壁以治疗开角型青光眼。地点:多中心手术部位。设计:非随机多中心临床试验。方法:这项研究包括成人开角型青光眼患者,他们接受了管腔成形术或白内障-管腔成形术联合手术。合格的术前眼压(IOP)至少为16 mm Hg,历史IOP至少为21 mm Hg。使用柔性的微导管对运河的整个圆周进行粘膜扩张并放置小梁张紧缝合线。主要结局指标包括眼压,青光眼用药和不良事件。结果:术后三年,所有研究眼(n = 157)的平均眼压为15.2 mm Hg +/- 3.5(SD),平均青光眼药物使用率为0.8 +/- 0.9,而基线眼压为23.8 +/-在1.8 +/- 0.9药物剂量下为5.0毫米汞柱。白内障-管腔联合手术的眼睛在0.3 +/- 0.5药物下的平均IOP为13.6 +/- 3.6 mm Hg,而在1.5 +/- 1.0药物下的平均IOP为23.5 +/- 5.2 mm Hg。在每个时间点,所有眼睛的眼内压和药物使用结果均较基线显着降低(P <.001)。术后晚期并发症包括白内障(12.7%),眼压升高(6.4%)和通过小梁网部分缝合线挤压(0.6%)。结论:对于患有开角型青光眼的成年患者,泪管成形术可显着且持续地降低眼压,并具有良好的短期和长期术后安全性。财务披露:没有任何作者对所提及的任何材料或方法有财务或所有权利益。在脚注中可以找到其他披露内容。

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