Cornea: Keratitis Flashcards

1
Q

How do you tell which type of keratitis it is?

A

If in centre of cornea (central 3-4mm) it is more likely to be infectious
If in periphery (near limbus with conj vessels) it is more likely to be sterile (e.g. marginal keratitis, peripheral ulcerative keratitis)

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2
Q

Describe marginal keratitis & its treatment?

A
  • More common
  • Immune mediated inflammation as result of blepharitis & lid margin disease
  • Usually occurs where lid touch globe/cornea
    o More likely to be 4 to 5 o’clock position, 7 to 8
    o’clock position, 10 to 11 o’clock position, 2 to
    3 o’clock position
  • Always a small area of clear cornea between the limbus
    and the infiltrate
  • Infiltrate may appear as white patch
    Treatment:
  • Ongoing lid hygiene advice
  • Combo of antibiotic & steroid (as inflammatory)
    –> antibiotic: chloramphernicol 4x a day for 2 weeks
    After that lid hygiene & ocular lubricants for any associated dry eye
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3
Q

Describe Superficial Punctate Keratitis?

A
  • Common
  • Descriptive term
  • Pebble-dashed appearance of epithelium
  • Endothelium becomes oedematous & NaFl can gather in between unhealthy epithelial cells
  • Common in dry eye & people who wear CLs
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4
Q

Describe the most common ways that ocular surface infections are spread?

A
  • Opportunistic exposure and contact
    o Airborne
    o Finger
    o Contact lenses – majority in young pxs – easy to transfer pathogens into eye, any micro abrasion can lead to the pathogen causing an infection – since cornea is avascular, infection can take hold quite quickly & cause significant
    degree of damage before body can amount a
    immune response
    o Extension from lids
    o Upper respiratory tract infection
    o Sexual contact
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5
Q

Describe molluscum contagiosum?

A

Px can have ongoing ocular signs of inflammation - doesn’t matter what put on eye - this will continue to shed pox virus causing recurrent infections
Needs moluscum removed

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6
Q

Describe Peripheral keratitis?

A

If BVs growing over cornea, then know it has been there for a while - BVs do not just grow over night - take weeks or months
If infection encroaching on centre then more likely to be immune mediated –> px will have dermatitis so do not just look at the eye
Look at the px too

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7
Q

Describe herpes simplex virus (HSV) keratitis?

A
  • Symptoms:
    o FB sensation
    o Photophobia
    o Redness
    o Blurred vision – if ulcer involves central cornea & visual axis
  • Can involve just the eyelid – get small white vesicles
  • Epithelial Ulcer:
    o Dendritic pattern – multiple small branches with small bulbs
    o Stain w/ NaFl
    o Terminal bulbs
    o Swollen adjacent epithelium
    o If edges of ulcer start to separate & whole thing starts to enlarge  geographic ulcer
  • Assess for corneal sensation – just use tip of tissue & ask px if they can feel it when you touch the surface of their eye (will be able to tell as they would blink if they could feel it)
    o These pxs would not blink and may not feel anything
    o If unsure, use other end of tissue and test other eye
  • Reduced corneal sensation:
    o Focal or diffuse
  • Conjunctival injection
  • Underlying stromal oedema – due to break in epithelium
  • After resolution:
    o Stromal scarring
    o Ghost dendrite – scar in pattern of dendritic ulcer
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8
Q

Describe the management for HSV keratitis?

A

o Referral of acute episodes w/ no history
o Recurrent cases:
 Clear diagnosis
 Only epithelial involvement
 Commence topical antiviral therapy – acyclovir/ganciclovir 5 times a day
o Refer if non-healing after 1 week or if there is stromal involvement
o Topical antiviral therapy:
 Acyclovir 3% ointment 5 times daily
 Review one week
 Therapy longer than 2 weeks induces keratopathy
o Debridement w/ cotton bud
o Oral acyclovir:
 800mg 5 times daily
 Maintenance dose of 400mg 2 times daily in recurring disease
o Topical steroids must be discontinued
 If px on topical steroids when present to you w/ epithelial HSV then DISCONTINUE as will affect healing process

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9
Q

Describe HSV Disciform keratitis?

A
  • Endotheliitis
  • Often has circular lesion (disc)
  • Associated uveitis
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10
Q

Describe HSV Stromal keratitis?

