Minckler Don S, Francis Brian A, Hodapp Elizabeth A, Jampel Henry D, Lin Shan C, Samples John R, Smith Scott D, Singh Kuldev
Ophthalmology. 2008 Jun;115(6):1089-98. doi: 10.1016/j.ophtha.2008.03.031.
To provide an evidence-based summary of commercially available aqueous shunts currently used in substantial numbers (Ahmed [New World Medical, Inc., Rancho Cucamonga, CA], Baerveldt [Advanced Medical Optics, Inc., Santa Ana, CA], Krupin [Eagle Vision, Inc, Memphis, TN], Molteno [Molteno Ophthalmic Ltd., Dunedin, New Zealand]) to control intraocular pressure (IOP) in various glaucomas.
Seventeen previously published randomized trials, 1 prospective nonrandomized comparative trial, 1 retrospective case-control study, 2 comprehensive literature reviews, and published English language, noncomparative case series and case reports were reviewed and graded for methodologic quality.
Aqueous shunts are used primarily after failure of medical, laser, and conventional filtering surgery to treat glaucoma and have been successful in controlling IOP in a variety of glaucomas. The principal long-term complication of anterior chamber tubes is corneal endothelial failure. The most shunt-specific delayed complication is erosion of the tube through overlying conjunctiva. There is a low incidence of this occurring with all shunts currently available, and it occurs most frequently within a few millimeters of the corneoscleral junction after anterior chamber insertion. Erosion of the equatorial plate through the conjunctival surface occurs less frequently. Clinical failure of the various devices over time occurs at a rate of approximately 10% per year, which is approximately the same as the failure rate for trabeculectomy.
Based on level I evidence, aqueous shunts seem to have benefits (IOP control, duration of benefit) comparable with those of trabeculectomy in the management of complex glaucomas (phakic or pseudophakic eyes after prior failed trabeculectomies). Level I evidence indicates that there are no advantages to the adjunctive use of antifibrotic agents or systemic corticosteroids with currently available shunts. Too few high-quality direct comparisons of various available shunts have been published to assess the relative efficacy or complication rates of specific devices beyond the implication that larger-surface-area explants provide more enduring and better IOP control. Long-term follow-up and comparative studies are encouraged.
对目前大量使用的市售水性分流器(艾哈迈德分流器[新视野医疗公司,加利福尼亚州兰乔库卡蒙加]、贝尔维尔德特分流器[先进医疗光学公司,加利福尼亚州圣安娜]、克鲁平分流器[鹰视公司,田纳西州孟菲斯]、莫尔滕诺分流器[莫尔滕诺眼科有限公司,新西兰达尼丁])进行循证总结,以控制各种青光眼的眼压(IOP)。
回顾了17项先前发表的随机试验、1项前瞻性非随机对照试验、1项回顾性病例对照研究、2篇综合文献综述以及已发表的英文非对照病例系列和病例报告,并对其方法学质量进行分级。
水性分流器主要用于药物、激光和传统滤过性手术治疗青光眼失败后,已成功控制了多种青光眼的眼压。前房引流管的主要长期并发症是角膜内皮功能衰竭。最常见的与分流器相关的延迟并发症是引流管穿过覆盖的结膜发生侵蚀。目前所有可用分流器发生这种情况的发生率都很低,且在前房植入后最常发生在角膜巩膜交界处几毫米范围内。赤道板穿过结膜表面的侵蚀较少发生。随着时间的推移,各种装置的临床失败率约为每年10%,这与小梁切除术的失败率大致相同。
基于一级证据,在复杂青光眼(先前小梁切除术失败后的有晶状体眼或人工晶状体眼)的治疗中,水性分流器似乎具有与小梁切除术相当的益处(眼压控制、益处持续时间)。一级证据表明,对于目前可用的分流器,辅助使用抗纤维化药物或全身皮质类固醇并无优势。已发表的高质量直接比较各种可用分流器的研究太少,无法评估特定装置的相对疗效或并发症发生率,仅能推断出更大表面积的植入物能提供更持久且更好的眼压控制。鼓励进行长期随访和比较研究。