Drugs of the Heart Part I
- Cardiovascular disorders
- Congestive heart failure (CHF)
- Cardiac arrhythmias
- Angina pectoris
- MI
- Hypertension or hypotension
- Shock
- Drug classes
- Vasopressors
- Inotropes
- Vasodilators
- Antiarrhythmia
- Tachycardia
- Bradycardia
- Electrolytes
- Anti-thrombotic
- Sedatives and paralytics
- Pain management
- Sepsis
- Associated
terms you should know
- CO
(CO) = Heart Rate x stroke volume
- Preload
– Volume coming in - filling pressures of the cardiac chambers
- Afterload
– Volume going out - resistance
- Contractility
– result in ejection fraction (EF)
- Terms
associated with cardiac medication
- Inotropic
– affects contractility
- Chronotropic
– affects heart rate (increase or decrease)
- Positive chronotropic drugs increase heart rate
- Negative chronotropic drugs decrease the heart rate
- Dopaminergic
– may increase urine output and mesenteric vasodilation
- Receptors
in the heart - Two basic types alpha α and β
- Alpha
- Found in vascular smooth muscle and heart muscle
- Two
types
- Alpha
1
- Vasoconstriction of smooth muscle
- Increases
Inotropic
- Decreases chronotropic
- Alpha
2
- Prevents
release of norepinephrine
- Counters
alpha 1
- Modulates
vascular tone of large vessels
- Alpha
effects
- Increases
blood flow to brain, heart, and skeletal muscles
- Increases
cellular metabolism
- Increases
O2 consumption and CO2 production
- Causes
pupil dilation
- Beta
- Found in vascular smooth muscle and heart
- Two
types
- Beta
1
- Increases chronotropic and decreases Inotropic
- Increases
conduction
- Found
mostly in heart tissue
- Beta
2
- Vasodilation of smooth muscle
- Relaxes
bronchioles and gut smooth muscles
- Found
mostly in bronchioles and gland cells
- Overall
effect
- Increases
heart rate and contractility
- Increases
sweat production
- Decreases
GI tone and motility
- Causes
urinary retention
- Causes
bronchial relaxation
- Specific
Drugs that effect the heart - There are 5 general categories
- Vasopressors (Category I)
- Characteristics
- Maintain
tissue perfusion by keeping the systolic pressure @ 90 mmHg
- Note: 60 mmHg required to keep all major organs
perfused, but the brain needs 70 mmHg
- Affects
patient’s fight or flight response
- If
the patient electrolytes are low, low blood volume, and/or acidosis this drug
will be less effective
- Tissue
necrosis occurs if injected subcutaneously
- Increases
O2 supply to cardiac tissue (MVO2)
- There are 5 different drugs in the category
- Vasopressin
- Alternative
to epinephrine
- Potent
peripheral vasoconstrictor
- Lasts
2 – 8 hours
- Epinephrine
(Adrenalin)
- Effects
both Alpha and Beta receptors
- Heart
becomes more responsive to fibrillation
- Stimulates
pacemaker activity and conductivity in cardiac resting state
- Immediate
treatment for anaphylaxis or any hypersensitive response
- Dose
can be given initially during cardiac rest and then IV drip as needed
- Norepinephrine
(Levophed)
- Effects
Alpha significantly more than Beta receptors
- Causes
vasoconstriction and decreases renal, visceral, and skeletal blood flow
- Used
on patients that have: hypotensive
states, cardiogenic and septic shock
- Dose
is best given through a central line
- Is
not a first line drug
- Dopamine
(Intropin)
- Pending
dose level it effects Alpha and Beta receptors, dopaminergically
- Low
dose should no longer be used (2-3 mcg/kg/min)
- Moderate
dose 5-10 mcg/kg/min
-Stimulates
beta receptors to increase: HR,
contractility, BP, and CO
- High
Dose: 10-20 mcg/kg/min
- Beta
activity remains and Alpha activity is overwhelmed by Dopaminergic actions
- Above
results cause vasoconstriction
- Indication: hypotension (not volume related), shock,
septicemia, CHF
- Usually
a first line drug
- Phenylephrine
(Neosynephrine)
- Alpha
1 stimulant causing vasoconstriction (does not effect the heart)
- Reduces
renal and mesenteric blood flow, which limits its long term use
- Used
