E. Souied, A. El Ameen, O. Semoun, A. Miere, G. Querques, S. Cohen
{"title":"Optical Coherence Tomography Angiography of Type 2 Neovascularization in Age-Related Macular Degeneration.","authors":"E. Souied, A. El Ameen, O. Semoun, A. Miere, G. Querques, S. Cohen","doi":"10.1159/000442777","DOIUrl":"https://doi.org/10.1159/000442777","url":null,"abstract":"Well-defined choroidal neovascularization, known as type 2 neovascularization (NV) or classic NV, is the least representative phenotype of exudative age-related macular degeneration. Clinical aspects of type 2 NV have been widely described in the literature, and to date fluorescein angiography remains the gold standard for imaging age-related macular degeneration at initial presentation. Optical coherence tomography angiography (OCT-A) can be used to image vessels based on flow characteristics without any dye injection. Type 2 NV can be visualized using OCT-A with very typical patterns. A neovascular membrane appears as either a medusa-shaped complex or a glomerulus-shaped lesion in the outer retina and the choriocapillaris layer. Furthermore, in the choriocapillaris layer, the external borders of the lesion appear as a dark ring in most cases, and one or more central feeder vessels that extend deeply into the more profound choroidal layers are visible. Identification of type 2 NV is easily feasible for any clinician using OCT-A, especially in areas where there are normally no vessels, like in subretinal space, if the interpretation rules are respected.","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"56 1","pages":"52-6"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000442777","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64987885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
B. Lumbroso, M. Rispoli, M. Savastano, Yali Jia, O. Tan, David Huang
{"title":"Optical Coherence Tomography Angiography Study of Choroidal Neovascularization Early Response after Treatment.","authors":"B. Lumbroso, M. Rispoli, M. Savastano, Yali Jia, O. Tan, David Huang","doi":"10.1159/000442782","DOIUrl":"https://doi.org/10.1159/000442782","url":null,"abstract":"AIMS Study the choroidal neovascularization (CNV) morphological evolution after treatment using optical coherence tomography angiography (OCTA). METHOD We used Optovue XR Avanti, with split-spectrum amplitude-decorrelation angiography algorithm. RESULTS OCT Angiography allows to recognize better the CNV type. In our series all our cases seem to follow a 45 to 60 days cycle, after intra vitreal injection. After each injection a pruning of smaller vessels is seen immediately (after 24 hours) that increases for 6 to 12 days when it reaches a maximum. It is followed by a reopening or new sprouting of the vessels 20 to 50 days later. The later cycles seem longer. Our results on early CNV evolution seem to confirm previous observations of CNV abnormalization and arterialization. Pruning the small peripheral branches seems to strengthen the trunk. In OCTA, closing terminal vessels (anti-VEGF effects) seems to cause an increased flow in trunk after the CNV reactivation.","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"56 1","pages":"77-85"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000442782","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64988296","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aniruddha Agarwal, Nithya Rajagopalan, Muhammad Hassan, Mohammad Ali Sadiq, Mohamed K Soliman, Rubbia Afridi, Yasir Jamal Sepah, Quan Dong Nguyen
{"title":"Sirolimus for Retinal and Uveitic Diseases.","authors":"Aniruddha Agarwal, Nithya Rajagopalan, Muhammad Hassan, Mohammad Ali Sadiq, Mohamed K Soliman, Rubbia Afridi, Yasir Jamal Sepah, Quan Dong Nguyen","doi":"10.1159/000438951","DOIUrl":"https://doi.org/10.1159/000438951","url":null,"abstract":"<p><p>Chronic inflammation plays an important role in the pathogenesis of ocular diseases such as diabetic retinopathy, uveitis and age-related macular degeneration. Activation and proliferation of naïve T cells may result in pathological changes responsible for significant visual morbidity. Sirolimus (earlier termed rapamycin) is a novel drug that inhibits cellular kinases and, thereby, inhibits T-cell proliferation. Preclinical studies in experimental models have shown promising results with the use of this pharmacological agent in various ocular conditions. Subsequently, early phase I/II studies have provided encouraging safety and efficacy data. This chapter focuses on the mechanisms of action, preclinical study results and data from human clinical trials of sirolimus in human eye diseases. Key highlights from ongoing phase III clinical trials are also provided. Sirolimus, thus, appears to be an important addition to the armamentarium of steroid-sparing therapeutic agents that act on various steps in the inflammatory pathway.</p>","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"55 ","pages":"276-81"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000438951","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34184509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jose R Maya, Mohammad Ali Sadiq, Aniruddha Agarwal, Peter K Kaiser, Glenn L Stoller, Yasir Jamal Sepah, Quan Dong Nguyen
