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Assessing Agreement of Intraocular Pressure from Four Mechanistically Different Tonometers in the Eye Dynamics and Engineering Network Clinical Trial 在EDEN临床试验中评估四种机械不同眼压计的眼压一致性。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.07.010
Max Liu BS , David M. Reed PhD , Shan Fan MD , Arash Kazemi MD , Vikas Gulati MD, PhD , Arthur J. Sit SM, MD , Sayoko E. Moroi MD, PhD , Carol B. Toris PhD

Purpose

To compare the measurements of intraocular pressure (IOP) by four mechanistically different tonometers in healthy participants from the Eye Dynamics and Engineering Network Aqueous Humor Dynamics clinical trial using the mean difference estimation, equivalence statistics, and adjusting for proparacaine’s effects on IOP.

Design

Multicenter open-label clinical trial in healthy adults (NCT01677507).

Participants

Enrolled were 122 participants (55.2 ± 8.8 years; 92 women and 30 men), 121 of which had measurements with and without proparacaine.

Methods

Participants from 3 sites had their IOPs measured with iCare rebound tonometer (RT), ocular response analyzer corneal-compensated (CC), pneumatonometer (PN), and Goldmann applanation tonometer (GAT). Intraocular pressure readings with RT and CC were collected with and without proparacaine.

Main Outcome Measures

Effect sizes and agreement in IOP measurements from the four tonometers was analyzed with Data analysis using Bootstrap-Coupled ESTimation, Bland–Altman Limits of Agreement (LoAs), Lin's concordance correlation coefficient (CCC), and robust equivalence two 1-sided t-tests in tandem with null hypothesis significance testing. Data analysis using bootstrap-Coupled ESTimation was used to analyze differences in IOP readings from RT and CC before and after administering proparacaine.

Results

Data analysis using Bootstrap-Coupled ESTimation, LoA, and CCC showed greatest effect size and poorest agreement between PN and the other tonometers. The lowest mean difference was seen when comparing GAT and CC. However, LoA and CCC found the strongest agreement between RT and GAT. Two 1-sided tests revealed tonometers can be considered equivalent to one another at ± 2 mmHg, except for PN. After applying proparacaine, IOP decreased significantly (P < 0.0001) by RT (1.2 ± 1.9 mmHg right eye [OD]; 1.1 ± 1.7 mmHg left eye [OS]), and CC (1.4 ± 1.8 mmHg OD; 1.3 ± 2.3 mmHg OS).

Conclusions

When adjusted for proparacaine’s effect on IOP, 3 tonometers were equivalent between each other when determined by equivalence statistical testing with equivalence bounds ± 2 mmHg. The PN reads >2 mmHg higher than RT, CC, or GAT. Therefore, when comparing IOP data from different tonometers, one should consider that not all tonometer measurements are interchangeable and the proparacaine effect should be considered.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:比较来自眼动力学和工程网络(EDEN)房水动力学(AHD)临床试验的健康受试者使用四种机械不同的眼压计测量的眼内压(IOP),采用均差估计、等效统计和调整丙帕卡因对IOP的影响。设计:健康成人多中心开放标签临床试验(NCT01677507)。受试者:纳入122名受试者(55.2±8.8 y;92名女性,30名男性),其中121人在服用和不服用丙帕卡因时进行了测量。方法:来自三个地点的参与者使用iCare™反弹眼压计(RT)、眼反应分析仪角膜补偿眼压计(CC)、气压计(PN)和Goldmann眼压计(GAT)测量眼压。使用和不使用丙帕卡因时分别收集RT和CC的IOP读数。主要结果测量:采用自举耦合估计(DABEST)、Bland-Altman协议限(LoA)、Lin’s一致性相关系数(CCC)和稳健等效性(tost -两个单侧检验)结合零假设显著性检验的数据分析,分析四种眼压计测量的效应大小和一致性。使用DABEST分析给予丙帕卡因前后RT和CC的IOP读数的差异。结果:DABEST、LoA和CCC在PN和其他眼压计之间的效应值最大,一致性最差。比较GAT和CC的平均差异最小,而LoA和CCC发现RT和GAT之间的一致性最强。除了PN外,TOST显示的眼压计在±2 mmHg时可以被认为是等效的。应用丙帕卡因后,眼压随RT(1.2±1.9 mmHg OD)显著降低(p < 0.0001);1.1±1.7 mmHg OS), CC(1.4±1.8 mmHg OD;1.3±2.3 mmHg OS)。结论:在考虑了丙帕卡因对IOP的影响后,采用等效界±2 mmHg的等效统计检验,三种眼压计之间是等效的。气压计读数比RT、CC或GAT高2mmhg以上。因此,在比较不同眼压计的IOP数据时,应考虑到并非所有眼压计的测量值都是可互换的,并应考虑丙帕卡因的作用。
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引用次数: 0
On the Feasibility of Accelerating Glaucoma Clinical Trials Using Portable Perimetry 浅谈便携式眼周仪加速青光眼临床试验的可行性。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.08.004
Jeremy C.K. Tan MD , Giovanni Montesano MD, PhD , Jonathan Crowston MBBS, PhD , Katharina Bell MD, PhD , David P. Crabb PhD , Pete R. Jones PhD

Purpose

To model whether more frequent (weekly, monthly) visual field (VF) assessments using portable “home” perimetry might more quickly detect glaucoma progression in a clinical trial context.

Design

Cross-sectional with additional simulations

Participants

Forty patients (78 eyes; n = 21 healthy, n = 16 glaucoma suspects, n = 41 manifest glaucoma).

Methods

Participants performed an interleaved sequence of 2 portable (Eyecatcher v3.0; EC3) and 2 reference (Humphrey Field Analzyer [HFA] SITA-Fast) VF tests (4 tests total per eye). Linear mixed modeling was then applied to one randomly selected eye per patient to mathematically predict the expected proportion of progressors detected by EC3/HFA over a 3-year period, given different testing regimens (from weekly to every 4 months), levels of variability, and underlying rates of true progression.

Main Outcome Measures

Test–retest variability and proportion of progressors detected.

Results

The portable perimeter was significantly less reliable: the Bland–Altman 95% coefficient of repeatability for mean deviation (CoRMD95%) was 6.37 dB for EC3 and 4.25 dB for the HFA. Statistical simulations, however, predicted that this lower reliability would be offset by more frequent testing. Thus, modeling indicated one EC3 test per month would detect a higher proportion of slow (–0.5 dB/year), moderate (–1 dB/year), and fast (–2 dB/year) progressors compared to one HFA test every 4 months. Implications for trial sample sizes were also modeled, with the number of participants required to evidence a 20% reduction in baseline progression over 2 years (following a hypothetical intervention) predicted to decrease by 24.3%/36.3% with the addition of monthly/fortnightly home testing. There was no significant difference in mean test duration between the EC3 and HFA (226 vs. 225 seconds, P = 0.78), and participants rated the EC3 as somewhat easier to use (system usability scale; P = 0.004).

