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Race and Gender Shift among Academic Glaucoma Specialists in the Last 5 Decades. 过去50年学术青光眼专家的种族和性别转变。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1407
Kasra Afzali, Dylann K Fujimoto, Seyed Omid Mohammadi, Ken Y Lin

Purpose: To evaluate the demographic composition of academic glaucoma specialists currently practicing in the United States.

Design: Retrospective and observational study.

Subjects: Academic glaucoma specialists identified from ophthalmology residency programs listed on the Doximity database.

Methods: The American Board of Ophthalmology (ABO) membership directory, Doximity database, publicly available data, and direct communications were used to identify academic glaucoma specialists and their demographics. Information collected included-name, gender, race/ethnicity, geographic location, board certification date, academic affiliation, and academic rank. Ophthalmic age was defined as the number of years since ophthalmology board certification. Underrepresented minority (URM) groups were defined as Hispanics, Black or African Americans, Latinos, American Indians, or Alaskan Natives as defined by San Francisco match. In addition, the temporal, geographic, and academic rank distributions among females and URMs were explored.

Main outcome measures: Women and URMs representations among academic glaucoma specialists across academic ranks, geographic regions, as well as ophthalmic age.

Results: There were 457 active academic glaucoma specialists identified from 110 institutions in 38 states. Among them, 185 (40.5%) were women and 42 (9.2%) were URM. The proportion of women glaucoma specialists in academia had increased significantly with a rate of 1.049 in odds ratio (OR) per year (p < 0.001). However, there were no significant changes in the proportion of URMs over time. The earliest year of certification was 1,964 for males and 1,974 for females. When controlled for ophthalmic age, there were no significant differences in the distribution of women or URMs between the different academic ranks (p = 0.572 and p = 0.762, respectively). Among assistant professors, women had a significantly higher ophthalmic age compared to men (p < 0.001), but there was no significant difference in ophthalmic age in both the associate and full professor groups. There were no significant differences in the geographic distribution of gender (p = 0.516) and URM across United States regions (p = 0.238).

Conclusion: The proportion of women among academic glaucoma specialists has significantly increased over the past 5 decades; however, the proportion of URMs has been stagnant in the same period. Enhancing URM representation among academic glaucoma specialists deserves to be a future priority.

How to cite this article: Afzali K, Fujimoto DK, Mohammadi SO, et al. Race and Gender Shift among Academic Glaucoma Specialists in the Last 5 Decades. J Curr Glaucoma Pract 2023;17(2):98-103.

目的:评估目前在美国执业的学术青光眼专家的人口构成。设计:回顾性和观察性研究。受试者:从Doximity数据库中列出的眼科住院医师项目中确定的学术性青光眼专家。方法:使用美国眼科委员会(ABO)会员目录、Doximity数据库、公开数据和直接沟通来确定学术青光眼专家及其人口统计数据。收集的信息包括姓名、性别、种族/民族、地理位置、董事会认证日期、学术关系和学术等级。眼科年龄定义为自眼科委员会认证以来的年数。根据旧金山比赛的定义,代表性不足的少数族裔(URM)群体被定义为西班牙裔、黑人或非裔美国人、拉丁裔、美洲印第安人或阿拉斯加原住民。此外,还探讨了女性和URM的时间、地理和学术等级分布。主要结果指标:不同学术级别、地理区域以及眼科年龄的学术青光眼专家中女性和URM的代表性。结果:共有457名活跃的学术青光眼专家,来自38个州的110个机构。其中女性185例(40.5%),URM 42例(9.2%)。学术界女性青光眼专家的比例显著增加,比值比(OR)每年为1.049(p<0.001)。然而,随着时间的推移,URM的比例没有显著变化。最早的认证年份是1964年(男性)和1974年(女性)。当对照眼科年龄时,不同学术级别的女性或URM的分布没有显著差异(分别为p=0.572和p=0.762)。在助理教授中,女性的眼科年龄明显高于男性(p<0.001),但副教授组和正教授组的眼科年龄没有显著差异。美国各地区的性别地理分布(p=0.516)和URM(p=0.238)没有显著差异。结论:在过去50年中,学术青光眼专家中女性的比例显著增加;然而,URM的比例在同一时期一直停滞不前。加强URM在学术青光眼专家中的代表性应该成为未来的优先事项。如何引用这篇文章:Afzali K,Fujimoto DK,Mohammadi SO等。过去50年学术青光眼专家的种族和性别转变。青光眼临床杂志2023;17(2):98-103。
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引用次数: 0
New-onset Glaucoma Following Moderna COVID-19 Vaccination. 莫德纳新冠肺炎疫苗接种后新发性青光眼。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1408
Yi-Wen Su, Shih-Jung Yeh, Mei-Ju Chen

Aim: To report a case of new-onset glaucoma following administration of the Moderna (mRNA-1273) vaccine.

