Pub Date : 2025-12-10DOI: 10.1177/24741264251400694
Jonathan N Levenson, Carla G Dias, Jaffer Shah, Kyle D Kovacs
Purpose: Diabetes and its microvascular complications have significant social and economic impact, and targeted prevention strategies are paramount. Wearable technology may play an important role in personalized diabetes management. This study assesses the association between physical activity measured by wearable activity trackers and the presence of diabetic retinopathy (DR) in individuals with diabetes. Methods: Retrospective chart review of accelerometer data obtained on personal fitness (Fitbit) trackers from adults with diabetes who had >1 month of linked activity tracking data registered in the All of Us Research Program Registered Tier dataset (version 7). Binary logistic regression models were used to assess adjusted associations between presence of DR and physical activity measures of mean number of daily steps and mean number of daily minutes spent on moderate-to-vigorous activities. Results: Of the 668 participants, 63% were female and 37% were male, 80% were non-Hispanic White, and 42.5% had a history of smoking. Mean age was 64.3 years (range, 25-91 years). A unit increase of 1000 daily steps walked by participants was significantly associated with a 45% reduction in the odds of having DR (odds ratio [OR] 0.55, 95% CI 0.33-0.91). A 1-minute unit increase in the mean number of daily minutes spent on moderate-to-vigorous activity was significantly associated with a 24% reduction in the odds of having DR (OR 0.76, 95% CI 0.63-0.92). Conclusions: These findings demonstrate that increased physical activity, as measured through objective quantification of both daily steps and minutes of activity, is inversely correlated with the presence of DR. This may indicate a role for wearable technology in personalizing diabetes management.
目的:糖尿病及其微血管并发症具有重大的社会和经济影响,有针对性的预防策略至关重要。可穿戴技术可能在个性化糖尿病管理中发挥重要作用。本研究评估了可穿戴活动追踪器测量的身体活动与糖尿病患者糖尿病视网膜病变(DR)之间的关系。方法:对个人健身(Fitbit)追踪器上获得的加速度计数据进行回顾性图表回顾,这些数据来自糖尿病成年人,他们在All of Us Research Program注册Tier数据集(版本7)中注册了100个月的相关活动跟踪数据。使用二元逻辑回归模型来评估DR的存在与平均每日步数和平均每天花在中等到高强度活动上的分钟数的体力活动测量之间的调整相关性。结果:在668名参与者中,63%为女性,37%为男性,80%为非西班牙裔白人,42.5%有吸烟史。平均年龄64.3岁(25-91岁)。参与者每天步行1000步与DR的几率降低45%显著相关(比值比[OR] 0.55, 95% CI 0.33-0.91)。中度至剧烈运动的平均每日分钟数每增加1分钟,发生DR的几率就会降低24% (OR 0.76, 95% CI 0.63-0.92)。结论:这些研究结果表明,通过对每日活动步数和分钟数的客观量化测量,增加的身体活动与dr的存在呈负相关。这可能表明可穿戴技术在个性化糖尿病管理中的作用。
{"title":"Association of Accelerometer Measured Physical Activity with Presence of Diabetic Retinopathy.","authors":"Jonathan N Levenson, Carla G Dias, Jaffer Shah, Kyle D Kovacs","doi":"10.1177/24741264251400694","DOIUrl":"10.1177/24741264251400694","url":null,"abstract":"<p><p><b>Purpose:</b> Diabetes and its microvascular complications have significant social and economic impact, and targeted prevention strategies are paramount. Wearable technology may play an important role in personalized diabetes management. This study assesses the association between physical activity measured by wearable activity trackers and the presence of diabetic retinopathy (DR) in individuals with diabetes. <b>Methods:</b> Retrospective chart review of accelerometer data obtained on personal fitness (Fitbit) trackers from adults with diabetes who had >1 month of linked activity tracking data registered in the All of Us Research Program Registered Tier dataset (version 7). Binary logistic regression models were used to assess adjusted associations between presence of DR and physical activity measures of mean number of daily steps and mean number of daily minutes spent on moderate-to-vigorous activities. <b>Results:</b> Of the 668 participants, 63% were female and 37% were male, 80% were non-Hispanic White, and 42.5% had a history of smoking. Mean age was 64.3 years (range, 25-91 years). A unit increase of 1000 daily steps walked by participants was significantly associated with a 45% reduction in the odds of having DR (odds ratio [OR] 0.55, 95% CI 0.33-0.91). A 1-minute unit increase in the mean number of daily minutes spent on moderate-to-vigorous activity was significantly associated with a 24% reduction in the odds of having DR (OR 0.76, 95% CI 0.63-0.92). <b>Conclusions:</b> These findings demonstrate that increased physical activity, as measured through objective quantification of both daily steps and minutes of activity, is inversely correlated with the presence of DR. This may indicate a role for wearable technology in personalizing diabetes management.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251400694"},"PeriodicalIF":0.8,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12698458/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145756998","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-29DOI: 10.1177/24741264251396437
Wendy J Li, Maura Di Nicola, Basil K Williams
Purpose: To describe a rare case of spontaneous resolution and subsequent recurrence of subretinal fluid (SRF) associated with circumscribed choroidal hemangioma. Methods: A single case was reviewed. Results: A 67-year-old woman presented with a circumscribed choroidal hemangioma and visually significant SRF. Three weeks after initial presentation and before planned treatment, the patient's vision returned to baseline, and imaging confirmed complete resolution of SRF. She was observed without intervention. Two months later, the SRF recurred, and the patient was successfully treated with photodynamic therapy, achieving complete resolution. Conclusions: Spontaneous resolution of SRF secondary to circumscribed choroidal hemangioma can occur, albeit rarely. At the time of treatment planning, reassessment of symptoms and repeat imaging may help identify such spontaneous improvement. If resolution occurs, patients should be closely followed up for the possibility of fluid recurrence.
