- •Preface
- •Contents
- •1.1.1 The Vitreous
- •1.1.1.1 Embryology
- •1.1.1.2 The Anatomy
- •1.1.1.3 Anatomical Attachments of the Vitreous to the Surrounding Structures
- •1.1.2 The Retina
- •1.1.2.1 Embryology
- •1.1.2.2 Anatomy
- •Retinal Pigment Epithelium (RPE)
- •Photoreceptor Layer
- •Intermediary Neurones
- •Ganglion Cells
- •Retinal Blood Vessels
- •Other Fundal Structures
- •1.1.3 The Physiology of the Vitreous
- •1.2 Clinical Examination and Investigation
- •1.2.1 Using the Database
- •1.2.2 Examination of the Eye
- •1.2.2.1 Examination Technique
- •Visual Acuity
- •1.2.2.2 The Slit Lamp
- •1.2.2.3 Binocular Indirect Ophthalmoscope
- •1.2.2.4 Using the Indenter
- •1.2.2.5 Ultrasonography
- •Posterior Vitreous Detachment (PVD)
- •Retinal Tear
- •Retinal Detachment
- •Subretinal Haemorrhage
- •Retinoschisis
- •Choroidal Elevation
- •Trauma
- •1.2.2.6 Optical Coherence Tomography
- •Time-Domain OCT
- •Colour Coding
- •Frequency-Domain OCT
- •Full-Field OCT
- •Scan Resolution
- •Images and Measurements
- •Performing the Scan
- •Macular Scan Patterns
- •Central Retinal Thickness
- •Inner Segment and Outer Segment Junction and External Limiting Membrane
- •1.2.3 Subjective Tests
- •1.2.4 The Preoperative Assessment
- •1.3 Summary
- •References
- •2: Introduction to Vitreoretinal Surgery
- •2.1 Introduction
- •2.2 Choice of Anaesthesia
- •2.3 Pars Plana Vitrectomy
- •2.3.1 Sclerotomies
- •2.3.2 Where to Place the Sclerotomies
- •2.3.3 Securing the Infusion Cannula
- •2.3.4 Checking the Infusion
- •2.3.6 The Superior Sclerotomies
- •2.3.6.1 Where to Place
- •2.3.7 Checking the View
- •2.3.8 The Independent Viewing System
- •2.3.9 Removing the Vitreous
- •2.4 Vitrectomy Cutters
- •2.5 Handling the Light Pipe
- •2.6 Use of Sclerotomy Plugs
- •2.7 The Internal Search
- •2.8 Endolaser
- •2.9 Using a Contact Lens
- •2.10 Maintaining a View
- •2.10.1 Microscope
- •2.10.3 Cornea
- •2.10.4 Blood in the Anterior Chamber
- •2.10.5 Condensation on an Intraocular Lens Implant
- •2.10.6 Cataract Formation
- •2.10.7 Pupillary Dilation
- •2.11 Closing
- •2.12 Peroperative Complications
- •2.12.1 Iatrogenic Breaks
- •2.12.1.1 Causes
- •2.12.2 Choroidal Haemorrhage
- •2.12.3 Haemorrhage from Retinal or Other Blood Vessels
- •2.12.4 Lens Touch
- •2.12.5 Hypotony
- •2.13 Postoperative Complications
- •2.13.1 Cataract
- •2.13.2 Endophthalmitis
- •2.13.3 Corneal Changes
- •2.13.4 Choroidal Haemorrhage
- •2.13.5 Raised Intraocular Pressure
- •2.13.6 Retinal Breaks and RRD
- •2.13.7 Hypotony
- •2.13.8 Scleritis
- •2.13.9 Sympathetic Uveitis
- •2.14 Adjustments for 20 Gauge Vitrectomy
- •2.14.1 Construction of Superior Sclerotomies
- •2.14.2 Priming
- •2.14.3 Self-Sealing Sclerotomies
- •2.15 Adjustments for 23 and 25 Gauge Vitrectomy
- •2.15.1 Instrumentation
- •2.15.2 Surgical Technique
- •2.15.2.1 Vitrectomy Technique
- •2.15.3 Flexibility
- •2.15.4 Indentation
- •2.15.5 Flow Rates
- •2.15.6 Trochar Internal Protrusion
- •2.15.7 Silicone Oil
- •2.16 Complications
- •2.16.1 Peroperative
- •2.16.1.1 Extrusion of the Trochar on Removal of Instrumentation
- •2.16.1.2 Conjunctival Chemosis
- •2.16.1.3 Hypotony
- •2.16.1.4 Endophthalmitis
- •2.16.2 Postoperative Retinal Break Formation
- •2.17 Advantages and Disadvantages of 23 and 25 G Systems
- •2.18 Combined Cataract Extraction and PPV