Background: Previous studies have reported a low incidence of ocular adverse events induced by the coronavirus disease 2019 (COVID-19) vaccine. The literature on open-angle glaucoma associated with COVID-19 vaccination is limited.

Case description: The patient complained of blurred vision 2 days following the administration of the second dose of the Moderna vaccine in July 2021. At presentation, the ophthalmic examination showed elevated intraocular pressure (IOP) of 30 mm Hg in her right eye (OD) and 18 mm Hg in her left eye (OS). There were no signs of intraocular inflammation or glaucomatous optic neuropathy at the initial presentation. She was treated with a topical β-blocker first. In addition, 1 month later, her IOPs were 28 mm Hg OD and 26 mm Hg OS. Although treated with multiple antiglaucoma medications, her optic cup-to-disc ratios were increased in both eyes (OU) compared to May 2019. She developed a glaucomatous visual field (VF) defect OD in October 2021. Optical coherence tomography (OCT) revealed progressive retinal nerve fiber layer (RNFL) thinning in OU.

Conclusion: Glaucoma may be a rare but severe ocular adverse event of the Moderna vaccines. The ophthalmologist should pay attention to the risk of increased IOP following COVID-19 vaccination.

Clinical significance: We reported a case of new-onset open-angle glaucoma presumably associated with COVID-19 vaccination.

How to cite this article: Su Y, Yeh S, Chen M. New-onset Glaucoma Following Moderna COVID-19 Vaccination. J Curr Glaucoma Pract 2023;17(2):106-109.

目的:报告一例接种莫德纳(mRNA-1273)疫苗后新发青光眼的病例。背景:先前的研究报告称,2019冠状病毒病(新冠肺炎)疫苗诱导的眼部不良事件发生率较低。关于与新冠肺炎疫苗接种相关的开角型青光眼的文献有限。病例描述:患者在2021年7月接种第二剂莫德纳疫苗后2天抱怨视力模糊。在介绍时,眼科检查显示她的右眼(OD)和左眼(OS)的眼压分别升高了30毫米汞柱和18毫米汞柱。在最初的表现中没有眼内炎症或青光眼性视神经病变的迹象。她首先接受了局部β-阻滞剂治疗。此外,1个月后,她的眼压为外径28毫米汞柱,OS 26毫米汞柱。尽管接受了多种抗青光眼药物的治疗,但与2019年5月相比,她的双眼视杯与视盘的比例有所增加。她于2021年10月出现青光眼视野(VF)缺陷OD。光学相干断层扫描(OCT)显示OU中进行性视网膜神经纤维层(RNFL)变薄。结论:青光眼可能是一种罕见但严重的莫德纳疫苗眼部不良反应。眼科医生应注意接种新冠肺炎疫苗后眼压升高的风险。临床意义:我们报告了一例新发的开角型青光眼,可能与新冠肺炎疫苗接种有关。如何引用本文:Su Y,Yeh S,Chen M.莫德纳新冠肺炎疫苗接种后新发性青光眼。青光眼临床杂志2023;17(2):106-109。
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引用次数: 1
Profile of Childhood Glaucoma Attending a Tertiary Eye Care Center in Northern India. 印度北部一家三级眼科护理中心的儿童青光眼简介。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1400
Suneeta Dubey, Kanika Jain, Julie Pegu, Saptarshi Mukherjee

Purpose: To ascertain the prevalence and clinical features of the various types of childhood glaucoma at a tertiary eye care hospital in Northern India.

Materials and methods: Retrospective chart review of all children less than 16 years of age with childhood glaucoma who presented from 1st April 2014 to 31st March 2019, who was diagnosed to have any subtype of childhood glaucoma as per Childhood Glaucoma Research Network (CGRN) classification and advised appropriate management.

