The Diagnosis and Management of Corneal Dystrophies
Transcript of The Diagnosis and Management of Corneal Dystrophies
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The Diagnosis and Management of Corneal Dystrophies
Susan J. Gromacki, O.D., M.S., F.A.A.O., F.S.L.S.Diplomate
Cornea, Contact Lenses, and Refractive TechnologiesThe American Academy of Optometry
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The Diagnosis and Management of Corneal Dystrophies
Susan J. Gromacki, O.D., M.S., F.A.A.O., F.S.L.S.
Disclosures: AccuLens, Alcon, Alden, Allergan, Bausch + Lomb, Bioscience Communications, Blanchard, CIBA Vision, CooperVision, Danker, Focus Labs, Glaukos,
GPLI, Inspire, Johnson & Johnson, Osmotica/RVL, Pilkington Barnes-Hind, Sauflon, SLES, Sunsoft, SynergEyes, Valeant, Visionary Optics, Vistakon, Wesley-Jessen, and Westcon
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Corneal Dystrophy
•Bilateral
•Symmetric
•Centrally located
•Avascular
•Hereditary (autosomal dominant) and usually unrelated to systemic disease
•Early in onset
•Only slowly progressive
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Corneal Degeneration
• A deterioration or change in the corneal tissue, making it less functional
• Secondary to aging, trauma, inflammation, or systemic disease
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Corneal Degeneration
•Unilateral
•Asymmetric
•Peripheral or eccentric
•Vascularization
•No inheritance pattern or genetic predisposition
•Onset middle life or later
• Lesions are progressive
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Corneal Dystrophies
Newest Classification: IC3D (International Committee for Classification of Corneal Dystrophies) edition 2; Cornea 2015
•Epithelial and Subepithelial
•Epithelial-Stromal TGFBI (transforming growth factor beta induced)
•Stromal
•Endothelial
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Epithelial and SubepithelialDystrophies
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Epithelial Basement Membrane Dystrophy(EBMD)
•Most common anterior dystrophy
•Third + decade of life: maps, dots, and/or fingerprints
• Map-Dot-Fingerprint Dystrophy
• Anterior Basement Membrane Dystrophy (ABMD)
• Cogan’s Microcystic Corneal Dystrophy
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Epithelial Basement Membrane Dystrophy(EBMD)
•Visual loss usually minimal
•Treatment: early cases, AT;
•Debridement; debridement + amniotic membrane; Phototherapeutic Keratectomy (PTK)→ but can recur
• Later, tx recurrent corneal erosions (10%)
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Treating a Recurrent Corneal Erosion
• Acute: cyclopentolate or homatropine 2%; topical antibiotic qid. Bandage SCL if large
• Topical or oral anti-inflammatories (personal preference)
• After healed: AT 4-8X/day & AT ung qhs X 3mos+ or 5%NaCl gtt 4-8X/day & ung qhs
• If corneal epithelium loose: debridement
• If non-responsive: consider anterior stromal puncture, Phototherapeutic Keratectomy (PTK), or amniotic membrane
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Phototherapeutic keratectomy (PTK)
• Excimer laser sequentially ablates uniformly thin layers of anterior corneal tissue
• Similar to PRK but only approved by the FDA for:• Corneal dystrophies
• Irregular corneal surfaces
• Corneal scars and opacities
• May be performed in-office with topical anesthetic drops
• Removes anterior stromal opacities or eliminates elevated corneal lesions
• Creates a smooth stromal surface to improve postoperative corneal clarity, decrease existing scarring and facilitate epithelial adhesion
• Complications: refractive errors (most commonly hyperopia) corneal scarring, and glare
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PTK for Corneal Dystrophies
• Less aggressive and faster visual rehabilitation than PKP
• If stromal deposits, laser ablation may result in an irregular surface• Deposits may be ablated at different rate than normal
stroma• Corneal surface not smooth prior to ablation
• AT should be used prior to procedure to help by pooling in the valleys
•May remove superficial opacities and leave deeper ones→ delay corneal transplantation
• If attempt deep stromal ablation, higher chance of permanent haze
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Meesman Dystrophy (Juvenile Hereditary Epithelial Dystrophy)
•Clear vesicles interpalpebral -> fine lines t/o cornea
• “Peculiar Substance”
•Visual loss usually minimal
•Tx: recurrent corneal erosions
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Epithelial-Stromal TGFBI Dystrophies
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Reis-Bucklers Dystrophy
• Bluish-white ring-shaped opacities
• Fishnet or honeycomb appearance
• Painful recurrent corneal erosions (3-4X/year)
• 4th decade: replacement of Bowman layer by scar tissue
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Reis-Bucklers Dystrophy
• Tx: RCE; irregular astigmatism: GP CL,
PTK, Penetrating
Keratoplasty
(“PKP” or “PK”)
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Corneal TransplantationManagement Strategies:
• Indications: • When all non-surgical options have
been exhausted
• Patient vision still poor
• Selecting a surgeon: • Experience and reputation
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Penetrating Keratoplasty (PKP)
•Full-thickness corneal transplant
•Excellent visual outcomes
•Most common complication is astigmatism (30% specs, 47% CL)
•Rejection rate 8-39%• Most often due to the endothelial
layer being replaced
•Do not last forever!Joslin C, Wilson B, Barr JT, et al. Clinical Outcomes in
Keratoconus Following Penetrating Keratoplasty. Optometry
and Vision Science Supplement, December 2003: 221.
