Pub Date : 2025-01-16eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S502181
Achim Fieß, Sandra Gißler, Stephanie Grabitz, Philipp S Wild, Karl J Lackner, Manfred E Beutel, Michael S Urschitz, Oliver Tüscher, Thomas Münzel, Jörn M Schattenberg, Stavros V Konstantinides, Norbert Pfeiffer, Alexander K Schuster
This study investigates the association between self-reported birth weight (BW) and the frequency of cataract and pseudophakia in a large population-based cohort in Germany, as part of the Gutenberg Health Study (GHS). Slit lamp examination and Scheimpflug imaging of 8205 participants, aged 35 to 74, were assessed and signs of cataract or pseudophakia analyzed. The research aimed to explore the correlation between fetal growth restriction and/or prematurity indicated by BW and the frequency of cataract and pseudophakia. In the univariable analysis, cataract was initially associated with low and high BW, but this association disappeared after adjusting for age, sex, examiner and cardiovascular risk factors. No association was found between low BW and pseudophakia or the frequency of cataract surgery within 5 years. The study reveals novel insights from a large population-based study specifically exploring this association.
{"title":"Short Report - Birth Weight is Not Associated With Cataracts or Pseudophakia - Results from the Gutenberg Health Study.","authors":"Achim Fieß, Sandra Gißler, Stephanie Grabitz, Philipp S Wild, Karl J Lackner, Manfred E Beutel, Michael S Urschitz, Oliver Tüscher, Thomas Münzel, Jörn M Schattenberg, Stavros V Konstantinides, Norbert Pfeiffer, Alexander K Schuster","doi":"10.2147/OPTH.S502181","DOIUrl":"https://doi.org/10.2147/OPTH.S502181","url":null,"abstract":"<p><p>This study investigates the association between self-reported birth weight (BW) and the frequency of cataract and pseudophakia in a large population-based cohort in Germany, as part of the Gutenberg Health Study (GHS). Slit lamp examination and Scheimpflug imaging of 8205 participants, aged 35 to 74, were assessed and signs of cataract or pseudophakia analyzed. The research aimed to explore the correlation between fetal growth restriction and/or prematurity indicated by BW and the frequency of cataract and pseudophakia. In the univariable analysis, cataract was initially associated with low and high BW, but this association disappeared after adjusting for age, sex, examiner and cardiovascular risk factors. No association was found between low BW and pseudophakia or the frequency of cataract surgery within 5 years. The study reveals novel insights from a large population-based study specifically exploring this association.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"153-156"},"PeriodicalIF":0.0,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11745053/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143018375","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 : 2025-01-16eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S513309
Anjali Rani, Rakesh Kumar Yadav
{"title":"The Distribution and Influence Factors of Non-Invasive Tear Film Break-Up Time in Children [Letter].","authors":"Anjali Rani, Rakesh Kumar Yadav","doi":"10.2147/OPTH.S513309","DOIUrl":"https://doi.org/10.2147/OPTH.S513309","url":null,"abstract":"","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"151-152"},"PeriodicalIF":0.0,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11745070/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143018378","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 : 2025-01-16eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S498431
Savak Teymoorian, Jasmin Kaur
Purpose: To assess real-world efficacy and safety of standalone travoprost intracameral implant (iDose TR) implantation by a US glaucoma surgeon in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT).
Methods: This non-randomized, retrospective, unmasked, consecutive case series included all cases of standalone iDose TR implantation from a single US glaucoma surgeon since the product's approval by the US Food and Drug Administration (FDA) in December 2023. Patients were pseudophakic, had OAG or OHT, and had undergone prior SLT and/or bimatoprost intracameral implant injection (Durysta). Intraocular pressure (IOP), medications, and adverse events were evaluated through 3 months postoperatively.
Results: All patients (n=65 eyes) were implanted with iDose TR and experienced no intraoperative complications. In the consistent cohort of eyes with 3-month follow-up data (n=54), mean IOP reduced from 19.6±3.8 mmHg preoperatively to 13.1±2.5 mmHg at 3 months (33.2% reduction, p=0.001). The percentage of eyes with IOP ≤15 mmHg increased from 11.1% preoperatively to 83.3% at 3 months (p=0.001). Mean number of IOP-reducing medications reduced from 0.28±0.71 preoperatively to 0.0±0.0 at 3 months (100% reduction; p=0.006). The percentage of eyes off topical medication increased from 85% preoperatively to 100% at 3 months. One eye was reported to have mild iritis at 1-2 weeks postoperatively, and was treated with a topical prednisolone acetate taper. No secondary procedures occurred in any eye.
Conclusion: Standalone implantation of the travoprost intracameral implant yielded statistically and clinically significant IOP and medication reductions through 3 months in eyes with prior SLT and/or bimatoprost intracameral implant injection with favorable safety.
