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Comparison of a Novel Head-mounted Perimeter vs. the Humphrey Field Analyzer 新型头戴式周长仪与汉弗莱场强分析仪的比较。
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2024.11.007
Wisam O. Najdawi BS , Fangfang Jiang MSc , Gideon K.D. Zamba PhD , Chris A. Johnson PhD , Andrew E. Pouw MD

Purpose

Perimetry is a critical tool for the diagnosis and monitoring of glaucomatous visual field defects. The Humphrey Field Analyzer (HFA) is a large, relatively expensive device that does not normally allow for examination outside of the clinic, and it can be ergonomically difficult to tolerate for some patients. The present study compared the novel Smart System Virtual Reality (SSVR) perimetric headset test to that of the HFA in a group of patients with glaucoma.

Design

Prospective comparative study.

Subjects

Seventy-two eyes from 36 patients with glaucoma recruited at the University of Iowa Hospitals and Clinics.

Methods

Patients completed both HFA and SSVR visual field tests on the same day, with the order of tests randomized. After completing both visual field tests, subjects completed a survey regarding their subjective experience using each perimeter. Visual fields were analyzed using a linear mixed model to assess differences between devices accounting for intereye correlation and Bland–Altman analysis.

Main Outcome Measures

Primary outcome measures included mean deviation (MD), pattern standard deviation (PSD), and test duration.

Results

No statistically significant difference in MD was observed between the SSVR (−7.17 ± 6.36 dB) and HFA (−6.88 ± 6.78 dB; P = 0.859). Statistically significant differences in PSD were observed between the SSVR (4.26 ± 2.37 dB) and HFA (6.38 ± 4.51 dB; P < 0.001) and test duration (323.44 ± 72.27 seconds and 372.20 ± 61.44 seconds, respectively; P < 0.001). Subjectively, the SSVR was the preferred perimeter by 88.5% of patients.

Conclusions

The SSVR headset is a novel visual field testing device that produces similar results to the HFA with a shorter testing duration. The SSVR was the preferred perimeter by the majority of patients. Future study is required to determine if the SSVR can identify visual field progression.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.
目的:周边视力测定是诊断和监测青光眼视野缺损的重要工具。汉弗莱视野分析仪(Humphrey Field Analyzer,HFA)是一种大型、相对昂贵的设备,通常不允许在诊室外进行检查,而且从人体工程学角度来看,有些患者可能难以忍受。本研究对一组青光眼患者进行了新型智能系统虚拟现实(SSVR)周边测量耳机测试与 HFA 的比较:设计:前瞻性比较研究:方法:患者同时完成 HFA 和 SSVR 测试:患者在同一天完成 HFA 和 SSVR 视野测试,测试顺序随机。在完成这两项视野测试后,受试者填写了一份调查问卷,内容涉及他们使用每种视力表的主观感受。使用线性混合模型对视野进行分析,以评估不同设备之间的差异,并考虑到眼间相关性和布兰-阿尔特曼分析:主要结果测量指标包括平均偏差(MD)、模式标准偏差(PSD)和测试持续时间:结果:SSVR(-7.17±6.36 dB)和 HFA(-6.88±6.78,P=0.859)之间的 MD 无统计学差异。在 SSVR(4.26±2.37 dB)和 HFA(6.38±4.51,p=结论)之间观察到 PSD 有统计学意义的差异:SSVR 头戴式耳机是一种新型视野测试设备,其测试结果与 HFA 相似,但测试时间更短。SSVR是大多数患者的首选。今后还需要进行研究,以确定 SSVR 是否能识别视野进展。
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引用次数: 0
Protection from Steroid-Induced Glaucoma via iStent Inject in a Patient with Behçet’s Disease iStent注射剂对behalet病患者类固醇性青光眼的保护作用
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2024.12.001
Milton Louca MD , David Z. Wechsler MBBS (Hons), FRANZCO
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引用次数: 0
Minimally Invasive Glaucoma Surgery and the Distal Aqueous Outflow System: The Final Frontier? 微创青光眼手术和远端水流出系统:最后的前沿?
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2024.11.006
Clemens A. Strohmaier MD, PhD, Martin Kallab MD, PhD, Saige Oechsli BSc, Alex S. Huang MD, PhD, Osamah J. Saeedi MD, MS
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引用次数: 0
Agreement and Reliability of Transpalpebral Tonometers with Goldmann Applanation Tonometer 经眼压计与戈德曼眼压计的一致性和可靠性 - 系统综述和元分析。
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2024.11.001
Selvaraj Jerrome MSc, MPhil , Sanil Joseph MHA, MSc , Balasubramaniam Niranjana MS , Majumdar Arkaprava MSc , Pooludaiyar Lakshmanan MSc , Sundar Balagiri MSc , Thandavarayan Kumaragurupari PhD , S. Vidya DO , Vijayalakshmi A. Senthilkumar MS , Subbaiah R. Krishnadas DO, DNB