Conclusions

Home VF assessments, despite poorer reliability than current reference standard (“in-clinic”) devices, would allow faster or greater detection of glaucoma progression via an increased frequency of testing, and could reduce the sample size requirements of future clinical trials. Implications on duration, access and overall cost are discussed.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:在临床试验背景下,模拟使用便携式“家庭”验光仪进行更频繁(每周、每月)的视野评估是否可以更快地检测青光眼的进展。参与者:40例患者(78只眼;n=21健康,n=16青光眼疑似,n=41明显青光眼)方法:参与者进行两次便携式(Eyecatcher v3.0; EC3)和两次参考(HFA SITA-Fast)视野测试的交叉序列(每只眼共4次测试)。然后将线性混合模型应用于每个患者随机选择的一只眼睛,以数学方式预测3年内EC3/HFA检测到的进展者的预期比例,给予不同的测试方案(从每周一次到每4个月一次),变异性水平和潜在的真实进展率。主要结果测量:测试-再测试变异性。检测到进展者的比例。结果:便携式周长的可靠性明显降低:EC3的平均偏差(CoRMD95%)的Bland-Altman 95%重复性系数为6.37 dB, HFA为4.25 dB。然而,统计模拟预测,这种较低的可靠性将被更频繁的测试所抵消。因此,建模表明,与每四个月进行一次HFA测试相比,每月一次EC3测试将检测到较慢(-0.5 dB/年),中度(-1dB/年)和快速(-2dB/年)进展者的比例更高。对试验样本量的影响也进行了建模,两年内(假设干预后)需要证明基线进展减少20%的参与者数量预计会减少24.3%/36.3%,加上每月/两周的家庭测试。EC3和HFA的平均测试持续时间没有显著差异(226 vs 225秒,P = 0.78),参与者认为EC3更容易使用(系统可用性量表;P = 0.004)。结论:家用VF评估尽管比目前的参考标准(“临床”)设备可靠性差,但通过增加检测频率,可以更快/更好地检测青光眼的进展,和/或可以减少未来临床试验的样本量要求。讨论了对持续时间、获取途径和总成本的影响。
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引用次数: 0
Widefield OCT Angiography and Euclidian Distance Analysis of Microvascular Deficits in Glaucomatous Eyes 青光眼微血管缺损的宽视场光学相干断层血管造影和欧氏距离分析。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.08.010
Diogo F. Muller MD, Yingying Shi MD, Maria J. Chaves-Samaniego MD, Khushali Shah MD, Gustavo Rosa Gameiro MD, PhD, Giovanni Gregori MD, PhD, Steven J. Gedde MD, Luis E. Vazquez MD, PhD
<div><h3>Purpose</h3><div>To evaluate superficial microvascular deficits of glaucomatous eyes with widefield OCT angiography (OCTA) and Euclidian distance (ED) analysis.</div></div><div><h3>Design</h3><div>Cross-sectional study.</div></div><div><h3>Subjects</h3><div>Swept-source OCTA (SS-OCTA) images of healthy and glaucomatous eyes.</div></div><div><h3>Methods</h3><div>Twelve-by-twelve mm scans of healthy and glaucomatous eyes were acquired with SS-OCTA (PLEX Elite 9000, ZEISS). The en face images of the superficial retina segmentation were exported and analyzed with ImageJ software. A fixed threshold that predicted the size of the foveal avascular zone was used to generate binarized images with vascular (white) or deficient (black) pixels. Four vascular parameters were measured within a macula-centered 9 × 10.8 mm ellipse: vascular density (VD), average ED (ED<sub><em>avg</em></sub>), maximum ED (ED<sub><em>max</em></sub>), and nonperfusion density (NPD). Euclidian distance values were visualized with a heatmap color scale. The vascular parameters were compared between healthy and glaucomatous eyes (Student t-test). Person coefficients were calculated to test correlations between the vascular parameters and retinal nerve fiber layer (RNFL) thickness, macular ganglion cell and inner plexiform layer (GCIPL) thickness, and visual field mean deviation in glaucomatous eyes. <em>P</em> < 0.05 was considered significant.</div></div><div><h3>Main Outcome Measures</h3><div>Vascular density, ED<sub><em>avg</em></sub>, ED<sub><em>max</em></sub>, and NPD</div></div><div><h3>Results</h3><div>Forty glaucomatous and twenty-five healthy eyes were included. Vascular density (fraction) was 0.442 ± 0.029 vs 0.320 ± 0.072 (<em>P</em> < 0.001), ED<sub><em>avg</em></sub> (μm) was 17.37 ± 0.55 vs 32.62 ± 9.54 (<em>P</em> < 0.001), ED<sub><em>max</em></sub> (μm) was 153.7 ± 49.1 vs 248.5 ± 156.6 (<em>P</em> = 0.005), and NPD (%) was 0.97 ± 0.82 vs 7.09 ± 5.99 (<em>P</em> < 0.001) in healthy vs glaucomatous eyes. Vascular density, ED, and NPD were better in optic nerve head sectors than in temporal macula and retinal periphery sectors in both groups, but were worse in the glaucoma group across all sectors of the ellipse (<em>P</em> < 0.01 for all sectors). Microvascular deficits in glaucomatous eyes often exceeded structural and functional glaucomatous damage, and there was modest correlation between the vascular and structural or functional parameters. Pearson ρ of the correlation with average RNFL and GCIPL were highest for VD (ρ = 0.46, <em>P</em> = 0.002 and ρ = –0.49, <em>P</em> = 0.001, respectively) and lowest for ED<sub><em>max</em></sub> (ρ = –0.19, <em>P</em> = 0.24 and ρ = –0.23, <em>P</em> = 0.16, respectively).</div></div><div><h3>Conclusions</h3><div>Vascular density, ED, and NPD were worse in glaucomatous compared to healthy eyes throughout the widefield OCTA image. High ED and NPD values accentuate regions of inadequate perfusion.</div></
目的:应用宽视场光学相干断层血管造影(OCTA)和欧氏距离(ED)分析评价青光眼浅表微血管缺损。设计:横断面研究。受试者:健康眼和青光眼的扫描源OCTA (SS-OCTA)图像。方法:采用SS-OCTA (PLEX®Elite 9000,蔡司)对健康眼和青光眼进行12x12mm扫描。利用ImageJ软件导出视网膜浅面分割的人脸图像并进行分析。预测中央凹无血管区(FAZ)大小的固定阈值用于生成血管(白色)或缺陷(黑色)像素的二值化图像。在以黄斑为中心的9 × 10.8mm椭圆范围内测量4项血管参数:血管密度(VD)、平均ED (EDavg)、最大ED (EDmax)和非灌注密度(NPD)。用热图色标显示ED值。比较健康眼和青光眼的血管参数(学生t检验)。计算Person系数,检验青光眼血管参数与视网膜神经纤维层(RNFL)厚度、黄斑神经节细胞及内丛状层(GCIPL)厚度、视野平均偏差(VFMD)的相关性。主要结局:VD、EDavg、EDmax和NPD结果:纳入40只青光眼和25只健康眼。VD(分数)为0.442±0.029 vs 0.3205±0.072;Pavg (μm)为17.37±0.549 vs 32.62±9.545;Pmax (μm)为153.7±49.15 vs 248.5±156.6 (P=0.005); NPD(%)为0.97±0.82 vs 7.09±5.99 (Pmax (r=-0.19, P=0.24和r=-0.23, P=0.16)。结论:在宽视场OCTA图像上,青光眼患者的VD、ED和NPD比健康人更严重。高ED和NPD值突出了灌注不足的区域。
{"title":"Widefield OCT Angiography and Euclidian Distance Analysis of Microvascular Deficits in Glaucomatous Eyes","authors":"Diogo F. Muller MD,&nbsp;Yingying Shi MD,&nbsp;Maria J. Chaves-Samaniego MD,&nbsp;Khushali Shah MD,&nbsp;Gustavo Rosa Gameiro MD, PhD,&nbsp;Giovanni Gregori MD, PhD,&nbsp;Steven J. Gedde MD,&nbsp;Luis E. Vazquez MD, PhD","doi":"10.1016/j.ogla.2025.08.010","DOIUrl":"10.1016/j.ogla.2025.08.010","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Purpose&lt;/h3&gt;&lt;div&gt;To evaluate superficial microvascular deficits of glaucomatous eyes with widefield OCT angiography (OCTA) and Euclidian distance (ED) analysis.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Design&lt;/h3&gt;&lt;div&gt;Cross-sectional study.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Subjects&lt;/h3&gt;&lt;div&gt;Swept-source OCTA (SS-OCTA) images of healthy and glaucomatous eyes.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;Twelve-by-twelve mm scans of healthy and glaucomatous eyes were acquired with SS-OCTA (PLEX Elite 9000, ZEISS). The en face images of the superficial retina segmentation were exported and analyzed with ImageJ software. A fixed threshold that predicted the size of the foveal avascular zone was used to generate binarized images with vascular (white) or deficient (black) pixels. Four vascular parameters were measured within a macula-centered 9 × 10.8 mm ellipse: vascular density (VD), average ED (ED&lt;sub&gt;&lt;em&gt;avg&lt;/em&gt;&lt;/sub&gt;), maximum ED (ED&lt;sub&gt;&lt;em&gt;max&lt;/em&gt;&lt;/sub&gt;), and nonperfusion density (NPD). Euclidian distance values were visualized with a heatmap color scale. The vascular parameters were compared between healthy and glaucomatous eyes (Student t-test). Person coefficients were calculated to test correlations between the vascular parameters and retinal nerve fiber layer (RNFL) thickness, macular ganglion cell and inner plexiform layer (GCIPL) thickness, and visual field mean deviation in glaucomatous eyes. &lt;em&gt;P&lt;/em&gt; &lt; 0.05 was considered significant.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Main Outcome Measures&lt;/h3&gt;&lt;div&gt;Vascular density, ED&lt;sub&gt;&lt;em&gt;avg&lt;/em&gt;&lt;/sub&gt;, ED&lt;sub&gt;&lt;em&gt;max&lt;/em&gt;&lt;/sub&gt;, and NPD&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;Forty glaucomatous and twenty-five healthy eyes were included. Vascular density (fraction) was 0.442 ± 0.029 vs 0.320 ± 0.072 (&lt;em&gt;P&lt;/em&gt; &lt; 0.001), ED&lt;sub&gt;&lt;em&gt;avg&lt;/em&gt;&lt;/sub&gt; (μm) was 17.37 ± 0.55 vs 32.62 ± 9.54 (&lt;em&gt;P&lt;/em&gt; &lt; 0.001), ED&lt;sub&gt;&lt;em&gt;max&lt;/em&gt;&lt;/sub&gt; (μm) was 153.7 ± 49.1 vs 248.5 ± 156.6 (&lt;em&gt;P&lt;/em&gt; = 0.005), and NPD (%) was 0.97 ± 0.82 vs 7.09 ± 5.99 (&lt;em&gt;P&lt;/em&gt; &lt; 0.001) in healthy vs glaucomatous eyes. Vascular density, ED, and NPD were better in optic nerve head sectors than in temporal macula and retinal periphery sectors in both groups, but were worse in the glaucoma group across all sectors of the ellipse (&lt;em&gt;P&lt;/em&gt; &lt; 0.01 for all sectors). Microvascular deficits in glaucomatous eyes often exceeded structural and functional glaucomatous damage, and there was modest correlation between the vascular and structural or functional parameters. Pearson ρ of the correlation with average RNFL and GCIPL were highest for VD (ρ = 0.46, &lt;em&gt;P&lt;/em&gt; = 0.002 and ρ = –0.49, &lt;em&gt;P&lt;/em&gt; = 0.001, respectively) and lowest for ED&lt;sub&gt;&lt;em&gt;max&lt;/em&gt;&lt;/sub&gt; (ρ = –0.19, &lt;em&gt;P&lt;/em&gt; = 0.24 and ρ = –0.23, &lt;em&gt;P&lt;/em&gt; = 0.16, respectively).&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusions&lt;/h3&gt;&lt;div&gt;Vascular density, ED, and NPD were worse in glaucomatous compared to healthy eyes throughout the widefield OCTA image. High ED and NPD values accentuate regions of inadequate perfusion.&lt;/div&gt;&lt;/","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"9 1","pages":"Pages 117-125"},"PeriodicalIF":3.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145006935","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
Likelihood of Corneal Transplantation after Tube versus Trabeculectomy 角膜移植与小梁切除术的可能性:IRIS®注册(视力智能研究)研究。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.09.001
Anna Marie Dickinson MD , Luke Leidy , Md Enamul Haque PhD , Helene Lam MD , Kuldev Singh MD , Ann Caroline Fisher MD , Bethlehem Mekonnen MD , Suzann Pershing MD, MS

