Pub Date : 2024-09-14DOI: 10.1177/24741264241275283
Dilraj S Grewal, Ella Leung, Miguel Busquets, Philip Niles, Dan A Gong, Anton M Kolomeyer, Nitika Aggarwal, Nick Boucher, Jill Blim, Judy E Kim, Reginald Sanders, Paul Hahn
Purpose: To compare the modeled costs of the Protocol AC bevacizumab-first treatment protocol (with a switch to aflibercept for sub-responders) with real-world costs for treatment-naïve patients with diabetic macular edema (DME) over a 2-year period. Methods: Published data from the Diabetic Retinopathy Clinical Research Network (DRCR) Protocol AC bevacizumab-first arm (154 eyes) were used to model 2-year treatment costs. Real-world costs were modeled using data from the Vestrum Health electronic medical records database from a 2016 to 2018 cohort of treatment-naïve eyes with DME (n = 1062) treated with antivascular endothelial growth factor monotherapy. The visual acuity (VA) before treatment in the real-world cohort was matched to Protocol AC. A secondary cost analysis further matched VA gains after treatment in the real-world cohort (n = 346) to Protocol AC. Results: In Protocol AC, the modeled 2-year DME treatment cost in the bevacizumab-first arm was $18,952, with a mean of 16.1 injections over 22.5 visits and 70% of eyes being switched to aflibercept by year 2. (Within 2 years, 57% of injections were bevacizumab and 43% were aflibercept.) Over the same period, the modeled 2-year real-world cost ($11,459) was 40% lower, with a mean of 8.6 injections over 13.8 visits (42% bevacizumab, 45% aflibercept, 13% ranibizumab). Even when matched for baseline VA and a 14-letter VA gain over 2 years, the real-world cost ($15,394) was still 19% lower than the modeled cost in the Protocol AC bevacizumab-first arm. Conclusions: The real-world cost of treating DME over 2 years was significantly lower than the Protocol AC bevacizumab-first cost. Application of Protocol AC findings into real-world utilization, as with step therapy mandates, should only be considered if the same intensive protocol could be followed. These data suggest that existing real-world costs that reflect physician choice are already significantly lower than protocol-mandated step therapy, even when controlling for similar VA outcomes.
目的:比较糖尿病黄斑水肿(DME)患者在两年内接受 AC 方案贝伐珠单抗先行治疗方案(反应不佳者改用阿夫利百普)的模型成本与实际成本。研究方法利用糖尿病视网膜病变临床研究网络(DRCR)AC方案贝伐珠单抗先行组(154只眼)已公布的数据建立2年治疗成本模型。使用Vestrum Health电子病历数据库中2016年至2018年队列中接受抗血管内皮生长因子单药治疗的DME(n = 1062)治疗无效眼的数据,对真实世界的成本进行建模。真实世界队列中治疗前的视力(VA)与协议 AC 匹配。次要成本分析进一步将真实世界队列(n = 346)治疗后的视力提高与 AC 方案进行匹配。结果显示在AC方案中,贝伐珠单抗先用组的模型2年DME治疗成本为18,952美元,22.5次就诊中平均注射16.1次,70%的眼睛在第2年转为阿弗利贝赛普(2年内,57%的注射为贝伐珠单抗,43%为阿弗利贝赛普)。同期,模拟的 2 年实际费用(11,459 美元)降低了 40%,在 13.8 次就诊中平均注射 8.6 次(42% 为贝伐珠单抗,45% 为阿弗利百普,13% 为雷尼珠单抗)。即使根据基线视力和2年内14个字母的视力增益进行匹配,实际成本(15,394美元)仍比AC方案贝伐珠单抗先用组的模型成本低19%。结论2年内治疗 DME 的实际成本明显低于先用贝伐珠单抗的 AC 方案成本。将 AC 方案的研究结果应用于真实世界的使用情况,就像阶梯疗法的规定一样,只有在可以遵循相同的强化方案时才应考虑。这些数据表明,即使控制了类似的退伍军人疗效,反映医生选择的现有真实世界成本已经明显低于方案规定的阶梯疗法。
