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Patient Attitudes toward Distress Screening and Referral in Glaucoma Care 青光眼护理中患者对窘迫筛查和转诊的态度。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.09.004
Eun Young Choi MD , Natalie Chou BS , Hannah M. Fisher PhD , Davina Malek MD , Alessandro A. Jammal MD, PhD , Tamara Somers PhD , Kelly Muir MD , Felipe A. Medeiros MD, PhD , Samuel I. Berchuck PhD
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引用次数: 0
Intraocular Pressure Fluctuations Recorded by a Telemetric Sensor after Nonpenetrating Glaucoma Surgery in Primary Open-Angle Glaucoma 原发性开角型青光眼非穿透性青光眼手术后用遥测传感器记录眼压波动。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.07.007
Colya N. Englisch MD , André M. Trouvain MD , Philip Wakili MD , Kaweh Mansouri MD , H. Burkhard Dick MD , Esther M. Hoffmann MD , Marc J. Mackert MD , Achim Langenbucher PhD , Karl T. Boden MD , Peter Szurman MD

Objective

To investigate short- and long-term intraocular pressure (IOP) fluctuations in patients with primary open-angle glaucoma (POAG) after successful nonpenetrating glaucoma surgery (NPGS, canaloplasty or deep sclerectomy).

Design

A prospective, open-label, multicenter interventional study.

Subjects

A total of 20 patients with POAG who underwent NPGS combined with permanent implantation of a suprachoroidal telemetric IOP sensor (EyeMate-SC, Implandata Ophthalmic Products GmbH). The mean age of the cohort was 66.9 ± 10.6 years. Half were female, and half were male.

Methods

Telemetric IOP measurements were obtained over a 3-year period, excluding the first 180 postoperative days and those during which ocular glaucoma medications were applied. One day was divided into 8 time-of-day (TOD) periods. The median absolute difference (MAD) in IOP between day χ and day χ + 7, 30, 90, 180, and 360 was calculated for each TOD and each eye, in which sequential IOP measurements were accordingly available.

Main Outcome Measures

Intraocular pressure fluctuations.

Results

The mean follow-up duration was 952.8 ± 276.6 days. For analysis, a total of 139 512 mean IOP values were paired. Overall, diurnal IOP decreased by 20.7%, from 11.1 ± 5.0 mmHg in the “early morning” to 8.8 ± 3.2 mmHg in the “late evening,” followed by a nocturnal IOP increase of 13.6% to 10.0 ± 3.8 mmHg in the “late night.” Independently of the TOD, fluctuations were smallest during the 7-day interval and largest during the 360-day interval. The awake period, lasting from early morning to early evening, displayed increasing MADs with growing time intervals, resulting in moderate IOP fluctuations in the short term (1.5 mmHg < MAD < 2.0 mmHg) and large fluctuations in the long term (MAD > 2.0 mmHg). The late-night TOD displayed the lowest fluctuation amplitude.

Conclusions

Nychthemeral IOP fluctuations persist in eyes with an average IOP of 10 mmHg after successful NPGS. Short-term IOP fluctuations were moderate, whereas long-term fluctuations were large. Irregular IOP measurements are insufficient to assess IOP fluctuation and thus to determine optimal glaucoma management. The implementation of safe and accurate telemetric sensors has the potential to enhance glaucoma management.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:探讨原发性开角型青光眼(POAG)患者非穿透性青光眼手术(NPGS)成功后的短期和长期眼压(IOP)波动。设计:前瞻性、开放标签、多中心介入研究。受试者:共有20例POAG患者接受了NPGS联合脉络膜上遥测IOP传感器的永久植入(EyeMate-SC, Implandata Ophthalmic Products GmbH, Hanover, Germany)。该队列的平均年龄为66.9±10.6岁。其中一半是男性,一半是女性。方法:遥测IOP测量时间为3年,不包括术后前180天和使用青光眼药物期间。一天被分为八个时间段(TODs)。计算每个TOD和每只眼的眼内眼压中位绝对差(MAD),分别为day χ和day χ + 7、30、90、180和360,并相应地获得连续的眼内眼压测量。主要结果:眼压波动。结果:平均随访时间952.8±276.6 d。为了进行分析,共配对了139,512个平均IOP值。总体而言,白天的IOP下降了20.7%,从“清晨”的11.1±5.0 mmHg下降到“深夜”的8.8±3.2 mmHg,随后“深夜”的夜间IOP上升13.6%至10.0±3.8 mmHg。与TOD无关,波动在7天间隔期间最小,在360天间隔期间最大。清醒期从清晨持续到傍晚,随着时间间隔的增加,MADs增加,导致IOP短期中度波动(1.5 mmHg < MAD < 2.0 mmHg),长期大幅波动(MAD > 2.0 mmHg)。夜间TOD波动幅度最小。结论:NPGS成功后,平均眼压为10 mmHg的眼内持续夜热性眼压波动。短期眼压波动适中,而长期波动较大。不规则的IOP测量不足以评估IOP波动,从而确定最佳青光眼治疗。安全、准确的遥测传感器的实施有可能提高青光眼的管理。
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引用次数: 0
Causes and Treatments of Malignant Glaucoma in the United States 美国恶性青光眼的病因和治疗:IRIS®Registry (Intelligent Research in Sight)的分析。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.08.006
Asahi Fujita MD , William C. Kearney MS , David S. Friedman MD, PhD , Prashit Parikh BA , Elizabeth Ciociola Kelly MD , Yusrah Shweikh MD , Connor Ross BS , Tobias Elze PhD , Alice C. Lorch MD, MPH , Joan W. Miller MD , Nazlee Zebardast MD, MPH

Purpose

To investigate the causes and treatments of malignant glaucoma (MG) in the United States.

Design

Retrospective cohort study

Subjects

Eyes with diagnosis codes for MG between 2014 and 2023 in the IRIS® Registry (Intelligent Research in Sight).

Methods

Precipitating procedures and treatment modality were identified using procedure codes and medication data. Using generalized estimating equations, we investigated factors associated with initial treatment with pars plana vitrectomy (PPV), those associated with undergoing laser or incisional surgeries after medication, and those associated with undergoing surgery or cyclophotocoagulation after laser hyaloidotomy.

Main Outcome Measures

The primary outcomes were a breakdown of precipitating procedures and treatment modalities. The secondary outcomes included factors associated with initial treatment with PPV and those associated with undergoing additional procedures after medication or laser hyaloidotomy.

