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Associations between Clustered Visual Field Progression and Locations of Disc Hemorrhages in Glaucoma 青光眼聚集性视野进展与椎间盘出血部位的关系:一项为期三年的前瞻性研究。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.04.009
Tadamichi Akagi MD, PhD , Takeo Fukuchi MD, PhD , Tomomi Higashide MD, PhD , Sachiko Udagawa PhD , Shinji Ohkubo MD, PhD , Kazuhisa Sugiyama MD, PhD , Hidenobu Tanihara MD, PhD , Makoto Araie MD, PhD , Goji Tomita MD, PhD , Chota Matsumoto MD, PhD , Atsuo Tomidokoro MD, PhD , Masanori Hangai MD, PhD , Hisashi Kawata MS , Maya Inai MS , Yuki Tanaka MS , SVF Prospector Study Group

Purpose

To evaluate the impact of disc hemorrhages (DHs) at different locations on clustered visual field (VF) progression in patients with primary open-angle glaucoma (POAG) over a 3-year prospective study.

Design

A prospective multicenter cohort study.

Participants

Patients diagnosed with POAG and intraocular pressure (IOP) ≤18 mmHg undergoing prostaglandin analog monotherapy.

Methods

Visual field testing, IOP measurements, fundus photography, and OCT scans were conducted quarterly over a 3-year period. Disc hemorrhage locations were categorized into superior, inferior, temporal, and nasal quadrants. The VF was subdivided into superior, inferior, and central regions, with the central VF further divided into superior central and inferior central zones. A multivariable linear mixed-effects model with random intercepts and slopes was employed to analyze the relationship between DH history at specific locations and progressive changes in clustered total deviation (TD).

Main Outcome Measures

Association between DH location and the rate of clustered VF progression.

Results

Among 186 eyes from 109 patients, DH occurred in 61 eyes (32.8%). Superior, inferior, temporal, and nasal DH were observed in 19, 31, 21, and 2 eyes, respectively. A faster superior TD slope was significantly associated with inferior DH (P = 0.032), but not with superior or temporal DH. A faster inferior TD slope was significantly associated with a worse inferior baseline TD value (P = 0.009) and marginally associated with superior DH (P = 0.053) but not with inferior or temporal DH. A faster central TD slope was significantly associated with temporal DH (P < 0.001) and inferior DH (P = 0.034) but not with superior DH. Detailed analysis revealed that inferior DH was significantly associated with the superior central TD slope (P = 0.010) but not with the inferior central TD slope. Although DH recurrence was observed in 37 eyes, the number of DH events did not show an additive effect on corresponding clustered VF progression.