Topic

The systematic review and meta-analysis consolidates the extant body of evidence comparing reliability and agreement between transpalpebral tonometers (TTs) and Goldmann applanation tonometer (GAT).

Clinical Relevance

With a global prevalence of 3.54 percent, glaucoma stands as the second leading cause of preventable blindness. Projections indicate a rise to 111 million cases by 2040. Existing literature presents inconsistent findings while comparing TT and GAT. The derivation of summary estimates assessing their agreement holds significance, given TT’s multifaceted applicability in clinical, community, and home settings.

Methods

Systematic review was conducted using PubMed, Cochrane Library, and Google Scholar from January 2000 to December 2022. Two reviewers independently evaluated, enumerated, and extracted studies and data based on eligibility criteria. The Quality Assessment for Diagnostic Accuracy Studies checklist was used to assess study quality. The summary measures were pooled using the random-effects model as mean difference (MD), and 95% limits of agreement (LoA). We assessed heterogeneity using the I2 statistic. The study protocol was registered with the International Prospective Register of Systematic Reviews (CRD42022321693).

Results

A total of 26 methods comparison studies (3577 eyes) were included in the meta-analysis. The overall random-effects MD (TT – GAT) and standard deviation (SD) for intraocular pressure (IOP) were −0.70 ± 4.32 mmHg (95% LoA: −8.74 to 7.33 mmHg). In the subgroup analysis based on index test devices used, Easyton showed the lowest MD, SD, (−0.29 ± 2.35 mmHg), and 95% LoA (−4.90 to 4.32 mmHg). In the univariate meta-regression model, we found that, on average, studies examining normal eyes reported a statistically significant lower MD of 2.67 mmHg (95% confidence interval: 0.27–5.07 mmHg; P = 0.03) between TT and GAT, compared to studies that assessed eyes with mixed ocular condition.

Conclusion

In the current meta-analysis, we found a small MD in the measured IOP between the 2 tonometers. However, given the high heterogeneity and a wider LoA, it is not advisable to use TT interchangeably with GAT.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.
主题:该系统综述和荟萃分析整合了现有证据,比较了经眼睑眼压计(TT)和戈德曼角膜曲率计(GAT)之间的可靠性和一致性:青光眼的全球发病率为 3.54%,是导致可预防性失明的第二大原因。据预测,到 2040 年,患病人数将增至 1.11 亿。现有文献对 TT 和 GAT 的比较结果并不一致。鉴于 TT 在临床、社区和家庭环境中的多方面适用性,得出评估两者一致性的简要估计值具有重要意义:从 2000 年 1 月到 2022 年 12 月,我们使用 PubMed、Cochrane Library 和 Google Scholar 进行了系统回顾。两名审稿人根据资格标准对研究和数据进行了独立评估、列举和提取。采用诊断准确性研究质量评估(QUADAS-2)核对表评估研究质量。采用随机效应模型对汇总指标进行了平均差(MD)和 95% LoA(一致性限值)汇总。我们使用 I2 统计量评估异质性。研究方案已在国际系统综述前瞻性注册中心(PROSPERO - CRD42022321693)注册:荟萃分析共纳入了 26 项方法对比研究(3577 只眼)。眼压的总体随机效应 MD (TT - GAT)、SD 和 95% LoA 为 -0.70 ± 4.15 mmHg (-8.83 至 7.43 mmHg)。在基于所用指数测试设备的亚组分析中,Easyton 显示出最低的 MD、SD(-0.29 ± 2.35 mmHg)和 95% LoA(-4.90 至 4.32 mmHg)。在单变量荟萃回归模型中,我们发现,平均而言,与评估混合眼状态的研究相比,检查正常眼的研究报告显示,TT 和 GAT 之间的平均差异为 2.67 mmHg(95% CI:0.27 至 5.07 mmHg;P = 0.03),具有显著的统计学意义:在当前的荟萃分析中,我们发现两种眼压计测得的眼压差异很小。然而,鉴于高度异质性和较宽的 LoA,不宜将 TT 与 GAT 互换使用。
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引用次数: 0
Influence of Social Determinants of Health on Presentation and Outcomes of Primary Congenital Glaucoma 社会健康因素对原发性先天性青光眼的表现和预后的影响
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2025.02.001
David A. Ramirez MD , Blair Shaman MA , Jennifer L. Rossen MD , Adam Jacobson MD , Brenda L. Bohnsack MD, PhD