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Deep Anterior Lamellar Keratoplasty (DALK)
•Partial-thickness cornea transplant that involves selective transplantation of the corneal stroma, leaving the patient’s Descemet membrane and endothelium in place
•Trephinate the host cornea to a depth of 90%
• Inject fluid or air to separate layers
•Remove patient stroma
•Remove donor Descemet and endothelium and trephinate
•Place donor tissue in bed and suture into place
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DALK (compared with PKP)
Advantages:
•*Endothelium maintained• Need a healthy, functioning
endothelium prior to the procedure
• Decreased risk of endothelial rejection
•No “open sky”
•Prev. inferior visual outcomes d/t interface, now equal
Disadvantages:
•Technically more demanding and time consuming• If Descemet perforates, convert to PKP
(9-14%)
•Epithelial rejection 2-15%, Stromal rejection 1-2%, Infection 0.8%, similar astigmatism
•More opacification at the interface layers
Macintyre R, Chow SJ, Chan E et al. Long-term outcomes of deep anterior lamellar keratoplasty versus
penetrating keratoplasty in Australian keratoconus patients. Cornea. 2014 Jan; 33(1): 6-9.
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Granular Dystrophy Type 1
•White opacities in superficial stroma of central cornea
• 7th-8th decade: opacities enlarge, coalesce and deepen
•Hyaline
•Good VA since stroma b/w lesions remains clear
• Tx: RCE; irregular astigmatism: GP CL, PTK, PKP (recur)
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62 yo wf, Judge
•Granular Type 1 Dystrophy
•PKP→ dystrophy recurred
•20/60, 20/70 specs
• Irregular astigmatism
•Oblate corneal shape after transplant
•Poor comfort and retention with corneal GP lens
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Solution:
• Scleral GP lenses OU
• Rigid surface provides a new refracting surface and excellent optics
• Lens vaults the cornea, protecting the lesions
• Tear reservoir underneath the lens fills in imperfections of the cornea• Corrects irregular astigmatism• Use a non-preserved artificial tear for this purpose to provide extra
lubrication
• Lens rests on the conjunctiva/sclera to provide excellent centration• Excellent retention
• Excellent comfort
• VA 20/25, 20/30
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Lattice Dystrophy
• Refractile lines, anterior-to-mid-stromal dots and faint central haze, subepithelial round opacities
• Stroma b/w remains clear until later in life
• Amyloid
• 6-7 different mutations (“types”)
• Tx: RCE; irregular astigmatism: GP CL, PTK (some), DALK or PKP (recur)
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Granular Dystrophy Type 2(formerly Avellino Dystrophy)
• Granular (early onset) and lattice (later) changes in same eye
• Hyaline and amyloid
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Stromal Dystrophies
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Macular Dystrophy
•Diffuse, grayish-white spots in central portion of anterior stroma→ 3rd
decade: extends to endothelium and limbus→ Descemet membrane opacified and endothelial guttata
•Mucopolysaccaride
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Macular Dystrophy
•Autosomal recessive
•Severe vision loss
•Tx: RCE (infrequent), irregular astigmatism: GP CL, PKP• Lamellar not indicated
since leaves damaged endothelium→ recurrence
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Schnyder (Crystalline) Corneal Dystrophy
•Round, oval, discoid, or annular central opacity composed of needle-shaped crystals, sometimes with arcus and limbal girdle
•Cholesterol
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Schnyder (Crystalline) Corneal Dystrophy
•AD- also assoc. with systemic disorder: hyperlipidemia
•Vision remains good despite appearance
•Tx: rare (PTK, PKP)
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Fleck Dystrophy
•Small, discrete, dandruff-like specs in the stroma that extend to the periphery
•VA good
•Tx: none
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Endothelial Dystrophies
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Congenital Hereditary Endothelial Dystrophy (CHED)
• Least common endo. dystrophy• No longer CHED 1 (too rare) and
CHED 2
• Epithelial and stromal edema t/o cornea
• Defective formation of the endothelium in utero
• AD (1st few years of life) or AR (at birth, nystagmus)
• Tx: hypertonic agents, hair dryer (dehydrates the cornea), PKP (d/t stromal “ground glass opacification”)
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Posterior Polymorphous Dystrophy
• 2018: localized the variation to the DNA on gene GRHL2• Genome sequencing using