{"title":"Temporary Spontaneous Resolution of Subretinal Fluid in a Circumscribed Choroidal Hemangioma.","authors":"Wendy J Li, Maura Di Nicola, Basil K Williams","doi":"10.1177/24741264251396437","DOIUrl":"10.1177/24741264251396437","url":null,"abstract":"<p><p><b>Purpose:</b> To describe a rare case of spontaneous resolution and subsequent recurrence of subretinal fluid (SRF) associated with circumscribed choroidal hemangioma. <b>Methods:</b> A single case was reviewed. <b>Results:</b> A 67-year-old woman presented with a circumscribed choroidal hemangioma and visually significant SRF. Three weeks after initial presentation and before planned treatment, the patient's vision returned to baseline, and imaging confirmed complete resolution of SRF. She was observed without intervention. Two months later, the SRF recurred, and the patient was successfully treated with photodynamic therapy, achieving complete resolution. <b>Conclusions:</b> Spontaneous resolution of SRF secondary to circumscribed choroidal hemangioma can occur, albeit rarely. At the time of treatment planning, reassessment of symptoms and repeat imaging may help identify such spontaneous improvement. If resolution occurs, patients should be closely followed up for the possibility of fluid recurrence.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251396437"},"PeriodicalIF":0.8,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12665586/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145661411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-26DOI: 10.1177/24741264251393958
Niranjana Kesavamoorthy, Maria Sibug Saber, Erin Su, Jason A Junge, Narsing Rao, Hossein Ameri
Purpose: Stargardt disease is an inherited form of retinal degeneration characterized by early-onset central vision loss. This report describes the long-term retinal histologic characteristics of a patient with Stargardt disease after human embryonic stem cell-derived retinal pigment epithelium (hESC-RPE) transplantation. Methods: Eyes were obtained postmortem from an 80-year-old legally blind male patient with Stargardt disease. The patient had previously undergone hESC-RPE transplantation of his left eye, and the right eye (untransplanted) served as a control. Fluorescence lifetime imaging microscopy was used to study retinal structure and metabolic activity. Staining of the retina for lipofuscin was performed using the Armed Forces Institute of Pathology method. Results: Metabolic analysis showed that the macular area had more oxidative phosphorylation relative to the mid-peripheral retina, in both the transplanted and untransplanted eye. Melanin-laden RPE cells were detected in the transplanted eye, which correlated with a pigment band present on fundus images post-hESC-RPE transplantation. Conclusions: This case description illustrates the long-term survival of subretinal hESC-RPE cells post-transplantation in a patient with Stargardt disease.
{"title":"Postmortem Retinal Structural and Metabolic Analysis After Human Embryonic Stem Cell-derived Retinal Pigment Epithelium Transplantation in a Patient With Stargardt Disease.","authors":"Niranjana Kesavamoorthy, Maria Sibug Saber, Erin Su, Jason A Junge, Narsing Rao, Hossein Ameri","doi":"10.1177/24741264251393958","DOIUrl":"10.1177/24741264251393958","url":null,"abstract":"<p><p><b>Purpose:</b> Stargardt disease is an inherited form of retinal degeneration characterized by early-onset central vision loss. This report describes the long-term retinal histologic characteristics of a patient with Stargardt disease after human embryonic stem cell-derived retinal pigment epithelium (hESC-RPE) transplantation. <b>Methods:</b> Eyes were obtained postmortem from an 80-year-old legally blind male patient with Stargardt disease. The patient had previously undergone hESC-RPE transplantation of his left eye, and the right eye (untransplanted) served as a control. Fluorescence lifetime imaging microscopy was used to study retinal structure and metabolic activity. Staining of the retina for lipofuscin was performed using the Armed Forces Institute of Pathology method. <b>Results:</b> Metabolic analysis showed that the macular area had more oxidative phosphorylation relative to the mid-peripheral retina, in both the transplanted and untransplanted eye. Melanin-laden RPE cells were detected in the transplanted eye, which correlated with a pigment band present on fundus images post-hESC-RPE transplantation. <b>Conclusions:</b> This case description illustrates the long-term survival of subretinal hESC-RPE cells post-transplantation in a patient with Stargardt disease.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251393958"},"PeriodicalIF":0.8,"publicationDate":"2025-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12657203/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145648867","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-24DOI: 10.1177/24741264251393968
Landon J Rohowetz, Matthew J McSoley, Humberto Salazar, Jesse D Sengillo, Julia Hudson, Nicolas A Yannuzzi, Audina M Berrocal, Thomas A Albini, Harry W Flynn