{"title":"Travoprost Intracameral Implant in Eyes with Glaucoma or Ocular Hypertension: Early Short-Term Real-World Outcomes.","authors":"Savak Teymoorian, Jasmin Kaur","doi":"10.2147/OPTH.S498431","DOIUrl":"10.2147/OPTH.S498431","url":null,"abstract":"<p><strong>Purpose: </strong>To assess real-world efficacy and safety of standalone travoprost intracameral implant (iDose TR) implantation by a US glaucoma surgeon in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT).</p><p><strong>Methods: </strong>This non-randomized, retrospective, unmasked, consecutive case series included all cases of standalone iDose TR implantation from a single US glaucoma surgeon since the product's approval by the US Food and Drug Administration (FDA) in December 2023. Patients were pseudophakic, had OAG or OHT, and had undergone prior SLT and/or bimatoprost intracameral implant injection (Durysta). Intraocular pressure (IOP), medications, and adverse events were evaluated through 3 months postoperatively.</p><p><strong>Results: </strong>All patients (n=65 eyes) were implanted with iDose TR and experienced no intraoperative complications. In the consistent cohort of eyes with 3-month follow-up data (n=54), mean IOP reduced from 19.6±3.8 mmHg preoperatively to 13.1±2.5 mmHg at 3 months (33.2% reduction, p=0.001). The percentage of eyes with IOP ≤15 mmHg increased from 11.1% preoperatively to 83.3% at 3 months (p=0.001). Mean number of IOP-reducing medications reduced from 0.28±0.71 preoperatively to 0.0±0.0 at 3 months (100% reduction; p=0.006). The percentage of eyes off topical medication increased from 85% preoperatively to 100% at 3 months. One eye was reported to have mild iritis at 1-2 weeks postoperatively, and was treated with a topical prednisolone acetate taper. No secondary procedures occurred in any eye.</p><p><strong>Conclusion: </strong>Standalone implantation of the travoprost intracameral implant yielded statistically and clinically significant IOP and medication reductions through 3 months in eyes with prior SLT and/or bimatoprost intracameral implant injection with favorable safety.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"157-166"},"PeriodicalIF":0.0,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11747201/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143018380","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 : 2025-01-13eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S503337
Ben Connell, Ben LaHood
Background: The Eyhance Toric intraocular lens (IOL) builds upon the Tecnis Toric platform, initially associated with considerable post-operative rotational instability. Version 2, the Eyhance Toric IOL has been modified to enhance rotational stability. This study evaluates the post-operative rotational stability of the Eyhance Toric IOL compared to the Clareon Toric IOL, recognized for its stable performance.
Methods: Patients undergoing cataract surgery received either the Eyhance or Clareon Toric IOLs. Placement was guided by the Barrett Toric Calculator at baseline (P0). IOL stability, uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), and refractive astigmatism were assessed at 6-24 hours (P1) and 3 weeks to 6 months (P2) post-operatively. IOL rotational measurements were recorded at each interval.
Results: The study included 187 patients (median age: 74 for Clareon, 79 for Eyhance, p = 0.004). No significant differences were found in UDVA, CDVA, or refractive astigmatism at P2. Median rotation from P0 to P1 (3.0 vs 4.0 degrees, p = 0.091) and P0 to P2 (1.0 vs -0.5 degrees, p = 0.482) were not statistically different. However, the Clareon IOL showed less rotation between P1 and P2 (0.0 vs 1.0 degrees, p = 0.049). Absolute rotation from P0 to P1 (4.0 degrees), P1 to P2 (1.0 vs 2.0 degrees, p = 0.064), and P0 to P2 (4.0 vs 3.5 degrees, p = 0.095) were comparable.
Conclusion: The Eyhance Toric IOL demonstrated comparable rotational stability and visual outcomes to the Clareon Toric IOL. Modifications in the Eyhance design have successfully improved its rotational stability, positioning it as a viable alternative to the Clareon Toric IOL in clinical practice.
