• CKD is defined as:
o Abnormalities in kidney structure or function >3 months (e.g. ↓ eGFR, albuminuria, structural anomalies)
• Staging based on eGFR (mL/min/1.73 m²):
o Stage 1: ≥90 + evidence of renal damage (e.g. proteinuria, imaging)
o Stage 2: 60–89 + evidence of damage
o Stage 3a: 45–59
o Stage 3b: 30–44
o Stage 4: 15–29
o Stage 5: <15 (end-stage renal disease, ESRD)
• Albuminuria grading (ACR):
o A1: <3 mg/mmol
o A2: 3–30
o A3: >30
• Diabetes mellitus (most common)
• Hypertension
• Glomerulonephritis (e.g. IgA nephropathy)
• Polycystic kidney disease
• Obstructive uropathy (e.g. BPH, stones)
• Chronic pyelonephritis
• Vascular disease (e.g. renal artery stenosis)
o Normocytic, normochromic due to ↓ erythropoietin
o Contributing factors: inflammation, iron deficiency, bleeding
o Rx: erythropoiesis-stimulating agents (ESAs), iron (IV/oral)
o ↓ 1α-hydroxylation of vitamin D → ↓ Ca²⁺ → ↑ PTH (secondary hyperparathyroidism)
o Features: bone pain, fractures, vascular calcification
o Labs: ↑ PTH, ↑ phosphate, ↓ calcium, ↑ ALP
o Rx: phosphate binders, vitamin D analogues (e.g. calcitriol), cinacalcet
o Major cause of mortality in CKD
o Risk factors: HTN, dyslipidaemia, anaemia, inflammation
o ↑ risk of: LV hypertrophy, heart failure, MI, stroke
o Rx: BP control (target <130/80), statins, antiplatelets if indicated
o Hyperkalaemia, metabolic acidosis, hyponatraemia, hypocalcaemia
o Require dietary restriction, bicarbonate supplementation
o Oedema, hypertension, pulmonary congestion
o Salt and fluid restriction, loop diuretics
o Symptoms: nausea, anorexia, pruritus, pericarditis, encephalopathy
o Dialysis indicated if symptomatic
• Indications:
o ESRD (CKD 5) or refractory complications (e.g. hyperkalaemia, acidosis, fluid overload)
o Most common modality
o Requires arteriovenous (AV) fistula (takes ~6 weeks to mature)
o Schedule: typically 3×/week
o Risks: hypotension, infection, dialysis disequilibrium syndrome
o Continuous Ambulatory Peritoneal Dialysis (CAPD) or Automated (APD)
o Performed at home; uses peritoneum as semi-permeable membrane
o Risks: peritonitis (cloudy dialysate, abdominal pain), exit site infections, inadequate clearance
o Best long-term option for eligible patients
o Types: living related, living unrelated, deceased donor
o Requires lifelong immunosuppression (e.g. tacrolimus, mycophenolate, steroids)
o Risks:
Acute rejection: T-cell mediated, occurs days–months post-op
Chronic rejection: interstitial fibrosis and tubular atrophy
Infections: CMV, BK virus
Drug toxicities: calcineurin inhibitors (CNI) → nephrotoxicity, hypertension, diabetes
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Author & Educational Disclaimer
Author:
Dr Phillip Cockrell BM FRCP DipClinEd
Dr Phillip Cockrell is a UK Consultant Physician in Internal Medicine, currently working at Queen Alexandra Hospital, Portsmouth University Hospitals NHS Trust. He has previously worked as a registrar across Intensive Care Medicine, Gastroenterology, Cardiology, Stroke Medicine, Acute Medicine, and Respiratory Medicine.
He has held senior leadership roles including Associate Clinical Director of the Acute Medical Unit, Clinical Director of Internal Medicine, and Chief of Medicine. Dr Cockrell has over 15 years’ experience in postgraduate medical education, having lectured extensively across the MRCP syllabus and contributed to MRCP revision teaching and course development.
Dr Cockrell holds a Bachelor of Medicine (BM), Fellowship of the Royal College of Physicians (FRCP), and a Diploma in Clinical Education (DipClinEd). His teaching approach is based on structured consolidation of complex medical topics to support efficient and effective revision for postgraduate examinations.
Purpose of this content:
The material on this page is intended solely for educational purposes to support revision for the MRCP (UK) Part 1 examination. It reflects examination-relevant principles of internal medicine and is designed to aid learning and pattern recognition.
Medical disclaimer:
This content is designed for postgraduate medical examination revision and does not constitute medical advice, diagnosis, or treatment guidance and must not be used as a substitute for professional clinical judgement, local guidelines, or specialist consultation. Clinical decisions should always be made in the context of individual patient circumstances and current national guidance.