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.

Proteinuria and albuminuria

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

RapidFull
!
Escalate

Heavy new proteinuria with rapid renal decline, active haematuria, severe hypertension, pulmonary oedema, suspected systemic vasculitis or nephrotic syndrome complicated by thrombosis, infection or AKI needs urgent nephrology assessment. Pregnancy after 20 weeks with new hypertension and proteinuria enters the obstetric pre-eclampsia pathway.

Synopsis

Detect and quantify urinary protein accurately, distinguish albumin, tubular and overflow mechanisms, recognise nephrotic or nephritic urgency and use albuminuria to guide CKD risk and treatment.

  • Use urine albumin-to-creatinine ratio as the first-line quantitative test in non-pregnant adults because it detects lower-level albumin leakage better than dipstick or PCR.
  • NICE classifies A1 as ACR below 3 mg/mmol, A2 as 3 to 30 mg/mmol and A3 as above 30 mg/mmol; albuminuria changes risk even when eGFR is preserved.
  • Confirm an ACR from 3 to 70 mg/mmol on a subsequent early-morning sample in a stable adult. NICE does not require confirmation before action when the initial ACR is at least 70 mg/mmol.
  • Fever, strenuous exercise, UTI, decompensated heart failure, hyperglycaemia, menstruation and marked hypertension can cause transient albuminuria; resolve context without ignoring a very high result.
  • Glomerular protein is predominantly albumin. Tubular disease loses low-molecular-weight proteins, while overflow protein such as immunoglobulin light chains may produce a high PCR with relatively modest ACR.
  • A negative or weak dipstick does not exclude light-chain proteinuria. Suspected myeloma requires serum free light chains, immunoglobulins and protein electrophoresis/immunofixation under the local pathway.
  • Nephrotic syndrome combines heavy protein loss with hypoalbuminaemia and oedema, often hyperlipidaemia, and increases venous thrombosis and infection risk. The cause still requires biopsy-led nephrology assessment.
  • Blood plus protein, hypertension and impaired renal function is nephritic until assessed; this pattern is more urgent than isolated stable albuminuria in diabetes.
  • ACE inhibitors or ARBs and SGLT2 inhibitors reduce albuminuria and kidney risk in defined NICE populations, but require potassium, creatinine, volume and pregnancy review.
  • Monitor proportional and absolute ACR change with the same collection conditions. Small fluctuations are biological noise; disappearance of protein during severe filtration loss is not necessarily recovery.

Key red flags

Nephrotic syndrome

Generalised oedema, very heavy proteinuria, low serum albumin and often high lipids suggests nephrotic syndrome. Unilateral leg swelling, pleuritic pain, fever or abdominal pain may indicate thrombosis or infection.

Nephritic proteinuria

Albuminuria with haematuria, red-cell casts, hypertension, oliguria and rising creatinine supports inflammatory glomerular disease. Pulmonary or systemic features make it a renal emergency.

Overflow protein

Bone pain, anaemia, hypercalcaemia, recurrent infection or AKI with discordantly high PCR and low ACR suggests a non-albumin protein such as monoclonal free light chain.

Investigation priorities

01
Early-morning urine ACRFirst step

Confirm and classify albumin leakage while reducing postural and concentration variation.

Management branches

Incidental albuminuriaConfirm and classify risk

Positive dipstick protein or ACR at least 3 mg/mmol without current severe illness.

  1. Check UTI, menstruation, exercise, fever, glucose and heart failure, then confirm ACR 3 to 70 using an early-morning sample; do not delay action for ACR at least 70.
  2. Assign A category with eGFR G category, check blood pressure and diabetes, review medicines and calculate progression or KFRE where NICE applies.
  3. Start indicated kidney-protective treatment and monitoring, referring for high ACR, haematuria, rapid decline, resistant hypertension, young age or uncertain cause.

Key medicines

ACE inhibitor or angiotensin receptor blockerTitrate to the highest licensed dose tolerated when NICE indications are met, using blood pressure, potassium, creatinine and volume-status monitoring.Avoid combination ACE inhibitor plus ARB. Review pregnancy, potassium above 5, bilateral renovascular disease and AKI risk; check renal profile before and after initiation or dose increase.
SGLT2 inhibitorSelect the licensed agent and dose using current NICE indication, eGFR range, diabetes status and SmPC, alongside standard kidney-protective care.Provide genital infection, volume, ketoacidosis and peri-procedure sick-day advice. Glycosuria is expected; temporarily review during severe acute illness and never use eGFR outside the licence.
Open full textbook →Answer 2 questions
Sources and review status4 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 NG203 chronic kidney disease recommendationsACR categories, confirmation, treatment and referral rules.
  • UKKA measurement of kidney functionACR and PCR interpretation for UK practice.
  • UKKA CKD staging guideCombined G/A risk, progression and referral framework.
  • NICE CKD proteinuria visual summaryRAAS and SGLT2 treatment pathways.

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