{"title":"Comparing Rotational Stability of Clareon and Eyhance Toric IOLs in a Real-World Setting.","authors":"Ben Connell, Ben LaHood","doi":"10.2147/OPTH.S503337","DOIUrl":"https://doi.org/10.2147/OPTH.S503337","url":null,"abstract":"<p><strong>Background: </strong>The Eyhance Toric intraocular lens (IOL) builds upon the Tecnis Toric platform, initially associated with considerable post-operative rotational instability. Version 2, the Eyhance Toric IOL has been modified to enhance rotational stability. This study evaluates the post-operative rotational stability of the Eyhance Toric IOL compared to the Clareon Toric IOL, recognized for its stable performance.</p><p><strong>Methods: </strong>Patients undergoing cataract surgery received either the Eyhance or Clareon Toric IOLs. Placement was guided by the Barrett Toric Calculator at baseline (P0). IOL stability, uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), and refractive astigmatism were assessed at 6-24 hours (P1) and 3 weeks to 6 months (P2) post-operatively. IOL rotational measurements were recorded at each interval.</p><p><strong>Results: </strong>The study included 187 patients (median age: 74 for Clareon, 79 for Eyhance, p = 0.004). No significant differences were found in UDVA, CDVA, or refractive astigmatism at P2. Median rotation from P0 to P1 (3.0 vs 4.0 degrees, p = 0.091) and P0 to P2 (1.0 vs -0.5 degrees, p = 0.482) were not statistically different. However, the Clareon IOL showed less rotation between P1 and P2 (0.0 vs 1.0 degrees, p = 0.049). Absolute rotation from P0 to P1 (4.0 degrees), P1 to P2 (1.0 vs 2.0 degrees, p = 0.064), and P0 to P2 (4.0 vs 3.5 degrees, p = 0.095) were comparable.</p><p><strong>Conclusion: </strong>The Eyhance Toric IOL demonstrated comparable rotational stability and visual outcomes to the Clareon Toric IOL. Modifications in the Eyhance design have successfully improved its rotational stability, positioning it as a viable alternative to the Clareon Toric IOL in clinical practice.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"141-149"},"PeriodicalIF":0.0,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11740591/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143018371","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 : 2025-01-11eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S489585
Grace Baldwin, John B Miller
Purpose of review: Intimate partner violence (IPV) is a leading cause of death and disability across the world. We sought to investigate the prevalence and clinical presentation of ocular injuries in IPV.
Recent findings: Literature review revealed 16 published studies that evaluated ocular injuries in IPV, of which the study types included 9 retrospective studies, 2 prospective, 1 review, 1 invited commentary, 2 case reports, and 1 population-based cross-sectional survey. These studies suggest that 45% of IPV incidents involve ocular injury. Various injury types have been described including traumatic cataract, dislocated lens, retinal detachment, intraocular hemorrhage, orbital and zygomaticomaxillary complex fractures, optic nerve avulsion, and open globe injuries. Implementation of IPV screening programs in various clinical settings, including an emergency department evaluating ocular trauma, suggests a positive association with identification of IPV and improving access to resources.
Summary: Within IPV, ocular injuries are a prevalent and important cause of vision loss. Various injuries have been reported affecting nearly every anatomical region of the eye. Routine screening for IPV among patients that present with ocular injuries and evaluating for visual complaints among patients experiencing IPV are both important. Future work focused on prospective studies and evaluation of screening techniques may be impactful.
{"title":"Ocular Injuries and Intimate Partner Violence: A Review of the Literature.","authors":"Grace Baldwin, John B Miller","doi":"10.2147/OPTH.S489585","DOIUrl":"10.2147/OPTH.S489585","url":null,"abstract":"<p><strong>Purpose of review: </strong>Intimate partner violence (IPV) is a leading cause of death and disability across the world. We sought to investigate the prevalence and clinical presentation of ocular injuries in IPV.</p><p><strong>Recent findings: </strong>Literature review revealed 16 published studies that evaluated ocular injuries in IPV, of which the study types included 9 retrospective studies, 2 prospective, 1 review, 1 invited commentary, 2 case reports, and 1 population-based cross-sectional survey. These studies suggest that 45% of IPV incidents involve ocular injury. Various injury types have been described including traumatic cataract, dislocated lens, retinal detachment, intraocular hemorrhage, orbital and zygomaticomaxillary complex fractures, optic nerve avulsion, and open globe injuries. Implementation of IPV screening programs in various clinical settings, including an emergency department evaluating ocular trauma, suggests a positive association with identification of IPV and improving access to resources.</p><p><strong>Summary: </strong>Within IPV, ocular injuries are a prevalent and important cause of vision loss. Various injuries have been reported affecting nearly every anatomical region of the eye. Routine screening for IPV among patients that present with ocular injuries and evaluating for visual complaints among patients experiencing IPV are both important. Future work focused on prospective studies and evaluation of screening techniques may be impactful.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"119-127"},"PeriodicalIF":0.0,"publicationDate":"2025-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11737344/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143018373","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 : 2025-01-10eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S494531
Mingrui Chen, Jianhua Li, Qinyun Chen, Yuan Zhao
Objective: To assess the visual quality in patients with primary angle-closure glaucoma (PACG) complicated by cataracts after cataract phacoemulsification with intraocular lens (IOL) implantation and goniosynechialysis, and to explore the relationship between pupil size and visual quality.
