Cvintal Victor, Moster Marlene R, Shyu Andrew P, McDermott Katie, Ekici Feyzahan, Pro Michael J, Waisbourd Michael
Glaucoma Research Center, Wills Eye Hospital, Philadelphia, PA.
J Glaucoma. 2016 May;25(5):e475-80. doi: 10.1097/IJG.0000000000000324.
To evaluate the clinical outcomes of the new Ahmed glaucoma valve (AGV) model M4. The device consists of a porous polyethylene shell designed for improved tissue integration and reduced encapsulation of the plate for better intraocular pressure (IOP) control.
Medical records of patients with an AGV M4 implantation between December 1, 2012 and December 31, 2013 were reviewed. The main outcome measure was surgical failure, defined as either (1) IOP<5 mm Hg or >21 mm Hg and/or <20% reduction of IOP at last follow-up visit, (2) a reoperation for glaucoma, and/or (3) loss of light perception.
Seventy-five eyes of 73 patients were included. Postoperative IOP at all follow-up visits significantly decreased from a baseline IOP of 31.2 mm Hg (P<0.01). However, IOP increased significantly at 3 months (20.4 mm Hg), 6 months (19.3 mm Hg), and 12 months (20.3 mm Hg) compared with 1 month (13.8 mm Hg) postoperatively (P<0.05). At 6 months and 1 year, the cumulative probability of failure was 32% and 72%, respectively.
The AGV M4 effectively reduced IOP in the first postoperative month, but IOP steadily increased thereafter. Consequently, failure rates were high after 1 year of follow-up.
评估新型艾哈迈德青光眼引流阀(AGV)M4型的临床疗效。该装置由多孔聚乙烯外壳组成,旨在改善组织整合并减少引流盘的包封,以更好地控制眼压(IOP)。
回顾了2012年12月1日至2013年12月31日期间植入AGV M4型的患者的病历。主要观察指标为手术失败,定义为:(1)末次随访时眼压<5 mmHg或>21 mmHg和/或眼压降低<20%;(2)因青光眼再次手术;和/或(3)光感丧失。
纳入73例患者的75只眼。所有随访时的术后眼压均较基线眼压31.2 mmHg显著降低(P<0.01)。然而,与术后1个月(13.8 mmHg)相比,术后3个月(20.4 mmHg)、6个月(19.3 mmHg)和12个月(20.3 mmHg)时眼压显著升高(P<0.05)。在6个月和1年时,失败的累积概率分别为32%和72%。
AGV M4型在术后第1个月有效降低了眼压,但此后眼压稳步升高。因此,随访1年后失败率较高。