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Antiarrhythmic Drugs
Arrhythmia
• Definition:
– Disturbances in the heart rate, rhythm, impulse
generation or conduction of electrical impulses
responsible for membrane depolarization
– These disturbances can lead to alterations in
overall cardiac function that can be life
threatening.
• Antiarrhythmic drugs:
– Compounds used to prevent or treat cardiac
arrhythmias
1. Arrhythmia
2. Tachycardia
3. Bradycardia
4. PSVT
5. Atrial flutter
6. Atrial fibrillation
7. Ventricular fibrillation
Mechanism of arrhythmias
• Disturbances in impulse generation may be
due to
– Abnormal automaticity
– Delayed after depolarizations
• Disturbances of impulse conduction
– The impulse may recirculate in heart causing
repeated activation (re-entry)
– Conduction blocks
Re-entry phenomenon
Phases of action potential of cardiac cells
• Phase 0 rapid depolarisation
(inflow of Na+)
• Phase 1 early repolarisation
(inward Na+ current
deactivated, outflow of K+)
• Phase 2 plateau (slow inward
calcium current)
• Phase 3 rapid repolarisation
(calcium current inactivates, K+
outflow)
• Phase 4 slow diastolic
depolarization (Slow Na+
inflow, slowing of K+ outflow)
Phase 4
II
Phase 0
Phase 1
Phase 3
0 mV
-80mV
I
III
IV
Phase 2
Classification of antiarrhythmics
• Class I: Sodium channel blockers
• Class II: β-Adrenergic blockers
– Propranolol, acebutolol, esmolol
• Class III: Potassium channel blockers
– Amiodarone, bretylium, sotalol
• Class IV: calcium channel blockers
– Verapamil, diltiazem
• Miscellaneous
– PSVT: Adenosine, Digoxin
– AV block: Atropine
Class I: Sodium channel blockers
• IA: Prolong repolarization
– Quinidine, procainamide, disopyramide, morcizine
• IB: Shorten repolarization
– Lignocaine, mexiletine, phenytoin
• 1C: Little effect on repolarization
– Encainide, flecainide, propafenone
Class IA
Quinidine
• D- isomer of quinine obtained from cinchona bark
• MOA: blocks sodium channels
– ↓ automaticity , conduction velocity and prolongS
repolarization
– ↓phase 0 depolarization , ↑ APD & ↑ERP
• Other actions:
– ↓ BP (α block), skeletal muscle relaxation
• Uses: Atrial and ventricular arrhythmias
• Adverse effects:
– Arrhythmias and heart block , hypotension, QT prolongation
– GIT , thrombocytopenia, hepatitis , idiosyncratic reactions
– High doses – cinchonism like quinine
• Procainamide:
– Derivative of procaine
– No vagolytic or α-blocking action unlike quinidine
– Better tolerated
– Adverse effects:
• Nausea, vomiting and hypersensitivity reactions
• Higher doses can cause hypotension, heart block and
QT prolongation
• Disopyramide:
– Significant anticholinergic properties:
• Dry mouth, blurred vision, constipation, urinary
retention
Class IB drugs
Lignocaine, phenytoin,
mexiletine
Block sodium channels
also shorten
repolarization
Lignocaine
• Local anaesthetic
• Raises threshold for action potential,
↓automaticity at ectopic sites
• Suppress electrical activity of arrhythmogenic
tissues, normal tissues less effected
• High first pass metabolism so given
parenterally
• Use: ventricular arrhythmias
• Adverse effects:
– Drowsiness, hypotension, blurred vision,
confusion and convulsions
• Phenytoin:
– Antiepileptic also useful in ventricular arrhythmias
(not preferred) and digitalis induced arrhythmias
• Mexiletine:
– Can be used orally causes dose related
neurological adverse events like tremors and
blurred vision
– Nausea is common
– Used as alternative to lignocaine in ventricular
arrhythmias
Class I C drugs
Encainide, Flecainide, Propafenone
Have minimal effect on
repolarization
Are most potent sodium
channel blockers
Prophylaxis in PSVT
•Risk of cardiac arrest ,
sudden death so not used
commonly
•May be used in severe
ventricular arrhythmias
Class II drugs
• Supress adrenergically mediated ectopic activity
• Antiarrhythmic action due to of β blockade
• Depress myocardial contractility, automaticity and
conduction velocity
• Depress phase-4 depolarization
• Propranolol:
– Treatment & prevention of supraventricular
arrhythmias especially associated with exercise,
emotion or hyperthyroidism
• Esmolol:
– IV short acting can be used to treat arrhythmias
during surgery , following MI & other emergencies
Class III drugs
↑APD & ↑RP by
blocking the K+ channels