Conclusions

The location of DH was strongly associated with corresponding clustered VF progression in patients with POAG. Both temporal and inferior DH represent risk factors for central VF progression.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:在一项为期3年的前瞻性研究中,评估不同部位的椎间盘出血(DHs)对原发性开角型青光眼(POAG)患者聚集性视野(VF)进展的影响。设计:前瞻性、多中心队列研究。参与者:诊断为POAG且眼压(IOP)≤18 mmHg且接受前列腺素类似物单药治疗的患者。方法:VF测试,IOP测量,眼底摄影,光学相干断层扫描(OCT)扫描,为期3年。DH位置分为上象限、下象限、颞象限和鼻象限。VF又分为上、下、中央区,中央VF又分为上中央区和下中央区。采用随机截距和斜率的多变量线性混合效应模型,分析了特定位置DH历史与聚类总偏差(TD)渐进变化的关系。主要结局指标:DH位置与聚集性VF进展率之间的关系。结果:109例患者186只眼发生DH 61只眼(32.8%)。分别观察19眼、31眼、21眼和2眼的上、下、颞和鼻腔DH。更快的上TD斜率与下DH显著相关(P=0.032),但与上DH或时间DH无关。更快的下道TD斜率与较差的下道基线TD值显著相关(P=0.009),与较高的DH值略有相关(P=0.053),但与较低的或时间的DH值无关。更快的中央TD斜率与时间DH显著相关(结论:DH的位置与POAG患者相应的聚集性VF进展密切相关。颞部和下壁DH都是中枢性心室颤动进展的危险因素。
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引用次数: 0
Intraocular Pressure Matters 眼压很重要。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.07.008
Sasan Moghimi MD, Christopher Girkin MD, MSPH, Robert N. Weinreb MD
To date, evidence from multiple randomized controlled trials has shown that effective intraocular pressure (IOP)-lowering therapy significantly reduces the risk of glaucomatous progression across all stages of the disease. Changes in IOP have a substantial impact on the load-bearing connective tissues of the optic nerve head (ONH), as well as the overlying neurovascular tissues of the ONH and retina. An initial treatment goal of reducing IOP by 25% to 35%—and possibly more in advanced cases—can help prevent progression. Additionally, maintaining stable IOP by minimizing both diurnal and long-term fluctuations may further enhance disease control and reduce the risk of worsening.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
迄今为止,来自多个随机对照试验的证据表明,有效的降低眼压(IOP)治疗可显著降低青光眼在疾病所有阶段进展的风险。IOP的变化对视神经头(ONH)的承重结缔组织以及ONH和视网膜的上覆神经血管组织有重大影响。最初的治疗目标是将IOP降低25%到35%,在晚期患者可能会降低更多,这有助于防止病情恶化。此外,通过尽量减少昼夜和长期波动来维持稳定的IOP可能进一步加强疾病控制并降低恶化的风险。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
Then and Now: Medical Therapy for Glaucoma 过去和现在:青光眼的药物治疗。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.08.002
Eydie Miller-Ellis MD , Gloria P. Fleming MD
There has been a remarkable evolution of medical therapy for glaucoma over the 4 decades since the founding of the American Glaucoma Society in 1985. The therapeutic landscape has undergone a transformation from limited, poorly tolerated treatment options to sophisticated patient-centered approaches that prioritize efficacy, convenience, and improved quality of life. This evolution was propelled not only by advances in pharmacological understanding and drug delivery innovation, but also by a growing recognition of how medication-related side effects contribute to nonadherence and the overall burden of disease. Key developments have included the transition from systemic to topical formulations, which mitigated several systemic side effects; the expansion of drug classes targeting alternate pathways of outflow; the advent of once-daily dosing regimens improving patient compliance; and the evolution of sustained-release delivery models, potentially reducing or eliminating the dependency of patient daily participation. Our understanding of the critical importance of ocular surface health in long-term treatment success gave rise to the development of preservative-free formulations. This four-decade journey from limited treatment options to evolutionary paradigm shifts in medical management demonstrates the power of scientific innovation in the quest to preserve vision while also enhancing quality of life measures for our patients with chronic disease. As interventions like minimally invasive glaucoma surgeries evolve, the role of glaucoma medical management may shift, but currently remains a dependable cornerstone in our treatment algorithms.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
自1985年美国青光眼协会成立以来,在过去的40年里,青光眼的医学治疗有了显著的发展。治疗领域经历了从有限的、耐受性差的治疗选择到复杂的以患者为中心的方法的转变,这些方法优先考虑疗效、便利性和改善生活质量。这一演变不仅受到药理学理解和药物传递创新的推动,也受到药物相关副作用如何导致不依不从和整体疾病负担的日益认识的推动。主要的发展包括从全身剂型向局部剂型的转变,这减轻了一些全身副作用;扩大药物类别,以替代流出途径为目标;每日一次给药方案的出现改善了患者的依从性;以及持续释放给药模式的发展,可能会减少或消除患者对日常参与的依赖。我们对眼表健康在长期治疗成功中至关重要的认识促使了无防腐剂配方的发展。从有限的治疗选择到医疗管理的进化范式转变,这四十年的历程证明了科学创新在寻求保护视力的同时也提高了慢性病患者的生活质量。随着微创青光眼手术等干预措施的发展,青光眼医疗管理的作用可能会发生变化,但目前仍是我们治疗算法的可靠基石。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