Methods: A retrospective, non-randomized study was conducted, including 65 PACG patients (75 eyes) who underwent cataract surgery with IOL implantation and goniosynechialysis from July 2021 to June 2023, as well as a control group of cataract-only patients. Visual quality was evaluated using objective and subjective methods at least 3 months postoperatively. PACG patients were divided into large-pupil (≥5 mm) and normal-pupil (<5 mm) groups. Visual quality parameters were compared among groups, and correlations between pupil size and objective visual quality measures were analyzed.
Results: Visual Parameters: The large-pupil PACG group showed significantly higher higher-order aberrations, including coma and spherical aberrations, compared to both the cataract and normal-pupil groups. Contrast sensitivity was also worse in the large-pupil group. Visual Quality Questionnaire: The large-pupil group reported higher scores for night glare and difficulty driving at night. Correlations: Pupil size was positively correlated with higher-order aberrations and negatively correlated with contrast sensitivity.
Conclusion: Pupil dilation is a major factor affecting postoperative visual quality in PACG patients, even after surgery. Larger pupil size significantly increases higher-order aberrations and reduces contrast sensitivity. Techniques like pupil suturing may help improve visual quality in these patients.
{"title":"Study on Visual Quality After Cataract Surgery and Goniosynechialysis in Patients with Primary Angle-Closure Glaucoma and Cataracts.","authors":"Mingrui Chen, Jianhua Li, Qinyun Chen, Yuan Zhao","doi":"10.2147/OPTH.S494531","DOIUrl":"10.2147/OPTH.S494531","url":null,"abstract":"<p><strong>Objective: </strong>To assess the visual quality in patients with primary angle-closure glaucoma (PACG) complicated by cataracts after cataract phacoemulsification with intraocular lens (IOL) implantation and goniosynechialysis, and to explore the relationship between pupil size and visual quality.</p><p><strong>Methods: </strong>A retrospective, non-randomized study was conducted, including 65 PACG patients (75 eyes) who underwent cataract surgery with IOL implantation and goniosynechialysis from July 2021 to June 2023, as well as a control group of cataract-only patients. Visual quality was evaluated using objective and subjective methods at least 3 months postoperatively. PACG patients were divided into large-pupil (≥5 mm) and normal-pupil (<5 mm) groups. Visual quality parameters were compared among groups, and correlations between pupil size and objective visual quality measures were analyzed.</p><p><strong>Results: </strong>Visual Parameters: The large-pupil PACG group showed significantly higher higher-order aberrations, including coma and spherical aberrations, compared to both the cataract and normal-pupil groups. Contrast sensitivity was also worse in the large-pupil group. Visual Quality Questionnaire: The large-pupil group reported higher scores for night glare and difficulty driving at night. Correlations: Pupil size was positively correlated with higher-order aberrations and negatively correlated with contrast sensitivity.</p><p><strong>Conclusion: </strong>Pupil dilation is a major factor affecting postoperative visual quality in PACG patients, even after surgery. Larger pupil size significantly increases higher-order aberrations and reduces contrast sensitivity. Techniques like pupil suturing may help improve visual quality in these patients.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"129-139"},"PeriodicalIF":0.0,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11733163/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143018376","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 : 2025-01-09eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S498985
Ryan B Rush, Westin Klein, Sloan W Rush, Robert Reinauer
Purpose: To assess the 12-month outcomes in subjects developing macular neovascularization (MNV) during intravitreal avacincaptad pegol (IVA) treatment for geographic atrophy (GA) secondary to age-related macular degeneration (AMD).
Methods: This research was conducted as a case-controlled, retrospective study of AMD subjects undergoing IVA treatment for GA from two private practice institutions. Subjects were divided into 1) a Study Group of patients who developed MNV and then underwent anti-vascular endothelial growth factor (VEGF) therapy during the study period, and 2) a Control Group of patients who were complication-free during the study period. Both cohorts had a baseline Snellen visual acuity of ≥ 20/200, a baseline GA total area of ≥ 1 mm2and ≤ 17.5 mm2, and 12 months of follow-up after initiation of IVA for GA.
Results: There were 56 patients analyzed. There were no significant differences in baseline features between cohorts. The Study Group had a greater decrease in visual acuity [-0.22 logMAR (-0.27 to -0.17) versus -0.06 logMAR (-0.12 to 0.00); p=<0.0001], and greater GA total lesion growth [1.78 mm2 (1.53-2.03) versus 0.78 mm2 (0.54-1.02); p=<0.0001] during the 12-month study period compared to the Control Group.
Conclusion: Patients developing MNV while undergoing IVA treatment for GA secondary to AMD have worse clinical outcomes despite undergoing anti-VEGF therapy compared to patients who were complication-free at 12-months. This highlights the seriousness of MNV in this patient population and may help specialists counsel patients when considering treatment for GA secondary to AMD.