Purpose

Assess the effect of social determinants of health on presentation and outcomes in primary congenital glaucoma (PCG).

Design

Retrospective case series.

Subjects

Patients with PCG presenting between 2011 and 2023 with > 3 months follow-up.

Methods

The percentage of households with 0, 1–2, or > 3 community resilience estimates (CREs) risk factors and median income for the census tract of residence for each patient were collected. Initial details and final outcomes were correlated with race, ethnicity, insurance type, and census tract data.

Main Outcome Measures

Final best-corrected visual acuity (BCVA).

Results

Of 59 patients (105 eyes, 68% male), the presenting average age was 294 ± 365 days. Black patients (n = 16) were younger (P < 0.001) than White (n = 31) or other race patients (n = 12). Although there was no racial or ethnic differences in initial intraocular pressure (IOP), IOP > 30 mmHg was associated with worse final BCVA. Patients with Medicaid (n = 31) required more glaucoma surgeries compared with those with commercial insurances (n = 28, P = 0.0305), respectively. Linear regression analysis demonstrated that census tracts with higher percentage of households with > 3 CRE risk factors correlated with worse visual acuity (ß = 0.02, P = 0.0028, R2 = 0.2). There were no racial, ethnic, insurance type, tract median income, or CRE risk factor differences in IOP, number of glaucoma medications, spherical equivalent, or cup-to-disc ratio at final follow-up.

Conclusions

Type of insurance and census data as markers for social determinants of health demonstrated increased risk factors can be associated with worse visual outcomes in PCG.

Financial Disclosure(s)

