Altinel Meltem Guzin, Kanra Ayse Yagmur, Karadag Remzi, Bayramlar Huseyin
Department of Ophthalmology, Fatih Sultan Mehmet Training and Research Hospital, Icerenkoy Atasehir 34752, Istanbul, Turkey.
Dunyagoz Hospitals Group, Sultanbeyli 34337, Istanbul, Turkey.
Int J Ophthalmol. 2019 Aug 18;12(8):1290-1297. doi: 10.18240/ijo.2019.08.09. eCollection 2019.
To evaluate the clinical results, efficacy and safety of Ex-PRESS P200 glaucoma shunt implant in different types of medically uncontrolled glaucoma.
The study included 31 eyes of 31 patients that were unresponsive to medical antiglaucomatous therapy in whom Ex-PRESS P200 glaucoma shunt implantation was performed. The demographic characteristics of the patients, type of glaucoma, complete ocular examination results, number of antiglaucomatous drugs before and after surgery, early and late complications of surgery, additional surgical and nonsurgical medical interventions, and success rates were investigated from the patients' files, retrospectively.
The mean postoperative follow-up time was 16.4±7.5mo. The preoperative mean corrected intraocular pressure (IOP) was 28.7±10.3 mm Hg and postoperative mean corrected IOP was 15.3±5.2 mm Hg (<0.05) at the last visit. The mean IOP reduction was 39.9% when the preoperative and postoperative values of the last visits were compared. The average number of antiglaucomatous drug use decreased from 3.9±0.3 to 1.7±1.7 postoperatively (<0.05). The use of antiglaucomatous medications at the last visit was more than in other studies in the literature. The most common complication was conjunctival leakage, which was seen in 7 patients. Other early complications were iris touch, intravitreal hemorrhage, hyphema, choroidal effusion, early transient hypotonia and corneal edema. One of the late complications was endophthalmitis which was seen in one case 6mo after the operation, and the other late complication was opacification of the cornea in one patient. Twelve additional surgical operations associated to Ex-PRESS surgery and 3 bleb needling have done. At the last visit, the complete success rate was 32.3% and the qualified success rate was 77.5% in all patients.
Ex-PRESS P200 glaucoma shunt implantation may be an effective procedure for medically uncontrolled glaucoma with significantly lower use of antiglaucomatous medications.
评估Ex-PRESS P200青光眼分流植入物在不同类型药物治疗无法控制的青光眼患者中的临床结果、疗效及安全性。
本研究纳入31例患者的31只眼,这些患者对青光眼药物治疗无反应,均接受了Ex-PRESS P200青光眼分流植入术。回顾性地从患者病历中调查患者的人口统计学特征、青光眼类型、完整的眼部检查结果、手术前后抗青光眼药物的使用数量、手术的早期和晚期并发症、额外的手术及非手术药物干预措施以及成功率。
术后平均随访时间为16.4±7.5个月。末次随访时,术前平均矫正眼压(IOP)为28.7±10.3 mmHg,术后平均矫正眼压为15.3±5.2 mmHg(P<0.05)。比较术前和末次随访时的眼压值,平均眼压降低了39.9%。术后抗青光眼药物的平均使用数量从3.9±0.3降至1.7±1.7(P<0.05)。末次随访时抗青光眼药物的使用情况高于文献中的其他研究。最常见的并发症是结膜渗漏,7例患者出现该情况。其他早期并发症包括虹膜接触、玻璃体内出血、前房积血、脉络膜渗漏、早期短暂性低眼压和角膜水肿。晚期并发症之一是1例患者术后6个月发生眼内炎,另1例晚期并发症是1例患者角膜混浊。与Ex-PRESS手术相关的另外12次手术及3次滤泡针刺术已完成。末次随访时,所有患者的完全成功率为32.3%,合格成功率为77.5%。
Ex-PRESS P200青光眼分流植入术对于药物治疗无法控制的青光眼可能是一种有效的手术方法,且抗青光眼药物的使用量显著降低。