Management of Vitreoretinal Interface Disorders · Management of Vitreoretinal Interface Disorders...

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1 Cole Eye Institute | Cleveland Clinic Cole Eye Institute | Cleveland Clinic Management of Vitreoretinal Interface Disorders Justis P. Ehlers, MD Assistant Professor Cole Eye Institute Cleveland Clinic Justis P. Ehlers, MD Assistant Professor Cole Eye Institute Cleveland Clinic Cole Eye Institute | Cleveland Clinic Cole Eye Institute | Cleveland Clinic Financial Disclosures Bioptigen (P) Synergetics (P) Thrombogenics (C,R,S) Genentech (R) Regeneron (S) Bioptigen (P) Synergetics (P) Thrombogenics (C,R,S) Genentech (R) Regeneron (S) Cole Eye Institute | Cleveland Clinic Cole Eye Institute | Cleveland Clinic Off-label Discussion Ocriplasmin (Jetrea) Indocyanine green Brilliant blue Zeiss RESCAN 700 Ocriplasmin (Jetrea) Indocyanine green Brilliant blue Zeiss RESCAN 700 Cole Eye Institute | Cleveland Clinic Cole Eye Institute | Cleveland Clinic Case Presentation 60 year old female: Decreased vision OS Moderate distortion OS Mild floaters OS No flashes All for several months VA: 20/50 60 year old female: Decreased vision OS Moderate distortion OS Mild floaters OS No flashes All for several months VA: 20/50

Transcript of Management of Vitreoretinal Interface Disorders · Management of Vitreoretinal Interface Disorders...

Page 1: Management of Vitreoretinal Interface Disorders · Management of Vitreoretinal Interface Disorders Justis P. Ehlers, MD Assistant Professor Cole Eye Institute Cleveland Clinic ...

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Management of Vitreoretinal

Interface Disorders

Justis P. Ehlers, MDAssistant ProfessorCole Eye InstituteCleveland Clinic

Justis P. Ehlers, MDAssistant ProfessorCole Eye InstituteCleveland Clinic

Cole Eye Institute | Cleveland ClinicCole Eye Institute | Cleveland Clinic

Financial Disclosures

● Bioptigen (P)

● Synergetics (P)

● Thrombogenics (C,R,S)

● Genentech (R)

● Regeneron (S)

● Bioptigen (P)

● Synergetics (P)

● Thrombogenics (C,R,S)

● Genentech (R)

● Regeneron (S)

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Off-label Discussion

● Ocriplasmin (Jetrea)

● Indocyanine green

● Brilliant blue

● Zeiss RESCAN 700

● Ocriplasmin (Jetrea)

● Indocyanine green

● Brilliant blue

● Zeiss RESCAN 700

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Case Presentation

● 60 year old female:

● Decreased vision OS

● Moderate distortion OS

● Mild floaters OS

● No flashes

● All for several months

● VA: 20/50

● 60 year old female:

● Decreased vision OS

● Moderate distortion OS

● Mild floaters OS

● No flashes

● All for several months

● VA: 20/50

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Diagnosis

Epiretinal MembraneEpiretinal Membrane

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Epiretinal Membrane

• Etiology

• Idiopathic

• Secondary– Uveitis

– Trauma

– Retinal breaks

– Intraocular surgery, part of the PVR spectrum

– Retinal vascular occlusions

– Others

• Etiology

• Idiopathic

• Secondary– Uveitis

– Trauma

– Retinal breaks

– Intraocular surgery, part of the PVR spectrum

– Retinal vascular occlusions

– Others

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Epiretinal Membrane

• Symptoms:– Asymptomatic

– Metamorphopsia

– Micropsia

– Monocular Diplopia

– Photopsia

– Reduced visual acuity (20/20 to 20/200)

• Symptoms:– Asymptomatic

– Metamorphopsia

– Micropsia

– Monocular Diplopia

– Photopsia

– Reduced visual acuity (20/20 to 20/200)

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Epiretinal Membrane

• Symptoms:– Appearance and visual acuity remain stable in

majority of patients

– 75% of patients maintain VA 20/50 or better

– Over 2 years 10-25% lose one or two lines of VA

• Symptoms:– Appearance and visual acuity remain stable in

majority of patients

– 75% of patients maintain VA 20/50 or better

– Over 2 years 10-25% lose one or two lines of VA

Epiretinal Membrane

• Diagnostic Testing– FA:

• Vascular tortuosity/straightening

• Leakage usually irregular and corresponds to area covered by the membrane

• Facilitates evaluation for concurrent disease

• Diagnostic Testing– FA:

• Vascular tortuosity/straightening

• Leakage usually irregular and corresponds to area covered by the membrane

• Facilitates evaluation for concurrent disease

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Epiretinal Membrane

• Diagnostic Testing– OCT:

• Hyperreflective preretinal band

• Cystic and/or noncystic thickening

• Irregular inner retinal surface consistent with retinal striae/folds

• Evaluate subretinal pathology and integrity of the ellipsoid zone

• Diagnostic Testing– OCT:

• Hyperreflective preretinal band

• Cystic and/or noncystic thickening

• Irregular inner retinal surface consistent with retinal striae/folds

• Evaluate subretinal pathology and integrity of the ellipsoid zone

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Epiretinal Membrane

Example of Noncystic Thickening

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Epiretinal Membrane

Example of Cystic Thickening

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Epiretinal Membrane

• Prognostic Factors– RPE disruption poor prognostic factor

– Long-standing leakage or cystoid edema may be poor prognostic factor

– Membranes following RD may have poorer prognosis

• Prognostic Factors– RPE disruption poor prognostic factor

– Long-standing leakage or cystoid edema may be poor prognostic factor

– Membranes following RD may have poorer prognosis

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Epiretinal Membrane

● Treatment

● Observation

● Pars plana vitrectomy with membrane peeling

● Consider for patients with VA < 20/40 or with other severe symptoms and VA > 20/40

● Treatment

● Observation

● Pars plana vitrectomy with membrane peeling

● Consider for patients with VA < 20/40 or with other severe symptoms and VA > 20/40

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Epiretinal Membrane

● Procedure:

● Pars plana vitrectomy

● Core vitrectomy performed, PVD induced if not present

● Chromovitrectomy may be used to highlight surgical anatomy:

● Indocyanine green (ICG), membrane blue, brilliant blue, triamcinolone, and others

● Differential staining (ERM vs ILM)

• Example: Negative staining ERM with ICG

● Procedure:

● Pars plana vitrectomy

● Core vitrectomy performed, PVD induced if not present

● Chromovitrectomy may be used to highlight surgical anatomy:

● Indocyanine green (ICG), membrane blue, brilliant blue, triamcinolone, and others

● Differential staining (ERM vs ILM)

• Example: Negative staining ERM with ICG

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Epiretinal Membrane

● Procedure● Forceps, membrane scraper, pick, or barbed MVR

blade can be used to elevate an edge from the retinal surface

● ERM peeled gently off the retinal surface, with close attention to removal over the fovea

● Consider ILM Peel:

● Simultaneous

● Sequential

● Reduces ERM recurrence, does not appear to change final visual outcome

● Consider image-assisted/guided surgery with intraoperative OCT (iOCT)

● Procedure● Forceps, membrane scraper, pick, or barbed MVR

blade can be used to elevate an edge from the retinal surface

● ERM peeled gently off the retinal surface, with close attention to removal over the fovea

● Consider ILM Peel:

● Simultaneous

● Sequential

● Reduces ERM recurrence, does not appear to change final visual outcome

● Consider image-assisted/guided surgery with intraoperative OCT (iOCT)

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iOCT and ERM: Exploring a new view

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iOCT and ERM: Exploring a new view

Zeiss RESCAN 700

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Epiretinal Membrane

● Surgical Complications:– Increased nuclear sclerosis

– Retinal tears occur in 1-6% of cases

– Retinal detachment is seen in 1-7%

– Visually significant recurrent ERMs occur in 5%

● Recent study suggested iOCT may change surgical decision-making in > 10% of cases (e.g., more peeling, completed surgical objectives).

● Surgical Complications:– Increased nuclear sclerosis

– Retinal tears occur in 1-6% of cases

– Retinal detachment is seen in 1-7%

– Visually significant recurrent ERMs occur in 5%

● Recent study suggested iOCT may change surgical decision-making in > 10% of cases (e.g., more peeling, completed surgical objectives).