A
  • Herpetic Eye Disease Study (HEDS)
  • Oral antiviral – acyclovir – systemic preferred as topical normally doesn’t penetrate deeper than epithelium
  • Topical steroid – Pred forte 4x day – to control inflammation
  • Reduces persistence / progression
  • Shortens duration
  • Long term prophylaxis – reduced no. of recurrences px can have and lessens severity of episode if it does occur
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11
Q

Describe Herpes Zoster Ophthalmicus (HZO)?

A
  • Reactivation of latent virus – px had chicken pox in past
  • Associated w/ altered immunity
  • Zoster dermatitis:
    o Vesicular rash – respects vertical midline
    o General malaise
    o Multitude of ophthalmicus signs
  • Hutchinson’s Sign: rash extending to tip of nose, if see this then the nasociliary nerve has been involved & as that travels through orbit, px is more likely to have ocular signs
  • Investigations:
    o Detailed history & symptoms
    o Full examination – dilated to make sure no evidence of vitritis, retinitis or optic neuritis
    o Pxs can also have cranial nerve palsies so important to investigate ocular motility too
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12
Q

Describe the management for Herpes Zoster Ophthalmicus?

A

o Rest & supportive advice
o Advice on avoiding contact with immunocompromised patients
 Consider elderly, infants, pregnant females (in 1st trimester)
o Epithelial disease – lubricants
o Analgesia
o Limited to epithelium – Manage jointly with GP if have ongoing neuralgic pain
o Referral if deeper layers involved

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13
Q

Compare the epithelial changes of HSK vs VZV?

A
  • Dendrites:
    o HSV – Central ulceration with terminal bulbs. Geographic if steroids used
    o VZV – Smaller without central ulceration or terminal bulbs
  • Dermatomal distribution – respects midline
  • Skin scarring
  • Neuralgia – often after initial rash settles there is on going inflammation of the dermatomal distribution causing significant neuralgic type pain – can be ongoing for many months, px will need neuralgic type analgesia
  • Iris atrophy
  • Recurrent disease
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14
Q

Describe bacterial keratitis? & ulcers?

A
  • Sight and eye threatening condition
  • Variable speed of onset
  • Rapid onset with significant inflammation
  • Can progress to corneal perforation
  • Requires urgent referral
  • Take appropriate history
  • Associated with epithelial disruption:
    o Contact lens wear – send the CL to microbiology lab
    o Trauma
    o Contaminated topical ocular medications – send this to microbiology lab
    o Impaired defence mechanisms
    o Altered structure of corneal surface – hx of chronic corneal erosions? Chronic dry eye?
  • Ulcers:
    o Sharp epithelial demarcation
    o Underlying dense, suppurative stromal inflammation Indistinct edges surrounded by stromal oedema
    o Presentation can vary from quick onset and aggressive course to slow, indolent course
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15
Q

Describe CL related keratopathy management?

A
  • Discontinue of lens wear 2-14 days
  • Advice against extended wear – if start CLs again wear for short time
  • Lid hygiene in presence of blepharitis
  • Appropriate type of contact lens wear
  • Refer if infective component suspected
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16
Q

Describe the clinical presentation of bacterial keratitis?

A
  • Rapid onset of pain
  • Conjunctival injection
  • Photophobia
  • Decreased vision – if ulcer is on visual axis
  • Rate of progression depends on virulence of organism
17
Q

Describe the clinical presentation of pseudomonas bacterial keratitis?

A
  • Pseudomonas typically produces stromal necrosis with a shaggy surface and adherent mucopurulent exudate
  • V aggressive
  • Endothelial inflammatory plaque
  • Marked anterior chamber reaction
  • Hypopyon – can develop over course of an hour
  • Slow growing, fastidious organisms
    o Mycobacterium
    o Anaerobes
    o Non-suppurative infiltrate
    o Intact epithelium
18
Q

What is the management for non-vision threatening bacterial keratitis?