目的:评估年龄相关性黄斑变性(AMD)继发地理性萎缩(GA)患者在玻璃体静脉注射avacincaptad pegol (IVA)治疗期间发生黄斑新生血管(MNV)的12个月结果。方法:本研究是一项病例对照的回顾性研究,来自两家私人执业机构的AMD患者因GA接受IVA治疗。研究对象分为两组:1)研究组为研究期间发生MNV并接受抗血管内皮生长因子(VEGF)治疗的患者;2)对照组为研究期间无并发症的患者。两个队列的基线Snellen视力≥20/200,基线GA总面积≥1 mm2和≤17.5 mm2, GA IVA开始后随访12个月。结果:共分析56例患者。各组间基线特征无显著差异。研究组的视力下降幅度更大[-0.22 logMAR(-0.27至-0.17)相比-0.06 logMAR(-0.12至0.00);P =2 (1.53-2.03) vs 0.78 mm2 (0.54-1.02);p=结论:与12个月无并发症的患者相比,尽管接受了抗vegf治疗,但在接受IVA治疗时发生MNV的患者的临床结果更差。这突出了MNV在这一患者群体中的严重性,可能有助于专家在考虑治疗继发于AMD的GA时为患者提供建议。
{"title":"One-Year Outcomes in Subjects Developing Macular Neovascularization While Undergoing Avacincaptad Pegol Therapy for Geographic Atrophy.","authors":"Ryan B Rush, Westin Klein, Sloan W Rush, Robert Reinauer","doi":"10.2147/OPTH.S498985","DOIUrl":"10.2147/OPTH.S498985","url":null,"abstract":"<p><strong>Purpose: </strong>To assess the 12-month outcomes in subjects developing macular neovascularization (MNV) during intravitreal avacincaptad pegol (IVA) treatment for geographic atrophy (GA) secondary to age-related macular degeneration (AMD).</p><p><strong>Methods: </strong>This research was conducted as a case-controlled, retrospective study of AMD subjects undergoing IVA treatment for GA from two private practice institutions. Subjects were divided into 1) a Study Group of patients who developed MNV and then underwent anti-vascular endothelial growth factor (VEGF) therapy during the study period, and 2) a Control Group of patients who were complication-free during the study period. Both cohorts had a baseline Snellen visual acuity of ≥ 20/200, a baseline GA total area of ≥ 1 mm<sup>2</sup>and ≤ 17.5 mm<sup>2</sup>, and 12 months of follow-up after initiation of IVA for GA.</p><p><strong>Results: </strong>There were 56 patients analyzed. There were no significant differences in baseline features between cohorts. The Study Group had a greater decrease in visual acuity [-0.22 logMAR (-0.27 to -0.17) versus -0.06 logMAR (-0.12 to 0.00); p=<0.0001], and greater GA total lesion growth [1.78 mm<sup>2</sup> (1.53-2.03) versus 0.78 mm<sup>2</sup> (0.54-1.02); p=<0.0001] during the 12-month study period compared to the Control Group.</p><p><strong>Conclusion: </strong>Patients developing MNV while undergoing IVA treatment for GA secondary to AMD have worse clinical outcomes despite undergoing anti-VEGF therapy compared to patients who were complication-free at 12-months. This highlights the seriousness of MNV in this patient population and may help specialists counsel patients when considering treatment for GA secondary to AMD.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"111-118"},"PeriodicalIF":0.0,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11727320/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142981006","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 : 2025-01-08eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S487047
Elaine M Tran, Ninel Z Gregori, Aleksandra Rachitskaya, Abhishek Nandan, Suzann Pershing, Jeffrey L Goldberg
Purpose: To investigate the influence of systemic and serum measures and hypoglycemic medications on the initial presentation and ongoing development of diabetic retinopathy (DR) and diabetic macular edema (DME).
Design: Using Veterans Affairs electronic health records, we identified patients with a diabetes mellitus diagnosis and at least one eye examination between 1997 and 2010. After adjusting for sociodemographic factors, we used multivariable Cox regression models to evaluate the association of hemoglobin A1c (HbA1c) levels, blood pressure, albuminuria, blood urea nitrogen (BUN), and prescribed medications with the subsequent diagnosis of 1) any diabetic eye disease (defined for this analysis as DR and/or DME, 2) diabetic retinopathy, and 3) diabetic macular edema.
Results: Of 4089 diabetic Veteran patients, 821 (20%) were subsequently diagnosed with diabetic retinopathy and 88 (2%) had macular edema. Patients were more likely to receive a diabetic retinopathy diagnosis if they presented with HbA1c > 8.5 (HR=2.66, 95% CI 1.88-3.77, p<0.01), systolic blood pressure > 140 mmHg (HR=1.45, 95% CI 1.26-1.66, p<0.01), blood urea nitrogen (BUN) > 35 mg/dL (HR=2.17, 95% CI 1.60-2.93, p<0.01), and/or used insulin (HR=2.04, 95% CI 1.74-2.40, p<0.01). Patients were more likely to be diagnosed with diabetic macular edema if they had systolic blood pressure > 140 mmHg (HR=2.00, CI 1.29-3.08, p<0.01) and/or used insulin (HR=2.48, CI 1.53-4.03, p<0.01).