{"title":"Future Perspectives: Agents on the Horizon.","authors":"Jose R Maya, Mohammad Ali Sadiq, Aniruddha Agarwal, Peter K Kaiser, Glenn L Stoller, Yasir Jamal Sepah, Quan Dong Nguyen","doi":"10.1159/000439037","DOIUrl":"https://doi.org/10.1159/000439037","url":null,"abstract":"<p><p>As demonstrated in the previous chapters of this textbook, retinal pharmacotherapeutics is a rapidly developing area. The enormous burden of disease in an aging population will hopefully be met by significant improvements in our understanding and treatment of disease processes such as age-related macular degeneration (AMD) and diabetic retinopathy. This chapter will provide perspectives on select anti-angiogenic drugs currently in development, as well as therapies directed against the complement cascade for the treatment of AMD, and an anti-inflammatory monoclonal antibody for the treatment of diabetic macular edema, among others, that have not been discussed elsewhere in this book. The mechanism of action of a number of drugs under discussion differs enough to have the potential to control neovascularization in several different ways, potentially allowing for more effective management of this process with fewer treatments.</p>","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"55 ","pages":"391-8"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000439037","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34185007","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
David Huang, Yali Jia, Simon S. Gao, B. Lumbroso, M. Rispoli
{"title":"Optical Coherence Tomography Angiography Using the Optovue Device.","authors":"David Huang, Yali Jia, Simon S. Gao, B. Lumbroso, M. Rispoli","doi":"10.1159/000442770","DOIUrl":"https://doi.org/10.1159/000442770","url":null,"abstract":"Optovue AngioVue system technology for optical coherence tomography (OCT) angiography is based on the AngioVue Imaging System (Optovue, Inc., Freemont, CA), using split-spectrum amplitude-decorrelation angiography (SSADA) algorithm. This algorithm was developed to minimize scanning time. It detects motion in blood vessel lumen by measuring the variation in reflected OCT signal amplitude between consecutive cross-sectional scans. The novelty of SSADA lies in how the OCT signal is processed to enhance flow detection and reject axial bulk motion noise. Specifically, the algorithm splits the OCT image into different spectral bands, thus increasing the number of usable image frames. Each new frame has a lower axial resolution that is less susceptible to axial eye motion caused by blood pulsation. Optovue AngioVue system technology allows quantitative analysis. It provides numerical data about flow area and non-flow area. It can also generate a flow density map. These metrics may serve as biomarkers in diagnosis and for tracking disease progression or treatment response. Flow area: the software will calculate the drawn area and vessel area in mm(2). It allows for comparison of all measurements for a given participant. Non-flow area: the software shows the non-perfused areas by mouse click selection. Ischemic areas will be shown in yellow. These areas may be saved and matched with others in the study. Flow density tool is able to measure the percentage of vascular areas on en face angiograms. This analysis is based on an ETDRS grid centered on the macula as with the thickness map. This tool works both on inner and outer vascular plexus.","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"56 1","pages":"6-12"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000442770","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64987671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
P. Stanga, E. Tsamis, A. Papayannis, Francesco Stringa, Tim Cole, A. Jalil
{"title":"Swept-Source Optical Coherence Tomography Angio™ (Topcon Corp, Japan): Technology Review.","authors":"P. Stanga, E. Tsamis, A. Papayannis, Francesco Stringa, Tim Cole, A. Jalil","doi":"10.1159/000442771","DOIUrl":"https://doi.org/10.1159/000442771","url":null,"abstract":"Optical coherence tomography (OCT) angiography (OCTA) is a novel, noninvasive, three-dimensional imaging technique that allows for the visualization of intravascular flow in the microvasculature. Swept-source OCT technology utilizes longer-wavelength infrared light than conventional spectral-domain OCT. This enables improved penetration into tissue and imaging through optical opacities and is invisible to the subject. Topcon has recently developed an innovative OCTA algorithm, OCTARA (OCTA Ratio Analysis), which benefits from being paired with swept-source OCT. OCTARA aims to provide improved detection sensitivity of low blood flow and reduced motion artifacts without compromising axial resolution. In this chapter, we describe the implementation of OCTARA with swept-source OCT technology, the technical specifications of acquisition (e.g. the number of scans, area of examination field, etc.) along with the algorithm's function and principles for analysis of B-scan data to achieve angiographic visualization. Examples of OCTA scans performed using the OCTARA algorithm and a comparison of these scans with images obtained using other technologies are also presented.","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"56 1","pages":"13-7"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000442771","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64987791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E. Souied, A. Miere, S. Cohen, O. Semoun, G. Querques