Results: Out of 405 children with childhood glaucoma, 36% had primary glaucoma, whereas the rest had secondary glaucoma. Primary congenital glaucoma (PCG) was the most common form of primary glaucoma. Glaucoma associated with acquired conditions was the most common cause of secondary glaucoma. Primary glaucoma was mostly bilateral in contrast to secondary glaucoma. The most common age of presentation with primary glaucoma was <1 year of age, and in children with secondary glaucoma was 11-16 years. On presentation, 80% of eyes had intraocular pressure (IOP) of >20 mm Hg and 70% had cupping of >0.7. Eyes with PCG were primarily managed surgically.

Conclusion: In our cohort, PCG was the most common primary childhood glaucoma. Traumatic glaucoma was the most common secondary glaucoma. Since childhood glaucoma is an important cause of visual morbidity in children, its timely diagnosis and prompt management are essential to prevent irreversible visual loss.

Clinical significance: Understanding the disease pattern, their presenting features, and the proportion of different types of childhood glaucoma can help in planning appropriate eye care services, create awareness and better allocate resources to plan appropriate management strategies. Screening programs and counseling of parents should also be strengthened.

How to cite this article: Dubey S, Jain K, Pegu J, et al. Profile of Childhood Glaucoma Attending a Tertiary Eye Care Center in Northern India. J Curr Glaucoma Pract 2023;17(2):68-74.

目的:确定印度北部一家三级眼科医院各种类型儿童青光眼的患病率和临床特征。材料和方法:对2014年4月1日至2019年3月31日期间出现的所有16岁以下儿童青光眼的回顾性图表回顾,根据儿童青光眼研究网络(CGRN)的分类,被诊断为患有任何儿童青光眼亚型,并建议进行适当的治疗。结果:405名儿童期青光眼患儿中,36%为原发性青光眼,其余为继发性青光眼。原发性先天性青光眼是最常见的原发性青光眼。与后天条件相关的青光眼是继发性青光眼最常见的原因。与继发性青光眼相比,原发性青光眼多为双侧。原发性青光眼最常见的发病年龄为20毫米汞柱,70%的患者拔火罐>0.7。PCG眼主要通过手术治疗。结论:在我们的队列中,PCG是最常见的原发性儿童青光眼。外伤性青光眼是最常见的继发性青光眼。由于儿童期青光眼是儿童视力发病的重要原因,因此及时诊断和及时治疗对于预防不可逆转的视力损失至关重要。临床意义:了解疾病模式、其表现特征和不同类型儿童青光眼的比例,有助于规划适当的眼部护理服务,提高意识,并更好地分配资源来规划适当的管理策略。还应加强对家长的筛查和咨询。如何引用这篇文章:Dubey S,Jain K,Pegu J等。印度北部一家三级眼科护理中心的儿童青光眼简介。青光眼临床杂志2023;17(2):68-74。
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引用次数: 0
Agreement between Two Swept-source Optical Coherence Tomography: Optic Nerve Head, Retinal Nerve Fiber Layer and Ganglion Cell Layers in Healthy Eyes. 健康眼视神经头、视网膜神经纤维层和神经节细胞层扫描源光学相干断层扫描的一致性。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1409
Angelica M Prada, Alejandro Tello, Carlos M Rangel, Virgilio Galvis, Gustavo Espinoza

Aim and background: Precision of optical coherence tomography (OCT) measurements of the optic nerve head (ONH), retinal nerve fiber layer (RNFL), and macular ganglion cell layer (GCL) is essential for the diagnosis and monitoring of glaucoma. The purpose of this research was to evaluate the repeatability and reproducibility of retinal and ONH parameters measured with two identical swept-source optical coherence devices.

Methods: A cross-sectional study was conducted. A total of 30 eyes of 15 healthy subjects were included. Two technicians performed four OCT-wide protocol scans in the same visit using two identical Triton swept-source OCT (DRI-OCT) instruments. The interdevice and interobserver reproducibility and the repeatability of both instruments for all ONH, RNFL, and macular GCL parameters were evaluated by the intraclass correlation coefficient (ICC). Additionally, Bland-Altman test analysis was used for repeatability and reproducibility measurements.

Results: Intraclass correlation coefficient (ICCs) of the ONH, RNFL, and GCL measurements were excellent for repeatability and interdevice reproducibility (>0.9). Interobserver reproducibility was good for all parameters except for RNFL clock hour 11 (ICC = 0.72). The variability of the average RNFL was from -4.103 to 4.97 µm, with a mean percentage of the difference (PD) of 0.37 ± 2.03%. Among GCL parameters, the greatest variability was found in the inferior sector (PD = -0.88 ± 5.39%, limits of agreement (LoA) = -8.345-7.078 μm).

