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Referral and warning signs
When to refer
Referral to Nephrologist/Specialist recommended for: GFR <30 ml/min (Stage 4/5). Rapidly declining GFR. Persistent significant albuminuria (>300mg/day or ACR >30mg/mmol). CKD with refractory hypertension or complications (anaemia, MBD, electrolyte issues). Need for RRT planning. Children with CKD. Suspected glomerular disease or familial kidney disease.
Red flags
- Rapid decline in GFR
- Symptoms/signs of uraemia (confusion, pericardial rub, severe nausea/vomiting)
- Severe electrolyte abnormalities (esp. hyperkalaemia >6.0-6.5 mmol/L)
- Refractory fluid overload / Pulmonary oedema
- Severe uncontrolled hypertension
Signs and symptoms
- Often asymptomatic until advanced stages (GFR <30).
- Early stages may have symptoms of underlying cause (e.g., hypertension, diabetes).
- Later stages (Advanced CKD / Uraemia):
- - Fatigue, lethargy, weakness.
- - Anorexia, nausea, vomiting.
- - Pruritus (itching).
- - Peripheral oedema, pulmonary oedema (fluid overload).
- - Hypertension (often worsens).
- - Pallor (due to anaemia).
- - Metallic taste, foetor uraemicus (urine-like breath odour).
- - Difficulty concentrating, drowsiness, confusion (uraemic encephalopathy).
- - Muscle cramps, restless legs.
- - Bone pain (renal osteodystrophy).
- - Shortness of breath.
Risk factors
- Diabetes Mellitus (leading cause)
- Hypertension (leading cause)
- Glomerulonephritis
- Polycystic Kidney Disease (ADPKD)
- Chronic Pyelonephritis / Reflux Nephropathy
- Obstructive Uropathy (stones, BPH, strictures)
- Nephrotoxic drugs (long-term NSAID use)
- HIV-Associated Nephropathy (HIVAN)
- Sickle Cell Nephropathy
- Cardiovascular disease
- Older age (>50 years)
- Family history of kidney disease
- Obesity
Diagnosis
Clinical assessment
Suspect in patients with risk factors, especially those with long-standing diabetes or hypertension. Often detected via screening (urine dipstick, serum creatinine). Assess for symptoms/signs of uraemia and complications. Differentiate from AKI (duration >3 months needed for CKD diagnosis).
Investigations
- Serum Creatinine: Calculate estimated Glomerular Filtration Rate (eGFR) using formulas (e.g., CKD-EPI, MDRD). GFR determines CKD stage (Stage 1: ≥90 + kidney damage; Stage 2: 60-89 + damage; Stage 3a: 45-59; Stage 3b: 30-44; Stage 4: 15-29; Stage 5: <15 or dialysis).
- Urinalysis: Dipstick for protein, blood. Microscopy for cells, casts.
- Urine Albumin-to-Creatinine Ratio (ACR) or Protein-to-Creatinine Ratio (PCR): Quantify proteinuria/albuminuria (key marker of kidney damage and progression risk).
- Kidney Ultrasound: Assess kidney size (typically small/echogenic in CKD, except in PCKD/diabetic nephropathy), rule out obstruction, assess structure.
- Blood tests: Urea, Electrolytes (check K+, bicarbonate - acidosis), Calcium, Phosphate, Parathyroid Hormone (PTH) (assess bone mineral disease), CBC (anaemia), HbA1c (diabetes control), Lipid profile.
- Investigations for underlying cause: e.g., Viral serology (HBV, HCV, HIV), Autoimmune screen, Protein electrophoresis.
Diagnostic criteria
Presence of kidney damage (e.g., albuminuria ≥30mg/day or ACR ≥3mg/mmol) OR GFR <60 ml/min/1.73m² for ≥3 months.
Management
Non-pharmacological management
- Slowing Progression & Managing Co-morbidities:
- - Blood Pressure Control: Crucial. Target typically <130/80 mmHg (or per specific guidelines). ACE inhibitors or ARBs are first-line, especially if proteinuria/diabetes.
- - Glycaemic Control (Diabetes): Target HbA1c <7% (or individualized target).
- - Lifestyle Modifications: Weight loss, smoking cessation, regular exercise, low salt diet (<2g/day).
