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Potassium Chloride

Table of Contents > Drugs > Potassium Chloride     Print

Pronunciation
U.S. Brand Names
Synonyms
Generic Available
Canadian Brand Names
Use
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Overdosage/Toxicology
Drug Interactions
Stability
Compatibility
Mechanism of Action
 
Pharmacodynamics/Kinetics
Dosage
Administration
Monitoring Parameters
Dietary Considerations
Patient Education
Cardiovascular Considerations
Dental Health: Effects on Dental Treatment
Dental Health: Vasoconstrictor/Local Anesthetic Precautions
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Dosage Forms
References
International Brand Names

Pronunciation

(poe TASS ee um KLOR ide)

U.S. Brand Names

K+8; K+10; Kaon-Cl-10®; Kaon-Cl® 20; Kay Ciel®; K+ Care®; K-Dur® 10; K-Dur® 20; K-Lor™; Klor-Con®; Klor-Con® 8; Klor-Con® 10; Klor-Con®/25; Klor-Con® M; Klotrix®; K-Tab®; microK®; microK® 10; Rum-K®

Synonyms

KCl

Generic Available

Yes

Canadian Brand Names

Apo-K®; K-10®; K-Dur®; K-Lor®; K-Lyte®/Cl; Micro-K Extencaps®; Roychlor®; Slow-K®

Use

Treatment or prevention of hypokalemia

Pregnancy Risk Factor

A

Contraindications

Severe renal impairment, untreated Addison's disease, heat cramps, hyperkalemia, severe tissue trauma; solid oral dosage forms are contraindicated in patients in whom there is a structural, pathological, and/or pharmacologic cause for delay or arrest in passage through the GI tract; an oral liquid potassium preparation should be used in patients with esophageal compression or delayed gastric emptying time

Warnings/Precautions

Use with caution in patients with cardiac disease, severe renal impairment, hyperkalemia

Adverse Reactions

>10%: Gastrointestinal: Diarrhea, nausea, stomach pain, flatulence, vomiting (oral)

1% to 10%:

Cardiovascular: Bradycardia

Endocrine & metabolic: Hyperkalemia

Local: Local tissue necrosis with extravasation, pain at the site of injection

Neuromuscular & skeletal: Weakness

Respiratory: Dyspnea

<1%: Abdominal pain, alkalosis, arrhythmia, chest pain, heart block, hypotension, mental confusion, paralysis, paresthesia, phlebitis, rash, throat pain

Overdosage/Toxicology

Symptoms of overdose include muscle weakness, paralysis, peaked T waves, flattened P waves, prolongation of QRS complex, ventricular arrhythmias

Removal of potassium can be accomplished by various means; removal through the GI tract with Kayexalate® administration; by way of the kidney through diuresis, mineralocorticoid administration or increased sodium intake; by hemodialysis or peritoneal dialysis; or by shifting potassium back into the cells by insulin and glucose infusion or sodium bicarbonate; calcium chloride reverses cardiac effects.

Drug Interactions

Increased effect/levels with potassium-sparing diuretics, salt substitutes, ACE inhibitors

Stability

Store at room temperature, protect from freezing; use only clear solutions; use admixtures within 24 hours

Compatibility

Stable in dextran 6% in dextrose, dextran 6% in NS, D5LR, D51/4NS, D51/2NS, D5NS, D5W, D10W, D20W, LR, 1/2NS, NS, sodium chloride 3%; variable compatibility (consult detailed reference) in fat emulsion 10%, mannitol

Y-site administration: Compatible: Acyclovir, alatrofloxacin, aldesleukin, allopurinol, amifostine, aminophylline, amiodarone, ampicillin, atropine, aztreonam, betamethasone sodium phosphate, calcium gluconate, chlordiazepoxide, chlorpromazine, ciprofloxacin, cisatracurium, cladribine, clarithromycin, cyanocobalamin, dexamethasone sodium phosphate, digoxin, diltiazem, diphenhydramine, dobutamine, docetaxel, dopamine, doxorubicin liposome, droperidol, edrophonium, enalaprilat, epinephrine, esmolol, estrogens (conjugated), ethacrynate, etoposide, famotidine, fentanyl, fentanyl and droperidol, filgrastim, fludarabine, fluorouracil, furosemide, gatifloxacin, gemcitabine, granisetron, heparin, hydralazine, idarubicin, inamrinone, indomethacin, insulin (regular), isoproterenol, kanamycin, labetalol, lidocaine, linezolid, lorazepam, magnesium sulfate, melphalan, menadiol, meperidine, methoxamine, methylergonovine, midazolam, milrinone, minocycline, morphine, neostigmine, norepinephrine, ondansetron, oxacillin, oxytocin, paclitaxel, penicillin G potassium, pentazocine, phytonadione, piperacillin/tazobactam, procainamide, prochlorperazine edisylate, propofol, propranolol, pyridostigmine, remifentanil, sargramostim, scopolamine, sodium bicarbonate, succinylcholine, tacrolimus, teniposide, theophylline, thiotepa, tirofiban, trimethaphan, trimethobenzamide, vinorelbine, warfarin, zidovudine. Incompatible: Amphotericin B cholesteryl sulfate complex, diazepam, ergotamine, phenytoin. Variable (consult detailed reference): Methylprednisolone sodium succinate, promethazine