Purpose: To report the clinical features and outcomes in eyes with fishing-related ocular injury. Methods: We performed a retrospective, consecutive case series of all eyes evaluated at Bascom Palmer Eye Institute between January 1, 2013, and January 1, 2023, with a history of fishing-related ocular trauma. Results: The study cohort included 75 eyes. The cause of injury included contact with a fishhook in 27 eyes (37%), sinker in 26 (35%), and fishing pole in 7 (10%). Open-globe injury occurred in 17 (23%) eyes, and endophthalmitis was suspected preoperatively or intraoperatively in 3 (18%) of these eyes. Eyes with fishhook injuries were more likely to sustain an open-globe injury (13/24 [54%]) compared with those with non-fishhook injuries (4/44 [9%]; P < .001). Eyes with open-globe injury had worse mean best-corrected visual acuity during their last follow-up examination (1.4 logMAR [Snellen equivalent 20/501]) compared with eyes without open-globe injury (0.46 logMAR [Snellen equivalent 20/58]; P = .002). When documented, 5 (42%) of 12 eyes with open-globe injuries received intraoperative intravitreal antibiotics, while 5 (42%) eyes with injuries localized to the anterior segment received intracameral antibiotics. Eleven (92%) of 12 patients with open-globe injury underwent repair on an outpatient basis and were discharged on the day of surgery without intravenous antibiotics. There were no newly diagnosed cases of endophthalmitis in the postoperative period. Conclusions: Poor visual outcomes occurred most commonly after open-globe injuries caused by fishhooks. Most eyes with open-globe injuries received intracameral or intravitreal antibiotics at the time of surgical treatment, without postoperative inpatient admission or intravenous antibiotics, and no cases of postoperative endophthalmitis were observed.
{"title":"Clinical Features and Outcomes of Fishing-Related Ocular Injuries.","authors":"Landon J Rohowetz, Matthew J McSoley, Humberto Salazar, Jesse D Sengillo, Julia Hudson, Nicolas A Yannuzzi, Audina M Berrocal, Thomas A Albini, Harry W Flynn","doi":"10.1177/24741264251393968","DOIUrl":"https://doi.org/10.1177/24741264251393968","url":null,"abstract":"<p><p><b>Purpose:</b> To report the clinical features and outcomes in eyes with fishing-related ocular injury. <b>Methods:</b> We performed a retrospective, consecutive case series of all eyes evaluated at Bascom Palmer Eye Institute between January 1, 2013, and January 1, 2023, with a history of fishing-related ocular trauma. <b>Results:</b> The study cohort included 75 eyes. The cause of injury included contact with a fishhook in 27 eyes (37%), sinker in 26 (35%), and fishing pole in 7 (10%). Open-globe injury occurred in 17 (23%) eyes, and endophthalmitis was suspected preoperatively or intraoperatively in 3 (18%) of these eyes. Eyes with fishhook injuries were more likely to sustain an open-globe injury (13/24 [54%]) compared with those with non-fishhook injuries (4/44 [9%]; <i>P</i> < .001). Eyes with open-globe injury had worse mean best-corrected visual acuity during their last follow-up examination (1.4 logMAR [Snellen equivalent 20/501]) compared with eyes without open-globe injury (0.46 logMAR [Snellen equivalent 20/58]; <i>P</i> = .002). When documented, 5 (42%) of 12 eyes with open-globe injuries received intraoperative intravitreal antibiotics, while 5 (42%) eyes with injuries localized to the anterior segment received intracameral antibiotics. Eleven (92%) of 12 patients with open-globe injury underwent repair on an outpatient basis and were discharged on the day of surgery without intravenous antibiotics. There were no newly diagnosed cases of endophthalmitis in the postoperative period. <b>Conclusions:</b> Poor visual outcomes occurred most commonly after open-globe injuries caused by fishhooks. Most eyes with open-globe injuries received intracameral or intravitreal antibiotics at the time of surgical treatment, without postoperative inpatient admission or intravenous antibiotics, and no cases of postoperative endophthalmitis were observed.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251393968"},"PeriodicalIF":0.8,"publicationDate":"2025-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12643895/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145635270","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-21DOI: 10.1177/24741264251390000
Danny Varghese, Giovanni Campagna, Kevin Elwood, Kaitlyn Timmons, Chirag Jhaveri, Saradha Chexal, Brian Berger, Gowtham Jonna
Purpose: Central serous chorioretinopathy (CSCR) typically resolves spontaneously within 4-6 months. Observation is the mainstay of management, but low-fluence photodynamic therapy (PDT) is a well-established treatment. This study investigates risk factors for CSCR recurrence in patients managed with observation versus PDT. Methods: This retrospective case-control study included patients with a first-time CSCR diagnosis between January 2014 and January 2018. All patients were initially managed with 4-6 months of observation and followed up for at least 1 year to monitor CSCR resolution or recurrence, defined as presence of new subretinal fluid after prior resolution. For patients who received PDT following initial observation, an additional year of follow-up post-PDT was required. Demographics, medical history, and retinal imaging findings were analyzed for recurrence associations. Results: Among 90 patients with CSCR, 56 (62.2%) were managed with observation alone, and 34 (37.8%) received PDT. The groups had comparable demographic characteristics. Exogenous hormone use was higher in the PDT group than in the observation group (17.6% vs 3.6%; P = .025). Recurrence occurred in 25 patients (27.8%): 14 (25.0%) in the observation group and 11 (32.4%) in the PDT group (P = .57). Post-PDT recurrence was noted in 5 patients (14.7%). Baseline visual acuity was worse in the PDT group than in the observation group (mean ± SD 0.41 ± 0.33 vs 0.23 ± 0.27 logMAR; P < .001), but baseline central retinal thickness was similar between groups (mean ± SD 403 ± 169 vs 398 ± 166 µm; P = .89). Exogenous hormone use was a significant predictor of CSCR recurrence (odds ratio 5.2, 95% confidence interval 1.1-23.6; P = .034). Conclusions: Patients with exogenous hormone exposure may be at increased risk of recurrent CSCR and may be more likely to receive PDT. Reducing or avoiding exogenous hormones may lower CSCR recurrence risk.