Amiodarone
• Iodine containing long acting drug
• Mechanism of action: (Multiple actions)
– Prolongs APD by blocking K+ channels
– blocks inactivated sodium channels
– β blocking action , Blocks Ca2+ channels
– ↓ Conduction, ↓ectopic automaticity
• Pharmacokinetics:
– Variable absorption 35-65%
– Slow onset 2days to several weeks
– Duration of action : weeks to months
– Many drug interactions
Amiodarone
• Uses:
– Can be used for both supraventricular and ventricular
tachycardia, AF, WPW syndrome, Tachyarrhythmia's,
resistant arrhythmias
• Adverse effects:
– Cardiac: heart block , QT prolongation, bradycardia,
cardiac failure, hypotension
– Pulmonary: pneumonitis leading to pulmonary fibrosis
– Bluish discoloration of skin
– GIT disturbances, hepatotoxicity
– Blocks peripheral conversion of T4to T3 can cause
hypothyroidism or hyperthyroidism
• Bretylium:
– Adrenergic neuron blocker used in resistant
ventricular arrhythmias
• Sotalol:
– Beta blocker
• Dofetilide:
– Selective K+ channel blocker, less adverse events
– Oral use in AF to convert or maintain sinus rhythm
• Ibutilide:
– K+ channel blocker used as IV infusion in AF or
flutter can cause QT prolongation
Calcium channel blockers (Class IV)
• Inhibit the inward
movement of calcium
↓ contractility,
automicity , and AV
conduction.
• Verapamil & diltiazem
Verapamil
• Uses:
– Terminate PSVT
– control ventricular rate in atrial flutter or
fibrillation
• Drug interactions:
– Displaces digoxin from binding sites
– ↓ renal clearance of digoxin
Other antiarrhythmics
• Adenosine :
– Purine nucleotide having short and rapid action
– Mechanism of action: AcetylCholine sensitive K+ channels
and causes membrane hyperpolarization through
interaction with A1 type of adenosine GPCRs on SA node
– IV suppresses automaticity, AV conduction and dilates
coronaries
– Drug of choice for PSVT
– Adverse events:
• Nausea, dyspnoea, flushing, headache
• Atropine: Used in sinus bradycardia
• Digitalis: Atrial fibrillation and atrial flutter
• Magnesium SO4: digitalis induced arrhythmias

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Antiarrhythmic Drugs: Classification and Mechanisms

  • 2. Arrhythmia • Definition: – Disturbances in the heart rate, rhythm, impulse generation or conduction of electrical impulses responsible for membrane depolarization – These disturbances can lead to alterations in overall cardiac function that can be life threatening. • Antiarrhythmic drugs: – Compounds used to prevent or treat cardiac arrhythmias
  • 3. 1. Arrhythmia 2. Tachycardia 3. Bradycardia 4. PSVT 5. Atrial flutter 6. Atrial fibrillation 7. Ventricular fibrillation
  • 4. Mechanism of arrhythmias • Disturbances in impulse generation may be due to – Abnormal automaticity – Delayed after depolarizations • Disturbances of impulse conduction – The impulse may recirculate in heart causing repeated activation (re-entry) – Conduction blocks
  • 6. Phases of action potential of cardiac cells • Phase 0 rapid depolarisation (inflow of Na+) • Phase 1 early repolarisation (inward Na+ current deactivated, outflow of K+) • Phase 2 plateau (slow inward calcium current) • Phase 3 rapid repolarisation (calcium current inactivates, K+ outflow) • Phase 4 slow diastolic depolarization (Slow Na+ inflow, slowing of K+ outflow) Phase 4 II Phase 0 Phase 1 Phase 3 0 mV -80mV I III IV Phase 2
  • 7. Classification of antiarrhythmics • Class I: Sodium channel blockers • Class II: β-Adrenergic blockers – Propranolol, acebutolol, esmolol • Class III: Potassium channel blockers – Amiodarone, bretylium, sotalol • Class IV: calcium channel blockers – Verapamil, diltiazem • Miscellaneous – PSVT: Adenosine, Digoxin – AV block: Atropine
  • 8. Class I: Sodium channel blockers • IA: Prolong repolarization – Quinidine, procainamide, disopyramide, morcizine • IB: Shorten repolarization – Lignocaine, mexiletine, phenytoin • 1C: Little effect on repolarization – Encainide, flecainide, propafenone
  • 10. Quinidine • D- isomer of quinine obtained from cinchona bark • MOA: blocks sodium channels – ↓ automaticity , conduction velocity and prolongS repolarization – ↓phase 0 depolarization , ↑ APD & ↑ERP • Other actions: – ↓ BP (α block), skeletal muscle relaxation • Uses: Atrial and ventricular arrhythmias • Adverse effects: – Arrhythmias and heart block , hypotension, QT prolongation – GIT , thrombocytopenia, hepatitis , idiosyncratic reactions – High doses – cinchonism like quinine