- •2.18.1 How to Decide Whether to Perform Combined Surgery
- •2.18.1.1 Accommodation
- •2.19 Biometry
- •2.20 Chandelier Systems and Bimanual Surgery
- •2.20.1 Possible Complications
- •2.21 Dyes
- •2.22 Intravitreal Injections
- •2.22.1 Injection Medications
- •2.23 Slow Release Preparations
- •2.24 Summary
- •References
- •3: Principles of Internal Tamponade
- •3.1 Gases
- •3.1.1 Principles
- •3.1.1.1 Properties
- •3.1.1.2 A Safe Method for Drawing Up Gas
- •3.1.2 Complications
- •3.1.2.1 Vision
- •3.1.2.2 Refraction
- •3.1.2.3 Cataract
- •3.1.2.5 Loss of the Gas Bubble
- •3.1.2.6 Gas in the Wrong Place
- •3.1.3 Important Postoperative Information
- •3.1.3.1 Flying or Travel to High Altitude
- •3.1.3.2 General Anaesthesia
- •3.2 Silicone Oil
- •3.2.1 Properties
- •3.2.3 Complications of Silicone Oil
- •3.2.3.1 Refractive Changes
- •3.2.3.2 Cataract
- •3.2.3.5 Cornea
- •3.2.3.6 Macular Toxicity
- •3.2.3.7 Oil in the Wrong Place
- •3.2.3.8 Emulsion
- •3.2.3.9 IOLs
- •3.2.4 Silicone Oil Removal
- •3.2.4.1 Alternative Methods
- •3.2.4.2 Retinal Redetachment Rates After Oil Removal
- •3.2.5 Heavy Silicone Oils
- •3.2.6 Heavy Liquids
- •3.2.7 ‘Light’ Heavy Liquids
- •3.3 Summary
- •References
- •4: Posterior Vitreous Detachment
- •4.1 Introduction
- •4.1.1 Symptoms
- •4.1.1.1 Floaters
- •4.1.1.2 Flashes
- •Introduction
- •Clinical Characteristics
- •4.1.2 Signs
- •4.1.2.1 Detection of PVD
- •4.1.2.2 Shafer’s Sign
- •4.1.2.3 Vitreous Haemorrhage
- •4.1.2.4 Ophthalmoscopy
- •4.1.3 Retinal Tears
- •4.1.3.1 U Tears
- •4.1.3.2 Atrophic Round Holes
- •4.1.3.3 Other Breaks
- •4.1.3.4 Progression to Retinal Detachment
- •4.1.4 Peripheral Retinal Degenerations
- •4.2 Summary
- •References
- •5: Vitreous Haemorrhage
- •5.1 Introduction
- •5.2 Aetiology
- •5.3 Natural History
- •5.4 Erythroclastic Glaucoma
- •5.5 Investigation
- •5.6 Ultrasound
- •5.7 Management
- •5.8 Surgery
- •5.9 Vitrectomy
- •5.10 Summary
- •References
- •6: Rhegmatogenous Retinal Detachment
- •6.1 Introduction
- •6.1.1 Tears with Posterior Vitreous Detachment
- •6.1.2 Breaks Without Posterior Vitreous Detachment
- •6.1.3 Natural History
- •6.1.3.1 Chronic RRD
- •6.1.3.2 Risk to the Other Eye
- •6.2 Clinical Features
- •6.2.1 Anterior Segment Signs
- •6.2.2 Signs in the Vitreous
- •6.2.3 Subretinal Fluid Accumulation
- •6.2.4 Retinal Break Patterns in RRD
- •6.2.5 Macula Off or On
- •6.3 Surgery
- •6.3.1 Flat Retinal Breaks
- •6.3.1.1 Retinopexy
- •6.3.1.2 Cryotherapy
- •6.3.1.3 Cryotherapy in the Clinic Setting
- •6.3.1.4 Laser
- •6.3.1.5 Laser in the Clinic Setting
- •6.3.2 Retinal Detachment
- •6.3.2.1 Principles
- •6.3.2.2 Break Closure
- •6.3.2.3 Relief of Traction
- •6.3.2.4 Alteration of Fluid Currents
- •6.3.2.5 Retinopexy
- •6.3.3 Pars Plana Vitrectomy
- •6.3.3.1 Introduction
- •6.3.3.2 Finding the Breaks
- •6.3.3.4 Draining Subretinal Fluid
- •6.3.3.5 When to Use Heavy Liquids
- •6.3.3.6 Removal of Heavy Liquid
- •6.3.3.7 Choice of Tamponade
- •6.3.3.8 Avoiding Retinal Folds
- •6.3.3.9 Inferior Breaks
- •6.3.3.10 Posterior Breaks
- •6.3.3.11 Multiple Breaks
- •6.3.3.12 Medial Opacities
- •6.3.3.13 Complications
- •6.3.3.14 Surgery for Eyes with No Breaks Found
- •6.3.3.15 Use of 360° Laser or Routine 360° Encirclage
- •6.3.3.16 Posturing
- •6.3.4.1 Operative Stages
- •6.3.4.2 Postoperative Care
- •6.3.4.3 Complications
- •6.3.4.4 Peroperative