The authors have no proprietary or commercial interest in any materials discussed in this article.
目的:评估健康的社会决定因素对原发性先天性青光眼(PCG)的表现和结局的影响设计:回顾性病例系列研究对象:2011年至2023年间出现的PCG患者,随访3个月。方法:收集每个患者居住的人口普查区具有0、1-2或>3个社区恢复力评估(CRE)风险因素和收入中位数的家庭百分比。最初的细节和最终的结果与种族、民族、保险类型和人口普查区数据相关。主要观察指标:最终最佳矫正视力(BCVA)结果:59例患者(105眼,68%为男性),平均呈现年龄为294±365天。黑色患者(n=16)较年轻(p30 mmHg与较差的最终BCVA相关)。有医疗补助的患者(n=31)比有商业保险的患者(n=28, p=0.0305)需要更多的青光眼手术。线性回归分析表明,人口普查区存在bbbb3 CRE危险因素的家庭比例越高,VA越差(ß=0.02, p=0.0028, R2=0.2)。在最后随访时,在IOP、青光眼药物数量、球形当量或杯盘比方面,没有种族、民族、保险类型、眼道收入中位数或CRE危险因素的差异。结论:保险类型和人口普查数据作为健康社会决定因素的标志表明,风险因素的增加可能与PCG患者视力结果的恶化有关。
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引用次数: 0
Eye Drop Instillation Success and Hand Function in Adults with Glaucoma 成人青光眼滴眼液滴注成功与手功能的关系
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2024.12.008
Madeline K. Weber BS , Gül G. Kabil BS , Leslie M. Niziol MS , Daniel Duque Urrego BSE , Cameron Haire BSE , Stephen M. Cain PhD , Alanson P. Sample PhD , David T. Burke PhD , Susan H. Brown PhD , Paula Anne Newman-Casey MD
<div><h3>Purpose</h3><div>To investigate hand function and eye drop instillation success in adults with and without glaucoma.</div></div><div><h3>Design</h3><div>Cross-sectional pilot study.</div></div><div><h3>Subjects</h3><div>Adults aged ≥ 65 years with glaucoma who use eye drops daily and adults aged 65+ without glaucoma who do not regularly use eye drops.</div></div><div><h3>Methods</h3><div>Hand function was evaluated using the Saehan Hydraulic Pinch Gauge, Jamar Hand Dynamometer, Grooved Pegboard Test (GPT), Arthritis Hand Function Tests (AHFT), Semmes-Weinstein Monofilament Test, and a tactile pattern recognition device. Eye drop instillation success was analyzed through videography.</div></div><div><h3>Main Outcome Measures</h3><div>Proportion of successful eye drop instillation trials assessed by (1) overall success in getting at least one drop in the eye; (2) average number of drops dispensed; and (3) bottle tip contact with the eye, eyelashes, or skin. Hand function measures: mean pinch and grip strength, GPT and AHFT completion times, smallest detected monofilament, tactile pattern identification time, and accuracy.</div></div><div><h3>Results</h3><div>A total of 25 participants with glaucoma and 79 participants without glaucoma were included. There was no difference in the proportion of trials where at least one drop was successfully instilled, disregarding bottle tip contact (glaucoma: 0.95, nonglaucoma: 0.91; <em>P</em> = 0.88). Participants with glaucoma were more likely to make contact between the bottle tip and the eye, eyelashes, or skin compared with those without (glaucoma: 0.49, nonglaucoma: 0.28; <em>P</em> = 0.01). Participants with glaucoma dispensed a similar number of drops as those without (glaucoma: 1.37, nonglaucoma: 1.46; <em>P</em> = 0.47). Participants with glaucoma had significantly reduced pinch strength (glaucoma: 4.8 kg, nonglaucoma 6.1 kg, <em>P</em> = 0.01), grip strength (glaucoma: 23.4 kg, nonglaucoma: 27.7 kg, <em>P</em> = 0.02), longer completion times for the GPT (glaucoma: 113.5 seconds, nonglaucoma: 85.5 seconds, <em>P</em> = 0.02), and specific AHFT tasks of fastening/unfastening buttons (glaucoma: 36.6 seconds, nonglaucoma: 27.7 seconds, <em>P</em> = 0.03) and pinning/unpinning safety pins (glaucoma: 35.4 seconds, nonglaucoma: 27.3 seconds, <em>P</em> = 0.02), and worse tactile acuity on monofilament (<em>P</em> = 0.04) compared with participants without glaucoma.</div></div><div><h3>Conclusions</h3><div>Despite hand function deficits, in this exploratory pilot study, adults with glaucoma demonstrated eye drop instillation success comparable to those without glaucoma, though with higher rates of bottle tip contact with the eye, skin, or eyelashes, suggesting an increased risk of potential eye drop bottle contamination. These findings suggest that though regular practice may help mitigate the effects of hand function deficits on the targeted activity of getting the eye drop in the eye, the deficits
目的观察青光眼患者和非青光眼患者的手功能和滴眼液滴注效果。设计横断面试验研究。受试者年龄≥65岁的青光眼患者,每日使用滴眼液;65岁以上的青光眼患者,不定期使用滴眼液。方法采用Saehan液压夹钳仪、Jamar手测力仪、沟槽钉板测试(GPT)、关节炎手功能测试(AHFT)、Semmes-Weinstein单丝测试和触觉模式识别装置对手部功能进行评估。通过录像分析滴眼液滴注成功情况。主要观察指标滴眼液试验成功的比例通过(1)至少滴入1滴眼液的总体成功来评估;(2)平均滴药数;(3)瓶尖接触眼睛、睫毛或皮肤。手功能测量:平均捏握强度,GPT和AHFT完成时间,最小检测单丝,触觉模式识别时间,准确性。结果共纳入25例青光眼患者和79例非青光眼患者。不管药瓶尖端接触与否,至少滴入一滴成功的试验比例没有差异(青光眼:0.95,非青光眼:0.91;p = 0.88)。与没有青光眼的参与者相比,患有青光眼的参与者更有可能接触到瓶子尖端和眼睛、睫毛或皮肤(青光眼:0.49,非青光眼:0.28;P = 0.01)。患有青光眼的参与者与没有青光眼的参与者分配了相似数量的滴剂(青光眼:1.37,非青光眼:1.46;p = 0.47)。青光眼患者的捏紧强度(青光眼:4.8 kg,非青光眼:6.1 kg, P = 0.01)、握力(青光眼:23.4 kg,非青光眼:27.7 kg, P = 0.02)显著降低,GPT完成时间(青光眼:113.5秒,非青光眼:85.5秒,P = 0.02)延长,以及固定/解开纽扣(青光眼:36.6秒,非青光眼:27.7秒,P = 0.03)和固定/解开安全别针(青光眼:35.4秒,非青光眼:35.4秒,非青光眼:35.4秒,非青光眼:35.4秒,非青光眼:35.4秒)等特定AHFT任务的完成时间延长。27.3秒,P = 0.02),单丝触觉敏锐度较无青光眼者差(P = 0.04)。结论:尽管有手功能缺陷,在这项探索性的初步研究中,青光眼患者滴眼液的成功率与没有青光眼的患者相当,但滴眼液瓶尖接触眼睛、皮肤或睫毛的几率更高,这表明滴眼液瓶污染的风险增加。这些发现表明,尽管经常练习可能有助于减轻手功能缺陷对滴眼液这一目标活动的影响,但手功能缺陷可能会使这项活动变得困难。财务披露专有或商业披露可在本文末尾的脚注和披露中找到。
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引用次数: 0
Agreement between the ICare HOME Tonometer and the Goldmann Applanation Tonometer in the Assessment of the Peak Intraocular Pressure in the Water-Drinking Test Icare HOME眼压计与Goldmann眼压计在饮水试验中评估眼压峰值的一致性。
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2024.11.008
Carolina N. Susanna MD , Fernanda N. Susanna MD , Laura Goldfarb Cyrino MD , Renato Antunes Schiave Germano MD, PhD , Remo Susanna Jr. MD, PhD , Pradeep Y. Ramulu MD, PhD , Marcelo Hatanaka MD, PhD

