Cardiac Drugs Flashcards
Blood pressure
MAP = 2(DBP) + SBP / 3
MAP = HR x SV x SVR
Phases of contraction
Phase 0: rapid depolarization, influx of Na through “fast” channels
Phase 1: beginning of depolarization, Na channels close, K and Cl open
Phase 2: Plateau, balance btwn Ca influx and K efflux
Phase 3: Ca channels close, cellular repolarization
Phase 4: Resting state returns Na influx, K efflux
Chronotropic and Inotropic
Chronotropic: changes HR, affects nerves controlling heart, postive increases HR, negative decreases HR
Inotropic: Affects force of contraction, can be - or +
Hypotension Drugs (Shock)
Fluids are first-line therapy
Catecholamines
NE, Isoproterenol, dopamine, phenylephrine, vasopressin
Inotropes
Dobutamine, Phosphodiesterase inhibitors cardiac glycosides
Catecholamines
NE (Levophed) and EPI (Adrenalin)
endogenous catecholamines secreted by adrenal medulla
Net response is tachycardia and vasoconstriction
Isoproterenol Synthetic catecholamine Treats symptomatic bradycardia or torsades de pointes B receptor agonist Limited use because of HR effects
Dopamine
Precursor to NE, Stimulates B receptors increases after load and myocardial oxygen demand
Phenylephrine
Purely a-agonist, vasoconstriction elevates total peripheral resistance
Vasopressin
Increases BP and water retention effect, aka anti diuretic hormone
Inotropic agents
Dobutamine (dobutrex)
Short term treatment of heart failure
R-isomer causes positive Inotropic effects, vasodilation
Phosphodiesterase inhibitors (Inamrinone and milrinone) Inotropic vasodilator, increases cAMP
Cardiac glycosides (digoxin)
Management of CHF
Inotropic effect, inhibits Na/K ATPase pump
Narrow therapeutic margin
Advanced cardiac life support pharmacotherapy
Epinephrine
1mg dose of 10 mL solution
Stimulates a-receptors and B Adrenergic effects
Decrease affinity in metabolic acidosis
Sodium bicarbonate
Dose 1mEq/kg
Limited use, will increase CO 2 levels
Used to keep pH above 7.2
Vasopressin
1 x dose of 40 units (substitute of dose of epinephrine)
Affinity not compromised in metabolic acidosis
Atropine
1mg IV push in asystole or PEA along with EPI or Vasopressin
Blocks acetylcholine
Magnesium sulfate
Used for torsades de pointes (caution in renal impairment)
Alternative administration routes
Interosseous
for use in children especially and neonates
ETT
NAVEL…Naloxone, Atropine, Vassopressin, EPI, Lidocaine
Double the dose with dilute in 10 mL of NS or water, follow with vent.
Hypertensive drugs
First line agents Angiotensin-converting enzyme inhibitors Angiotensin II receptor blockers Calcium channel blockers B-blockers Thiazide diuretics
Second line Vasodilators a-blockers a2 agonists anti-adrenergics
Angiotensin-converting enzyme inhibitors
Indications
Hypertension, heart failure, systolic dysfunction, MI prevention, LV dysfunction, and diabetic neuropathy
Common side effect is dry cough (treated with cromolyn sodium)
Significant interaction with NSAIDS
Mode of action Block conversion of angiotensin I to II Reduce peripheral arterial resistance Increase CO Increase renal blood flow
Angiotensin II receptor blockers
Slightly weaker than ACEI’s
Indicated for hypertension and heart failure
Calcium channel blockers
Indirect dilation of vasculature by blocking vasoconstriction via calcium channel blockade
Coronary and peripheral dilation
Verapamil and diltiazem (negative chronotropic/inotropic effects)
B-blockers
Mode of action
Blockade of B receptors on renal juxtaglomerular cells, myocardial, and CNS receptors
May induce bronchospasm and render B-agonist ineffective