Influence of CYP1B1 Variants on Phenotypic Characteristics and Therapeutic Outcomes in Primary Congenital Glaucoma CYP1B1变异对原发性先天性青光眼表型特征和治疗结果的影响
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.04.012
Rita Rodrigues MD , David Alves MD , João Esteves-Leandro MD , Marta Silva MD , João Barbosa-Breda MD, PhD , João Tavares-Ferreira MD , Joana Araújo MD , Susana Fernandes PhD , Renata Oliveira MD , António Melo MD , Flávio Alves MD , Augusto Magalhães MD , José Cotta MD , Sérgio Estrela-Silva MD
<div><h3>Purpose</h3><div>To identify <span><span>CYP1B1</span></span><span> variants in primary congenital glaucoma (PCG) patients from Northern Portugal and examine genotype–phenotype correlations.</span></div></div><div><h3>Design</h3><div>Cross sectional observational study.</div></div><div><h3>Participants</h3><div>Seventy-one patients diagnosed and treated for PCG at ULS São João, Porto, Portugal, were included. These patients met the following criteria: available genetic testing data, a minimum follow-up period of 1 year, and the last appointment between January 2022 and January 2024.</div></div><div><h3>Methods</h3><div>Demographic and clinical data were collected. <em>CYP1B1</em><span> variants were screened using DNA sequencing. A next-generation sequencing (NGS) glaucoma panel was performed in patients with heterozygous or absent </span><em>CYP1B1</em> variants in the screening. Genotype–phenotype correlations were assessed by comparing clinical characteristics between patients with identified biallelic plausible disease-causing variants in <em>CYP1B1</em> variants and those with negative genetic testing results.</div></div><div><h3>Main Outcome Measures</h3><div><em>CYP1B1</em><span> variants, sex, laterality, age at diagnosis, age at first surgery, number of surgical procedures, number of intraocular pressure (IOP)-lowering medications, IOP at last follow-up, and final best-corrected visual acuity (BCVA).</span></div></div><div><h3>Results</h3><div><span>Sixty-six unrelated probands and 5 affected relatives (133 eyes) were analyzed. Two plausible disease-causing </span><em>CYP1B1</em> variants were identified in 60.6% (43/71) of patients. Nineteen distinct <em>CYP1B1</em> variants were identified, including 4 novel variants. The most frequent variants were c.535del (43.5%) and c.1200_1209dup (28.2%). Compared with negative genetic testing group (n = 22), patients with <em>CYP1B1</em> variants (n = 43) showed significantly higher rates of bilateral disease (100% vs. 68%, <em>P</em> < 0.001), earlier disease onset (median 0 vs. 5.5 months, <em>P</em> < 0.001), poorer final BCVA (median 0.5 vs. 0.25 logarithm of the minimum angle of resolution, <em>P</em> = 0.025), higher IOP at last follow-up (median 16 vs. 12 mmHg, <em>P</em> < 0.001), and greater need for surgical interventions (median 2 vs. 1, <em>P</em> = 0.014) and IOP-lowering medications (median 2 vs. 0, <em>P</em> = 0.005). Next-generation sequencing testing in <em>CYP1B1</em>-negative patients identified 3 novel heterozygous variants of uncertain significance in the TEK gene.</div></div><div><h3>Conclusions</h3><div>Primary congenital glaucoma patients from Northern Portugal with <em>CYP1B1</em> variants are more likely to present with bilateral disease, earlier onset, and a more severe clinical phenotype, suggesting a strong genotype–phenotype correlation.</div></div><div><h3>Financial Disclosure(s)</h3><div>The authors have no proprietary or commercial interest in a
目的:鉴定葡萄牙北部原发性先天性青光眼(PCG)患者的CYP1B1变异,并检查基因型与表型的相关性。设计:横断面观察性研究。参与者:71例在葡萄牙波尔图的 o jo s诊断和治疗的PCG患者。这些患者符合以下标准:可获得基因检测数据,至少随访1年,最后一次预约时间为2022年1月至2024年1月。方法:收集人口学和临床资料。使用DNA测序筛选CYP1B1变异体。下一代测序(NGS)青光眼小组在筛选中杂合或缺失CYP1B1变异的患者中进行。通过比较在CYP1B1变异中确定的双等位基因似是而非的致病变异的患者与基因检测结果为阴性的患者的临床特征,评估基因型-表型相关性。主要观察指标:CYP1B1变异、性别、侧边、诊断时年龄、首次手术年龄、手术次数、降眼压药物次数、最后随访时眼压、最终最佳矫正视力(BCVA)。结果:对66例无血缘关系先证者和5例患病亲属(133眼)进行分析。60.6%(43/71)的患者发现了两种可能致病的CYP1B1变异。鉴定出19种不同的CYP1B1变异,包括4种新的变异。最常见的变异是c.535del(43.5%)和c.1200_1209dup(28.2%)。与基因检测阴性组(n=22)相比,CYP1B1变异患者(n=43)的双侧疾病发生率明显更高(100% vs 68%, p结论:来自葡萄牙北部的CYP1B1变异的PCG患者更容易出现双侧疾病,发病更早,临床表型更严重,提示基因型-表型相关性强。
