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73 Cards in this Set

  • Front
  • Back
Defence mechanisms against ocular infections
-Skin and mucosal membranes act as barriers
-Tear anti-microbial agents eg. lysozyme (dissolves cell wall of bacteria-> esp. gram +ve), beta-lysin (affects cell membrane)
-Beta-Lysin in aqueous humour
-Immune system, tear immunoglobulins IgA, IgG, IgM
Factors and situations that increase risk of ocular infections
-Corneal abrasions (CL wear), trauma, depressed immune system
-Increased risk areas: farming, gardening, 3rd world countries
Biological Processes in Tears
-64 Proteases (enzyme that breaks down proteins and peptides)
-18 Anti-oxidant enzymes

-Most involved in defence of eye -> immune response against external agents, wound healing, blood coagulation.
Antimicrobial Activity of Tears
Tear components with antimicrobial activity (mainly from lacrimal gland, cells of ocular surface)
-AMPS= Antimicrobial Peptides
-slgA= Secretory immunoglobulin A
-sPLA2= Secretory phosopholipase A2
-SLPI= Secretory leukocyte protease inhibitor
-SP-D= Surfactant protein D
Cellular Classification of Organisms
Prokaryotes= Cells without nuclei (bacteria)
Eukaryotes= Cells with nuclei (fungi, protozoa, helminths)
Viruses= Don't really have cells but take over the host biochemical machinery
Bacteria Classification and Examples
Single-celled, produce own energy + components, gram dividing on shape
Gram +ve -> simple cell wall structure, easy passage of +vely charged compounds, layered peptidoglycan cell wall, Purple stain
Gram -ve -> more complex cell wall, thin peptidoglycan cell wall, outer membrane outside cell wall
Eg.
Gram +ve Cocci= Staphylocci-> lives in skin, Streptococci-> sore throat
Gram -ve Cocci= Neisseriae-> ophthalmia neonatorum (conjunctivitis at birth)
Gram +ve rods= Corynebacteria-> membranous conjunctivitis
Gram -ve rods= Pseudomonas Aeruginosa-> water contaminant (green pus), Haemophilus
Virus Examples
Herpes Viruses= Zoster, Simplex, cytomegalovirus
Adenovirus 8= EKC-> common cause of acute conjunctivitis
Rubella= Microphthalmia, Cataracts, Glaucoma
HIV
Fungi Examples
Candida
Aspergillus
Chlamydia Examples
Trachoma
Amoeba Examples
Acanthomoeba
Choice of Agent
Intelligent guess on type of organism and most effective agent for that
Base treatment on cultures (time issue)
Least toxic drug
Surface Infection-> absorption characteristics not important
Internal infection-> drug penetration/ injection
Drops easiest to use
Ointments longer action but smear vision, good for children, lid infections
Choice of Dosage
Concentration high enough for bacterial effect-> higher than minimum inhibitory concentration (MIC)
Increase frequency to increase dose
Antibiotics half life ~8min, little left after 1hr-> hourly admin may be ok
Compromise between what is required and what Px compliance
Treat for right length of time
Addition to physical procedures
Resistance and Cross Resistance
Bacteria are resistant if growth is not stopped by maximum level of antibiotic tolerated by host
Bacteria are resistant to one antibiotic will be resistant to the whole class (cross-resistance)
Genetic changes in bacteria (many generations in short periods)
Mechanisms of Bacterial Resistance
-Drug inactivation or modification
-Alteration of target site
-Alteration of metabolic pathway
-Reduce drug accumulation
Multidrug Antibiotic Resistance Examples
Staphylococci-> resistant to nearly all available
Mycobacterium-> resistant to most antituberculosis agents = death