Conclusion: Using two identical swept-source OCT instruments for the evaluation of the structural parameters of the ONH, RNFL, and macular GCL showed high repeatability and reproducibility. This allows the clinician to make a therapeutic decision based on OCT findings coupled with the clinical evaluation of the patient. When evaluating RNFL clock hours measurements, interobserver reproducibility might decrease.

Clinical significance: The understanding of measurement variability while using different devices and the impact of the observer capturing the images, is clinically relevant.

How to cite this article: Prada AM, Tello A, Rangel CM, et al. Agreement between Two Swept-source Optical Coherence Tomography: Optic Nerve Head, Retinal Nerve Fiber Layer and Ganglion Cell Layers in Healthy Eyes. J Curr Glaucoma Pract 2023;17(2):85-90.

目的和背景:光学相干断层扫描(OCT)对视神经头(ONH)、视网膜神经纤维层(RNFL)和黄斑神经节细胞层(GCL)的精确测量对于青光眼的诊断和监测至关重要。本研究的目的是评估用两个相同的扫频源光学相干设备测量的视网膜和ONH参数的可重复性和再现性。方法:采用横断面研究。共纳入15名健康受试者的30只眼睛。两名技术人员在同一次访问中使用两台相同的Triton扫描源OCT(DRI-OCT)仪器进行了四次全OCT方案扫描。通过组内相关系数(ICC)评估两种仪器对所有ONH、RNFL和黄斑GCL参数的设备间和观察者间再现性以及可重复性。此外,Bland-Altman测试分析用于重复性和再现性测量。结果:ONH、RNFL和GCL测量的组内相关系数(ICCs)具有良好的重复性和设备间再现性(>0.9)。除RNFL时钟小时11(ICC=0.72)外,所有参数的观察者间再现性均良好。平均RNFL的变异性为-4.103至4.97µm,平均差异百分比(PD)为0.37±2.03%。在GCL参数中,下段变异性最大(PD=-0.88±5.39%,一致性极限(LoA)=-8.345-7.078μm)。结论:使用两个相同的扫描源OCT仪器评估ONH、RNFL、,黄斑GCL具有较高的重复性和再现性。这使得临床医生能够根据OCT的发现以及对患者的临床评估做出治疗决定。当评估RNFL时钟小时测量值时,观察者之间的再现性可能会降低。临床意义:在使用不同设备时对测量可变性的理解以及观察者捕捉图像的影响与临床相关。如何引用这篇文章:Prada AM,Tello A,Rangel CM等。两扫描源光学相干断层扫描之间的协议:健康眼睛中的视神经头、视网膜神经纤维层和神经节细胞层。青光眼临床杂志2023;17(2):85-90。
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引用次数: 0
Use of Ocular Response Analyzer Output Data in the Management of Low Intraocular Pressure after Glaucoma Filtration Surgery. 眼反应分析仪输出数据在青光眼滤过术后低眼压管理中的应用。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1402
Sarah Dawson, Abhijit Mohite

Aim: To highlight potential benefits of using Reichert's ocular response analyzer (ORA) for intraocular pressure (IOP) measurement following glaucoma filtering surgery (GFS), especially in cases of low IOP.

Background: Goldmann applanation tonometry (GAT) is widely regarded as the gold standard of IOP measurement in clinical practice. The ORA also calculates corneal biomechanics, which is used in the calculation of the cornea-compensated IOP (IOPcc).1 This useful, previously unknown information can be used to guide management in challenging clinical cases.

Case description: A 78-year-old lady underwent right trabeculectomy with mitomycin C. During the first 9 months postoperatively, IOP's when measured with GAT, were found to be low (ranging between 2 mm Hg and 5 mm Hg). The patient displayed no clinical features of hypotony and visual acuity remained stable throughout. IOP was also measured with Reichert's ORA, which gives readings for corneal hysteresis (CH), corneal resistance factor and corneal corrected IOP. IOPcc measurements obtained with ORA were consistently higher, ranging from 6.7 mm Hg to 9.3 mm Hg and were more in keeping with the clinical features of the case.

Conclusion: This case highlights the possibility that GAT can underestimate the true IOP in eyes with low IOP following GFS, as it does not account for corneal biomechanical properties.

Clinical significance: Ocular response analyzer (ORA)-measured IOPcc may be a useful adjunct in reassuring surgeons to manage postoperative numerical hypotony conservatively in the absence of any clinical signs of hypotony.