Results

A total of 3554 eyes were diagnosed with MG, among which pre-existing glaucoma was identified in 54.5%. Cataract surgery was the most common precipitating surgery (26.6%), and estimated incidence rate was the highest after tube shunt surgery (23.8/10 000). First-recorded treatment was medication in 54.8%, laser hyaloidotomy in 8.9%, and PPV in 31.9%. Higher intraocular pressure (IOP) at onset (odds ratio: 1.08 [95% confidence interval: 1.03–1.12] per 10 mmHg) and worse visual acuity at onset (odds ratio: 1.27 [95% confidence interval: 1.19–1.35] per 1 unit higher logarithm of the minimum angle of resolution) were associated with initial PPV; 34% and 24% of the eyes underwent additional procedures after medication and laser hyaloidotomy, respectively. Factors associated with subsequent procedures among medically treated eyes included aphakia or pseudophakia (odds ratio: 1.33 [95% confidence interval: 1.09–1.63]) and higher IOP at onset (odds ratio: 1.11 [95% confidence interval: 1.05–1.17] per 10 mmHg). Higher IOP at onset (odds ratio: 1.19 [95% confidence interval: 1.03–1.38] per 10 mmHg) was also associated with additional procedures after laser hyaloidotomy.

Conclusions

More than half of the eyes with MG had a pre-existing glaucoma diagnosis. Tube shunt surgery had the highest incidence rate of MG. More than half were initially treated with medication, and one-third were initially treated with PPV. Higher IOP at onset was associated with a higher likelihood of being initially treated with PPV as well as a higher likelihood of requiring additional procedures when initially treated with medication or laser hyaloidotomy.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:探讨美国恶性青光眼(MG)的病因及治疗方法。设计:回顾性队列研究受试者:在IRIS®注册表(视力智能研究)中2014年至2023年间诊断为MG的眼睛。方法:采用程序代码和用药资料确定沉淀程序和治疗方式。利用广义估计方程,我们研究了与玻璃体切割(PPV)初始治疗相关的因素,与药物治疗后进行激光或切口手术相关的因素,以及与激光玻璃体切开术后进行手术或光凝治疗相关的因素。主要结局指标:主要结局是沉淀程序和治疗方式的分解。次要结局包括与初始PPV治疗相关的因素,以及在药物或激光玻璃体切开术后接受额外手术相关的因素。结果:恶性青光眼3554眼,其中已有青光眼占54.5%。白内障手术是最常见的沉淀手术(26.6%),估计发病率最高的是分流手术(23.8/10,000)。首次记录的治疗方法为药物治疗占54.8%,激光玻璃体切开术占8.9%,PPV占31.9%。发病时较高的眼内压(IOP)(比值比:1.08[95%可信区间:1.03-1.12]/ 10 mmHg)和发病时较差的视力(比值比:1.27[1.19-1.35]/ 1单位高logMAR)与初始PPV相关。34%和24%的眼睛分别在药物治疗和激光玻璃体切开术后接受了额外的手术。在治疗过的眼睛中,与后续手术相关的因素包括无晶状体或假性晶状体(1.33[1.09-1.63])和发病时较高的IOP (1.11 [1.05-1.17] / 10 mmHg)。起病时较高的IOP (1.19 [1.03-1.38] / 10mmhg)也与激光玻璃体切开术后的附加手术有关。结论:超过一半的MG患者有先前的青光眼诊断。导管分流术中MG的发生率最高。超过一半的患者最初接受药物治疗,三分之一的患者最初接受PPV治疗。起病时较高的IOP与最初接受PPV治疗的可能性较高以及最初接受药物治疗或激光玻璃体切开术时需要额外手术的可能性较高相关。
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引用次数: 0
Predictors of Selective Laser Trabeculoplasty Efficacy 选择性激光小梁成形术疗效的预测因素来自瑞典最佳SLT多中心随机对照试验。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.08.008
Tobias Dahlgren MD , Marcelo Ayala MD, PhD , Madeleine Zetterberg MD, PhD
<div><h3>Purpose</h3><div>To investigate the impact of potential predictor variables on selective laser trabeculoplasty (SLT) efficacy in the Swedish Optimal SLT (OSLT) trial.</div></div><div><h3>Design</h3><div>Post hoc analysis of a multicenter, masked, randomized controlled trial.</div></div><div><h3>Subjects</h3><div>Five hundred twelve eyes from 399 patients enrolled in the OSLT trial.</div></div><div><h3>Methods</h3><div>Patients were randomized to one of 4 SLT variants, differing in treatment extent (180° or 360°), and laser power (standard or high). Analyses were performed with linear mixed models, which allowed optimal use of all the data and applied comprehensive adjustment to the results. A wide selection of potential predictors for SLT efficacy were first analyzed separately regarding their association with intraocular pressure reduction (IOPR). Predictors meeting a threshold of <em>P</em> < 0.1 were then included in a multivariable candidate model, which was refined through manual stepwise backwards selection until only significant variables (<em>P</em> < 0.05) remained. Thereafter, other variables of interest were evaluated in this model.</div></div><div><h3>Main Outcome Measures</h3><div>The mean IOPR 1 to 6 months after SLT.</div></div><div><h3>Results</h3><div>Selective laser trabeculoplasty performed in 360 degrees, at an energy level giving a 50% to 75% cavitation bubble frequency (the 360/high protocol) remained the most efficacious SLT variant after adjustment for predictors (<em>P <</em> 0.001). The coefficient estimate (CE) of 360/high SLT was 2.0; SLT performed in 360 degrees, at an energy level titrated just below the cavitation bubble threshold (360/standard) CE was 0.9; and SLT performed in 180 degrees, at an energy level giving a 50% to 75% cavitation bubble frequency (180/high) CE was –0.1, with SLT performed in 180 degrees, at an energy level titrated just below the cavitation bubble threshold (180/low) as the reference. Higher baseline IOP was a positive predictor for both absolute IOPR (CE 0.35; <em>P</em> < 0.001) and relative IOPR (CE 0.72; <em>P</em> < 0.001). A larger IOPR from the prior SLT (CE 0.18; <em>P</em> = 0.004), as well as IOPR in the contralateral eye (CE 0.57; <em>P</em> < 0.001), were also highly significant positive predictors. Conversely, the present analyses suggest that SLT efficacy is diminished by pseudoexfoliations (CE –0.69; <em>P</em> = 0.02), the number of prior SLTs (CE –0.54; <em>P</em> = 0.004), and increased corneal thickness (CE –0.01; <em>P</em> < 0.002). Consultants/specialists and residents achieved similar SLT results, but individual surgeon performance mattered (<em>P</em> = 0.003), as well as if the surgeon used the dominant hand (CE 0.35; <em>P</em> = 0.050). However, age, glaucoma medication, cataract surgery, anterior chamber angle pigmentation, inflammatory symptoms, or postoperative anterior chamber flare had no correlation with SLT efficacy.</div></di