{"title":"Influence of CYP1B1 Variants on Phenotypic Characteristics and Therapeutic Outcomes in Primary Congenital Glaucoma","authors":"Rita Rodrigues MD ,&nbsp;David Alves MD ,&nbsp;João Esteves-Leandro MD ,&nbsp;Marta Silva MD ,&nbsp;João Barbosa-Breda MD, PhD ,&nbsp;João Tavares-Ferreira MD ,&nbsp;Joana Araújo MD ,&nbsp;Susana Fernandes PhD ,&nbsp;Renata Oliveira MD ,&nbsp;António Melo MD ,&nbsp;Flávio Alves MD ,&nbsp;Augusto Magalhães MD ,&nbsp;José Cotta MD ,&nbsp;Sérgio Estrela-Silva MD","doi":"10.1016/j.ogla.2025.04.012","DOIUrl":"10.1016/j.ogla.2025.04.012","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Purpose&lt;/h3&gt;&lt;div&gt;To identify &lt;span&gt;&lt;span&gt;CYP1B1&lt;/span&gt;&lt;/span&gt;&lt;span&gt; variants in primary congenital glaucoma (PCG) patients from Northern Portugal and examine genotype–phenotype correlations.&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Design&lt;/h3&gt;&lt;div&gt;Cross sectional observational study.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Participants&lt;/h3&gt;&lt;div&gt;Seventy-one patients diagnosed and treated for PCG at ULS São João, Porto, Portugal, were included. These patients met the following criteria: available genetic testing data, a minimum follow-up period of 1 year, and the last appointment between January 2022 and January 2024.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;Demographic and clinical data were collected. &lt;em&gt;CYP1B1&lt;/em&gt;&lt;span&gt; variants were screened using DNA sequencing. A next-generation sequencing (NGS) glaucoma panel was performed in patients with heterozygous or absent &lt;/span&gt;&lt;em&gt;CYP1B1&lt;/em&gt; variants in the screening. Genotype–phenotype correlations were assessed by comparing clinical characteristics between patients with identified biallelic plausible disease-causing variants in &lt;em&gt;CYP1B1&lt;/em&gt; variants and those with negative genetic testing results.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Main Outcome Measures&lt;/h3&gt;&lt;div&gt;&lt;em&gt;CYP1B1&lt;/em&gt;&lt;span&gt; variants, sex, laterality, age at diagnosis, age at first surgery, number of surgical procedures, number of intraocular pressure (IOP)-lowering medications, IOP at last follow-up, and final best-corrected visual acuity (BCVA).&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;&lt;span&gt;Sixty-six unrelated probands and 5 affected relatives (133 eyes) were analyzed. Two plausible disease-causing &lt;/span&gt;&lt;em&gt;CYP1B1&lt;/em&gt; variants were identified in 60.6% (43/71) of patients. Nineteen distinct &lt;em&gt;CYP1B1&lt;/em&gt; variants were identified, including 4 novel variants. The most frequent variants were c.535del (43.5%) and c.1200_1209dup (28.2%). Compared with negative genetic testing group (n = 22), patients with &lt;em&gt;CYP1B1&lt;/em&gt; variants (n = 43) showed significantly higher rates of bilateral disease (100% vs. 68%, &lt;em&gt;P&lt;/em&gt; &lt; 0.001), earlier disease onset (median 0 vs. 5.5 months, &lt;em&gt;P&lt;/em&gt; &lt; 0.001), poorer final BCVA (median 0.5 vs. 0.25 logarithm of the minimum angle of resolution, &lt;em&gt;P&lt;/em&gt; = 0.025), higher IOP at last follow-up (median 16 vs. 12 mmHg, &lt;em&gt;P&lt;/em&gt; &lt; 0.001), and greater need for surgical interventions (median 2 vs. 1, &lt;em&gt;P&lt;/em&gt; = 0.014) and IOP-lowering medications (median 2 vs. 0, &lt;em&gt;P&lt;/em&gt; = 0.005). Next-generation sequencing testing in &lt;em&gt;CYP1B1&lt;/em&gt;-negative patients identified 3 novel heterozygous variants of uncertain significance in the TEK gene.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusions&lt;/h3&gt;&lt;div&gt;Primary congenital glaucoma patients from Northern Portugal with &lt;em&gt;CYP1B1&lt;/em&gt; variants are more likely to present with bilateral disease, earlier onset, and a more severe clinical phenotype, suggesting a strong genotype–phenotype correlation.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Financial Disclosure(s)&lt;/h3&gt;&lt;div&gt;The authors have no proprietary or commercial interest in a","PeriodicalId":19519,"journal":{"name":"Ophthalmology. Glaucoma","volume":"8 5","pages":"Pages 457-465"},"PeriodicalIF":3.2,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144043049","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
Meaningful Patient Partnerships 有意义的患者伙伴关系:青光眼手术患者观点和共同决策的定性研究。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.04.006
Zayn Al-Timimi BMed, MD , Samrat Sarkar BOptom, MAppSc , Sapna Nand BAppSc(Orth) , Simon E. Skalicky MBBS, PhD , Sartaj Sandhu MBBS , Hamish Dunn MBBS, PhD , Lisa Keay MPH, PhD

