Sodium plays a key role in the body in muscle contraction, conduction of nerve impulses and maintenance of electrolyte balance. It maintains the extracellular fluid volume by affecting the distribution of water between intracellular and extracellular compartments by osmosis and is part of the bicarbonate buffer system. Average dietary salt intake generally exceeds requirements in western diets, and excess is primarily excreted in perspiration and urine. A normal blood sodium level is between 135 and 145 mmol/L.
Sodium
Sodium
Sodium is an essential electrolyte, and the main extracellular cation in the blood.
Sodium is responsible for maintaining the extracellular fluid volume. Serum sodium concentration is kept within range by number of various mechanisms which adjust the amount excreted in the urine or increase the intake of water to prevent a rise in serum sodium levels.
Hypernatraemia
This is a level > 145mmol/L. The most common causes include
- Inadequate intake causing dehydration.
- Excessive GI loss without fluid replacement through severe vomiting and/or diarrhoea.
- Loop diuretic use which increases urine output.
- Thirst impairment (elderly, dementia patients).
- Diabetes insipidus.
- Dermal skin losses – burns, excessive perspiration in athletes, eg long distance runners.
- Renal dysfunction.
- Incorrect IV fluid replacement (excessive saline).
- Osmotic diuresis for diabetic coma.
- Primary aldosteronism.
- Hypernatraemic dehydration in breastfed infants.
Hyponatraemia
Hyponatremia is a low plasma sodium level < 135mmol/L, and is usually caused by a failure to excrete water normally. It can be categorised as mild (Na 125 – 134mmol/L), moderate (120 – 124mmol/L) or severe (<120mmol/L). Normally the release of ADH regulates the water balance with excess water being excreted in the kidneys.
The causes of hyponatremia are typically classified according to a person’s body fluid status. There are 3 types: hypovolaemic, euvolaemic or hypervolaemic hyponatraemia.
Hypovolaemic hyponatraemia
This occurs when there is depletion of both total body water and sodium with a relative excess of sodium loss. Common causes include:
- Medications – particularly thiazide & loop diuretics.
- GI loss: prolonged vomiting, chronic diarrhoea, pancreatitis, peritonitis, bowel obstruction.
- Addisons Disease.
- Congenital adrenal hypoerplasia.
- Renal impairment – nephropathy.
- Haemorrhage.
- Exercise induced – excessive perspiration with prolonged endurance type of exercise.
- Rhabdomyolysis.
- Severe burns.
Euvolaemic hyponatraemia occurs when there is relative absolute increase in body water with a concurrent reduction in serum sodium, with no clinical oedema. Common causes include:
- SIADH.
- Adrenal insufficiency.
- Hypothyroidism.
- Excessive water intake.
- Normal physiologic change of pregnancy.
Hypervolaemic Hyponatraemia occurs with both sodium and water content increase. Common causes include:
- Congestive cardiac failure.
- Liver cirrhosis.
- Renal dysfunction particularly nephrotic syndrome.
- Hyperglycaemic states.
Drugs that may cause hyponatraemia: Diuretics (thiazide, combination, loop diuretics), anti convulsants (carbamazepine), ACE inhibitors, Psychotropics – antidepressants: SSRI, MAOIs; antipsychotics, mood stabilisers, sedatives, hypnotics, COX 2 inhibitor, Sulphonylureas , PPIs, Desmopressin, oxytocin
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5mL venous serum or plasma
Enfer Medical
Tests/Assays
Enfer Medical offers Ion Selective Electrode (indirect) technology for the quantitative assay for Chloride, Sodium & Potassium. This test is CE-IVD certified.
Patient
Request Form
For clients using the Enfer Medical Client Portal, the Enfer Medical Patient Request Form (PRF) will be generated when you have completed your “Test Request” within the portal linked below.
Please note that samples suspected of containing high risk pathogens such as Mycobacterium tuberculosis should be clearly identified on the form and packed separately from other samples.
Results are available next working day.
This assay is available seven days a week.
Packaging
The packaging/preparation of samples for delivery to the laboratory are required to be in adherence to all national regulations for the safe transport of biological materials. HSE guidance can be reviewed HERE.
There are specific packaging instructions and labelling requirements requiring triple packaging including:
- Primary leak-proof container – tube or vial containing the sample.
- Secondary watertight container, with absorbent material, intended to protect the primary container.
- Outer container protects the secondary container.
- Patient Request forms must be placed between the secondary container and the outer shipping container.
Further information on the packaging/preparation of samples for delivery to the laboratory is contained within the Enfer Medical Laboratory User Manual which clients are provided with.
Storage & Stability
Specimens must be tested within 7 days of collection and stored at 2-8°C.
Samples
In addition to the packaging of samples, the transport/delivery of clinical samples to the laboratory is required to be in adherence to all national regulations for the safe transport of biological materials. Enfer Medical provides a fully compliant logistics service, aligned with clients’ testing requirements.
Prompt transport of specimens:
To ensure prompt testing of samples and release of results within the published test turnaround times, samples should arrive to the laboratory by 18:00. Test turnaround time is measured from receipt of the sample at the laboratory until the time the authorised results are reported to users.
of Samples
In rare cases specimens may not be suitable for testing on arrival to the laboratory. In that case the sample will be rejected at the receipt stage and the service user will be notified immediately and an explanation as to why the sample could not be processed will be provided. Reasons why samples cannot be processed include but are not limited to:
- Samples received beyond the stability limits and/or not at the correct temperature indicated for each test.
- Incorrect sample type received.
- Leaking samples, sample not received or sample insufficient for analysis as stated below within sample requirements.
- Non-compliant samples or request forms i.e. those missing sample date information, missing sample test request and/or missing sample site/type information.
- Samples received without the necessary patient identifiers.
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Quantitative results for Sodium are reported in numeric value in mmol/L. Critical results are communicated in accordance with the Communication of critical results for patients in the community- national laboratory handbook CSP041/2019
Accessing
Your Results
Following receipt at the Laboratory, results should be available on the next working day and will be reported to the referring clinician via the Enfer Medical Client Portal or in a format agreed with clients.
Established clients can login to the portal using the link above.