Osman Essam A, Al-Muammar Abdulrahman, Mousa Ahmed, Al-Mezaine Hani, Al-Obeidan Saleh A
Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Saudi J Ophthalmol. 2010 Jan;24(1):9-13. doi: 10.1016/j.sjopt.2009.12.002. Epub 2010 Jan 7.
To evaluate the clinical efficacy and safety of controlled contact transscleral diode laser Cyclophotocoagulation (COCO) procedure in reducing the Intraocular Pressure (IOP) among patients with refractory glaucoma.
Thirty two patients (35 eyes) with refractory glaucoma in prospective clinical studies were treated with trans-sclera diode laser in a controlled manner. The energy power used was 5 W in adults and 3 W in children, exposure time was 0.5 s, a total of 16 shots were applied over ciliary body and four shots in each quadrant. Pre and postoperative IOP were measured at different postoperative visits. Snellen visual acuity, the number of anti-glaucoma medications and associated complications were also recorded. Student T test was used to compare the pre and post intervention IOPs, while Wilcoxon Signed Ranks test was used, to detect significance change in medication dependency.
The mean (SD) follow up time was 80.2(±9.6) months, range (36-84) m, where the mean IOP was significantly reduced from 35.1 mm Hg (±10.7) before intervention to 18.8 mm Hg (±7.3) after intervention, in the final visit (P < 0.0001). Complete success was achieved in seven eyes (20%), 22 eyes (62.8%) showed qualified successes and complete failure was reported in six eyes (17.1%). The overall success rate was 82.8% (95% CI: 70.4-95.3). Visual acuity improved in three eyes (8.5%), no change took place in 27 eyes (77.1%) and decreased in five eyes (14.2%). The number of anti-glaucoma medications has significantly changed between pre and post intervention (P < 0.0001). No cases of hypotony, phthisis bulbi or sympathetic ophthalmia were reported.
Controlled COCO is a simple procedure, safe with minimal complications and fewer side effects.
评估可控接触式经巩膜二极管激光睫状体光凝术(COCO)降低难治性青光眼患者眼压的临床疗效及安全性。
对32例(35只眼)难治性青光眼患者进行前瞻性临床研究,采用可控方式经巩膜二极管激光治疗。成人使用的能量功率为5W,儿童为3W,曝光时间为0.5秒,在睫状体上共进行16次照射,每个象限4次。在术后不同时间点测量术前和术后眼压。记录Snellen视力、抗青光眼药物使用数量及相关并发症。采用学生t检验比较干预前后眼压,采用Wilcoxon符号秩检验检测药物依赖的显著变化。
平均(标准差)随访时间为80.2(±9.6)个月,范围为(36 - 84)个月,末次随访时,平均眼压从干预前的35.1mmHg(±10.7)显著降至干预后的18.8mmHg(±7.3)(P < 0.0001)。7只眼(20%)完全成功,22只眼(62.8%)显示合格成功,6只眼(17.1%)报告完全失败。总体成功率为82.8%(95%CI:70.4 - 95.3)。3只眼(8.5%)视力提高,27只眼(77.1%)无变化,5只眼(14.2%)视力下降。干预前后抗青光眼药物使用数量有显著变化(P < 0.0001)。未报告低眼压、眼球痨或交感性眼炎病例。
可控COCO是一种简单的手术,安全,并发症少,副作用小。