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treatment goals
achieve ≥25% reduction in intraocular pressure from pretreatment with fewest meds and minimal adverse fx
drug classes
prostaglandin analogues
b-adrenergic blockers
a-adrenergic agonists
carbonic anhydrase inhibitors
cholinergic agonists
rho kinase inhibitors
classes that increase aq humor outflow
prostaglandin analogues
a-adrenergic agonists
cholinergic agonists
rho kinase inhibitors
classes that decrease aq humor production
b-adrenergic blockers
a-adrenergic agonists
carbonic anhydrase inhibitors
rho kinase inhibitors
prostaglandin analogue pearls
decreases IOP by 25-33%
ocular side fx and HA ~ well tolerated
contraindicated in pregnancy (miscarriage or induce early birth)
prostaglandin analogue meds
latanoprost
bimatoprost
travoprost
tafluprost (PF)
prostaglandin analogue side fx
eyelash lengthening (reversible)
iris darkening (irreversible)
dark circles (reversible)
herpes activation
b-adrenergic blocker pearls
decreases IOP by 20-25%
ocular & more systemic fx
caution (not avoid) with chronic resp. & CV conditions
less potent than prostagladin analogues
b-adrenergic blocker meds
selective:
betaxolol
nonselective:
timolol
carteolol
levobunolol
metipranolol
nasolacrimal occlusion technique
reduces risk & severity of systemic adverse fx
put pressure on tear ducts & close eyes after admin eye drops so more is absorbed
a-adrenergic agonists pearls
decreased IOP by 20-25%
ocular & systemic side fx
caution with CV meds, MAOIs, TCAs (ddi)
safest in pregnancy
less potent than prostaglandin analogues
use nasolacrimal occlusion technique
a-adrenergic agonist meds
selective:
brimonidine
apraclonidine
carbonic anhydrase inhibitors pearls
decrease IOP by 15-20% (top) & 20-30% (oral)
ocular & systemic side fx (bad taste)
avoid in sulfonamide allergy
carbonic anhydrase inhibitor meds
ocular:
brinzolamide
dorzolamide
oral:
acetazolamide
methazolamide
cholinergic agent pearls
decreases IOP by 20-25%
ocular & systemic side fx
caution acute ocular inflammation
use nasolacrimal occlusion technique
cholinergic agent med
pilocarpine
lines of drug therapy
first line - prostaglandin analogues then beta blockers
second line - a-agonists, carbonic anhydrase inhibitors, cholinergics, rho kinase inhibitors
initiation & titration of therapy
start with single agent
if target IOP not reach switch to another in same class before adding a 2nd drug of different class
if second drug monotherapy ineffective then add second agent of diff class
if 2 drugs ineffective then add third agent of diff class
monitor IOP every 4-6 wks after starting new med
surgery or laser procedure if nothing effective
rho kinase inhibitor pearls
decreases IOP by 15-25%
only ocular side fx (conjunctival hyperemia very common)
1x daily dosing
rho kinase inhibitor meds
netarsudil
cannabinoid pearls
decrease bp ~ blood flow to eye & optic nerve
decreases aq humor production & increase outflow
surgical treatment
laser: increases aq humor outflow by poking holes, little scarring can be repeated, for pts that fail drug therapy
surgery: creates pathway for aq flow, first line txt for pts with severe visual loss
eye drop admin counseling
wash hands to avoid contaminating bottle tip
tilt head back and pull lower eyelid to form pocket
admin 1 drop and gently close eyes
nasolacrimal occlusion technique
wait for 3-5 min between eyedrops if taking multiple
blot excess liquid or wash if prostaglandin analogue
refrigerate product if pt struggles to hit the eye
managing side fx
use artificial tears before eye drops to decrease burning/stinging
brimonidine tartrate if conjunctival hyperemia (redness)
storage
store away from other drop bottle items
keep in box
know name and cap colors
read name out loud
take eye & ear drops at diff times
throw away leftover bottles
POAG epidemiology
second leading cause of blindness worldwide
age 70’s most common
women more likely
white ppl more likely
risk factors
high IOP ~ >22 mmHg
family hx
type 2 diabetes
very nearsighted
hx of eye trauma
CV diseases
male smokers
POAG pathophysiology
imbalanced aq humor production & drainage —> increased IOP causing stress on posterior of eye —> optic nerve cells & fibers damage/die —> reduced peripheral visual field and enlarged blind spots
increased IOP is not defining criterion for POAG
POAG diagnosis
tonometry
air pulse (non-contact)
ophthalmoscopy (fundus exam)
perimetry - measure visual field
POAG prognosis
slow progression (mos to yrs)
functional loss irreversible
earlier discover the better
POAG pharm therapy
eye drops & oral meds
POAG txt goals
goal: preserve remaining visual field & maintain QOL
POAG drug