Objective

Utilization of glaucoma drainage devices (tube shunts) has increased. In this analysis we evaluate long-term likelihood and time-to-event for corneal transplantation after trabeculectomy versus tube shunt glaucoma surgeries.

Design

Retrospective cohort study.

Participants

American Academy of Ophthalmology IRIS® Registry (Intelligent Research In Sight) patients who underwent glaucoma surgery between 2001 and 2021.

Methods

Patients with glaucoma who underwent isolated trabeculectomy, isolated tube shunt, or both surgeries in a given eye were identified by procedure codes. Subsequent corneal transplantation procedures performed in the same eye were similarly identified. Multivariable Cox proportional hazard regression models were used to evaluate the likelihood of corneal transplantation and time from first glaucoma surgery to corneal transplantation.

Main Outcome Measures

Hazard ratios and 95% confidence intervals (CIs) for corneal transplantation.

Results

We identified 246 521 eyes among 197 910 patients with glaucoma surgery meeting study inclusion criteria. Corneal transplantation was most frequently observed among patients who previously underwent both trabeculectomy and tube shunt (5.00%, n = 672), followed by isolated tube shunt (2.97%, n = 3473) and isolated trabeculectomy (0.80%, n = 929). Eyes that only underwent tube shunts had a mean time to corneal transplantation of 2.49 years (standard deviation [SD], 2.4), compared with 3.75 years (SD, 3.3) for isolated trabeculectomy eyes and 3.21 years (SD, 2.6) for eyes that received both trabeculectomy and tube shunt. Adjusted likelihood of corneal transplantation was highest with both trabeculectomy and tube shunt (hazard ratio [HR], 5.88; 95% CI, 5.34–6.48), and isolated tube shunt (HR, 3.97; 95% CI, 3.69–4.26), compared with isolated trabeculectomy.

