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Outcome Of MicroPulse ? Transscleral Photocoagulation In Different Types Of Glaucoma

机译:微孔的结果?不同类型的青光眼的过载光凝

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Purpose: To evaluate the safety and efficacy of MicroPulsesup?/sup transscleral cyclophotocoagulation (μP-TSCPC) up to 24-months follow-up using a standardized fixed protocol in patients with various types of glaucoma. Methods: Prospective, nonrandomized, non-comparative interventional case series of μP-TSCPC performed by a single glaucoma surgeon at tertiary hospitals between May 2017 and May 2019. Results: A total of 71 eyes of 68 patients (39 males, 29 females) aged 60.0 years (13–89 years) were treated with μP-TSCPC. The most common diagnosis was neovascular glaucoma. The safety index of corrected distance visual acuity (CDVA) was 1.0, i.e. there was no significant change in CDVA postoperatively compared to baseline CDVA. The median baseline IOP was 35.0 mmHg (21.0–70.0 mmHg), which was reduced to 16 mmHg (8–32 mmHg) at 12 months/last follow-up postoperatively (p0.001, Wilcoxon signed-rank test). The median reduction in IOP was 52% (0.0–89%) at 12 months/last follow-up postoperatively compared to baseline. The median number of medications was 5 (3–5) at baseline compared to 4 (2–4) at 12 months/last follow-up postoperatively (p0.001, Wilcoxon signed-rank test). The percent of eyes treated with systemic glaucoma medication was 62% (44) at baseline compared to 0% (0) at 12 months/last follow-up postoperatively. The postoperative surgical success of 90%, 91.4%, and 95.7% at 2 weeks, 3 months, and 6 months respectively then remains unchanged. No significant adverse events or complications were observed. Conclusion: μP-TSCPC demonstrated good efficacy and safety profiles with minimal vision-threatening complications in treating a variety of glaucoma types.
机译:目的:评估微孔的安全性和功效 transcrencleral环晶(μp-tscpc),在各种类型青光眼患者中使用标准化的固定方案使用标准化的固定方案进行后续行动。方法:在2017年5月和2019年5月5日星期四的第三届医院的单一青光眼外科医生进行的前瞻性,非扫描,非比较介入案例系列μp-TSCPC。结果:68名患者(39名男性,29名女性)共有71只眼睛用μP-TSCPC治疗60.0岁(13-89岁)。最常见的诊断是新生血管型青光眼。矫正距离视力(CDVA)的安全指数为1.0,即术后CDVA没有显着变化与基线CDVA相比。中位数基线IOP为35.0 mmHg(21.0-70.0mmHg),在术后12个月/最后一次随访时将其降至16mmHg(8-32mmHg)(P <0.001,WILCOXON签名试验)。与基线相比,IOP的中位数减少为12个月/最后一次随访时间为52%(0.0-89%)。在术后12个月/最后一次随访时,基线中,药物的中位数为5(3-5)),术后12个月/最后一次随访(P <0.001,Wilcoxon签名 - 秩检验)。在术后12个月/最后一次随访时,在基线下,用全身青光眼药物治疗的眼睛的百分比为62%(44)。/最后一次随访。术后外科90%,91.4%和95.7%,3个月和6个月分别保持不变。没有观察到显着的不良事件或并发症。结论:μP-TSCPC呈现出良好的疗效和安全性,具有最小的视力威胁性并发症,治疗各种青光眼类型。

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