How to cite this article: Dawson S, Mohite A. Use of Ocular Response Analyzer Output Data in the Management of Low Intraocular Pressure after Glaucoma Filtration Surgery. J Curr Glaucoma Pract 2023;17(2):104-105.

目的:强调使用Reichert的眼反应分析仪(ORA)测量青光眼滤过术后眼压(IOP)的潜在益处,特别是在低眼压的情况下。背景:Goldmann压平眼压计(GAT)被广泛认为是临床上测量眼压的金标准。ORA还计算角膜生物力学,用于计算角膜补偿IOP(IOPC)。1这些有用的、以前未知的信息可用于指导具有挑战性的临床病例的管理。病例描述:一位78岁的女士用丝裂霉素C进行了右小梁切除术。术后前9个月,用GAT测量的IOP较低(范围在2毫米汞柱至5毫米汞柱之间)。患者没有表现出低眼压的临床特征,视力始终保持稳定。还使用Reichert的ORA测量眼压,该ORA提供角膜滞后(CH)、角膜阻力因子和角膜校正眼压的读数。ORA获得的IOPcc测量值始终较高,范围从6.7毫米汞柱到9.3毫米汞柱,更符合病例的临床特征。结论:该病例强调了GAT可能低估了GFS后低眼压眼的真实眼压,因为它没有考虑角膜生物力学特性。临床意义:眼部反应分析仪(ORA)测量的IOPcc可能是一种有用的辅助手段,可以让外科医生在没有任何临床低眼压迹象的情况下,保守地管理术后数字低眼压。如何引用这篇文章:Dawson S,Mohite A.在青光眼滤过术后低眼压管理中使用眼部反应分析仪输出数据。青光眼临床杂志2023;17(2):104-105。
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引用次数: 0
Prevalence of Glu323Lys Mutation of the TIGR/MYOC Gene and Risk Factors amongst Primary Open-angle Glaucoma Patients in Ouagadougou, Burkina Faso. 布基纳法索瓦加杜古原发性开角型青光眼患者TIGR/MYOC基因Glu323Lys突变的患病率和危险因素。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1403
Lassina Traoré, Jérôme Sanou, Bélélé S Bakyono, Abdou A Zoure, Théodora M Zohoncon, Hermann K Sombié, Albert T Yonli, Guertrude Meda-Hien, Ezechiel B Tibiri, Florencia W Djigma, Jacques Simpore

Aim: Glaucoma is a group of degenerative diseases of the optic nerve whose predisposing factors may be genetic. The objective of this study was to estimate the frequency of the Glu323Lys mutation as a genetic risk factor for glaucoma.

Materials and methods: A cross-sectional study over 6 months from October 2020 to March 2021 in Ouagadougou, Burkina Faso. A total of 89 samples of patients with primary open-angle glaucoma (POAG) were collected. The frequency of the Glu323Lys mutation of the myocilin, trabecular meshwork inducible glucocorticoid response (TIGR/MYOC) gene by polymerase chain reaction (PCR)-restriction fragment length polymorphism.

Results: In glaucoma patients, only homozygous nonmutated guanine-guanine (GG) and heterozygous mutated adenine-guanine (AG) genotypes were found in 96.63 and 3.37% of cases, respectively. Around 69.66% of patients had a family history of glaucoma, 28.09% had a history of hypertension, and 7.86% had a history of diabetes.

Conclusion: The frequency of the Glu323Lys mutation of the TIGR/MYOC gene was 3.37% in the glaucoma population in Ouagadougou. A case-control study is necessary to know the contribution of the Glu323Lys mutation as a genetic risk factor for glaucoma in our study population.

Clinical significance: This study constituted the beginning of genetic investigations of glaucoma in our context and showed a low Glu323Lys mutation.

How to cite this article: Traoré L, Sanou J, Bakyono BS, et al. Prevalence of Glu323Lys Mutation of the TIGR/MYOC Gene and Risk Factors amongst Primary Open-angle Glaucoma Patients in Ouagadougou, Burkina Faso. J Curr Glaucoma Pract 2023;17(2):79-84.

