Pillunat Karin R, Herber Robert, Haase Maike A, Jamke Melanie, Jasper Carolin S, Pillunat Lutz E
Department of Ophthalmology, Medical Faculty Carl Gustav Carus, Technische Universität, Dresden, Germany.
Acta Ophthalmol. 2022 May;100(3):e779-e790. doi: 10.1111/aos.14968. Epub 2021 Jul 31.
To report efficacy and safety outcomes of the PRESERFLO™ MicroShunt compared with trabeculectomy, the current gold-standard treatment for advanced glaucoma, in the early and intermediate postoperative period.
Institutional prospective interventional cohort study of primary open-angle glaucoma (POAG) patients scheduled for the PRESERFLO™ MicroShunt. The comparison group were POAG patients who had had received trabeculectomy and were matched for age, known duration of disease, number and classes of intraocular pressure (IOP)-lowering medications to ensure a similar conjunctival condition. The study is part of the Dresden Glaucoma and Treatment Study (DGTS), was not randomized, but used a uniform study design, with the same inclusion and exclusion criteria as well as standardized definitions of success and failure.
mean diurnal IOP (mdIOP, mean of 6 measurements), diurnal peak IOP, diurnal IOP fluctuations, glaucoma medical therapy, success rates, visual acuity, visual fields, surgical complications and interventions, and severe adverse events.
Fifty-two eyes of 52 patients, 26 in each group, were analysed. At 6 months, median [Q25, Q75] mdIOP was 10.8 [9.5-12.2] mmHg in the microshunt and 10.3 [7.6-11.8] mmHg in the trabeculectomy group. Reduction in mdIOP (p = 0.458), peak diurnal IOP (p = 0.539), and median diurnal fluctuation (p = 0.693) was not statistically significantly different between groups. The rate of interventions was statistically significantly higher in the trabeculectomy compared with the microshunt group (p = 0.004). None of the patients experienced severe adverse events.
Both procedures are equally effective and safe in lowering mdIOP in patients with POAG. Because the microshunt is less invasive with less follow-up and interventions needed postoperatively, it might be recommended earlier in the treatment of glaucoma.
报告PRESERFLO™微型分流器与小梁切除术(目前晚期青光眼的金标准治疗方法)相比,在术后早期和中期的疗效和安全性结果。
对计划接受PRESERFLO™微型分流器治疗的原发性开角型青光眼(POAG)患者进行机构前瞻性干预队列研究。对照组为接受过小梁切除术的POAG患者,根据年龄、已知病程、降低眼压(IOP)药物的数量和类别进行匹配,以确保结膜状况相似。该研究是德累斯顿青光眼与治疗研究(DGTS)的一部分,未进行随机分组,但采用统一的研究设计,具有相同的纳入和排除标准以及成功和失败的标准化定义。
平均日眼压(mdIOP,6次测量的平均值)、日眼压峰值、日眼压波动、青光眼药物治疗、成功率、视力、视野、手术并发症及干预措施,以及严重不良事件。
分析了52例患者的52只眼,每组26只。在6个月时,微型分流器组的mdIOP中位数[Q25,Q75]为10.8[9.5 - 12.2]mmHg,小梁切除术组为10.3[7.6 - 11.8]mmHg。两组间mdIOP降低幅度(p = 0.458)、日眼压峰值降低幅度(p = 0.539)和日眼压波动中位数降低幅度(p = 0.693)差异均无统计学意义。小梁切除术组的干预率在统计学上显著高于微型分流器组(p = 0.004)。所有患者均未发生严重不良事件。
两种手术在降低POAG患者mdIOP方面同样有效且安全。由于微型分流器侵入性较小,术后随访和干预需求较少,因此在青光眼治疗中可能更早被推荐使用。