Purpose

To investigate the agreement between the ICare HOME tonometer and the Goldmann Applanation Tonometer (GAT) in assessing the peak intraocular pressure (IOP) during the water-drinking test (WDT).

Design

Prospective cross-sectional study.

Subjects

Seventy-nine eyes of 41 open-angle glaucoma patients were included in the study.

Methods

All of the included patients underwent a training session provided by ophthalmologist specialists to use the ICare HOME tonometer. Then the IOP was first measured with the GAT (AT900; Haag-Streit) by a trained physician, immediately followed by ICare HOME tonometer (TA022, ICare Oy) measurement by the patient. Four measurements were taken with each device with 15-minute differences as established by the WDT.

Main Outcome Measures

The agreement and degree of correlation of the peak IOP by both tonometers were assessed.

Results

The agreement between the ICare HOME and GAT was high during the WDT: the intraclass correlation coefficient (r) between the 2 methods from basal to 45 minutes: 0.94 (P < 0.001), at basal: 0.91 (P < 0.001), at 15 minutes: 0.94 (P < 0.001), at 30 minutes: 0.94 (P < 0.001), at 45 minutes: 0.95 (P < 0.001), and for peak IOP: 0.94 (P < 0.001). There was no significant difference between peak IOP with the GAT and ICare HOME (18.3 ± 4.6 [10–33] and 18.5 ± 5.0 [0–33], respectively, P = 0.533), nor between the delta of fluctuation between basal and peak IOP with the GAT and ICare HOME (3.96 ± 3.22 and 4.54 ± 3.92, P = 0.054).

Conclusions

Our study demonstrated a high agreement between the ICare HOME and the GAT during the WDT in a clinical environment with supervision.

Financial Disclosure(s)