目的:中枢性浆液性脉络膜视网膜病变(CSCR)通常在4-6个月内自行消退。观察是治疗的主要方法,但低通量光动力疗法(PDT)是一种成熟的治疗方法。本研究调查了观察与PDT治疗患者CSCR复发的危险因素。方法:本回顾性病例对照研究纳入了2014年1月至2018年1月期间首次诊断为CSCR的患者。所有患者最初进行了4-6个月的观察,并随访至少1年,以监测CSCR的消退或复发,定义为在先前消退后存在新的视网膜下积液。对于在初始观察后接受PDT的患者,PDT后需要额外的一年随访。分析了人口统计学、病史和视网膜成像结果与复发的关系。结果:90例CSCR患者中,56例(62.2%)采用单纯观察治疗,34例(37.8%)采用PDT治疗。两组人口统计学特征具有可比性。PDT组外源激素使用高于观察组(17.6% vs 3.6%; P = 0.025)。复发25例(27.8%),其中观察组14例(25.0%),PDT组11例(32.4%)(P = 0.57)。pdt术后复发5例(14.7%)。PDT组的基线视力差于观察组(平均±SD 0.41±0.33 vs 0.23±0.27 logMAR; P < .001),但两组之间基线视网膜中央厚度相似(平均±SD 403±169 vs 398±166µm; P = .89)。外源性激素的使用是CSCR复发的显著预测因子(优势比5.2,95%可信区间1.1-23.6;P = 0.034)。结论:外源性激素暴露的患者复发CSCR的风险可能增加,可能更容易接受PDT。减少或避免外源性激素可降低CSCR复发风险。
{"title":"Exogenous Hormone Use as a Predictor of Central Serous Chorioretinopathy Recurrence: A Comparative Analysis of Observation Versus Low-Fluence Photodynamic Therapy.","authors":"Danny Varghese, Giovanni Campagna, Kevin Elwood, Kaitlyn Timmons, Chirag Jhaveri, Saradha Chexal, Brian Berger, Gowtham Jonna","doi":"10.1177/24741264251390000","DOIUrl":"10.1177/24741264251390000","url":null,"abstract":"<p><p><b>Purpose:</b> Central serous chorioretinopathy (CSCR) typically resolves spontaneously within 4-6 months. Observation is the mainstay of management, but low-fluence photodynamic therapy (PDT) is a well-established treatment. This study investigates risk factors for CSCR recurrence in patients managed with observation versus PDT. <b>Methods:</b> This retrospective case-control study included patients with a first-time CSCR diagnosis between January 2014 and January 2018. All patients were initially managed with 4-6 months of observation and followed up for at least 1 year to monitor CSCR resolution or recurrence, defined as presence of new subretinal fluid after prior resolution. For patients who received PDT following initial observation, an additional year of follow-up post-PDT was required. Demographics, medical history, and retinal imaging findings were analyzed for recurrence associations. <b>Results:</b> Among 90 patients with CSCR, 56 (62.2%) were managed with observation alone, and 34 (37.8%) received PDT. The groups had comparable demographic characteristics. Exogenous hormone use was higher in the PDT group than in the observation group (17.6% vs 3.6%; <i>P</i> = .025). Recurrence occurred in 25 patients (27.8%): 14 (25.0%) in the observation group and 11 (32.4%) in the PDT group (<i>P</i> = .57). Post-PDT recurrence was noted in 5 patients (14.7%). Baseline visual acuity was worse in the PDT group than in the observation group (mean ± SD 0.41 ± 0.33 vs 0.23 ± 0.27 logMAR; <i>P</i> < .001), but baseline central retinal thickness was similar between groups (mean ± SD 403 ± 169 vs 398 ± 166 µm; <i>P</i> = .89). Exogenous hormone use was a significant predictor of CSCR recurrence (odds ratio 5.2, 95% confidence interval 1.1-23.6; <i>P</i> = .034). <b>Conclusions:</b> Patients with exogenous hormone exposure may be at increased risk of recurrent CSCR and may be more likely to receive PDT. Reducing or avoiding exogenous hormones may lower CSCR recurrence risk.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251390000"},"PeriodicalIF":0.8,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12638235/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145588188","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-21DOI: 10.1177/24741264251388105
Russel H Dinh, Howard Zhang, Rebecca Pan, Jose Rico-Jimenez, Shravika Lam, Xiangyu Ji, Margaret Comer, Farozan Noori, Sean Berkowitz, Mohsin H Ali, Qingxia Chen, Yuankai K Tao, Avni P Finn
Purpose: To investigate the relationship between preoperative volumetric optical coherence tomography (OCT) features of full-thickness macular holes (FTMHs), including intraretinal cysts and 3-dimensional hole symmetry, and both visual acuity outcomes and surgical prognosis in patients with FTMH. Methods: This multicenter, retrospective cohort study assessed patients with FTMH who underwent pars plana vitrectomy from 2017 to 2022. In-depth manual segmentation of each pre- and postoperative OCT volumetric scan (60 B-scans per volume) was performed by 3 graders. Correlations between preoperative cystoid volume and FTMH symmetry and preoperative visual acuity, preoperative minimum linear diameter (MLD), improvement in visual acuity at 6 months postsurgery, and FTMH closure rate postsurgery were assessed using linear regression models, adjusted for baseline lens status, duration of symptoms, and MLD. Results: A total of 69 eyes of 69 patients with FTMH were included. Mean (± SD) visual acuity was 0.69 ± 0.44 logMAR (Snellen 20/98) before surgery, and improved to 0.39 ± 0.23 logMAR at 6 months after surgery (Snellen 20/49). FTMH closure after a single surgery was 96%. Greater cystoid volume before surgery was associated with larger FTMH MLD (P < .001), worse preoperative visual acuity (P = .003), and greater visual acuity improvement at 6 months after surgery (P = .02). Greater hole asymmetry before surgery was associated with smaller MLD (P = .04), but not associated with preoperative visual acuity (P = .74) or postoperative FTMH closure rates (P = .19). Conclusions: This study on OCT volumetric measurements showed that intraretinal cystoid volume correlated with larger macular holes and greater visual acuity improvement while smaller macular holes tended to be more asymmetric.
