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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Hyperkalaemia

Endocrinology and metabolism · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

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Serum potassium at least 6.5 mmol/L, hyperkalaemic ECG change, rapid rise, paralysis or clinical instability is life-threatening. Obtain an urgent ECG, continuous monitoring, senior and renal help, and use the current UK Kidney Association hospital algorithm. Give intravenous calcium immediately for toxic ECG changes while potassium-shifting and removing measures are prepared; cardiac arrest follows the RCUK hyperkalaemia algorithm.

Synopsis

Confirm and risk-stratify raised potassium, stabilise cardiac membranes, shift potassium safely and secure definitive removal with rebound surveillance.

  • UKKA defines hyperkalaemia from 5.5 mmol/L and recommends an urgent 12-lead ECG for every hospitalised adult with potassium at least 6.0 mmol/L.
  • Use continuous three-lead monitoring at 6.5 mmol/L or above, with any hyperkalaemic ECG feature, or at 6.0–6.4 mmol/L when the patient is unwell or a rapid rise is expected.
  • Repeat a potentially haemolysed or surprising sample promptly, but never delay treatment when the ECG, potassium and clinical context indicate genuine severe toxicity.
  • Intravenous calcium stabilises the myocardium within minutes but does not lower serum potassium; potassium-shifting and removal treatment must proceed alongside it.
  • UKKA’s standard insulin–glucose regimen is 10 units soluble insulin with 25 g glucose, with extra glucose infusion when pretreatment glucose is below 7 mmol/L and scheduled monitoring for six hours.
  • Nebulised salbutamol is an adjunct, not monotherapy for severe disease, and response may be limited in patients taking non-selective beta-blockers.
  • Shift therapies wear off: repeat potassium at 1, 2, 4, 6 and 24 hours under UKKA guidance and arrange definitive gastrointestinal or dialysis removal when indicated.
  • After stabilisation, preserve beneficial renin–angiotensin or heart-failure therapy where possible through cause correction, dietary review and specialist potassium binders rather than automatic permanent withdrawal.

Key red flags

Electrical toxicity

Peaked T waves, prolonged PR, flattened or absent P waves, widening QRS, bradycardia, sine wave or ventricular arrhythmia demands immediate calcium treatment.

Neuromuscular effect

Paraesthesia, ascending weakness, flaccid paralysis or ventilatory compromise can accompany severe hyperkalaemia and should not be mistaken for a primary neurological disorder.

Renal failure context

Oliguria, acute kidney injury, missed dialysis or access dysfunction predicts impaired removal and lowers the threshold for urgent renal replacement planning.

Cell breakdown

Crush injury, prolonged seizure, burns, rhabdomyolysis, tumour lysis or haemolysis can release potassium continuously and cause rapid rebound after temporary shifting.

Investigation priorities

01
Urgent twelve-lead ECGFirst step

Detect cardiac membrane toxicity and determine the immediate need for intravenous calcium.

Management branches

ConfirmRisk-stratify without delaying rescue

A laboratory or point-of-care result shows raised potassium or the ECG suggests hyperkalaemia.

  1. Use ABCDE, repeat potassium appropriately, obtain an urgent 12-lead ECG at 6.0 mmol/L or above and establish continuous monitoring for UKKA high-risk categories.
  2. Review renal output, acid–base state, glucose, medicines, cell injury and dialysis history while stopping exogenous potassium and avoidable causal agents.
  3. If severe potassium or toxic ECG change is present, activate the hospital algorithm immediately and call senior, renal and critical-care teams before confirmation delays treatment.

Key medicines

Intravenous calcium salts for ECG toxicityUKKA recommends 30 mL calcium gluconate 10% over 10 minutes for non-arrest patients, or 10 mL calcium chloride 10% over 5 minutes in cardiac arrest or peri-arrest; reassess the ECG and repeat only through the algorithm.Calcium does not lower potassium and its protection is temporary. Confirm the salt and concentration because elemental calcium differs, use a secure line, avoid extravasation and obtain expert toxicology advice when digoxin poisoning is suspected.
Soluble insulin with glucoseGive 10 units soluble insulin with 25 g glucose under UKKA guidance; if pretreatment glucose is below 7 mmol/L, follow with 10% glucose at 50 mL/hour for five hours and titrate to the monitored glucose target.Check glucose before treatment and at 0, 30, 60, 90, 120, 180, 240, 300 and 360 minutes. Hypoglycaemia risk is increased by renal failure, low body weight, non-diabetes and repeat dosing; treat lows immediately.
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Sources and review status5 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • UKKA acute hyperkalaemia guideline pageCurrent October 2023 UK clinical guideline, with review date October 2026.
  • UKKA full adult hyperkalaemia guidelineExact ECG, calcium, insulin–glucose, salbutamol and monitoring recommendations.
  • RCUK 2025 special circumstancesCurrent UK resuscitation modifications for hyperkalaemic cardiac arrest and peri-arrest care.
  • BNF hyperkalaemia treatment summaryUK formulary treatment options and links to the current specialty algorithm.
  • Calcium gluconate 10% SmPCCurrent licensed adult hyperkalaemia administration, onset and repeat-dose safety.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftAwaiting review
Clinical state
JurisdictionUnited Kingdom