The authors have no proprietary or commercial interest in any materials discussed in this article.
目的:探讨Icare家用眼压计与Goldmann眼压计(GAT)在饮水试验(WDT)中评估眼压峰值的一致性。设计:前瞻性横断面研究。研究对象:41例开角型青光眼患者79只眼。方法:所有纳入的患者都接受了由眼科专家提供的使用Icare®家用眼压仪的培训课程。然后用Goldmann眼压计(AT900;Haag-Streit;由训练有素的医生(Köniz, suia)进行测量,紧接着由患者进行Icare®家用血压仪(TA022, Icare Oy, Vanda, Finland)测量。根据WDT确定,每个装置进行了四次测量,相差15分钟。主要观察指标:评估两种眼压计测量的峰值眼压的一致性和相关程度。结果:在WDT期间,iCare与Goldmann压血压计之间的一致性很高:两种方法在基线至45 min之间的类内相关系数(r)为0.94 (p < 0.001),在基线时为0.91 (p < 0.001),在15 min时为0.94 (p < 0.001),在30 min时为0.94 (p < 0.001),在45 min时为0.95 (p < 0.001),在IOP峰值时为0.94 (p < 0.001)。GAT和iCare的IOP峰值分别为18.3±4.6(10-33)和18.5±5.0(0-33),差异无统计学意义(p = 0.533); GAT和iCare的基础IOP与峰值的波动δ值分别为3.96±3.22和4.54±3.92,差异无统计学意义(p = 0.054)。结论:我们的研究表明,iCare HOME和Goldmann眼压计在临床环境监督下,在WDT期间具有很高的一致性。
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引用次数: 0
Re: Lee et al.: Associations between statin use and glaucoma in the All of Us Research Program (Ophthalmol Glaucoma. 2024;7:563–571) Re: Lee等人:他汀类药物与青光眼的相关性研究(Ophthalmol glaucoma . 2024;7:563-571)。
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2025.01.005
Ayushi S. Shah BS , Pranav Vasu MPH
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引用次数: 0
Effect of Blood Pressure on Rates of Progression in Focal Ischemic vs. Generalized Cup Enlargement Glaucoma Phenotypes 血压对局灶性缺血性青光眼与全身性杯状增大青光眼表型进展率的影响。
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2025.01.001
Marcus Guerreiro-Filho MD , Alessandro A. Jammal MD, PhD , Rohit Muralidhar BA , Rafael Scherer MD, PhD , Luiz F. Beniz MD , Douglas R. da Costa MD , Ivan M. Tavares MD, PhD , Felipe A. Medeiros MD, PhD

Purpose

To investigate the impact of blood pressure (BP) on rates of retinal nerve fiber layer (RNFL) thinning in glaucomatous eyes with focal ischemic (FI) vs. generalized cup enlargement (GE) optic disc phenotypes.

Design

Prospective cohort study.

Participants

The study included 122 eyes from 101 patients diagnosed with primary open-angle glaucoma. Eyes were classified as FI (n = 31, 25%) or GE (n = 91, 75%) based on masked grading of stereophotographs at baseline.

Methods

Subjects underwent comprehensive ophthalmic examinations, including intraocular pressure (IOP) measurement and spectral-domain OCT scans, every 6 months for an overall mean follow-up of 4.2 years ± 1.5 years. Brachial artery BP was measured concurrently, and mean arterial pressure (MAP), systolic arterial pressure (SAP), and diastolic arterial pressure (DAP) were calculated. Rates of global RNFL thickness change over time were assessed using linear mixed models, evaluating the impact of BP parameters in each optic disc phenotype, adjusting for IOP and other confounders. Interaction terms were used to test for differences in the effects of BP and IOP between the FI and GE phenotypes.

Main Outcome Measures

Effect of MAP, SAP, and DAP on rates of RNFL loss over time in FI and GE optic disc phenotypes.

Results

In the adjusted FI group models, each 10 mmHg decrease in MAP, SAP, and DAP was associated with −0.397 μm/year (P = 0.006), −0.211 μm/year (P = 0.029), and −0.471 μm/year (P = 0.005) faster RNFL thinning, respectively. In contrast, BP parameters were not significantly associated with RNFL loss in the GE group. In the multivariable model with interaction terms, the interaction between DAP and phenotype was statistically significant (P = 0.019), indicating the FI phenotype exhibited greater sensitivity to lower diastolic pressure compared to GE eyes. In contrast, interaction terms between IOP and optic disc phenotype were not significant in any of the models, suggesting a similar effect of IOP in both phenotypes.