{"title":"Bevacizumab First in DRCR Protocol AC vs Real-World Physician Treatment Choice for Diabetic Macular Edema: Two-Year Cost Analysis.","authors":"Dilraj S Grewal, Ella Leung, Miguel Busquets, Philip Niles, Dan A Gong, Anton M Kolomeyer, Nitika Aggarwal, Nick Boucher, Jill Blim, Judy E Kim, Reginald Sanders, Paul Hahn","doi":"10.1177/24741264241275283","DOIUrl":"10.1177/24741264241275283","url":null,"abstract":"<p><p><b>Purpose:</b> To compare the modeled costs of the Protocol AC bevacizumab-first treatment protocol (with a switch to aflibercept for sub-responders) with real-world costs for treatment-naïve patients with diabetic macular edema (DME) over a 2-year period. <b>Methods:</b> Published data from the Diabetic Retinopathy Clinical Research Network (DRCR) Protocol AC bevacizumab-first arm (154 eyes) were used to model 2-year treatment costs. Real-world costs were modeled using data from the Vestrum Health electronic medical records database from a 2016 to 2018 cohort of treatment-naïve eyes with DME (n = 1062) treated with antivascular endothelial growth factor monotherapy. The visual acuity (VA) before treatment in the real-world cohort was matched to Protocol AC. A secondary cost analysis further matched VA gains after treatment in the real-world cohort (n = 346) to Protocol AC. <b>Results</b>: In Protocol AC, the modeled 2-year DME treatment cost in the bevacizumab-first arm was $18,952, with a mean of 16.1 injections over 22.5 visits and 70% of eyes being switched to aflibercept by year 2. (Within 2 years, 57% of injections were bevacizumab and 43% were aflibercept.) Over the same period, the modeled 2-year real-world cost ($11,459) was 40% lower, with a mean of 8.6 injections over 13.8 visits (42% bevacizumab, 45% aflibercept, 13% ranibizumab). Even when matched for baseline VA and a 14-letter VA gain over 2 years, the real-world cost ($15,394) was still 19% lower than the modeled cost in the Protocol AC bevacizumab-first arm. <b>Conclusions:</b> The real-world cost of treating DME over 2 years was significantly lower than the Protocol AC bevacizumab-first cost. Application of Protocol AC findings into real-world utilization, as with step therapy mandates, should only be considered if the same intensive protocol could be followed. These data suggest that existing real-world costs that reflect physician choice are already significantly lower than protocol-mandated step therapy, even when controlling for similar VA outcomes.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241275283"},"PeriodicalIF":0.5,"publicationDate":"2024-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556346/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142622847","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 : 2024-09-14DOI: 10.1177/24741264241276602
Amit V Mishra, Shangjun Jiang, Matthew T S Tennant, Mark E Seamone
Purpose: To describe a single case of systemic lymphoma recurring in the iris and ciliary body. Methods: A retrospective case review was performed. Results: A 75-year-old woman presented to the retina service with an iris mass in the left eye. Her medical history was significant for previous systemic diffuse large B-cell lymphoma treated with systemic chemotherapy. Aqueous sampling was significant for recurrence of the disease. Local therapy with intravitreal (IVT) methotrexate was initiated. Although there was initial improvement, an increased interval between injections led to disease recurrence. External beam radiation to the left eye was then applied, leading to a complete clinical remission. Conclusions: Systemic lymphoma presenting in the iris is a rare manifestation that should be considered on the differential for an amelanotic iris lesion. Although monotherapy with IVT methotrexate did not control the ocular disease in this patient, subsequent external beam radiation resulted in complete clinical remission.
