ImportantCar Flashcards

1
Q

cardiac output

A

the quantity of blood pumped into the systemic circulation by the ventricle each minute
- dependent upon the heart rate and stroke volume

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2
Q

Stroke volume

A

the amount of blood ejected by the left ventricle with each heart beat or contraction

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3
Q

Preload

A

time for the heart to fill with blood + enough volume of blood entering the right side of the heart; necessary for adequate stroke volume

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4
Q

Afterload

A

describes the force needed to push blood out of the ventricles or arterial pressure against which the ventricle must pump

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5
Q

what factors influence cardiac output?

A

high blood pressure and/or constriction of the vasculature

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6
Q

in response to hypotension the sympathetic nervous system releases ?

A

Renin-Angiotensin-Aldosterone system + norepinephrine to increase heart rate and cause vasoconstriction of small arteries as a short term solution to raise blood pressure

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7
Q

What does the Renin-Angiotensin-Aldosterone system do in response to hypotension?

A

activated when the kidney detects hypotension and the juxtaglomerular cells release renin and angiotensinogen

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8
Q

How are Angiotensinogen and ACE related/work together?

A

Angiotensinogen converts angiotensin1 to angiotensin2 which is a potent vasoconstrictor, and supports blood pressure. The enzyme that enables conversion of angiotensin1 to angiotensin2 is called angiotensin converting enzyme also known as “ACE”

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9
Q

How does the RAA system influence blood pressure?

A

causes the release of the mineralcorticoid hormone aldosterone from the adrenal gland –> the kidney conserves sodium and water –> blood pressure maintenance

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10
Q

Clinical signs of advanced heart disease are caused by?

A

response to decreased cardiac function, low cardiac output and poor venous return, thus the body tissues no longer receive sufficient blood and oxygenation

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11
Q

RAA cascade as a short term vs long term solution

A

short term - good solution to low blood pressure and cardiac output
long term - increase in sodium and water retention as well as vasoconstriction eventually makes it more difficult for the heart to work against the systemic pressure and weakens the heart muscle

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12
Q

What are important treatments of CHF /focus of cardiac drug therapy

A

inhibinting the RAA system and/or vasodialation by other mechanisms of action, diuresis to remove excess fluid, and strengthenign the force of heart muscle contration

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13
Q

What are the (important) sympathetic adrenergic receptors involved with cardiac function?

A

Alpha-1 (peripheral vessel constriction, increase BP)
Beta-1 (increase HR, force of constriction and blood glucose)
Beta-2 (bronchodilation)

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14
Q

compare the functions of the different sympathetic adrenergic receptors involoved with cardiac function

A

Alpha-1 (peripheral vessel constriction, increase BP)
Beta-1 (increase HR, force of constriction and blood glucose)
Beta-2 (bronchodilation)

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15
Q

What compensatory mechanisms will the heart take on to decrease workload on the heart and increase cardac output in response to a failing heart?

A

the heart will enlarge in an attempt to pump out more blood (dilated cariomyopathy and hypertrophic cardiomyopathy)

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16
Q

compare dilated cardiomyopathy and hypertrophic cardiomyopathy

A

DC- heart chamber dilation
HC- thickened myocardium

17
Q

Postitive Inotropes

A
  • Drugs that increase the heart’s stroke volume by increased force of heart muscle contraction
  • are used if the heart muscle is too weak to adequately pump
  • Drugs in this category include the cardiac glycosides, and sympathomimetic drugs which mimic the action of adrenergic sympatheticstimulation.
18
Q

What am I?
- cardiac glycoside
- derivative of purple foxglove plant (Digitalis purpurea)
- treat CHF and arrhytmias (atrial fibrillation and supraventricular tachycardia)
- narrow margin of safety
- interact with many other drugs
- must be dosed based on lean body mass and monitored through periodic blood testing (due to adverse effects and toxicity)
- fallen out of favor with the development of less toxic drugs

A

digoxin (Cardoxin) and Digitoxin (Crystodigin)

19
Q

What am I?
- sympathomimetic
- directly stimulates the heart
- used in cases of shock, severe allergic reactions and cardiac asystole emergencies
- affects both alpha and beta adrenergic receptors –> increased heart rate and contractility, increased blood pressure, increased blood glucose, bronchodilation, constriction of peripheral vessels and antagonizes the effects of histamine
- immediate onset when administered intracardiac, IV or intratracheal in emergency situations

A

Epinephrine (Adrenalin)

20
Q

What is a contraindication of Epinephrine?

A

use cautiously due to caridac side effect of causing arrhythmias (ventricular fibrillation and hypertension)

21
Q

Why would Epi be added to a local anesthetic?

A

The solution (Epi) is available in various strengths and is an ingredient found in local anesthetics such as lidocaine for its ability to constrict local vessels allowing the lidocaine to remain in the area.

22
Q

Pay attention! Theres a cardiovascular emergency, why should you pause before administering Epi (solutions)?

A

Lidocaine is also used to correct ventricular arrhythmias such as PVCs and ventricular tachycardia, therefore DO NOT USE lidocaine intended for local anesthesia in these cases since it contains epinephrine as it will cause tachycardia and worsen arrythmias!!

