Exam 3 chapter 28 Diuretic drugs Flashcards
Diuretics are drugs that accelerate the rate of?
urine formation via a variety of mechanisms, resulting in the removal of sodium and water from the body.
The five main types of diuretics are
(1) carbonic anhydrase inhibitors (CAIs)
(2) loop diuretics
(3) osmotic diuretics
(4) potassium-sparing diuretics
(5) thiazide and thiazide-like diuretics.
most commonly used Diuretics
The loop, potassium-sparing, and thiazide diuretics are the most commonly used. Remember that the loop diuretics are more potent than the thiazides, combination diuretics, and potassium-sparing diuretics.
The Seventh Joint National Committee on the Detection, Evaluation, and Treatment of Hypertension reaffirmed the role of diuretics, especially the thiazides, as?
first-line drugs in the treatment of hypertension.
All diuretics work primarily in the?
kidney
The kidney filters out toxic waste products from the blood while simultaneously conserving essential substances. This delicate balance between elimination of toxins and retention of essential chemicals is maintained by the nephron. The nephron is the?
main structural unit of the kidney, and each kidney contains approximately 1 million nephrons.
The initial filtering of the blood takes place in the glomerulus, a cluster of capillaries surrounded by the glomerular capsule. The rate at which this filtering occurs is referred to as?
The glomerular filtration rate and it is used as a gauge of how well the kidneys are functioning as filters.
It is important to have a thorough knowledge of renal anatomy and physiology and how it relates to the action of the various diuretics; for example, if a loop diuretic is given, its site of action is the?
loop of Henle and it causes the excretion of sodium, potassium, and chloride into the urine.
The various diuretics are classified according to their?
sites of action within the nephron, their chemical structure, and their diuretic potency.
The most potent diuretics are the loop diuretics, followed by mannitol, metolazone (a thiazide-like diuretic), the thiazides, and the potassium-sparing diuretics. The potency of these diuretics is a function of?
where they work in the nephron to inhibit sodium and water resorption. The more sodium and water they inhibit from resorption, the greater the amount of diuresis and therefore the greater the potency.
Carbonic Anhydrase Inhibitors (CAIs) are chemical derivatives of sulfonamide antibiotics. They inhibit the activity of?
the enzyme carbonic anhydrase, which is found in the kidneys, eyes, and other parts of the body.
- work at the location of the carbonic anhydrase enzyme system along the nephron, primarily the proximal tubule
The carbonic anhydrase system in the kidney is located?
just distal to the glomerulus in the proximal tubules, where roughly two thirds of all sodium and water is resorbed into the blood.
For sodium and water to be resorbed back into the blood what must happen?
hydrogen must be exchanged for it.
- without hydrogen, this cannot occur & the sodium and water will be eliminated w/urine
- carbonic anhydrase makes hydrogen ions available for this exchange
The CAIs reduce the formation of?
hydrogen and bicarbonate ions from carbon dioxide and water through the noncompetitive, reversible inhibition of carbonic anhydrase activity, resulting in a reduction in the availability of the ions, mainly hydrogen, for use by active transport system
An undesirable effect of CAIs is?
elevation of the blood glucose level and glycosuria in diabetic patients. This may be due in part to CAI enhanced potassium loss through the urine.
Therapeutic use of CAIs is in treatment of?
glaucoma, edema, and high-altitude sickness.
Undesirable effects of carbonic anhydrase inhibitors are?
metabolic abnormalities such as acidosis and hypokalemia, as well as drowsiness, anorexia, paresthesias, hematuria, urticaria, photosensitivity, and melena.
Because CAIs can cause hypokalemia, an increase in?
digoxin toxicity may occur when they are combined with digoxin. Use with corticosteroids may also cause hypokalemia.
-the effects of amphetamines, carbamazepine, cyclosporine, phenytoin, and quinidine may be increased when these drugs are taken concurrently w/CAIs
Loop diuretics (bumetanide, ethacrynic acid, furosemide, and torsemide) are very potent diuretics.
.
Loop diuretics have what effects?
These drugs act primarily along the?
Loop diuretics have renal, cardiovascular, and metabolic effects. These drugs act primarily along the thick ascending limb of the loop of Henle, blocking chloride and, secondarily, sodium resorption. They are also thought to activate renal prostaglandins, which results in dilatation of the blood vessels of the kidneys, the lungs, and the rest of the body.
Loop diuretics are used for?
edema associated with heart failure and hepatic or renal disease, hypertension, and to increase the renal excretion of calcium in patients with hypercalcemia. They may also be indicated for heart failure resulting from diastolic dysfunction.
Loop diuretics produce a potent diuresis and subsequent loss of fluid. The resulting decreased fluid volume leads to a?
decreased return of blood to the heart, or decreased filling pressures resulting in reduced blood pressure, pulmonary vascular resistance, systemic vascular resistance, central venous pressure, and left ventricular end-diastolic pressure.
Loop diuretics are particularly useful when?
rapid diuresis is needed because of their rapid onset of action. The diuretic effect lasts at least 2 hours.
Loop diuretics have a distinct advantage over thiazide diuretics in that?
their diuretic action continues even when creatinine
clearance decreases below 25 mL/min.
-this means that when kidney function diminishes, loop diuretics can still work
The major adverse effect of loop diuretics is?
electrolyte disturbances.
Prolonged administration of high dosages can also result in hearing loss stemming from ototoxicity.
Hypokalemia is of serious clinical importance. To prevent
hypokalemia, patients often receive?
potassium supplements along with furosemide.
main toxic effects of loop diuretics that require attention.
Electrolyte loss and dehydration, can result in circulatory failure, are main toxic effects of loop diuretics that require attention. Treatment involves electrolyte and fluid replacement.
Loop diuretics: Furosemide can produce?
erythema multiforme, exfoliative dermatitis, photosensitivity, and in rare cases, aplastic anemia.
Loop diuretics: Torsemide may rarely cause?
blood disorders, including thrombocytopenia, agranulocytosis, leukopenia, neutropenia, and Stevens-Johnson syndrome.
Interactions: Loop diuretics exhibit both?
neurotoxic and nephrotoxic properties, and they produce additive effects when given in combination with drugs that have similar toxicities.
Loop diuretics also affect certain laboratory results, which are?
increasing serum levels of uric acid, glucose, alanine aminotransferase, and aspartate aminotransferase.
The osmotic diuretics include?
mannitol, urea, organic acids, and glucose. Mannitol, a nonabsorbable solute, is the most commonly used of these drugs.
Mannitol works along the entire nephron, but primarily in the?
proximal tubule and descending limb of the loop of
Henle. Because it is nonabsorbable, it increases osmotic pressure in the glomerular filtrate, which in turn pulls fluid into the renal tubules from the surrounding tissues. This process also inhibits the tubular resorption of water and solutes, which produces a rapid diuresis.