- •6.3.4.5 Postoperative
- •6.3.5 Drainage Air Cryotherapy and Explant (DACE)
- •6.3.5.1 Subretinal Fluid (SRF) Drainage
- •6.3.5.2 Air Insertion
- •6.3.5.3 Complications
- •6.3.6 Pneumatic Retinopexy
- •6.3.6.1 Surgical Steps
- •6.3.6.2 Complications
- •6.4 Success Rates
- •6.5 Causes of Failure
- •6.6 Surgery for Redetachment
- •6.7 Secondary Macular Holes
- •6.8 Detachment with Choroidal Effusions
- •6.9 Removal of Explant
- •6.9.1 Diplopia
- •6.9.2 Erosion Through Conjunctiva
- •6.9.3 Infection
- •6.9.4 Cosmesis
- •6.9.5 Irritation
- •6.9.6 Surgery for Removal of the Explant
- •6.10 Summary
- •References
- •7.2 Atrophic Hole RRD with Attached Vitreous
- •7.3 Pseudophakic RRD
- •7.4 Aphakic RRD
- •7.5 Retinal Dialysis
- •7.5.1 Clinical Features
- •7.5.2 Surgery for Retinal Dialysis
- •7.5.2.1 Search
- •7.5.2.2 Cryotherapy
- •7.5.2.3 Marking the Break
- •7.5.2.4 Plombage
- •7.5.2.5 Checking the Indent
- •7.5.3 Complications
- •7.5.4 Giant Retinal Dialysis
- •7.5.5 Dialysis and PVR
- •7.5.6 Par Ciliaris Tear
- •7.6 Giant Retinal Tear
- •7.6.1 Clinical Features
- •7.6.2 Stickler’s Syndrome
- •7.6.3 Surgery for Giant Retinal Tear
- •7.6.3.1 Heavy Liquids
- •7.6.3.2 Retinopexy
- •7.6.3.3 Trans-scleral Illumination Technique
- •7.6.3.4 Silicone Oil Insertion
- •7.6.3.5 Choice of Endotamponade
- •7.6.3.6 Success Rates
- •7.6.3.7 Removal of the Silicone Oil
- •7.6.3.8 The Other Eye
- •7.7 Retinal Detachment in High Myopes
- •7.7.1 Clinical Features
- •7.7.2 Surgery
- •7.8.1 Clinical Features
- •7.8.1.1 Infantile Retinoschisis
- •7.8.1.2 Senile Retinoschisis
- •7.8.1.4 Retinal Detachment in Retinoschisis
- •7.8.2 Surgery
- •7.9 Juvenile Retinal Detachment
- •7.10 Atopic Dermatitis
- •7.11 Refractive Surgery
- •7.12 Congenital Cataract
- •7.13 Others
- •7.14 Summary
- •References
- •8: Proliferative Vitreoretinopathy
- •8.1 Introduction
- •8.2 Pathogenesis
- •8.3 Clinical Features
- •8.3.1 Introduction
- •8.3.2 Grading
- •8.3.3 Risk of PVR
- •8.4 Surgery
- •8.4.1 Mild PVR
- •8.4.2 Moderate PVR
- •8.4.3 Severe PVR
- •8.4.3.1 The Relieving Retinectomy
- •8.4.4 Radial Retinotomy
- •8.4.5 Silicone Oil Injection
- •8.4.6 Applying Laser
- •8.4.7 ROSO Plus
- •8.4.8 Very Severe PVR
- •8.4.9 Choice of Endotamponade
- •8.4.9.1 Silicone Oil or Perfluoropropane Gas
- •8.4.9.2 Heavy Oils
- •8.4.10 Removal of Subretinal Bands
- •8.4.11 Adjunctive Therapies
- •8.4.12 Success Rates
- •8.4.13 Postoperative Complications
- •8.5 Summary
- •References
- •9: Macular Hole
- •9.1 Introduction
- •9.2 Idiopathic Macular Hole
- •9.2.1 Clinical Features
- •9.2.1.1 Introduction
- •9.2.1.2 Watzke–Allen Test
- •9.2.1.3 Grading
- •9.2.1.4 Natural History
- •9.2.1.5 Optical Coherence Tomography
- •9.2.2 Secondary Macular Holes
- •9.2.3 Lamellar and Partial Thickness Holes
- •9.2.4 Surgery
- •9.2.4.1 Introduction
- •9.2.4.2 Surgery
- •9.2.4.3 Peeling the Posterior Hyaloid Membrane
- •9.2.4.4 ILM Peel and Other Adjunctive Therapies
- •9.2.4.5 Choice of Tamponade
- •9.2.4.6 Postoperative Posturing of the Patient
- •9.2.4.9 Visual Field Loss
- •9.2.5 Success Rates
- •9.2.6 Reoperation
- •9.3 Microplasmin
- •9.4 Summary
- •References
- •10.1 Clinical Features
- •10.1.1 Other Conditions
- •10.1.2 Secondary Macular Pucker
- •10.2 Surgery
- •10.3 Success Rates
- •10.5 Membrane Recurrence
- •10.6 Summary
- •References
- •11: Choroidal Neovascular Membrane