目的:在瑞典最佳激光小梁成形术(OSLT)试验中,探讨潜在预测变量对选择性激光小梁成形术(SLT)疗效的影响。设计:一项多中心、盲法、随机对照试验的事后分析。受试者:参加OSLT试验的399例患者的512只眼睛。方法:根据治疗程度(180°或360°)和激光功率(标准或高)的不同,将患者随机分为四种SLT变体之一。采用线性混合模型(lmm)进行分析,使所有数据得到最佳利用,并对结果进行综合调整。我们首先对SLT疗效的多种潜在预测因素分别分析了它们与眼压降低(IOPR)的关系。主要结果测量:SLT后1-6个月的平均IOPR。结果:以180/标准为参考,调整预测因子(系数估计(CE) 360/高2.0、360/标准0.9和180/高-0.1)后,360/高方案仍然是最有效的SLT变体;结论:在调整多个预测因子后,360/high方案仍然是最有效和可靠的技术。没有证据表明反对针对任何特定患者群体的360/高SLT。选择性激光小梁成形术(SLT)是治疗开角型青光眼和高眼压的一线治疗方法。1-3 SLT可以用不同的技术(治疗方案)进行,主要在治疗区域的范围、激光光斑的数量和设置激光功率的原则上有所不同多年来,一直缺乏最佳治疗技术的证据。因此,我们设计了最优SLT (OSLT)试验,这是一项在瑞典进行的大型随机对照多中心试验。该研究包括来自400名患者的513只眼睛,随机分配到四种不同治疗程度(180度或360度)和激光功率(标准或高)的SLT方案之一。该研究的参与者构成了世界上最大的前瞻性SLT队列之一。OSLT的方法和初步结果已在以前报告过360/高SLT方案显示出更大的眼压(IOP)降低(IOPR),更高的成功率,更长的效果持续时间,而不降低安全性。
{"title":"Predictors of Selective Laser Trabeculoplasty Efficacy","authors":"Tobias Dahlgren MD ,&nbsp;Marcelo Ayala MD, PhD ,&nbsp;Madeleine Zetterberg MD, PhD","doi":"10.1016/j.ogla.2025.08.008","DOIUrl":"10.1016/j.ogla.2025.08.008","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Purpose&lt;/h3&gt;&lt;div&gt;To investigate the impact of potential predictor variables on selective laser trabeculoplasty (SLT) efficacy in the Swedish Optimal SLT (OSLT) trial.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Design&lt;/h3&gt;&lt;div&gt;Post hoc analysis of a multicenter, masked, randomized controlled trial.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Subjects&lt;/h3&gt;&lt;div&gt;Five hundred twelve eyes from 399 patients enrolled in the OSLT trial.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;Patients were randomized to one of 4 SLT variants, differing in treatment extent (180° or 360°), and laser power (standard or high). Analyses were performed with linear mixed models, which allowed optimal use of all the data and applied comprehensive adjustment to the results. A wide selection of potential predictors for SLT efficacy were first analyzed separately regarding their association with intraocular pressure reduction (IOPR). Predictors meeting a threshold of &lt;em&gt;P&lt;/em&gt; &lt; 0.1 were then included in a multivariable candidate model, which was refined through manual stepwise backwards selection until only significant variables (&lt;em&gt;P&lt;/em&gt; &lt; 0.05) remained. Thereafter, other variables of interest were evaluated in this model.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Main Outcome Measures&lt;/h3&gt;&lt;div&gt;The mean IOPR 1 to 6 months after SLT.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;Selective laser trabeculoplasty performed in 360 degrees, at an energy level giving a 50% to 75% cavitation bubble frequency (the 360/high protocol) remained the most efficacious SLT variant after adjustment for predictors (&lt;em&gt;P &lt;&lt;/em&gt; 0.001). The coefficient estimate (CE) of 360/high SLT was 2.0; SLT performed in 360 degrees, at an energy level titrated just below the cavitation bubble threshold (360/standard) CE was 0.9; and SLT performed in 180 degrees, at an energy level giving a 50% to 75% cavitation bubble frequency (180/high) CE was –0.1, with SLT performed in 180 degrees, at an energy level titrated just below the cavitation bubble threshold (180/low) as the reference. Higher baseline IOP was a positive predictor for both absolute IOPR (CE 0.35; &lt;em&gt;P&lt;/em&gt; &lt; 0.001) and relative IOPR (CE 0.72; &lt;em&gt;P&lt;/em&gt; &lt; 0.001). A larger IOPR from the prior SLT (CE 0.18; &lt;em&gt;P&lt;/em&gt; = 0.004), as well as IOPR in the contralateral eye (CE 0.57; &lt;em&gt;P&lt;/em&gt; &lt; 0.001), were also highly significant positive predictors. Conversely, the present analyses suggest that SLT efficacy is diminished by pseudoexfoliations (CE –0.69; &lt;em&gt;P&lt;/em&gt; = 0.02), the number of prior SLTs (CE –0.54; &lt;em&gt;P&lt;/em&gt; = 0.004), and increased corneal thickness (CE –0.01; &lt;em&gt;P&lt;/em&gt; &lt; 0.002). Consultants/specialists and residents achieved similar SLT results, but individual surgeon performance mattered (&lt;em&gt;P&lt;/em&gt; = 0.003), as well as if the surgeon used the dominant hand (CE 0.35; &lt;em&gt;P&lt;/em&gt; = 0.050). However, age, glaucoma medication, cataract surgery, anterior chamber angle pigmentation, inflammatory symptoms, or postoperative anterior chamber flare had no correlation with SLT efficacy.&lt;/div&gt;&lt;/di","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"9 1","pages":"Pages 15-25"},"PeriodicalIF":3.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145002057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical Outcomes of Hydrus Microstent Implantation for Open-Angle Glaucoma 水合液微支架植入术治疗开角型青光眼的临床效果:来自一个大型学术中心的结果。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.08.011
Natalie R. Hamilton PhD , Anam Akhlaq MBBS , Patrick O. Nnoromele BS , Nicolas Gasquet MPH , Catalina Garzon MD , Yulia Nam MD , Leangelo Hall MD , Pradeep Y. Ramulu MD, PhD , Ian Pitha MD, PhD , Mona Kaleem MD , Jella An MD , Elyse J. McGlumphy MD , Jacob A. Kanter MD , Thomas V. Johnson MD, PhD

