Cornea Flashcards
(29 cards)
Four quantitative videokeratographic indices for screening keratoconic patients
- central corneal power >47.2 D
- inferior-superior dioptric asymmetry >1.2 D
- Sim-K astigmatism >1.5 D
- skewed radial axes >21°
Why is immune status important when treating HSV/HZV?
Valacyclovir, a pro-drug of acyclovir, can cause TTP/HUS in severely immuno-compromised patients such as those with AIDS; thus, it must be used with caution if the immune status is unknown.
Minimum normal inferior forniceal depth
> 8 mm
Define keratomalacia
softening and necrosis of the cornea associated with vitamin A deficiency.
Ddx of peripheral K ulcers
- Mooren’s
- staph marginal
- terrien’s
- PUK
- Fuchs superficial marginal keratitis
- HSV epithelial keratitis
Bacteria that can penetrate intact epithelium
“No Hard or Soft Contact Lenses”
Neisseria (both types), haemophilus aegypti, shigella, corynebacterium, listeria
Types of HSV keratitis and treatment
Primary:
1. Unilateral blepahroconjunctivitis (bilateral in kids, immunosuppressed, atopes) – self limited, but can use po antivirals
Recurrent
- Epithelial keratitis (dendritic, geographic): po or topical antiviral +/- debridement
- Stromal keratitis s ulceration- prophylactic dose po antiviral, topical steroid
- Stromal keratitis c ulceration-tx dose po antiviral, topical steroid
- Endothelial (Disciform) keratitis- tx dose po antiviral, topical steroid
HEDS Study Conclusions
- topical steroids effective in stromal keratitis when combined c trifluridine prophylaxis
- oral ACV provides no addt’l benefit in pts with stromal keratitis tx c topical steroids and trifluridine
- study terminated early, but trend toward benefit of oral ACV in HSV Iridocyclitis
- in epi keratitis tx’ed c trifluridine, oral ACV provides no addt’l benefit in dec risk of stromal keratitis or iritis
- oral ACV dec risk of recurrent heretic dz esp in pts with stromal dz
- H/o epi keratitis not a RF for recurrent epi dz, but stromal keratitis inc risk of recurrent stromal keratitis
Filamentous fungi
Aka molds –> form hyphae
Septate: aspergillus, curvularia, fusarium, penicillium, phialophora, paecilomyces
Non-septate: mucor
RF: trauma c vegetable matter, scl wear
Yeasts
Aka non-filamentous and don’t form hyphae
Candida
Cryptococcus
RFs: scl wear, topical steroids, PED, immunocompromise
Dimorphic fungi
Non-filamentous –> no hyphae
Histoplasma
Blastomyces
Coccidioides
Post refractive sx historic method for IOL calls
Ave preoperative Ks
Calculate SE for pre nd postoperative mrx
Add/subt to ave preoperative k depending on whether LASIK was myopic or hyperopia (see OQ #6, 1/28)
Axis of greatest astigmatism in pellucid
180 (nasal/temp thinning lead to ATR cyl –> crab claw)
Gene defect in Schnyder’s dystrophy
UbiA prenyltransferase domain-containing protein 1 (UBIAD1)
Ts of Terrien’s
T: Thinning of the cornea
T: Top (superior)
T: Traversing pannus over area of thinning
T: Thirties
T: Can take Turns (mostly unilateral but can be bilateral)
T: Treatment: Transplantation (cresent shaped lamellar) if perforation occurs
Corneal side FX of topical NSAIDs
MELT and also PEE
K thickness above which endothelial cell damage is likely
640 microns
Protein defect in Reis-Buckler
Keratoepithelin
DDX acute and chronic follicular conjunctivitis
Acute: Adeno hardly happens to careful nuns
Adeno, HSV, hemorrhagic, chlamydia, Newcastle (Neisseria?– not according to Friedman #8)
Chronic: Passing tough tests means mostly late cramming
Parinauds, trachoma, toxic, molluscum, moraxella, Lyme, chlamydia
DDX verticillata
Amiodarone, indomethacin, chloroquine, chlorpromazine
Fabrys
Eye findings in Fabry’s
Vortex keratopathy
Tortuous/telangiectasia vessels of conj AND retina
Granular lens opacities
Describe ocular vs oculodermal melanocytosis
Ocular: congenital blue Nevus of episclera; more common in whites; 10% risk of ipsilateral glc and 1/400 risk of uveal melanoma
Oculodermal melanocytosis: ocular melanocytosis + peri ocular cutaneous melanocytosis; more common in AA/Asians, but malignant transformation occurs almost exclusively in whites
Gland type: Krause Wolfring Zeis Meibomian Moll
Krause: eccrine; lacrimal Wolfring: eccrine; lacrimal Zeis: holocrine; sebaceous (a/w cilia) Meibomian: holocrine; sebaceous Moll: apocrine
DDX K crystals
K dystrophy (macular, granular, lattice dystrophy, Schnyder), Bietti’s, ciloxan deposits, Strep Viridans (ICK), cystinosis, multiple myeloma, and monoclonal gammopathy