- •11.1 Age-Related Macular Degeneration
- •11.1.1 Clinical Features
- •11.1.2 Vitreous Haemorrhage and CNV
- •11.1.3 Pneumatic Displacement of Subretinal Haemorrhage
- •11.1.4 Surgery for Failed Anti-VEGF Therapy
- •11.1.4.1 Introduction
- •11.1.4.2 360° Macular Translocation
- •11.1.6 Success Rates
- •11.2 Choroidal Neovascular Membrane Not from ARMD
- •11.2.1 Introduction
- •11.2.2 Surgery
- •11.3 Summary
- •References
- •12: Diabetic Retinopathy
- •12.1 Introduction
- •12.2 Diabetic Retinopathy
- •12.2.1 Introduction
- •12.2.1.1 Diabetic Retinopathy Grading
- •12.2.2 Diabetic Vitreous Haemorrhage
- •12.2.3 Progression to Vitreous Haemorrhage and Tractional Retinal Detachment
- •12.2.3.1 Clinical Features
- •12.2.3.2 Surgery
- •12.2.4 Diabetic Retinal Detachment
- •12.2.4.1 Clinical Features
- •12.2.4.2 Surgery
- •12.2.4.3 Tractional Retinal Detachment
- •12.2.4.4 Peroperative Panretinal Photocoagulation
- •12.2.4.6 Bimanual Surgery
- •12.2.4.7 Dealing with Bleeding Vessels
- •12.2.4.8 Iatrogenic Breaks
- •12.2.4.9 Silicone Oil
- •12.2.4.10 Combined TRD and RRD
- •12.2.5 Postoperative Complications
- •12.2.5.1 Vitreous Haemorrhage
- •12.2.5.2 Rhegmatogenous Retinal Detachment
- •12.2.5.3 Iris Neovascularisation
- •12.2.5.4 Phthisis Bulbi
- •12.2.5.5 Maculopathy
- •12.2.5.6 Survival After Surgery
- •12.2.6 Success Rates
- •12.2.7 Diabetic Maculopathy
- •References
- •13: Other Vascular Disorders
- •13.1 Introduction
- •13.2 Retinal Vein Occlusion
- •13.2.1 Chorioretinal Anastomosis
- •13.2.2 Arteriovenous Decompression
- •13.2.3 Radial Optic Neurotomy
- •13.2.4 Intravitreal Steroid and Anti-VEGF Agents
- •13.2.5 Tissue Plasminogen Activator
- •13.3 Sickle-Cell Disease
- •13.3.1 Introduction
- •13.3.2 Types of Sickle-Cell Disease
- •13.3.3 Systemic Investigation
- •13.3.4 Inheritance and Race
- •13.3.5 Systemic Manifestations
- •13.3.6 Ophthalmic Presentation
- •13.3.7 Laser Therapy
- •13.3.8 Surgery
- •13.3.9 Visual Outcome
- •13.3.10 Screening
- •13.3.11 Survival
- •13.4 Retinal Vasculitis
- •13.5 Central Retinal Artery Occlusion
- •13.6 Summary
- •References
- •14: Trauma
- •14.1 Introduction
- •14.3 Contusion Injuries
- •14.3.1 Clinical Presentation
- •14.3.2 Types of Retinal Break
- •14.3.2.1 Dialysis
- •14.3.2.2 Pars Ciliaris Tears
- •14.3.2.3 Ragged Tear in Commotio Retinae
- •14.3.2.4 Giant Retinal Tears
- •14.3.3 Surgery
- •14.3.4 Visual Outcome
- •14.4 Rupture
- •14.4.1 Clinical Presentation
- •14.4.2 Surgery
- •14.4.3 Visual Outcome
- •14.5 Penetrating Injury
- •14.5.1 Clinical Presentation
- •14.5.1.1 Endophthalmitis
- •14.5.1.2 Retinal Detachment
- •14.5.2 Surgery
- •14.5.3 Visual Outcome
- •14.6 Trauma Scores
- •14.7 Intraocular Foreign Bodies
- •14.7.1 Clinical Presentation
- •14.7.1.1 Diagnostic Imaging
- •14.7.2 IOFB Materials
- •14.7.3 Surgery
- •14.7.4 The Primary Procedure
- •14.7.5 PPV: The Anterior Segment
- •14.7.5.1 The Lens
- •14.7.6 PPV: The Posterior Segment
- •14.7.7 The Magnet
- •14.7.8 Visual Outcome
- •14.7.9 Siderosis
- •14.8 Perforating Injury
- •14.9 Sympathetic Ophthalmia
- •14.10 Proliferative Vitreoretinopathy
- •14.11 Phthisis Bulbi
- •14.12 When Not to Operate
- •14.12.1 At Presentation
- •14.12.2 Postoperatively
- •14.13 Summary
- •References
- •15.1 Introduction
- •15.2 Dropped Nucleus
- •15.2.1 Clinical Features
- •15.2.2 Surgery
- •15.2.2.1 Primary Management