Purpose

To assess the clinical outcomes of Hydrus Microstent implantation with cataract extraction for the treatment of open-angle glaucoma (OAG) over a maximum of 4 years.

Design

A retrospective, single-center, single-arm, longitudinal cohort study.

Subjects

Three hundred eight patients (464 eyes) with OAG who underwent Hydrus Microstent implantation with cataract extraction between February 2019 and December 2021, followed for a median of 2.0 (interquartile range [IQR], 1.3–2.8) years.

Methods

Medical records were reviewed to collect demographic and clinical data. After assessment for Gaussian distribution, mean and standard deviation (SD) or median and IQR were calculated. Change from baseline was calculated with mixed-effects models and expressed as mean change and standard error.

Main Outcome Measures

(1) Intraocular pressure (IOP); (2) number of glaucoma medications; (3) need for additional glaucoma procedures; and (4) rate of glaucoma progression, calculated using mean deviation (MD) from standard automated perimetry and OCT peripapillary retinal nerve fiber layer (RNFL) thickness.

Results

Among 308 patients, 60.7% (n = 187) were White, and 50.6% (n = 156) were female. The median age was 74 (IQR, 68–78) years. Most eyes had mild (63.8%) or moderate (23.9%) OAG. Of 464 eyes, 99 (21.4%) had undergone prior procedures for glaucoma. At baseline, the mean (±SD) IOP was 16.0 ± 3.7 mmHg while taking 1.9 ± 1.1 glaucoma medications. After Hydrus implantation, a sustained reduction was observed in mean IOP [mean change ± standard error]: –1.9 ± 0.3 at 6 months (P < 0.0001), –1.2 ± 0.2 at 1 year (P < 0.0001), –1.2 ± 0.2 at 2 years (P < 0.0001), –1.6 ± 0.3 at 3 years (P < 0.0001), and –1.2 ± 0.7 at 4 years (P = 0.02). Glaucoma medications were reduced by 1.2 ± 0.1 at 6 months (P < 0.0001), 1.1 ± 0.1 at 1 year (P < 0.0001), 1.0 ± 0.1 at 2 years (P < 0.0001), 0.9 ± 0.1 at 3 years (P < 0.0001), and 0.5 ± 0.2 at 4 years (P = 0.03). Only 14 eyes (3.2%) required additional glaucoma procedures. Compared to the lookback period, the rates of visual field MD and RNFL loss decreased in the postoperative period by 0.18 ± 0.08 dB/year (–0.18 ± 0.02 vs. 0.004 ± 0.08 dB/year, P = 0.02) and 0.51 ± 0.29 μm/year (–0.47 ± 0.12 vs. 0.04 ± 0.21 μm/year, P = 0.07), respectively.

Conclusions

In this nontrial setting, cataract surgery with Hydrus Microstent implantation was associated with sustained reductions in IOP, glaucoma medication burden, and disease progression rate.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:评价水合显微支架植入术联合白内障摘出术治疗开角型青光眼(OAG)最长4年的临床疗效。设计:回顾性、单中心、单臂、纵向队列研究。研究对象:2019年2月至2021年12月期间,308例(464只眼)OAG患者接受了Hydrus Microstent植入术并摘除白内障,随访中位数(四分位数间距,IQR)为2.0(1.3,2.8)年。方法:回顾医疗记录,收集人口学和临床资料。经高斯分布评估后,计算平均值和标准差(SD)或中位数和IQR。使用混合效应模型计算基线变化,并以平均变化和标准误差(SE)表示。主要观察指标:1)眼压(IOP);2)青光眼用药次数;3)需要额外的青光眼手术;4)青光眼的进展率,使用标准自动视距测量和光学相干断层扫描乳头周围视网膜神经纤维层(RFNL)厚度的平均偏差(MD)计算。结果:308例患者中白人占60.7% (n=187),女性占50.6% (n=156)。中位(IQR)年龄为74(68,78)岁。大多数眼睛为轻度(63.8%)或中度(23.9%)OAG。在464只眼睛中,99只(21.4%)曾经接受过青光眼手术。基线时,平均(±SD) IOP为16.0±3.7 mmHg,同时服用1.9±1.1种青光眼药物。在Hydrus植入术后,6个月平均IOP持续降低[平均变化±SE]: -1.9±0.3](结论:在非试验环境下,白内障手术植入Hydrus微支架与IOP、青光眼药物负担和疾病进展率持续降低相关。
{"title":"Clinical Outcomes of Hydrus Microstent Implantation for Open-Angle Glaucoma","authors":"Natalie R. Hamilton PhD ,&nbsp;Anam Akhlaq MBBS ,&nbsp;Patrick O. Nnoromele BS ,&nbsp;Nicolas Gasquet MPH ,&nbsp;Catalina Garzon MD ,&nbsp;Yulia Nam MD ,&nbsp;Leangelo Hall MD ,&nbsp;Pradeep Y. Ramulu MD, PhD ,&nbsp;Ian Pitha MD, PhD ,&nbsp;Mona Kaleem MD ,&nbsp;Jella An MD ,&nbsp;Elyse J. McGlumphy MD ,&nbsp;Jacob A. Kanter MD ,&nbsp;Thomas V. Johnson MD, PhD","doi":"10.1016/j.ogla.2025.08.011","DOIUrl":"10.1016/j.ogla.2025.08.011","url":null,"abstract":"<div><h3>Purpose</h3><div>To assess the clinical outcomes of Hydrus Microstent implantation with cataract extraction for the treatment of open-angle glaucoma (OAG) over a maximum of 4 years.</div></div><div><h3>Design</h3><div>A retrospective, single-center, single-arm, longitudinal cohort study.</div></div><div><h3>Subjects</h3><div>Three hundred eight patients (464 eyes) with OAG who underwent Hydrus Microstent implantation with cataract extraction between February 2019 and December 2021, followed for a median of 2.0 (interquartile range [IQR], 1.3–2.8) years.</div></div><div><h3>Methods</h3><div>Medical records were reviewed to collect demographic and clinical data. After assessment for Gaussian distribution, mean and standard deviation (SD) or median and IQR were calculated. Change from baseline was calculated with mixed-effects models and expressed as mean change and standard error.</div></div><div><h3>Main Outcome Measures</h3><div>(1) Intraocular pressure (IOP); (2) number of glaucoma medications; (3) need for additional glaucoma procedures; and (4) rate of glaucoma progression, calculated using mean deviation (MD) from standard automated perimetry and OCT peripapillary retinal nerve fiber layer (RNFL) thickness.</div></div><div><h3>Results</h3><div>Among 308 patients, 60.7% (n = 187) were White, and 50.6% (n = 156) were female. The median age was 74 (IQR, 68–78) years. Most eyes had mild (63.8%) or moderate (23.9%) OAG. Of 464 eyes, 99 (21.4%) had undergone prior procedures for glaucoma. At baseline, the mean (±SD) IOP was 16.0 ± 3.7 mmHg while taking 1.9 ± 1.1 glaucoma medications. After Hydrus implantation, a sustained reduction was observed in mean IOP [mean change ± standard error]: –1.9 ± 0.3 at 6 months (<em>P</em> &lt; 0.0001), –1.2 ± 0.2 at 1 year (<em>P</em> &lt; 0.0001), –1.2 ± 0.2 at 2 years (<em>P</em> &lt; 0.0001), –1.6 ± 0.3 at 3 years (<em>P</em> &lt; 0.0001), and –1.2 ± 0.7 at 4 years (<em>P</em> = 0.02). Glaucoma medications were reduced by 1.2 ± 0.1 at 6 months (<em>P</em> &lt; 0.0001), 1.1 ± 0.1 at 1 year (<em>P</em> &lt; 0.0001), 1.0 ± 0.1 at 2 years (<em>P</em> &lt; 0.0001), 0.9 ± 0.1 at 3 years (<em>P</em> &lt; 0.0001), and 0.5 ± 0.2 at 4 years (<em>P</em> = 0.03). Only 14 eyes (3.2%) required additional glaucoma procedures. Compared to the lookback period, the rates of visual field MD and RNFL loss decreased in the postoperative period by 0.18 ± 0.08 dB/year (–0.18 ± 0.02 vs. 0.004 ± 0.08 dB/year, <em>P</em> = 0.02) and 0.51 ± 0.29 μm/year (–0.47 ± 0.12 vs. 0.04 ± 0.21 μm/year, <em>P</em> = 0.07), respectively.</div></div><div><h3>Conclusions</h3><div>In this nontrial setting, cataract surgery with Hydrus Microstent implantation was associated with sustained reductions in IOP, glaucoma medication burden, and disease progression rate.</div></div><div><h3>Financial Disclosure(s)</h3><div>Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.</div></div>","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"9 1","pages":"Pages 48-61"},"PeriodicalIF":3.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145008680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Obstructive Sleep Apnea as a Potentiator of Primary Open-Angle Glaucoma and Necessity for Interventional Therapy 阻塞性睡眠呼吸暂停作为原发性开角型青光眼的增强剂及介入治疗的必要性。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-11-01 DOI: 10.1016/j.ogla.2025.05.005
Pranav Vasu MPH , Isabella V. Wagner BS , Paul Connor Lentz MD , Priyanka Gumaste MD , Yazan Abubaker MD , Bryan C.H. Ang MD , Abhimanyu S. Ahuja MD , Emily Dorairaj BS , Ibrahim Qozat MD , Darby D. Miller MD, MPH , Syril Dorairaj MD

