Diagnosis of cause of hyponatraemia
A definitive diagnosis of the underlying aetiology of hyponatraemia is not always possible at the time of initial presentation
- an accurate history should be taken
- look for signs and symptoms of hyponatraemia
- inquire about any medication (e.g. - diuretics, antidepressants), recently received intravenous fluids, vomiting, diarrhea and about any associated diseases (1)
- measure serum osmolality (2)
- if serum osmolality is normal (275 – 295 mOsmol/l) or high (>295 mOsmol/l) consider causes such as hyperglycaemia, hyperlipidaemia, hyperprotinaemia and renal failure
- in cases of low osmolality (<275 mOsmol/l) assess volume status of the patient,
- hypovolaemia – tachycardia, postural hypotension, dry skin, reduced skin turgor, raised blood urea, raised plasma rennin
- euvolaemia – blood urea normal or slightly reduced
- hypervolaemia – oedema (peripheral, sacral, pulmonary), ascites, increased JVP or CVP (3)
- the three major classifications of hypotonic hyponatraemia based on the patients ECF volume status:
- hypovolaemic hyponatraemia
- normovolaemic (euvolaemic) hyponatraemia
- hypervolaemic hyponatraemia
- plasma glucose and lipids, renal function, thyroid function and adrenal function test should be done if clinically indicated (1,2)
Reference
- Adrogué HJ, Tucker BM, Madias NE. Diagnosis and management of hyponatremia: a review. JAMA. 2022 Jul 19;328(3):280-91.
- Spasovski G, Vanholder R, Allolio B, et al; Hyponatraemia Guideline Development Group. Clinical practice guideline on diagnosis and treatment of hyponatraemia. Eur J Endocrinol. 2014 Feb 25;170(3):G1-47.
Related pages
Create an account to add page annotations
Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.