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HIGH YIELD NOTES Updated June 2026 · ~5 min read

Core Concepts

Nephrology encompasses the study of normal kidney function and kidney diseases, their diagnosis, and treatment. Key areas include acute kidney injury (AKI), chronic kidney disease (CKD), glomerular diseases (nephrotic and nephritic syndromes), hypertension (especially renovascular), electrolyte and acid-base disorders, inherited kidney diseases, and renal replacement therapy (dialysis and transplantation). Understanding GFR estimation, albuminuria, and the progression of kidney disease is fundamental.

Clinical Presentation

  • Acute Kidney Injury (AKI): Rapid decline in kidney function. Presents with oliguria/anuria, peripheral/pulmonary edema, nausea, vomiting, fatigue, altered mental status (uremia).
  • Chronic Kidney Disease (CKD): Often asymptomatic until advanced stages. Symptoms include fatigue, weakness, pruritus, anorexia, nocturia, peripheral edema, muscle cramps, bone pain (renal osteodystrophy), neuropathy.
  • Nephrotic Syndrome: Characterized by heavy proteinuria (>3.5g/day), hypoalbuminemia, generalized edema (anasarca), hyperlipidemia, and thrombotic tendency.
  • Nephritic Syndrome: Presents with hematuria (often microscopic, but can be macroscopic/coca-cola urine), hypertension, mild proteinuria, oliguria, and often AKI (rapidly progressive glomerulonephritis, RPGN).
  • Electrolyte/Acid-Base Disorders:
    • Hyperkalemia: Palpitations, muscle weakness, arrhythmias (peaked T waves, wide QRS).
    • Hypokalemia: Muscle cramps, weakness, fatigue, arrhythmias (U waves).
    • Hyponatremia: Headache, nausea, confusion, seizures.
    • Hypernatremia: Thirst, lethargy, seizures, coma.
    • Metabolic Acidosis: Kussmaul breathing, fatigue, confusion.
  • Hypertension: Often asymptomatic. May present with headache, visual changes, epistaxis, or symptoms of end-organ damage (e.g., flash pulmonary edema in renal artery stenosis).

Diagnosis (Gold Standard)

  • AKI: Defined by KDIGO criteria: increase in serum creatinine by ≥0.3 mg/dL within 48 hours, or ≥1.5 times baseline within 7 days, or urine volume <0.5 mL/kg/h for 6 hours.
  • CKD: GFR <60 mL/min/1.73m² for ≥3 months, or markers of kidney damage (e.g., albuminuria, hematuria, structural abnormalities) for ≥3 months, irrespective of GFR.
  • Glomerular Diseases (Nephrotic/Nephritic Syndromes, RPGN): Renal biopsy is the gold standard for definitive diagnosis and classification, guiding specific therapy.
  • Renovascular Hypertension: Renal angiography is the gold standard; non-invasive tests include duplex ultrasound, CT angiography, and MRA.
  • Electrolyte/Acid-Base Disorders: Serum electrolyte panel, arterial blood gas (ABG) analysis.
  • Urinary Tract Obstruction: Renal ultrasound, CT KUB.

Management (First Line)

  • AKI:
    • Address underlying cause (e.g., stop nephrotoxic drugs, rehydrate in prerenal, relieve obstruction in postrenal).
    • Optimize hemodynamics and fluid balance.
    • Manage electrolyte abnormalities (e.g., hyperkalemia).
    • Renal Replacement Therapy (RRT) if indicated (AEIOU: Acidosis, Electrolytes, Intoxications, Overload, Uremia).
  • CKD:
    • Blood pressure control: Target <130/80 mmHg; ACEi/ARB are first-line, especially with albuminuria (caution in advanced CKD/AKI).
    • Glycemic control: HbA1c target 6.5-7.5% in diabetics; SGLT2 inhibitors (e.g., empagliflozin, dapagliflozin) are now standard for kidney and cardiovascular protection in eligible patients.
    • Lifestyle modifications: Diet (low salt, protein moderation), exercise, smoking cessation.
    • Manage complications: Anemia (iron supplementation, ESAs), CKD-MBD (phosphate binders, vitamin D analogs), acidosis (sodium bicarbonate).
    • Delay progression: SGLT2i, finerenone (for CKD with T2DM and albuminuria).
  • Glomerular Diseases:
    • Symptomatic relief: Diuretics for edema, ACEi/ARB for proteinuria/BP.
    • Immunosuppression: Tailored to specific biopsy diagnosis (e.g., corticosteroids, cyclophosphamide, mycophenolate mofetil, rituximab).
  • Hypertension:
    • Lifestyle modification.
    • Pharmacotherapy: ACEi/ARB, CCB, thiazide diuretics. Alpha-blockers, beta-blockers as add-on.
    • Target BP <130/80 mmHg for most CKD patients.
  • End-Stage Kidney Disease (ESKD): Prepare for RRT (hemodialysis, peritoneal dialysis) or kidney transplantation.