{"title":"Volumetric Optical Coherence Tomography Analysis of Visual and Surgical Outcomes in Patients With Full-Thickness Macular Hole.","authors":"Russel H Dinh, Howard Zhang, Rebecca Pan, Jose Rico-Jimenez, Shravika Lam, Xiangyu Ji, Margaret Comer, Farozan Noori, Sean Berkowitz, Mohsin H Ali, Qingxia Chen, Yuankai K Tao, Avni P Finn","doi":"10.1177/24741264251388105","DOIUrl":"10.1177/24741264251388105","url":null,"abstract":"<p><p><b>Purpose:</b> To investigate the relationship between preoperative volumetric optical coherence tomography (OCT) features of full-thickness macular holes (FTMHs), including intraretinal cysts and 3-dimensional hole symmetry, and both visual acuity outcomes and surgical prognosis in patients with FTMH. <b>Methods</b>: This multicenter, retrospective cohort study assessed patients with FTMH who underwent pars plana vitrectomy from 2017 to 2022. In-depth manual segmentation of each pre- and postoperative OCT volumetric scan (60 B-scans per volume) was performed by 3 graders. Correlations between preoperative cystoid volume and FTMH symmetry and preoperative visual acuity, preoperative minimum linear diameter (MLD), improvement in visual acuity at 6 months postsurgery, and FTMH closure rate postsurgery were assessed using linear regression models, adjusted for baseline lens status, duration of symptoms, and MLD. <b>Results:</b> A total of 69 eyes of 69 patients with FTMH were included. Mean (± SD) visual acuity was 0.69 ± 0.44 logMAR (Snellen 20/98) before surgery, and improved to 0.39 ± 0.23 logMAR at 6 months after surgery (Snellen 20/49). FTMH closure after a single surgery was 96%. Greater cystoid volume before surgery was associated with larger FTMH MLD (<i>P</i> < .001), worse preoperative visual acuity (<i>P</i> = .003), and greater visual acuity improvement at 6 months after surgery (<i>P</i> = .02). Greater hole asymmetry before surgery was associated with smaller MLD (<i>P</i> = .04), but not associated with preoperative visual acuity (<i>P</i> = .74) or postoperative FTMH closure rates (<i>P</i> = .19). <b>Conclusions:</b> This study on OCT volumetric measurements showed that intraretinal cystoid volume correlated with larger macular holes and greater visual acuity improvement while smaller macular holes tended to be more asymmetric.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251388105"},"PeriodicalIF":0.8,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12638230/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145587670","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-17DOI: 10.1177/24741264251383397
Irina Sverdlichenko, Safwan Tayeb, Miguel Cruz Pimentel, Charbel Wahab, Anarsaikhan Narmandakh, Peng Yan
Purpose: To present a sequential surgical approach for macular hole (MH)-associated retinal detachment using preoperative pneumatic retinopexy followed by pars plana vitrectomy, and to review the published literature on surgical strategies for this condition. Methods: A retrospective chart review was conducted for 2 patients who developed MH-associated retinal detachment. For the literature review, PubMed was used as the primary reference database to identify relevant studies. Results: Two patients with MH-associated retinal detachment were described. Both underwent pneumatic retinopexy to treat the retinal detachment, followed by pars plana vitrectomy with amniotic membrane plug or internal limiting membrane (ILM) peel, achieving successful MH closure. The literature review included 502 cases of MH-associated retinal detachment. Of these, 65% (333/502) were female and 90% were myopic. Fewer than 2% of patients underwent sequential repair of the retinal detachment and MH. In 7% of cases, laser photocoagulation was performed around the MH following vitrectomy. More than half the eyes underwent conventional ILM peel, with other techniques including ILM peel with insertion into the MH, ILM inverted and draped over or inserted into the MH, or amniotic membrane plug. The overall MH closure rate was 64%, and the initial retinal reattachment rate was 95%. Conclusions: We reviewed 2 cases that underwent a sequential surgical approach for the treatment of MH-associated retinal detachment, converting an emergent retinal detachment into an elective MH case and enhancing the likelihood of hole closure.