Purpose

Patient-centered care is key to successful clinical outcomes and meaningful clinician–patient relationships. Accordingly, a comprehensive understanding of patient perspectives is essential to aligning the clinician's focus and patient's goals. However, our understanding of patients' perceptions of glaucoma surgery and involvement in surgical decision-making has not kept pace with the rapid treatment advances in the field and move toward earlier surgery with the advent of minimally invasive glaucoma surgery devices. The purpose of this study was to understand the perspectives and priorities of people with glaucoma when considering glaucoma surgery through qualitative analysis of semistructured interviews.

Design

A qualitative study.

Participants

Individuals diagnosed with glaucoma, above 18 years of age, and able to communicate effectively in English. Interviews were conducted with 40 participants: 23 participants who had undergone glaucoma surgery and 17 who had not.

Methods

Interviews were conducted over telephone, using an interview guide developed in consultation with people with glaucoma and surgeons. The cohort was purposely sampled to ensure representation across age, sex, socioeconomic status, remoteness, glaucoma severity, clinic settings, and treatment histories. Transcripts were iteratively analyzed to identify key themes pertaining to perceptions of glaucoma surgery and involvement in decision-making.

Main Outcome Measures

Surgical perception and involvement themes, including barriers and bridges to confidence in glaucoma surgery.

Results

Six key themes were identified: (1) patients feeling rushed; (2) onus on the patient to seek information; (3) undercurrents of anxiety; (4) perceptions of surgery shaped by understanding and expectations of the disease and its treatment paradigm; (5) trust in surgeon imbuing confidence in surgery; and (6) empowerment through understanding of alternatives. Key barriers to patient involvement included patient anxiety, time pressures (real or perceived), and perceived urgency of intervention.