in short-term management of hypotension or septic shock
- Side
effects of Vasopressors
- May
cause ventricular dysrhythmias
- Palpitations
and tachycardia are possible
- Hypertension
- Angina
- Decreased
urinary output
- Headaches
are common
- Inotropics (Category 2)
- Characteristics
- Increases
the force of myocardial contraction
- Major
role in the clinical treatment of CHF
- Dobutamine
(Dobutrex)
- Works
mostly on Beta 1 receptors
- Mild
effect on Beta 2 receptors
- Increases
contractility, effecting the stroke volume, and CO with little effect on heart
rate
- Increases
coronary blood flow and MVO2
- Due
to the increase in CO causes increase in blood supply to peripheral areas and the
kidneys
- First
line drug
- Indicators
- Heart
failure
- Cardiogenic
shock
- Low
CO states: RV infarcts and LV
failure
- Side
effects
- Palpitations
and/or tachycardia
- Arrhythmias
- Angina
- Hypertension
- Milrinone
(Primacor)
- Phosphodiesterase inhibitor without adrenergic effect
- prolong and enhances the effects of
physiological processes mediated by these cyclic nucleotides. cAMP and
cGMP
- Analog
to amrinone (vasodilator) with similar actions, but more effective and fewer
side effects
- Positive inotropic and causes vasodilator
- Indications
- CHF
- Low
cardiac output (for whatever reason)
- Side
effects
- Hypotension
- Angina/arrhythmias
- Thrombocytopenia
- Sulfite
allergy (amrinone only)
- Isoproterenol (Isuprel)
- Action
- Stimulates
beta 1 and 2
- Potent inotropic and chronotropic
- Stimulates
heart, dilates vessels in skeletal muscles, and relaxes bronchial smooth
muscles
- Indications
- Transplants
and pediatrics
- Might
be used in cardiogenic shock except if caused by MI
- Respiratory
drug for bronchospasm
- Side
effects
- Proarrrhythmia – antiarrhythmic that causes new arrhythmias which may result in V-Tack
- Palpitations
and angina
- Headache
and anxiety
- Hypotension
- Digoxin (Lanoxin)
- Action
- Increases
myocardial contractility
- Reduces
heart rate
- Side
effects
- Excess
amount may cause toxicity
- Symptoms
include: nausea, vomiting, anorexia,
blurred or yellow vision, fatigue, bradycardia, and
heart blocks
- Imbalances
of K, Mg, and Ca increase the toxic effect
- Digibind (Digoxin immune Fab)
- Used to eliminates
the toxic effect of digoxin
- Peripheral
Vasodilators (Category 3)
- Characteristics
- Relaxation
of smooth muscles in blood vessels
- May
decrease BP
- Increases
CO by reduces blood flow (afterload reduction)
- Nitroglycerin
(Tridil)
- Action
- Veno/arterial dilation
- Decreases
venous return, preload, MVO2, BP, CVP, PCWP
- Improves
coronary artery flow and O2
- Indications
- Angina
and/or MI
- HTN
- CHF
- Preload/afterload
reduction
- Side
effects
- Hypotension
- Headache
and dizziness
- Bradycardia
or reflex tachycardia
- Na
Nitroprusside (Nipride)
- Action
- Dilates venous and arterial smooth muscles
- Reduces
BP and PVR
- Initially
decreases afterloading and also decreases preload
- Indications
- Hypertensive
crisis
- Afterload
reduction – CHF, cardiogenic shock, and LV
failure
- Side
effects
- Hypotension
- Thiocyanate toxicity
- Reflex
tachycardia
- Angina
- Fenoldopam (Corlopam)
- Action
- Decreases
PVR
- Increases
renal blood flow, diuretics, and attributes
- Is
an agonist to dopamine
- Indications
- HTN
- Renal
Compromise
- CHF
- Nesiritide (Natrecor)
- Action
- Form
of human B-type natriuretic peptide hBNP)
- Relaxes
smooth muscles
- Acts
as a vasodilator, diuretic, natriuretic, and causes
dose dependency
- Indications
- Acutely decompensates CHF patients that have dyspnea at rest or with minimal activity
- Do
not use with patient on NTG or Nipride
- Side
effects
- Hypotension
- Renal
Dysfunction
- Ventricular
arrhythmias
- Angina
- Bradycardia
- Headache
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For additional information on cardiac pharmacology upload this PDF file
http://deptmed.queensu.ca/clerkship/assets/cardiac_pharmacology_clerk_lecture.pdf