Nursing Pharmacology Chapter 26: Renal Pharmacology
Acetazolamide (Diamox)
Glaucoma
Decreases rate of aqueous humor production leads to a declining in intraocular pressure.
Most common indication for use of carbonic anhydrase inhibitors.
Dorzolamide (Trusopf) is a topical carbonic anhydrase inhibitor.
No diuretic or systemic metabolic effects.
Reduction in intraocular pressure comparable to oral agents.
Urinary Alkalinization
Increased uric acid and cystine solubility by alkalinizing the urine by increasing bicarbonate excretion.
For prophylaxis of uric acid renal stones, bicarbonate administration (baking soda) may be required.
Metabolic Alkalosis
Results from:
Decreased total potassium with reduced vascular volume
High mineralocorticoid levels
These conditions are usually managed by treating the underlying causes; however, in certain clinical settings acetazolamide may assist in correcting alkalosis {e.g. alkalosis due to excessive diuresis in CHF patients}
Acute Mountain Sickness
Symptoms: weakness, insomnia, headache, nausea, dizziness (rapid ascension of all of 3000 meters); symptoms are usually mild.
In serious cases: life-threatening cerebral or pulmonary edema
Acetazolamide (Diamox) reduces the rate of CSF formation and decreases cerebral spinal fluid pH.
Prophylaxis against acute mountain sickness may be appropriate
Other Uses
Some role in management of epilepsy
Hypokalemia periodic paralysis
Increase urinary phosphate excretion during severe hyperphosphatemia.
Furosemide (Lasix), bumetanide (Bumex), torsemide (Demadex), ethacrynic acid (Edecrin)
Major Clinical uses:
Acute pulmonary edema
Acute hypercalcemia
Management of edema
Other uses
Hyperkalemia
Loop diuretics increase potassium excretion
Effect increased by concurrent administration of NaCl and water.
Acute renal failure
May increase rate of urine flow and increase potassium excretion.
May convert oligouric to non-oligouric failure which is easier to clinically manage.
Renal failure duration is not affected
Anion overload
Bromide, chloride, iodide: all reabsorbed by the thick ascending loop:
Systemic toxicity may be reduced by decreasing reabsorption
Concurrent administration of sodium chloride and fluid is required to prevent volume depletion.
Thiazides
Major Clinical Uses
Hypertension
Congestive heart failure
Nephrolithiasis (due to idiopathic hypercalciuria)
Nephrogenic diabetes insipidus
Bendroflumethazide |
Benzthiazide |
Chlorothiazide (Diuril) |
Chlorthalidone (Hygroton) |
Hydrochlorothiazide (HCTZ, Esidrix, HydroDIURIL) |
Hydroflumethiazide |
Indapamide (Lozol) |
Methyclothiazide |
Metolazone (Zaroxolyn, Mykrox) |
Polythiazide |
Quinethazone |
Trichlomethiazide |
Mannitol (Osmitrol)
To increase urine volume:
May be used to prevent anuria if the kidney due to hemolysis or rhabdomyolysis is presented with a large pigmented load.
When renal hemodynamics are compromised
To decrease intracranial or intraocular pressure:
Mannitol extract water from intracellular compartments, reducing total body water
Following IV administration, intracranial pressure falls within 60-90 minutes.
Amiloride (Midamor), triamterene (Dyrenium), spironolactone (Aldactone)
Reduction of potassium loss associated with thiazide or loop diuretic administration
Mineralocorticoid excess:
Conn's syndrome (primary hypersecretion)
Ectopic ACTH production (primary hypersecretion)
Secondary aldosteronism caused by:
Congestive heart failure
Hepatic cirrhosis
Nephrotic syndrome
Conditions that cause renal salt retention with reduced intravascular volume
other diuretics may further reduce intravascular volume thus worsening secondary aldosteronism
Cardiac glycosides |
Oral hypoglycemics |
Aminoglycoside antibiotics |
Uricosuric drugs |
Non-steroidal anti-inflammatory drugs |
Jackson, E.K. Diuretics In, Goodman and Gillman's The Pharmacological Basis of Therapeutics,(Hardman, J.G, Limbird, L.E, Molinoff, P.B., Ruddon, R.W, and Gilman, A.G.,eds) The McGraw-Hill Companies, Inc.,1996, pp. 685- 713
Jackson, E.K. Vasopressin and Other Agents Affecting the Renal Conservation of Water In, Goodman and Gillman's The Pharmacological Basis of Therapeutics, (Hardman, J.G, Limbird, L.E, Molinoff, P.B., Ruddon, R.W, and Gilman, A.G.,eds) The McGraw-Hill Companies, Inc.,1996, pp.715-732