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Handbook Of Vitreo-retinal Disorder Management: A Practical Reference Guide

Handbook Of Vitreo-retinal Disorder Management: A Practical Reference Guide

Park Susanna Soon-chun

(2015)

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Book Details

Abstract

This unique one-volume handbook provides a quick and concise reference guide for practising ophthalmologists, retinal specialists, vitreo-retinal fellows, ophthalmology residents and optometrists on the latest recommendations for managing common vitreo-retinal disorders seen in everyday retina practise. It provides comprehensive and essential information on diagnosis and management in outline and table format for conciseness and quick access. Color illustrations of important clinical manifestations are provided in an appendix.Dr Susanna Park is a Professor of ophthalmology and Director of Vitreo-retinal Fellowship and Ocular Oncology at the University of California Davis Eye Center. She has over 20 years clinical experience as a vitreo-retinal specialist and published over 100 journal papers and book chapters on the subject.

Table of Contents

Section Title Page Action Price
Contents xi
Preface v
Contributing Authors vii
Section 1: Diagnostic Testing 1
Chapter 1: Retinal Imaging 3
1. Optical Coherence Tomography (OCT) 3
2. Fluorescein Angiography (FA) 8
3. Indocyanine Green (ICG) Angiography 12
4. Fundus Autofluoresence (AF) 14
References 15
Chapter 2: Electroretinography 16
1. Electroretinogram (ERG) 16
2. Multifocal Electroretinogram 19
References 21
Chapter 3: Genetic Testing 22
1. Advantages of Genetic Testing 22
2. Limitations of Genetic Testing 22
3. American Academy of Ophthalmology Recommendations for Genetic Testing 22
4. Inherited Retinal Diseases (Refer to Section 4 for more details) 23
5. Ocular Tumors (Refer to Section 8 for more details) 26
Points to Remember about Genetic Testing 28
References 29
Section 2: Acquired Macular Disorders 31
Chapter 4: Age-related Macular Degeneration 33
1. Epidemiology of Age-related Macular Degeneration (AMD) 33
2. Initial Evaluation: Pertinent Details 33
3. Major Differential Diagnosis of NV-AMD 34
4. Diagnostic Testing 35
5. Management of Non-exudative ( dry) AMD 38
6. Management of Exudative AMD (NV-AMD) 38
7. Prognosis is Based on Severity of AMD 39
References 41
Chapter 5: Central Serous Chorioretinopathy 43
1. Epidemiology: Central Serous Chorioretinopathy (CSCR) 43
2. Initial Evaluation: Pertinent History 43
3. Presenting Signs and Symptoms 43
4. Clinical Findings 44
5. Differential Diagnosis for Intra Retinal or Sub Retinal Macular Fluid 44
6. Diagnostic Testing (Figure 1) 44
7. Management 46
8. Follow-up and Monitoring 48
9. Prognosis 48
References 49
Chapter 6: Epiretinal Membrane 50
1. Epidemiology of Epiretinal Membrane (ERM) 50
2. Pertinent Signs and Symptoms 50
3. Major Non-idiopathic Causes 51
4. Diagnostic Testing 51
5. Management 52
6. Follow-up and Monitoring 53
7. Prognosis for ERM 53
References 54
Chapter 7: Macular Holes 55
1. Epidemiology of Full-thickness Macular Hole (FTMH) 55
2. Signs and Symptoms 55
3. Major Differential Diagnosis 56
4. Diagnostic Testing 56
5. Management of Macular Hole 56
6. Follow-up and Monitoring 59
7. Prognosis after Vitrectomy for Macular Hole 59
References 60
Chapter 8: Toxic Maculopathy/Retinopathy 61
AMINOQUINOLINE ( CHLOROQUINE AND HYDROXYCHLOROQUINE) TOXICITY 61
1. Epidemiology 61
2. Indications for Chloroquine or Hydroxychloroquine Use 61
3. Risk Factors for Macular Toxicity 62
4. Clinical Signs and Symptoms 62
5. Differential Diagnosis for Bull’s Eye Maculopathy 63
6. Clinical Examination and Diagnostic Testing 63
7. 2011 Screening Guidelines and Management 65
8. Prognosis 65
PHENOTHIAZINE TOXICITY 66
1. Phenothiazine Subtypes 66
2. Indications for Phenothiazine Use 66