目的:描述一例复发于虹膜和睫状体的全身淋巴瘤。方法:对病例进行回顾性分析:对病例进行回顾性分析。结果一名 75 岁的妇女因左眼虹膜肿块到视网膜科就诊。病史显示她曾患全身性弥漫大 B 细胞淋巴瘤并接受过全身化疗。水样检查显示疾病复发。她开始接受玻璃体内甲氨蝶呤(IVT)局部治疗。虽然最初病情有所好转,但注射间隔的延长导致疾病复发。随后对左眼进行了体外放射治疗,临床症状完全缓解。结论:出现在虹膜上的全身性淋巴瘤是一种罕见的表现,应与虹膜褪色性病变鉴别考虑。虽然单用静脉滴注甲氨蝶呤无法控制该患者的眼部疾病,但随后的体外放射治疗使其临床症状完全缓解。
{"title":"Isolated Recurrence of Diffuse Large B-Cell Lymphoma Predominantly in the Iris and Ciliary Body.","authors":"Amit V Mishra, Shangjun Jiang, Matthew T S Tennant, Mark E Seamone","doi":"10.1177/24741264241276602","DOIUrl":"10.1177/24741264241276602","url":null,"abstract":"<p><p><b>Purpose:</b> To describe a single case of systemic lymphoma recurring in the iris and ciliary body. <b>Methods:</b> A retrospective case review was performed. <b>Results:</b> A 75-year-old woman presented to the retina service with an iris mass in the left eye. Her medical history was significant for previous systemic diffuse large B-cell lymphoma treated with systemic chemotherapy. Aqueous sampling was significant for recurrence of the disease. Local therapy with intravitreal (IVT) methotrexate was initiated. Although there was initial improvement, an increased interval between injections led to disease recurrence. External beam radiation to the left eye was then applied, leading to a complete clinical remission. <b>Conclusions:</b> Systemic lymphoma presenting in the iris is a rare manifestation that should be considered on the differential for an amelanotic iris lesion. Although monotherapy with IVT methotrexate did not control the ocular disease in this patient, subsequent external beam radiation resulted in complete clinical remission.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241276602"},"PeriodicalIF":0.5,"publicationDate":"2024-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556293/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142623035","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 : 2024-09-14DOI: 10.1177/24741264241276601
Saima Khan, Cole A Martin, Shannon Scarboro, Edward Wood, Clio A Harper
Purpose: To report a pediatric case of Coats plus syndrome that initially presented resembling familial exudative vitreoretinopathy (FEVR). Methods: A single case was analyzed. Results: A pediatric patient was referred at 2 years of age to the retina clinic for exotropia and decreased visual acuity in the right eye and was found to have a dense vitreous hemorrhage. She later developed persistent gastrointestinal bleeding requiring regular blood transfusions and intravenous bevacizumab. Treatment with systemic bevacizumab resolved the patient's cystoid macular edema (CME). Although her presentation and examination were initially suggestive of FEVR, genetic analysis revealed heterozygous biallelic mutations in the STN1 gene, mutations that are known to be associated with Coats plus syndrome. Conclusions: Coats plus syndrome is a rare and life-threatening microangiopathy that affects the retina, central nervous system, and gastrointestinal system. The patient's resulting CME significantly improved with intravenous bevacizumab.
目的:报告一例最初表现类似家族性渗出性玻璃体视网膜病变(FEVR)的科茨加综合征儿科病例。方法:对一个病例进行分析:分析一个病例。结果:一名两岁大的儿童患者因右眼外斜和视力下降被转诊至视网膜诊所,发现其右眼有致密玻璃体出血。后来,她出现了持续性消化道出血,需要定期输血和静脉注射贝伐单抗。全身使用贝伐珠单抗治疗后,患者的囊样黄斑水肿(CME)得到了缓解。虽然她的表现和检查最初提示为 FEVR,但基因分析发现 STN1 基因存在杂合双倍重复突变,而已知这种突变与 Coats plus 综合征有关。结论:科茨加综合征是一种罕见的危及生命的微血管病变,会影响视网膜、中枢神经系统和胃肠道系统。静脉注射贝伐单抗后,患者的CME症状明显改善。
{"title":"Improvement in Cystoid Macular Edema Secondary to Systemic Bevacizumab in a Patient With Coats Plus Syndrome.","authors":"Saima Khan, Cole A Martin, Shannon Scarboro, Edward Wood, Clio A Harper","doi":"10.1177/24741264241276601","DOIUrl":"10.1177/24741264241276601","url":null,"abstract":"<p><p><b>Purpose:</b> To report a pediatric case of Coats plus syndrome that initially presented resembling familial exudative vitreoretinopathy (FEVR). <b>Methods:</b> A single case was analyzed. <b>Results:</b> A pediatric patient was referred at 2 years of age to the retina clinic for exotropia and decreased visual acuity in the right eye and was found to have a dense vitreous hemorrhage. She later developed persistent gastrointestinal bleeding requiring regular blood transfusions and intravenous bevacizumab. Treatment with systemic bevacizumab resolved the patient's cystoid macular edema (CME). Although her presentation and examination were initially suggestive of FEVR, genetic analysis revealed heterozygous biallelic mutations in the <i>STN1</i> gene, mutations that are known to be associated with Coats plus syndrome. <b>Conclusions:</b> Coats plus syndrome is a rare and life-threatening microangiopathy that affects the retina, central nervous system, and gastrointestinal system. The patient's resulting CME significantly improved with intravenous bevacizumab.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241276601"},"PeriodicalIF":0.5,"publicationDate":"2024-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556374/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142623009","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 : 2024-09-14DOI: 10.1177/24741264241276606
Hao-Tinh Le, Natasha Kesav, Ankur Mehra, Mohamed Soliman, Warren Sobol
Purpose: To describe the early presentation of successive acute retinal necrosis (ARN) decades after the initial infection. Methods: A single case and its findings were analyzed. Results: A 62-year-old man with a remote history of left-sided ARN presented for evaluation of right-sided blurry vision. An examination showed 1+ anterior chamber cells and mild vitritis with multiple small patches of white retinitis. The lesions progressed despite treatment with oral antivirals, eventually requiring multiple doses of intravitreal antiviral agents and hospitalization for intravenous antiviral therapy. Despite a characteristic clinical picture consistent with ARN, multiple aqueous samples tested negative for viral etiologic agents. Conclusions: ARN is a rapidly progressive disease, and the diagnosis is clinical. Our patient was treated aggressively with antiviral therapy on the basis of the clinical picture without confirmatory testing, which remained negative. The lesions responded well to treatment and 20/25 visual acuity was maintained. Regardless of confirmatory testing, timely treatment is critical in cases of suspected ARN.