Conclusions

The likelihood of corneal transplantation is over 4 times higher after tube shunts compared with trabeculectomies. This may reflect factors such as chronic, cumulative corneal endothelial mechanical trauma from the tube shunt, changes to aqueous humor fluid circulation, altered aqueous humor composition and associated signaling pathways, differences in use of antimetabolites as adjunctive therapy, tube material, and tube movement or migration over time. Further research is needed to understand causes of corneal compromise, and consideration of corneal health is warranted in glaucoma surgical decision-making.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:青光眼引流装置(分流管)的使用率越来越高。在本分析中,我们评估了小梁切除术后角膜移植与管分流青光眼手术后角膜移植的长期可能性和时间。设计:回顾性队列研究。参与者:2001年至2021年间接受青光眼手术的美国眼科学会IRIS®注册(视力智能研究)患者。方法:青光眼患者接受孤立小梁切除术,孤立管分流术,或两种手术在一个给定的眼睛被识别的程序代码。在同一只眼睛中进行的后续角膜移植手术也同样确定。采用多变量Cox比例风险回归模型评估角膜移植的可能性,以及从首次青光眼手术到角膜移植的时间。主要结局指标:角膜移植的风险比和95%置信区间(ci)。结果:我们在197910例青光眼手术患者中发现246521只眼睛符合研究纳入标准。在既往行小梁切除术和分流术的患者中,角膜移植最为常见(5.00%,n = 672),其次为孤立性分流术(2.97%,n = 3,473)和孤立性小梁切除术(0.80%,n = 929)。仅行分流手术的患者平均角膜移植时间为2.49年(SD 2.4),而单纯行小梁切除术的患者平均角膜移植时间为3.75年(SD 3.3),同时行小梁切除术和分流手术的患者平均角膜移植时间为3.21年(SD 2.6)。与孤立小梁切除术相比,小梁切除术和分流术的调整后角膜移植的可能性最高(HR, 5.88; 95% CI, 5.34-6.48),孤立分流术的调整后可能性最高(HR, 3.97; 95% CI, 3.69-4.26)。结论:与小梁切除术相比,管分流术后角膜移植的可能性高出4倍以上。这可能反映了一些因素,如由管分流引起的慢性累积性角膜内皮机械损伤、房水液体循环的改变、房水成分和相关信号通路的改变、抗代谢物作为辅助治疗使用的差异、管的材料和/或随时间的管的移动或迁移。需要进一步的研究来了解角膜损害的原因,在青光眼手术决策时考虑角膜健康是必要的。
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引用次数: 0
Re: Figueroa et al.: Association of blood pressure and retinal nerve fiber layer rates of thinning in patients with moderate to advanced glaucoma (Ophthalmol Glaucoma. 2025;8:285–292) Re: Figueroa等人:血压与中晚期青光眼患者视网膜神经纤维层变薄率的关系(Ophthalmol glaucoma . 2025; 8:285-292)。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.09.005
Parth Aphale PhD, Himanshu Shekhar BHMS, Shashank Dokania BHMS
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引用次数: 0
Intrastromal Fluid Cavity in Corneal Hydrops Secondary to Congenital Glaucoma 先天性青光眼继发性角膜积液的星间液腔。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.09.008
Marie Michele Macaron MD, Ta Chen Peter Chang MD
{"title":"Intrastromal Fluid Cavity in Corneal Hydrops Secondary to Congenital Glaucoma","authors":"Marie Michele Macaron MD,&nbsp;Ta Chen Peter Chang MD","doi":"10.1016/j.ogla.2025.09.008","DOIUrl":"10.1016/j.ogla.2025.09.008","url":null,"abstract":"","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"9 1","pages":"Page e3"},"PeriodicalIF":3.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145357008","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
Quantitative Classification of Visual Field Defects in Early Glaucoma 早期青光眼视野缺损的定量分类。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.09.010
Jeremy C.K. Tan MD, FRANZCO , Jack Phu PhD

Objective

While qualitative visual field (VF) grading systems enable the classification and description of VF defects in glaucoma, they may be prone to subjective interpretation and interobserver disagreement. In this study, we characterize the types and frequencies of VF defects in a large cohort of subjects with early glaucomatous loss, using a quantitative method based on the Ocular Hypertension Treatment Study (OHTS) VF classification system.

Design

Cross-sectional study.

Subjects

One thousand three hundred thirty eyes of 733 subjects with healthy, suspect or early glaucoma.

Methods

We translated the OHTS system into an objective, quantitative method to classify the VF of each eye into nerve fiber bundle (bundle) and nonbundle defects comprising 14 patterns. This was applied to VF tests from subjects who received two 24-2 Swedish Interactive Thresholding Algorithm-Faster VF tests per eye on the same visit.

Main Outcome Measures

Distribution of initial and repeatable VF patterns across cohort and the relationship with mean deviation (MD) and test reliability.

Results

The mean baseline MD and pattern standard deviation (SD) was –1.08 (SD, 1.83) and 2.26 (SD, 1.26), respectively. The most common repeatable pattern was the inferior nasal step (22.6%), followed by the inferior enlarged blind spot (19.1%), superior nasal step (12.6%), and superior enlarged blind spot (11.6%). The frequency of occurrence of initial defects was significantly higher than repeatable defects for the majority of patterns. The frequency of nasal step defects decreased as MD worsened, with a corresponding increase in the frequency of arcuate defects. There was a consistently higher frequency of bundle and nonbundle defects in unreliable versus reliable tests based on a false-positive rate above 15%, including an inferior enlarged blind spot (30.0% vs. 20.8%, P < 0.001), superior central defect (13.7% vs. 5.5%, P < 0.001), and partial superonasal quadrant (14.4% vs. 7.2%, P < 0.001) defects.

Conclusions

In a large cohort of suspect and early glaucoma, the most common VF defects were nasal step, enlarged blind spot and arcuate defects, with a significant difference in distribution between initial versus repeatable defects and reliable versus unreliable tests. Application of quantitative criteria may improve the accuracy and consistency of classifying VF defects.