- - Dietary Protein Restriction: Moderate restriction may be beneficial in later stages (specialist guidance).
- - Avoid Nephrotoxins: NSAIDs, aminoglycosides, IV contrast (use cautiously).
- Management of Complications:
- - Anaemia: Iron supplements (oral/IV), Erythropoiesis-Stimulating Agents (ESAs - e.g., Epoetin alfa, Darbepoetin alfa) if Hb <10-11 g/dL (Target Hb 10-12 g/dL). Requires specialist initiation/monitoring.
- - Mineral and Bone Disorder (CKD-MBD): Phosphate binders (e.g., Calcium carbonate/acetate), Vitamin D analogues (e.g., Calcitriol, Alfacalcidol), Calcimimetics (specialist). Control phosphate, calcium, PTH levels.
- - Fluid Overload: Sodium/fluid restriction, Loop diuretics (Furosemide - often requires high doses).
- - Metabolic Acidosis: Oral sodium bicarbonate.
- - Hyperkalaemia: Dietary potassium restriction, review medications, potentially potassium binders.
- Renal Replacement Therapy (RRT) Planning (Stage 4/5):
- - Education about options: Haemodialysis, Peritoneal dialysis, Kidney transplantation.
- - Vascular access creation (AV fistula/graft) well in advance of needing haemodialysis.
- - Referral for transplant evaluation.
Pharmacological treatment
- Antihypertensives: ACE inhibitors (e.g., Enalapril, Lisinopril) or ARBs (e.g., Losartan, Valsartan) preferred, especially with proteinuria/diabetes. Add other agents (CCBs, diuretics, beta-blockers) as needed to reach target BP. Adjust doses for GFR.
- Diuretics: Loop diuretics (Furosemide) for fluid overload (Thiazides generally ineffective if GFR <30).
- Medications for Complications: Iron, ESAs, Phosphate binders, Vitamin D analogues, Sodium bicarbonate (as above).
- Dosage Adjustment: Many drugs require dose adjustment based on eGFR. Consult drug information resources.
Monitoring
Regular monitoring (e.g., 3-12 monthly depending on stage/stability) of: GFR/Creatinine, Electrolytes (esp. K+), Bicarbonate, Calcium, Phosphate, PTH, Hb, BP control, Albuminuria/Proteinuria, Volume status, Nutritional status.
Complications
- Progression to End-Stage Renal Disease (ESRD) requiring dialysis or transplantation
- Cardiovascular Disease (MI, Stroke, HF, Sudden Death - leading cause of death in CKD)
- Anaemia
- CKD-Mineral and Bone Disorder (Renal Osteodystrophy, vascular calcification)
- Fluid overload / Hypertension
- Electrolyte abnormalities (Hyperkalaemia, Hyperphosphataemia, Hypocalcaemia)
- Metabolic Acidosis
- Malnutrition
- Uraemia and its complications (encephalopathy, pericarditis, neuropathy, bleeding)
- Increased susceptibility to infections
Prevention
- Screening high-risk individuals (diabetes, hypertension, family history).
- Optimal control of diabetes and hypertension.
- Avoidance of nephrotoxic drugs.
- Treatment of underlying kidney diseases (e.g., glomerulonephritis).
Patient education
- Explain CKD, its chronic nature, and staging.
- Importance of controlling BP and diabetes.
- Lifestyle modifications (diet - salt/potassium/phosphate/protein restriction as advised, fluid limits, exercise).
- Medication adherence and potential side effects.
- Avoidance of nephrotoxins (NSAIDs, certain herbs).
- Recognizing symptoms of worsening kidney function or complications.
- Need for regular monitoring (blood tests, urine tests, BP).
- Options for Renal Replacement Therapy (dialysis, transplant) when nearing ESRD.
Uganda-specific notes
Diabetes and hypertension are major drivers. HIVAN also significant. Late presentation common. Access to diagnostics (eGFR calculation, ACR, ultrasound), specialist care, and especially RRT (dialysis/transplant) is severely limited and costly. Focus on BP control, diabetes management, avoiding nephrotoxins, and managing complications like anaemia/fluid overload with available means.
References
- Uganda Clinical Guidelines (UCG) 2023
Chapter 7, Section 7.1.2