Compatibility when admixed: Compatible: Aminophylline, amiodarone, atracurium, bretylium, calcium gluconate, cefepime, ceftazidime, chloramphenicol, cimetidine, ciprofloxacin, clindamycin, corticotropin, cytarabine, dimenhydrinate, dopamine, enalaprilat, erythromycin lactobionate, floxacillin, fluconazole, foscarnet, fosphenytoin, furosemide, heparin, hydrocortisone sodium succinate, hydrocortisone sodium succinate with isoproterenol, lidocaine, metaraminol, methyldopate, metoclopramide, mitoxantrone, nafcillin, norepinephrine, oxacillin, penicillin G potassium, penicillin G potassium with vitamin B complex with C, phenylephrine, piperacillin, propafenone, ranitidine, sodium bicarbonate, thiopental, vancomycin, verapamil, vitamin B complex with C. Incompatible: Amphotericin B. Variable (consult detailed reference): Amikacin, dobutamine, etoposide with cisplatin and mannitol, penicillin G sodium

Mechanism of Action

Potassium is the major cation of intracellular fluid and is essential for the conduction of nerve impulses in heart, brain, and skeletal muscle; contraction of cardiac, skeletal and smooth muscles; maintenance of normal renal function, acid-base balance, carbohydrate metabolism, and gastric secretion

Pharmacodynamics/Kinetics

Absorption: Well absorbed from upper GI tract

Distribution: Enters cells via active transport from extracellular fluid

Excretion: Primarily urine; skin and feces (small amounts); most intestinal potassium reabsorbed

Dosage

I.V. doses should be incorporated into the patient's maintenance I.V. fluids; intermittent I.V. potassium administration should be reserved for severe depletion situations in patients undergoing ECG monitoring.

Normal daily requirements: Oral, I.V.:

Premature infants: 2-6 mEq/kg/24 hours

Term infants 0-24 hours: 0-2 mEq/kg/24 hours

Infants >24 hours: 1-2 mEq/kg/24 hours

Children: 2-3 mEq/kg/day

Adults: 40-80 mEq/day

Prevention during diuretic therapy: Oral:

Children: 1-2 mEq/kg/day in 1-2 divided doses

Adults: 20-40 mEq/day in 1-2 divided doses

Treatment of hypokalemia: Children:

Oral: 1-2 mEq/kg initially, then as needed based on frequently obtained lab values. If deficits are severe or ongoing losses are great, I.V. route should be considered.

I.V.: 1 mEq/kg over 1-2 hours initially, then repeated as needed based on frequently obtained lab values; severe depletion or ongoing losses may require >200% of normal limit needs

I.V. intermittent infusion: Dose should not exceed 1 mEq/kg/hour, or 40 mEq/hour; if it exceeds 0.5 mEq/kg/hour, physician should be at bedside and patient should have continuous ECG monitoring; usual pediatric maximum: 3 mEq/kg/day or 40 mEq/m2/day

Treatment of hypokalemia: Adults:

I.V. intermittent infusion: 5-10 mEq/hour (continuous cardiac monitor recommended for rates >5 mEq/hour), not to exceed 40 mEq/hour; usual adult maximum per 24 hours: 400 mEq/day.

Potassium dosage/rate of infusion guidelines:

Serum potassium >2.5 mEq/L: Maximum infusion rate: 10 mEq/hour; maximum concentration: 40 mEq/L; maximum 24-hour dose: 200 mEq

Serum potassium <2.5 mEq/L: Maximum infusion rate: 40 mEq/hour; maximum concentration: 80 mEq/L; maximum 24-hour dose: 400 mEq

Potassium >2.5 mEq/L:

Oral: 60-80 mEq/day plus additional amounts if needed

I.V.: 10 mEq over 1 hour with additional doses if needed

Potassium <2.5 mEq/L:

Oral: Up to 40-60 mEq initial dose, followed by further doses based on lab values

I.V.: Up to 40 mEq over 1 hour, with doses based on frequent lab monitoring; deficits at a plasma level of 2 mEq/L may be as high as 400-800 mEq of potassium

Administration

Parenteral: Potassium must be diluted prior to parenteral administration; maximum recommended concentration (peripheral line): 80 mEq/L; maximum recommended concentration (central line): 150 mEq/L or 15 mEq/100 mL; in severely fluid-restricted patients (with central lines): 200 mEq/L or 20 mEq/100 mL has been used; maximum rate of infusion, see Dosage, I.V. intermittent infusion

Oral: Wax matrix tablets must be swallowed and not allowed to dissolve in mouth.

Monitoring Parameters

Serum potassium, glucose, chloride, pH, urine output (if indicated), cardiac monitor (if intermittent infusion or potassium infusion rates >0.25 mEq/kg/hour)

Dietary Considerations

Administer with plenty of fluid and/or food because of stomach irritation and discomfort.

Patient Education

Long-acting and wax matrix tablets should be swallowed whole; do not crush or chew. Powder must be dissolved in water before use. Take with food. Liquid can be diluted or dissolved in water or juice.

