Department of Ophthalmology, Meir Medical Center, Kfar Saba, Israel.
J Glaucoma. 2012 Mar;21(3):193-8. doi: 10.1097/IJG.0b013e3181f7b14f.
To evaluate the efficacy of CO2 laser-assisted sclerectomy surgery (CLASS) in primary and pseudoexfoliative open-angle glaucoma.
Patients for primary filtration surgery underwent CLASS with a CO2 laser system (OT-134-IOPtiMate, IOPtima Ltd., Ramat Gan, Israel). This self-controlled system gradually ablates and removes scleral layers until percolating fluid absorbs the energy, attenuating further tissue ablation. Intraocular pressure (IOP) was measured at baseline, 1, 2, 4, and 6 weeks, and 3, 6, and 12 months, respectively. Complete success was defined as 5≤IOP≤18 mm Hg and 20% IOP reduction with no medication at a 12-month endpoint visit, and qualified success as the same IOP range with or without medication.
Thirty of 37 patients completed 12 months of follow-up. Mitomycin C was used in 25 procedures (83.3%). The mean baseline IOP of 26.3±7.8 mm Hg (mean±SD) dropped to 14.4±3.4 and 14.3±3.1 mm Hg at 6 and 12 months, respectively, with 42.4% and 40.7% IOP reduction at 6 and 12 months, respectively (P<0.001). Complete success was achieved by 76.7% and 60% of the patients at 6 and 12 months, respectively, whereas qualified success was achieved by 83.3% and 86.6% of the patients at 6 and 12 months, respectively. Complications were mild and transitory with no sequela.
Short-term and intermediate results suggest that CLASS may become a simple, safe, and effective means of choice for the treatment of open-angle glaucoma.
评估二氧化碳激光辅助巩膜切除术(CLASS)治疗原发性和假性剥脱性开角型青光眼的疗效。
接受原发性滤过手术的患者接受了 CO2 激光系统(OT-134-IOPtiMate,IOPtima Ltd.,Ramat Gan,以色列)的 CLASS。这个自我控制的系统逐渐消融和去除巩膜层,直到渗透液吸收能量,减弱进一步的组织消融。分别在基线、1、2、4 和 6 周以及 3、6 和 12 个月测量眼内压(IOP)。完全成功定义为 5≤IOP≤18 mm Hg,且在 12 个月的终点访视时无需药物治疗,IOP 降低 20%;合格成功定义为相同的 IOP 范围,无论是否使用药物。
37 例患者中有 30 例完成了 12 个月的随访。25 例(83.3%)使用丝裂霉素 C。平均基线 IOP 为 26.3±7.8 mm Hg(均值±标准差),分别在 6 和 12 个月时降至 14.4±3.4 和 14.3±3.1 mm Hg,分别在 6 和 12 个月时 IOP 降低 42.4%和 40.7%(P<0.001)。分别有 76.7%和 60%的患者在 6 和 12 个月时达到完全成功,而 83.3%和 86.6%的患者在 6 和 12 个月时达到合格成功。并发症轻微且短暂,无后遗症。
短期和中期结果表明,CLASS 可能成为治疗开角型青光眼的一种简单、安全、有效的方法。