Financial Disclosure(s)

The authors have no proprietary or commercial interest in any materials discussed in this article.
目的:虽然定性视野(VF)分级系统可以对青光眼的VF缺陷进行分类和描述,但它们可能容易产生主观解释和观察者之间的分歧。在这项研究中,我们使用基于高眼压治疗研究(OHTS) VF分类系统的定量方法,描述了大量早期青光眼丧失受试者的VF缺陷的类型和频率。设计:横断面研究对象:733例健康、可疑或早期青光眼患者的1330只眼。方法:我们将OHTS系统转化为一种客观、定量的方法,将每只眼的VF分为神经纤维束(束)和非束状缺损,包括14种模式。这适用于在同一次访问中每只眼睛接受两次24-2 SITA-Faster视距测试的受试者的视距测试。主要结果测量:初始和可重复VF模式在整个队列中的分布,以及与平均偏差和测试信度的关系。结果:平均基线MD和PSD分别为-1.08 (SD 1.83)和2.26 (SD 1.26)。最常见的重复形态为下鼻步(22.6%),其次为下鼻步增大(19.1%)、上鼻步增大(12.6%)和上鼻步增大(11.6%)。对于大多数模式,初始缺陷的出现频率明显低于可重复缺陷。随着MD的恶化,鼻步缺损的频率降低,弓形缺损的频率相应增加。在假阳性率高于15%的不可靠检测和可靠检测中,束状缺损和非束状缺损的出现频率始终较高,包括下位扩大盲点(30.0%比20.8%,P < 0.001)、上位中心缺损(13.7%比5.5%,P < 0.001)和部分鼻上象限缺损(14.4%比7.2%,P < 0.001)。结论:在大量可疑和早期青光眼患者中,最常见的VF缺损是鼻步、盲点扩大和弓形缺损,在初始与可重复缺损、可靠与不可靠试验之间的分布有显著差异。客观标准的应用可以提高VF缺陷分类的准确性和一致性。
{"title":"Quantitative Classification of Visual Field Defects in Early Glaucoma","authors":"Jeremy C.K. Tan MD, FRANZCO ,&nbsp;Jack Phu PhD","doi":"10.1016/j.ogla.2025.09.010","DOIUrl":"10.1016/j.ogla.2025.09.010","url":null,"abstract":"<div><h3>Objective</h3><div>While qualitative visual field (VF) grading systems enable the classification and description of VF defects in glaucoma, they may be prone to subjective interpretation and interobserver disagreement. In this study, we characterize the types and frequencies of VF defects in a large cohort of subjects with early glaucomatous loss, using a quantitative method based on the Ocular Hypertension Treatment Study (OHTS) VF classification system.</div></div><div><h3>Design</h3><div>Cross-sectional study.</div></div><div><h3>Subjects</h3><div>One thousand three hundred thirty eyes of 733 subjects with healthy, suspect or early glaucoma.</div></div><div><h3>Methods</h3><div>We translated the OHTS system into an objective, quantitative method to classify the VF of each eye into nerve fiber bundle (bundle) and nonbundle defects comprising 14 patterns. This was applied to VF tests from subjects who received two 24-2 Swedish Interactive Thresholding Algorithm-Faster VF tests per eye on the same visit.</div></div><div><h3>Main Outcome Measures</h3><div>Distribution of initial and repeatable VF patterns across cohort and the relationship with mean deviation (MD) and test reliability.</div></div><div><h3>Results</h3><div>The mean baseline MD and pattern standard deviation (SD) was –1.08 (SD, 1.83) and 2.26 (SD, 1.26), respectively. The most common repeatable pattern was the inferior nasal step (22.6%), followed by the inferior enlarged blind spot (19.1%), superior nasal step (12.6%), and superior enlarged blind spot (11.6%). The frequency of occurrence of initial defects was significantly higher than repeatable defects for the majority of patterns. The frequency of nasal step defects decreased as MD worsened, with a corresponding increase in the frequency of arcuate defects. There was a consistently higher frequency of bundle and nonbundle defects in unreliable versus reliable tests based on a false-positive rate above 15%, including an inferior enlarged blind spot (30.0% vs. 20.8%, <em>P</em> &lt; 0.001), superior central defect (13.7% vs. 5.5%, <em>P</em> &lt; 0.001), and partial superonasal quadrant (14.4% vs. 7.2%, <em>P</em> &lt; 0.001) defects.</div></div><div><h3>Conclusions</h3><div>In a large cohort of suspect and early glaucoma, the most common VF defects were nasal step, enlarged blind spot and arcuate defects, with a significant difference in distribution between initial versus repeatable defects and reliable versus unreliable tests. Application of quantitative criteria may improve the accuracy and consistency of classifying VF defects.</div></div><div><h3>Financial Disclosure(s)</h3><div>The authors have no proprietary or commercial interest in any materials discussed in this article.</div></div>","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"9 1","pages":"Pages 96-105"},"PeriodicalIF":3.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145182450","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 in Primary Congenital Glaucoma, 2011–2023 原发性先天性青光眼的预后,2011-2023:L V Prasad眼科研究所,海德拉巴。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.07.005
Anil K. Mandal MD , Vijaya K. Gothwal PhD , Mohammed Hasnat Ali PhD

Purpose

To report the clinical outcomes in patients with primary congenital glaucoma (PCG) managed over a period of 13 years.

Design

Retrospective cohort study.

Participants

One thousand one hundred fifty eyes of 704 patients undergoing surgery for PCG between January 2011 and December 2023 with a minimum follow-up of 6 months.

Methods

Medical records of children with PCG were reviewed, and demographic and clinical data were collected. Patients who underwent primary combined trabeculotomy-trabeculectomy (CTT) without mitomycin-C (MMC) as an initial procedure were included (n = 1128 eyes). Complete success was defined as intraocular pressure (IOP) ≥ 6 mmHg and ≤ 16 mmHg without glaucoma medications and qualified success when 1 glaucoma medication was required. Failure was defined as uncontrolled IOP with more than 1 glaucoma medication, need for repeat surgery, chronic hypotony (IOP < 6 mmHg on 2 consecutive visits at 1 month interval) or any sight-threatening complications.

Main Outcome Measures

Intraocular pressure control, number of glaucoma medications, visual acuity (VA), and success rate.

Results

The mean age of patients at first surgery was 23.1 (standard deviation [SD]: 44.7) months (range, 9 days to 233 months; median, 5 months) and mean follow-up was 60.1 (SD: 49.6) months. Infantile-onset PCG was the most common form (61%) of presentation. Primary CTT without MMC was performed in 1128 eyes (98.1%). Complete success rate was 85.9%, 69.7%, and 37.8%, at the 1st, 5th, and 10th year, respectively. The corresponding complete plus qualified success rate was 98.2%, 93.3%, and 84.1%, respectively. Overall, infantile-onset PCG showed better success rates than other 2 groups. There was a significant reduction in IOP at last follow-up (43.4%; P < 0.0001). Preoperatively, majority of eyes (n = 937; 81.5%) were using glaucoma medications, whereas at last follow-up, 388 eyes (41.4%) required medications (P < 0.0001). Of the 690 eyes (60%) that presented with corneal edema, 622 eyes (90%) had clear cornea at last follow-up (P < 0.0001). At last follow-up, 190 eyes (23.1%) had VA of ≥20/40. Multivariate Cox proportional hazards analysis revealed level of IOP and corneal diameter to be independent risk factors for poor surgical outcome.

Conclusions

Our large cohort study treated by CTT without MMC is encouraging and may be considered as the initial surgical procedure in PCG. The outcomes were more favorable in children with infantile-onset PCG.