Cardiovascular Considerations

Hypokalemia is highly arrhythmogenic, particularly in the setting of ischemia or digitalis toxicity. ECG evidence of hypokalemia includes flattening of the T wave. As the T wave shrinks, U waves may appear. There is no prolongation of the QT interval. Hyperkalemia may present as tall peaked symmetrical T waves. S-T elevation may present in severe hyperkalemia. QRS complex progressively widens with eventual apparent sine waves on the ECG. Hyperkalemia will also induce cardiac slowing and AV conduction abnormalities.

Dental Health: Effects on Dental Treatment

No significant effects or complications reported

Dental Health: Vasoconstrictor/Local Anesthetic Precautions

No information available to require special precautions

Mental Health: Effects on Mental Status

None reported

Mental Health: Effects on Psychiatric Treatment

None reported

Dosage Forms

Capsule, extended release: 10 mEq [800 mg]

microK® [microencapsulated]: 8 mEq [600 mg]

microK® 10 [microencapsulated]: 10 mEq [800 mg]

Infusion [premixed in D5W]: 20 mEq (1000 mL); 30 mEq (1000 mL); 40 mEq (1000 mL)

Infusion [premixed in D5W and LR]: 20 mEq (1000 mL); 30 mEq (1000 mL)

Infusion [premixed in D5W and 1/4NS]: 10 mEq (500 mL, 1000 mL); 20 mEq (1000 mL); 30 mEq (1000 mL); 40 mEq (1000 mL)

Infusion [premixed in D5W and 1/2NS]: 20 mEq (1000 mL); 40 mEq (1000 mL)

Infusion [premixed in D5 and NS]: 20 mEq (1000 mL); 40 mEq (1000 mL)

Infusion [premixed in D5W and sodium chloride 0.3%]: 10 mEq (500 mL); 20 mEq (1000 mL)

Infusion [premixed in NS]: 20 mEq (1000 mL); 40 mEq (1000 mL)

Infusion [premixed in SWFI]: 10 mEq (50 mL, 100 mL); 20 mEq (50 mL, 100 mL); 30 mEq (100 mL); 40 mEq (100 mL)

Injection, solution [concentrate]: 2 mEq/mL (5 mL, 10 mL, 15 mL, 20 mL, 250 mL)

Powder, for oral solution: 20 mEq/packet (30s, 100s, 1000s)

K+ Care®: 20 mEq/packet (30s) [fruit or orange flavor]

K-Lor®: 20 mEq/packet (30s, 100s)

Kay Ciel® 10%: 20 mEq/packet (30s, 100s) [sugar free]

Klor-Con®: 20 mEq/packet (30s, 100s) [sugar free]

Klor-Con®/25: 25 mEq/packet (30s, 100s) [sugar free]

Solution, oral: 20 mEq/15 mL (480 mL); 40 mEq/15 mL (480 mL)

Kaon-Cl® 20: 40 mEq/15 mL (480 mL) [sugar free; contains alcohol; cherry flavor]

Kay Ciel®: 10%: 20 mEq/15 mL (120 mL, 480 mL) [sugar free; contains alcohol]

Rum-K®: 20 mEq/10 mL (480 mL) [alcohol free, sugar free; butter/rum flavor]

Tablet, extended release: 8 mEq [600 mg]; 10 mEq [800 mg]; 20 mEq [1500 mg]

K+8: 8 mEq [600 mg]

K+10: 10 mEq [800 mg]

K-Dur® 10 [microencapsulated]: 10 mEq [800 mg]

K-Dur® 20 [microencapsulated]: 20 mEq [1500 mg; scored]

K-Tab®: 10 mEq [800 mg]

Kaon-Cl® 10 [film coated]: 10 mEq [800 mg

Klor-Con® 8: 8 mEq [600 mg; wax matrix]

Klor-Con® 10: 10 mEq [800 mg; wax matrix]

Klor-Con® M10 [microencapsulated]: 10 mEq [800 mg]

Klor-Con® M15 [microencapsulated]: 15 mEq [1125 mg]

Klor-Con® M20 [microencapsulated]: 20 mEq [1500 mg; scored]

Tablet, slow release [film coated] (Klotrix®): 10 mEq [800 mg; wax matrix]

References

Hamill RJ, Robinson LM, Wexler HR, et al, "Efficacy and Safety of Potassium Infusion Therapy in Hypokalemic Critically Ill Patients,"Crit Care Med, 1991, 19(5):694-9.

Khilnani P, "Electrolyte Abnormalities in Critically Ill Children,"Crit Care Med, 1992, 20(2):241-50.

Joint Commission on Accreditation of Healthcare Organizations, "2005 National Patient Safety Goals," available at http://www.jcaho.org/accredited+organizations/patient+safety/05_npsg_guidelines Last accessed October 15, 2004.

International Brand Names

Apo-K® (CA); K-10® (CA); K-Dur® (CA); K-Lor® (CA); K-Lyte®/Cl (CA); Micro-K Extencaps® (CA); Roychlor® (CA); Slow-K® (CA)

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