Conclusion: Markers of systemic health may be useful predictors for incident diabetic retinopathy or diabetic macular edema, evaluated collectively in Veteran patients. Higher HbA1c levels, systolic blood pressure, BUN levels, and insulin use (suggestive of more severe and/or long-standing diabetes) appear to be highly associated with the development of diabetic eye disease, and, in particular, diabetic retinopathy.
目的:探讨全身和血清测量及降糖药物对糖尿病视网膜病变(DR)和糖尿病黄斑水肿(DME)的初始表现和持续发展的影响。设计:使用退伍军人事务部的电子健康记录,我们确定了1997年至2010年间诊断为糖尿病并至少进行过一次眼科检查的患者。在调整社会人口统计学因素后,我们使用多变量Cox回归模型来评估血红蛋白A1c (HbA1c)水平、血压、蛋白尿、血尿素氮(BUN)和处方药物与随后诊断的相关性:1)任何糖尿病性眼病(在本分析中定义为DR和/或DME), 2)糖尿病性视网膜病变,3)糖尿病性黄斑水肿。结果:4089例糖尿病退伍军人患者中,821例(20%)随后诊断为糖尿病视网膜病变,88例(2%)出现黄斑水肿。如果患者出现HbA1c bbb8.5 (HR=2.66, 95% CI 1.88-3.77, p140 mmHg) (HR=1.45, 95% CI 1.26-1.66, p35 mg/dL (HR=2.17, 95% CI 1.60-2.93, p140 mmHg (HR=2.00, CI 1.29-3.08)),患者更有可能被诊断为糖尿病视网膜病变。结论:在退伍军人患者中进行集体评估,全身健康指标可能是糖尿病视网膜病变或糖尿病黄斑水肿的有用预测因素。较高的HbA1c水平、收缩压、BUN水平和胰岛素使用(提示更严重和/或长期糖尿病)似乎与糖尿病性眼病的发展高度相关,特别是糖尿病性视网膜病变。
{"title":"Systemic Predictors of Diabetic Retinopathy and Diabetic Macular Edema in an Adult Veteran Population.","authors":"Elaine M Tran, Ninel Z Gregori, Aleksandra Rachitskaya, Abhishek Nandan, Suzann Pershing, Jeffrey L Goldberg","doi":"10.2147/OPTH.S487047","DOIUrl":"10.2147/OPTH.S487047","url":null,"abstract":"<p><strong>Purpose: </strong>To investigate the influence of systemic and serum measures and hypoglycemic medications on the initial presentation and ongoing development of diabetic retinopathy (DR) and diabetic macular edema (DME).</p><p><strong>Design: </strong>Using Veterans Affairs electronic health records, we identified patients with a diabetes mellitus diagnosis and at least one eye examination between 1997 and 2010. After adjusting for sociodemographic factors, we used multivariable Cox regression models to evaluate the association of hemoglobin A1c (HbA1c) levels, blood pressure, albuminuria, blood urea nitrogen (BUN), and prescribed medications with the subsequent diagnosis of 1) any diabetic eye disease (defined for this analysis as DR and/or DME, 2) diabetic retinopathy, and 3) diabetic macular edema.</p><p><strong>Results: </strong>Of 4089 diabetic Veteran patients, 821 (20%) were subsequently diagnosed with diabetic retinopathy and 88 (2%) had macular edema. Patients were more likely to receive a diabetic retinopathy diagnosis if they presented with HbA1c > 8.5 (HR=2.66, 95% CI 1.88-3.77, p<0.01), systolic blood pressure > 140 mmHg (HR=1.45, 95% CI 1.26-1.66, p<0.01), blood urea nitrogen (BUN) > 35 mg/dL (HR=2.17, 95% CI 1.60-2.93, p<0.01), and/or used insulin (HR=2.04, 95% CI 1.74-2.40, p<0.01). Patients were more likely to be diagnosed with diabetic macular edema if they had systolic blood pressure > 140 mmHg (HR=2.00, CI 1.29-3.08, p<0.01) and/or used insulin (HR=2.48, CI 1.53-4.03, p<0.01).</p><p><strong>Conclusion: </strong>Markers of systemic health may be useful predictors for incident diabetic retinopathy or diabetic macular edema, evaluated collectively in Veteran patients. Higher HbA1c levels, systolic blood pressure, BUN levels, and insulin use (suggestive of more severe and/or long-standing diabetes) appear to be highly associated with the development of diabetic eye disease, and, in particular, diabetic retinopathy.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"101-110"},"PeriodicalIF":0.0,"publicationDate":"2025-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11725239/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142973526","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 : 2025-01-08eCollection Date: 2025-01-01DOI: 10.2147/OPTH.S481124
Caroline Guerrero-de Ferran, Daniel Bastán-Fabián, Alfredo Del Castillo-Morales, I Jocelyn Rivera-Alvarado, Jorge E Valdez García
Purpose: To compare the meibographies and dry eye parameters of paretic vs non-paretic sides of patients with a facial palsy diagnosis.