- •15.2.2.2 Vitrectomy Surgery
- •15.2.2.4 Success Rates
- •15.3 Intraocular Lens Dislocations
- •15.3.1 Clinical Presentation
- •15.3.2 Surgery
- •15.3.2.1 Removal of the IOL
- •15.4 Surgical Options for the Aphakic Eye
- •15.4.1 McCannell Sutured IOL
- •15.4.2 Iris-Clip IOL
- •15.4.3 Haptic Capture Method
- •15.4.4 Anterior Chamber IOL
- •15.4.5 Sutured Posterior Chamber IOLs
- •15.4.6 The Aphakic and Aniridic Eye
- •15.5 Postoperative Endophthalmitis
- •15.5.1 Clinical Features
- •15.5.2 Surgery
- •15.5.2.1 Vitreous Tap
- •15.5.2.2 Vitreous Biopsy
- •15.5.3 Infective Organisms
- •15.5.4 Antibiotics
- •15.5.5 The Role of Vitrectomy
- •15.5.6 Success Rates
- •15.6 Chronic Postoperative Endophthalmitis
- •15.7 Needlestick Injury
- •15.7.1 Clinical Features
- •15.7.2 Surgery
- •15.8 Intraocular Haemorrhage
- •15.9 Retinal Detachment
- •15.10 Chronic Uveitis
- •15.11 Postoperative Cystoid Macular Oedema
- •15.12 Postoperative Vitreomacular Traction
- •15.13 Postoperative Choroidal Effusion
- •15.13.1 External Drainage
- •15.14 Summary
- •References
- •16: Uveitis and Allied Disorders
- •16.1 Introduction
- •16.2 Non-infectious Uveitis of the Posterior Segment
- •16.2.2 Retinal Detachment
- •16.2.3 Cystoid Macular Oedema
- •16.2.4 Hypotony
- •16.2.5 The Vitreous Biopsy
- •16.2.6 Sampling at the Beginning of a PPV
- •16.2.6.1 Special Situations
- •16.3 Acute Retinal Necrosis
- •16.3.1 Clinical Features
- •16.3.2 Surgery
- •16.3.2.1 For Diagnosis
- •16.3.2.2 For Treatment
- •16.3.3 Visual Outcome
- •16.4 Cytomegalovirus Retinitis
- •16.4.1 Clinical Features
- •16.4.2 Surgery
- •16.4.2.1 For Diagnosis
- •16.4.2.2 For Treatment
- •16.4.3 Visual Outcome
- •16.5 Fungal Endophthalmitis
- •16.5.1 Clinical Features
- •16.5.2 Surgery
- •16.5.2.1 For Diagnosis
- •16.5.2.2 For Treatment
- •16.5.3 Visual Outcome
- •16.6 Other Infections
- •16.6.1 Clinical Features
- •16.6.2 Surgery
- •16.6.2.1 For Diagnosis
- •16.6.2.2 Chorioretinal Biopsy
- •16.6.2.3 For Treatment
- •16.6.3 Visual Outcome and Survival
- •16.7 Paraneoplastic Retinopathy
- •16.8 Summary
- •References
- •17: Miscellaneous Conditions
- •17.1 Vitrectomy for Vitreous Opacities
- •17.2 Vitreous Anomalies
- •17.2.1 Persistent Hyperplastic Primary Vitreous
- •17.2.2 Asteroid Hyalosis
- •17.2.3 Amyloidosis
- •17.3 Retinal Haemangioma and Telangiectasia
- •17.4 Optic Disc Anomalies
- •17.4.1 Optic Disc Pits and Optic Disc Coloboma
- •17.4.2 Morning Glory Syndrome
- •17.5 Retinochoroidal Coloboma
- •17.6 Marfan’s Syndrome
- •17.7 Retinopathy of Prematurity
- •17.8 Uveal Effusion Syndrome
- •17.8.1 Clinical Features
- •17.8.2 Surgery
- •17.9 Terson’s Syndrome
- •17.10 Disseminated Intravascular Coagulation
- •17.11 Retinal Prosthesis
- •17.12 Summary
- •References
- •Glossary of Abbreviations
- •Others in Database
- •Appendices
- •Useful Formulae and Rules
- •Cryotherapy
- •Fluids (i.e. Both Gases and Liquids)
- •Gases
- •Liquids
- •Ultrasound
- •Diffusion and Viscosity
- •Visual Acuity
- •Diffusion
- •Fick’s Law
- •Stokes-Einstein
- •Darcy’s Law
- •Starling’s Law
- •Index
276 |
12 Diabetic Retinopathy |
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Fig. 12.18 Traction on the retina can create a retinal break as in this patient who has an avulsed blood vessel and an operculum on the nasal side of the disc overlying a retinal hole. Often as in this eye, progression to RRD does not occur; this may be due to the stiff, immobile vitreous in diabetes. The immobility of the vitreous prevents the creation of ßuid currents thought to be necessary for SRF to accumulate
