Errico Donato, Scrimieri Francesca Luigia, Riccardi Roberta, Iarossi Giancarlo
Ophthalmology Unit, Azienda Ospedaliera "Cardinale G. Panico", Lecce, Italy.
Department of Ophthalmology, Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Middle East Afr J Ophthalmol. 2016 Apr-Jun;23(2):177-82. doi: 10.4103/0974-9233.175889.
To compare the outcomes of Ex-PRESS device implantation versus trabeculectomy in patients with ocular hypertension after pars plana vitrectomy and silicone oil injection (SOI).
Twenty-six consecutive eyes with ocular hypertension after pars plana vitrectomy and SOI were included in this study and randomized to one of two groups: A group treated with Ex-PRESS (model P50) placed under a scleral flap (Ex-PRESS group), and a group treated with trabeculectomy (trabeculectomy group). Complete success (intraocular pressure [IOP] <21 mmHg without medication) and qualified success rates (IOP <21 mmHg with one or two glaucoma medications) at 2 years postoperatively were analyzed. Between-groups comparison was performed with the Mann-Whitney U-test for continuous variables, and Fischer exact test for categorical data. Success rates between groups were compared using Kaplan-Meier life analysis and the log-rank test. P < 0.05 was considered statistically significant.
In the Ex-PRESS group, complete success was achieved in 73% eyes and qualified success in 81.8% of eyes. In the trabeculectomy group, complete success was achieved in 40% and qualified success was achieved in 60% of eyes. The difference in mean IOP between groups was statistically significant from the 3(rd) postoperative month onward (P = 0.007 at 3 months, P = 0.003 at 6 months, and P = 0.03 at 24 months).
Ex-PRESS implantation was more effective than trabeculectomy in controlling IOP in ocular hypertensives after pars plana vitrectomy and SOI, but the surgical technique may require improvement.
比较扁平部玻璃体切除术联合硅油注入(SOI)后高眼压患者植入Ex-PRESS装置与小梁切除术的效果。
本研究纳入26例连续的扁平部玻璃体切除术联合SOI后出现高眼压的患眼,并随机分为两组:一组采用巩膜瓣下植入Ex-PRESS(P50型号)进行治疗(Ex-PRESS组),另一组采用小梁切除术进行治疗(小梁切除术组)。分析术后2年的完全成功率(眼压[IOP]<21 mmHg且无需药物治疗)和合格成功率(眼压<21 mmHg且使用一种或两种青光眼药物)。连续变量采用Mann-Whitney U检验进行组间比较,分类数据采用Fischer精确检验。采用Kaplan-Meier生存分析和对数秩检验比较两组的成功率。P<0.05被认为具有统计学意义。
Ex-PRESS组中,73%的患眼实现了完全成功,81.8%的患眼实现了合格成功。小梁切除术组中,40%的患眼实现了完全成功,60%的患眼实现了合格成功。两组之间平均眼压的差异从术后第3个月起具有统计学意义(3个月时P = 0.007,6个月时P = 0.003,24个月时P = 0.03)。
在扁平部玻璃体切除术联合SOI后的高眼压患者中,植入Ex-PRESS比小梁切除术在控制眼压方面更有效,但手术技术可能需要改进。