Conclusions

Lower systemic BP levels were associated with faster RNFL thinning in the FI optic disc phenotype but not in the GE phenotype. These findings highlight the importance of considering both IOP and systemic BP when managing patients with the FI optic disc phenotype.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:探讨血压(BP)对伴有局灶性缺血性(FI)和全身性增大(GE)视盘表型的青光眼视网膜神经纤维层(RNFL)变薄率的影响。设计:前瞻性队列研究。参与者:该研究包括101例原发性开角型青光眼患者的122只眼睛。根据基线立体照片的模糊分级,将眼睛分为FI (n= 31,25%)或GE (n= 91,75%)。方法:每6个月进行一次全面眼科检查,包括眼内压(IOP)测量和光谱域光学相干断层扫描(SD-OCT),平均随访4.2年±1.5年。同时测量肱动脉血压,计算平均动脉压(MAP)、收缩压(SAP)和舒张压(DAP)。使用线性混合模型评估全球RNFL厚度随时间变化的比率,评估BP参数对每种视盘表型的影响,调整IOP和其他混杂因素。相互作用项用于测试FI和GE表型之间BP和IOP影响的差异。主要结局指标:MAP、SAP和DAP随时间对FI和GE视盘表型中RNFL损失率的影响。结果:在调整后的FI组模型中,MAP、SAP和DAP每降低10 mmhg分别与-0.397 μm/年(p=0.006)、-0.211 μm/年(p=0.029)和-0.471 μm/年(p=0.005)的RNFL变薄速度相关。相比之下,GE组的BP参数与RNFL损失无显著相关。在具有相互作用项的多变量模型中,DAP与表型之间的相互作用具有统计学意义(p=0.019),表明FI表型比GE眼对低舒张压表现出更大的敏感性。相比之下,IOP和视盘表型之间的相互作用项在任何模型中都不显著,表明IOP在两种表型中的作用相似。结论:在FI视盘表型中,较低的全身BP水平与更快的RNFL变薄有关,而在GE表型中则与此无关。这些发现强调了在治疗FI视盘表型患者时同时考虑IOP和全身性血压的重要性。
{"title":"Effect of Blood Pressure on Rates of Progression in Focal Ischemic vs. Generalized Cup Enlargement Glaucoma Phenotypes","authors":"Marcus Guerreiro-Filho MD ,&nbsp;Alessandro A. Jammal MD, PhD ,&nbsp;Rohit Muralidhar BA ,&nbsp;Rafael Scherer MD, PhD ,&nbsp;Luiz F. Beniz MD ,&nbsp;Douglas R. da Costa MD ,&nbsp;Ivan M. Tavares MD, PhD ,&nbsp;Felipe A. Medeiros MD, PhD","doi":"10.1016/j.ogla.2025.01.001","DOIUrl":"10.1016/j.ogla.2025.01.001","url":null,"abstract":"<div><h3>Purpose</h3><div>To investigate the impact of blood pressure (BP) on rates of retinal nerve fiber layer (RNFL) thinning in glaucomatous eyes with focal ischemic (FI) vs. generalized cup enlargement (GE) optic disc phenotypes.</div></div><div><h3>Design</h3><div>Prospective cohort study.</div></div><div><h3>Participants</h3><div>The study included 122 eyes from 101 patients diagnosed with primary open-angle glaucoma. Eyes were classified as FI (n = 31, 25%) or GE (n = 91, 75%) based on masked grading of stereophotographs at baseline.</div></div><div><h3>Methods</h3><div>Subjects underwent comprehensive ophthalmic examinations, including intraocular pressure (IOP) measurement and spectral-domain OCT scans, every 6 months for an overall mean follow-up of 4.2 years ± 1.5 years. Brachial artery BP was measured concurrently, and mean arterial pressure (MAP), systolic arterial pressure (SAP), and diastolic arterial pressure (DAP) were calculated. Rates of global RNFL thickness change over time were assessed using linear mixed models, evaluating the impact of BP parameters in each optic disc phenotype, adjusting for IOP and other confounders. Interaction terms were used to test for differences in the effects of BP and IOP between the FI and GE phenotypes.</div></div><div><h3>Main Outcome Measures</h3><div>Effect of MAP, SAP, and DAP on rates of RNFL loss over time in FI and GE optic disc phenotypes.</div></div><div><h3>Results</h3><div>In the adjusted FI group models, each 10 mmHg decrease in MAP, SAP, and DAP was associated with −0.397 μm/year (<em>P</em> = 0.006), −0.211 μm/year (<em>P</em> = 0.029), and −0.471 μm/year (<em>P</em> = 0.005) faster RNFL thinning, respectively. In contrast, BP parameters were not significantly associated with RNFL loss in the GE group. In the multivariable model with interaction terms, the interaction between DAP and phenotype was statistically significant (<em>P</em> = 0.019), indicating the FI phenotype exhibited greater sensitivity to lower diastolic pressure compared to GE eyes. In contrast, interaction terms between IOP and optic disc phenotype were not significant in any of the models, suggesting a similar effect of IOP in both phenotypes.</div></div><div><h3>Conclusions</h3><div>Lower systemic BP levels were associated with faster RNFL thinning in the FI optic disc phenotype but not in the GE phenotype. These findings highlight the importance of considering both IOP and systemic BP when managing patients with the FI optic disc phenotype.</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 3","pages":"Pages 293-301"},"PeriodicalIF":2.8,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142973497","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
Risk Factors for Diagnostic Change from Glaucoma Suspect to Primary Open-Angle Glaucoma and Vice Versa Over 2 Years 两年内青光眼从疑似青光眼转为原发性开角型青光眼的危险因素。
IF 2.8 Q1 OPHTHALMOLOGY Pub Date : 2025-05-01 DOI: 10.1016/j.ogla.2024.12.006
Lillian K. To MD, MS , Nicole V. Carrabba MD , Chaitanya G. Kalathuru MD , Alice Z. Chuang PhD , Logan Smith MD , Robert M. Feldman MD