Fig. 12.19 Unfortunately, despite the advantages in screening and in treatment by panretinal photocoagulation, patients still attend with very severe tractional retinal detachments as seen in this picture. The appearance can be deceptive with dissections easier than at Þrst apparent. As with all diabetic tractional retinal detachments, the key is determining the right layer and getting behind the posterior hyaloid, membrane and cortex. Elevation of cortex remnants in a vitreoschisis aids removal of the vitreous gel and reattachment of the retina
12.2.4 Diabetic Retinal Detachment
12.2.4.1 Clinical Features
As in other epiretinal membranes, Þbroblasts within the vascularised membranes contract, and the tangential traction so produced is stabilised and consolidated by collagen synthesis. The tangential traction results initially in folding of the inner retinal layers (internal limiting membrane and nerve Þbre layer) and can then progress to traction retinal detachment.
Contraction of the neovascular membranes both anteroposteriorly and tangentially combined with shrinkage of the vitreous gel pulls the retina at its points of adhesion into the centre of the eye. Without a retinal hole to allow accumulation of subretinal ßuid, the retina detaches with a concave conÞguration. Two forces are acting on the retina, one the action of the RPE to keep the retina ßat and two the action of the shrinking vitreous and neovascular membranes pulling the retina centrally into the vitreous cavity.
During this process, the vitreous cortex often splits, leaving a thin layer on the retina that can be elevated during surgery to allow easier dissection of the Þbrotic neovascular membranes (Schwatz et al. 1996; Chu et al. 1996). The vitreous detachment on the inner surface of the vitreoschisis is taut and stretches from the vitreous base to the neovascular membranes and between the membranes. The areas of detachment surround neovascularisation on the retinal arcades and are often multifocal. Eventually the macula detaches severely reducing the visual acuity, whilst the
Fig. 12.20 The membranes in diabetic TRD usually form over the retinal vasculature, the optic disc and temporal to the macula encircling the macula. However, membranes can be seen anywhere in the retina
periphery remains ßat. The extent of tractional retinal detachment (TRD) varies from a single focus to large areas of the retina. Similarly and more important to the surgeon, the areas of adhesion of the neovascular membrane to the retina vary, often being most pronounced on the vascular arcades and around the optic disc.
12.2 Diabetic Retinopathy |
277 |
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Fig. 12.24 See previous Þgure
Fig. 12.21 The fovea is just being elevated by the TRD in this patient as shown by the OCT image (see Fig. 12.22)
Traction on the disc can reduce vision by damaging the superÞcial nerve Þbres (Kroll et al. 1999); indeed, axons are found in tissue removed from the disc surgically (Pendergast et al. 1995).
Traction on the retina may split the retina causing retinoschisis (Pendergast et al. 1995).
