Hypotonic sodium chloride
- Drugs List
- Therapeutic Indications
- Dosage
- Administration
- Contraindications
- Precautions and Warnings
- Pregnancy and Lactation
- Side Effects
- Monograph
Presentation
Solution for infusion containing sodium chloride 0.18%.
Solution for infusion containing sodium chloride 0.45%.
Drugs List
Therapeutic Indications
Uses
Hypotonic sodium chloride 0.18% and 0.45% is used in the treatment of dehydration associated with hyperosmolarity (hypernatraemia).
Dosage
Adults
The rate of administration and volume infused will depend upon the requirements of the individual patient and the judgement of the physician.
Elderly
The rate of administration and volume infused will depend upon the requirements of the individual patient and the judgement of the physician.
Care should be taken to avoid circulatory overload especially if the patient has either renal or cardiac insufficiency.
Do not administer rapidly or for prolonged periods, particularly in the elderly.
Children
The rate of administration and volume infused will depend upon the requirements of the individual patient and the judgement of the physician.
Do not administer rapidly or for prolonged periods, particularly in infants.
Patients with Renal Impairment
Additional Dosage Information
The clinical effect of hypotonic saline can often be assessed from relief of symptoms, observation of blood pressure and measurement of the volume and concentration of urine output.
Administration
For intravenous infusion.
Contraindications
None known.
Precautions and Warnings
Do not use for protracted periods unless there is a heavy and continued loss of electrolytes. In such circumstances the clinician should continue therapy with great caution and with due regard to the patient's electrolyte balance.
Too rapid correction can induce cerebral oedema.
Administer potassium supplements to patients deficient in potassium as sodium chloride solutions will increase potassium loss.
Use with caution in patients susceptible to sodium overload due to cardiac failure and renal impairment.
In the first 5 or 6 days after surgery or severe trauma, patients may be unable to excrete excess sodium so caution is required to avoid administration of excess sodium chloride.
Use with caution in cardio-respiratory diseases, hepatic cirrhosis and children receiving glucocorticoids.
Use with caution in patients with:
Peripheral oedema
Pulmonary oedema
Hypertension
Toxaemia of pregnancy
Avoid fluid and electrolyte overload in infants and the elderly.
Do not administer rapidly or for prolonged periods, particularly in infants and the elderly.
During fluid therapy, monitor fluid and electrolyte status, blood pressure, volume and concentration of urine output.
Pregnancy and Lactation
Pregnancy
Sodium chloride infusion/injection in pregnancy is usually considered safe.
However caution should be exercised in pre-eclampsia / toxaemia of pregnancy.
The use of all medication in pregnancy should be avoided whenever possible; particularly in the first trimester. Non-drug treatments should also be considered. When essential, a medication with the best safety record over time should be chosen, employing the lowest effective dose for the shortest possible time. Polypharmacy should be avoided. Teratogens taken in the pre-embryonic period, often quoted as lasting until 14-17 days post-conception, are believed to have an all-or-nothing effect. Where drugs have a short half-life, and when the date of conception is certain, this may allow women to be reassured where drug exposure has occurred within this time frame. Further advice may be available from the UK National Teratology Information Service (NTIS) and through ToxBase, available via password on the internet ( www.toxbase.org ) or if this is unavailable at the backup site ( www.toxbasebackup.org ).
Lactation
Sodium chloride infusion/injection in during lactation is usually considered safe.
Neonates, infants born prematurely, those with low birth weight, those with an unstable gastrointestinal function or who have serious illnesses may require special consideration. For any infant, if a drug is prescribed to the nursing mother, it should be at the lowest practical dose and for the shortest time. When drug administration is unavoidable and breastfeeding is to continue, minimisation of exposure of the infant to the drug may sometimes be achieved by timing the maternal doses to just after a feeding episode. Infants exposed to drugs via breast milk should be monitored for unusual signs or symptoms. Interactions between the drug received by the infant from the mother's milk and medication prescribed for the infant should also be considered, for example, when the drug given to the infant may prevent metabolism of the drug received via breast milk.
Specialist advice is available from the UK Drugs in Lactation Advisory Service at https://www.midlandsmedicines.nhs.uk/content.asp?section=6&subsection=17&pageIdx=1
Side Effects
Nausea
Vomiting
Diarrhoea
Thrombosis
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 (https://www.toxbase.org/).
Shelf Life and Storage
Store at 2 to 25 degrees C.
Reference Sources
British National Formulary, 62nd Edition (2011) Pharmaceutical Press, London.
BNF for Children (2011-2012) Pharmaceutical Press, London.
Martindale: The Complete Drug Reference, 37th edition (2011) ed. Sweetman, S. Pharmaceutical Press, London.
Summary of Product Characteristics: Sodium Chloride 0.18% Intravenous infusion, Fresenius Kabi. Revised February 2010.
Summary of Product Characteristics: Sodium Chloride 0.45% Intravenous Infusion BP as Steriflex No.2, Fresenius Kabi. Revised August 2006.
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