  • 11. • Procainamide: – Derivative of procaine – No vagolytic or α-blocking action unlike quinidine – Better tolerated – Adverse effects: • Nausea, vomiting and hypersensitivity reactions • Higher doses can cause hypotension, heart block and QT prolongation • Disopyramide: – Significant anticholinergic properties: • Dry mouth, blurred vision, constipation, urinary retention
  • 12. Class IB drugs Lignocaine, phenytoin, mexiletine Block sodium channels also shorten repolarization
  • 13. Lignocaine • Local anaesthetic • Raises threshold for action potential, ↓automaticity at ectopic sites • Suppress electrical activity of arrhythmogenic tissues, normal tissues less effected • High first pass metabolism so given parenterally • Use: ventricular arrhythmias • Adverse effects: – Drowsiness, hypotension, blurred vision, confusion and convulsions
  • 14. • Phenytoin: – Antiepileptic also useful in ventricular arrhythmias (not preferred) and digitalis induced arrhythmias • Mexiletine: – Can be used orally causes dose related neurological adverse events like tremors and blurred vision – Nausea is common – Used as alternative to lignocaine in ventricular arrhythmias
  • 15. Class I C drugs Encainide, Flecainide, Propafenone Have minimal effect on repolarization Are most potent sodium channel blockers Prophylaxis in PSVT •Risk of cardiac arrest , sudden death so not used commonly •May be used in severe ventricular arrhythmias
  • 16. Class II drugs • Supress adrenergically mediated ectopic activity • Antiarrhythmic action due to of β blockade • Depress myocardial contractility, automaticity and conduction velocity • Depress phase-4 depolarization • Propranolol: – Treatment & prevention of supraventricular arrhythmias especially associated with exercise, emotion or hyperthyroidism • Esmolol: – IV short acting can be used to treat arrhythmias during surgery , following MI & other emergencies
  • 17. Class III drugs ↑APD & ↑RP by blocking the K+ channels
  • 18. Amiodarone • Iodine containing long acting drug • Mechanism of action: (Multiple actions) – Prolongs APD by blocking K+ channels – blocks inactivated sodium channels – β blocking action , Blocks Ca2+ channels – ↓ Conduction, ↓ectopic automaticity • Pharmacokinetics: – Variable absorption 35-65% – Slow onset 2days to several weeks – Duration of action : weeks to months – Many drug interactions
  • 19. Amiodarone • Uses: – Can be used for both supraventricular and ventricular tachycardia, AF, WPW syndrome, Tachyarrhythmia's, resistant arrhythmias • Adverse effects: – Cardiac: heart block , QT prolongation, bradycardia, cardiac failure, hypotension – Pulmonary: pneumonitis leading to pulmonary fibrosis – Bluish discoloration of skin – GIT disturbances, hepatotoxicity – Blocks peripheral conversion of T4to T3 can cause hypothyroidism or hyperthyroidism
  • 20. • Bretylium: – Adrenergic neuron blocker used in resistant ventricular arrhythmias • Sotalol: – Beta blocker • Dofetilide: – Selective K+ channel blocker, less adverse events – Oral use in AF to convert or maintain sinus rhythm • Ibutilide: – K+ channel blocker used as IV infusion in AF or flutter can cause QT prolongation
  • 21. Calcium channel blockers (Class IV) • Inhibit the inward movement of calcium ↓ contractility, automicity , and AV conduction. • Verapamil & diltiazem
  • 22. Verapamil • Uses: – Terminate PSVT – control ventricular rate in atrial flutter or fibrillation • Drug interactions: – Displaces digoxin from binding sites – ↓ renal clearance of digoxin
  • 23. Other antiarrhythmics • Adenosine : – Purine nucleotide having short and rapid action – Mechanism of action: AcetylCholine sensitive K+ channels and causes membrane hyperpolarization through interaction with A1 type of adenosine GPCRs on SA node – IV suppresses automaticity, AV conduction and dilates coronaries – Drug of choice for PSVT – Adverse events: • Nausea, dyspnoea, flushing, headache • Atropine: Used in sinus bradycardia • Digitalis: Atrial fibrillation and atrial flutter • Magnesium SO4: digitalis induced arrhythmias