Occasionally a hole appears in the fragile ischaemic retina, allowing subretinal ßuid accumulation. The retinal detachment then takes on a convex conÞguration and may extend further anteriorly in a bullous fashion. Application of panretinal photocoagulation to eyes with tractional retinal detachment can cause further contraction of the
Fig. 12.22 See previous Þgure membranes and macular detachment (Ghoraba 2002). Therefore, in patients with established TRDs but with no PRP, it is often safer to proceed to PPV rather than try PRP alone.
12.2.4.2 Surgery
Table 12.3 DifÞculty rating for diabetic tractional retinal detachment
DifÞculty rating |
High |
Success rates |
Moderate |
Complication rates |
High |
When to use in training |
Late |
Fig. 12.23 If you see asymmetrical disease, fellow eye (Fig. 12.24) check the eye with less retinopathy for a PVD or check the carotids for stenosis (the worse stenosis is on the same side as the eye with less retinopathy)
278 |
12 Diabetic Retinopathy |
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12.2.4.3 Tractional Retinal Detachment
Additional surgical steps
Remove vitreous haemorrhage as above but retain any traction on the retina.
Create holes in the posterior hyaloid to allow easy access to the areas of retinal elevation and vitreoretinal adhesion.
Detect and elevate the posterior layer of any vitreoschisis.
Dissect the tractional membranes off the retina. Complete the removal of the vitreous.
Apply panretinal photocoagulation.
Where signiÞcant neovascular membranes exist or retinal detachment is present dissection by delamination of any membranes is required. The membranes are best removed in total (Ôen blocÕ) to prevent future reproliferation and subsequent detachment (Kakehashi 2002; Williams et al. 1989; Abrams and Williams 1987). The core of the vitreous is removed whilst retaining the taut peripheral gel thereby maintaining traction upon the membrane. A hole is made in the cortical gel to allow access of instruments to the retinal surface. The outer portion of the vitreous cortex on the retinal surface is then elevated to Þnd the plane of cleavage of the internal limiting membrane and posterior hyaloid membrane. The posterior hyaloid and the neovascular membranes are then dissected away from the retina to relieve traction and allow the retina to reattach. Modern cutters especially small gauge have oriÞces which are nearer the tip end of the cutter shaft.
Note: In less complex TRD, the membranes can be trimmed down by these cutters effectively shaving down the membrane until the retina is cleared to membrane rather than using scissors to dissect off the membrane.
Elevating the cortical gel and posterior hyaloid which is still attached to the surface of the retina is the key manoeuvre of the operation. Having made the hole in the elevated vitreous cortex, use the edge of the scissors to run along the slope of an area of TRD. may catch the posterior hyaloid and see it lift both outwards towards the equator and towards the TRD. Elevate the PHM up to the edge of the TRD and then use the plane between this and the retina to elevate the membranes. Alternatively, the correct plane can sometimes be found by starting in the macular area and working outwards towards the arcades.
Note: The PHM very often ends in the peripheral retina and does not often extend to the vitreous base in severe TRD.
In this plane, the membranes will separate much more easily. Cutting through cortical gel is much more difÞcult and will leave membrane on the retina, allowing later
Fig. 12.25 The membranes can cause traction and damage on the optic nerve, reducing visual recovery postoperatively
Fig. 12.26 A combination of rhegmatogenous and tractional retinal detachment may occur. Particular problems exist when the patient has a rhegmatogenous element in addition producing PVR. Other indicators of relative poor prognosis are subretinal haemorrhage and iris neovascularisation
reproliferation. Some of the membrane will lift off, but sites of adhesion that will not lift must be cut. Keep your visualisation to a maximum by trimming any elevated membrane with the cutter whilst maintaining some anteroposterior traction on the TRD. As with any membrane, work around points of adhesion, lifting the membrane around a difÞcult site before tackling it. Usually I will elevate and PHM around the TRD 360¡, if I can, before dissecting the area of TRD itself. When lifting the PHM, lift close to the edge of the TRD and then move tangentially out to elevate the PHM in the periphery.
