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Cornea - I Free Papers - aioseducation

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<strong>Cornea</strong> <strong>Free</strong> <strong>Papers</strong><br />

A common protocol was applied to all cases. Each patient was examined<br />

under Slit Lamp biomicrocope by an ophthalmologist. Ulcer is stained by<br />

Sterile fluorescein strip touched at the lower fornix to make out the extent of<br />

epithelial breech and recorded in mm in its longest and shortest diameter.<br />

Other details like depth, zone of stromal infiltrate, <strong>Cornea</strong>l edema etc are<br />

noted with proper color coding. Hypopyon is measured in mm and number of<br />

days for its resolution is noted.<br />

Healed Ulcer<br />

An ulcer is defined healed where fluorescein staining is negative and there is<br />

no stromal infiltrate.<br />

Meticulous data was collected on the following:<br />

1. Date of first visit.<br />

2. Date at which ulcer has healed .<br />

3. Size of ulcer at first visit<br />

4. Site of ulcer (central , inferior temporal , inferior nasal , superior temporal,<br />

inferior temporal)<br />

5. Hypopyon present on presentation and its resolution time.<br />

6. Best corrected visual acuity at first visit.<br />

7. Best corrected visual acuity at end of treatment.<br />

Exclusion criteria<br />

Associated systemic ailments like Diabetes etc.<br />

Associated ocular conditions like dry eye, dacryocystitis, blepharitis, lid<br />

pathologies etc. Typical viral ulcers, healing ulcers, moorens , interstitial<br />

keratitis, neurotropic ulcer, bullous keratopathy, exposure keratopathy etc.<br />

Scraping<br />

The cornea and conjunctival sac are anesthetized with proparacaine<br />

hydrochloride (0.5%), Epithelium is scraped from over the ulcer and beyond.<br />

Ulcer is scraped by an ophthalmologist under aseptic conditions ,at the slit<br />

lamp, using sterile Bard Parker Blade no 15.<br />

Material is obtained from<br />

1. The bed of the ulcer<br />

2. Leading edge of the ulcer and a KOH mount prepared for examination<br />

under microscope first under 10 x and then finally under 40x.<br />

Detailed microbiological examinations like fungal and bacterial culture etc<br />

are done as part of hospital protocol but has not been taken into consideration<br />

in this study as these are not feasible at the grass roots level. It is obviously<br />

ideal to inoculate into several media but this is not always possible due to<br />

473

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