{"title":"Sequential Management of Macular Hole-Associated Rhegmatogenous Retinal Detachment: Case Report and Literature Review.","authors":"Irina Sverdlichenko, Safwan Tayeb, Miguel Cruz Pimentel, Charbel Wahab, Anarsaikhan Narmandakh, Peng Yan","doi":"10.1177/24741264251383397","DOIUrl":"10.1177/24741264251383397","url":null,"abstract":"<p><p><b>Purpose:</b> To present a sequential surgical approach for macular hole (MH)-associated retinal detachment using preoperative pneumatic retinopexy followed by pars plana vitrectomy, and to review the published literature on surgical strategies for this condition. <b>Methods:</b> A retrospective chart review was conducted for 2 patients who developed MH-associated retinal detachment. For the literature review, PubMed was used as the primary reference database to identify relevant studies. <b>Results:</b> Two patients with MH-associated retinal detachment were described. Both underwent pneumatic retinopexy to treat the retinal detachment, followed by pars plana vitrectomy with amniotic membrane plug or internal limiting membrane (ILM) peel, achieving successful MH closure. The literature review included 502 cases of MH-associated retinal detachment. Of these, 65% (333/502) were female and 90% were myopic. Fewer than 2% of patients underwent sequential repair of the retinal detachment and MH. In 7% of cases, laser photocoagulation was performed around the MH following vitrectomy. More than half the eyes underwent conventional ILM peel, with other techniques including ILM peel with insertion into the MH, ILM inverted and draped over or inserted into the MH, or amniotic membrane plug. The overall MH closure rate was 64%, and the initial retinal reattachment rate was 95%. <b>Conclusions:</b> We reviewed 2 cases that underwent a sequential surgical approach for the treatment of MH-associated retinal detachment, converting an emergent retinal detachment into an elective MH case and enhancing the likelihood of hole closure.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251383397"},"PeriodicalIF":0.8,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12623219/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145557163","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-17DOI: 10.1177/24741264251387554
Amira Abbas, Janani Singaravelu, Jordana G Fein
Purpose: To examine the clinical usage and safety profile in real-world patients with age-related macular degeneration (AMD) receiving intravitreal pegcetacoplan (Syfovre) for the treatment of geographic atrophy, and to explore the effect of intravitreal pegcetacoplan on neovascular AMD (nAMD) disease activity. Methods: Information on patient demographics, AMD classification, treatment history, visual acuity, and ocular adverse events were extracted from the electronic medical records. Results: A total of 1069 patients (1451 eyes) initiated intravitreal pegcetacoplan treatment between February 2023 and October 2023 and were followed up until March 2024. Patients received a mean (±SD) 3.3 ± 2.1 injections, and the mean (±SD) follow-up after pegcetacoplan administration was 7.5 ± 2.3 months. The majority of this cohort displayed stable visual acuity throughout treatment, with logMAR values in 821 patients remaining within 0.20 of the initial value. Ocular hypertension occurred in 36 patients (2.5% of eyes). Seventy-six patients (5.2% of eyes) with non-neovascular AMD at treatment initiation subsequently developed nAMD. Five patients (0.34% of eyes) had intraocular inflammation, including 3 with anterior uveitis, 1 with nonocclusive retinal vasculitis, and 1 with hemorrhagic occlusive retinal vasculitis with subsequent poor outcomes. A rate of retinal vasculitis of 0.03% per injection and a rate of overall intraocular inflammation of 0.1% per injection were observed. In total, 460 patients with nAMD received intravitreal pegcetacoplan. Stability of the anti-vascular endothelial growth factor (anti-VEGF) treatment interval was observed in 289 of 396 patients (73%). Preserved or improved visual acuity while undergoing anti-VEGF therapy was noted in 384 of 396 patients (97%). Conclusions: Real-world data on intravitreal pegcetacoplan treatment identifies clinician practice patterns and demonstrates an acceptable safety profile, with complications leading to long-term vision loss following pegcetacoplan administration being rare in this cohort.