{"title":"Early Presentation of Successive Acute Retinal Necrosis Decades After Initial Infection.","authors":"Hao-Tinh Le, Natasha Kesav, Ankur Mehra, Mohamed Soliman, Warren Sobol","doi":"10.1177/24741264241276606","DOIUrl":"10.1177/24741264241276606","url":null,"abstract":"<p><p><b>Purpose:</b> To describe the early presentation of successive acute retinal necrosis (ARN) decades after the initial infection. <b>Methods:</b> A single case and its findings were analyzed. <b>Results:</b> A 62-year-old man with a remote history of left-sided ARN presented for evaluation of right-sided blurry vision. An examination showed 1+ anterior chamber cells and mild vitritis with multiple small patches of white retinitis. The lesions progressed despite treatment with oral antivirals, eventually requiring multiple doses of intravitreal antiviral agents and hospitalization for intravenous antiviral therapy. Despite a characteristic clinical picture consistent with ARN, multiple aqueous samples tested negative for viral etiologic agents. <b>Conclusions:</b> ARN is a rapidly progressive disease, and the diagnosis is clinical. Our patient was treated aggressively with antiviral therapy on the basis of the clinical picture without confirmatory testing, which remained negative. The lesions responded well to treatment and 20/25 visual acuity was maintained. Regardless of confirmatory testing, timely treatment is critical in cases of suspected ARN.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241276606"},"PeriodicalIF":0.5,"publicationDate":"2024-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556361/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142622994","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 : 2024-09-14DOI: 10.1177/24741264241271733
Cuneyt Ozkardes, Riley N Sanders, H Logan Brooks, Ahmed Shakarchi
Purpose: To describe the spontaneous closure of a chronic, persistent, stage 4 full-thickness macular hole (FTMH) that did not respond to surgical treatment but closed after an episode of cystoid macular edema (CME) secondary to acute iritis. Methods: A single case was evaluated. Results: A 71-year-old woman presented with decreased vision in the left eye for 6 months. A chronic stage 4 FTMH was identified. Surgical treatment consisting of pars plana vitrectomy and internal limiting membrane peeling was unsuccessful, and the patient declined a repeat operation. Two months later, she presented with acute iritis and CME. Imaging showed incidental closure of the FTMH. The iritis resolved after a sub-Tenon triamcinolone injection. At the 3-month follow-up, the FTMH remained closed without CME or iritis. Conclusions: This case highlights the potential importance of CME in the closure of a chronic FTMH after unsuccessful primary surgical repair and suggests clinicians should consider this mechanism in the management of chronic FTMH.
