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Chapter 24- heart failure drugs

Melissa Mathews

Heart Failure Drugs

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4._____ is a potassium sparing diuretic
6._______ may increase the risk of cardiac toxicity due to potassium loss
8.This study shows that the 5 year survival rate in patients with heart failure is about 50%
10.amiodarone, quinidine and verapamil can ______ digoxin levels by 50%
11.other adverse effects of _________ hypotension, angina, hypokalemia, tremor and thrombocytopenia
12.ACE inhibitors are beneficial in the treatment of heart failure because they prevent sodium and water resorption by inhibiting ________ secretion
13.________ ejection fraction is about 65%
15.______ ______ heart failure leads to systemic venous congestion, pedal edema, jugular venous distension, ascites and hepatic congestion
17.______ used to be the mainstay of heart failure treatment but has been replaced by other drugs with fewer adverse side affects and drug interactions
20.has many effects including acting as a nonselective beta blocker, an alpha 1 blocker, and possible a calcium channel blocker and antioxident
21.a complete medication history should be completed including ________ _______
22.an example of an angiotension 2 receptor blocker (ARBs)
24.________ should be part of your assessment before giving drugs to treat heart failure
29.the approach to treating chronic heart failure revolves around _______ the effects of the renin-angiotension-aldosterone system and the sns
32.are used to decrease systemic vascular resistance
33.digixon is used to treat atrial fibrillation, 2nd or 3rd degree heart block, ventricular tachycardia, heart failure from dystolic dysfunction and subaortic stenosis depending on the patient's ________ ________
36.__ ______ _______ may reduce digoxin levels
40.________ _______ tests should be done before giving heart failure drugs
43.______ ______ drugs increase the rate at which the heart beats
44.________ also has a negative chronotropic and dromotropic effects, increases stroke volume, reduces heart size during diastole, decreases venous BP and vein engorgement, increase in coronary circulation, promotes tissue perfusion and diuresis, improved blood circulation and other effects
45.the only drug in the B-type natriuretic peptide class
46.The primary adverse effect of PDIs are ________
47.______ ______ heart failure leads to pulmonary edema, coughing, shortness of breath and dyspnea
48.the beneficial effect of digoxin is _________
49.symptoms of heart failure in _______ may include poor growth, difficulty in feeding, tachypnea, inability to tolerate exercise and other activities, need to rest more often and dyspnea
Down
1.inhibition of phosphodiesterase results in a __________
2._______ _______ work by reducing or blocking SNS stimulation to the heart and the heart's conduction system
3.the only drug in the phosphodiesterase inhibitor class
5.________ may potentiate the effects of digoxin
7.patient should take _____ _____ before each dose of digoxin
9.digoxin is primarily used in the treatment of _____ heart failure and atrial fibrallation
14.________ may precipitate digoxin toxicity
16.______ ______ drugs reduce the force of contraction
18.PDIs are primarily used in the ____ for the short term management of acute heart failure
19.________ may increase digoxin levels
23.examples of _____ ________ are spironolactone and eplerenone
25.patients should avoid antacids, dairy products and bran products 2 hours before and 2 hours after drug administration to avoid decreased ________
26.when large amounts of ______ are ingested, the absorption of oral digoxin may be decreased
27.is used to treat digoxin toxicity
28.contraindications of PDIs include the presence of severe aortic or pulmonary valvular disease and heart failure resulting from ______ ________
30.an assessment of _____ ______ and all meal and snacks consumed in the last 24 hours
31.the beneficial effects of milrinone come form the intracellular increase in _____
34.______ ______ drugs increase the force of myocardial contractions
35.______ ______ drugs accelerate conduction
37.______ _______ is a pathological state in which the heart is unable to pump blood in sufficient amounts from the ventricles to meet the body's metabolic needs
38.the beta blocker most commonly used to treat heart failure
39.concurrent use of ________ may cause significant hypovolemia and decreased cardiac filling pressure
41.Mechanism of action PDIs differs from other ________ drugs such as digoxin and the catcholamines
42.the symptoms of ______ ______ include bradycardia, headache, dizziness, confusion, nausea and visual disturbances

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