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保罗和贝伐尔德青光眼植入物治疗一年后的疗效比较。

Treatment Outcomes Comparing the Paul and Baerveldt Glaucoma Implants After One Year of Follow-Up.

机构信息

Department of Ophthalmology, University Hospitals of Leuven.

Department of Ophthalmology, Hospital de Santa Maria, CHULN.

出版信息

J Glaucoma. 2024 Aug 1;33(8):594-600. doi: 10.1097/IJG.0000000000002366. Epub 2024 May 6.

Abstract

PRCIS

In reducing intraocular pressure (IOP), Paul (PGI) and Baerveldt (BGI) glaucoma implants are safe and effective in patients with glaucoma.

OBJECTIVE

To compare efficacy and safety profiles of the PGI and BGI in the treatment of medically uncontrolled glaucoma at 1 year of follow-up.

METHODS

Retrospective analysis of patients implanted with a PGI or BGI with a minimum of 12 months follow-up. The primary outcome was surgical success defined as IOP ≥6 and ≤18 mm Hg and at least 20% IOP reduction from baseline. Secondary outcomes included IOP measurements, number of medications, and complications.

RESULTS

Twenty-three patients implanted with PGI and 27 with BGI were included. At last visit (12 mo), mean IOP had decreased from 23.7 ± 6.9 to 0.1 ± 2.9 mm Hg in the PGI group versus 26 ± 7.3 to 10.4 ± 4.9 mm Hg with the BGI ( P < 0.001 for both comparisons). Overall qualified success rates were similar between groups (PGI 91% vs BGI 89%, P = 0.784). IOP was significantly lower in the PGI at week 1 and month 1 of follow-up versus the BGI (13.6 ± 6.1 vs 20.1 ± 7.4; 14.6±3.8 vs 21.2 ± 5.8 mm Hg; P < 0.002 for both) with a lower number of medications (1.57 ± 1.47 vs 2.52 ± 1.16 at mo 1, P = 0.015). Most complications were minor and similar in both groups.

CONCLUSION

Both PGI and BGI are safe and effective in reducing IOP in patients with glaucoma, with similar success rates.

摘要

PRCIS

在降低眼内压(IOP)方面,Paul(PGI)和 Baerveldt(BGI)青光眼植入物在青光眼患者中安全且有效。

目的

比较 1 年随访时 PGI 和 BGI 在治疗药物控制不佳的青光眼患者中的疗效和安全性。

方法

回顾性分析了至少随访 12 个月、植入 PGI 或 BGI 的患者。主要结局是手术成功,定义为眼压(IOP)≥6 且≤18mmHg,且与基线相比至少降低 20%的 IOP。次要结局包括眼压测量值、药物使用数量和并发症。

结果

共纳入 23 例植入 PGI 和 27 例植入 BGI 的患者。末次随访(12 个月)时,PGI 组的平均 IOP 从 23.7±6.9mmHg 降至 0.1±2.9mmHg,BGI 组从 26±7.3mmHg 降至 10.4±4.9mmHg(两组比较均 P<0.001)。两组的总体合格成功率相似(PGI 91% vs BGI 89%,P=0.784)。PGI 在随访第 1 周和第 1 个月的 IOP 明显低于 BGI(13.6±6.1 对比 20.1±7.4;14.6±3.8 对比 21.2±5.8mmHg;均 P<0.002),且药物使用数量较少(1 个月时 P=0.015,1.57±1.47 对比 2.52±1.16)。大多数并发症轻微且两组相似。

结论

PGI 和 BGI 均安全有效,可降低青光眼患者的眼压,成功率相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea8/11319072/07860708e8f3/ijg-33-594-g001.jpg

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