TextbookRenal MedicineElectrolyte Disorders

Electrolyte Disorders

Disturbances in serum sodium, potassium, calcium, magnesium, and phosphate concentrations that can cause significant morbidity and mortality. Hyponatraemia is the most common electrolyte disorder in hospitalised patients, while hyperkalaemia is the most immediately life-threatening.

Key Facts

Hyponatraemia (<135 mmol/L) is the most common electrolyte disorder in hospitalised patients (~20-30%); causes include SIADH, heart failure, cirrhosis, diuretics Severe hyponatraemia (<120 mmol/L): risk of seizures, cerebral oedema; correct slowly (≤10 mmol/L/24h) to avoid osmotic demyelination syndrome (ODS) Hyperkalaemia (>5.5 mmol/L): most dangerous electrolyte disorder; treat urgently if ECG changes or K+ >6.5 mmol/L Hypocalcaemia: Chvostek sign (facial nerve tap → facial twitch), Trousseau sign (BP cuff → carpopedal spasm), prolonged QT Hypercalcaemia: bones, stones, groans, moans (bone pain, renal stones, abdominal pain, psychiatric symptoms); most common causes: primary hyperparathyroidism and malignancy Hypomagnesaemia: often coexists with hypokalaemia and hypocalcaemia; must correct Mg²⁺ first Hyperphosphataemia: hallmark of CKD stage 4-5; managed with phosphate binders (sevelamer, calcium acetate) All electrolyte corrections require monitoring every 2-6 hours during acute treatment

Overview

Key Facts

Electrolyte disorders are ubiquitous in hospital medicine and require systematic assessment of volume status, underlying cause, and severity to guide safe correction.

Epidemiology

  • Hyponatraemia: 20-30% of hospitalised patients
  • Hyperkalaemia: 10% of hospitalised patients
  • Hypokalaemia: 10-20% of hospitalised patients
  • Electrolyte disorders are associated with increased length of stay, ICU admission, and mortality

Classification of Hyponatraemia by Volume Status

Hypovolaemic (low total body water + low Na): diarrhoea, vomiting, Addison disease, diuretics Euvolaemic (normal total body water): SIADH (most common euvolaemic cause), hypothyroidism, cortisol deficiency Hypervolaemic (high total body water): heart failure, cirrhosis, nephrotic syndrome, CKD

Pathophysiology

  • Sodium determines plasma osmolality and ECF volume
  • Potassium maintains resting membrane potential – critical for cardiac and neuromuscular function
  • Calcium: 50% protein-bound (correct for albumin); ionised calcium is physiologically active
  • Magnesium: cofactor for Na-K-ATPase; deficiency causes refractory hypokalaemia and hypocalcaemia

Clinical Presentation

Hyponatraemia

  • Mild (130-134): often asymptomatic
  • Moderate (125-129): nausea, headache, confusion
  • Severe (<120): seizures, coma, respiratory arrest
  • Chronic hyponatraemia: may be surprisingly well-tolerated due to brain adaptation

Hypokalaemia

  • Muscle weakness, cramps, paralysis
  • U-wave on ECG, flattened T waves, ST depression
  • Cardiac arrhythmias (especially with digoxin)
  • Constipation, ileus

Hypercalcaemia

  • "Bones, stones, groans, and psychic moans"
  • Polyuria, polydipsia, dehydration
  • Short QT on ECG
  • Confusion, depression, coma in severe cases

Hypocalcaemia

  • Perioral and distal paraesthesiae
  • Muscle cramps, tetany, carpopedal spasm
  • Chvostek and Trousseau signs
  • Prolonged QT → risk of torsades de pointes
  • Seizures in severe cases

Red Flags

  • Na <120 with neurological symptoms → hypertonic saline (3% NaCl)
  • K+ >6.5 with ECG changes → emergency protocol
  • Corrected calcium >3.5 mmol/L → IV saline + zoledronic acid/calcitonin
  • Symptomatic hypocalcaemia → IV calcium gluconate 10% 10-20mL over 10 minutes

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
SIADHEuvolaemic hyponatraemia, concentrated urine, low urine Na >30Serum/urine osmolality
Addison diseaseHyponatraemia + hyperkalaemia, hypotensionShort Synacthen test
Diabetes insipidusHypernatraemia, dilute urine, polyuriaWater deprivation test
Primary hyperparathyroidismHypercalcaemia, raised PTHPTH, calcium
Malignancy-related hypercalcaemiaPTHrP elevated, low PTHPTHrP, CT staging
Gitelman syndromeHypokalaemia, metabolic alkalosis, hypomagnesaemiaUrinary electrolytes

