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Potassium chloride in glucose 10% parenteral

Presentation

Infusion containing potassium chloride and glucose 10%.

Drugs List

  • potassium chloride 0.15% (10mmol potassium) in glucose 10% 500ml infusion
  • Therapeutic Indications

    Uses

    Electrolyte imbalance
    Hypokalaemia - severe
    Rehydration in patients with high carbohydrate need
    Severe hypoglycaemia

    Prevention and treatment of potassium depletion and/or hypokalaemia in cases where supply of water, potassium chloride and carbohydrates is required due to restricted fluid and electrolyte intake via normal routes.

    Supply of potassium and carbohydrate during parenteral nutrition.

    Prevention and treatment of hypoglycaemia.

    Rehydration in case of water loss and dehydration states in patients with high carbohydrate need.

    Dosage

    Adults

    Treatment of carbohydrate depletion, rehydration in case of water loss or dehydration and prevention and treatment of hypoglycaemia
    500ml to 3 litres/24 hours (7ml/kg/24 hours to 40ml/kg/24 hours).
    Rate: Maximum 5mg/kg/minute (3ml/kg/hour).

    Prevention of potassium depletion
    Up to 50mmoles/24 hours. The maximal recommended dose of potassium is 2mmol/kg/24 hours to 3mmol/kg/24 hours.

    Treatment of potassium depletion
    20mmoles of potassium over 2 to 3 hours (7mmol/hour to 10mmol/hour) under ECG control.
    Rate: Maximum 15mmol/hour to 20mmol/hour.

    Children

    Treatment of carbohydrate depletion, rehydration in case of water loss or dehydration and prevention and treatment of hypoglycaemia

    Weight more than 20kg: 1500ml + (20ml/kg over 20kg) per 24 hours.
    Weight between 10kg and 20kg: 1000ml + (50ml/kg over 10kg) per 24 hours.
    Weight less than 10kg: 100ml/kg per 24 hours.

    Maximum dose 10 to 18mg/kg/minute depending on the age and the total body mass.

    Prevention of potassium depletion
    Up to 50mmoles/24 hours. The maximal recommended dose of potassium is 2mmol/kg/24 hours to 3mmol/kg/24 hours.

    Treatment of potassium depletion
    20mmoles of potassium over 2 to 3 hours (7mmol/hour to 10mmol/hour) under ECG control.
    Rate: Maximum 15mmol/hour to 20mmol/hour.

    Patients with Renal Impairment

    Patients with renal impairment should receive lower doses.

    Administration

    For slow intravenous infusion only.

    Contraindications

    Baseline serum potassium above 5 mmol/L
    Diabetic hyperosmolar coma
    Impaired glucose tolerance
    Oedema
    Addison's disease
    Anuria
    Cardiac failure
    Diabetes insipidus
    Hepatic cirrhosis with ascites
    Hyperchloraemia
    Hyperglycaemia
    Hyperlactataemia
    Hypervolaemia
    Oliguria
    Severe renal impairment
    Uncontrolled diabetes mellitus

    Precautions and Warnings

    Acute illness
    Burns
    Cardiopulmonary disorder
    Children under 18 years
    Females of childbearing potential
    Recent head trauma
    Shock
    Adrenal insufficiency
    Breastfeeding
    Cardiac disorder
    Chronic alcoholism
    Diabetes mellitus
    Gastrointestinal disorder
    Hepatic impairment
    Hyperaldosteronism
    Metabolic alkalosis
    Pregnancy
    Recent cerebrovascular accident
    Renal impairment
    Severe dehydration
    Severe malnutrition
    Thyrotoxicosis

    Reduce dose in patients with renal impairment
    Avoid rapid infusion rates
    Do not give blood products in same intravenous line
    Diabetic control may need adjustment
    Ensure adequate hydration prior to infusion
    Monitor acid-base balance
    Monitor blood / urinary glucose concentrations in diabetic patients
    Monitor children closely for signs and symptoms of hyponatraemia
    Monitor creatinine, blood urea nitrogen (BUN) and urinary output
    Monitor ECG
    Monitor fluid and electrolyte status
    Monitor renal function in patients with renal impairment
    Monitor serum glucose in newborns
    Monitor serum potassium regularly
    Discontinue if hypersensitivity reactions occur

    Intravenous potassium should be administered via a large peripheral or central vein to reduce the risk of causing sclerosis. If infused through a central vein, ensure that the catheter is not in the atrium of ventricle in order to avoid localised hyperkalaemia.

    The intravenous infusion device and administration equipment must be frequently monitored.

    If hyperglycaemia occurs during therapy, reduce the rate of infusion or administer insulin.

    Do not use plastic containers connected in series as this can result in air embolism. This is due to residual air being drawn from the primary container before the administration of the fluid from the secondary container is completed.

    Acute hyponatraemia can lead to acute hyponatraemic encephalopathy. Children, women in the fertile age, patients with brain oedema or with reduced cerebral compliance are all at particular risk of life threatening brain swelling caused by acute hyponatraemia.

    Pregnancy and Lactation

    Pregnancy

    Use potassium chloride in glucose 10% with caution during pregnancy.

    The manufacturer advises caution if potassium chloride in glucose 10% is used during pregnancy as it may result in foetal hyperglycaemia and metabolic acidosis as well as rebound neonatal hypoglycaemia due to foetal insulin production.

    Hyperkalaemic and hypokalaemic states lead to impaired cardiac function of the maternal and foetal hearts. Maternal electrolyte levels must therefore be controlled regularly.

    Potassium chloride in glucose 10% should be used with caution if administered in combination with oxytocin due to the risk of hyponatraemia.

    Lactation

    Use potassium chloride in glucose 10% with caution during breastfeeding.

    The manufacturer advises caution if potassium chloride in glucose 10% is used when breastfeeding. There presence of potassium chloride in glucose 10% in human breast milk and the effects on exposed infants are unknown. The potential risk and benefits for each specific patient should be carefully considered prior to administration.

    Side Effects

    Anaphylactic reaction
    Cardiac arrest
    Chills
    Electrolyte disturbances
    Extravasation
    Glycosuria
    Hyperglycaemia
    Hyperkalaemia
    Hypersensitivity reactions
    Hypervolaemia
    Hypokalaemia
    Hyponatraemia
    Irritation (injection site)
    Local infection at injection site
    Over-hydration
    Pain / soreness (injection site)
    Phlebitis (injection site)
    Pyrexia

    Overdosage

    It is strongly recommended that the UK National Poisons Information Service be consulted on cases of suspected or actual overdose where there is doubt over the degree of risk or about appropriate management.

    The following number will direct the caller to the relevant local centre (0844) 892 0111

    Information may be obtained if you have access to ToxBase the primary clinical toxicology database of the National Poisons Information Service. This is available via password on the internet ( www.toxbase.org ) or if this is unavailable at the backup site ( www.toxbasebackup.org ).

    Further Information

    Last Full Review Date: November 2020.

    Reference Sources

    Summary of Product Characteristics: Potassium chloride 0.15% w/v and glucose 10% w/v solution for infusion. Baxter Healthcare Ltd. Revised October 2019.

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