Conclusions

Shared decision-making in glaucoma surgery remains aspirational. This study provides valuable insights into patient perceptions of glaucoma surgery, which can help inform patient-centered care. Readily applicable “practice points” are proposed to optimize patient involvement and empowerment.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:以患者为中心的护理是成功的临床结果和有意义的医患关系的关键。因此,全面了解患者的观点对于调整临床医生的重点和患者的目标至关重要。然而,随着微创青光眼手术设备的出现,我们对患者对青光眼手术的看法和参与手术决策的理解并没有跟上该领域治疗的快速发展,也没有向早期手术发展。本研究的目的是通过半结构化访谈的定性分析,了解青光眼患者在考虑青光眼手术时的观点和优先事项。设计:定性研究。参与者:被诊断为青光眼的个体,18岁以上,能够用英语进行有效沟通。对40名参与者进行了访谈:23名参与者接受了青光眼手术,17名没有。方法:采用与青光眼患者和外科医生协商制定的访谈指南,通过电话进行访谈。该队列的抽样是有目的的,以确保年龄、性别、社会经济地位、偏远地区、青光眼严重程度、诊所设置和治疗史的代表性。反复分析转录本,以确定与青光眼手术和参与决策有关的关键主题。主要结果测量:手术感知和受累主题,包括青光眼手术信心的障碍和桥梁。结果:确定了6个关键主题:(1)患者感觉匆忙;(二)患者查询信息的责任;(3)焦虑潜流;(4)对手术的认知受对疾病及其治疗模式的理解和期望的影响;(五)对外科医生的信任,对手术充满信心;(6)通过理解替代方案来授权。患者参与的主要障碍包括患者焦虑,时间压力(真实的或感知的),以及感知到的干预紧迫性。结论:青光眼手术的共同决策仍然是理想的。本研究为患者对青光眼手术的看法提供了有价值的见解,有助于为以患者为中心的护理提供信息。提出了易于应用的“实践点”,以优化患者参与和授权。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
Female Authorship Trends in Ophthalmology Glaucoma 眼科学青光眼的女性作者趋势。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.06.005
Sophia S. Lam MD, Tak Yee Tania Tai MD, Nisha Chadha MD
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引用次数: 0
The Evolution of Visual Field Testing 视野测试的演变:40年来青光眼的现代视野测量。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.08.001
Anfei Li MD, PhD , C. Gustavo De Moraes MD, PhD
The assessment of the human visual field, a concept explored since ancient Greece, underwent a critical transformation in the 19th century with the advent of objective measurement techniques. Early methodologies concentrated on mapping the outer limits of vision, a practice known as perimetry. However, the focus soon shifted toward campimetry (although the name perimetry remained), which involves assessing defects within the central/paracentral visual field—a crucial development for diagnosing diseases such as glaucoma. Although historical methods such as Bjerrum tangent screen and Goldmann kinetic perimetry were foundational, the last 4 decades have been defined by the rise of static automated perimetry (SAP). Coinciding with the inception of the American Glaucoma Society, the 1980s marked a pivotal transition from manual techniques to computerized, automated testing. Static automated perimetry, exemplified by the Humphrey Field Analyzer (HFA), has since become the clinical standard, offering a precise and reproducible method for quantifying visual field sensitivities, which is indispensable for the detection and management of glaucoma. This review examines the evolution of modern visual field testing over the past 40 years, focusing on the technological advancements in hardware, software algorithms, and novel testing paradigms that have reshaped our approach to glaucoma care.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
人类视野的评估是一个自古希腊以来就被探索的概念,随着客观测量技术的出现,在19世纪经历了一个关键的转变。早期的方法集中于绘制视觉的外部界限,这种做法被称为视野测量。然而,焦点很快转向了视野测量(尽管名称仍然保留),它涉及评估中央/副中央视野内的缺陷——这是诊断青光眼等疾病的关键发展。虽然Bjerrum切线筛和Goldmann动力学视野测量等历史方法是基础,但在过去的40年里,静态自动视野测量(SAP)的兴起定义了这一方法。20世纪80年代恰逢美国青光眼协会成立,标志着从手工技术到计算机化、自动化测试的关键转变。以汉弗莱视场分析仪(Humphrey Field Analyzer, HFA)为代表的静态自动视场测量从此成为临床标准,提供了一种精确、可重复的量化视野灵敏度的方法,这对于青光眼的检测和治疗是不可或缺的。本文回顾了过去40年来现代视野检测的发展,重点介绍了硬件、软件算法和新的检测范式方面的技术进步,这些技术进步重塑了我们对青光眼的治疗方法。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
Appendix 合同附件。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.07.003
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引用次数: 0
American Glaucoma Society 40th Anniversary 美国青光眼协会成立40周年:前言。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.08.007
Carla J. Siegfried MD, Gregory L. Skuta MD
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引用次数: 0
Association of Eye Drop–Treated Diseases and Conditions That Can Impair Eye Drop Self-Administration 眼药水治疗的疾病和状况会损害眼药水的自我管理。
IF 3.2 Q1 OPHTHALMOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.ogla.2025.04.001
Tianyi Wang BA , Hong Su An PhD , Jaqueline Stoutin MD , Alexander D. Valentine MD , Leah K. Depperschmidt RN , Matthew Callewaert OD , Michael Goldstein MD , Joshua D. Stein MD, MS

Objective

Eye drops are often first-line treatment for glaucoma and dry eye disease (DED). Unfortunately, proper eye drop self-administration is difficult, and this is likely magnified in persons with comorbid rheumatological, neurological, or cognitive disorders. This study investigates the association between ocular conditions often treated with eye drops (glaucoma and DED) and medical conditions that may impair proper eye drop self-administration.