a large family from the Czech Republic
• 2-20 vesicles surrounded by a diffuse gray halo
• Collagen
• Severe cases: stromal and epithelial edema
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Posterior Polymorphous Dystrophy
•VA normal in most patients
•Tx: hypertonic agents, hair dryer
•Surgical intervention dictated by amount of corneal edema
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Evolution of Corneal Transplantation for Endothelial Dystrophies
• 10 yrs ago PKP→ DSEK/DSAEK→ DMEK today
• DSEK=Descemet stripping endothelial keratoplasty
• DSAEK=Descemet stripping automated endothelial keratoplasty• “A”= automated
• Uses microkeratome to cut the tissue
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DMEK=Descemet membrane endothelial keratoplasty •Vs. PKP: decreased likelihood of graft rejection, less
induced astig, and avoids potential suture removal
•Vs. DSAEK: eliminates the stromal carrier used→results in lower higher order aberrations and faster visual recovery
•Thinner, so more difficult to perform, resulting in complications if not performed correctly (graft loss during preparation, rebubbling, and endothelial cell loss)
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DMEK Tissue
•Several eye banks throughout the US process the tissue, facilitating the procedure
•Available to any US surgeon
• “Pre-loaded” or “patient ready” tissue:• Eye bank strips the donor tissue, stains it, cuts it to size
and even loads it into the injector• Ships to surgeon in nutrient solution
•Surgeon does not have to prepare the tissue in the operating room• Takes the risk out of the surgeon damaging the tissue
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Contact Lens Spectrum, Volume: 29, Issue: August 2014, page(s): 36-38, 40, 42
Normal Cornea
Full thickness PKP
DALK
DSAEK
DMEK
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Fuchs Dystrophy
•Most common corneal dx in the US, 4% over age 40
•Rare prior to age 50
•Symptoms: glare and blurred vision, worse upon awakening
•Risk factors:• European descent• Female (3X male)• Smoking• Diabetes• Exposure to UV light
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Fuchs Dystrophy
• Pigment dusting and guttata
• Can lead to focal excrescences of Descemet m.-> stromal and epithelial edema-> large epithelial bullae (rupture: severe pain)
• Collagen (thin layer DM, early onset cases)
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Fuchs Dystrophy
•Very slowly progressing
•RTC q 3 (if edema causing increased IOP) to 12 mos.
•Tx: hypertonic agents, hair dryer, antiglaucoma gtt, BCL, PKP→DSEK/DSAEK→DMEK
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Graft Rejection Classification*
Definite:
• Mild:• 1 to 5 keratic precipitates (KPs: collections of inflammatory cells on the
endothelium)
• Increase in cells within the aqueous
• Less than a 10% increase in total corneal thickness ultrasonically compared with previous visit
*Corneal Preservation Time Study (CPTS)
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Graft Rejection Classification*
Definite:
•Severe:• >5 KPs • Cells in the stroma• >10% increase in total corneal thickness ultrasonically
compared with previous visit• Clinically apparent decrease in stromal clarity• Endothelial rejection line• OR increased corneal thickness >10% from previous visit
AND increased aqueous cells
*Corneal Preservation Time Study (CPTS)
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Graft Rejection Classification*
Possible/Probable:
• In a previously clear graft, clinically apparent stromal edema affecting stromal clarity with inflammation (KP, aqueous cells, ciliary injection) without an endothelial rejection line
•OR possible presence of a new KP with difficulty distinguishing between KP and pigment
*Corneal Preservation Time Study (CPTS)
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New Development for Corneal Dystrophy Diagnosis:AvaGen (Avellino Labs)
• 1st commercially available genetic diagnostic test of its kind for keratoconus and corneal dystrophies
• Next generation sequencing (NGS) technology: examines over 1,000 variants across 75 genes for keratoconus and over 70 mutations of the TGFBI gene for corneal dystrophies
• In-office cheek swab
• Initial launch Oct. 2019; nationwide launch mid-2021
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Traditional Methods of Detecting Corneal Abnormalities:
• Slit lamp microscopy: 1910
• Genetic sequencing: 2020 and beyond
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USING GENETIC TESTING TO IDENTIFY PATIENTS AT RISK
Avagen Testing Protocol:
EXTRACTION SEQUENCING
REFERENCING &
VARIANT RISK
SCORES
PATIENT
REPORT