Financial Disclosure(s)

The authors have no proprietary or commercial interest in any materials discussed in this article.
目的:报告原发性先天性青光眼(PCG)患者治疗13年的临床结果。设计:回顾性队列研究。参与者:2011年1月至2023年12月期间接受PCG手术的704例患者的1150只眼睛,至少随访6个月。方法:回顾患儿PCG病历,收集人口学资料和临床资料。接受初级联合小梁切除术-小梁切除术(CTT)而不使用丝裂霉素c (MMC)作为初始手术的患者(n=1128只眼睛)。完全成功的定义是在没有青光眼药物的情况下眼压(IOP)≥6 mmHg和≤16 mmHg,并且在需要一种青光眼药物的情况下成功。失败定义为使用一种以上青光眼药物控制IOP,需要重复手术,慢性低眼压(IOP)。主要观察指标:IOP控制,青光眼药物数量,视力和成功率。结果:首次手术患者的平均(SD)年龄为23.1(44.7)个月(范围:9天至233个月;中位(5个月)和平均(SD)随访时间为60.1(49,6)个月。婴儿起病的PCG是最常见的表现形式(61%)。无MMC的原发性CTT 1128眼(98.1%)。第1年、第5年和第10年的完全成功率分别为85.9%、69.7%和37.8%。相应的完全+合格成功率分别为98.2%、93.3%和84.1%。总体而言,婴儿起病PCG的成功率高于其他两组。最后一次随访时IOP显著降低(43.4%;P < 0.0001)。术前,大多数眼睛(n=937, 81.5%)使用青光眼药物,而在最后随访时,388只眼睛(41.4%)需要药物治疗(结论:我们的大型队列研究是令人鼓舞的,可以考虑作为PCG的初始手术方法。在婴儿起病的PCG患儿中,结果更为有利。
{"title":"Outcomes in Primary Congenital Glaucoma, 2011–2023","authors":"Anil K. Mandal MD ,&nbsp;Vijaya K. Gothwal PhD ,&nbsp;Mohammed Hasnat Ali PhD","doi":"10.1016/j.ogla.2025.07.005","DOIUrl":"10.1016/j.ogla.2025.07.005","url":null,"abstract":"<div><h3>Purpose</h3><div>To report the clinical outcomes in patients with primary congenital glaucoma (PCG) managed over a period of 13 years.</div></div><div><h3>Design</h3><div>Retrospective cohort study.</div></div><div><h3>Participants</h3><div>One thousand one hundred fifty eyes of 704 patients undergoing surgery for PCG between January 2011 and December 2023 with a minimum follow-up of 6 months.</div></div><div><h3>Methods</h3><div>Medical records of children with PCG were reviewed, and demographic and clinical data were collected. Patients who underwent primary combined trabeculotomy-trabeculectomy (CTT) without mitomycin-C (MMC) as an initial procedure were included (<em>n</em> = 1128 eyes). Complete success was defined as intraocular pressure (IOP) ≥ 6 mmHg and ≤ 16 mmHg without glaucoma medications and qualified success when 1 glaucoma medication was required. Failure was defined as uncontrolled IOP with more than 1 glaucoma medication, need for repeat surgery, chronic hypotony (IOP &lt; 6 mmHg on 2 consecutive visits at 1 month interval) or any sight-threatening complications.</div></div><div><h3>Main Outcome Measures</h3><div>Intraocular pressure control, number of glaucoma medications, visual acuity (VA), and success rate.</div></div><div><h3>Results</h3><div>The mean age of patients at first surgery was 23.1 (standard deviation [SD]: 44.7) months (range, 9 days to 233 months; median, 5 months) and mean follow-up was 60.1 (SD: 49.6) months. Infantile-onset PCG was the most common form (61%) of presentation. Primary CTT without MMC was performed in 1128 eyes (98.1%). Complete success rate was 85.9%, 69.7%, and 37.8%, at the 1st, 5th, and 10th year, respectively. The corresponding complete plus qualified success rate was 98.2%, 93.3%, and 84.1%, respectively. Overall, infantile-onset PCG showed better success rates than other 2 groups. There was a significant reduction in IOP at last follow-up (43.4%; <em>P</em> &lt; 0.0001). Preoperatively, majority of eyes (<em>n</em> = 937; 81.5%) were using glaucoma medications, whereas at last follow-up, 388 eyes (41.4%) required medications (<em>P</em> &lt; 0.0001). Of the 690 eyes (60%) that presented with corneal edema, 622 eyes (90%) had clear cornea at last follow-up (<em>P</em> &lt; 0.0001). At last follow-up, 190 eyes (23.1%) had VA of ≥20/40. Multivariate Cox proportional hazards analysis revealed level of IOP and corneal diameter to be independent risk factors for poor surgical outcome.</div></div><div><h3>Conclusions</h3><div>Our large cohort study treated by CTT without MMC is encouraging and may be considered as the initial surgical procedure in PCG. The outcomes were more favorable in children with infantile-onset PCG.</div></div><div><h3>Financial Disclosure(s)</h3><div>The authors have no proprietary or commercial interest in any materials discussed in this article.</div></div>","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"9 1","pages":"Pages 62-74"},"PeriodicalIF":3.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144700462","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
Ab-Externo MicroShunt vs. Trabeculectomy in Primary Open-Angle Glaucoma Ab-Externo MicroShunt与小梁切除术治疗原发性开角型青光眼:一项随机、多中心研究的5年安全性结果
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.08.009
Joseph F. Panarelli MD , Marlene R. Moster MD , Julian Garcia-Feijoo MD, PhD , Brian E. Flowers MD , N. Douglas Baker MD , Howard S. Barnebey MD , Davinder S. Grover MD, MPH , Michael C. Stiles MD , James D. Brandt MD , Henny J.M. Beckers MD, PhD , Nicholas G. Strouthidis MD, PhD

Purpose

To compare the long-term safety of MicroShunt implantation with trabeculectomy in eyes with primary open-angle glaucoma.

Design

A 3-year observational extension of a 2-year prospective randomized trial.

Participants

The extension study enrolled 279 patients (217 MicroShunt, 62 trabeculectomy), with 256 (198 and 58, respectively) completing the month 60 visit.

Methods

This trial compared clinical outcomes of MicroShunt implantation with trabeculectomy, both augmented with mitomycin C. Adverse events (AEs), intraocular pressure (IOP), and IOP-lowering medication use were recorded 36, 48, and 60 months after initial randomization.

Main Outcome Measures

The primary outcome was the cumulative incidence of sight-threatening AEs. Secondary outcomes included all other AEs/complications, secondary interventions, and reductions in IOP and number of glaucoma medications.

Results

Rates of sight-threatening AEs were 2% (n = 4) in the MicroShunt group and 0% in the trabeculectomy group, with 1 eye each in the MicroShunt group having central retinal artery occlusion, choroidal hemorrhage (after placement of a glaucoma drainage device), progressive endothelial cell loss, and pseudophakic bullous keratopathy. Only 2 of the 4 sight-threatening AEs in the MicroShunt group were deemed related to the study device or procedure. Four eyes in the MicroShunt group experienced device erosion through the conjunctiva. Increased IOP requiring treatment was more frequent (26% vs. 8%, P = 0.0017), whereas hypotony (3% vs. 13%, P = 0.038), epiretinal membrane formation (2% vs. 8%; P = 0.028), and blepharoptosis (4% vs. 11%, P = 0.048) were less frequent in the MicroShunt group. Four patients in the trabeculectomy group required surgical revision for hypotony. Changes in endothelial cell density were similar in the MicroShunt (–19% ± 22%) and trabeculectomy (–19% ± 22%) groups, with a mean between-group difference of 0.1% (P = 0.98). In the mean ± standard deviation, IOP was reduced from 20.8 ± 4.9 mmHg at baseline to 14.2 ± 4.1 mmHg at month 60 in MicroShunt eyes (mean reduction, 5.5 mmHg [26%]) and from 20.1 ± 3.9 mmHg to 10.4 ± 3.7 mmHg in trabeculectomy eyes (mean reduction, 9.1 mmHg [45%]), with a between-group difference of –4.6 mmHg (P < 0.0001).