Design

A retrospective database study.

Participants

From 6 health systems, 1 446 229 patients participated in the Sight Outcomes Research Collaborative between January 2012 and December 2021.

Methods

We determined the proportion of patients with glaucoma or DED with medical conditions that may limit proper eye drop self-administration and created multivariable logistic regression models assessing associations between glaucoma or DED and comorbid conditions.

Main Outcome Measures

Adjusted odds ratios (aORs) with 95% confidence intervals (CIs) of glaucoma or DED.

Results

Among 247 899 patients with glaucoma (mean [standard deviation] age: 60.1 [15.1] years, 56.2% female, 19.5% Black), 106 927 (43%) had ≥ 1 comorbid condition that could affect eye drop self-administration. Among 321 941 patients with DED (mean [standard deviation] age: 55.9 [16.1] years, 66.4% female, 12.6% Black), 156 811 (49%) had ≥ 1 such condition. Patients with ≥ 1 impairment affecting eye drop self-administration had 17% greater odds of glaucoma (aOR: 1.17, CI: 1.16–1.18) and 66% greater odds of DED (aOR: 1.66, CI: 1.65–1.68), compared with other patients. Persons with 2, 3, and ≥ 4 conditions that may affect eye drop administration had 27%, 39%, and 53% higher odds of glaucoma, respectively, compared with persons without such conditions (P < 0.0001). Persons with 2, 3, and ≥ 4 health conditions that may impair eye drop administration had 76%, 121%, and 156% higher odds of DED, respectively (P < 0.0001).

Conclusions

Nearly half of all patients with glaucoma or DED have ≥ 1 medical condition that may impair eye drop self-administration. Clinicians should assess patients' physical and mental capacity to self-administer topical ocular therapy. Some patients may benefit from alternative therapies that reduce or eliminate the need for eye drops.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
目的:青光眼和干眼病(DED)的一线治疗通常是滴眼液。不幸的是,适当的滴眼液自我给药是困难的,这在患有风湿病、神经或认知障碍的患者中可能会更加严重。本研究调查了经常用眼药水治疗的眼部疾病(青光眼和DED)与可能损害适当滴眼液自我给药的医疗状况之间的关系。设计:回顾性数据库研究参与者:2012年1月至2021年12月期间参加视力结局研究合作(SOURCE)的6个卫生系统的1,446,229名患者。方法:我们确定了青光眼或DED患者中存在可能限制适当滴眼液自我使用的医疗条件的比例,并创建了多变量logistic回归模型,评估青光眼或DED与合并症之间的关系。结果:在247899例青光眼患者(平均(SD)年龄:60.1(15.1)岁,56.2%为女性,19.5%为黑人)中,106927例(43%)患者存在≥1种影响滴眼液自我给药的合并症。在321,941例DED患者中(平均(SD)年龄:55.9(16.1)岁,女性66.4%,黑人12.6%),156,811例(49%)有≥1种可能妨碍滴眼液自我给药的情况。与无上述情况的患者相比,有≥1种损害影响滴眼液自我给药的患者发生青光眼的几率(aOR)高17% (1.17,CI(1.16-1.18)),发生DED的几率高66% (aOR 1.66, CI 1.65-1.68))。患有2、3、4+种可能影响滴眼液给药的疾病的患者患青光眼的几率分别比没有这些疾病的患者高27%、39%和53%(结论:近一半的青光眼或DED患者患有≥1种可能影响滴眼液自我给药的疾病)。这突出了临床医生评估患者的重要性,以确保他们在身体和精神上能够自我使用眼药水。其中一些患者可能会受益于替代疗法,减少或消除对滴眼液的需求。
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引用次数: 0
期刊
Ophthalmology. Glaucoma
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