Patients and methods: Twenty patients with unilateral facial palsy were recruited and the severity of the disease was staged using the House-Brackmann scale. A comprehensive dry eye evaluation was performed using the Oculus 5M Keratograph. A Pearson correlation coefficient was performed to determine correlation strength between House-Brackmann score and Meibomian gland atrophy. Meibographies were analyzed via ImageJ software to determine the affected area, and they were compared to the observer manual score. Cohen's Kappa coefficient was calculated to compare agreement between manual and ImageJ meibography scoring.
Results: Tear breakup time was reduced in the affected side (p = 0.21), tear meniscus height was much greater in the non-affected side (p = 0.02). Finally, Meibomian gland alterations were more evident in the affected side, with upper Meibomian glands having a loss of 29.55 ± 13.31% (p = 0.03) and lower glands presenting a loss of 44.44 ± 16.9% (p =< 0.001). Pearson correlation coefficient between House-Brackmann score and Meibomian gland atrophy was 0.841 (p < 0.001 [95% CI: 0.64-0.94]). Cohen's kappa coefficient was 0.643 (p < 0.001).
Conclusion: A clear difference in Meibomian gland and tear film dynamics can be observed in paretic vs non-paretic sides. A greater House-Brackmann score was correlated with a greater Meibomian gland atrophy area. A strong positive correlation is seen between the House-Brackmann score and Meibomian gland atrophy. Software-based analysis also showed a greater glandular area loss when compared to clinician's analysis. The level of agreement was moderate, so disparities are observed, especially in grade 2 Meibomian gland dropout where the least level of agreement was seen in cross tabulation. This study further incentivizes multimodal patient evaluation, which has been a growing area of interest in healthcare.
{"title":"Epidemiology, Tear Film, and Meibomian Gland Dysfunction in Facial Palsy: A Comparative Analysis.","authors":"Caroline Guerrero-de Ferran, Daniel Bastán-Fabián, Alfredo Del Castillo-Morales, I Jocelyn Rivera-Alvarado, Jorge E Valdez García","doi":"10.2147/OPTH.S481124","DOIUrl":"10.2147/OPTH.S481124","url":null,"abstract":"<p><strong>Purpose: </strong>To compare the meibographies and dry eye parameters of paretic vs non-paretic sides of patients with a facial palsy diagnosis.</p><p><strong>Patients and methods: </strong>Twenty patients with unilateral facial palsy were recruited and the severity of the disease was staged using the House-Brackmann scale. A comprehensive dry eye evaluation was performed using the Oculus 5M Keratograph. A Pearson correlation coefficient was performed to determine correlation strength between House-Brackmann score and Meibomian gland atrophy. Meibographies were analyzed via ImageJ software to determine the affected area, and they were compared to the observer manual score. Cohen's Kappa coefficient was calculated to compare agreement between manual and ImageJ meibography scoring.</p><p><strong>Results: </strong>Tear breakup time was reduced in the affected side (p = 0.21), tear meniscus height was much greater in the non-affected side (p = 0.02). Finally, Meibomian gland alterations were more evident in the affected side, with upper Meibomian glands having a loss of 29.55 ± 13.31% (p = 0.03) and lower glands presenting a loss of 44.44 ± 16.9% (p =< 0.001). Pearson correlation coefficient between House-Brackmann score and Meibomian gland atrophy was 0.841 (p < 0.001 [95% CI: 0.64-0.94]). Cohen's kappa coefficient was 0.643 (p < 0.001).</p><p><strong>Conclusion: </strong>A clear difference in Meibomian gland and tear film dynamics can be observed in paretic vs non-paretic sides. A greater House-Brackmann score was correlated with a greater Meibomian gland atrophy area. A strong positive correlation is seen between the House-Brackmann score and Meibomian gland atrophy. Software-based analysis also showed a greater glandular area loss when compared to clinician's analysis. The level of agreement was moderate, so disparities are observed, especially in grade 2 Meibomian gland dropout where the least level of agreement was seen in cross tabulation. This study further incentivizes multimodal patient evaluation, which has been a growing area of interest in healthcare.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"93-100"},"PeriodicalIF":0.0,"publicationDate":"2025-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11725262/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142973759","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}
Purpose: To develop a comprehensively deep learning algorithm to differentiate between bacterial keratitis, fungal keratitis, non-infectious corneal lesions, and normal corneas.