目的:青光眼是一组视神经退行性疾病,其诱发因素可能是遗传性的。本研究的目的是估计Glu323Lys突变作为青光眼遗传危险因素的频率。材料和方法:2020年10月至2021年3月在布基纳法索瓦加杜古进行的为期6个月的横断面研究。共收集了89例原发性开角型青光眼(POAG)患者的样本。应用聚合酶链式反应(PCR)-限制性片段长度多态性检测肌球蛋白、小梁网诱导型糖皮质激素反应(TIGR/MYOC)基因Glu323Lys突变频率。结果:在青光眼患者中,分别有96.63%和3.37%的病例发现纯合的非突变鸟嘌呤(GG)和杂合的突变腺嘌呤-鸟嘌呤(AG)基因型。约69.66%的患者有青光眼家族史,28.09%有高血压史,7.86%有糖尿病史。结论:瓦加杜古青光眼患者TIGR/MYOC基因Glu323Lys突变频率为3.37%。有必要进行病例对照研究,以了解Glu323Lys突变作为我们研究人群中青光眼的遗传危险因素的作用。临床意义:这项研究是我们对青光眼基因研究的开始,并显示了低Glu323Lys突变。如何引用这篇文章:TraoréL,Sanou J,Bakyono BS等。布基纳法索瓦加杜古原发性开角型青光眼患者TIGR/MYOC基因Glu323Lys突变的患病率和危险因素。青光眼临床杂志2023;17(2):79-84。
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引用次数: 0
Goldmann Applanation Tonometry: Comparison of Intraocular Pressure Values Obtained with Disposable Tip and Conventional Applanation Prism in the Population without Clinical Signs of Glaucoma. Goldmann应用眼压计:在没有青光眼临床症状的人群中,使用一次性尖端和常规应用棱镜获得的眼压值的比较。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1401
Pedro Henrique Alves Soares, Rafael de Oliveira Santos, Celso Ribeiro Angelo De Menezes Filho, Sebastião Pimenta Moraes Neto, João Antonio Prata Junior

Aim: Comparing intraocular pressure (IOP) measurements using Goldmann applanation prism and TonoSafe® in the population without signs of glaucoma.

Material and methods: Patients with no ocular pathologies, except ametropia (until ± 4 D) or IOP of <30 mm Hg without signs of glaucoma by optic disc structural analysis by fundus biomicroscopy. The IOP was measured sequentially using the traditional cone and the TonoSafe®, according to a randomization list to determine which device would be used first. The measurements from the right and left eyes were compared separately. Since there was no statistical difference, both eyes were considered in this study.

Results: A total of 385 eyes of 194 patients with a mean age of 66.4 ± 11.2 years old were included. The mean IOP with conventional prism was 14.2 ± 3.6 and 14.3 ± 3.6 mm Hg with TonoSafe®. Differences were not statistically significant by the Wilcoxon test (p = 0.3). The median was 14.0 mm Hg for both groups. The mean difference between measurements was 0.04 mm Hg, with the median equal to zero. There was no statistical difference in IOP readings according to which device was the first measurement.

Conclusion: No statistical difference was found in IOP was measured with conventional prism or TonoSafe® in the population without signs of glaucoma.

Clinical significance: The data provided by our study support the efficacy and safety of the disposable tonometer compared to the Goldman tonometer in measuring IOP in patients without glaucoma.

How to cite this article: Soares PHA, Santos RDO, Filho CRADM, et al. Goldmann Applanation Tonometry: Comparison of Intraocular Pressure Values Obtained with Disposable Tip and Conventional Applanation Prism in the Population without Clinical Signs of Glaucoma. J Curr Glaucoma Pract 2023;17(2):75-78.

目的:比较使用Goldmann压平棱镜和TonoSafe®在没有青光眼迹象的人群中测量的眼压。材料和方法:除屈光不正(至±4D)或IOP外,无眼部疾病的患者。结果:194例患者中,共385眼,平均年龄66.4±11.2岁。传统棱镜的平均眼压为14.2±3.6毫米汞柱,而TonoSafe®的平均眼压则为14.3±3.6毫米Hg。通过Wilcoxon检验,差异无统计学意义(p=0.3)。两组的中位数均为14.0毫米汞柱。测量值之间的平均差值为0.04毫米汞柱,中位数等于零。根据哪种设备是第一次测量,IOP读数没有统计学差异。结论:在没有青光眼迹象的人群中,使用传统棱镜或TonoSafe®测量眼压没有统计学差异。临床意义:我们的研究提供的数据支持一次性眼压计与Goldman眼压计相比在测量无青光眼患者眼压方面的有效性和安全性。如何引用这篇文章:Soares PHA,Santos RDO,Filho CRADM,et al.Goldmann Applanation Tonometry:在没有青光眼临床症状的人群中,使用一次性尖端和常规Applanation棱镜获得的眼压值的比较。青光眼临床杂志2023;17(2):75-78。
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引用次数: 0
Can We Ever Win with a Suprachoroidal Implant? 我们能用脉络膜上植入物获胜吗?
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1410
Leon Au, Shibal Bhartiya

How to cite this article: Au L, Bhartiya S. Can We Ever Win with a Suprachoroidal Implant? J Curr Glaucoma Pract 2023;17(2):55-57.

