Potassium Flashcards
Hyperkalemia
Work up
- Confirm it with a repeat blood draw. In setting of extreme leukocytosis or thrombocytosis, check plasma K+
- Spot urine K+:
- Less than 20 mEq/L (while urine osmolality is about 300 mOsm/kg) suggests impaired renal function
- More than 40 mEq/L (while urine osmolality is about 300 mOsm/kg) suggests high intake or shift
Hyperkalemia
Causing Drugs
- Aldosterone resistance:
- K+-sparing diuretics
- Trimethoprim-sulfamethoxazole
- Decrease aldosterone production:
- NSAIDs
- ACEIs and ARBs
- Cyclosporine (Also shifts K+ out of cells) and Tacrolimus
- Heparin (decrease aldosterone production)
- Shifts K+ out of cells
- Beta-blockers
- Digoxin and Fluoride toxicity (also venom of Bufo gargarizans toad that is used in Chinese folk medicine which acts like digoxin)
- Methotrexate
- Propofol infusion syndrome
- Succinylcholine
- Pentamidine
- Ketokonazole
- Metyrapone (reversible inhibitor of 11-beta hydroxylase, which stimulates ACTH secretion)
- Herbs:
- Alfalfa
- Dandelion
- Horsetail
- Stinging Nettle
Hyperkalemia
Shifting of K+ into extracellular space Causes
- Metabolic acidosis
- Acute tubular necrosis
- Electrical and thermal burns
- Head trauma
- Rabdomyolysis
- Tumor lysis syndrome
- Hypertonicity states
Hypomagnesemia
Treatment
- IV and oral supplements
- Hypokalemia and hypocalcemia will not correct without magnesium correction
Hypokalemia
Treatment
- Stop ongoing losses like administration of H2 blockers in patients receiving NG suction and control hyperglycemia if glycosuria is present
- Replacement of K+ through oral or IV route or both in addition to correction of Mg++
Hypomagnesemia
Presentation
In severe cases:
- Paresthesias
- Irritability, confusion, and lethargy
- Seizures
- Tetany
- Arrhythmias
- Hyperactive reflexes
Hyperkalemia
Decreased Excretion Causes
It is due to Type IV renal tubular acidosis which can be caused by the following:
- DM
- Sickle cell disease or trait
- Lower urinary tract obstruction
- Adrenal insufficiency
- Primary Addison syndrome
- Enzyme deficiencies
Hyperkalemia
ECG Findings
- Tall peaked T waves
- Wide QRS complex
- Prolongation of PR interval
- Low or loss of P waves
- Can progress to sine waves, VF and cardiac arrest
Hypokalemia
Inadequate potassium intake Causes
- Eating disorders: anorexia, bulimia, starvation, pica, and alcoholism
- Dental: impaired ability to chew
- Poverty and “tea-and-toast” diet of elderly individuals
- Hospitalization: potassium-poor TPN
Hypomagnesemia
Decrease intake Causes
Serum Mg++ < 1.5 mEq/L
- Malnutrition
- Malabsorption
- Short bowel syndrome
- TPN
Hypokalemia
ECG Findings
- T-wave flattening
- U waves (an additional wave after T wave)
- ST segment depression
- AV block and subsequent cardiac arrest
Hypokalemia
Genetic Causes
- Congenital adrenal hyperplasia (11-beta hydroxylase or 17-alpha hydroxylase deficiency)
- Glucocorticoid-remediable hypertension (AD disorder; fusion of regulatory region of 11-beta hydroxylase to coding region of aldosterone synthase [both on Chrom. 8] which results in an aldosterone synthase that is directly sensitive to ACTH; it responds to Rx with dexamethasone, spironolactone and eplerenone)
- Bartter syndrome
- Gitelman syndrome
- Liddle syndrome
- Gullner syndrome
- Glucocorticoid receptor deficiency
- Hypokalemic period paralysis
- Thyrotoxic periodic paralysis (TTPP)
- SeSAME syndrome
Hypokalemia
Potassium shift to intracellular space Causes
- Alkalosis
- Insulin or glucose administration (glucose stimulates insulin release)
- Intensive beta-adrenergic stimulation
- Hypokalemic period paralysis
- Thyrotoxic periodic paralysis (TTPP)
- Refeeding: prolonged starvation, eating disorders and alcoholism
- Hypothermia
Hypomagnesemia
Increased loss Causes
- Diuretics
- Diarrhea
- Vomiting
- Hypercalcemia
- Alcoholism
Hypomagnesemia
Diagnosis
- There may be a concurrent hypocalcemia and hypokalemia
- ECG may reveal prolonged PR and QT intervals