{"title":"Real-World Clinical Usage and Safety Profile of Intravitreal Pegcetacoplan in Age-Related Macular Degeneration-Associated Geographic Atrophy.","authors":"Amira Abbas, Janani Singaravelu, Jordana G Fein","doi":"10.1177/24741264251387554","DOIUrl":"10.1177/24741264251387554","url":null,"abstract":"<p><p><b>Purpose:</b> To examine the clinical usage and safety profile in real-world patients with age-related macular degeneration (AMD) receiving intravitreal pegcetacoplan (Syfovre) for the treatment of geographic atrophy, and to explore the effect of intravitreal pegcetacoplan on neovascular AMD (nAMD) disease activity. <b>Methods:</b> Information on patient demographics, AMD classification, treatment history, visual acuity, and ocular adverse events were extracted from the electronic medical records. <b>Results:</b> A total of 1069 patients (1451 eyes) initiated intravitreal pegcetacoplan treatment between February 2023 and October 2023 and were followed up until March 2024. Patients received a mean (±SD) 3.3 ± 2.1 injections, and the mean (±SD) follow-up after pegcetacoplan administration was 7.5 ± 2.3 months. The majority of this cohort displayed stable visual acuity throughout treatment, with logMAR values in 821 patients remaining within 0.20 of the initial value. Ocular hypertension occurred in 36 patients (2.5% of eyes). Seventy-six patients (5.2% of eyes) with non-neovascular AMD at treatment initiation subsequently developed nAMD. Five patients (0.34% of eyes) had intraocular inflammation, including 3 with anterior uveitis, 1 with nonocclusive retinal vasculitis, and 1 with hemorrhagic occlusive retinal vasculitis with subsequent poor outcomes. A rate of retinal vasculitis of 0.03% per injection and a rate of overall intraocular inflammation of 0.1% per injection were observed. In total, 460 patients with nAMD received intravitreal pegcetacoplan. Stability of the anti-vascular endothelial growth factor (anti-VEGF) treatment interval was observed in 289 of 396 patients (73%). Preserved or improved visual acuity while undergoing anti-VEGF therapy was noted in 384 of 396 patients (97%). <b>Conclusions:</b> Real-world data on intravitreal pegcetacoplan treatment identifies clinician practice patterns and demonstrates an acceptable safety profile, with complications leading to long-term vision loss following pegcetacoplan administration being rare in this cohort.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251387554"},"PeriodicalIF":0.8,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12623228/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145557100","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-17DOI: 10.1177/24741264251393951
Jacob Sperber, Sandra Hoyek, Celine Chaaya, Srujay Pandiri, Nimesh A Patel
Purpose: To describe a rare case of late reactivation of retinopathy of prematurity (ROP) in a treatment-naive adult female patient. Methods: Clinical examination and multimodal imaging techniques were used to diagnose the patient and guide the treatment, and genetic saliva testing was performed. Results: We describe a 30-year-old female patient who presented with late reactivation of treatment-naive ROP. She was born prematurely and never received a diagnosis of ROP. She presented at the age of 30 years with new onset of flashes and floaters. Fundoscopic examination was consistent with a diagnosis of ROP, with peripheral avascularity evident in the temporal retina bilaterally, a temporal ridge in the right eye, and focal leakage seen bilaterally on fluorescein angiography. The patient was treated with panretinal photocoagulation laser therapy. Genetic testing demonstrated a heterozygous mutation in ZNF408. Conclusions: Retinopathy associated with prematurity may reactivate in adulthood. This late reactivation may be influenced by a history of untreated ROP or by mutations associated with familial exudative vitreoretinopathy.