如何引用这篇文章:Au L,Bhartiya S.我们能用脉络膜上植入物获胜吗?青光眼临床杂志2023;17(2):55-57。
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引用次数: 0
Efficacy and Safety Outcomes of XEN Implantation and Gonioscopy-assisted Transluminal Trabeculotomy for the Management of Advanced Open-angle Glaucoma. XEN植入术和性腺镜辅助经腔小梁切除术治疗晚期开角型青光眼的疗效和安全性结果。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1394
Sunil Ruparelia, Mohammed Sharif, Nir Shoham-Hazon

Aim: Minimally invasive glaucoma surgery (MIGS) is not typically used in patients with advanced-stage glaucoma. This study describes the outcomes and complications of patients with advanced open-angle glaucoma (OAG) who underwent XEN implantation with cataract surgery or gonioscopy-assisted transluminal trabeculotomy (GATT) with cataract surgery.

Methods: This retrospective study identified patients who had undergone XEN implantation or GATT for the management of advanced OAG. Outcomes included surgical success, intraocular pressure (IOP) reduction, number of topical IOP-lowering drops, visual field mean deviation (MD), best-corrected visual acuity (BCVA), and complications. Surgical success was defined as an IOP of <14 mm Hg and a 20% reduction at 12 months without topical IOP-lowering drops (complete success) or with topical IOP-lowering drops (qualified success).

Results: Exactly 70 eyes were enrolled in this study, including 35 who had undergone XEN implantation and 35 who had undergone GATT. The overall surgical success rate was 74.3% (26 of 35) for eyes that underwent XEN implantation and 71.4% (25 of 35) for eyes that underwent GATT. Percent IOP reduction from baseline to 12 months postoperatively was 48% in the XEN cohort and 32% in the GATT cohort. Significant reduction in the use of topical IOP-lowering drops was demonstrated for both XEN (3.26 ± 1.15-1.23 ± 1.28) (p < 0.001) and GATT (2.46 ± 1.12-0.43 ± 0.78) (p < 0.001) cohorts at 12 months postoperatively. The only complication reported was transient hyphema, which occurred in three patients from the XEN group and four from the GATT group, and resolved spontaneously.

Conclusions: Both XEN implantation and GATT may be safe and effective management options when treating patients with advanced OAG. However, larger sample sizes are required to make direct statistical comparisons between these techniques.

Clinical significance: In this study, XEN implantation and GATT combined with cataract surgery were each associated with favorable outcomes in patients with advanced OAG.

How to cite this article: Ruparelia S, Sharif M, Shoham-Hazon N. Efficacy and Safety Outcomes of XEN Implantation and Gonioscopy-assisted Transluminal Trabeculotomy for the Management of Advanced Open-angle Glaucoma. J Curr Glaucoma Pract 2023;17(2):63-67.

目的:微创青光眼手术(MIGS)通常不用于晚期青光眼患者。本研究描述了晚期开角型青光眼(OAG)患者接受XEN植入白内障手术或角镜辅助的腔内小梁切开术(GATT)白内障手术的结果和并发症。方法:本回顾性研究确定了接受XEN植入或GATT治疗晚期OAG的患者。结果包括手术成功率、眼压(IOP)降低、局部IOP下降次数、视野平均偏差(MD)、最佳矫正视力(BCVA)和并发症。手术成功被定义为IOP。结果:本研究共有70只眼睛入选,其中35只接受了XEN植入,35只接受过GATT。接受XEN植入的眼睛的总手术成功率为74.3%(26/35),接受GATT的眼睛的手术成功率则为71.4%(25/35)。XEN队列中从基线到术后12个月的IOP降低百分比为48%,GATT队列中为32%。XEN(3.26±1.15-1.23±1.28)(p<0.001)和GATT(2.46±1.12-0.43±0.78)(p>0.001)两组患者在术后12个月时,局部降眼压滴剂的使用显著减少。据报道,唯一的并发症是短暂性前房积血,XEN组有3名患者,GATT组有4名患者出现,并自行消退。结论:XEN植入和GATT可能是治疗晚期OAG患者安全有效的治疗选择。然而,需要更大的样本量来对这些技术进行直接的统计比较。临床意义:在这项研究中,XEN植入术和GATT联合白内障手术均与晚期OAG患者的良好结果相关。如何引用这篇文章:Ruparelia S,Sharif M,Shoham Hazon N.XEN植入和性腺镜辅助下小梁切除术治疗晚期开角型青光眼的疗效和安全性结果。青光眼临床杂志2023;17(2):63-67。
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引用次数: 0
Evaluation of the Hypertensive Phase after Ahmed Glaucoma Valve Implantation in Neovascular Glaucoma. 新血管性青光眼Ahmed青光眼瓣膜植入术后高血压期的评估。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5005/jp-journals-10078-1406
Sunidhi Ramesh, Wesam S Shalaby, Jonathan S Myers, Leslie J Katz, Natasha N Kolomeyer, Daniel Lee, Reza Razeghinejad, Marlene R Moster, Aakriti G Shukla