A

Non-vision threatening = epithelial defects or infiltrate 1mm or less in size, pxs vision is not reduced and no hypopyon  still needs aggressive treatment
* Topical Quinolones – broad spectrum
o Ofloxacin
o Ciprofloxacin
* Every 1 – 2 hourly from at least 7am to 10pm
* Cyclopentolate 1% TDS (three times a day) – to reduce ciliary spasm & to increase comfort
* Review within 48 hours – over 1st day or 2 eye can feel worse especially if treating gram -ve bacteria
* Tapering as necessary
* Mild topical steroids once infection controlled ± organism identified (not 1st line tx) – too many steroids can make it worse

19
Q

What is the management for vision threatening bacterial keratitis?

A

Vision threatening = Larger epithelial defects affecting central visual axis – vision dropping down to hand movements or light perception – may have hypopyon
* Tx must be more aggressive
* Consider admission – depends on individual – e.g. if px is 80, lives on own, has rheumatoid arthritis and can’t put drops in then they would be more likely to be admitted than a 20/30 year old who lives near by
* Hourly:
o Day and night is needed
o Preservative free Cefuroxime 5%
o Preservative free Gentamicin 1.5%
o Taper after 48hours
* Cycloplegic
* Systemic antibiotics
o Oral ciprofloxacin 750mg BD

20
Q

What are the signs of improvement in bacterial keratitis?

A
  • Blunting of perimeter of infiltrate
  • Decreased density of stromal infiltrate – starts to fade, becomes more greyish
  • Reduction of stromal oedema
  • Reduction of anterior chamber activity – hypopyon starts to shrink and disappear, cells will disappear too
  • Epithelial recover
  • Cessation of corneal thinning
  • Eventually left with mild corneal scar
21
Q

Describe fungal keratitis?

A
  • Less common
  • Warmer, more humid areas
  • Predisposing risk factors:
    o Trauma to cornea
    o Contamination w/ organic material (gardners)
    o Topical steroid use
  • Gardeners
  • Immunocompromised
  • Fewer inflammatory signs & symptoms in initial phase – can manifest self over many weeks
  • Minimal conjunctival injection – less redness
  • Filamentous fungus:
    o Gray-white infiltrate w/ feathery margins
    o May elevate corneal surface
    o Satellite lesions may be present
    o Endothelial plaque +/- hypopyon w/ rapid progression
  • Candida:
    o Superficial white lesions
22
Q

Describe the management for fungal keratitis?

A

o Very difficult
o Initial tx probably for bacterial keratitis until diagnosis proven by biopsy
o Antifungals:
 Amphoteracin B
 Fluconazole
 Itraconazole
 Ketoconazole
 Clotrimazole

23
Q

Describe acanthamoebic keratitis?

A
  • Protozoa
  • Commonly associated w/ CL wear & swimming
  • Severe pain disproportionate to signs
  • Initial punctate keratopathy or dendrite
  • Ring ulcer – develops in later stages
  • Diagnosed by corneal scrape
  • Often diagnosed late
  • Suspected if non-responding to unconventional bacterial keratitis therapy
  • Management:
    o Have suspicion for acanthamoeba if see px who is not responding to conventional bacterial keratitis tx
    o Urgent referral – do not delay
    o Stop CL wear & bring w/ solution for culture
    o Corneal scrape
    o Topical amoebicides
    o Topical steroids – ABSOLUTE NOT TO BEGIN WITH – wait at least a fortnight if not a month to control the infectious part before treating inflammatory part
24
Q

Describe neurotrophic keratitis and the three stages?

A
  • Reduced corneal sensation resulting in corneal ulceration
  • Cornea needs good nerve supply for epithelium to continually regenerate – if nerve supply compromised epithelium can break down  leads to ulceration & non-healing defects
  • Can be due to HSV keratitis and lots of other infectious/metabolic causes
  • Stage 1:
    o Early stage
    o Punctate corneal epithelium (Gaule spots)
    o Superficial vascularization
    o Stromal scarring
    o Decreased tear break up time
    o Increased tear mucus viscosity
    o Epithelial hyperplasia and irregularity
    o Hyperplastic precorneal membrane
    o Staining of palpebral conjunctiva with Rose Bengal
  • Stage 2:
    o Epithelial defect, usually in superior half of cornea
    o Smooth and rolled epithelial defect edges
    o Surrounding rim of loose epithelium
    o Stromal oedema
    o Anterior chamber inflammation
  • Stage 3:
    o Corneal ulcer
    o Stromal melting
    o Perforation
    o Difficult to treat