Medical Forum 09/11

Page 6

By Dr Wayne Smit, General Pathologist

Perth Pathology

Dr Wayne Smit is a General Pathologist. He completed his Fellowship in Melbourne in 1996 and has worked in Perth since 1999, including a term as CEO at Clinipath Pathology (Sonic). Wayne co-founded Perth Pathology with like-minded ‘corporate refugees’ in 2006 and remains Managing Partner.

(Perth Medical Laboratories Pty Ltd APA) 152 High Street Fremantle WA 6160 Ph 9433 5696 Fax 9433 5472

www.perthpathology.com.au Collection centres throughout the Perth metropolitan area including: Fremantle (Main Lab); Perth CBD, Atwell, Bedford, Belmont, Bentley, East Perth, Ellenbrook, Hilton, Joondalup, Kardinya, Kinross, Maddington, Malaga, Palmyra, South Lake, South Perth, Southern River, Subiaco, West Leederville

Hyponatraemia By Dr Wayne Smit, General Pathologist

H

yponatraemia (low serum sodium) is the most common electrolyte disorder. Maintenance of sodium is important to sustain blood pressure and normal nerve and muscle function. In its most severe form, hyponatraemia is associated with significant morbidity and mortality. While the list of causes is long (see Table 1), unexpected cases can usually be resolved with clinical assessment and some basic laboratory investigations.

Clinical presentation Most patients with hyponatraemia are asymptomatic, especially if the fall in sodium has been slow. Symptoms may not develop until the [Na+] falls to 120mmol/L or less, and even then may be nonspecific (e.g. lethargy, headache, and nausea). However when reduction in sodium has been rapid, patients may be symptomatic well before a level of 120mmol/L is reached. In severe hyponatraemia neurological symptoms predominate. As the level of sodium outside the cells falls, there is movement of water from the extracellular fluids into the cells in an attempt to maintain the normal sodium concentration. Most tissues can

accommodate this cellular swelling but the brain is more sensitive because of the confinement by the skull bones. The risk of seizures and coma increases as the sodium level decreases.

Assessment & Investigation The identification of hyponatraemia should be followed by clinical assessment of the patient for symptoms but particularly to exclude important causes including CCF, liver or renal failure, malignancy, hypothyroidism, Addison’s, and IV or irrigation fluid administration. The patient’s hydration status should also be assessed and hydration status is important to help distinguish causes of hypotonic hyponatraemia.

In many cases the underlying cause will be evident following clinical assessment but where the aetiology is less clear, further investigation may be indicated. Applicable laboratory tests may vary with the clinical situation but serum osmolality, urine osmolality and urine sodium concentration are frequently useful. LFTs, TFTs, cortisol, glucose and lipids may be helpful to narrow the differential diagnoses. Assay of ADH (antidiuretic hormone) is rarely helpful.

Management Treatment, if indicated, is generally directed at the underlying cause of the hyponatraemia. Water restriction may be useful. In euvolaemic hyponatraemic patients, hypertonic saline may also be used but the risks of osmotic pontine demyelination caused by rapid restoration of sodium levels should be considered. References are available on request.

Table 1: Common Causes of Hyponatraemia: (after Walmsley) Pseudohyponatraemia (normal plasma osmolality)

Hyperlipidaemia Hyperproteinaemia

Hypertonic hyponatraemia (high plasma osmolality)

Hyperglycaemia (Diabetes)

Hypotonic hyponatraemia (low plasma osmolality) Hypovolaemia

- Extrarenal (urine Na <20mmol/L) GI loss: diarrhea, vomiting Skin loss: excessive sweating - Renal (urine Na >20mmol/L) Diuretic Rx Salt losing nephritis Addision’s disease

Euvolaemia (urine Na <20mmol/L) Acute water overload

Increased intake PLUS hypovolaemia: haemorrage, burns, drugs including IV hypotonic fluids Stress: post surgery, psychogenic Renal insufficiency

Euvolaemia (urine Na>20mmol/L) Chronic water overload

SIADH Drugs Chronic renal failure Endocrine: hypothyroidism, cortisol deficiency

Hypervolaemia (urine Na <20mmol/L): Oedematous states

Cardiac failure Hepatic cirrhosis Nephrotic syndrome

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Perth Pathology General Pathologist / Managing Partner: Dr Wayne Smit 0410-488736 Histology / Cytology: Dr Michael Armstrong Dr Tony Barham Dr Bruce Latham

0417-094799 0416-577619 0407-080608

Infectious Diseases (Microbiology): Dr Laurens Manning 0400-783194 Haematology: Dr Rebecca Howman

0417-935873

Laboratory Director: Paul Schneider

0417-931850

Providing phone advice to clinicians and a comprehensive range of medical pathology investigations, including: • • • •

Histology (Skin, GI, etc) Cytology (incl. Paps and FNAs) Haematology (yes, we do lab controlled INRs) B iochemistry (including hormones and markers) • Microbiology and Serology Professional personalised service from a noncorporate, pathologist owned and operated laboratory practice 5


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