Diuretics Flashcards

1
Q

Intracellular Fluid

A

-Inside the cell
-Largest compartment and holds 2/3 of the total body water

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2
Q

Extracellular fluid

A

-Outside of the cell
-1/3 of the total body water.
-Divided into vascular compartments (blood vessels) and the interstitial space (gaps between the cells)

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3
Q

Abnormal fluid loss

A

-Vomiting
-Diarrhea
-Hemorrhage

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4
Q

Signs and symptoms of fluid loss

A

-Low blood pressure
-Weak
-Dry skin
-Treatment- Give fluids

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5
Q

Abnormal retention of fluids

A

-Congestive heart failure
-Kidney failure

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6
Q

Signs and Symptoms of fluid retention

A

-Crackles in lungs
-Dyspnea (difficulty breathing)
-Edema

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7
Q

Nursing interventions

A

-Assess patient
-Daily weights
-Monitor intake and output
-IV fluids

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8
Q

3 basic functions of diuretics

A

-Cleansing of extracellular fluid and maintenance of ECF volume and composition.
-Maintenance of acid-base balance.
-Excretion of metabolic wastes and foreign substances.

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9
Q

Aldosterone

A

-Principal mineralocorticoid of the adrenal cortex, stimulates reabsorption of sodium from the distal nephron.
-At the same time, aldosterone causes potassium to be secreted.

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10
Q

Two major applications of diuretics

A

-Treatment of hypertension- helps to regulate fluid and blood pressure.
-Mobilization of edematous fluid to prevent renal failure.

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11
Q

Diuretics mechanism of action

A

-Blockade of sodium and chloride reabsorption.

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12
Q

Adverse effects of diuretics- too much fluid is pulled off

A

-Hypovolemia
-Acid-base imbalance
-Electrolyte imbalance

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13
Q

Loop Diuretics

A

Mechanism of action
-Acts on ascending loop of henle to block reabsorption of sodium and chloride.

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14
Q

Furosemide (Lasix)

A

-Most prescribed loop diuretic
-Rapid onset (PO 60 min, IV 5 min)

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15
Q

Therapeutic use of furosemide

A

-Pulmonary edema from CHF
-Edema of cardiac, hepatic or renal origin that has been unresponsive to less efficacious diuretics
-Hypertension that cannot be controlled with other diuretics

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16
Q

Adverse Effects of Furosemide

A

-Hyponatremia, hypochloremia, and dehydration.
-If dehydration occurs, hold
furosemide

17
Q
A

-Hypotension due to loss of volume and relaxation of venous smooth muscle; which reduces venous return to the heart.

18
Q
A

Hypokalemia- potassium is lost through increased secretion in the distal nephron.
-Low potassium can cause cardiac dysrhythmias.

19
Q
A

-Ototoxicity- deafness is transient.
-Hyperglycemia- can interfere with glucose metabolism.
-Hyperuricemia- Gout
-Don’t give during pregnancy.

20
Q

Drug interactions of Furosemide

A

-Digoxin- In the presence of low potassium, the risk of digoxin-induced toxicity (ventricular dysrhythmias) is increased. Loop diuretics promote potassium loss.
-Ototoxic drugs
-Potassium-sparing diuretics
-Lithium
-Antihypertensive drugs
-NSAIDS

21
Q

Preparations, dosage, and administration of Furosemide

A

-Oral
-Parenteral
-Given IV, administer slowly over 1-2 min
-If pushed fast it can cause hearing loss.

22
Q

Thiazides

A

-Used for newly diagnosed pt. with hypertension.
-Also know as benzothiadiazides
-Diuresis is considerably lower than that produced by loops.

23
Q

Thiazide mechanism of action

A

-Promotes urine production by blocking the reabsorption of sodium and chloride in the early segment of the distal convoluted tubule.
-Because only 10% of filtered sodium and chloride is normally absorbed at the site where thiazides act, the maximum urine flow these drugs can produce is lower than with loops.

24
Q

Hydrochlorothiazide (Hydrodiuril)

A

-Diuresis begins about 2 hours after oral administration.
-Effects peak within 4 to 6 hours

25
Q

Therapeutic uses of Hydrochlorothiazide

A

-Hypertension
-Edema
-Diabetes insipidus

26
Q

Adverse effects of Hydrochlorothiazide

A

-Hyponatremia
-Hypochloremia
-Dehydration
-Hypokalemia
-Hyperglycemia
-Hyperuricemia
-Impact on lipids, calcium and magnesium.
-Can be used during pregnancy

27
Q

Hydrochlorothiazide drug interactions

A

-Digoxin
-Augments effects of hypertensive medication
-Reduction of renal excretion of lithium (leading to accumulation)
-NSAIDs can blunt diuretic effects
-Can be combined with ototoxic agents without increased risk of hearing loss.

28
Q

Potassium-sparing diuretics

A

-Modest increase in urine production
-Decrease in potassium excretion

29
Q

Two groups of potassium-sparing diuretics

A

-Aldosterone Antagonist- Spironolactone
-Non-aldosterone antagonist- Triamterene and Amiloride

30
Q

Spironolactone Mechanism of Action

A

-Blocks aldosterone in the distal nephron
-Retention of potassium
-Increased secretion of sodium
-Diuresis for spironolactone is scant because most of the filtered sodium load has already been reabsorbed by the time the filtrate reaches the distal nephron.

31
Q

Therapeutic Uses of Spironolactone

A

-Hypertension
-Edematous states
-Heart failure (decreases mortality in severe failure)
-Primary hyperaldosteronism
-Premenstrual syndrome
-Polycystic ovary syndrome
-Acne in young women

32
Q

Adverse Effects of Spironolactone

A

-Hyperkalemia
-Benign and malignant tumors
-Endocrine effects
-Draw blood to know potassium levels

33
Q

Drug Interactions

A

-Thiazide and loop diuretics
-Agents that raise potassium levels

34
Q

Osmotic Diuretic
Mannitol (Osmitrol)

A

-Promotes diuresis by creating osmotic force within lumen of the nephron.
-Mannitol has no significant effect on the excretion of potassium and other electrolytes.

35
Q

Mannitol (Osmitrol)

A

-Drug must be given parentally!
-Given IV
-Does not diffuse across the GI epithelium and cannot be transported by the reuptake systems that absorb dietary sugars.
-Diuresis begins in 30 to 60 min and persists 6 to 8 hours.

36
Q

Therapeutic Uses of Mannitol (Osmitrol)

A

-Prophylaxis of renal failure
-Reduction of intracranial pressure
-Reduction of intraocular pressure

37
Q

Adverse Effects of Mannitol (Osmitrol)

A

-Edema
-Headache
-Nausea and vomiting
-fluid and electrolyte imbalance