Purpose

To evaluate the rate of progression of primary open-angle glaucoma (POAG) in patients with obstructive sleep apnea (OSA) compared with non-OSA mild-moderate POAG comparators and to assess the utilization of surgical and laser intervention.

Design

A retrospective cohort study of the TriNetX US Collaborative Network was conducted by analyzing international electronic health record data from January 2004 to October 2024.

Participants

Patients in the TriNetX US Collaborative Network with a diagnosis of mild-moderate POAG, stratified with respect to OSA status.

Methods

Patients were assessed for outcomes at 3, 5, and 10 years. Propensity score matching was conducted between cohorts matched for baseline demographics, comorbidities, and medication use. Odds ratios (ORs) and 95% confidence intervals (CIs) were subsequently calculated.

Main Outcome Measures

Risk of development of severe POAG.

Results

After propensity score matching, 5277 patients with, and 5277 patients without OSA were included in final analysis. At 3 (OR, 2.791; 95% CI, 2.289–3.403), 5 (OR, 2.300; 95% CI, 1.947–2.717), and 10 years (OR, 2.198; 95% CI, 1.873–2.578), the OSA cohort demonstrated significantly higher odds of developing severe POAG than the non-OSA comparators. Secondary outcomes of minimally invasive glaucoma surgery and trabeculectomy surgery yielded no significant difference between both cohorts (P > 0.05) at all follow-up times. However, laser therapy and tube shunt surgery demonstrated a significantly greater incidence in the OSA cohort at each time point.

Conclusions

The rate of glaucoma surgery appears similar between patients with POAG with and without OSA, despite those with OSA demonstrating a greater risk of rapid progression and vision loss. Future practice patterns should pay special attention to patients with OSA and consider offering more aggressive or earlier intervention, which may aid in limiting disease progression.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:评价阻塞性睡眠呼吸暂停(OSA)患者原发性开角型青光眼(POAG)与非OSA轻、中度POAG比较者的进展率,并评价手术和激光干预的应用情况。设计:通过分析2004年1月至2024年10月的国际电子健康记录(EHR)数据,对TriNetX美国协作网络进行回顾性队列研究。参与者:TriNetX美国合作网络中诊断为轻中度POAG的患者,根据OSA状态分层。方法:对患者进行3年、5年和10年的预后评估。倾向评分匹配(PSM)在基线人口统计学、合并症和药物使用匹配的队列之间进行。随后计算优势比(OR)和95%置信区间(CI)。主要观察指标:发生严重POAG的风险。结果:经PSM后,5277例OSA患者和5277例无OSA患者被纳入最终分析。在3年(OR 2.791, 95% CI: 2.289 - 3.403)、5年(OR 2.300, 95% CI: 1.947 - 2.717)和10年(OR: 2.198, 95% CI: 1.873 - 2.578)时,与非OSA比较者相比,OSA队列发生严重POAG的几率明显更高。微创青光眼手术(MIGS)和小梁切除术的次要结局在所有随访时间内两组间无显著差异(P < 0.05)。然而,在每个时间点,激光治疗和导管分流手术在OSA队列中的发病率都明显更高。结论:伴有和不伴有OSA的POAG患者青光眼手术率相似,尽管伴有OSA的患者表现出更大的快速进展和视力丧失的风险。未来的实践模式应特别关注阻塞性睡眠呼吸暂停患者,并考虑提供更积极或更早的干预,这可能有助于限制疾病进展。
{"title":"Obstructive Sleep Apnea as a Potentiator of Primary Open-Angle Glaucoma and Necessity for Interventional Therapy","authors":"Pranav Vasu MPH ,&nbsp;Isabella V. Wagner BS ,&nbsp;Paul Connor Lentz MD ,&nbsp;Priyanka Gumaste MD ,&nbsp;Yazan Abubaker MD ,&nbsp;Bryan C.H. Ang MD ,&nbsp;Abhimanyu S. Ahuja MD ,&nbsp;Emily Dorairaj BS ,&nbsp;Ibrahim Qozat MD ,&nbsp;Darby D. Miller MD, MPH ,&nbsp;Syril Dorairaj MD","doi":"10.1016/j.ogla.2025.05.005","DOIUrl":"10.1016/j.ogla.2025.05.005","url":null,"abstract":"<div><h3>Purpose</h3><div>To evaluate the rate of progression of primary open-angle glaucoma (POAG) in patients with obstructive sleep apnea (OSA) compared with non-OSA mild-moderate POAG comparators and to assess the utilization of surgical and laser intervention.</div></div><div><h3>Design</h3><div>A retrospective cohort study of the TriNetX US Collaborative Network was conducted by analyzing international electronic health record data from January 2004 to October 2024.</div></div><div><h3>Participants</h3><div>Patients in the TriNetX US Collaborative Network with a diagnosis of mild-moderate POAG, stratified with respect to OSA status.</div></div><div><h3>Methods</h3><div>Patients were assessed for outcomes at 3, 5, and 10 years. Propensity score matching was conducted between cohorts matched for baseline demographics, comorbidities, and medication use. Odds ratios (ORs) and 95% confidence intervals (CIs) were subsequently calculated.</div></div><div><h3>Main Outcome Measures</h3><div>Risk of development of severe POAG.</div></div><div><h3>Results</h3><div>After propensity score matching, 5277 patients with, and 5277 patients without OSA were included in final analysis. At 3 (OR, 2.791; 95% CI, 2.289–3.403), 5 (OR, 2.300; 95% CI, 1.947–2.717), and 10 years (OR, 2.198; 95% CI, 1.873–2.578), the OSA cohort demonstrated significantly higher odds of developing severe POAG than the non-OSA comparators. Secondary outcomes of minimally invasive glaucoma surgery and trabeculectomy surgery yielded no significant difference between both cohorts (<em>P</em> &gt; 0.05) at all follow-up times. However, laser therapy and tube shunt surgery demonstrated a significantly greater incidence in the OSA cohort at each time point.</div></div><div><h3>Conclusions</h3><div>The rate of glaucoma surgery appears similar between patients with POAG with and without OSA, despite those with OSA demonstrating a greater risk of rapid progression and vision loss. Future practice patterns should pay special attention to patients with OSA and consider offering more aggressive or earlier intervention, which may aid in limiting disease progression.</div></div><div><h3>Financial Disclosure(s)</h3><div>Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.</div></div>","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"8 6","pages":"Pages 553-559"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144144614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Outcomes of Hydrus Microstent with Cataract Surgery in Asian and Non-Asian Eyes with Normal Tension Glaucoma 亚洲和非亚洲眼正常张力性青光眼白内障手术中水合微支架的疗效。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-11-01 DOI: 10.1016/j.ogla.2025.06.006
Debbie S. Kuo MD , Sharon Y.H. Lee OD , Christos N. Theophanous MD, MBA

