Determining the Origin of Hypokalemic Paralysis

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Using the Transtubular Potassium Concentration Gradient

to Determine the Origin of Hypokalemic Paralysis

Many patients with hypokalemic paralysis live in diagnostic limbo for years without appropriate testing and therapy. Since time is muscle in the channelopathies, patients need speedy diagnosis and treatment. Repeated studies have shown that the transtubular potassium concentration gradient (TTKG), easily performed in the ER during an attack, can be used to distinguish between hypokalemia caused by renal (urinary) losses and hypokalemia caused by the intracellular shift of serum potassium into skeletal muscle, as in channelopathy HKPP.

The principle behind the test is that when faced with a low serum K+ level, the kidneys should excrete as little K+ as possible, unless the kidneys are the cause of the hypokalemia. A urinary K+ concentration greater than 20 mmol/L during hypokalemia indicates urinary loss of K+, i.e. hypokalemia of renal origin.

Clues which might indicate hypokalemia associated with intracellular shift are: weakness/paralysis which developed over a short time span (i.e. an hour or less) or during sleep, a low rate of K+ excretion, the absence of a metabolic acid base disorder, large intake of carbohydrate within past 48 hours, life crisis or stress, or signs of hyperthyroidism.

For example: A 13 year-old boy with familial hypokalemic periodic paralysis was observed during a paralytic attack and recovery. On the day of the attack the boy awoke at 5:00 am with complete paralysis. Because he vomited and could not take oral potassium he was admitted to the hospital at 11:00 am for observation and treatment with IV K+. Laboratory tests were done beginning at 11:00 am and for the next 22 hours, until 9:00 am the following day, when he was fully recovered.

SK+ = serum potassium, Total UK+ex = total urine potassium excreted. Urine was collected at 14:00 after 15 hours without urination.

Time in Hours Serum K+ Total UK+ ex
11:00 2.3 mmol/l ------
14:00 3.3 mmol/l 5 mmol
17:00 4.6 mmol/l 8 mmol
22:00 4.6 mmol/l 10 mmol
9:00 4.7 mmol/l 25 mmol

The normal renal response when hypokalemia is due to non-renal causes is a TTKG less than 2, where a TTKG greater than 5 is indicative of increased secretion of K+ in the cortical collecting ducts. Thus a transtubular potassium concentration gradient (TTKG) of greater than 3.0 indicates hypokalemia of renal origin, while a value below 2.0 indicates intracellular shift of K+, as found in ion channelopathy hypokalemic periodic paralysis.

The transtubular K+ concentration ([K+]) gradient (TTKG) is calculated using the following formula: TTKG = [K+]urine/(urine/plasma)/osmol/[K+]plasma History

1. Eliminate dietary inadequacy, diuretic, thyroid hormone or caffeine abuse, herbal usage (i.e. licorice root) or "body-building" supplements as potential causes of hypokalemia.

2. Recent history of ?: a) Unusual intensity of exercise; b) high carbohydrate intake (inc. alcohol) ; c) stress or life crisis; d) chilling; or e) combination of these factors. Signs consistent with hyperthyroidism or excess of beta-adrenergic activity; recent weight loss, diaphoresis, tachycardia, systolic hypertension, and wide pulse pressure. Has patient experienced exercise intolerance, weakness or paralysis in past, especially on awakening? (Patients sometimes do not recognize exercise intolerance or paralysis on awakening as abnormal.) Family history: Family members, including cousins, aunts, uncles, grandparents with similar symptoms or unexplained weakness, exercise intolerance, late development of myopathy in legs? (Sometimes called "spells", or believed to be "polio" or a "stroke" which was miraculously "cured" in hours.)


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8. Links TP; Muscle Fiber Conduction Velocity and Serum Muscle Enzymes in a Patient With an Attack of HypoKalemic Periodic Paralysis, Familial Hypokalemic Periodic Paralysis; ISBN 90-9005053-1, Chap 4.4 pp 113 - 122