Bolek Bartłomiej, Wylęgała Adam, Rebkowska-Juraszek Małgorzata, Wylęgała Edward
Chair and Clinical Department of Ophthalmology, School of Medicine in Zabrze, Medical University of Silesia in Katowice, 40-760 Katowice, Poland.
Clinical Department of Ophthalmology, District Railway Hospital, 40-760 Katowice, Poland.
Biomedicines. 2024 Jan 15;12(1):186. doi: 10.3390/biomedicines12010186.
this study aimed to assess the effectiveness and safety of phaco-endocyclophotocoagulation (phaco-ECP) in patients with glaucoma over five consecutive years.
Thirty-eight patients (38 eyes) with primary and secondary glaucoma were enrolled to undergo phaco-ECP (Endo Optiks URAM E2, Beaver-Visitec International, Waltham, MA, USA). The primary outcome measures were intraocular pressure (IOP) reduction, success rates, glaucoma medication use, and visual acuity after phaco-ECP. An IOP reduction of 20% compared to the baseline value without re-intervention was considered a successful treatment. Complete success was defined as a cessation of antiglaucoma medications. Secondary outcome measures included intraoperative and postoperative complications. Measurements were performed preoperatively and in the first week and 1, 3, 6, 12, 18, 24, 30, 36, 42, 48, 54, and 60 months postoperatively.
The mean ± SD values of IOP preoperatively, at 12, 24, 36, 48, and 60 months postoperatively were 22.6 ± 6.7 mmHg, 15.9 ± 3.9 mmHg ( < 0.001), 15.9 ± 2.9 mmHg ( < 0.001), 15.6 ± 2.7 mmHg ( < 0.001), 15.5 ± 3.8 mmHg ( < 0.001), and 15.2 ± 2.6 mmHg ( < 0.001), respectively. The mean IOP at the last follow-up was reduced by 32.7%. The decrease in the number of antiglaucoma medications was statistically significant at each follow-up visit compared to the baseline. The qualified success rate was 40.6%. All patients at the 60-month follow-up visit required the use of antiglaucoma medications-none of the patients achieved complete success. During the follow-up period, nine patients (28.3%) that required retreatment due to nonachievement of the target IOP were considered failures. Six patients (15.8%) were lost from the follow-up. A total of 23 patients were evaluated 60 months after their phaco-ECP. Complications directly associated with the procedure, such as corneal edema (25.6%), IOP spikes (20.5%), IOL dislocation (2.6%), and uveitis (12.8%), were observed in our patients. Hypotony was not observed in any of our patients.
The phaco-ECP procedure was effective, well-tolerated, and safe for reducing IOP in glaucoma patients with cataracts over a long-term follow-up. Randomized, larger-scale studies are required to validate the results obtained.
本研究旨在评估连续五年内超声乳化-睫状体光凝术(phaco-ECP)治疗青光眼患者的有效性和安全性。
纳入38例(38只眼)原发性和继发性青光眼患者,接受phaco-ECP治疗(使用美国马萨诸塞州沃尔瑟姆市比弗-维西泰克国际公司的Endo Optiks URAM E2)。主要观察指标为超声乳化-睫状体光凝术后的眼压降低情况、成功率、青光眼药物使用情况及视力。与基线值相比眼压降低20%且无需再次干预被视为治疗成功。完全成功定义为停用抗青光眼药物。次要观察指标包括术中及术后并发症。术前、术后第1周、1、3、6、12、18、24、30、36、42、48、54和60个月进行测量。
术前、术后12、24、36、48和60个月的眼压均值±标准差分别为22.6±6.7 mmHg、15.9±3.9 mmHg(P<0.001)、15.9±2.9 mmHg(P<0.001)、15.6±2.7 mmHg(P<0.001)、15.5±3.8 mmHg(P<0.001)和15.2±2.6 mmHg(P<0.001)。最后一次随访时的平均眼压降低了32.7%。与基线相比,每次随访时抗青光眼药物使用数量的减少具有统计学意义。合格成功率为40.6%。60个月随访时所有患者均需使用抗青光眼药物,无一例患者达到完全成功。随访期间,9例(28.3%)因未达到目标眼压而需要再次治疗的患者被视为治疗失败。6例(15.8%)患者失访。共有23例患者在接受超声乳化-睫状体光凝术60个月后接受评估。在我们的患者中观察到与手术直接相关的并发症,如角膜水肿(25.6%)、眼压峰值(20.5%)、人工晶状体脱位(2.6%)和葡萄膜炎(12.8%)。未观察到任何患者出现低眼压。
在长期随访中,超声乳化-睫状体光凝术对于降低白内障合并青光眼患者的眼压是有效、耐受性良好且安全的。需要进行随机、大规模研究以验证所得结果。