Conclusions

Both filtering procedures demonstrated favorable safety profiles over 5 years. Most AEs through 5 years did neither necessitate reoperation nor result in vision-threatening complications.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:比较微分流植入与小梁切除术治疗原发性开角型青光眼(POAG)的长期安全性。方法:这是一项为期2年的前瞻性随机试验的3年观察延伸,比较MicroShunt植入与小梁切除术的临床结果,两者都增加了丝裂霉素c。在初始随机化后的36、48和60个月记录不良事件(ae)、眼压(IOP)和降低眼压的药物使用情况。主要结局是视力威胁不良事件的累积发生率。次要结局包括所有其他不良反应/并发症、二次干预、IOP降低和青光眼药物的数量。结果:扩展研究纳入279例患者(217例MicroShunt, 62例小梁切除术),其中256例(分别为198例和58例)完成了第60个月的随访。MicroShunt组视力威胁不良事件发生率为2% (n=4),小梁切除术组为0%,其中MicroShunt组各有一只眼视网膜中央动脉闭塞、脉络膜出血(放置青光眼引流装置后)、进行性内皮细胞丢失和假性大泡性角膜病变。在MicroShunt组中,四例威胁视力的ae中只有两例被认为与研究设备或程序有关。MicroShunt组有4只眼出现结膜糜烂现象。需要治疗的IOP增加更频繁(26%对8%,P=0.0017),而在MicroShunt组中,低眼压(3%对13%,P=0.038)、视网膜前膜形成(2%对8%,P=0.028)和上睑下垂(4%对11%,P=0.048)的发生率较低。小梁切除术组4例患者因低斜视需要手术矫正。内皮细胞密度的变化在MicroShunt组(-19%±22%)和小梁切除术组(-19%±22%)相似,组间平均差异为0.1% (P=0.98)。MicroShunt眼的平均±SD IOP从基线时的20.8±4.9 mmHg降至第60个月时的14.2±4.1 mmHg(平均降低5.5 mmHg[26%]),小梁切除术眼的平均IOP从20.1±3.9 mmHg降至10.4±3.7 mmHg(平均降低9.1 mmHg[45%]),两组间差异为-4.6 mmHg(结论:两种过滤方法在5年内均表现出良好的安全性。大多数ae在5年内不需要再手术,也不会导致视力威胁并发症。
{"title":"Ab-Externo MicroShunt vs. Trabeculectomy in Primary Open-Angle Glaucoma","authors":"Joseph F. Panarelli MD ,&nbsp;Marlene R. Moster MD ,&nbsp;Julian Garcia-Feijoo MD, PhD ,&nbsp;Brian E. Flowers MD ,&nbsp;N. Douglas Baker MD ,&nbsp;Howard S. Barnebey MD ,&nbsp;Davinder S. Grover MD, MPH ,&nbsp;Michael C. Stiles MD ,&nbsp;James D. Brandt MD ,&nbsp;Henny J.M. Beckers MD, PhD ,&nbsp;Nicholas G. Strouthidis MD, PhD","doi":"10.1016/j.ogla.2025.08.009","DOIUrl":"10.1016/j.ogla.2025.08.009","url":null,"abstract":"<div><h3>Purpose</h3><div>To compare the long-term safety of MicroShunt implantation with trabeculectomy in eyes with primary open-angle glaucoma.</div></div><div><h3>Design</h3><div>A 3-year observational extension of a 2-year prospective randomized trial.</div></div><div><h3>Participants</h3><div>The extension study enrolled 279 patients (217 MicroShunt, 62 trabeculectomy), with 256 (198 and 58, respectively) completing the month 60 visit.</div></div><div><h3>Methods</h3><div>This trial compared clinical outcomes of MicroShunt implantation with trabeculectomy, both augmented with mitomycin C. Adverse events (AEs), intraocular pressure (IOP), and IOP-lowering medication use were recorded 36, 48, and 60 months after initial randomization.</div></div><div><h3>Main Outcome Measures</h3><div>The primary outcome was the cumulative incidence of sight-threatening AEs. Secondary outcomes included all other AEs/complications, secondary interventions, and reductions in IOP and number of glaucoma medications.</div></div><div><h3>Results</h3><div>Rates of sight-threatening AEs were 2% (n = 4) in the MicroShunt group and 0% in the trabeculectomy group, with 1 eye each in the MicroShunt group having central retinal artery occlusion, choroidal hemorrhage (after placement of a glaucoma drainage device), progressive endothelial cell loss, and pseudophakic bullous keratopathy. Only 2 of the 4 sight-threatening AEs in the MicroShunt group were deemed related to the study device or procedure. Four eyes in the MicroShunt group experienced device erosion through the conjunctiva. Increased IOP requiring treatment was more frequent (26% vs. 8%, <em>P</em> = 0.0017), whereas hypotony (3% vs. 13%, <em>P</em> = 0.038), epiretinal membrane formation (2% vs. 8%; <em>P</em> = 0.028), and blepharoptosis (4% vs. 11%, <em>P</em> = 0.048) were less frequent in the MicroShunt group. Four patients in the trabeculectomy group required surgical revision for hypotony. Changes in endothelial cell density were similar in the MicroShunt (–19% ± 22%) and trabeculectomy (–19% ± 22%) groups, with a mean between-group difference of 0.1% (<em>P</em> = 0.98). In the mean ± standard deviation, IOP was reduced from 20.8 ± 4.9 mmHg at baseline to 14.2 ± 4.1 mmHg at month 60 in MicroShunt eyes (mean reduction, 5.5 mmHg [26%]) and from 20.1 ± 3.9 mmHg to 10.4 ± 3.7 mmHg in trabeculectomy eyes (mean reduction, 9.1 mmHg [45%]), with a between-group difference of –4.6 mmHg (<em>P</em> &lt; 0.0001).</div></div><div><h3>Conclusions</h3><div>Both filtering procedures demonstrated favorable safety profiles over 5 years. Most AEs through 5 years did neither necessitate reoperation nor result in vision-threatening complications.</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 37-47"},"PeriodicalIF":3.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145006949","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
Long-Term Follow-Up on a Juvenile Open-Angle Glaucoma Pedigree with a Novel EFEMP1 Mutation (c.1313, p.Tyr438Cys) 对一个具有新型EFEMP1突变(c.1313, p.Tyr438Cys)的少年开角型青光眼家系进行长期随访。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2026-01-01 DOI: 10.1016/j.ogla.2025.08.003
Brian P. Young BS , Angela W. Nyunt BS , Molly A. Clymer OD , Mallory R. Tollefson PhD , Ben R. Roos BS , Michael J. Schnieders PhD , Alan L. Robin MD , John H. Fingert MD, PhD

Purpose

Determine the genetic cause of glaucoma in a juvenile open-angle glaucoma (JOAG) pedigree of European ancestry.