Purpose

To evaluate the efficacy and safety of the Hydrus Microstent in conjunction with cataract surgery in patients with normal tension glaucoma (NTG) with minimum 12-month follow-up.

Design

Retrospective cohort study.

Subjects

Normal tension glaucoma eyes having Hydrus with cataract surgery and cataract-only controls.

Methods

Glaucoma was staged by the Hodapp–Parrish–Anderson criteria. Generalized estimating equations were used to account for intraocular correlation in regression analyses.

Main Outcome Measures

The primary outcome was medication reduction from baseline at 1 year. Secondary outcomes were medication reduction in subsequent years, mean intraocular pressure (IOP) change from baseline, proportion of eyes meeting IOP targets, and percentage of eyes requiring secondary surgical interventions (SSI) at yearly time points.

Results

Sixty-four eyes of 40 patients undergoing Hydrus Microstent and cataract surgery were included in the analysis, of which 32 eyes were from Asian patients. Thirty-nine eyes of 25 patients were used as cataract-only controls. Glaucoma severity was mild (37.5%), moderate (40.6%) and severe (21.9%) in treated eyes. The median follow-up available was 2.5 years (range: 1–5 years). Baseline IOP was 13.83 ± 2.93 mmHg on 2.11 ± 1.04 medication classes in treated eyes. At year 1, there was a mean reduction of medication classes by 1.25 ± 0.84 (P < 0.0010) and IOP by 0.89 ± 2.61 mmHg (P = 0.02). Medication class reduction remained significant through year 4 and IOP reduction through year 3. Compared to controls, treated eyes had significant differences in mean medication change (−1.25 vs. −0.03 at year 1, P < 0.001) and percentage of eyes with medication reduction (85.9% vs. 5.3% at year 1, P < 0.001), which were sustained through at least year 4. There were no significant differences in medication reduction and IOP observed between treated Asian and non-Asian eyes at any time point. In treated eyes, IOP was 16 mmHg or less on same or fewer medications in more than 90% (range: 90.6%–100%) of eyes at all time points and medication-free in more than 31% (range: 31.3%–54.5%) at all time points. No SSI occurred during the study period.

Conclusions

Hydrus Microstent was safe and effective in all NTG eyes with a significant, sustained reduction in medication use through at least 4 years of follow-up.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:通过至少12个月的随访,评价Hydrus微支架联合白内障手术治疗正常张力性青光眼(NTG)患者的疗效和安全性。设计:回顾性队列研究。方法:青光眼按照Hodapp-Parrish-Anderson标准进行分期。在回归分析中使用广义估计方程来解释眼内相关性。主要转归指标:主要转归指标为1年时基线用药减少。次要结果是随后几年的药物减少,平均IOP从基线变化,达到IOP目标的眼睛比例,以及每年时间点需要二次手术干预(SSI)的眼睛百分比。结果:40例行水合显微支架和白内障手术的患者64只眼纳入分析,其中32只眼来自亚洲患者。25例患者39只眼作为单纯白内障对照。青光眼严重程度分别为轻度(37.5%)、中度(40.6%)和重度(21.9%)。中位随访时间为2.5年(范围:1-5年)。基线IOP为13.83±2.93 mmHg,用药等级为2.11±1.04。在第1年,药物类别平均减少1.25±0.84 (p < 0.0010), IOP平均减少0.89±2.61 mmHg (p = 0.02)。在第4年,药物等级的降低仍然很明显,在第3年,IOP的降低也很明显。与对照组相比,接受治疗的眼睛在平均药物变化方面存在显著差异(1年时为-1.25 vs -0.03)。结论:Hydrus微支架在所有NTG眼睛中都是安全有效的,在至少4年的随访中,药物使用显著持续减少。
{"title":"Outcomes of Hydrus Microstent with Cataract Surgery in Asian and Non-Asian Eyes with Normal Tension Glaucoma","authors":"Debbie S. Kuo MD ,&nbsp;Sharon Y.H. Lee OD ,&nbsp;Christos N. Theophanous MD, MBA","doi":"10.1016/j.ogla.2025.06.006","DOIUrl":"10.1016/j.ogla.2025.06.006","url":null,"abstract":"<div><h3>Purpose</h3><div>To evaluate the efficacy and safety of the Hydrus Microstent in conjunction with cataract surgery in patients with normal tension glaucoma (NTG) with minimum 12-month follow-up.</div></div><div><h3>Design</h3><div>Retrospective cohort study.</div></div><div><h3>Subjects</h3><div>Normal tension glaucoma eyes having Hydrus with cataract surgery and cataract-only controls.</div></div><div><h3>Methods</h3><div>Glaucoma was staged by the Hodapp–Parrish–Anderson criteria. Generalized estimating equations were used to account for intraocular correlation in regression analyses.</div></div><div><h3>Main Outcome Measures</h3><div>The primary outcome was medication reduction from baseline at 1 year. Secondary outcomes were medication reduction in subsequent years, mean intraocular pressure (IOP) change from baseline, proportion of eyes meeting IOP targets, and percentage of eyes requiring secondary surgical interventions (SSI) at yearly time points.</div></div><div><h3>Results</h3><div>Sixty-four eyes of 40 patients undergoing Hydrus Microstent and cataract surgery were included in the analysis, of which 32 eyes were from Asian patients. Thirty-nine eyes of 25 patients were used as cataract-only controls. Glaucoma severity was mild (37.5%), moderate (40.6%) and severe (21.9%) in treated eyes. The median follow-up available was 2.5 years (range: 1–5 years). Baseline IOP was 13.83 ± 2.93 mmHg on 2.11 ± 1.04 medication classes in treated eyes. At year 1, there was a mean reduction of medication classes by 1.25 ± 0.84 (<em>P</em> &lt; 0.0010) and IOP by 0.89 ± 2.61 mmHg (<em>P</em> = 0.02). Medication class reduction remained significant through year 4 and IOP reduction through year 3. Compared to controls, treated eyes had significant differences in mean medication change (−1.25 vs. −0.03 at year 1, <em>P</em> &lt; 0.001) and percentage of eyes with medication reduction (85.9% vs. 5.3% at year 1, <em>P</em> &lt; 0.001), which were sustained through at least year 4. There were no significant differences in medication reduction and IOP observed between treated Asian and non-Asian eyes at any time point. In treated eyes, IOP was 16 mmHg or less on same or fewer medications in more than 90% (range: 90.6%–100%) of eyes at all time points and medication-free in more than 31% (range: 31.3%–54.5%) at all time points. No SSI occurred during the study period.</div></div><div><h3>Conclusions</h3><div>Hydrus Microstent was safe and effective in all NTG eyes with a significant, sustained reduction in medication use through at least 4 years of follow-up.</div></div><div><h3>Financial Disclosure(s)</h3><div>Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.</div></div>","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"8 6","pages":"Pages 589-598"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144327813","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Survey of Patient Understanding and Satisfaction in Glaucoma Filtering Surgery 青光眼滤过手术患者认识及满意度调查。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-11-01 DOI: 10.1016/j.ogla.2025.06.007
Farid Akkouche MD , Paul Bastelica MD , Christophe Baudouin MD, PhD , Shaya Sable MD , Antoine Labbe MD, PhD