12.2 Diabetic Retinopathy |
279 |
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|
Fig. 12.27 Occasionally an eye in which neovascularisation has been stabilised by laser will have inactive membrane overlying the macula
Fig. 12.28 Despite only minimal PRP, these membranes are stable perhaps indicating a Ôburnt outÕ retinopathy
Fig. 12.29 Try to work along a ridge of adhesion (a, often along a large blood vessel) rather than across it because the scissors can straddle the ridge (b) and keep away from the retina, and any forces (arrows) are applied to the relatively strong blood vessel (F arrow). Going across the ridge risks the tips of the scissors incising the retina (c and d), and the forces are applied to the weak retina on the slope of the ridge
a
c
b
F
d
F
280 |
12 Diabetic Retinopathy |
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a
b
a
b
Fig. 12.30 When using the posterior hyaloid to lift a membrane (e.g. TRD membrane) to look for pegs at site (b), stay close to the edge of the membrane. Lifting further away from the membrane requires a vertical movement to avoid traction at point (a) to see the pegs. This will also put a force on pegs deeper under the membrane which you cannot see. If you stay close to the membrane edge, a tangential motion is possible without undue force at point (a) and only applying force to pegs at the edge of the membrane
Normal
Force required to tear the retina |
Force allowed to detach membranes |
Force required to tear the retina |
Force allowed to detach membranes |
Diabetic |
|
Fig. 12.31 The balancing act between pulling on an ERM and avoiding a retinal tear. In the normal eye, a large force is required before the retina tears, so that a relatively large force can be applied to pull off an ERM. In the ischaemic diabetic retina, a small force may tear the retina; therefore, only a small force can be applied to ERM to remove it
If using the PHM to lift the edge of the TRD, stay close to the TRD to achieve a large angle on the edge of the TRD without applying forces on the vitreous base.
Most TRDs are made up of peg attachments except: at the optic disc where a larger area of adhesion approximately ½ a disc area is seen. This will usually peel off the disc with some
Vitreous
Membrane
Retina
Fig. 12.32 It is important to dissect under the outer layer of a vitreoschisis which is easier than cutting through the vitreous to get to pegs of membranous attachment and avoids leaving vitreous on the retina
Fig. 12.33 The OCT of this patient shows the pegs of attachment between the membranes and the retina see 12.34.
cutting with scissors surprisingly easily though; be aware of the major blood vessels and vulnerability of the surface of the optic nerve head.
Where there is schitic retina, there can sometimes be a sheet of adhesion of the membrane to the retina.
Retinoschisis is an occasional feature in retina in TRD and is presumably due to splitting of the retina from traction. It may prevent ßattening of the retina at the end of the operation and application of laser. Often partial-thickness inner retinal holes are seen. Dissection of membrane is often difÞcult from the surface of the schitic area.
12.2 Diabetic Retinopathy |
281 |
|
|
Fig. 12.34 See previous Þgure
Fig. 12.35 TRDs are characterised by a triangular-shaped elevation of the retina with attachment to the vitreous. The vitreous is usually immobile in these patients
Entry holes
a |
b |
|
|
Area of posterior |
Pegs |
|
layer of vitreochisis |
Scissors
c |
d |
Fig. 12.36 Try to Þnd a route through the posterior hyaloid membrane to allow easy dissection of the membranes and insertion of your scissors underneath the posterior hyaloid membrane to aid dissection. These can be found conveniently in locations such as superotemporally or superonasally (a), so that you have access with right or left hand to the membranes or over the macula itself where it is possible to start centrally and work peripherally through the membranes (b). Once you have found your appropriate layer, 45o angle scissors can be used to dissect off the membrane from the retina. You must cut pegs of attachment of the membrane to the retina (c and d). Cutting, rather than pulling these apart, reduces bleeding and improves your postoperative re-bleed rate whilst minimising any chance of iatrogenic tears. Once you have made your access incisions in the posterior vitreous, work around the most severe membranes which are often on the arcades and disc, lifting the hyaloid around these sites, so that you can determine the most adherent foci before working down onto the most severe membranes themselves. Often these are found concentrated around blood vessels and the optic disc, but also can be found sporadically around the retina
282 |
12 Diabetic Retinopathy |
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a
Split in vitreous cortex
Retina
Subretinal space
b
Separation of vitreous from retina
Fig. 12.38 A peroperative picture shows a membrane which may tempt the surgeon into performing a dissection off only the anterior layer, but in fact, re-examination of the eye shows another layer indicated by the position of the scissors; a more posterior layer which is attached to the retina. This is the posterior hyaloid membrane and cortical remnants that make up the posterior leaf of the vitreoschisis. These must be elevated to Þnd the right plane for removal of the membranes
c
Separation of vitreous from retina
d
Fig. 12.37 (aÐd) Lift the vitreoschisis (a) on either side of the line of adhesion (b and c) before working along the line of adhesion (d) to detach the membrane
Fig. 12.39 Occasionally when dissections are difÞcult use bimanual surgery with illuminated forceps to hold membranes so that pegs can be seen and cut with scissors
Surgical Pearl of Wisdom
For diabetic tractional detachments: Sometimes it can be difÞcult (but necessary) to dissect and elevate midperipheral hyaloid in complex cases of diabetic tractional retinal detachments. Even when not necessary for visualisation, skilled scleral depression can be quite useful to relax the hyaloid and open a potential subhyaloid space. This can convert a challenging bimanual