Diagnosis / Investigation

For All Electrolyte Disorders

  • Serum electrolytes: Na, K, Ca (adjusted for albumin), Mg, PO4
  • Renal function: U&Es
  • Serum osmolality: key for hyponatraemia workup
  • Urine osmolality and urine Na: essential for hyponatraemia classification
  • ECG: K+ and Ca²⁺ abnormalities
  • ABG/VBG: acid-base status

Specific

  • Hyponatraemia: serum/urine osmolality, urine Na, TFTs, cortisol, volume status assessment
  • Hyperkalaemia: ECG, exclude pseudohyperkalaemia, CK (rhabdomyolysis), cortisol
  • Hypercalcaemia: PTH, vitamin D, myeloma screen, PTHrP, CXR
  • Hypocalcaemia: PTH, vitamin D, magnesium, phosphate
  • Hypomagnesaemia: serum Mg, urinary Mg (renal vs GI loss)

Management

Hyponatraemia

  • Acute symptomatic (<48h or seizures): 3% hypertonic saline 100-150mL IV over 20 min (repeat ×2 if needed); aim ↑Na by 4-6 mmol/L in first 6 hours
  • Chronic: correct by ≤10 mmol/L per 24 hours (risk of ODS if too fast)
  • Hypovolaemic: IV 0.9% NaCl
  • SIADH: fluid restriction (750-1000mL/day); tolvaptan 15mg OD if refractory; demeclocycline (less used)
  • Hypervolaemic: fluid restriction + treat underlying cause (diuretics for HF)

Hyperkalaemia

  • See dedicated hyperkalaemia topic for emergency protocol

Hypercalcaemia

  • Mild (<3.0): oral hydration, avoid thiazides
  • Moderate-severe (>3.0): IV 0.9% NaCl 3-4L/24h (rehydration) + IV zoledronic acid 4mg over 15 min (onset 2-4 days)
  • Life-threatening (>3.5): add calcitonin 4IU/kg SC/IM 12-hourly (rapid onset but tachyphylaxis)
  • Denosumab: if refractory to bisphosphonates
  • Treat underlying cause: parathyroidectomy (PHPT), chemo/radio (malignancy)

Hypocalcaemia

  • Symptomatic: 10% calcium gluconate 10-20mL IV over 10 minutes (with cardiac monitoring); may need continuous infusion
  • Chronic: oral calcium (Calcichew 1-2 tablets TDS) + alfacalcidol/calcitriol
  • Correct magnesium if low (IV MgSO4 8mmol over 15-20 min)

Hypomagnesaemia

  • IV MgSO4 8-20mmol over 2-4 hours (severe/symptomatic)
  • Oral Mg glycerophosphate 1-2 tablets TDS (chronic)
  • Must correct before hypokalaemia/hypocalcaemia will respond to treatment

Referral Criteria

  • Severe/symptomatic electrolyte disorder → acute medicine/ICU
  • Recurrent hyponatraemia → endocrinology (SIADH workup)
  • Hypercalcaemia with raised PTH → endocrine surgery
  • Refractory hypokalaemia → nephrology (Bartter/Gitelman)

Prognosis

  • Severe hyponatraemia (<120): mortality 10-25% if acute; osmotic demyelination syndrome if corrected too rapidly (irreversible brain damage)
  • Severe hyperkalaemia (>7.0): mortality >50% if untreated
  • Severe hypercalcaemia (>3.5): can cause cardiac arrest; good prognosis if treated promptly
  • Chronic electrolyte disorders: prognosis depends on underlying cause
  • ODS (from rapid sodium correction): devastating neurological outcome; classically pontine myelinolysis

Other Relevant Information

Hyponatraemia Management Algorithm

Volume StatusUrine NaUrine OsmolalityLikely CauseTreatment
Hypovolaemic<30>500GI/skin lossesIV 0.9% NaCl
Hypovolaemic>30>500Addison, diureticsTreat cause
Euvolaemic>30>100SIADHFluid restriction
Hypervolaemic<30>100HF, cirrhosisFluid restriction + treat cause

ECG Changes in Electrolyte Disorders

DisorderECG Finding
HyperkalaemiaTall tented T waves → widened QRS → sine wave
HypokalaemiaFlat T waves, U waves, ST depression
HypercalcaemiaShort QT
HypocalcaemiaProlonged QT
HypomagnesaemiaProlonged QT, torsades de pointes