Purpose: To compare Ahmed glaucoma valve (AGV) outcomes in neovascular glaucoma (NVG) eyes with and without a postoperative (PO) hypertensive (HTN) phase.

Design: Retrospective study at a single tertiary care center of patients who underwent AGV implantation for NVG treatment with ≥6-month follow-up.

Methods: Main outcome measures included intraocular pressure (IOP), number of glaucoma medications (GM), and failure at month 6 or at the most recent visit. Failure was defined as decline to no light perception (NLP) vision, IOP >21 mm Hg, or need for glaucoma reoperations (all with GM).

Results: A total of 76 eyes of 74 patients (37 without HTN phase and 39 with HTN phase) with a mean follow-up duration of 28.9 ± 25.7 months (p = 0.602) were included. Both groups had similar demographics, visual acuity (VA), number of GM, etiology of NVG, and retina treatment perioperatively. Baseline IOP was significantly higher in the HTN phase group (p = 0.001). Compared to eyes without an HTN phase, HTN phase eyes more commonly met failure criteria at month 6 (33.3 vs 9.1%; p = 0.01), but both groups had a comparable cumulative failure for the entire follow-up period (p = 0.180). At the most recent visit, the number of GM was higher in the HTN phase group (p = 0.019), but IOP was similar in both groups. PO complications were comparable and uncommon in both groups.

Conclusion: Hypertensive (HTN) phase following AGV implantation for NVG is associated with higher preoperative IOP and greater failure by PO month (POM) 6. However, eyes with and without the HTN phase had similar needs for GM and failure rates over the long term.

How to cite this article: Ramesh S, Shalaby WS, Myers JS, et al. Evaluation of the Hypertensive Phase after Ahmed Glaucoma Valve Implantation in Neovascular Glaucoma. J Curr Glaucoma Pract 2023;17(2):91-97.

目的:比较有和无术后(PO)高血压(HTN)期的新生血管性青光眼(NVG)眼的Ahmed青光眼瓣膜(AGV)结果。设计:在单个三级护理中心对接受AGV植入NVG治疗的患者进行回顾性研究,随访时间≥6个月。方法:主要的结果指标包括眼压(IOP)、青光眼药物的数量(GM)以及第6个月或最近一次就诊时的失败。失败被定义为无光感(NLP)视力下降、IOP>21 mm Hg或需要青光眼再次手术(均为GM)。结果:74例患者共76眼(37例无HTN期,39例有HTN期),平均随访时间为28.9±25.7个月(p=0.602)。两组患者在人口统计学、视力(VA)、GM数量、NVG病因和围手术期视网膜治疗方面相似。HTN期组的基线IOP明显更高(p=0.001)。与没有HTN期的眼睛相比,HTN期眼睛在第6个月更常见地达到失败标准(33.3%对9.1%;p=0.01),但两组在整个随访期的累积失败率相当(p=0.0180),但两组的IOP相似。PO并发症在两组中具有可比性且不常见。结论:NVG植入AGV后的高血压(HTN)期与术前IOP升高和PO月(POM)失败率增加有关6。然而,有和没有HTN期的眼睛对GM的需求和长期的失败率相似。如何引用这篇文章:Ramesh S,Shalaby WS,Myers JS,et al.新血管性青光眼Ahmed青光眼瓣膜植入术后高血压期的评估。青光眼临床杂志2023;17(2):91-97。
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引用次数: 0
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Journal of Current Glaucoma Practice
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