Department of Ophthalmology, University Hospital, CHU Grenoble, Joseph Fourier University, Grenoble, France.
Department of Ophthalmology, University Hospital, Lyon, France.
Acta Ophthalmol. 2016 Aug;94(5):e268-77. doi: 10.1111/aos.12913. Epub 2015 Nov 7.
To evaluate the efficacy and safety of the ultrasonic circular cyclocoagulation procedure in patients with open-angle glaucoma naïve of previous filtering surgery.
Prospective non-comparative interventional clinical study conducted in five French University Hospitals. Thirty eyes of 30 patients with open-angle glaucoma, intra-ocular pressure (IOP) > 21 mmHg and with no previous filtering glaucoma surgeries were sonicated with a probe comprising six piezoelectric transducers. The six transducers were activated with a 6-s exposure time. Complete ophthalmic examinations were performed before the procedure and at 1 day, 1 week, 1, 2, 3, 6 and 12 months after the procedure. Primary outcomes were qualified surgical success (defined as IOP reduction from baseline ≥20% and IOP > 5 mmHg with possible re-intervention and without hypotensive medication adjunction) and complete surgical success (defined as IOP reduction from baseline ≥20%, IOP > 5 mmHg and IOP < 21 mmHg with possible re-intervention and without hypotensive medication adjunction) at the last follow-up visit and vision-threatening complications. Secondary outcomes were mean IOP at each follow-up visit compared with baseline, medication use, complications and re-interventions.
Intra-ocular pressure was significantly reduced (p < 0.05) from a mean pre-operative value of 28.2 ± 7.2 mmHg (n = 3.6 hypotensive medications) to 19.6 ± 7.9 mmHg at 12 months (n = 3.1 hypotensive medications and n = 1.1 procedures) (mean IOP reduction of 30%). Qualified success was achieved in 63% of eyes (19/30) (mean IOP reduction of 37% in these eyes) and complete success in 46.7% of eyes (14/30) (mean IOP reduction of 37% in these eyes) at the last follow-up. No major intra- or post-operative complications occurred.
The UC(3) procedure seems to be an effective and well-tolerated method to reduce IOP in patients with open-angle glaucoma without previous filtering surgery.
评估超声环形凝固术治疗既往无滤过性手术的开角型青光眼患者的疗效和安全性。
这是一项在法国五所大学医院进行的前瞻性非对照干预性临床研究。30 例(30 只眼)开角型青光眼患者,眼压(IOP)>21mmHg,且既往无滤过性青光眼手术史,使用包含 6 个压电换能器的探头对其进行超声治疗。6 个换能器的激活时间为 6s。在治疗前和治疗后 1 天、1 周、1、2、3、6 和 12 个月进行全面眼科检查。主要结局为合格手术成功率(定义为眼压从基线降低≥20%,IOP>5mmHg,可能需要再次干预,且无需添加降压药物)和完全手术成功率(定义为眼压从基线降低≥20%,IOP>5mmHg,IOP<21mmHg,可能需要再次干预,且无需添加降压药物)和视力威胁性并发症。次要结局为每次随访时的平均眼压与基线相比、药物使用、并发症和再次干预。
眼压从术前的 28.2±7.2mmHg(n=3.6 例使用降压药物)显著降低(p<0.05)至 12 个月时的 19.6±7.9mmHg(n=3.1 例使用降压药物和 n=1.1 例手术)(平均眼压降低 30%)。30 只眼中有 63%(19/30)(这些眼中的平均眼压降低 37%)达到合格手术成功率,46.7%(14/30)(这些眼中的平均眼压降低 37%)达到完全手术成功率。术中及术后无严重并发症发生。
UC(3)程序似乎是一种有效且耐受性良好的方法,可以降低既往无滤过性手术的开角型青光眼患者的眼压。