Ears And Eye Flashcards
Conjunctivitis
Newborns should be checked for ophthalmia neonatorum
Preschoolers have bacterial conjunctivitis
School aged have viral conjunctivitis with adenovirus
Adolescents/adult can have sexually active conjunctivitis, check for neisseria gonorrhea, can also be bacterial or viral
Chlamydia can also be seen in neonates
Miotics
Class: Antiglaucoma agents, Cholinesterase inhibits
MOA- Indirect acting agents that inhibit cholinesterase
Cause intense miosos and muscle contraction intraocular pressure is decreased by decreased resistance to aqueous outflow
Two types- reversible, and irreversible
Reversible - physostigmine and Demecarium with cholinesterase
Irreversible -echothiophate iodide binds to cholinesterase into a covalent bond that does not hydrolyze, cholinesterase must be obtained from other parts of the body for eye action to normalize
Direct acting parasympathetic drugs with muscarinic effects peoples will constrict , ciliary muscles are stimulated, and there is increased, aqueous humor outflow, outflow resistance is decreased from contraction of the iris sphincter
Pharmacokinetics- duration 6-8 hrs, direct acting 4-8 hrs
Contraindications with eye inflammation or with no construction, not warranted, such as with iritis, uveitis, secondary glaucoma
Adverse effect -corneal clouding, headache, retinal detachment may have systemic anticolic effects like headache, hypertension, salivation, sweating, nausea, vomiting
Drug-drug- echothiophate can have additive effects with system anticholineserase (MG meds)
Carbonic anhydrase inhibitors
Class- Anti glaucoma agent
MOA- Decrease aqueous humor, secretions by decreasing the formation of bicarbonate ions this decreases sodium and fluid transport leads to less aqueous humor production
Pharmacokinetics- Brinzolamide (azopt) absorbed systemically widely distributed, including in breastmilk, and can cross placenta, metabolize, and excreted in urine
Dorzolamide (trusopt) some systemic absorption primary excreted unchanged in urine
Methazolamide (nepatazane) oral agent, absorbed from G.I. tract distributed throughout extruded by the kidneys 25% unchanged in urine.
Dorzolamide and brinzolamide contain sulfa, and are absorbed in amounts great enough to cause hypersensitivity in those with allergy, pregnancy C category, contraindicated and lactation safety in children is not known. Methazolamide is contraindicated in those with low potassium, low sodium renal disease, liver disease, Supra renal gland disease, severe COPD, not recommended in children and pregnancy category C
Adverse effect - dysgeusia, can punctuate keratosis, oral agents like neptazane can cause melena, GI upset, glycosuria, urinary frequency, renal stones, or nephro toxicity
Drug-drug- concurrent use of other CAI and high dose salicylates may cause metabolic acidosis, and salicylate toxicity, Methazolamide and topamax can increase risk of renal stones
Sympathomimetics
Class- Anti glaucoma agent
MOA-Cause phase of construction pupillary dilation and decrease the intraocular pressure these drugs, decrease intraocular pressure by reducing production of aqueous humor and by increasing aqueous humor outflow
Pharmacokinetics- Apraclonidine (lopidine) is contraindicated in those allergic to clonidine, pregnancy category C
Dipivefrin (akpro, propine) is contraindicated in those with narrow angle glaucoma, pregnancy category B, not recommended for children or nursing moms
Adverse effects-conjunctival or corneal pigmentation, systemic effects such as headache, hypertension, elevated heart rate, cardiac arrhythmias
Drug-drug- no known drug interactions but apraclonidine do not use MOAI because of potential hypertensive crisis
Alpha adrenergic agents
Class-Anti glaucoma agents
MOA- Decrease intraocular pressure by reducing the production of aqueous humor by increasing uveoscleral outflow
Pharmacokinetics- Brimonidine (alphagan) peak levels in 1-4 hours metabolized in liver eliminates in urine
Brimonidine is contraindicated in those on MAOIs
do not instill with contact lenses in 15 minutes use before putting contacts in pregnancy category C
Adverse effect - feeling of foreign body and eye and pain can have systemic effects such as dry mouth, drowsiness, or headache
Drug-drug- do not use MAOIs, additive effect, if use with a central nervous system depressant, drugs, I can lower heart rate may have added effect of depressing heart rate rate and blood pressure if Brimonidine used with alpha adrenergic agonist
Prostaglandin agonists
Class- Anti glaucoma agents
Prototype- Lantanoprost (xalantan) MOA- selective agonist of a prostaglandin receptor FP, increases outflow of aqueous humor by acting on the receptors and thus decreasing intraocular pressure, absorbed through cornea, hydrolyzed to active form, not knowing if it crosses, placenta and animal studies there are adverse fetal effects metabolize in the urine
Bimatoprost (lumigan) is synthetic form, decreases intraocular pressure by increasing aqueous humor outflow
Unoprost (rescula) and travaprost (travatan) are also synthetic, F2 alpha analogues,
Pharmacokinetics- Bimatoprost- absorb and reach a steady state of plasma, metabolize by oxidation and exerted in urine and feces.
Travaprost- absorbed from cornea and peaks and plasma within 30 minutes hydrolyzed in cornea and rapidly cleared within 60 minutes
Unoprostone- rapidly absorbed from cornea and hydrolyzed into unoprostone free acid rapidly eliminated in urine
MOA is unknown- thought to decrease intraocular pressure by decreasing uveoscleral outflow
Bimatoprost is also marked as Latisse to treat lash hypotrichosis
Lantanoprost -do not instill with contacts in use caution in those with iritis, pregnancy category C
Brimatoprost pregnancy category C
Adverse effect - feeling a foreign body in eye, keratopathy, Iris discoloration, gradual, increase in amount of brown pigment from increase and number of melanosomes which is usually permanent, Bimatoprost can cause permanent brown iris, pigment, and hair growth outside of the treatment area must only be applied to upper lashes
Drug-drug- interacts with thimerosal, wait 5 between the two different drops
Beta blockers
Class- Anti glaucoma agent
Pharmacokinetics- Little is known, duration is 12 to 24 hours , systemic absorption does occur in a can be seen on the lungs and heart
Contraindicated and deal with asthma, COPD or other pulmonary diseases
Decreases conduction through atrial ventricular node topical beta blockers are contraindicated in those with bradycardia or AV blocks or those with a cystic blood pressure less than 100 use in caution with those with poorly control diabetes, raynauds, peripheral artery, occlusive, disease or CVA, pregnancy C category, topical beta blocker excrete in breastmilk so contraindicated in breast-feeding
Adverse effects -headache, dizziness, systemic, like bradycardia, hypotension, broncos spasm
Drug-drug- use with systemic beta blockers can’t cause additive effects, timolol can cause bradycardia and asystole, also interact with beta blocker, pressers, calcium channel blockers, amiodarone, quinidine, beta agonist
betaxolol/caretolol/metipranol interacts with beta blockers other pressers calcium channel blockers did Jackson amiodarone and beta agonist, levobunolol-interacts with other beta blockers and beta agonist
Adverse drug reactions for all antiglaucoma agents
All drugs may cause transient discomfort, or tearing blurred vision, photophobia, hyperemia may occur
Bacitracin (eye)
Class- bacteriostatic
Inhibits incorporation of amino acid and nucleotides into the cell
Active against gram positive staph, steep, clostridia, corynebacterium, anaerobes
Active against gram negative gonococci, meningococci, fusobacteria
Can cause blurred vision but transient
No drug to drug interactions
EES (eye)
Class- bacteriostatic
Marcolide that binds to 50S ribosomal subunits, inhibits bacterial protein synthesis
Active against gram positive staph aureus, strep pyogenes, strep pneumonia; strep viridians, corynebacterium diptheriae, chlamydia, trachomatis
Limited gram negative coverage
Safe in children
No drug drug interactions
Sulfacetamide (eye)
Class- sulfonamide
Inhibits bacterial Dihydrofolate synthesis
Active against strep, staph, ecoli, klebiseilla, pseudomonas, pyocynea, neisserria gonorrhea, chlamydia
Drainage can inactive
Not for those less than 2 mths old
Can cause hypersensitivity reactions in those all allergic to oral sulfa , can also cause burning or stinging
Drug-drug- Incompatible with silver preparations if use with zinc preparation it precipitates, interacts with -Caine drugs, can antagonize sulfa
Tobrmycin (eye)
Class- aminoglycoside
Active against staph, strep, corynebacterium, klebsiella, morakella, proteus, beta hemolytic strep, HI
Not active against Neisseria or chlamydia
Safe in children
Can cause local ocular, toxicity or hypersensitivity
No drug to drug interactions
Gentamycin (eye)
Class- aminoglycoside
Active against gram positive and negative pathogens
MOA unknown
Covers staph, strep pneumonia, beta hemolytic strep, ecoli, HI, n.gonorrhea, enterobacteria
Can cause local ocular, toxicity or hypersensitivity
Pregnancy category C
No drug to drug interactions
Azithromax (eye)
Gets 88% of gram positive and 92% of gram negative bacteria in RCT including 93% of HI
Age less that one safety not established
No drug to drug interactions
Fluoroquinolones (eye)
Bacterial cidal via inhibition of DNA gyrase
Active against staph, strep, HI, klebsiella, proteus, enterobacter, p.aeruginosa
Pregnancy category C
In those less than one year safety is not established
Moxifloxacin is ok for children for 4 moths and older
Can cause a white crystal precipitate in the cornea lid crusting crystal scales and sense of foreign body in the eye altered taste can also cause photophobia nausea decrease vision , conjunctival hyperemia, corneal straining
Drug-drug- increases theophyline and INR levels