{"title":"Macular Edema Causing Spontaneous Closure of a Macular Hole After Unsuccessful Primary Surgical Repair.","authors":"Cuneyt Ozkardes, Riley N Sanders, H Logan Brooks, Ahmed Shakarchi","doi":"10.1177/24741264241271733","DOIUrl":"10.1177/24741264241271733","url":null,"abstract":"<p><p><b>Purpose:</b> To describe the spontaneous closure of a chronic, persistent, stage 4 full-thickness macular hole (FTMH) that did not respond to surgical treatment but closed after an episode of cystoid macular edema (CME) secondary to acute iritis. <b>Methods:</b> A single case was evaluated. <b>Results:</b> A 71-year-old woman presented with decreased vision in the left eye for 6 months. A chronic stage 4 FTMH was identified. Surgical treatment consisting of pars plana vitrectomy and internal limiting membrane peeling was unsuccessful, and the patient declined a repeat operation. Two months later, she presented with acute iritis and CME. Imaging showed incidental closure of the FTMH. The iritis resolved after a sub-Tenon triamcinolone injection. At the 3-month follow-up, the FTMH remained closed without CME or iritis. <b>Conclusions:</b> This case highlights the potential importance of CME in the closure of a chronic FTMH after unsuccessful primary surgical repair and suggests clinicians should consider this mechanism in the management of chronic FTMH.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241271733"},"PeriodicalIF":0.5,"publicationDate":"2024-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556379/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142623037","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 : 2024-09-11DOI: 10.1177/24741264241275246
Graeme K Loh, Amit V Mishra, Mark Seamone, Matthew Tennant
Purpose: To analyze the outcomes and complications of immediate (within 24 hours) small-gauge (23-gauge, 25-gauge) pars plana vitrectomy (PPV) for all causes of exogenous endophthalmitis. Methods: A retrospective case series was evaluated. Results: The study included 107 patients who had immediate PPV for exogenous endophthalmitis between 2016 and 2022. The primary outcome measures were the change from baseline best-corrected visual acuity (BCVA) to the final follow-up and the complications after PPV. Causes of exogenous endophthalmitis included intravitreal injections (62.6%), PPV (18.7%), cataract surgery (11.2%), glaucoma surgery (5.6%), and trauma (1.9%). The most common complications were retinal detachment (17.8%) and secondary glaucoma (9.3%). The mean logMAR BCVA improved significantly from the initial diagnosis to the final follow-up (2.26 vs 1.21) (P < .0001). Conclusions: In most cases, immediate small-gauge vitrectomy for exogenous endophthalmitis leads to an improvement in VA, regardless of the VA at presentation. Patients should be counseled about the potential risks associated with PPV surgery.
目的:分析针对各种原因引起的外源性眼内炎立即(24 小时内)进行小号(23 号、25 号)玻璃体旁切除术(PPV)的结果和并发症。方法:对一个回顾性病例系列进行评估。结果:研究纳入了2016年至2022年间因外源性眼内炎而立即进行PPV手术的107例患者。主要结果指标是基线最佳矫正视力(BCVA)到最终随访的变化以及PPV后的并发症。外源性眼内炎的病因包括玻璃体内注射(62.6%)、PPV(18.7%)、白内障手术(11.2%)、青光眼手术(5.6%)和外伤(1.9%)。最常见的并发症是视网膜脱离(17.8%)和继发性青光眼(9.3%)。从最初诊断到最后随访,BCVA的平均logMAR值明显改善(2.26 vs 1.21)(P 结论:从最初诊断到最后随访,BCVA的平均logMAR值明显改善(2.26 vs 1.21):在大多数情况下,无论患者发病时的视力如何,立即进行小号玻璃体切割术治疗外源性眼内炎都能改善视力。应告知患者 PPV 手术的潜在风险。
{"title":"Unified Approach to Treating Exogenous Endophthalmitis With Immediate Vitrectomy.","authors":"Graeme K Loh, Amit V Mishra, Mark Seamone, Matthew Tennant","doi":"10.1177/24741264241275246","DOIUrl":"10.1177/24741264241275246","url":null,"abstract":"<p><p><b>Purpose:</b> To analyze the outcomes and complications of immediate (within 24 hours) small-gauge (23-gauge, 25-gauge) pars plana vitrectomy (PPV) for all causes of exogenous endophthalmitis. <b>Methods:</b> A retrospective case series was evaluated. <b>Results:</b> The study included 107 patients who had immediate PPV for exogenous endophthalmitis between 2016 and 2022. The primary outcome measures were the change from baseline best-corrected visual acuity (BCVA) to the final follow-up and the complications after PPV. Causes of exogenous endophthalmitis included intravitreal injections (62.6%), PPV (18.7%), cataract surgery (11.2%), glaucoma surgery (5.6%), and trauma (1.9%). The most common complications were retinal detachment (17.8%) and secondary glaucoma (9.3%). The mean logMAR BCVA improved significantly from the initial diagnosis to the final follow-up (2.26 vs 1.21) (<i>P</i> < .0001). <b>Conclusions:</b> In most cases, immediate small-gauge vitrectomy for exogenous endophthalmitis leads to an improvement in VA, regardless of the VA at presentation. Patients should be counseled about the potential risks associated with PPV surgery.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241275246"},"PeriodicalIF":0.5,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556366/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142623133","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 : 2024-08-31DOI: 10.1177/24741264241275247
