Potassium is a very significant mineral in the body, playing important roles in both cellular and electrical function. Its functions can be described as follows:
Regulation of water balance and acid-base balance in the blood and tissues, along with sodium. Potassium enters the cell more readily than does sodium and sets off the brief sodium-potassium exchange across the cell membranes. In the nerve cells, this sodium-potassium flux produces the electrical potential that is necessary for the conduction of nerve impulses. When potassium leaves the cell, it changes the membrane potential and allows the nerve impulse to progress. This electrical potential gradient, created by the "sodium-potassium pump," facilitates smooth muscle contractions and regulates the heartbeat. In addition, the pump prevents the swelling of cells. If sodium is not pumped out, water accumulates within the cell causing it to swell and ultimately burst.2Haas EM. Role of Potassium in Maintaining Health. Available at http://www.hkpp.org/general/potassium_health.html. Accessed on June 25, 2011.
Increased potassium excretion. Increased excretion of potassium, especially coupled with poor intake, is the most common cause of hypokalemia. It is usually due to the use of diuretics or to hyperaldosteronism.
Deficient potassium intake. This is an uncommon cause of hypokalemia, found in very elderly individuals who are unable to cook for themselves or have difficulty in chewing or swallowing. Patients receiving total parenteral nutrition (TPN) are also prone to hypokalemia if the potassium supplementation is inadequate for a prolonged period of time.
Gastrointestinal losses. Diarrhea and vomiting are the common causes of gastrointestinal potassium loss. Vomiting causes volume depletion and metabolic alkalosis. These two processes are accompanied by increased renal potassium excretion. Volume depletion leads to secondary hyperaldosteronism, which, in turn, leads to enhanced cortical collecting tubule secretion of potassium in response to enhanced sodium reabsorption. Metabolic alkalosis also increases collecting tubule potassium secretion due to the decreased availability of hydrogen ions for secretion in response to sodium reabsorption.
Shift from extracellular to intracellular space. This is also usually accompanied by increased excretion, leading to a potentiation of the hypokalemic effect of excessive loss. It is most commonly drug-induced; hence, it is important to review the patient's drug record while treating the condition.6Gennari FJ. Hypokalemia. N Engl J Med 1998;339:451-458.
Clinical features
The clinical features of hypokalemia are non-specific and varied, and their severity depends on the degree of hypokalemia. Symptoms seldom occur unless the plasma K+ concentration falls below 3 mEq/L. They are:7Harrison's Principles of Internal Medicine, 16th ed.
Fatigue
Myalgia
Muscular weakness of the lower extremities
More severe hypokalemia may lead to progressive weakness, hypoventilation (due to respiratory muscle involvement), and eventually complete paralysis
Increased risk of rhabdomyolysis, due to impaired muscle metabolism and the blunted hyperemic response to exercise associated with profound K+ depletion
Paralytic ileus, due to impairment of smooth-muscle function
Symptoms of metabolic alkalosis, such as confusion (which may progress to stupor or coma), hand tremor, light-headedness, muscle twitching, nausea, vomiting, numbness or tingling in the face or extremities, prolonged muscle spasms (tetany)
Symptoms of digitalis toxicity in patients taking digitalis. These symptoms include confusion, irregular pulse, loss of appetite, nausea, vomiting, diarrhea, palpitations, visual changes, impaired consciousness, decreased urine output, etc.
On physical examination, tachycardia or tachypnea may be found occasionally due to respiratory muscle weakness. Blood pressure may be raised because of primary hyperaldosteronism, renal artery stenosis, licorice ingestion, or the more unusual forms of genetically transmitted hypertensive syndromes such as congenital adrenal hyperplasia, glucocorticoid remediable hypertension, or Liddle syndrome. In addition, there may be muscle weakness and flaccid paralysis; deep-tendon reflexes may be depressed or absent.5Lederer E. Hypokalemia. Available at http://emedicine.medscape.com/article/242008-overview#showall. Accessed on June 25, 2011.
Clinical effects of hypokalemia
Effects of hypokalemia can vary from mild to severe. If not treated in time, it can have serious consequences, which may be life-threatening.
Hepatic effects: Hepatic encephalopathy or aggravation of its symptoms.10
CNS effects: Memory loss, seizures
Drug-induced hypokalemia
Diuretics
Diuretic therapy is the most common cause of hypokalemia. Loop diuretics like frusemide and torsemide prevent the reabsorption of sodium and chloride ions at the loop of Henle in the kidney. Thiazide diuretics like hydrochlorothiazide also prevent sodium and chloride reabsorption in the distal convoluted tubule.
Both these types of diuretics cause increased amounts of sodium and water to pass through the collecting tubules. This, in turn, causes a reflex secretion of potassium into the urine by increased aldosterone secretion. Also, volume depletion due to increased urine output as a result of the diuretic causes further increased secretion of aldosterone, which further increases the secretion of potassium into the collecting duct and into the urine (this is an effect of aldosterone action trying to maintain volume in the cardiovascular system). Thus, there is a two-way method of potassium loss through the urine which then causes hypokalemia.11Why do diuretics cause hypokalemia? Available at http://answers.yahoo.com/question/index?qid=20090509005839AAO7Ygh. Accessed on June 25, 2011.