Objective

This study investigates the incidence and causes of diagnostic changes from primary open-angle glaucoma suspect (POAGS) to primary open-angle glaucoma (POAG), and vice versa, in clinical practice.

Design

This is a retrospective, single-site, case-control study.

Participants

It includes patients > 40 years of age diagnosed with either POAG or POAGS between 2013 and 2020. Controls had a minimum of 24 months of follow-up without a diagnostic change, whereas cases underwent a diagnostic change from glaucoma to suspect (POAG to POAGS) or from suspect to glaucoma (POAGS to POAG) within 2 years.

Methods

At initial and follow-up visits, diagnosis, treatment, type of ophthalmic provider, and performance of pachymetry, visual fields (VFs), OCT, disc examination, and gonioscopy were recorded.

Main Outcome Measures

Data were then analyzed to determine if baseline characteristics, type of provider seen, or ophthalmic testing performed were protective or risk factors in regards to diagnostic change.

Results

Nine hundred twenty-two subjects were included, and the incidence of diagnostic changes was 13.8% (127/922), of which 99 (78%) were upstaged from POAGS to POAG and 28 (22%) changed from POAG to POAGS. Pre-existing nonglaucomatous VF defect (P < 0.001) was significantly higher in cases than controls. Cases were significantly less likely to be seen by a glaucoma specialist at the initial visit compared with controls (P < 0.001), and less cases underwent VF testing (P < 0.001), OCT testing (P = 0.017), or gonioscopy (P = 0.013) at the initial visit. On multivariate analysis, performing VFs or OCT at both visits reduced the odds of short-term diagnostic change, whereas changing providers from a nonglaucoma specialist to a glaucoma specialist between visits increased the odds of diagnostic change. In the POAG-to-POAGS cases, 39% (11/28) were treated with either medications or laser trabeculoplasty, whereas 72% (71/99) of the POAGS-to-POAG cases were left untreated between visits.

Conclusions

It is important to understand risk factors for diagnostic changes in glaucoma, in order to prevent undertreatment of disease and overtreatment of suspects. Here we find specialist type and adherence to American Academy of Ophthalmology (AAO) recommended testing to be important factors in preventing short term diagnostic changes.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.
目的:探讨原发性开角型青光眼(POAGS)与原发性开角型青光眼(POAG)在临床诊断中的变化及其原因。设计:这是一项回顾性、单地点、病例对照研究。参与者:包括2013-2020年间诊断为POAG或POAGS的40岁以上患者。对照组随访至少24个月,诊断无变化,而病例在2年内从青光眼转为疑似青光眼(POAG->POAGS)或从疑似青光眼转为青光眼(POAGS->POAG)。方法:记录患者初访及随访时的诊断、治疗、眼科医生类型、视厚测量、视野(VF)、光学相干断层扫描(OCT)、椎间盘检查和角膜镜检查结果。主要结果测量:然后对数据进行分析,以确定基线特征、所见提供者类型或所进行的眼科检查是有关诊断改变的保护因素还是危险因素。结果:纳入922例受试者,诊断改变发生率为13.8%(127/922),其中POAG->POAG抢镜99例(78%),POAG->POAG抢镜28例(22%)。非青光眼性VF缺损(POAGS)患者中,39%(11/28)采用药物治疗或激光小梁成形术治疗,而POAGS ->POAG患者中,72%(71/99)在两次访视之间未进行治疗。结论:了解青光眼诊断改变的危险因素,以防止疾病治疗不足和疑似患者过度治疗。在这里,我们发现专家类型和遵守AAO推荐的测试是预防短期诊断改变的重要因素。
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引用次数: 0
期刊
Ophthalmology. Glaucoma
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