Jaskirat S Takhar, Ankur A Mehra, Shree K Kurup, Warren M Sobol, Rabail Aslam, Kwadwo A Oduro, Jose J Echegaray
Purpose: To present a case of acute B-cell lymphoblastic leukemia (B-ALL) ocular relapse treated with chimeric antigen receptor T-cell (CAR T) therapy. Methods: A retrospective case review was evaluated. Results: A 69-year-old woman with a history of B-ALL presented with bilateral hypopyons and 3+ anterior chamber cells that responded to topical prednisolone. Six months later, she developed recurrent hypopyons, iris neovascularization, and iris nodularity in both eyes. A fine-needle aspiration biopsy confirmed ocular infiltration of B-ALL. A single infusion of CAR T therapy resulted in remission of the systemic and ocular findings. The clinical course was complicated by cytokine release syndrome and neurotoxicity, which improved with medical management. The patient remained in remission for 7 months after a single CAR T infusion. Conclusions: CAR T therapy may be effective in treating systemic leukemia and uveal infiltration, with an ocular side-effect profile and visual outcomes. The systemic side effects of CAR T therapy may be managed medically.
目的:介绍一例采用嵌合抗原受体 T 细胞(CAR T)疗法治疗的急性 B 细胞淋巴细胞白血病(B-ALL)眼部复发病例。研究方法对病例进行回顾性评估。结果一名 69 岁的女性患者曾患 B-ALL 病史,出现双侧眼睑下垂和 3+ 前房细胞,对局部强的松龙治疗有反应。6 个月后,她的双眼反复出现视力减退、虹膜新生血管和虹膜结节。细针穿刺活检证实了 B-ALL 的眼部浸润。单次输注 CAR T 疗法后,全身和眼部症状均得到缓解。临床过程因细胞因子释放综合征和神经毒性而变得复杂,但经过药物治疗后情况有所改善。单次输注 CAR T 治疗后,患者病情持续缓解了 7 个月。结论CAR T疗法可有效治疗全身性白血病和葡萄膜浸润,同时具有眼部副作用和视觉效果。CAR T疗法的全身副作用可通过药物控制。
{"title":"Resolution of Anterior Uveal Infiltration of Acute Lymphoblastic Leukemia After Chimeric Antigen Receptor T-Cell Therapy.","authors":"Jaskirat S Takhar, Ankur A Mehra, Shree K Kurup, Warren M Sobol, Rabail Aslam, Kwadwo A Oduro, Jose J Echegaray","doi":"10.1177/24741264241275247","DOIUrl":"10.1177/24741264241275247","url":null,"abstract":"<p><p><b>Purpose:</b> To present a case of acute B-cell lymphoblastic leukemia (B-ALL) ocular relapse treated with chimeric antigen receptor T-cell (CAR T) therapy. <b>Methods:</b> A retrospective case review was evaluated. <b>Results:</b> A 69-year-old woman with a history of B<b>-</b>ALL presented with bilateral hypopyons and 3+ anterior chamber cells that responded to topical prednisolone. Six months later, she developed recurrent hypopyons, iris neovascularization, and iris nodularity in both eyes. A fine-needle aspiration biopsy confirmed ocular infiltration of B-ALL. A single infusion of CAR T therapy resulted in remission of the systemic and ocular findings. The clinical course was complicated by cytokine release syndrome and neurotoxicity, which improved with medical management. The patient remained in remission for 7 months after a single CAR T infusion. <b>Conclusions:</b> CAR T therapy may be effective in treating systemic leukemia and uveal infiltration, with an ocular side-effect profile and visual outcomes. The systemic side effects of CAR T therapy may be managed medically.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241275247"},"PeriodicalIF":0.5,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11562240/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142648119","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 : 2024-08-31DOI: 10.1177/24741264241275285
Michael L Prairie, Shaina M Rubino, Peter H Tang
Purpose: To describe a case of lipemia retinalis, a rare ocular manifestation of hypertriglyceridemia that is characterized by a creamy-white to salmon-colored appearance to the fundus. Methods: A 55-year-old man was referred for an evaluation for diabetic retinopathy and was subsequently found to have marked lipemia retinalis. Results: The patient's triglyceride levels were 3141 mg/dL; therefore, treatment was initiated with high-intensity statin therapy and lifestyle modifications. At the 3-month follow-up, the patient had significantly reduced triglyceride levels (689 mg/dL) and full resolution of lipemia retinalis. Conclusions: Lipemia retinalis may be an initial finding of a severe systemic problem and a harbinger for more severe, and potentially fatal, consequences. Thus, a complete systemic assessment is warranted for any patient with signs of lipemia retinalis.
