Yazdani Shahin, Mahboobipour Hassan, Pakravan Mohammad, Doozandeh Azadeh, Ghahari Elham
*Ocular Tissue Engineering Research Center †Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
J Glaucoma. 2016 May;25(5):415-21. doi: 10.1097/IJG.0000000000000256.
To determine whether adjunctive mitomycin C (MMC) or amniotic membrane transplantation (AMT) improve the outcomes of Ahmed glaucoma valve (AGV) implantation.
This double-blind, stratified, 3-armed randomized clinical trial includes 75 eyes of 75 patients aged 7 to 75 years with refractory glaucoma. Eligible subjects underwent stratified block randomization; eyes were first stratified to surgery in the superior or inferior quadrants based on feasibility; in each subgroup, eyes were randomly assigned to the study arms using random blocks: conventional AGV implantation (group A, 25 eyes), AGV with MMC (group B, 25 eyes), and AGV with AMT (group C, 25 eyes).
The 3 study groups were comparable regarding baseline characteristics and mean follow-up (P=0.288). A total of 68 patients including 23 eyes in group A, 25 eyes in group B, and 20 eyes group C completed the follow-up period and were analyzed. Intraocular pressure was lower in the MMC group only 3 weeks postoperatively (P=0.04) but comparable at other time intervals. Overall success rate was comparable in the 3 groups at 12 months (P=0.217). The number of eyes requiring medications (P=0.30), time to initiation of medications (P=0.13), and number of medications (P=0.22) were comparable. Hypertensive phase was slightly but insignificantly more common with standard surgery (82%) as compared with MMC-augmented (60%) and AMT-augmented (70%) procedures (P=0.23). Complications were comparable over 1 year (P=0.28).
Although adjunctive MMC and AMT were safe during AGV implantation, they did not influence success rates or intraocular pressure outcomes. Complications, including hypertensive phase, were also comparable.
确定辅助使用丝裂霉素C(MMC)或羊膜移植(AMT)是否能改善艾哈迈德青光眼阀(AGV)植入术的疗效。
这项双盲、分层、三臂随机临床试验纳入了75例年龄在7至75岁的难治性青光眼患者的75只眼。符合条件的受试者进行分层区组随机化;首先根据可行性将眼睛分为上象限或下象限手术;在每个亚组中,使用随机区组将眼睛随机分配至各研究组:传统AGV植入术(A组,25只眼)、AGV联合MMC(B组,25只眼)和AGV联合AMT(C组,25只眼)。
3个研究组在基线特征和平均随访方面具有可比性(P = 0.288)。共有68例患者完成随访期并进行分析,其中A组23只眼、B组25只眼、C组20只眼。仅在术后3周时MMC组的眼压较低(P = 0.04),但在其他时间间隔时眼压相当。3组在12个月时的总体成功率具有可比性(P = 0.217)。需要用药的眼数(P = 0.30)、开始用药的时间(P = 0.13)以及用药数量(P = 0.22)均具有可比性。与MMC增强组(60%)和AMT增强组(70%)相比,标准手术的高血压期略为常见但无显著差异(82%)(P = 0.23)。1年内并发症具有可比性(P = 0.28)。
尽管在AGV植入术中辅助使用MMC和AMT是安全的,但它们并未影响成功率或眼压结果。包括高血压期在内的并发症也具有可比性。