Methods: This retrospective study collected slit-lamp photos of patients with bacterial keratitis, fungal keratitis, non-infectious corneal lesions, and normal cornea. Causative organisms of infectious keratitis were identified by either positive culture or clinical response to single treatment. Convolutional neural networks (ResNet50, DenseNet121, VGG19) and Ensemble with probability weighting were used to develop a deep learning algorithm. The performance including accuracy, precision, recall, F1 score, specificity and AUC has been reported.
Results: Total of 6478 photos from 2171 eyes, composed of 2400 bacterial keratitis, 1616 fungal keratitis, 1545 non-infectious corneal lesions, and 917 normal corneas were collected from hospital database. DenseNet121 demonstrated the best performance among three convolutional neural networks with the accuracy of 0.8 (95% CI 0.74-0.86). The ensemble technique showed higher performance than single algorithm with the accuracy of 0.83 (95% 0.78-0.88).
Conclusion: Convolutional neural networks with ensemble techniques provided the best performance in discriminating bacterial keratitis, fungal keratitis, non-infectious corneal lesions, and normal corneas. Our models can be used as a screening tool for non-ophthalmic health care providers and ophthalmologists for rapid provisional diagnosis of infectious keratitis.
目的:开发一种区分细菌性角膜炎、真菌性角膜炎、非感染性角膜病变和正常角膜的综合深度学习算法。方法:回顾性收集细菌性角膜炎、真菌性角膜炎、非感染性角膜病变和正常角膜患者的裂隙灯照片。通过培养阳性或对单一治疗的临床反应来鉴定感染性角膜炎的致病微生物。使用卷积神经网络(ResNet50, DenseNet121, VGG19)和概率加权的Ensemble来开发深度学习算法。准确度、精密度、召回率、F1评分、特异性和AUC等指标均有报道。结果:从医院数据库中共收集到2171只眼的照片6478张,其中细菌性角膜炎2400张,真菌性角膜炎1616张,非感染性角膜病变1545张,正常角膜917张。DenseNet121在三个卷积神经网络中表现最好,准确率为0.8 (95% CI 0.74-0.86)。集成技术的准确率为0.83(95% 0.78 ~ 0.88),优于单一算法。结论:卷积神经网络集成技术对细菌性角膜炎、真菌性角膜炎、非感染性角膜病变和正常角膜的鉴别效果最好。我们的模型可以作为非眼科保健提供者和眼科医生快速临时诊断感染性角膜炎的筛查工具。
{"title":"A Convolutional Neural Network Using Anterior Segment Photos for Infectious Keratitis Identification.","authors":"Vannarut Satitpitakul, Apiwit Puangsricharern, Surachet Yuktiratna, Yossapon Jaisarn, Keeratika Sangsao, Vilavun Puangsricharern, Ngamjit Kasetsuwan, Usanee Reinprayoon, Thanachaporn Kittipibul","doi":"10.2147/OPTH.S496552","DOIUrl":"10.2147/OPTH.S496552","url":null,"abstract":"<p><strong>Purpose: </strong>To develop a comprehensively deep learning algorithm to differentiate between bacterial keratitis, fungal keratitis, non-infectious corneal lesions, and normal corneas.</p><p><strong>Methods: </strong>This retrospective study collected slit-lamp photos of patients with bacterial keratitis, fungal keratitis, non-infectious corneal lesions, and normal cornea. Causative organisms of infectious keratitis were identified by either positive culture or clinical response to single treatment. Convolutional neural networks (ResNet50, DenseNet121, VGG19) and Ensemble with probability weighting were used to develop a deep learning algorithm. The performance including accuracy, precision, recall, F1 score, specificity and AUC has been reported.</p><p><strong>Results: </strong>Total of 6478 photos from 2171 eyes, composed of 2400 bacterial keratitis, 1616 fungal keratitis, 1545 non-infectious corneal lesions, and 917 normal corneas were collected from hospital database. DenseNet121 demonstrated the best performance among three convolutional neural networks with the accuracy of 0.8 (95% CI 0.74-0.86). The ensemble technique showed higher performance than single algorithm with the accuracy of 0.83 (95% 0.78-0.88).</p><p><strong>Conclusion: </strong>Convolutional neural networks with ensemble techniques provided the best performance in discriminating bacterial keratitis, fungal keratitis, non-infectious corneal lesions, and normal corneas. Our models can be used as a screening tool for non-ophthalmic health care providers and ophthalmologists for rapid provisional diagnosis of infectious keratitis.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"73-81"},"PeriodicalIF":0.0,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11724627/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142973843","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}