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41 Cards in this Set

  • Front
  • Back
what is the general function of Class I Drugs
Na+ channel blockers
what is the general function of Class II drugs
reduce adrenergic activityon the heart
what is the general function of Class III drugs
K+ channel blockers
what is the general function of Class IV drugs
Ca++ channel blockers
what is the general function of Class I A drugs
blocks activated Na+ channels
lengthens the duration of the action potential
inc ERP
what is the general function of Class I B drugs
blocks inactivated Na+ channels
shortens the duration of the action potential
dec ERP
what is the general function of Class I C drugs
blocks all Na+ channels
No effect on duration of the action potential
what is the Class I A drug of choice
Quinidine
what is the Class I B drug of choice
Lidocaine
what is the Class I C drug of choice
flecainide
what are the Class II drugs
B-blockers

Propranolol
what are the Class III drugs
Amiodarone
Sotalol
what is the Class IV drug of choice
Verapamil
what are the cardiac effects of quinidine (quinora)
prolongs the duration of the action potential
thus, dec automaticity
M receptor blockade (inc HR)
blocks Alpha receptors (vasodilation, poss reflex tachy)
Cinchonism- tinitis, vertigo, headache, allergy
whar are the pharmokinetics of quinidine (quinora)
orall
first pass metabo
t 1/2- 6 hours
what are the toxicitys of Quinidine (quinora)
low therapeutic index
cardiac toxicity
severe hypotension
paradoxical Tachy
Torsade de pointes
digitalis + quinidine = syncope and death
diarrhea
Cinchonism
what are the drug interactions to consider with quinidine
Q + digitalis= syncope and death
phenytoin decreases Q effectiveness
Q inc warfarins effect
Q + NTG= extra dec in BP
increases the effect of muscle relaxants
what extra toxicities does procainamide have over quinidine
SLE***
arthritis
inc ANA titer
hepatitis
How is disopyramide different from quinidine
negative inotropic effect
antichilenergic
what type of arrhythmias is lidocaine used to treat?
Ventricular arrhythmias
lidocaine's mech of action
binds inactivated Na+ channels
-block of the slow Na+ "window" currents
what are the benifits of using Lidocaine over Quinidine (or other Class I A)? Drawbacks?
benifits:
-less hypotension
-does not depress myocardial contractility (least neg inotropic of all antiarrhythmics)
-no vagal blocking

Drawbacks:
-only good for Ventricular arrhythmias
-only IV admin (I.E no outpatient)
lidocaine toxicities
convulsion
bradycardia & aggrivation of arrhythmias occasionally
what is flecainide used for
treatment of supraventricular tachy
life threatening ventricular arrhythmias

CHF clinicl study for its pro-arrhythmic effects**
gen facts about Flecainide
binds all Na+ channels
no ANS effects
orall, hepatic metab & renal excret
key points for propafenone (Class I C)
used for refractory pts c severe, life threatening arrhythmias
B-blocking activity as well
what is the mech of action for Amiodarone
Class III (K+) > Class I, IV activity
alpha blocking effects- vasodilation
What is the half life for Amiodarone
13-103 days

LD-15 to 30 days
toxicities associated with Amiodarone
brady
heart block, heart fail
pulmonary fibrosis
tissue deposition (yellow-eye, blue-skin)
photodermatitis
thyroid dysfxn
constipation
liver toxicity
use of Amiodarone
only approved for Ventricular arrhythmias
Sotalol (betapace) info
K+ blocker
nonselective Beta blocker
prolonged action potential
Oral, renal excre
SV arrhy and ventricular arrhythmias
Toxicity- Torsades de pointes, B-blockade
what are the mech of action and effects of Verapamil
Ca++ channel blocker (L-type)
dec AV conduction, dec HR
most benificial in SVTarrhythmias
antihypertensive
antianginal
pharmokinetics of Vermapimil
Oral or IV
first pass if oral
kidney excretion
what are the key toxicities assoc with verapamil
GI intolerance
bradycardia
neg inotropic effect
poss AV block (IV)
contraindicated in CHF
do not use with B-blockers
use of verapamil
reentrant SVT
reduces ventricular rate in aflutter and afib
uses of diltiazem
Prinzmetals angina
angina pectoris
HTN
following angioplasty
what is the mech of action for Adnosine (Adenocard)
enhanced K+ conductance
inhibit Ca++ influx
inhibits AV conduction
IV admin
toxicities of Adenosine (adenocard)
Flush, SOB, burning
hypotension, headache, nausea
what is the clinical use of Adenosine (adenocard)
Drug of choice for paroxysmal SVT
what is Magnesium sulfate used for
treatment of eclampsia and preeclampsia
digitalis (glycoside) induced arrhythmias
torsade de pointe
K+ and the heart
both hypo and hyperkalemia are arrhythmogenic
hypo- risk of afterdepolarization
hyper- membrane stabilizing to a point, then lethal arrhythmias