3. Risk Factor for Retinal Toxicity 66
4. Signs and Symptoms of Retinal Toxicity 66
5. Diagnostic Testing 66
6. Management 67
7. Prognosis and Follow-up 67
TAMOXIFEN TOXICITY 67
1. Indications for Tamoxifen Use 67
2. Risk Factors for Toxicity 67
3. Signs and Symptoms of Toxic Maculopathy from Tamoxifen 67
4. Major Differential Diagnosis for Toxic Crystalline Retinopathy 68
5. Diagnostic Tests 68
6. Management 69
7. Follow-up and Prognosis 69
References 70
Section 3: Retinal Vascular Disorder 71
Chapter 9: Proliferative Diabetic Retinopathy 73
1. Incidence of Proliferative Diabetic Retinopathy (PDR) 73
2. Clinical Features 73
3. Diagnostic Testing 75
4. Differential Diagnosis 76
5. Management 76
6. Follow-up Recommendations 79
References 80
Chapter 10: Diabetic Macular Edema 82
1. Incidence of Diabetic Macular Edema (DME) 82
2. Factors Associated with Severity of DME 82
3. Clinical Features of DME 82
4. Diagnostic Testing 83
5. Differential Diagnosis of DME 84
6. Management of DME 84
References 90
Chapter 11: Retinal Vein Occlusion 92
1. Incidence 92
2. Types 92
3. Risk Factors 92
4. Clinical Presentation 93
5. Differential Diagnosis 93
6. Evaluation and Diagnostic Testing 93
7. Prognosis 96
8. Management 96
References 99
Chapter 12: Retinal Artery Occlusion 100
Introduction 100
1. Incidence 100
2. Types Based on Location 100
3. Clinical Features 101
4. Clinical Findings 101
5. Differential Diagnosis 101
6. Diagnostic Testing 102
7. Management 102
8. Prognosis 103
References 104
Chapter 13: Ocular Ischemic Syndrome 105
1. Incidence 105
2. Clinical Features 105
3. Management 106
References 108
Chapter 14: Retinopathy of Prematurity 109
1. Incidence 109
2. Who and When to Screen 109
3. Staging 109
4. Follow-up Schedule 113
5. Differential Diagnosis 114
6. Photocoagulation 114
7. Controversy of Intravitreal Anti-Vascular Endothelial Growth Factor Treatment (VEGF) 114
8. Surgical Treatment 114
9. Common Late Sequelae of ROP 115
10. Telemedical ROP Screening 115
References 116
Section 4: Hereditary Retinal Degeneration 117
Chapter 15. Retinitis Pigmentosa 119
1. Incidence of Retinitis Pigmentosa (RP) 119
2. Inheritance Pattern of RP 119
3. Clinical Features 119
4. Diagnostic Testing 120
5. Clinical Course 121
6. Differential Diagnosis 121
7. Management 121
8. Rule out Retinal Degenerations Associated With Systemic Treatable Disease 122
References 126
Chapter 16. Hereditary Chorioretinal Dystrophies 127
Choroideremia 127
1. Incidence 127
2. Inheritance Pattern 127
3. Clinical Features 127
4. Diagnostic Testing 128
5. Clinical Course 129
6. Differential Diagnosis 129
7. Management 130
Gyrate Atrophy 130
1. Incidence 130
2. Inheritance Pattern 130
3. Clinical Features 130
4. Diagnostic Testing 130
5. Clinical Course 131
6. Differential Diagnosis 131
7. Diagnosis 131
8. Management 131
References 132
Chapter 17. Cone Dystrophy 133
Cone Dystrophy 133
1. Incidence 133
2. Inheritance Patterns 133
3. Clinical Features 133
4. Diagnostic Testing 134
5. Clinical Course 134
6. Differential Diagnosis 134
7. Management 134
References 135
Chapter 18. Hereditary Maculopathy 136
STARGARDT’S DISEASE 136
1. Incidence 136
2. Inheritance Pattern 136
3. Clinical Features 136
4. Diagnostic Testing 136
5. Clinical Course 138
6. Differential Diagnosis 138
BEST’S DISEASE 138
1. Inheritance Pattern 138
2. Clinical Features 138
3. Diagnostic Testing 139
4. Clinical Course 140
5. Differential Diagnosis 140
6. Management 140
PATTERN DYSTROPHY 140
1. Inheritance Pattern 140
2. Clinical Features 140
3. Diagnostic Testing 141
4. Clinical Course 141
5. Differential Diagnosis 141
6. Management 142
CENTRAL AREOLAR CHOROIDAL DYSTROPHY 142
1. Inheritance Pattern 142
2. Clinical Features 142
3. Clinical Course 142
4. Differential Diagnosis 143
5. Management 143
NORTH CAROLINA MACULAR DYSTROPHY 143
1. Inheritance Pattern 143
2. Clinical Features 143
