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Ex-PRESS微型青光眼植入物在技术上具有挑战性的晚期青光眼病例中的应用结果:一项临床试点研究。

Results of the use of the Ex-PRESS miniature glaucoma implant in technically challenging, advanced glaucoma cases: a clinical pilot study.

作者信息

Wamsley Sonja, Moster Marlene R, Rai Sushma, Alvim Heryberto S, Fontanarosa Joann

机构信息

William and Anna Goldberg Glaucoma Service and Research Laboratory, Wills Eye Hospital, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.

出版信息

Am J Ophthalmol. 2004 Dec;138(6):1049-51. doi: 10.1016/j.ajo.2004.06.024.

Abstract

PURPOSE

To report results of implantation of the Ex-PRESS Miniature Glaucoma Implant (Optonol, Neve Ilan, Israel) shunt directly under the conjunctiva in advanced glaucoma.

DESIGN

Noncomparative case series.

METHODS

Chart review of eleven cases of Ex-PRESS implantation. Outcome measures included intraocular pressure (IOP), complications, visual acuity, and additional interventions. Failure was defined as unacceptably high IOP requiring revision or explantation.

RESULTS

Four patients (36%) failed. Ten (91%) experienced hypotony during postoperative week one. In the seven nonfailures, mean pre and postoperative IOPs were 30.3 +/- 9.3 mm Hg and 13.6 +/- 4.4 mm Hg, respectively (P = .006). The logMAR visual acuity did not change significantly from baseline to follow up (logMAR 1.1 +/- 0.9 and 1.4 +/- 0.9, respectively, P = .13). There were no intraoperative complications. Postoperative complications in the 11 eyes included choroidal detachment in 3 (27%) and suprachoroidal hemorrhage in 2 (18%). Of the 7 successful cases, additional interventions were required in 4 (57%).

CONCLUSIONS

Despite significant IOP reduction, the incidence of complications following Ex-PRESS implantation directly under the conjunctiva was unacceptably high in this group of patients.

摘要

目的

报告在晚期青光眼患者中,将Ex-PRESS微型青光眼植入物(Optonol,以色列内韦伊兰)分流器直接植入结膜下的结果。

设计

非对照病例系列。

方法

对11例Ex-PRESS植入病例进行病历回顾。观察指标包括眼压(IOP)、并发症、视力和额外干预措施。失败定义为眼压高得无法接受,需要进行翻修或取出植入物。

结果

4例患者(36%)失败。10例(91%)在术后第一周出现低眼压。在7例未失败的患者中,术前和术后平均眼压分别为30.3±9.3mmHg和13.6±4.4mmHg(P = .006)。从基线到随访,对数最小分辨角视力(logMAR)无显著变化(分别为logMAR 1.1±0.9和1.4±0.9,P = .13)。术中无并发症。11只眼中的术后并发症包括3只眼(27%)发生脉络膜脱离,2只眼(18%)发生脉络膜上腔出血。在7例成功病例中,4例(57%)需要额外干预。

结论

尽管眼压显著降低,但在这组患者中,将Ex-PRESS植入物直接植入结膜下后的并发症发生率高得令人无法接受。

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