CVM drugs Flashcards

1
Q

ACE inhibitors are used for the treatment of

A

hypertension, heart failure, MI, nephropathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

ACE inhibitor approved for use in nephropathy is

A

Captopril

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Name 3 side effects from the use of ACE inhibitors

A

first dose hypotension, cough, hyperkalemia, renal failure, angioedema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

why is cough a side effect of ACE inhibitors but not a side effect of ARBs

A

ACE inhibitors facilitate breakdown of bradykinin - causes increase sensitivity and cause cough. But ARBs do not

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the Frank Sterling law?

A

Increase filling of ventricles will increase in contractility of heart > Increase cardiac output (fill more, pump more)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the 2 forms of heart failure?

A

Systolic heart failure (HFrEF) and diastolic heart failure (HFpEF)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the mechanism of action of beta-blockers in treatment of heart failure?

A
  • blocks B1 receptors on heart and decreases heart rate and contractility
  • blocks B1 receptors on juxtaglomerular cells in the kidney > reduce renin production > reduce BP > reduce afterload
  • blocks B1 receptors on juxtaglomerular cells in the kidney > reduce aldosterone production > reduce Na/H2o reabsorption > reduce plasma volume
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the mechanism of action of beta-blockers in treatment of angina

A
  • blocks B1 receptors > decrease in HR and contractility > reduce O2 demand, increase diastolic filling time > increase flow to coronaries
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Name 2 non selective beta blockers and 2 B1 selective beta blockers

A

Non selective: propanolol, carvediol

Selective B1: Bisoprolol, metoprolol, atenolol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Name the 3 beta blockers that have been shown to be effective in treatment of heart failure

A

Bisoprolol, metoprolol, carvediol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Contraindications of use of ACE inhibitors and ARBs

A

Pregnancy (drugs are teratogenic)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Name 3 medical conditions in which beta blockers are contraindicated

A

Asthma (due to B2 adrenoceptors - causing bronchoconstriction), diabetes (masking sympathetic effects during hypoglycemia), sick sinus syndrome/AV blocks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Name 3 side effects of beta-blockers

A

Hypotension, AV nodal blocks, CNS effects (sedation, vivid dreams, rarely depression), asthma exacerbation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the 2 types of calcium channel blockers?

A

Dihydropyridines and non-dihydropyridines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Name 2 examples of dihydropyridines and 2 examples of non-dihydropyridines

A

DHP: Nifedipine, Amlodipine

Non DHP: Verapamil, Dilitiazem

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Why is Nifedipine not useful in the treatment of arrthymias?

A

Nifedipine is a non-dihydropyridines - does not act on the cardiac myocytes to decrease contractility

17
Q

Name 3 side effects of calcium channel blockers

A

Hypotension, cardiac suppression (bradycardia, AV blocks, heart failure), constipation, vasodilatory effects (flushing, dizziness, headache, peripheral edema)

18
Q

What medical conditions can calcium channel blockers be used to treat?

A

1) Arrthymias (Non DHP)
2) Hypertension (both DHP and non DHP)
3) Angina (both DHP and non DHP)

19
Q

What drugs will interact with loop diuretics?

A

NSAIDs

Loop diuretics induce renal synthesis of prostaglandins > increasing renal blood flow

20
Q

At which site of the nephron does loop diuretics work?

A

Thick ascending limb of loop of Henle

21
Q

Why are loop diuretics most efficacious?

A

It works at the thick ascending limb of loop of Henle where about 25% of Na reabsorption takes place

22
Q

Name 3 side effects of loop diuretics

A

Hypotension, Hypokalemia, Hypomagnesemia, ototoxicity, hyperuricemia

23
Q

Name 3 side effects of thiazides

A

Hypokalemia, Metabolic alkalosis, Hyperglycaemia, Hyperlipidemia, Hyponatremia, Hypercalcemia

24
Q

At which site of the nephron does thiazides work on? Name of cotransporter which they work on?

A

Distal convoluted tubule. Na/Cl cotransporter

25
Q

What is the site of action of potassium-sparing diuretics?

A

Collecting tubules

26
Q

What are the 2 mechanism of actions of potassium-sparing diuretics?

A

1) Act by inhibiting Na ion channels > decrease Na reabsorption
2) Competitive antagonists at aldosterone receptors > decrease in synthesis of intracellular proteins > inhibit opening of Na channels > decrease Na reabsorption

27
Q

Name 2 examples of potassium-sparing diuretics

A

Spironolactone, Amiloride

28
Q

What is the mechanism of action of Digoxin?

A

Inhibits Na/K ATPase, keeping Na+ in the cells > leads to Na/Ca exchanger pumping Na+ out of cell and bringing Ca2+ into the cells > CICR >contraction

29
Q

Name a serious adverse effect of digoxin

A

Arrthymias (due to increase in intracellular Ca > issues with automaticity, extrasystoles)

30
Q

Management of digoxin toxicity?

A

1) Discontinue
2) Correct electrolyte abnormalities
3) Anti-arrthymias
4) Digoxin antibody > to dilute levels of digoxin in body

31
Q

Name 2 classes of lipid lowering drugs that will work on reducing LDLs

A

Statins, Bile acid sequestrants, cholesterol absorption inhibitors, PCSK9 inhibitors

32
Q

Mechanism of action of statins

A

1) Inhibitors of HMG-CoA reductase which is the rate limiting enzyme of cholesterol biosynthesis > decrease cholesterol production
2) upregulate LDL receptors > increase LDL uptake
3) decrease VLDL production, increase HDL production