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Comparison of ExPress Mini-Device Implantation Alone or Combined with Phacoemulsification for the Treatment of Open-Angle Glaucoma

机译:ExPress微型器械植入或超声乳化联合植入治疗开角型青光眼的比较

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摘要

We propose comparative assessment of the effectiveness of two surgical methods for the treatment of open-angle glaucoma: (1) ExPress mini-device implantation combined with phacoemulsification and (2) ExPress mini-device implantation alone. In this prospective study, 81 patients (88 phakic eyes) with uncontrolled open-angle glaucoma enrolled for surgery. They were assigned two groups, those with coexisting cataracts (46 eyes; P-ExPress group) and those with glaucoma alone (42 eyes; ExPress group). The follow-up period was 12.9 ± 0.4 months in P-ExPress and 12.2 ± 0.6 months in ExPress group. In both groups the following parameters were measured: best corrected visual acuity (BCVA), intraocular pressure (IOP), number of complications and necessary postoperative interventions, and number of glaucoma medications. The IOP at the end of follow-up was similar in both groups (18.8 ± 5.9 versus 18.1 ± 4.8 mmHg; P = 0.814). There were no statistical differences in the average number of glaucoma medications between ExPress and P-ExPress groups (0.9 ± 1.65 versus 1.3 ± 1.7; P = 0.419) as well as in the number of postoperative complications (26 versus 21%; P = 0.179 in the P-ExPress and ExPress groups, resp.). Both methods are safe and effective for the surgical treatment of open-angle glaucoma. Coexistence of cataracts does not constitute a compelling contraindication for combined surgery.
机译:我们建议比较评估两种手术方法治疗开角型青光眼的有效性:(1)联合超声乳化术的ExPress微型器械植入和(2)单独进行ExPress微型器械植入。在这项前瞻性研究中,有81例(88晶状体眼)失控的开角型青光眼参加了手术。他们分为两组,白内障并存者(46眼; P-ExPress组)和仅青光眼者(42眼; ExPress组)。 P-ExPress组的随访时间为12.9±0.4个月,ExPress组的随访时间为12.2±0.6个月。两组均测量以下参数:最佳矫正视力(BCVA),眼内压(IOP),并发症数和必要的术后干预措施以及青光眼药物治疗的数量。两组随访结束时的IOP相似(18.8±5.9对18.1±4.8mmHg; P = 0.814)。 ExPress和P-ExPress组之间的平均青光眼用药数量(0.9±1.65对1.3±1.7; P = 0.419)和术后并发症发生率(26对21%; P = 0.179)没有统计学差异在P-ExPress和ExPress组中)。两种方法对于开角型青光眼的手术治疗都是安全有效的。白内障并存并不构成联合手术的强制性禁忌症。

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