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GPManual/Blog/
Nephrology11 min readUpdated 28 February 2026

Chronic Kidney Disease in General Practice: Staging, Monitoring & Slowing Progression

From eGFR interpretation to ACEi/ARB prescribing, anaemia management, and referral criteria

Dr. James Okafor
Dr. James Okafor
GP with Special Interest in Diabetes & Metabolic Medicine
Published 20 August 2025
Chronic Kidney Disease in General Practice: Staging, Monitoring & Slowing Progression

CKD affects approximately 10% of the global population and is a major risk factor for cardiovascular disease and end-stage renal failure. This guide covers KDIGO staging, monitoring intervals, ACEi/ARB prescribing, anaemia of CKD, and referral criteria for primary care.

Clinical Decision Support: This article is for educational purposes and supports — not replaces — clinical judgment. Always verify with current national guidelines, BNF, and specialist consultation when needed.

Chronic kidney disease (CKD) affects approximately 10% of the global population and is a major independent risk factor for cardiovascular disease, with patients with CKD stage 3–5 having a 2–4 times higher cardiovascular mortality than the general population. In UK primary care, CKD is predominantly managed by GPs, with nephrology input reserved for advanced or complex cases.

KDIGO CKD Staging: eGFR and Albuminuria

CKD is defined as abnormalities of kidney structure or function, present for >3 months, with implications for health. Staging uses both eGFR (G stages) and albuminuria (A stages) — the combination determines prognosis and monitoring frequency.

G StageeGFR (mL/min/1.73m²)Description
G1≥90Normal or high (with kidney damage markers)
G260–89Mildly decreased
G3a45–59Mildly to moderately decreased
G3b30–44Moderately to severely decreased
G415–29Severely decreased
G5<15Kidney failure
A StageACR (mg/mmol)Description
A1<3Normal to mildly increased
A23–30Moderately increased (microalbuminuria)
A3>30Severely increased (macroalbuminuria)

A single low eGFR does not diagnose CKD — it must be confirmed on a repeat test at least 90 days later. Acute causes (dehydration, AKI, recent contrast) must be excluded before labelling as CKD.

Monitoring Intervals in CKD

CKD StageMonitoring FrequencyTests
G1–G2, A1AnnualeGFR, ACR, BP, electrolytes
G3a, A1–A2Every 6–12 monthseGFR, ACR, BP, electrolytes, Hb, calcium, phosphate
G3b–G4Every 3–6 monthsAbove + PTH, bicarbonate, uric acid
G5 (pre-dialysis)Every 1–3 monthsFull CKD panel; nephrology co-management

Slowing CKD Progression: Key Interventions

Blood Pressure Control

Hypertension is both a cause and consequence of CKD. Target BP in CKD is <140/90 mmHg (or <130/80 mmHg if ACR ≥70 mg/mmol). ACE inhibitors or ARBs are the preferred antihypertensives in CKD with proteinuria — they reduce intraglomerular pressure and slow progression independently of BP lowering.

SGLT2 Inhibitors in CKD

Dapagliflozin (Forxiga) is now licensed for CKD (eGFR 25–75 mL/min/1.73m²) regardless of diabetes status, following the DAPA-CKD trial. It reduces the risk of sustained eGFR decline, end-stage kidney disease, and cardiovascular death by approximately 39%. This is a major advance in CKD management in primary care.

Anaemia of CKD

  • Suspect CKD anaemia if Hb <130 g/L (men) or <120 g/L (women) with eGFR <60
  • Exclude other causes first: iron deficiency (ferritin, transferrin saturation), B12/folate deficiency, haemolysis
  • Iron deficiency is common in CKD — treat with oral iron first; IV iron if oral not tolerated or ineffective
  • Erythropoiesis-stimulating agents (ESAs): Refer to nephrology if Hb <100 g/L despite iron repletion
  • Target Hb with ESA: 100–120 g/L (avoid >130 g/L — increased cardiovascular risk)

Referral Criteria to Nephrology

  • eGFR <30 mL/min/1.73m² (G4–G5)
  • ACR >70 mg/mmol (A3)
  • Rapidly declining eGFR (>5 mL/min/1.73m² per year or >10 mL/min/1.73m² in 5 years)
  • Haematuria with proteinuria (possible glomerulonephritis)
  • Refractory hypertension despite 3+ antihypertensives
  • Suspected renal artery stenosis
  • Metabolic complications: refractory hyperkalaemia, acidosis, hyperphosphataemia

Key Clinical Takeaways

  • CKD requires two eGFR readings >90 days apart — do not diagnose on a single result
  • Stage using both eGFR (G1–G5) and albuminuria (A1–A3) — combination determines prognosis
  • ACEi/ARB are preferred antihypertensives in CKD with proteinuria — monitor eGFR and K+ closely
  • Dapagliflozin is now licensed for CKD regardless of diabetes — significant renoprotective benefit
  • Refer to nephrology if eGFR <30, ACR >70, or rapidly declining eGFR
  • Annual monitoring minimum for all CKD patients; more frequent for advanced stages
Topics:CKDChronic Kidney DiseaseeGFRACE inhibitorsNephrologyNICE NG203