Staphylococcus-> Methiciliin resistance
Prescribing for Microbial Resistance
-Do not use antibiotics if not necessary
-Appropriate use (antibiotic, dose, duration)
-Avoid chronic use
-Reserve newer antibiotics for corneal disease
-Less likely for ocular drugs
Microbial Resistance OBA Guidelines
Avoid:
-Inappropriate drug selection
-Insufficient therapeusis
-overuse
-Inappropriate dosage
-Don't use fluoroquinolones where older drug can be used
-Consider specialist opinion if requires long term use
Antimicrobial Failure Reasons
Inaccurate diagnosis
Resistant microorganism
Inadequate drug dosage
Patient noncompliance
Inadequate patient immune response
Sensitisation and Examples
Reaction when Px applies more of drug in attempt to decrease problem -> red eyes, contact dermatitis
Eg
-Neomycin
-Penicillin
-Streptomycin
-Gentamycin
-Some sulphonamides
5 Differences between Bacterial and Human cells
-Bacteria have a cell wall without which the bacteria undergoes lysis and dies (contain peptidoglycan)
-Slight differences in cell membranes (no sterols)
-Different size and structure of ribosomes
-Some different biosynthetic pathways (bacterial cells synthesis of their own folic acid)
-Differences in DNA gyrase (enzyme mediating coiling of DNA)
5 Antibacterial Drug Mechanisms
-Affect Cell Wall Structure
-Affect Cell Membrane
-Affect DNA Synthesis
-Affect Protein Synthesis
-Affect Intermediate Metabolism
Penicillin (Beta-lactam)
-antibacterial drug-> Inhibit cell wall synthesis
-Effective against gram +ve
-Acquired resistance (drug deactivating enzymes produced by bacteria)
-Allergic reaction problem
-Alter normal microflora of body
-25+ types (pneumonia, STDs, meningitis, tissue infections, UTIs, Bronchitis, Pharyngitis

-CAUTION OF HYPERSENSITIVITY REACTIONS-> CROSS SENSITIVITY
Cephalosporins (Beta-lactam)
-antibacterial drug-> Inhibit cell wall synthesis
-Similar structure to penicillins (action and resistance)
-Good against gram +ve bacteria, modest against gram –ve
-Broad spectrum, bactericidal, poor oral activity-> IV
-First, second, third generation compounds
-Septicaemia, pneumonia, meningitis, UTI, Sinusitis
Beta-Lactam (penicillin and cephalosporin) Action
Interferes with cross-linking of peptide chain (final step in bacterial cell wall formation)
Peptide chains give cells wall strength
Polymixin B
-Antibacterial drug-> affects cell membrane
-Cationic surfactant that interacts with cell membranes, increases permeability and causes cell leakage
-Effective against some gram –ve bacteria, some pseudomonas strains
-Popular for Tx of infections of the conjunctiva and lids
Risks: Neurotoxicity, nephrotoxicity
Gramicidin
-Antibacterial drug-> affects cell membrane
-Ineffective against gram –ve bacteria
Propamidine (Brolene)
-Action: Divalent cationic surfactant, affects cell membranes
-Activity: Active against Stap aureus, Streptococcus pyogenes, not active against Pseudomonas, some antifungal properties, action not inhibited by pus
-Use: Minor conjunctivitis blepharitis, acanthamoeba
-Adverse: Sensitization
-Pack: Eye drops 0.1%, 10mL bottle, ointment
-Dose: 2-3 times daily for ~1 week
-Available over the counter without Rx, S2
Drugs Affecting Intermediate Metabolism Action
Synthesis of folic acid in bacterial cells only (not human)
-Folate required for DNA synthesis -> humans obtain from diet
-Sulfonamides inhibit folic acid synthesis-> contains sulfanilamide -> competes with p- aminobenzoic acid (PABA) for the enzyme involved in folate synthesis