3. Diagnositic Testing 143
4. Clinical Course 144
5. Differential Diagnosis 144
6. Management 144
References 145
Section 5: Posterior Uveitis 147
Chapter 19. Work Up and Management of Uveitis 149
1. Nomenclature of Uveitis 149
2. Epidemiology of Uveitis 151
3. Initial Evaluation 151
4. Anterior Uveitis 152
5. Intermediate Uveitis 153
6. Posterior Uveitis 154
7. Panuveitis 159
8. Differential Diagnosis of Posterior and Panuveitis — in a Nutshell 162
9. Treatment of Uveitis 163
10. Surgical Interventions in Uveitis 164
References 166
Chapter 20. Infectious Uveitis 167
Toxoplasmosis 167
Syphilis 171
Tuberculosis (TB) 173
Herpetic Viral Retinochoroiditis 174
Cytomegalovirus (CMV) 177
Presumed Ocular Histoplasmosis Syndrome (POHS) 179
Toxocara 180
References 182
Chapter 21. Endophthalmitis 183
Post-Surgical 183
Post-Traumatic Endophthalmitis 189
Endogenous Endophthalmitis 191
Surgical Considerations and Pearls 195
References 197
Section 6: Trauma 199
Chapter 22. Surgical Management of Posterior Segment Trauma 201
Indications for Urgent Vitreo-retinal Surgical Intervention: 201
1. Intraocular Foreign Body (IOFB) 201
2. Traumatic Endophthalmitis 202
3. Macula-Sparing Traumatic Retinal Detachment 204
4. Open Globe Repair 205
Indications for Non-urgent Vitreoretinal Surgical Intervention: 205
1. Macula-involving Traumatic Retinal Detachment (RD) 205
2. Suprachoroidal Detachment or Hemorrhage 206
3. Non-clearing vitreous hemorrhage 207
4. Traumatic Cataract or Lens Subluxation 208
References 209
Chapter 23. Non-surgical Management of Posterior Segment Trauma 211
1. Traumatic Maculopathy/ Commotio Retinae 211
2. Traumatic Choroidal Rupture 212
3. Chorioretinitis Sclopetaria 213
4. Purtscher’s Retinopathy 214
References 215
Section 7: Retinal Detachment 217
Chapter 24. Retinal Detachment and Proliferative Vitreoretinopathy 219
Risk Factors 219
Etiology 219
Differential Diagnosis 220
Initial Evaluation: History 221
Initial Evaluation: Exam 222
Special Considerations 237
References 240
Section 8: Oncology 243
Chapter 25. Current Treatment Options for Intraocular Retinoblastoma 245
1. Retinoblastoma Epidemiology 245
2. Overall Treatment Approaches 245
3. Classification System (Grouping) 245
4. Systemic Chemotherapy 247
5. Periocular Chemotherapy Injection 248
6. Selective Intra-Arterial Chemotherapy (IAC) 248
7. Intravitreal Chemotherapy (IVC) 249
8. Laser Therapy 250
9. Cryotherapy 251
10. Brachytherapy 252
11. External Beam Radiotherapy (EBR) 252
12. Proton or Particle Beam Irradiation 253
13. Enucleation 254
14. Treatment Overview 254
15. Genetic Testing 255
16. Post-treatment Surveillance 256
References 257
Chapter 26. Choroidal Nevus and Melanocytoma 258
CHOROIDAL NEVUS 258
1. Incidence 258
2. Clinical Features 258
3. Differential Diagnosis & Clinical features 258
4. Initial Evaluation 259
5. Risk of Malignant Transformation 261
6. Good Prognostic Clinical Features 261
7. Management and Follow-up of Nevus 261
8. Management of Non-malignant Complications 262
MELANOCYTOMA 262
1. Incidence 262
2. Clinical Features 262
3. Differential Diagnosis 264
4. Management 264
References 265
Chapter 27. Choroidal Melanoma 266
1. Incidence 266
2. Risk Factors for Ocular Melanoma 266
3. Clinical Features 266
4. Diagnostic Testing 268
5. Metastasis Screening: At Baseline and Every 6 to 12 Months 269
6. Management of Ocular Melanoma 270
7. Long-term Follow-up 271
8. Prognosis 271
9. Metastatic Disease: Prognosis and Treatment 272
References 273
Chapter 28. Choroidal Metastasis 274
1. Choroidal Metastasis 274
2. Clinical Signs and Symptoms 274
3. Diagnostic Testing 275
4. Treatment 277
5. Management and Follow-up 277
6. Prognosis 278
References 279
Appendix: Intravitreal Injections 281
1. Technique 281
2. Indications for Intravitreal Injections 282
3. Adverse Effects of Intravitreal Injection 285
List of Abbreviations 287
Index 291