Medical Pharmacology: Antiarrhythmic Drugs
Practice Questions
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Classifications of antiarrhythmic drugs:
- sodium channel blockers
- calcium channel blockers
- potassium channel blockers
- beta-blockers
- all of the above
Antiarrhythmic drug classification: class II
- sodium channel blocker
- calcium channel blocker
- beta adrenergic receptor blocker
- potassium channel blocker
Factors that may precipitate or exacerbate arrhythmias:
- ischemia
- cardiac fiber stretching
- alkalosis
- A & C
- A, B & C
Factors that precipitate or exacerbate arrhythmias:
- abnormal electrolytes
- excess vagal tone
- antiarrhythmic drugs
- A & C
- A, B & C
Normal cardiac impulse propagation sequence:
- AV node, His-Purkinje, ventricle, SA node
- SA node, His-Purkinje, AV node, ventricle
- SA node, AV node, His-Purkinje, ventricle
- AV node, SA node, His-Purkinje, ventricle
- none of the above
Possible cause(s)/characteristic(s) of arrhythmias:
- Improper site of origination
- abnormal rate
- abnormal conduction characteristics
- A & B
- A & C
Principal ions involved in determining the cardiac transmembrane potential:
- chloride, sodium, potassium
- potassium, calcium, chloride
- sodium, calcium, large organic anions
- sodium, calcium, potassium
- sodium, potassium, large organic anions
Factors controlling membrane ionic "gates":
- ionic conditions
- metabolic conditions
- membrane potential
- A & B
- A, B & C
In reference to ionic gradients, the term "electrogenic" means:
- that a large membrane capacitance is present
- that the membrane is relatively permeable to potassium
- that net current flows as a result of ionic transport
- that current flows independent of membrane voltage
- none of the above
Concerning the ionic permeability state of the resting membrane:
- the membrane is relatively impermeable to potassium
- the membrane is relatively impermeable to sodium
- both
- neither
Cardiac cell permeability and conductance:
- conductance -- determined by characteristics of ion channel proteins
- current flow = voltage X conductance
- both
- neither
Cardiac cell membranes: "driving forces" acting on ions--
- Tendency for sodium to be driven out of the cell
- Limited tendency for potassium movement because of the balance between the potassium concentration and membrane electrical gradients
- The concentration gradient for potassium tends to drive potassium out
- B & C
- A, B & C
Principal determinant(s) of cardiac resting membrane potential:
- external potassium concentration
- inward potassium rectifier channel state
- both
- neither
Rapid upstroke characteristic of phase 0 depolarization in Purkinje and ventricular muscle cells:
- due to rapid increase in calcium permeability
- due to rapid decrease in potassium conductance
- due to rapid increase in sodium conductance
- due to significant outward chloride currents
Phase of the cardiac action potential (in SA nodal cells, for example) that is associated with "diastolic depolarization":
- phase 0
- phase 1
- phase 2
- phase 3
- phase 4
Factors which promotes ectopic pacemaker development:
- reduced autonomic, sympathetic activity
- reduced serum potassium
- both
- neither
Sequence of cardiac Purkinje fiber ion channel activation:
- calcium, potassium, sodium
- potassium, calcium, sodium
- sodium, calcium, potassium
Activation of this ion channel mainly associated with cardiac cell repolarization:
- calcium
- potassium
- sodium
Relationship between membrane resting potential when depolarization occurs and conduction velocities:
- increased membrane potential: reduced conduction velocity
- increased membrane potential: increased conduction velocity
Consequences of reduced sodium channel activation due to the reduced membrane potential (less negative) at the time and depolarization
- reduced of upstroke velocity (phase 0); i.e., reduced maximum rate of membrane potential change
- reduced conduction velocity
- increased of effective refractory period (prolongation of recovery)
- B & C
- A, B & C
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