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Epiretinal Membrane

● Recovery/Prognosis:

● Visual recovery takes months

● > 60% of patients improve 2 or more lines

● Many eyes have residual symptoms

● Metamorphopsia improved but typically not resolved

● Recovery/Prognosis:

● Visual recovery takes months

● > 60% of patients improve 2 or more lines

● Many eyes have residual symptoms

● Metamorphopsia improved but typically not resolved

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Case Presentation

● 55 year old male blurred VA OS for 6 months

● Main complaint is distortion

● VA 20/50

● Anterior exam is WNL

● Posterior exam as shown

● 55 year old male blurred VA OS for 6 months

● Main complaint is distortion

● VA 20/50

● Anterior exam is WNL

● Posterior exam as shown

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Case Presentation

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Diagnosis

Vitreomacular TractionVitreomacular Traction

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VMT Syndrome

• Diagnostic Tests

– FA:  May show leakage of fluorescein from vessels as well as optic nerve

– OCT:  Demonstrates vitreoretinal interface abnormalities.  Vitreous traction.  Cystic changes in the retina

• Clinical Course:

– Variable

– May be progresssive

– May spontaneously resolve

• Diagnostic Tests

– FA:  May show leakage of fluorescein from vessels as well as optic nerve

– OCT:  Demonstrates vitreoretinal interface abnormalities.  Vitreous traction.  Cystic changes in the retina

• Clinical Course:

– Variable

– May be progresssive

– May spontaneously resolve

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Progression ExamplesProgression Examples

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Progression Examples

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VMT

• Treatment:

– Observation

– Intravitreal ocriplasmin

– Pars plana vitrectomy with membrane peeling

– Elevate the posterior hyaloid

– Care to avoid unroofing foveal cyst

• Treatment:

– Observation

– Intravitreal ocriplasmin

– Pars plana vitrectomy with membrane peeling

– Elevate the posterior hyaloid

– Care to avoid unroofing foveal cyst

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Clinical Example 1

20/50 20/40

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Clinical Example 16 weeks later

20/5020/25

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Clinical Example 14 months later

20/2020/20

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Clinical Example 2

20/50

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Clinical Example 21 week later

20/50

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Clinical Example 24 months later

20/50

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Pharmacologic Vitreolysis

● Ocriplasmin (Jetrea, Thrombogenics)

● Approved in 2012 for the treatment of symptomatic vitremacular adhesion (e.g., VMT)

● Proteolytic enzyme with activity against proteins related to the vitreous and vitreoretinal interface (e.g., fibronectin, collagen, and laminin)

● Phase III studies included 464 eyes treated with ocriplasmin and 188 treated with vehicle

● Primary endpoint—resolution of VMA at 28 days

● 26.5% ocriplasmin vs 10.1% vehicle

● First pharmacologic alternative to surgical intervention for VMI condition

● Ocriplasmin (Jetrea, Thrombogenics)

● Approved in 2012 for the treatment of symptomatic vitremacular adhesion (e.g., VMT)

● Proteolytic enzyme with activity against proteins related to the vitreous and vitreoretinal interface (e.g., fibronectin, collagen, and laminin)

● Phase III studies included 464 eyes treated with ocriplasmin and 188 treated with vehicle

● Primary endpoint—resolution of VMA at 28 days

● 26.5% ocriplasmin vs 10.1% vehicle

● First pharmacologic alternative to surgical intervention for VMI condition

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Pharmacologic Vitreolysis

● Ocriplasmin (Jetrea, Thrombogenics)

● Patient selection and counseling critical.

● Advise of potential peri-injection symptoms:

• Blurred vision

• Photopsia

• Alterations in color vision

● Ocriplasmin (Jetrea, Thrombogenics)

● Patient selection and counseling critical.

● Advise of potential peri-injection symptoms:

• Blurred vision

• Photopsia

• Alterations in color vision

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Pharmacologic Vitreolysis

● Ocriplasmin (Jetrea, Thrombogenics)

● Advantages:

● Avoids concerns related to vitrectomy (e.g., anesthesia, increased nuclear sclerosis)

● Office-based procedure

● Potential predictors of response

● Lack of ERM

● Small adhesion width (<1500 microns)

● Phakic

● Age < 65

● Macular hole

● Ocriplasmin (Jetrea, Thrombogenics)

● Advantages:

● Avoids concerns related to vitrectomy (e.g., anesthesia, increased nuclear sclerosis)

● Office-based procedure

● Potential predictors of response

● Lack of ERM

● Small adhesion width (<1500 microns)