{"title":"Optical Coherence Tomography Angiography of Fibrosis in Age-Related Macular Degeneration.","authors":"E. Souied, A. Miere, S. Cohen, O. Semoun, G. Querques","doi":"10.1159/000442783","DOIUrl":"https://doi.org/10.1159/000442783","url":null,"abstract":"PURPOSE To describe the optical coherence tomography angiography (OCTA) features of subretinal fibrosis in the context of exudative age-related macular degeneration. METHODS Patients diagnosed exudative age-related macular degeneration presenting with subretinal fibrosis were imaged by conventional multimodal imaging and OCTA. The patients were divided into the following two groups: group A, for eyes with active exudative features over the last 6 months, and group B, for eyes without any sign of exudation for >6 months. RESULTS In almost all of the patients, a high-flow network was detected inside of the fibrotic scar. We divided the vascular networks into the following three patterns: the pruned vascular tree, tangled network and vascular loop patterns. Furthermore, two types of low-flow structures, for which we coined the terms large flow void and dark halo, were observed. Both active and inactive lesions demonstrated the abovementioned patterns either individually or together. No difference was found between the two groups in the prevalent vascular network pattern of low-flow areas. CONCLUSION OCTA of subretinal fibrosis revealed a perfused, abnormal vascular network, as well as collateral architectural changes in the outer retina and the choriocapillaris layer, in the majority of the studied eyes. These features are associated with both active and inactive fibrotic choroidal neovessels.","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"56 1","pages":"86-90"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000442783","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64988359","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
F. Bandello, Eleonora Corbelli, A. Carnevali, L. Pierro, G. Querques
{"title":"Optical Coherence Tomography Angiography of Diabetic Retinopathy.","authors":"F. Bandello, Eleonora Corbelli, A. Carnevali, L. Pierro, G. Querques","doi":"10.1159/000442801","DOIUrl":"https://doi.org/10.1159/000442801","url":null,"abstract":"PURPOSE To describe the optical coherence tomography angiography (OCTA) features of diabetic retinopathy. METHODS Literature review and case series. RESULTS Four cases are presented. CONCLUSION OCTA is an effective method for evaluating retinal changes in diabetic retinopathy and represents a novel complement or alternative to fluorescein angiography. Although OCTA should currently be considered an investigational technique, in the near future, it may play key roles in the diagnosis and management of diabetic retinopathy.","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"56 1","pages":"107-12"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000442801","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64989146","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Neuroprotection and Retinal Diseases.","authors":"Yannis M Paulus, J Peter Campbell","doi":"10.1159/000434703","DOIUrl":"https://doi.org/10.1159/000434703","url":null,"abstract":"Neuronal death is the primary cause of vision loss in most retinal diseases. Neuroprotection is the modification of neurons, and/or their surrounding environment, to promote the survival and function of the neurons, especially in environments that would normally be deleterious to their health. Through advances in antioxidative therapy, neurotrophic support and anti-apoptotic therapy, the field of neuroprotection is advancing with the therapeutic hope of improving vision and clinical outcomes for patients.","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"55 ","pages":"322-9"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000434703","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34117852","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Routes for Drug Delivery to the Retina: Topical, Transscleral, Suprachoroidal and Intravitreal Gas Phase Delivery.","authors":"Norihiro Yamada, Timothy W Olsen","doi":"10.1159/000431193","DOIUrl":"https://doi.org/10.1159/000431193","url":null,"abstract":"<p><p>Local drug delivery to the posterior segment, particularly the macula, represents a significant challenge. In this chapter, we review current challenges, barriers and limitations. Due to the local drug delivery to the retina and macula, systemic side effects are limited. In this chapter, we also discuss the historical approaches, key aspects of ideal drug delivery systems, the use of animal models to study pharmacokinetics, and the principles of transscleral, suprachoroidal and gas phase drug delivery.</p>","PeriodicalId":77107,"journal":{"name":"Developments in ophthalmology","volume":"55 ","pages":"71-83"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000431193","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34117923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}