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微脉冲经巩膜睫状体光凝术的疗效与安全性

Efficacy and Safety of Micropulse Transscleral Cyclophotocoagulation.

作者信息

de Vries Victor A, Pals Jan, Poelman Huub J, Rostamzad Parinaz, Wolfs Roger C W, Ramdas Wishal D

机构信息

Department of Ophthalmology, Erasmus Medical Center, 3000 CA Rotterdam, The Netherlands.

出版信息

J Clin Med. 2022 Jun 15;11(12):3447. doi: 10.3390/jcm11123447.

DOI:10.3390/jcm11123447
PMID:35743514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9224545/
Abstract

Background: Early studies have shown that micropulse transscleral cyclophotocoagulation (MP-TSCPC) might be an effective and safe treatment option for lowering intraocular pressure (IOP). These studies were, however, somewhat limited, in particular by their retrospective nature and the length of follow-up. Therefore, we assessed the efficacy and safety of this novel treatment in a large cohort for up to 4 years. Methods: We performed a prospective cohort study, including all patients who were treated with MP-TSCPC since November 2017. The primary outcome was a reduction of IOP and the number of IOP-lowering medications. Results: The mean ± standard deviation baseline IOP and number of IOP-lowering medications were 26.6 ± 10.8 mmHg and 3.3 ± 1.3. IOP was reduced by 8.2 ± 7.9 (31.8% reduction), 6.9 ± 8.7 (28.1% reduction), and 7.1 ± 8.4 (30.2% reduction) mmHg after 6, 12, and 24 months, respectively (p < 0.001). The mean postoperative number of IOP-lowering medications was significantly reduced after 6 months by 0.6 ± 1.5 (p = 0.002) but was not significantly different after 12 or 24 months. Oral acetazolamide was significantly reduced from 28 (29%) eyes before treatment, to 9 (9%) at the last follow-up visit (p < 0.001). No major complications were observed after treatment. Conclusions: MP-TSCPC is a safe and effective treatment option for lowering IOP, but only reduced IOP-lowering medications in the first 6 months after treatment. However, MP-TSCPC is especially effective in getting patients off oral IOP-lowering drugs.

摘要

背景

早期研究表明,微脉冲经巩膜睫状体光凝术(MP-TSCPC)可能是降低眼压(IOP)的一种有效且安全的治疗选择。然而,这些研究存在一定局限性,尤其是其回顾性性质以及随访时间长度。因此,我们在一个大型队列中评估了这种新疗法长达4年的疗效和安全性。

方法

我们进行了一项前瞻性队列研究,纳入自2017年11月起接受MP-TSCPC治疗的所有患者。主要结局是眼压降低以及降眼压药物的数量减少。

结果

眼压和降眼压药物数量的均值±标准差基线分别为26.6±10.8 mmHg和3.3±1.3。在6、12和24个月后,眼压分别降低了8.2±7.9(降低31.8%)、6.9±8.7(降低28.1%)和7.1±8.4(降低30.2%)mmHg(p<0.001)。术后6个月降眼压药物的平均数量显著减少了0.6±1.5(p = 0.002),但在12或24个月后无显著差异。口服乙酰唑胺从治疗前的28只眼(29%)显著减少至最后一次随访时的9只眼(9%)(p<0.001)。治疗后未观察到重大并发症。

结论

MP-TSCPC是降低眼压的一种安全有效的治疗选择,但仅在治疗后的前6个月减少了降眼压药物的使用。然而,MP-TSCPC在使患者停用口服降眼压药物方面特别有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bd/9224545/2c4759f9c733/jcm-11-03447-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bd/9224545/93e080f894c1/jcm-11-03447-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bd/9224545/03dd5aa5ced1/jcm-11-03447-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bd/9224545/2c4759f9c733/jcm-11-03447-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bd/9224545/93e080f894c1/jcm-11-03447-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bd/9224545/03dd5aa5ced1/jcm-11-03447-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bd/9224545/2c4759f9c733/jcm-11-03447-g003.jpg

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