Objectives

To assess patients' understanding of glaucoma surgery and their postoperative satisfaction, to study the factors that may influence them, and to investigate correlations between these 2 determining factors.

Design

A multicenter observational study.

Subjects

Patients scheduled for glaucoma filtration surgery were included.

Methods

Participants responded preoperatively to a questionnaire developed after literature review, evaluating their understanding of the surgery, and to a second questionnaire evaluating their postoperative satisfaction, between 2 and 3 months after surgery.

Main Outcome Measures

The primary outcomes were the mean scores for preoperative understanding and postoperative satisfaction. The influence of demographic, clinical, and surgical factors on comprehension and satisfaction was analyzed using univariate and multivariate models.

Results

In this study, 97 patients responded to the questionnaire evaluating their understanding of the surgery preoperatively. Postoperative satisfaction could be evaluated in 86 of them. The mean understanding score was 13.4 ± 5.4 (out of 25). Level of education (P < 0.01) and reading the French Society of Ophthalmology's information form on glaucoma filtering surgery (P < 0.05) were statistically correlated with a better understanding after multivariate analysis. The mean postoperative satisfaction score was 7.13 ± 3.0 (out of 10). Needling (P < 0.01) and resumption of hypotensive treatment (P < 0.001) were statistically correlated with poorer satisfaction after multivariate analysis. In addition, poorer preoperative understanding was correlated with lower postoperative satisfaction with a Pearson coefficient of 0.42 (95% confidence interval: 0.23–0.57 [P < 0.01]).

Conclusions

Overall, patient understanding was limited, and poor understanding negatively influenced postoperative satisfaction.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.
目的:了解患者对青光眼手术的了解程度和术后满意度,探讨可能影响青光眼手术满意度的因素,并探讨两者之间的相关性。设计:多中心观察性研究。对象:计划行青光眼滤过手术的患者。方法:术前,参与者在文献回顾后填写一份问卷,评估他们对手术的理解,并在术后2至3个月内填写第二份问卷,评估他们的术后满意度。主要结局指标:主要结局是术前理解和术后满意度的平均得分。采用单因素和多因素模型分析人口统计学、临床和手术因素对理解和满意度的影响。结果:本研究对97例患者进行了术前认知问卷调查。其中86例可评价术后满意度。平均理解得分为13.4±5.4分(满分25分)。结论:总体而言,患者理解有限,理解不足对术后满意度产生负面影响。
{"title":"Survey of Patient Understanding and Satisfaction in Glaucoma Filtering Surgery","authors":"Farid Akkouche MD ,&nbsp;Paul Bastelica MD ,&nbsp;Christophe Baudouin MD, PhD ,&nbsp;Shaya Sable MD ,&nbsp;Antoine Labbe MD, PhD","doi":"10.1016/j.ogla.2025.06.007","DOIUrl":"10.1016/j.ogla.2025.06.007","url":null,"abstract":"<div><h3>Objectives</h3><div>To assess patients' understanding of glaucoma surgery and their postoperative satisfaction, to study the factors that may influence them, and to investigate correlations between these 2 determining factors.</div></div><div><h3>Design</h3><div>A multicenter observational study.</div></div><div><h3>Subjects</h3><div>Patients scheduled for glaucoma filtration surgery were included.</div></div><div><h3>Methods</h3><div>Participants responded preoperatively to a questionnaire developed after literature review, evaluating their understanding of the surgery, and to a second questionnaire evaluating their postoperative satisfaction, between 2 and 3 months after surgery.</div></div><div><h3>Main Outcome Measures</h3><div>The primary outcomes were the mean scores for preoperative understanding and postoperative satisfaction. The influence of demographic, clinical, and surgical factors on comprehension and satisfaction was analyzed using univariate and multivariate models.</div></div><div><h3>Results</h3><div>In this study, 97 patients responded to the questionnaire evaluating their understanding of the surgery preoperatively. Postoperative satisfaction could be evaluated in 86 of them. The mean understanding score was 13.4 ± 5.4 (out of 25). Level of education (<em>P</em> &lt; 0.01) and reading the French Society of Ophthalmology's information form on glaucoma filtering surgery (<em>P</em> &lt; 0.05) were statistically correlated with a better understanding after multivariate analysis. The mean postoperative satisfaction score was 7.13 ± 3.0 (out of 10). Needling (<em>P</em> &lt; 0.01) and resumption of hypotensive treatment (<em>P</em> &lt; 0.001) were statistically correlated with poorer satisfaction after multivariate analysis. In addition, poorer preoperative understanding was correlated with lower postoperative satisfaction with a Pearson coefficient of 0.42 (95% confidence interval: 0.23–0.57 [<em>P</em> &lt; 0.01]).</div></div><div><h3>Conclusions</h3><div>Overall, patient understanding was limited, and poor understanding negatively influenced postoperative satisfaction.</div></div><div><h3>Financial Disclosure(s)</h3><div>The author(s) have no proprietary or commercial interest in any materials discussed in this article.</div></div>","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"8 6","pages":"Pages 634-642"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144487253","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ologen-Augmentation of Ahmed Valves in Pediatric Glaucomas 儿童青光眼艾哈迈德瓣膜的olog增强:2-6年随访。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-11-01 DOI: 10.1016/j.ogla.2025.06.008
Adam Jacobson MD , Brenda L. Bohnsack MD, PhD

Purpose

Determine 2- to 6-year outcomes of Ologen augmentation of Ahmed glaucoma devices (OAGDs) in children with glaucoma.