{"title":"Resolution of Lipemia Retinalis With Lifestyle Modification.","authors":"Michael L Prairie, Shaina M Rubino, Peter H Tang","doi":"10.1177/24741264241275285","DOIUrl":"10.1177/24741264241275285","url":null,"abstract":"<p><p><b>Purpose:</b> To describe a case of lipemia retinalis, a rare ocular manifestation of hypertriglyceridemia that is characterized by a creamy-white to salmon-colored appearance to the fundus. <b>Methods:</b> A 55-year-old man was referred for an evaluation for diabetic retinopathy and was subsequently found to have marked lipemia retinalis. <b>Results:</b> The patient's triglyceride levels were 3141 mg/dL; therefore, treatment was initiated with high-intensity statin therapy and lifestyle modifications. At the 3-month follow-up, the patient had significantly reduced triglyceride levels (689 mg/dL) and full resolution of lipemia retinalis. <b>Conclusions:</b> Lipemia retinalis may be an initial finding of a severe systemic problem and a harbinger for more severe, and potentially fatal, consequences. Thus, a complete systemic assessment is warranted for any patient with signs of lipemia retinalis.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241275285"},"PeriodicalIF":0.5,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11561956/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142648123","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 : 2024-08-31DOI: 10.1177/24741264241269479
Kyle B Thomson, Syed I Khalid, Naryan Sabherwal, Michael J Heiferman
Introduction: To explore the effect of cigarette smoking on the risk for developing diabetic macular edema (DME) among patients with diabetes. Methods: This retrospective exactly-matched cohort study used claims data for patients from all 50 states in the United States from 2010 through 2020. Patients with an initial diagnosis of diabetes were stratified into 3 cohorts as follows: active smokers, never smokers, and former smokers. After exact matching based on demographics and comorbidities, Kaplan-Meier survival functions for the 3 cohorts were compared using pairwise log-rank tests. Results: After matching, there were 42 298 patients in each cohort. Over 6 years of follow-up, the cumulative risk for DME was significantly higher among never smokers (1.18%) than among active smokers (0.88%) and former smokers (0.90%) (both P < .001). Conclusions: Among patients with diabetes, smoking may decrease the risk for developing DME. Although the harms of smoking far outweigh any potential protective benefits, further investigation into the mechanisms behind these findings has potential to uncover new therapeutic targets.
{"title":"Association Between Tobacco Smoking and the Development of Diabetic Macular Edema.","authors":"Kyle B Thomson, Syed I Khalid, Naryan Sabherwal, Michael J Heiferman","doi":"10.1177/24741264241269479","DOIUrl":"10.1177/24741264241269479","url":null,"abstract":"<p><p><b>Introduction:</b> To explore the effect of cigarette smoking on the risk for developing diabetic macular edema (DME) among patients with diabetes. <b>Methods:</b> This retrospective exactly-matched cohort study used claims data for patients from all 50 states in the United States from 2010 through 2020. Patients with an initial diagnosis of diabetes were stratified into 3 cohorts as follows: active smokers, never smokers, and former smokers. After exact matching based on demographics and comorbidities, Kaplan-Meier survival functions for the 3 cohorts were compared using pairwise log-rank tests. <b>Results:</b> After matching, there were 42 298 patients in each cohort. Over 6 years of follow-up, the cumulative risk for DME was significantly higher among never smokers (1.18%) than among active smokers (0.88%) and former smokers (0.90%) (both <i>P</i> < .001). <b>Conclusions:</b> Among patients with diabetes, smoking may decrease the risk for developing DME. Although the harms of smoking far outweigh any potential protective benefits, further investigation into the mechanisms behind these findings has potential to uncover new therapeutic targets.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241269479"},"PeriodicalIF":0.5,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11562456/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142647877","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 : 2024-08-31DOI: 10.1177/24741264241271649
