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与原发性开角型青光眼相比,选择性激光小梁成形术作为原发性剥脱性青光眼治疗的长期安全性和有效性。

Long-term safety and efficacy of selective laser trabeculoplasty as primary therapy for the treatment of pseudoexfoliation glaucoma compared with primary open-angle glaucoma.

作者信息

Shazly Tarek A, Smith Jan, Latina Mark A

机构信息

Ophthalmology Department, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA, USA.

出版信息

Clin Ophthalmol. 2010 Dec 16;5:5-10. doi: 10.2147/OPTH.S15952.

DOI:10.2147/OPTH.S15952
PMID:21311650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3032997/
Abstract

PURPOSE

To investigate the safety and efficacy of selective laser trabeculoplasty (SLT) to reduce intraocular pressure (IOP) in patients with pseudoexfoliation glaucoma (PXFG) compared with primary open-angle glaucoma (POAG).

DESIGN

Non-randomized, prospective, clinical trial.

METHODS

Nineteen eyes of 13 patients with POAG and 18 eyes of 13 patients with PXFG were treated with SLT. Patients were followed without antiglaucoma medications until additional medical, laser, or surgical intervention was initiated, at which time they were considered failures, had withdrawn from the study, or underwent a second SLT.

RESULTS

The POAG and PXFG eyes showed similar reductions of IOP over the 49 months of follow-up. At 30 months of follow-up the POAG group showed a mean IOP of 17.6 ± 2.8 mmHg and a mean IOP reduction of 5.7 ± 2.1 mmHg; the PXFG group showed a mean IOP of 18.3 ± 4.7 and a mean IOP reduction of 5.3 ± 3.0 mmHg. Four eyes in the PXFG group and three eyes in the POAG group failed by 30 months. The cumulative probability of success was 74% for the PXFG group and 77% for the POAG group. Four PXFG eyes underwent a second SLT after 30 months of follow-up with a final IOP of 17.6 ± 2.8 mmHg. There were no serious adverse events.

CONCLUSION

SLT is a safe and effective method to lower IOP in patients with PXFG as initial glaucoma therapy. Both groups showed similar IOP reductions and failure rates.

摘要

目的

与原发性开角型青光眼(POAG)相比,研究选择性激光小梁成形术(SLT)降低剥脱性青光眼(PXFG)患者眼压(IOP)的安全性和有效性。

设计

非随机、前瞻性临床试验。

方法

对13例POAG患者的19只眼和13例PXFG患者的18只眼进行SLT治疗。在不使用抗青光眼药物的情况下对患者进行随访,直到开始额外的药物、激光或手术干预,此时他们被视为治疗失败、退出研究或接受第二次SLT。

结果

在49个月的随访中,POAG组和PXFG组的眼压降低情况相似。在随访30个月时,POAG组的平均眼压为17.6±2.8 mmHg,平均眼压降低5.7±2.1 mmHg;PXFG组的平均眼压为18.3±4.7 mmHg,平均眼压降低5.3±3.0 mmHg。到30个月时,PXFG组有4只眼治疗失败,POAG组有3只眼治疗失败。PXFG组的累积成功率为74%,POAG组为77%。4只PXFG眼在随访30个月后接受了第二次SLT,最终眼压为17.6±2.8 mmHg。未发生严重不良事件。

结论

SLT作为PXFG患者青光眼初始治疗降低眼压是一种安全有效的方法。两组眼压降低情况和失败率相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629e/3032997/7d00eba56b6b/opth-5-005f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629e/3032997/d76e3f0bb16b/opth-5-005f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629e/3032997/7d00eba56b6b/opth-5-005f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629e/3032997/d76e3f0bb16b/opth-5-005f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629e/3032997/7d00eba56b6b/opth-5-005f2.jpg

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