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青光眼引流装置手术后高血压期的发生率和结局。

Incidence and Outcomes of Hypertensive Phase After Glaucoma Drainage Device Surgery.

机构信息

Department of Ophthalmology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Department of Preventive Medicine (Biostatistics), Northwestern University Feinberg School of Medicine, Chicago, Illinois.

出版信息

Ophthalmol Glaucoma. 2024 Jul-Aug;7(4):345-351. doi: 10.1016/j.ogla.2024.03.006. Epub 2024 Mar 26.

Abstract

PURPOSE

To describe the incidence, risk factors, clinical characteristics, and long-term outcomes of a hypertensive phase (HP) after glaucoma drainage device (GDD) implantation.

DESIGN

Retrospective cohort study.

PARTICIPANTS

Eyes that underwent implantation of their first GDD from January 2010 to October 2020 at a tertiary care center.

METHODS

Hypertensive phase was defined as intraocular pressure (IOP) >21 mmHg occurring at 2 consecutive visits in the first 90 days after the date of surgery for Ahmed Glaucoma Valve (AGV) or in the first 90 days after tube opening for Baerveldt Glaucoma Implant (BGI). Generalized estimating equations and Fisher exact tests were used to evaluate risk factors for HP and risk factors for failure of GDD surgery after occurrence of a HP.

MAIN OUTCOME MEASURES

Incidence and risk factors for HP. Overall surgical success rates, defined as the absence of failure criteria: IOP >21 mmHg, ≤5 mmHg, or <20% reduction below baseline IOP after 3 months for 2 consecutive visits, with or without adjunctive ocular hypotensive therapy; additional glaucoma surgery; or loss of light perception.

RESULTS

Among 419 eyes of 360 patients that underwent GDD implantation, 42 (10.0%) eyes developed HP. Onset of HP was 20.8 ± 10.5 days after AGV and 11.7 ± 20.3 days from the date of tube opening after BGI. Mean IOP during HP was 26.5 ± 3.2 mmHg with peak IOP of 30.0 ± 5.9 mmHg. Median follow-up duration was 21.5 months after onset of HP. Younger age and neovascular glaucoma were significant risk factors for HP occurrence in a multivariable model. Resolution of HP occurred in 32 eyes (76.2%) after a mean duration of 48.0 ± 53.0 days. Additional surgery with a second GDD or cyclophotocoagulation was performed for 12 eyes (28.6%). The overall success rate among eyes with a HP was 52.6% at 2 years, which was significantly lower than that observed among control eyes that did not experience HP (76.3%), P < 0.01.

CONCLUSIONS

The incidence of HP was 10.0%. Younger age and neovascular glaucoma were significant risk factors for HP in the multivariable model. The risk of surgical failure after HP is significantly higher compared to eyes that did not experience HP.

FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

摘要

目的

描述青光眼引流装置(GDD)植入后高血压期(HP)的发生率、风险因素、临床特征和长期结局。

设计

回顾性队列研究。

参与者

2010 年 1 月至 2020 年 10 月在一家三级护理中心接受首次 GDD 植入的眼睛。

方法

高血压期定义为 Ahmed Glaucoma Valve(AGV)手术后 90 天内或 Baerveldt Glaucoma Implant(BGI)开放后 90 天内连续 2 次就诊时眼压(IOP)>21mmHg。使用广义估计方程和 Fisher 确切检验评估 HP 的风险因素以及发生 HP 后 GDD 手术失败的风险因素。

主要观察指标

HP 的发生率和风险因素。总体手术成功率定义为无失败标准:IOP>21mmHg、≤5mmHg 或较基线 IOP 降低<20%,连续 2 次就诊,合并或不合并辅助降眼压治疗;额外的青光眼手术;或光感丧失。

结果

在 360 名患者的 419 只眼中,42 只(10.0%)眼发生 HP。AGV 后 HP 的发病时间为 20.8±10.5 天,BGI 后管开放后 11.7±20.3 天。HP 期间的平均 IOP 为 26.5±3.2mmHg,峰值 IOP 为 30.0±5.9mmHg。HP 发病后中位随访时间为 21.5 个月。年龄较小和新生血管性青光眼是多变量模型中 HP 发生的显著危险因素。在平均 48.0±53.0 天后,32 只眼(76.2%)HP 得到缓解。12 只眼(28.6%)行第二次 GDD 或睫状体光凝术。2 年时,有 HP 的眼总体成功率为 52.6%,明显低于未发生 HP 的对照眼(76.3%),P<0.01。

结论

HP 的发生率为 10.0%。年龄较小和新生血管性青光眼是多变量模型中 HP 的显著危险因素。与未发生 HP 的眼相比,发生 HP 后手术失败的风险显著增加。

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