Hypokalemia potentiates the effects of digitalis. Digitalis induces arrhythmias by changing the ion concentrations in the myocardial cells or changing the transcellular ion gradient. Both diuretic-induced hypokalemia and digitalis inhibit the membrane-Na+K+ATPase activity, leading to a fall in the intracellular potassium concentration. This may explain how cardiac arrhythmias occur during digitalis treatment and during severe hypokalemia, and also explain why myocardial sensitivity for digitalis increases in the presence of hypokalemia. The myocardial uptake of digitalis, however, is markedly increased at low extracellular potassium concentration and this may explain the interaction between digitalis and hypokalemia. Not only are the myocardial digoxin kinetics changed during hypokalemia but the renal excretion rate of digoxin is also markedly reduced, leading to increased serum digoxin concentration and thereby the risk of digitalis intoxication.12Steiness E. Diuretics, digitalis and arrhythmias. Acta Med Scand Suppl. 1981;647:75-8.
Corticosteroids can produce hypokalemia and other electrolyte disturbances via mineralocorticoid effects, the degree of which depends upon the agent and route of administration. However, large systemic doses
To determine the cause so as to prevent recurrences
Minimizing potassium losses
Treat diarrhea or vomiting.
Use H2 blockers to decrease nasogastric suction losses
Control hyperglycemia if glycosuria is present
Replenishing potassium stores
Every 1 mEq/L decrease in serum potassium creates a potassium deficit of approximately 200-400 mEq and patients with plasma levels under 3.0 mEq/L often require more than 600 mEq of potassium to correct the deficit.7Harrison's Principles of Internal Medicine, 16th ed. Therefore, the plasma potassium concentration should be monitored frequently when assessing the response to treatment.
The ready absorption of oral potassium allows the administration of relatively large doses safely because oral potassium enters the circulation more slowly, avoiding the risk of hyperkalemia.6Gennari FJ. Hypokalemia. N Engl J Med 1998;339:451-458.
The drug of choice is potassium chloride, as it promotes more rapid correction of hypokalemia and metabolic alkalosis.7Harrison's Principles of Internal Medicine, 16th ed. The oral preparation of potassium chloride available in the market contains 40 mEq of potassium in 30 ml.
Treatment should be tailored to the individual patient. For example, if diuretics cannot be discontinued due to an underlying disorder such as congestive heart failure, oral potassium supplements can be given. Typically, 40 to 100 mEq of supplemental potassium chloride is needed each day to maintain serum potassium concentrations near or within the normal range in patients receiving diuretics.6Gennari FJ. Hypokalemia. N Engl J Med 1998;339:451-458.
Monitoring for toxicity of hypokalemia
Hypokalemia is most detrimental to the heart. The patient should be monitored for evidence of cardiac arrhythmias.
References
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Haas EM. Role of Potassium in Maintaining Health. Available at http://www.hkpp.org/general/potassium_health.html. Accessed on June 25, 2011.
American Heart Association. Potassium and High Blood Pressure. Available at http://www.amhrt.org/HEARTORG/Conditions/ HighBloodPressure/PreventionTreatmentofHighBloodPressure/Potassium-and-High-Blood-Pressure_UCM_303243_Article.jsp. Accessed on July 07, 2011.
Nuble C. Potassium and Its Benefits to the Human Body. Available at: http://ezinearticles.com/?Potassium-and-Its-Benefits-to-the- Human-Body&id=74138. Accessed on June 25, 2011.
Lederer E. Hypokalemia. Available at http://emedicine.medscape.com/article/242008-overview#showall. Accessed on June 25, 2011.
Gennari FJ. Hypokalemia. N Engl J Med 1998;339:451-458.
Harrison's Principles of Internal Medicine, 16th ed.
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Steiness E. Diuretics, digitalis and arrhythmias. Acta Med Scand Suppl. 1981;647:75-8.
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Nagdeote AN, Pawade YR. The effect of oral salbutamol on the metabolism of electrolytes in asthmatic children. Journal of Clinical and Diagnostic Research. 2011;5(2):176-178.
How does salbutamol cause hypokalemia? Available at http://answers.yahoo.com/question/index?qid=20091005054329AAf75o C. Accessed on June 25, 2011.
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Holmes A, Hesling C, Wilson T. Drug-induced secondary hyperaldosteronism in patients with pulmonary tuberculosis. Q J Med 1970;154,299-315
Shin S, Furin J, Alcántara F, Hyson A, Joseph K, Sánchez E, Rich M. Hypokalemia among patients receiving treatment for multidrugresistant tuberculosis. Chest. 2004 Mar;125(3):974-80.
Drug interactions between Accuretic and prednisone. Available at: http://www.drugs.com/drug-interactions/accuretic-withprednisone-1266-1275-1936-0.html. Accessed on June 25, 2011.
Corticosteroids: A cause of low potassium (hypokalemia)? Available at http://www.riversideonline.com/health_reference/Questions-Answers/AN01385.cfm. Accessed on June 25, 2011.
Acetazolamide Drug Interactions. Available at http://www.hkpp.org/physicians/dr_acetazolamide.html. Accessed on June 25, 2011.
Introduction Irritable bowel syndrome (IBS) is a functional gastrointestinal disorder, characterized by recurrent abdominal pain, cramping, bloating, constipation and diarrhea, in the absence of detectable structural abnormalities. Although it causes a lot of discomfort and distress, it does not permanently harm the intestines and has no serious complications, such as cancer. IBS can be usually controlled with diet, stress management and prescribed medications, but sometimes may be disabling enough to prevent sufferers from working, attending social events or even travelling short distances.1Irritable bowel syndrome. Available at http://digestive.niddk.nih.gov/ddiseases/pubs/ibs/. Accessed on June 27, 2011. Epidemiology The prevalence of IBS varies by country and by age range examined. The disease is more common in women than in men in most parts of the world. In the Indian subcontinent, however, the trend is reversed, with men constituting almost 70-80% of patients with IBS.2Lehrer JK. Irritable Bowel Syndrome. Available at http://emedicine.medscape.com/article/180389-overview#showall. Accessed on June 27,…