Ali Khodor, Stephanie Choi, Tavish Nanda, Jonathan T Caranfa, Raul E Ruiz-Lozano, Shilpa H Desai, Michelle Liang, Caroline R Baumal, David C Reed, Tina S Cleary, Jeffrey S Heier, Chirag P Shah, Andre J Witkin
Purpose: To determine the efficacy of switching to intravitreal (IVT) faricimab in patients with treatment-resistant neovascular age-related macular degeneration (nAMD) and determine the rates of reversion to original antivascular endothelial growth factor (anti-VEGF) therapy. Methods: A retrospective chart review was performed of patients with nAMD and persistent fluid on optical coherence tomography previously treated with anti-VEGF injections who received at least 1 IVT faricimab injection between March 1, 2022, and January 31, 2023. Results: The study comprised 135 eyes of 119 patients. Before switching to IVT faricimab, the mean number of anti-VEGF injections in the previous 12 months was 10.7 ± 2.6 (SD) with a mean interval of 4.8 ± 1.3 weeks (range, 2-8). The mean follow-up was 11.6 ± 2 months. Thirty eyes (22.2%) switched to IVT faricimab returned to the original therapy. Of 105 eyes remaining on IVT faricimab, 66 (62.9%) had no fluid at the last follow-up. Compared with the original treatment, there was a significant improvement in logMAR visual acuity at the last follow-up in eyes on IVT faricimab (0.42 vs 0.38; P < .01) and in central subfield thickness (286 µm vs 246 µm; P < .0001). There was also a significant increase in the dosing interval after the third injection vs before IVT faricimab was prescribed (4.8 weeks vs 5.5 weeks; P < .001). Conclusions: Faricimab has a potent drying effect and potential for increasing the injection interval in many eyes with nAMD and persistent fluid on other anti-VEGF agents. Although nearly 25% of eyes reverted to the original therapy because of an insufficient response or adverse events, the majority did not achieve fluid resolution after reversion.
{"title":"Visual and Anatomic Responses in Patients With Neovascular Age-Related Macular Degeneration and a Suboptimal Response to Anti-VEGF Therapy Switched to Faricimab.","authors":"Ali Khodor, Stephanie Choi, Tavish Nanda, Jonathan T Caranfa, Raul E Ruiz-Lozano, Shilpa H Desai, Michelle Liang, Caroline R Baumal, David C Reed, Tina S Cleary, Jeffrey S Heier, Chirag P Shah, Andre J Witkin","doi":"10.1177/24741264241271649","DOIUrl":"10.1177/24741264241271649","url":null,"abstract":"<p><p><b>Purpose:</b> To determine the efficacy of switching to intravitreal (IVT) faricimab in patients with treatment-resistant neovascular age-related macular degeneration (nAMD) and determine the rates of reversion to original antivascular endothelial growth factor (anti-VEGF) therapy. <b>Methods:</b> A retrospective chart review was performed of patients with nAMD and persistent fluid on optical coherence tomography previously treated with anti-VEGF injections who received at least 1 IVT faricimab injection between March 1, 2022, and January 31, 2023. <b>Results:</b> The study comprised 135 eyes of 119 patients. Before switching to IVT faricimab, the mean number of anti-VEGF injections in the previous 12 months was 10.7 ± 2.6 (SD) with a mean interval of 4.8 ± 1.3 weeks (range, 2-8). The mean follow-up was 11.6 ± 2 months. Thirty eyes (22.2%) switched to IVT faricimab returned to the original therapy. Of 105 eyes remaining on IVT faricimab, 66 (62.9%) had no fluid at the last follow-up. Compared with the original treatment, there was a significant improvement in logMAR visual acuity at the last follow-up in eyes on IVT faricimab (0.42 vs 0.38; <i>P</i> < .01) and in central subfield thickness (286 µm vs 246 µm; <i>P</i> < .0001). There was also a significant increase in the dosing interval after the third injection vs before IVT faricimab was prescribed (4.8 weeks vs 5.5 weeks; <i>P</i> < .001). <b>Conclusions:</b> Faricimab has a potent drying effect and potential for increasing the injection interval in many eyes with nAMD and persistent fluid on other anti-VEGF agents. Although nearly 25% of eyes reverted to the original therapy because of an insufficient response or adverse events, the majority did not achieve fluid resolution after reversion.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264241271649"},"PeriodicalIF":0.5,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11562232/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142648155","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}