- •Foreword
- •Preface
- •Contents
- •Contributors
- •Acronyms
- •1.1 Introduction
- •1.2 Epidemiology
- •1.3 Risk Factors
- •1.3.1 Duration of Diabetes Mellitus
- •1.3.2 Glycemic Control
- •1.3.3 Hypertension
- •1.3.4 Ethnic Differences
- •1.3.5 Obesity
- •1.3.6 Socioeconomic Status
- •1.3.7 Other Risk Factors
- •1.4 Pathophysiology
- •Conclusion
- •References
- •2: Non-proliferative Diabetic Retinopathy
- •2.1 Clinical Overview
- •2.1.1 Clinical Findings
- •2.1.2 Classification of NPDR
- •2.1.3 Atypical Forms of NPDR
- •2.2 Diagnostic Tools
- •2.2.1 Telemedicine
- •2.2.2 Fundus Photography
- •2.2.3 Fluorescein Angiography
- •2.2.4 Ultrasonography
- •2.2.5 Optical Coherence Tomography
- •2.2.6 Adaptive Optics Scanning Laser Ophthalmoscope
- •2.2.7 Multifocal Electroretinogram
- •2.2.8 Pattern Visual Evoked Potentials
- •2.2.9 Other Diagnostic Tools
- •2.3 Present Therapies
- •2.3.1 Primary Interventions
- •2.3.1.1 Glycemic Control
- •2.3.1.2 Blood Pressure Control
- •2.3.1.3 Lipid-Lowering Therapy
- •2.3.2 Secondary Interventions
- •2.3.2.1 Protein Kinase C Inhibitors
- •2.4 Evolving Algorithms
- •2.4.1 Screening
- •2.4.2 Laser Photocoagulation
- •2.5 New Frontiers
- •References
- •3: Diabetic Macular Edema
- •3.1 Clinical Overview
- •3.1.1 Clinical Findings
- •3.1.2 Biomicroscopic Classification of DME
- •3.2 Diagnostic Tools
- •3.2.1 Fluorescein Angiography
- •3.2.2 Optical Coherence Tomography
- •3.2.3 Fundus Photography
- •3.2.4 Microperimetry
- •3.2.5 Multifocal Electroretinogram
- •3.2.6 Other Imaging Under Investigation
- •3.3 Present Therapies
- •3.3.1 Laser Photocoagulation
- •3.3.2 Intravitreal Pharmacotherapies
- •3.3.2.1 Intravitreal Steroids
- •3.3.2.2 Intravitreal Anti-VEGF
- •3.3.3 Pars Plana Vitrectomy
- •3.4 Evolving Algorithms
- •3.4.1 Therapeutic Algorithms
- •3.4.2 Factors Associated with Favorable Response to the Therapy
- •3.4.3 Treatment of DME Associated with Macular Ischemia
- •3.5 New Frontiers
- •References
- •4: Proliferative Diabetic Retinopathy
- •4.1 Clinical Overview
- •4.1.1 Clinical Findings
- •4.1.2 Classification of PDR
- •4.2 Diagnostic Tools
- •4.2.1 Fluorescein Angiography
- •4.2.2 Fundus Photography
- •4.2.3 Ultrasonography
- •4.2.4 Optical Coherence Tomography
- •4.2.5 Perimetry
- •4.2.6 Further Diagnostic Tools
- •4.3 Present Therapies
- •4.3.1 Panretinal Laser Photocoagulation
- •4.3.2 Intravitreal Injections
- •4.3.2.1 Intravitreal Steroids
- •4.3.2.2 Intravitreal Anti-VEGF Agents
- •4.4 Evolving Algorithms
- •4.5 New Frontiers
- •References
- •5.1 Introduction
- •5.2 Pathophysiology
- •5.3 Neovascular Glaucoma
- •5.4 Tractional Retinal Detachment
- •5.5 Treatment
- •5.5.1 Panretinal Laser Photocoagulation
- •5.5.2 Pars Plana Vitrectomy and Endophotocoagulation
- •5.5.4 Silicone Oil Tamponade
- •5.5.4.1 Viscodissection
- •Conclusion
- •References
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Metalloproteinases (MMPs) are modulators of inflammation and innate immunity involved in PDR and might be considered as a potential focus for the control of PDR [106]. Resveratrol, a polyphenol present in red wine, showed some activity in downregulating the levels of MMP-9 and protecting the retina from the ischemia [107].
An anti-angiogenic gene transfer of pigment epithelium-derived factor (PEDF) showed some benefits in the inhibition of NVE reducing the levels of MMP, VEGF, and connective tissue growth factor (CTGF) in an animal model of PDR [108].
Canakinumab is a novel monoclonal antibody against interleukin 1ß, which is currently used in rheumatic disorders. A pilot study evaluating the safety of 150 mg of canakinumab by subcutaneous injection in subjects affected by PDR is currently recruiting participants [109].
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Advanced Proliferative Diabetic |
5 |
Retinopathy |
Neelakshi Bhagat and Marco Attilo Zarbin
Contents
5.1 |
Introduction..................................................................................................................... |
164 |
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5.2 |
Pathophysiology.............................................................................................................. |
164 |
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5.3 |
Neovascular Glaucoma ................................................................................................... |
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5.4 |
Tractional Retinal Detachment ....................................................................................... |
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5.5 |
Treatment ........................................................................................................................ |
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5.5.1 |
Panretinal Laser Photocoagulation ..................................................................... |
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5.5.2 Pars Plana Vitrectomy and Endophotocoagulation ............................................ |
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5.5.3 |
Anti - VEGF Treatment ........................................................................................ |
168 |
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5.5.4 |
Silicone Oil Tamponade ..................................................................................... |
170 |
Conclusion |
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References.................................................................................................................... |
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N. Bhagat, MD, MPH, FACS
Institute of Ophthalmology and Visual Science, New Jersey Medical School, Rutgers University, Room 6156, Doctors OfÞce Center Suite 6100,
90 Bergen Street, Newark, NJ 07103, USA
e-mail: bhagatne@rutgers.edu, bhagatne@umdnj.edu
M.A. Zarbin, MD, PhD (*)
Institute of Ophthalmology and Visual Science, New Jersey Medical School, Rutgers University, Room 6156, Doctors OfÞce Center Suite 6100,
90 Bergen Street, Newark, NJ 07103, USA
Department of Ophthalmology, University Hospital,
Room 6156, Doctors OfÞce Center, 90 Bergen Street, Newark, NJ 07103, USA e-mail: zarbin@rutgers.edu, zarbin@earthlink.net
F. Bandello et al. (eds.), Clinical Strategies in the Management of Diabetic Retinopathy, |
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DOI 10.1007/978-3-642-54503-0_5, © Springer-Verlag Berlin Heidelberg 2014 |
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