Skip to textbook content
Doctor’s PassportTextbook
TopicsAll topics

Loading topic navigation…

Textbook navigation
TopicsAll topics

Loading topic navigation…

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.

Acute kidney injury: recognition and staging

Renal · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
!
Escalate

AKI with anuria, severe hyperkalaemia, pulmonary oedema, profound acidaemia, uraemic encephalopathy or pericarditis, shock, suspected infected obstruction or a rapidly progressive nephritic presentation needs immediate ABCDE treatment and urgent senior renal or urological involvement; do not wait for a higher creatinine stage.

Synopsis

Recognise acute kidney injury promptly, apply creatinine and urine-output staging correctly, identify immediate threats and start a cause-directed assessment before reversible injury progresses.

  • Diagnose AKI in an adult when serum creatinine rises by at least 26 micromol/L within 48 hours, rises to at least 1.5 times a known or presumed baseline within 7 days, or urine output falls below 0.5 mL/kg/hour for more than 6 hours.
  • Use the worst KDIGO creatinine or urine-output criterion. Stage 1: creatinine 1.5–1.9 times baseline or a rise of at least 26 micromol/L; urine output below 0.5 mL/kg/hour for 6–12 hours. Stage 2: creatinine 2.0–2.9 times baseline; urine output below 0.5 mL/kg/hour for at least 12 hours. Stage 3: creatinine at least 3 times baseline, an increase to at least 354 micromol/L with an acute rise of at least 44 micromol/L, or initiation of renal replacement therapy; urine output below 0.3 mL/kg/hour for at least 24 hours or anuria for at least 12 hours.
  • Creatinine is a delayed concentration marker influenced by muscle mass, fluid balance and laboratory timing; an apparently normal result cannot exclude evolving injury after shock, sepsis or toxin exposure.
  • Retrieve previous results and reconstruct the timeline. The same creatinine may represent stable CKD, AKI on CKD, or a major acute fall in filtration in a person with low muscle mass.
  • Measure and document urine output rather than relying on the phrase ‘passing urine’; non-oliguric AKI can still be severe, while blocked catheters and inaccurate fluid charts can mimic oliguria.
  • Classify the likely mechanism as impaired perfusion, intrinsic renal injury or urinary obstruction, while recognising that hospital AKI commonly has several concurrent causes.
  • Review every medicine for haemodynamic effect, direct nephrotoxicity, renal accumulation and the consequences of temporary interruption; create an explicit restart plan rather than allowing important long-term therapy to disappear.
  • Escalation follows physiology and trajectory, not a creatinine threshold alone: rapidly rising potassium, oxygen requirement, acidosis, altered cognition or worsening oliguria may demand action before stage 3 is reached.

Key red flags

Creatinine-defined AKI

A rise of at least 26 micromol/L within 48 hours or at least 50% above baseline within 7 days meets an adult AKI criterion. Search laboratory records for a credible baseline and state whether the timing is known, estimated or uncertain.

Urine-output-defined AKI

Output below 0.5 mL/kg/hour for over 6 hours is sufficient even before creatinine rises. Confirm measurement, catheter patency and body weight, and distinguish oliguria from complete anuria because anuria strongly raises obstruction or catastrophic vascular disease.

Intrinsic renal warning pattern

Blood and protein on urinalysis, red-cell casts if microscopy is available, hypertension, oedema, rash, pulmonary haemorrhage or systemic vasculitic features suggest glomerular or interstitial disease and warrant early nephrology discussion rather than repeated fluid challenges.

Complicated AKI

ECG change from hyperkalaemia, refractory pulmonary oedema, severe metabolic acidosis, uraemic pericarditic pain or encephalopathy, and a suspected infected obstructed system are time-critical complications whose treatment must begin while staging and cause are refined.

Investigation priorities

01
Serial serum creatinine, urea and electrolytesFirst step

Confirm an acute change, stage severity and expose dangerous potassium or bicarbonate disturbance.

Management branches

First hourStabilise and establish severity

A laboratory alert, new oliguria or clinical suspicion of acute renal dysfunction.

  1. 1. Perform ABCDE, obtain observations, assess perfusion and congestion, verify urine output and check the catheter or bladder when relevant.
  2. 2. Send urgent creatinine, electrolytes and venous gas, obtain an ECG if potassium may be raised, and begin treatment of any immediate physiological threat.
  3. 3. Retrieve baseline results, apply both creatinine and urine-output criteria, record the highest stage and document the direction and speed of change.
  4. 4. Review medicines and exposures, treat sepsis or shock promptly, and call renal, critical care or urology early when complications or diagnostic red flags are present.

Key medicines

Balanced isotonic crystalloidGive a cautious bolus only when clinical assessment supports intravascular depletion, then reassess immediately; use the current local resuscitation protocol rather than a fixed cumulative volume.Avoid automatic repeated boluses in pulmonary oedema, advanced cardiac failure or venous congestion. Document endpoints such as perfusion, blood pressure, lung findings and urine response; fluid is a treatment, not a diagnostic ritual.
Open full textbook →Answer 2 questions
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.

  • NICE NG148 acute kidney injury recommendationsNational criteria for detection, staging, investigation, referral and management.
  • UK Kidney Association acute kidney injury guidelineUK professional guideline and implementation resources for AKI care.
  • Think Kidneys secondary care AKI resourcesNHS care bundles, medication resources and discharge tools.
  • NHS acute kidney injury overviewCurrent NHS explanation of causes, diagnosis, treatment and recovery.
  • KDIGO 2012 clinical practice guideline for acute kidney injuryFinal 2012 adult stage 1–3 creatinine and urine-output table; NICE NG148 accepts KDIGO staging. The 2026 document remained a public-review draft at the August 2026 source check.

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

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom