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mechanism of class i drugs
block sodium channels in phase 0 of cardiac muscle action potential
influx of sodium, reduce speed of conduction in the heart
what drugs can be used if patient has atrial fibrillation/ flutter and no history of myocardial infarction, coronary heart disease
beta blockers -lol (type ii)
calcium channel blockers (type iv)
flecainide (type 1c sodium)
amiodarone (type iii potassium)
what drugs given if patient has atrial fib/flutter and has had myocardial infarction, chd
beta blockers
calcium channel blockers
amiodarone
what drugs given if patient has acute afib/flutter
potassium channel blockers
(amiodarone)
what drugs given for supraventricular tachycardia SVT
adenosine for acute treatment
beta blockers
verapamil
amiodarone
examples of class i drugs
lidocaine (1b)
flecainide (1c)
mechanism of class ii
inhibit sympathetic nervous system effects
slows down av node conduction
block calcium channels in phase 0 - prolonged refractory period
reduce slope of pacemaker potential (phase 4)
neg chronotropic
when are class ii drugs used
sinus tachycardia
ectopic pacemakers
atrial fibrillation
atrial flutter
side effects of class ii drugs
worsen heart block
cause bradycardia
precipitate heart failure
inc likelihood of diabetes
examples of class ii drugs
beta 1 adrenoreceptor antagonists, end in -lol
atenolol
bisprolol
class iii mechanism
potassium channel blockers
prolong phase 3 of cardiac action potential by inhibiting efflux, delays repolarisation
example of class iii drug
amiodarone (but also fits into many other classes)
class iv mechanism
calcium channel blcokers
effect on sa and av nodes in phase 0 depolarisation
slow firing rate of the SA node and delay conduction through the AV node
class iv example
verapamil
main example of cardio selective calcium channel blocker
when is lidocaine used
in emergency settings for ventricular dysrhythmias
intravenous administration IV
local anaesthetic
lidocaine action
rapid action
short duration
selectively targets inactivated channels - found in ischaemic tissues
side effects of lidocaine
seizures
coma
death at higher doses
when is flecainide used
supraventricular tachycardia
eg atrial fibrillation
not used in structural heart damage patients - can cause tachycardia/fibrillation
flecainide mechanism
binds to open state sodium channels
longer duration of action
used as tablet
fewer side effects than lidocaine
irony of antidysrhythmic drugs
can cause dysrhythmias
mechanism of amiodarone
potassium channel blocker
inhibits beta adrenoreceptors (Class ii)
blocks calcium channels (iv)
inhibits sodium channels (!a)
delays repolarisation - prolongs ap, refractory period
dec av node conduction
dec re entry circuit development
use of amiodarone
atrial fibrillation and flutter
ventricular and supraventricular tachycardias
cardioversion of ventricular fibrillation
limited by side effects and pharmacokinetics
pharmacokinetics of amiodarone
orally or iv administration
fat soluble so diff to establish stable plasma conc
100 days half life
metabolised by CYP3A4
side effects of amiodarone
lung fibrosis
visual problems
liver toxicity
skin discolouration
thyroid function interference due to iodine
bradycardia or av node block worsening
verapamil mechanism
acts on sa node, av node conduction is slowed
dec slope of phase 0 depolarisation
metabolised by CYP3A4
verapamil use
paroxsymal supraventricular tachycardia
av node re-entry tachycardia
NOT IN WOLFF PARKINSON WHITE WITH AFIB
side effects of verapamil
bradycardia
worsening of heart block
vasodilation - flush, hypotension, odeoma, headahce
constipation
dangerous if wolf parkinsons patient has atrial fibrillation
adenosine mechanism
short acting
gi protein - gabba subunit stimulates potassium channels, K+ efflux, hyperpolarisation
dec slope of phase 4
which drugs increase action potential duration
potassium channel blockers
drugs used to treat ventricular tachycardia, DAD, re-entry
primarily amiodarone
beta blockers
lidocaine
best drugs post myocardial infarction
lidocaine