Design

Retrospective interventional case series.

Subjects

Children (<18 years of age) with glaucoma requiring surgery for intraocular pressure (IOP) control with at least 2 years of postoperative follow-up.

Methods

Placement of OAGD between 2018 and 2022.

Main Outcome Measures

Change in IOP, number of glaucoma medications and best-corrected visual acuity from preoperative to final follow-up, and success of surgery (complete defined as IOP 5 to 20 mmHg without additional medications, visually devastating complication or additional IOP-lowering surgeries, qualified success defined as above except IOP control was maintained ± glaucoma medications).

Results

Forty eyes of 28 patients underwent OAGD at median age of 2.6 years (interquartile range [IQR], 0.6–7.8). Primary congenital glaucoma was the most common diagnosis (12 eyes of 9 patients), followed by glaucoma secondary to nonacquired ocular anomaly (11 eyes of 6 patients). Twenty-two eyes of 16 patients had prior glaucoma surgery (median 2, [interquatile range (IQR), 1–2]). Preoperative IOP was a median of 27 mmHg (IQR, 24–35) on a median of 3 (IQR, 2–3) glaucoma medications. At final follow-up (median 3.6 years [IQR, 2.9–4.3]), IOP (median, 15 mmHg [IQR, 13–17]) and glaucoma medications (median, 0 [IQR, 0–0]) were significantly decrease (P < 0.0001). Complete success at final follow-up was 55% (22 of 40 eyes) with 3- and 5-year survival rates of 75% (95% confidence interval [CI], 59–86) and 57% (95% CI, 35–74). Qualified success rate was 75% (30 of 40 eyes) with 3- and 5-year survival rates of 87% (95% CI, 71–95) and 67% (95% CI, 42–83), respectively.

Conclusions

Although OAGD decreased IOP and the number of glaucoma medications, the high survival rates seen over the first 3 years decreased by 5 years.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:确定Ahmed青光眼装置(OAGD)的ogen增强治疗儿童青光眼的2 - 6年预后。设计:回顾性介入病例系列研究对象:需要手术控制IOP(眼内压)的青光眼儿童(小于10岁),术后随访至少2年。方法:2018 - 2022年间放置OAGD。主要观察指标:术前至最终随访期间IOP的变化,青光眼药物的数量和最佳矫正视力(BCVA),手术成功(完全定义为IOP 5- 20mmhg,无额外药物,视力破坏性并发症或额外的降低眼压手术,除维持眼压控制外,上述定义的合格成功±青光眼药物。结果:28例患者40眼发生OAGD,中位年龄2.6岁[IQR 0.6, 7.8]。原发性先天性青光眼是最常见的诊断(9例12眼),其次是继发于非获得性眼部异常的青光眼(6例11眼)。16例患者中22只眼既往有青光眼手术史(中位数2,[IQR 1,2])。术前使用中位数3 [IQR 2,3]青光眼药物,IOP中位数为27 mmHg [IQR 24,35]。在最终随访(中位随访3.6年[IQR 2.9, 4.3])时,IOP(中位随访15 mmHg [IQR 13,17])和青光眼药物治疗(中位随访0 [IQR 0,0])均显著降低(p结论:OAGD降低了IOP和青光眼药物治疗的数量,前3年的高生存率下降了5年。
{"title":"Ologen-Augmentation of Ahmed Valves in Pediatric Glaucomas","authors":"Adam Jacobson MD ,&nbsp;Brenda L. Bohnsack MD, PhD","doi":"10.1016/j.ogla.2025.06.008","DOIUrl":"10.1016/j.ogla.2025.06.008","url":null,"abstract":"<div><h3>Purpose</h3><div>Determine 2- to 6-year outcomes of Ologen augmentation of Ahmed glaucoma devices (OAGDs) in children with glaucoma.</div></div><div><h3>Design</h3><div>Retrospective interventional case series.</div></div><div><h3>Subjects</h3><div>Children (&lt;18 years of age) with glaucoma requiring surgery for intraocular pressure (IOP) control with at least 2 years of postoperative follow-up.</div></div><div><h3>Methods</h3><div>Placement of OAGD between 2018 and 2022.</div></div><div><h3>Main Outcome Measures</h3><div>Change in IOP, number of glaucoma medications and best-corrected visual acuity from preoperative to final follow-up, and success of surgery (complete defined as IOP 5 to 20 mmHg without additional medications, visually devastating complication or additional IOP-lowering surgeries, qualified success defined as above except IOP control was maintained ± glaucoma medications).</div></div><div><h3>Results</h3><div>Forty eyes of 28 patients underwent OAGD at median age of 2.6 years (interquartile range [IQR], 0.6–7.8). Primary congenital glaucoma was the most common diagnosis (12 eyes of 9 patients), followed by glaucoma secondary to nonacquired ocular anomaly (11 eyes of 6 patients). Twenty-two eyes of 16 patients had prior glaucoma surgery (median 2, [interquatile range (IQR), 1–2]). Preoperative IOP was a median of 27 mmHg (IQR, 24–35) on a median of 3 (IQR, 2–3) glaucoma medications. At final follow-up (median 3.6 years [IQR, 2.9–4.3]), IOP (median, 15 mmHg [IQR, 13–17]) and glaucoma medications (median, 0 [IQR, 0–0]) were significantly decrease (<em>P</em> &lt; 0.0001). Complete success at final follow-up was 55% (22 of 40 eyes) with 3- and 5-year survival rates of 75% (95% confidence interval [CI], 59–86) and 57% (95% CI, 35–74). Qualified success rate was 75% (30 of 40 eyes) with 3- and 5-year survival rates of 87% (95% CI, 71–95) and 67% (95% CI, 42–83), respectively.</div></div><div><h3>Conclusions</h3><div>Although OAGD decreased IOP and the number of glaucoma medications, the high survival rates seen over the first 3 years decreased by 5 years.</div></div><div><h3>Financial Disclosure(s)</h3><div>Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.</div></div>","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"8 6","pages":"Pages 609-615"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144531323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Re: Han et al.: Comparison of structural changes after epiretinal membrane peeling between nonglaucomatous eyes and eyes with open-angle glaucoma (Ophthalmology Glaucoma. 2025;8:351-359) Re: Han等:非青光眼与开角型青光眼视网膜前膜剥离后结构变化的比较(眼科学青光眼,2025;8:351-359)。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-11-01 DOI: 10.1016/j.ogla.2025.09.002
Chun-Hsiang Chang MD, Fu-Chin Huang MD, I-Huang Lin MD
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引用次数: 0
期刊
Ophthalmology. Glaucoma
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