23
Q

Compare/contrast Dopamine and Dobutamine

A

Both :Dopamine and dobutamine are sympathomimetics used in critical care settings to increase cardiac output and have the effects of increasing heart rate, heart contractility and blood pressure.
- Due to their shortduration of action these drugs are given as a constant rate of infusion.
Dopamine is able to increase organ perfusion, especially blood flow to the kidney but is more likely to have tachycardia as a side effect.
Dobutamine is less likely to cause tachycardia as a side effect but does not have as much ability to increase blood flow to the viscera and kidney.

24
Q

Vasodilator

A

drugs used in cardiac therapy to bring about the vasodilation of arteries and/or veins to allow for improved cardiac output

25
Q

What are the two groups of vasodilators?

A

There are two groups of vasodilators that work by relaxing the smooth muscle of blood vessels or by inhibiting angiotensin converting enzyme, also known as ACE inhibitors.

26
Q

What is one side effect all vasodilators share?

A

All vasodilators have the side effect of producing hypotension and are contraindicated in patients with existing hypotension and/or hypovolemia, and dehydration.

27
Q

What am I?
- a venodilator that typically comes as an ointment or adhesive patch applied to the inner aspect of the pinna, axillary or inguinal regions.
- Clients should be warned to wear gloves when applying either the ointment or the patch
- an E-collar may be necessary to avoid licking or chewing of patches and ointments.

A

Nitroglycerin (Nitrol)

28
Q

What am I?
- an arterial dilator that reduces afterload in treatment of CHF
- Improves Cardiac Output
- Side Effects: Hypotension, GI signs

A

Hydralazine (Apresoline®)

29
Q

What am I?
- a “combined”vasodilator which means that it works by causing vasodilation of both the arteries and veins.
- Used to treat CHF, dilated cardiomyopathy, hypertension/pulmonary hypertension
- Side Effects: Hypotension, GI Signs

A

prazosin (Minipress®)

30
Q

What do enalapril (Enacard®) and captopril (Capoten®) have in common?

A
  • ACE inhibitors
  • are combined vasodilators that work on the arterial and venous vessels by blocking the angiotensin converting enzyme preventing the formation of the potent angiotensin II vasoconstrictor.
  • These drugs also act as diuretics by stopping the release of aldosterone, thereby reducing sodium and water retention.
31
Q

What are the preferred drugs of choice in early heart disease?

A
  • ACE inhibitors
  • are an effective treatment for cardiac disease involving either the right or left ventricles.
  • These drugs improve cardiac output with no change in heart rate and conserve potassium so can be used safely in conjunction with other diuretics commonly used for CHF such as furosemide (Lasix®).
32
Q

What am I?
- The newest FDA approved drug for management of mild to severe CHF
- This drug is an “inodilator” that works both as a balanced vasodilator (arterial and venous) and positive inotrope to strengthens the force of heart contraction.
- has become a popular drug of choice for CHF because it begins to act within one hour of dosing, has a duration of action up to 12 hours and is available in chewable tablets. (fast acting, 12hr duration, easy po admin)
- Since it is has positive inotropic activity, it may cause arrhythmias as a side effect, which is not the case with ACE inhibitors such as enalapril.
- can safely be used in conjunction with ACE inhibitors and with diuretics such as furosemide (Lasix®) in cases of more severe heart disease.

A

pimobendan (Vetmedin®).

33
Q

Antiarrhythmic (use and categorization)

A
  • used for the treatment of various arrhythmias in animals
  • categorized as Class I –IV according to their mechanism of action.
    [Class III drugs (potassium channel blockers) are not as commonly used in veterinary medicine and will not be discussed]
34
Q

what is the function of Class 1 antiarrhythmic agents?

A

stabilize cell myocardial cell membranes by inhibiting sodium influx and prevent cell depolarization.

35
Q

What is the drug of choice from the class 1 antiarrhythmic agents?

A

The drug of importance in this category is lidocaine.

36
Q

What am I?
- similar in action to lidocaine
- available orally to treat arrhythmias (PVC’s and ventricular tachycardia)

A

Tocainide (Tonocard®)

37
Q

How do Quinidine and procaninamide differ from lidocaine?

A

they are also used to treat some atrial arrythmias
- have less adverse effect of GI upset - > better tolerated in horses (cannot vomit)

38
Q

Beta-Blockers

A

AKA - Class II antiarrhythmic agents
- they work by blocking Beta-1 and Beta-2 adrenergic receptors –> decreased blood pressure and control of tachyarrhythmias by decreasing the heart rate and cardiac conduction.

39
Q

Class IV antiarrhythmic drugs (function and members)

A
  • work by blocking calcium channelsin smooth muscle.
  • Members of this group are all human products and include diltiazem (Cardizem®), verapamil (Isoptin®) and amlodipine (Norvasc®).
  • Of particular importance is amlodipine since it is now the drug of choice for systemic hypertension due to kidney disease, hyperthyroidism, and cardiomyopathy in cats, and due to its long half-life only requires once daily dosing.