Microbial Keratitis Flashcards

1
Q

What are the 5 layers of the cornea?

A
Epithelium
Bowman's Layers
Stroma ( ~90%)
Descemets Membrane
Endothelium
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2
Q

What are infiltrates?

A

yellow-grey-white opacities located within the anterior stroma.
Infiltrates are made from acute inflammation composed of inflammatory cells, cellular and extracellular debris (necrosis).

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3
Q

What is the classification for an Ulcer?

A

An ulcer is characterized by inflammation, necrosis, loss of tissue, progression and chronicity. (Yanoff)

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4
Q

What are the pathophys steps for the Bacterial Keratitis

A
  • Compromised epithelial layer allows bacteria access to the underlying tissue
  • Exo/Endo-toxins are released to aid this infestation.
  • The bacteria will begin its replication process within the stroma
  • This will further activate and release exotoxins that will damage the epithelial layer and initiate an inflammatory reaction.
  • WBC (specifically neutrophils) will arrive at the infected area and partnered up with the exotoxins, more damaged to the epithelial layer will be caused.
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5
Q

What are two ways that wearing Contact Lenses promote bacterial growth?

A
  1. Naturally occurring Lipid Rafts on the corneal epithelium cells help bind bacteria. Wearing CLs increases the number of Lipids Rafts thus increases the chances of bacteria attaching.
  2. Side chains of corneal mucin barriers block bacteria binding, and wearing CLs reduces the length of the side chains and thus less bacteria are blocked.
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6
Q

What type of bacteria can penetrate a healthy corneal epithelium?

A

Pseudomonas species can penetrate a healthy corneal epithelium in approximately 3 hours.

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7
Q

What helps stops the Pseudomonas species penetrate a healthy cornea?

A

Complete Lid closure
Tear FIlm
Tear Flow

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8
Q

Why is Microbial Keratitis more aggressive in Contact Lens wearers?

A

Wearing CLs predisposes the cornea to a “Pro inflammatory state”, which activates Langerhans Cells in the peripheral and central cornea.

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9
Q

What does Dk stand for?

A
The "Dk" value is a measure of their oxygen permeability of a CL. Materials with a high Dk transmit more oxygen to the eye than those with a low Dk value.
Low Dk is < 12
Medium Dk is 15-30
High Dk is 31-60
Super Dk is 61-100
Hyper Dk is > 100
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10
Q

How do Contact Lens solutions and cases effect the Cornea?

A

Contact lens cases and solutions harbor bacteria. The CL MPS decreases the epithelium layer turnover and thus older epithelium cells are held on on the cornea.

MPS promotes bacterial binding as it distrupts the ZO-1 proteins and thus decreases epithelial resistance.

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11
Q

What are the Risk Factors for MK?

A

Contact Lens Wear
Ocular trauma/surgeries
Ocular surface diseases

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12
Q

How do you differentiate between a Sterile and Infected ?

A

Use the PEDDAL mnemonic

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13
Q

What does the PEDDAL mnemonic stand for?

A

P - Pain (More pain the more likely it is Infected)
E - Epithelial Defect (If full thickness defect is seen its more likely infective) (Dendritic shape - Viral) (Larger than the infiltrate - more likely bacterial)
D- Discharge (Purulent - infected) (watery - viral)
D- Depth (If multiple layers are involved its more likely infected.
A - Anterior Chamber Reaction ( is present - infected)
L - Location (central - bacterial) (viral and fungal - numerous lesions

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14
Q

3 Other ways to differentiate between Infected and Sterile Keratitis

A
  1. Iris visibility? If iris is not visible more likely to be Bacterial
  2. Colour ( Grey-white, usually indicative of bacterial Infection, yellow is more likely just Bacterial.
  3. Borders of infiltrate - Indistinct usually means infective.
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15
Q

What is the clinical presentation of a Staph/Strep related Bacterial Keratitis?

A
Round/oval
Grey/white lesions
Distinct Margins
Mucopurulent discharge
Severe AC reaction
Initally may appear as a relatively clear surrounded cornea.
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16
Q

What is the Clinical presentation of Pseudomonus related Bacterial Keratitis?

A
Irregular shape and size
Yellow/green lesions
Soupy appearance with hazy cornea
Moderate AC reaction
Can perforate the cornea in 48 hours if not treated.
17
Q

When would you consider Lab testing before an empirical Approach?

A
You would consider lab testing in,
central ulcers
children
health care workers
history of trauma (vegetative)
patients using steroids 
immunocompromised patients
18
Q

What are the standard protols for treating MK?

A
  • Fluoroquinolone monotherapy ( ciprofloxacin 3mg/ml or Oflaxacin (0.3%))
  • Fortified combination therapy (1.3% gentamicin + 5% cephazolin - need 15minute gap between each dosage))
19
Q

What needs to be done by the optometrists so the px can gain PBS access for ciprofloxacin and/or ofloxacin?

A

The optom needs to be co-managing with an ophthalmologist

20
Q

what drugs are not suitable for empiric prescribing?

A

Cephalosporins

Aminoglycosides

21
Q

What is the dosing and review plan during the Sterilization phase?

A

Loading dose : 1 drop every 30 minutes for 4-6 hours (DAY AND NIGHT)

Intensive Therapy dosing: q1h (every hour) (day and night for 24 hours)

22
Q

What is the point of Intensive therapy dosing?

A

to keep the antibiotic within the therapeutic range and balance against corneal toxicity

23
Q

What is the dosing and review plan during the Healing phase?

A

Prophylactic coverage dose: Never less than q.i.d (4 times a day), ongoing until improvement is seen.

24
Q

How long is the review period for the first initial dose during empirical phase?

A

Always review in 24 hours, never 48 as this is sufficient time for bacterial species to perforate the cornea