Exam Red Flags

  • Rapidly Progressive Glomerulonephritis (RPGN): Acute decline in kidney function over weeks to months, often with nephritic features. Requires urgent renal biopsy and aggressive immunosuppression to preserve kidney function. Always consider ANCA-associated vasculitis, anti-GBM disease, or immune complex diseases.
  • Hyperkalemia with EKG changes (peaked T waves, wide QRS): Medical emergency requiring immediate treatment (IV calcium gluconate for cardiac stabilization, insulin/glucose, beta-agonists, loop diuretics, potassium binders).
  • AKI on CKD: Common and can accelerate CKD progression. Requires careful evaluation for reversible causes and optimization of management.
  • Malignant Hypertension (BP >180/120 mmHg with end-organ damage): Requires urgent, controlled BP reduction (not too rapid) with IV agents (e.g., labetalol, nicardipine, clevidipine).
  • Drug-Induced AKI: Always consider recent drug changes (NSAIDs, ACEi/ARBs in volume depletion/renal artery stenosis, contrast media, certain antibiotics).
  • Renal Artery Stenosis: Resistant hypertension, flash pulmonary edema, AKI with ACEi/ARB initiation, asymmetric kidney size.
  • Myeloma Kidney (Cast Nephropathy): AKI in a patient with paraproteinemia. Requires urgent plasma exchange and chemotherapy.
  • Thrombotic Microangiopathy (TMA): Presents with AKI, thrombocytopenia, microangiopathic hemolytic anemia. Consider TTP, HUS, atypical HUS, drug-induced TMA.

Sample Practice Questions

Question 1 FULLY WORKED EXAMPLE

A 34-year-old woman with biopsy-proven IgA nephropathy (MEST-C M1 E0 S1 T0) has persistent proteinuria of 1.4 g/24 h and eGFR 68 mL/min/1.73 m² despite 6 months of maximally tolerated ramipril. She has no macroscopic haematuria, BP is 122/76 mmHg, and serum albumin is 38 g/L. She is planning pregnancy within the next 12 months. Which is the most appropriate next step in management?

A) Add oral prednisolone 1 mg/kg/day for 6 months
B) Add mycophenolate mofetil and continue ramipril
C) Continue ramipril alone and reassess after delivery ✓ Correct
D) Add a second renin-angiotensin system blocker (valsartan)
Explanation:
The deciding finding is her active pregnancy plan within 12 months. KDIGO 2021 glomerular disease guidance supports a trial of immunosuppression for IgA nephropathy with proteinuria >1 g/day despite optimised RAS blockade, but both mycophenolate mofetil and high-dose corticosteroids are problematic in this setting: MMF is teratogenic and contraindicated in pregnancy planning, and steroid exposure near conception carries maternal and fetal risk. Continuing ramipril alone with reassessment after delivery is the safest option, accepting that her eGFR and proteinuria are only modestly abnormal. Prednisolone at 1 mg/kg/day is not appropriate when pregnancy is imminent and would not be first-line over optimised supportive care in this risk profile. MMF is absolutely contraindicated in a woman planning conception. Dual RAS blockade is not recommended because of increased hyperkalaemia and acute kidney injury without outcome benefit.
References: KDIGO Clinical Practice Guideline for the Management of Glomerular Diseases, IgA nephropathy section (2021)
Question 2 TRY IT — TAP AN ANSWER

A 58-year-old man with type 2 diabetes and CKD stage G4 (eGFR 22 mL/min/1.73 m²) is admitted with a non-ST-elevation myocardial infarction. He is on metformin, atorvastatin, and lisinopril. Troponin is elevated, ECG shows T-wave inversion in V4-V6, and he is haemodynamically stable. The cardiology team requests advice on contrast exposure. Which is the most appropriate recommendation regarding the planned coronary angiography?

A) Proceed with angiography using iso-osmolar contrast, with pre-procedure N-acetylcysteine
B) Proceed with angiography using low-osmolar contrast at the lowest volume, with pre- and post-hydration
C) Defer angiography until eGFR recovers above 30 mL/min/1.73 m²
D) Proceed with angiography but withhold lisinopril for 7 days beforehand
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Question 3 TRY IT — TAP AN ANSWER

A 27-year-old woman with systemic lupus erythematosus presents with new proteinuria of 3.2 g/24 h, active urinary sediment, and a rising anti-dsDNA titre. Renal biopsy shows class IV lupus nephritis with 40% cellular crescents. She has no extrarenal flares. She is 8 weeks pregnant. Which is the most appropriate initial immunosuppressive regimen?

A) Mycophenolate mofetil plus high-dose prednisolone
B) Cyclophosphamide plus high-dose prednisolone
C) Azathioprine plus high-dose prednisolone
D) Rituximab monotherapy
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Question 4 TRY IT — TAP AN ANSWER

A 72-year-old man with CKD stage G3b (eGFR 38 mL/min/1.73 m²) and type 2 diabetes is on metformin 1 g twice daily. He is admitted with sepsis from a urinary tract infection. Serum creatinine has risen from 1.6 to 2.4 mg/dL over 48 hours, lactate is 3.1 mmol/L, and he is hypotensive (BP 88/54 mmHg). Which is the most appropriate action regarding metformin?

A) Continue metformin at the same dose and monitor renal function daily
B) Reduce metformin to 500 mg twice daily
C) Withhold metformin and reassess renal function after acute illness resolves
D) Switch to gliclazide immediately
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Question 5 TRY IT — TAP AN ANSWER

A 45-year-old man with autosomal dominant polycystic kidney disease (ADPKD) has an eGFR of 52 mL/min/1.73 m², total kidney volume of 1,850 mL (height-adjusted 1,020 mL/m), and a Mayo imaging classification of 1C. He has well-controlled hypertension on amlodipine. He asks about tolvaptan. Which is the most appropriate response?

A) Tolvaptan is indicated and should be started now
B) Tolvaptan is contraindicated because of his hypertension
C) Tolvaptan should be deferred until eGFR falls below 30 mL/min/1.73 m²
D) Tolvaptan is not indicated because his eGFR is above 25 mL/min/1.73 m²
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