Design

Case series or pedigree analysis

Participants

A three-generation JOAG pedigree

Methods

We obtained clinical data and tested DNA for mutations in known JOAG-causing genes with Sanger sequencing for MYOC and whole exome sequencing for EFEMP1. We assessed identified mutations for pathogenicity by (1) frequency in control databases; (2) mutation analysis algorithms; (3) homology analyses; and (4) structural modeling of mutational effects on encoded proteins.

Main Outcome Measures

Detection of a mutation that is coinherited with glaucoma in the JOAG pedigree. Secondary measures include descriptions of glaucoma phenotype (age at presentation, maximum intraocular pressure [IOP], progression rate, and response to therapy).

Results

Clinical data from an average follow-up of 11.5 ± 7.05 years were available from four family members with JOAG. Members of this pedigree had a mean age of diagnosis of 32.5 ± 8.6 years (range 25–43 years) and a mean maximum treated IOP of 32.3 ± 12.0 (range 16–50) mmHg. Family members had visual field progression ranging from –0.25 to –1.1 dB/year and required an average of 1.8 ± 1.0 incisional glaucoma surgeries per eye for IOP control. No MYOC mutations were detected. A heterozygous missense mutation (c.1313A>G, p.Tyr438Cys) was detected in the EFEMP1 gene in all four family members with JOAG and is absent from control subjects. The p.Tyr438Cys mutation altered a highly conserved amino acid and was predicted to be pathogenic by 6 mutation analysis algorithms. Modeling of the p.Tyr438Cys mutation indicated it causes structural changes to EFEMP1 protein that are likely detrimental to its function.

Conclusions

This study identifies a novel mutation, p.Tyr438Cys, as the first known glaucoma-causing EFEMP1 mutation in a JOAG pedigree of European ancestry. Patients with the EFEMP1 mutation p.Tyr438Cys have an early-onset severe glaucoma phenotype with high maximum IOPs that require surgical interventions and may have rapid progression. These data underscore the severity of this type of JOAG and the need for further research into its pathogenic mechanisms and therapeutic management.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:确定欧洲血统的JOAG家系青光眼的遗传原因。方法:我们获得临床数据,并使用Sanger测序(MYOC)和EFEMP1全外显子组测序(EFEMP1)检测已知JOAG致病基因突变的DNA。我们通过对照数据库中的频率评估已鉴定突变的致病性;2)突变分析算法;3)同源性分析;4)编码蛋白突变效应的结构建模。主要结果测量:检测JOAG家系中与青光眼共同遗传的突变。次要指标包括青光眼表型描述(发病年龄、最大眼压(IOP)、进展率和对治疗的反应)。结果:4名患有JOAG的家庭成员平均随访11.5±7.05年,获得临床资料。该家族成员的平均诊断年龄为32.5±8.6岁(范围25至43岁),平均最大治疗IOP为32.3±12.0(范围20至50)mm Hg。家族成员的视野进展范围为-0.25至-1.1 dB /年,平均每只眼需要1.8±1.0切口青光眼手术来控制IOP。未检测到MYOC突变。四名JOAG家族成员的EFEMP1基因均存在杂合错义突变(c.1313A>G, p.Tyr438Cys),而对照组不存在该突变。p.Tyr438Cys突变改变了一个高度保守的氨基酸,通过6种突变分析算法预测该突变具有致病性。p.Tyr438Cys突变的建模表明,它会导致EFEMP1蛋白的结构变化,这可能对其功能有害。结论:本研究确定了一种新的突变p.Tyr438Cys,作为欧洲血统JOAG家系中第一个已知的导致青光眼的EFEMP1突变。EFEMP1突变p.Tyr438Cys的患者具有早发性严重青光眼表型,最大IOPs高,需要手术干预,并且可能有快速进展。这些数据强调了这种类型JOAG的严重性,以及对其致病机制和治疗管理进行进一步研究的必要性。
{"title":"Long-Term Follow-Up on a Juvenile Open-Angle Glaucoma Pedigree with a Novel EFEMP1 Mutation (c.1313, p.Tyr438Cys)","authors":"Brian P. Young BS ,&nbsp;Angela W. Nyunt BS ,&nbsp;Molly A. Clymer OD ,&nbsp;Mallory R. Tollefson PhD ,&nbsp;Ben R. Roos BS ,&nbsp;Michael J. Schnieders PhD ,&nbsp;Alan L. Robin MD ,&nbsp;John H. Fingert MD, PhD","doi":"10.1016/j.ogla.2025.08.003","DOIUrl":"10.1016/j.ogla.2025.08.003","url":null,"abstract":"<div><h3>Purpose</h3><div>Determine the genetic cause of glaucoma in a juvenile open-angle glaucoma (JOAG) pedigree of European ancestry.</div></div><div><h3>Design</h3><div>Case series or pedigree analysis</div></div><div><h3>Participants</h3><div>A three-generation JOAG pedigree</div></div><div><h3>Methods</h3><div>We obtained clinical data and tested DNA for mutations in known JOAG-causing genes with Sanger sequencing for <em>MYOC</em> and whole exome sequencing for <em>EFEMP1</em>. We assessed identified mutations for pathogenicity by (1) frequency in control databases; (2) mutation analysis algorithms; (3) homology analyses; and (4) structural modeling of mutational effects on encoded proteins.</div></div><div><h3>Main Outcome Measures</h3><div>Detection of a mutation that is coinherited with glaucoma in the JOAG pedigree. Secondary measures include descriptions of glaucoma phenotype (age at presentation, maximum intraocular pressure [IOP], progression rate, and response to therapy).</div></div><div><h3>Results</h3><div>Clinical data from an average follow-up of 11.5 ± 7.05 years were available from four family members with JOAG. Members of this pedigree had a mean age of diagnosis of 32.5 ± 8.6 years (range 25–43 years) and a mean maximum treated IOP of 32.3 ± 12.0 (range 16–50) mmHg. Family members had visual field progression ranging from –0.25 to –1.1 dB/year and required an average of 1.8 ± 1.0 incisional glaucoma surgeries per eye for IOP control. No <em>MYOC</em> mutations were detected. A heterozygous missense mutation (c.1313A&gt;G, p.Tyr438Cys) was detected in the <em>EFEMP1</em> gene in all four family members with JOAG and is absent from control subjects. The p.Tyr438Cys mutation altered a highly conserved amino acid and was predicted to be pathogenic by 6 mutation analysis algorithms. Modeling of the p.Tyr438Cys mutation indicated it causes structural changes to <em>EFEMP1</em> protein that are likely detrimental to its function.</div></div><div><h3>Conclusions</h3><div>This study identifies a novel mutation, p.Tyr438Cys, as the first known glaucoma-causing <em>EFEMP1</em> mutation in a JOAG pedigree of European ancestry. Patients with the <em>EFEMP1</em> mutation p.Tyr438Cys have an early-onset severe glaucoma phenotype with high maximum IOPs that require surgical interventions and may have rapid progression. These data underscore the severity of this type of JOAG and the need for further research into its pathogenic mechanisms and therapeutic management.</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 75-85"},"PeriodicalIF":3.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144980458","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
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Ophthalmology. Glaucoma
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