{"title":"Late Reactivation of Retinopathy in a Treatment-Naive Female Adult Patient With History of Prematurity and <i>ZNF408</i> Mutation.","authors":"Jacob Sperber, Sandra Hoyek, Celine Chaaya, Srujay Pandiri, Nimesh A Patel","doi":"10.1177/24741264251393951","DOIUrl":"10.1177/24741264251393951","url":null,"abstract":"<p><p><b>Purpose:</b> To describe a rare case of late reactivation of retinopathy of prematurity (ROP) in a treatment-naive adult female patient. <b>Methods:</b> Clinical examination and multimodal imaging techniques were used to diagnose the patient and guide the treatment, and genetic saliva testing was performed. <b>Results:</b> We describe a 30-year-old female patient who presented with late reactivation of treatment-naive ROP. She was born prematurely and never received a diagnosis of ROP. She presented at the age of 30 years with new onset of flashes and floaters. Fundoscopic examination was consistent with a diagnosis of ROP, with peripheral avascularity evident in the temporal retina bilaterally, a temporal ridge in the right eye, and focal leakage seen bilaterally on fluorescein angiography. The patient was treated with panretinal photocoagulation laser therapy. Genetic testing demonstrated a heterozygous mutation in <i>ZNF408</i>. <b>Conclusions:</b> Retinopathy associated with prematurity may reactivate in adulthood. This late reactivation may be influenced by a history of untreated ROP or by mutations associated with familial exudative vitreoretinopathy.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251393951"},"PeriodicalIF":0.8,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12623218/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145557095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-14DOI: 10.1177/24741264251388104
Daniel J Hu, Srujay Pandiri, Celine Chaaya, Emily D Cole, Jacob D Grodsky, Nathan L Scott, Audina M Berrocal, Thamolwan Surakiatchanukul, Judy E Kim, David F Chang, Geoffrey G Emerson, Emily Schehlein, Nimesh A Patel
Purpose: To analyze the financial cost and environmental impact of supplies used during routine intravitreal injection of antivascular endothelial growth factor (anti-VEGF) therapies. Methods: The authors conducted a life cycle assessment of all supplies consumed during intravitreal injections of bevacizumab, aflibercept 2 mg, aflibercept 8 mg, and faricimab at a single academic institution. Data collected included weight, material composition, and retail price of the supplies. Two models, including a process-based approach and a hybrid life cycle assessment featuring an economic input-output model, were used to estimate the environmental impact. Three procedural protocols were analyzed, with an increasing supply consumption from protocol 1 to protocol 3. Results: Excluding the anti-VEGF medication, protocols 1, 2, and 3 cost $12.05, $40.79, and $88.69 and resulted in 3, 11, and 20 kg carbon dioxide equivalents, respectively, using the hybrid life cycle assessment. Extrapolating averaged findings from the hybrid life cycle assessment to the national volume of 15 million injections per year, this procedure may yield 5200 metric tons of waste, approaching $27 billion in material costs and more than 7.2 million metric tons of carbon dioxide equivalents annually. Excluding the anti-VEGF medication pack, this amounts to a procedural supply cost of more than $710 million and an environmental impact of 170 000 metric tons of carbon dioxide equivalents. Limiting supply consumption for all injections to protocol 1 may save more than 800 tons in waste, more than $500 million in cost, and 120 000 metric tons of carbon dioxide equivalents annually. Conclusion: Decreasing supply consumption during intravitreal injections with procedural variations, including the removal of speculums, calipers, or sterile gloves, may yield significant reductions in financial costs and environmental impact.
{"title":"Environmental and Financial Cost Savings With Low-Consumption Intravitreal Injection Techniques.","authors":"Daniel J Hu, Srujay Pandiri, Celine Chaaya, Emily D Cole, Jacob D Grodsky, Nathan L Scott, Audina M Berrocal, Thamolwan Surakiatchanukul, Judy E Kim, David F Chang, Geoffrey G Emerson, Emily Schehlein, Nimesh A Patel","doi":"10.1177/24741264251388104","DOIUrl":"10.1177/24741264251388104","url":null,"abstract":"<p><p><b>Purpose:</b> To analyze the financial cost and environmental impact of supplies used during routine intravitreal injection of antivascular endothelial growth factor (anti-VEGF) therapies. <b>Methods:</b> The authors conducted a life cycle assessment of all supplies consumed during intravitreal injections of bevacizumab, aflibercept 2 mg, aflibercept 8 mg, and faricimab at a single academic institution. Data collected included weight, material composition, and retail price of the supplies. Two models, including a process-based approach and a hybrid life cycle assessment featuring an economic input-output model, were used to estimate the environmental impact. Three procedural protocols were analyzed, with an increasing supply consumption from protocol 1 to protocol 3. <b>Results:</b> Excluding the anti-VEGF medication, protocols 1, 2, and 3 cost $12.05, $40.79, and $88.69 and resulted in 3, 11, and 20 kg carbon dioxide equivalents, respectively, using the hybrid life cycle assessment. Extrapolating averaged findings from the hybrid life cycle assessment to the national volume of 15 million injections per year, this procedure may yield 5200 metric tons of waste, approaching $27 billion in material costs and more than 7.2 million metric tons of carbon dioxide equivalents annually. Excluding the anti-VEGF medication pack, this amounts to a procedural supply cost of more than $710 million and an environmental impact of 170 000 metric tons of carbon dioxide equivalents. Limiting supply consumption for all injections to protocol 1 may save more than 800 tons in waste, more than $500 million in cost, and 120 000 metric tons of carbon dioxide equivalents annually. <b>Conclusion:</b> Decreasing supply consumption during intravitreal injections with procedural variations, including the removal of speculums, calipers, or sterile gloves, may yield significant reductions in financial costs and environmental impact.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251388104"},"PeriodicalIF":0.8,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12618218/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145541016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}