(diagram in notes)
Sulfacetamide (Bleph-10 Allergan)
-Action: Sulfonamide, bacteriostatic
-Use: Conjunctivitis, trachoma, generally replaced by other agents, superseded
-Adverse: Allergic reactions common
-Pack: eye drops 10%, 15mL bottle
-Dose: every 2-3 hours during the day for ~1 week
-Available OTC
-S3, ask about sulphur allergies
-Irritant, avoid
Drugs Affecting Bacterial Protein Synthesis Action
-Takes place in ribosomes, differ eukaryotes and prokaryotes, sub-units in bacterial cells are 30S and 50S, human cells are 40S and 60S
-Some can interact with human mitochondrial ribosomes causing group toxic effects
Chloramphenical (Chloromycetin, Clorsig)
-Antibacterial drug-> affects bacterial protein synthesis
-Bind to 50S
-Action: Broad Spectrum (corynebacterium, E.coli, Haemophilus, streptoccoi), not effective against Pseudomonas, low toxicity (limits use), binds to bacterial ribosomes, inhibits protein synthesis
-Use: Prescribed for topical therapy, effective against gram +ve and –ve bacteria, chlamydia, mycoplasma, rickettsia and spirochetes, rarely used systemically (< resistance)
-Adverse: Toxicity, Anaemia, Optic neuropathy, bone marrow depression, fear of possible aplastic anaemia (may be fatal) limits use in some countries (USA), low systemic absorption, gray baby syndrome (child inability to excrete drug⇒ only in inappropriate dosing)
-Pack: eye drops 0.5%, 10mL bottle, fridge
minims, 20 per box
ointment 1%, 4g
-Dose: eye dorps 1-2 drops every 2-6 hrs for 2-3 days then reduce frequency
-S3, PBS
Tetracyclines (Optycin, Latycin)
-Antibacterial drug-> affects bacterial protein synthesis
-Bind to 30S
-Action: Broadest spectrum (gram +ve and –ve), bacteriostatic, resistance develops slowly, not effective against pseudomonas, poor corneal penetration
-Use: Ocular infections, chlamydial infection
-Adverse: Few side-effects topically, local reactions in isolated cases, oral tetracyclines can permanently yellow teeth and slow bone growth in children
-Pack: ointment 1%, 5g now compound pharmacy product (largely superseded by oral azithromycin for trachoma)
-Dose: Apply into lower conjunctival sac every 2 hrs, treatment duration depends on severity of condition
Macrolides
-Antibacterial drug-> affects bacterial protein synthesis
-Alternative to penicillins, similar effect
-Treat pneumonia, genital infections, legionnaires disease, chlamydial infections
-Resistant organisms
-Ear damage, GI disturbance
-Azithromycin, Erythromycin
Azithromycin
-Antibacterial drug-> affects bacterial protein synthesis
-Bind to 50S
-Action: Broad spectrum macrolid antibiotic with anti-inflammatory properties, inhibits protein synthesis, inhibits macrophage activity
-Use: Ocular infections, chlamydial infections, toxoplasma, STDs, malaria, respiratory infections
-Adverse: GI, HA, bitter taste, hypersensitivity
-Pack: 1.5% drops, compound pharmacy product (superseded by azithromycin)
-Dose: apply daily, treatment duration depends on severity of infection, long half life (68hrs)⇒ one high oral dose Tx, Oral 1g for adults, 20mg/kg for children
Erythromycin
-Antibacterial drug-> affects bacterial protein synthesis
-Bind to 50S
Aminoglycosides Action and Examples
-Antibacterial drug-> affects bacterial protein synthesis
-Bind to 30S unit of bacterial ribosome preventing protein synthesis
-Active against aerobic gram –ve and some gram +ve bacteria
-Rapid action, bacrtericidal
-If oral can cause nephrotoxicity (kidney damage) and otoxicity (ear damage)
-Not for systemic use
-Streptomycin, Framycetin, Gentamicin, Neomycin, Tobramycin
Framycetin
-Antibacterial drug-> affects bacterial protein synthesis
-Aminoglycoside

-Action: Isomer of neomycin, broad spectrum effective against gram-positive and –negative bacteria
-Use: Conjunctivitis, blepharitis, abrasions, styes, topical application, poor ocular penetrance
-Adverse: Kidney, ears affected, contact allergies
-Pack: eye drops 0.5%, 8mL bottle
-Dose: eye drops 2 drops every 1-2 hours decreasing to 3/times per day
Gentamicin
-Antibacterial drug-> affects bacterial protein synthesis
-Aminoglycoside

-Action: Broad Spectrum antibiotic, some resistant gram-positive organisms, bactericidal, poor ocular penetration when applied topically
-Use: Treatment of external eye and adnexal infection (bacterial conjunctivitis), prophylaxis following surgery or trauma (abrasions), suspected pseudomonas
-Adverse: Transient irritation, damage ears, kidneys, sensitisation reduced
-Pack: 0.3% 5mL bottle & minums
-Dose: 1-2 drops q4h, if severe 2 drops hourly
-1.3% fortified for bacterial keratitis
Neomycin
-Antibacterial drug-> affects bacterial protein synthesis
-Aminoglycoside

-Action: Broad spectrum antibiotic, some resistance from gram-positive organisms, bactericidal, not effective against pseudomonas
-Use: Bacterial infection, rarely used systemically, used prophylactically with steroid after surgery or for inflammation cover
-Adverse: ears, kidneys affected, hypersensitivity
-Pack: 0.5% minims, Neosporin drops, ointment, compound product
Tobramycin
-Antibacterial drug-> affects bacterial protein synthesis
-Aminoglycoside

-Action: Broad Spectrum, some resitance from gram +ve organisms, bactericidal
-Use: Treatment of external eye and adnexal infection (bacterial conjunctivitis), prophylaxis following ocular surgery or surface trauma, suspected pseudomonas
-Adverse: Ocular and systemic toxicity, superinfection ⇒ retarded corneal wound healing
-Pack: eye drops 0.3%, 5mL bottle
ointment 0.3%, 3.5g
-Dose: eye drops 1-2 drops every 4 hours
-Severe infection: 2 drops hourly until improvement
-1.3% fortified for bacterial keratitis
Drugs Affecting Bacterial DNA Synthesis
-New generation quinolones and fluorinated quinolones (fluoroquinolones)
-Broad Spectrum, little resistance
-Use only for microbial keratitis, extremely severe conjunctivitis
-Active against Pseudomonas & Staphylococcus
-Cause: Kidney stones, headache, nausea
-Not for use in children under 8yrs (cartilage damage)
Fluoroquinolones
-Antibacterial drug-> affects bacterial DNA synthesis
-Newest group, major area for new drugs
-Inhibit DNA synthesis during bacterial replication, unique mechanism means cross-resistance with other antibiotics less likely
-Well absorbed orally
-Inhibit DNA-gyrase, preventing supercoiling of DNA molecule
-Ciprofloxacin, Ofloxacin
Ciprofloxacin (Ciloxan, Ciloquin)
-Antibacterial drug-> affects bacterial DNA synthesis
-Action: Active against broad spectrum of gram+ve and –ve ocular pathogens
-Use: Bacterial keratitis, severe bacterial conjunctivitis, effective, safe, limit use to prevent resistance
-Adverse: Super infection, discomfort, burning, itching, hyperaemia, precipitates on corneal ulcers
-Pack: 0.3% 5mL bottle
-Dose:
-Corneal Ulcers= day 1: 2 drops every 15min for 6 hours then every 30min, Day 2: 2 drops every hour, Days 3-14: 2 drops every 4 hours
-Bacterial Conjunctivitis = Days 1-2: 1 drop every 2 hrs while awake, days 3-7: 1 drop every 4hrs while awake
Ofloxacin (Ocuflox)
-Antibacterial drug-> affects bacterial DNA synthesis
-Action: Active against broad spectrum of gram+ve and –ve ocular pathogens
-Use: Bacterial keratitis, severe bacterial conjunctivitis
-Adverse: Super infection, transient eye pain, hyperaemia,  risk of corneal perforation
-Pack: 0.3% 5mL bottle
-Dose:
-Bacterial conjunctivitis= Days 1-2: 1 drop every 4hrs while awake, Days 3-10: 1 drop every 6hrs
-Corneal Ulcers= Day 1: 2 drops every 15min for 6hrs then every 30min, Day 2: 2 drops every hour, Days 3-14: 2 drops every 4hrs
Antibacterial use for:
BACTERIAL CONJUNCTIVITIS
-Resolves in 10-14 days
-Staphylococcus aureus, staph. Epidermidis, Streptococcus pneumonia, hemophilus influenza
-Microbiological investigations (swabs) rarely needed
-Hygiene
-Topical antibiotics shorten course
-Broad spectrum antibiotic (gram+ive and –ve)
-4 times/day for 1 week
Antibacterial use for:
BACTERIAL KERATITIS
-Sight threatening
-CL wear and pseudomonas
-Microbial work up
-Broad spectrum antibiotic (immediately)
-Monotherapy with fluoroquinolone or dual therapy with fortified cephalosporin and aminoglycoside
-Drops hourly
-Ineffective corneal ulcers: Day1: 2 drops every 15min for 6hrs, then 30min, Day 2: 2 drops every hr, Days 3-14: 2 drops every 4hrs
Antibacterial use for:
CORNEAL ABRASION
-Heals spontaneously within few days
-Ice packs and oral analgesics for pain
-Subepithelial lesions referred immediately
-Broad-spectrum topical antibiotic used 4 times per day until epithelial healing
Antibacterial use for:
ANTERIOR BLEPHARITIS
-Anterior eye lid margin
-Chronic recurrent nature
-Lid hygiene, tear supplements
-Weak corticosteroids and antibiotics (chloramphenicol, erythromycin, gentamicin) ⇒ short term
Antibacterial use for:
POSTERIOR BLEPHARITIS
-Meibomian gland dysfunction
-Chronic recurrent nature
-As above treatment
-Systemic tetracyclines (doxycycline 100mg per day for 1 mth, then 50mg for 2 mths)
-Mild topical steroid (FML) and topical antibiotic 1-2 weeks to reduce inflammation and bacterial load
-Optimel antibacterial honey
Antibacterial use for:
CHLAMYDIAL CONJUNCTIVITIS
-Refer
-Oral doxycycline 100mg per day for 10-14 days
-one or two 1gm doses of azithromycin
-topical treatment ineffective
Antibacterial use for:
DACRYOCYSTITIS
-Bacterial or fungal infection of lacrimal sac and tear drainage system
-Oral broad-spectrum antibiotics
-Refer for aspiration if painful, surgical reconstruction
Antibacterial use for:
GONOCOCCAL KERATOCONJUNCTIVITIS
-Acute bilateral sight threatening disease caused by gram-ve diplococcus infection, Neisseria gonorrhoea ⇒ corneal perforation
-Lytic Enzymes in mucopurulent discharge must be washed away
-Systemic infection requiring systemic antibiotics
-Penecillin, 1gm ceftriaxone intramuscularly daily for 5 days, oral doxycycline, topical gentamycin 1.3% hourly
Antibacterial use for:
HORDEOLUM INTERNAL/ EXTERNAL
-Abscess of sebaceous gland
-Internal (acute staph infection of meibomian gland)
-External (acute staph infection of lash follicle and zeiss or moll gland)
-Resolve spontaneously
-Warm compresses, lid hygiene
-Broad-spectrum antibiotic 1 week course (external)
-1 week course of oral antibiotic if sig. cellulitis
-Epilation or curettage may assist drainage
Antibacterial use for:
PRESEPTAL CELLULITIS
-Infection of subcutaneous eyelid tissue anterior to orbital septum
-Requires urgent systemic treatment
-Haemophilus influenza, streptococcus pneumonia cause?
-Oral antibiotics for ~10days ⇒ penicillin, cephalosporin
-IV application may be required in children or if oral response does not occur
Antibacterial use for:
ROSACEA KERATITIS
-Inflammatory skin condition
-Butterfly rash of cheeks and nose
-Posterior blepharitis, corneal involvement
-Oral tetracycline(doxycycline 100mg/day for 1mth, 50mg/day for 2mths), erythromycin, or azithromycin
-Tear supplements and weak topical steroids helpful
Viruses
-Smallest infectious organisms
-Infect humans, animals, plants and bacteria
-Obligate intracellular parasites
-Depend on host cells for multiplication
-Invades metabolic machinery
-Acute disease limited by immune system
-Some can be latent (recurrent)
-Difficult to destroy without hurting host
-Immunisation only option (mostly)
Anti-Virals
-Target specific enzymes
-Difficult to develop (selective toxicity for viruses)
-Aciclovir, Vidarabine, Idoxuridine
-Many virus specific (in notes)
Aciclovir (Zovirax)
-ANTIVIRAL
-Zovirax, HSV, IV, tablets, ointment
-Analogue of guanosine
-Inhibits multiplication of herpes simplex virus, varicella zoster virus
-Activated by viral thymidine kinase (viral selectivity)
-Virus thinks it is a nucleotide
-Activated form inhibits DNA polymerase
-Minimal side effects
-Action: Antiviral agent, sig more effective than older agents
-Use: Herpes simplex keratitis
-Adverse: Transient mild stinging upon application, superficial punctate keratopathy
-Pack: Ointment 3% 30mg/g, 4.5g
-Dose: 1cm inside lower conjunctival sac 5 times daily for 14 days or minimum 3 days after healing
-Cold sore cream skin lesion versions available over the counter
Vidarabine (adenine arabinoside)
-ANTIVIRAL
-Action: Antiviral agent, nucleoside stops growth of nuclear chain, superseded by acyclovir
-Use: Herpes simplex virus
-Pack: Compound pharmacy product, 3% ointment
-Dose: 1 cm inside lower conjunctival sac 5 times daily for 14 days or minimum 3 days after healing
-First drug to become generally available for treatment of herpes simplex virus infections (1980s)
Idoxuridine
-ANTIVIRAL
-HSV, not for ocular use
Antiviral use for:
HERPES SIMPLEX
-Leading cause of corneal opacification and infection related visual loss
-Stromal keratitis or iritis can be present in serious forms
-Avoid triggers (sunglasses)
-Prompt presentation on recurrence of disease (Px education)
-Limit corneal scarring
-Topical antiviral agent, acyclovir ointment
-90% dendrites healed in 1 week
Antiviral use for:
HERPES ZOSTER
-Varicella zoster virus of trigeminal nerve (shingles)
-Treatment within 72hrs
-Early treatment reduces risk of post-herpetic neuralgia
-Irreversible ocular damage
-Contagious when vesicular lesions present
-Oral acyclovir 800mg 5x/day for 7 days
-reduces time for lesion healing
-reduces duration of viral shedding and new lesion formation
-Reduces duration of pain and incidence of other complications
-Poor oral bioavailability (poor water solubility)
-Valaciclovir 1g 3x/day for 7 days
-Enhanced bioavailability (prodrug of acyclovir)
-decreased duration of pain
-Greater effectiveness
-Topical antivirals have little effect
-Topical steroids, tear supplements, anti-glaucoma meds may be used to manage long term complications (virus never leaves)
Antiviral use for:
ADENOVIRAL CONJUNCTIVITIS (EKC)
-Broad range of adenoviruses causing it
-Upper respiratory tract infection
-Preauricular lymphadenopathy signals viral infection
-Gritty, watery, inflamed eyes, photophobia
-No effective treatment
-progression to viral keratitis
-AdenoPlus (diagnostic test)
-Highly contagious (hygiene)
-Resolution occurs within 2-4 weeks
-Antiviral agents ineffective
-Tear supplements to improve comfort
-Cold packs every 3-4 hours
-Topical steroids for early stages when opacities are inflammatory (not scars yet)
-Aspirin helpful if sig discomfort
-Povidone Iodine (betadine) wash suggested (limited evidence of effectiveness- stings)
Antiviral use for:
CYTOMEGALOVIRUS RETINITIS
-Inflammation of retina caused by human cytomegalovirus
-Occurs in immunocompromised individuals (AIDs)
-Cidofovir/ ganciclovir/foscarnet used intraveniously (or injected into eye) if active
-Intraocular ganciclovir device
-Inhibits viral DNA polymerases at concentrations too low to affect human DNA polymerases
-Discontinuation of use is common (Toxic!)
Antiviral use for:
MOLLUSCUM CONTAGIOSUM
-Localised skin infection caused by pox-wart-like viral skin infection
-Self-limiting (3-12mths)
-Raised, shiny, white-pink nodules
-Around eye can cause follicular conjunctivitis
-Good hygiene to avoid reinfection
-Treatment is excision not antiviral agents, upon removal lesion resolves
Antifungals
-No topical antifungal available
-Difficult to produce
-Ocular antifungal infections are rare
-Occur most after surgery or depressed immune system
-Fungal spores in farming areas can cause (doesn’t have to be from abrasion)
-Causes severe ocular damage
-Prompt and effective treatment to avoid loss of eye
-Fungal toxins cause damage after fungus eliminated
-Tablets and ointments (external)
Polyenes
-Antifungal agent
-Alter fungal cell membrane permeability, bind to sterol moiety of membrane
-Poor penetration, intravitreal for endophthalmitis
-Highly toxic⇒ retinal damage, renal toxicity, reversible anaemia, fevers, chills, hypotension
-Amphotericin B, Nystatin
Pyrimidines
-Antifungal agent
-Flucytosine
Imidazoles Azoles and Triazole Azoles
-Antifungal agent
-Alter fungal cell membrane permeability
-Miconazole, ketoconazole (IAs)
-Itraconazole, fluconazole (TAs)
Fungal Infections
-Uncommon ocular pathogens
-May be hard to distinguish from bacterial infections (won’t respond to antibiotics)
-Occurs in already compromised eye (ocular surface disease, long term steroid use)
-Slow, relentless infection
Antifungal use for:
FUNGAL KERATITIS
-Antibiotics inactive
-Ulcer with posterior corneal involvement
-pearls on back of cornea
-Refer to corneal specialist
-Send corneal scrape to lab
-Treat with antifungal agents when diagnosed (drugs are toxic to cornea)
-Topical and oral antifungal agents
-Amphotericin B, Ketoconzole, fluconazole, itraconozole, flucytosine
-Frequent administration for prolonged period (12 weeks at least)
-Topical corticosteroids are contraindicated
Antifungal use for:
ENDOPHTHALMITIS
-Ocular emergency, urgent referral
-Bacteria cause, unusual for fungi
-Entry to eye via wound (surgery, penetrating injury)
-Reduce post-operative risk by treating infections before surgery
-instil povidine iodine immediately post surgery (reduce risk)
-Intravitreal injection of antibiotics (vancomycin, ceftazidine) and steroid (dexamethasone)
-Topical, oral and IV antibiotics are ineffective on their own
Antifungal use for:
ACANTHAMOEBA KERATITIS
-Ubiquitous protozoan that rarely infects cornea
-Cease contact lens wear immediately (reintroduce after 6mths)
-Lab identification (scraping)
-Commence treatment using anti-amoebic drugs after confirmation (propamidine, neomycin and 0.02% polyhexamethylene-biguanide (PHMB) or topical chlorhexidine)
-Refer, reviewed weekly until clinical improvement seen