● Phakic

● Age < 65

● Macular hole

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Pharmacologic Vitreolysis

● Ocriplasmin (Jetrea, Thrombogenics)

● Possible safety concerns

● Dyschromatopsia

● ERG changes

● Vision changes

● Lens subluxation (animal studies)

● Retinal tear/retinal detachment (higher in vehicle group)

● Ocriplasmin (Jetrea, Thrombogenics)

● Possible safety concerns

● Dyschromatopsia

● ERG changes

● Vision changes

● Lens subluxation (animal studies)

● Retinal tear/retinal detachment (higher in vehicle group)

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Clinical Example 3

20/30

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Clinical Example 32 days later

20/200

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Clinical Example 32 days later

20/200

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Clinical Example 37 days later

20/80

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Clinical Example 31 month later

20/20

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Ocriplasmin: Cole Eye Initial Experience

• Nineteen eyes treated with ocriplasmin for symptomatic VMA

• 9/19 (47%) showed release

• Mean stability in vision

• No eyes lost > 2 lines at final follow-up

• Nineteen eyes treated with ocriplasmin for symptomatic VMA

• 9/19 (47%) showed release

• Mean stability in vision

• No eyes lost > 2 lines at final follow-up

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Ocriplasmin: Cole Eye Initial Experience

• Nineteen eyes treated with ocriplasmin for symptomatic VMA

• 10/19 (52%) showed ellipsoid zone attenuation

• Outer retinal thickness reduced significantly at 1 week but returned to baseline at 3 months.

• This reduction was related to changes in the ellipsoid changes

• Subretinal fluid accumulation was strongly associated with ellipsoid zone loss and symptomatic dyschromatopsia.

• Nineteen eyes treated with ocriplasmin for symptomatic VMA

• 10/19 (52%) showed ellipsoid zone attenuation

• Outer retinal thickness reduced significantly at 1 week but returned to baseline at 3 months.

• This reduction was related to changes in the ellipsoid changes

• Subretinal fluid accumulation was strongly associated with ellipsoid zone loss and symptomatic dyschromatopsia.

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Ocriplasmin: Cole Eye Initial Experience

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Ocriplasmin: Cole Eye Initial Experience

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VMT: Vitrectomy

● Procedure goal

● Release hyaloid traction

● Preserve inner retinal continuity

● Identify residual membranes

● Consider gas tamponade and ILM peeling

● Procedure goal

● Release hyaloid traction

● Preserve inner retinal continuity

● Identify residual membranes

● Consider gas tamponade and ILM peeling

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iOCT and VMT

● Immediate surgical feedback

● Release of traction

● Preservation of inner retinal wall

● Residual membrane

● New discoveries

● Increased subretinal hyporeflectivity

● Immediate surgical feedback

● Release of traction

● Preservation of inner retinal wall

● Residual membrane

● New discoveries

● Increased subretinal hyporeflectivity

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iOCT: Intraoperative Development of FTMHJPE20

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Case Presentation

● 60 y/o male with blindspot OS for 2 months

● VA 20/100 OS

● Anterior exam WNL

● Posterior exam as shown

● 60 y/o male with blindspot OS for 2 months

● VA 20/100 OS

● Anterior exam WNL

● Posterior exam as shown

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Case Presentation

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JPE20 Garbo for vitreous schisisVMT for butlerParsley for macula involving RDJustis P. EHlers, 10/16/2011

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Diagnosis

Primary Full-thickness Macular HolePrimary Full-thickness Macular Hole

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Primary Macular Hole

● Treatment options:

● Observation

● Ocriplasmin:

● Small holes with associated VMT

● Vitrectomy with gas tamponade

● Small holes: +/- ILM peeling

● Medium to large holes: ILM peeling

● Treatment options:

● Observation

● Ocriplasmin:

● Small holes with associated VMT

● Vitrectomy with gas tamponade

● Small holes: +/- ILM peeling

● Medium to large holes: ILM peeling

Primary Macular Hole

● Stage Zero: Configuration proposed in eyes at risk for macular hole development

● Fellow eyes with FTMH history

● At least one definitive perifoveal insertion of the posterior hyaloid

● Impending hole: Stage zero hole with associated VMT

● Stage Zero: Configuration proposed in eyes at risk for macular hole development

● Fellow eyes with FTMH history

● At least one definitive perifoveal insertion of the posterior hyaloid

● Impending hole: Stage zero hole with associated VMT

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Primary Macular Hole

• Vitreoretinal surgery:

• Core vitrectomy

• Elevate posterior hyaloid if not separated (may be sufficient with gas bubble for smaller holes)

• Consider internal limiting membrane peel

• May augment visualization with dyes or highlighting agents (e.g., ICG, triamcinolone) Circumferential peel around the hole, “maculorrhexis”

• Vitreoretinal surgery:

• Core vitrectomy

• Elevate posterior hyaloid if not separated (may be sufficient with gas bubble for smaller holes)

• Consider internal limiting membrane peel

• May augment visualization with dyes or highlighting agents (e.g., ICG, triamcinolone) Circumferential peel around the hole, “maculorrhexis”

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Primary Macular Hole

• Vitreoretinal surgery:

• Adjuncts used:

• ILM peeling

• Improves closure rates

• Dye‐assisted visualization

• Autologous serum

• Fibrinogen

• TGF‐beta

• Tamponade:  Air, SF6, C3F8, Silicone Oil

• Positioning:  Requirement and duration controversial

• Vitreoretinal surgery:

• Adjuncts used:

• ILM peeling

• Improves closure rates

• Dye‐assisted visualization

• Autologous serum

• Fibrinogen

• TGF‐beta

• Tamponade:  Air, SF6, C3F8, Silicone Oil

• Positioning:  Requirement and duration controversial

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Trans-tamponade OCT: Clinical Management

Postop Day 1

Postop Day 1

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Trans-Tamponade OCT Post-op Day 1

● Scan Classification Trans-Tamponade OCT

● Class 0: No image obtained

● Class 1: Tamponade/Retina Interface

● Class 2: TR Interface + RPE

● Class 3: Retinal architecture

● Class 4: Near-fluid filled quality

● Scan Classification Trans-Tamponade OCT

● Class 0: No image obtained

● Class 1: Tamponade/Retina Interface

● Class 2: TR Interface + RPE

● Class 3: Retinal architecture

● Class 4: Near-fluid filled quality

Class 1 Class 2

Class 4Class 3

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Trans-Tamponade OCT Case 1: Macular hole

Preop

Postop Day 1

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Trans-Tamponade OCT Case 2: Macular hole

Postop Day 1

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Trans-Tamponade OCT Case 3: Macular hole

Postop Hour 1

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Trans-Tamponade OCT Case 4: Macular hole

Postop Day 1

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Primary Macular Hole

• Surgical Complications

• Peripheral retinal breaks and rhegmatogenousretinal detachments

• RD occurs in approximately 2‐10% of cases

• Progression of nuclear sclerosis

• Others include endophthalmitis, increased IOP, progressive cataract

• Surgical Complications

• Peripheral retinal breaks and rhegmatogenousretinal detachments

• RD occurs in approximately 2‐10% of cases

• Progression of nuclear sclerosis

• Others include endophthalmitis, increased IOP, progressive cataract

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Other Macular Holes

● Lamellar Macular Hole

● Unique OCT features

● Partial thickness

● Surgical repair controversial

● Visual outcomes highly variable

● Management options

● Observation

● Vitrectomy with membrane peeling

• +/- ILM peeling and gas tamponade

● Lamellar Macular Hole

● Unique OCT features

● Partial thickness

● Surgical repair controversial

● Visual outcomes highly variable

● Management options

● Observation

● Vitrectomy with membrane peeling

• +/- ILM peeling and gas tamponade

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Clinical Example

20/200

30-50%“Thick”, “Dense” “LHEP”

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Clinical Example

20/200

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Clinical ExamplePost-op Week 1

20/60

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Clinical ExamplePost-op Month 3

20/30

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Other Macular Holes

● Traumatic Macular Hole

● May be associated with choroidal ruptures, subretinal hemorrhage

● Mechanism may be different:

● Direct foveal rupture

● Blunt trauma may result in retinal stretching, thinning and subsequent hole formation

● Direct vitreous traction during injury

● High rate of spontaneous hole closure.

● Traumatic Macular Hole

● May be associated with choroidal ruptures, subretinal hemorrhage

● Mechanism may be different:

● Direct foveal rupture

● Blunt trauma may result in retinal stretching, thinning and subsequent hole formation

● Direct vitreous traction during injury

● High rate of spontaneous hole closure.

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Thank you!Thank you!