Renal Failures Flashcards
What is the definition of renal failure?
A condition where the kidneys fail to maintain hydroelectrolytic and acid-base balance, leading to accumulation of metabolic waste (urea, creatinine, uric acid).
What are the two types of renal failure?
- Acute Kidney Injury (AKI) – Sudden onset, potentially reversible.
- Chronic Kidney Disease (CKD) – Progressive and irreversible kidney dysfunction.
What is acute kidney injury (AKI)?
A sudden loss of kidney function over hours to days, leading to electrolyte imbalances and waste accumulation.
What is oligoanuria, and how is it related to AKI?
- Oliguria: Urine output < 400 mL/24h
- Anuria: No urine output
- Important in AKI diagnosis!
What are the three main types of AKI?
- Prerenal (Functional) – Due to decreased kidney perfusion.
- Intrinsic (Renal/Parenchymal) – Due to direct kidney damage.
- Postrenal (Obstructive) – Due to urinary obstruction.
What are common causes of prerenal AKI?
Hypoperfusion due to dehydration, heart failure, shock, nephrotic syndrome, cirrhosis.
Can prerenal AKI be reversed?
Yes, if fluid balance is restored in time.
Intrinsic AKI (Renal)
What are common causes of intrinsic AKI?
Glomerulonephritis, infections, toxins, autoimmune diseases (ANCA, Anti-GBM), multiple myeloma, ischemia.
What investigations help diagnose intrinsic AKI?
- Hemolysis markers (LDH, haptoglobin).
- Autoimmune markers (ANCA, Anti-GBM, ANA).
- Renal biopsy (definitive test).
What are the main causes of postrenal AKI?
Urinary stones, prostate hypertrophy, bladder tumors, retroperitoneal fibrosis.
What are the main biochemical markers of AKI?
- Elevated creatinine (>50% increase).
- Increased blood urea nitrogen (BUN).
- Hyperkalemia, metabolic acidosis.
What electrolyte imbalances occur in AKI?
Hyperkalemia, hyponatremia, hyperchloremia.
What are the acid-base disturbances in AKI?
Metabolic acidosis (pH < 7.38).
What is the definition of chronic kidney disease (CKD)?
GFR < 60 mL/min/1.73m² for >3 months due to irreversible structural kidney damage.
What are the most common causes of CKD?
- Hypertension
- Diabetes (Diabetic Nephropathy)
- Glomerulonephritis
- Polycystic Kidney Disease (PKD)
Why is CKD a major public health issue?
Requires long-term management and can progress to dialysis or kidney transplant.
What are the key biochemical markers in CKD?
- Elevated serum creatinine.
- Reduced GFR (<60 mL/min).
- Proteinuria.
- Hyperkalemia, metabolic acidosis.
What is the best method for estimating GFR?
CKD-EPI formula (more accurate than MDRD).
What is the role of Cystatin C in CKD diagnosis?
Proposed as a better GFR marker but less commonly used than creatinine.
What is nephrotic syndrome?
A glomerular disease causing protein loss in urine due to increased glomerular permeability.
What are the four key biochemical features of nephrotic syndrome?
- Heavy proteinuria (>3g/24h).
- Hypoalbuminemia (<30 g/L).
- Hyperlipoproteinemia (high cholesterol & triglycerides).
- Edema (due to low oncotic pressure).
What are the key urinary findings in nephrotic syndrome?
Massive proteinuria (>3g/24h in adults, >50 mg/kg/day in children).
What are common blood findings in nephrotic syndrome?
- Hypoalbuminemia (<30 g/L).
- Hyperlipidemia.
- Hypercoagulability (high fibrinogen).
What are the most common symptoms of nephrotic syndrome?
- Generalized edema (soft, pitting).
- Fluid effusions (ascites, pleural effusion).
- Weight gain & oliguria.
Why do nephrotic patients have a high risk of thrombosis?
Increased fibrinogen and loss of anticoagulants in urine.
Why do nephrotic patients develop infections?
Loss of immunoglobulins in urine leads to immunodeficiency.
What are the key characteristics of pure nephrotic syndrome?
- Affects children (+).
- Selective proteinuria (Albumin >85%).
- Highly corticosteroid-sensitive (+++).
- No hypertension, hematuria, or renal failure.
What are the key characteristics of mixed nephrotic syndrome? (Glomerulonephritis, Systemic Disease)
- Corticosteroid-resistant.
- Non-selective proteinuria (includes albumin & other proteins).
- Associated with hypertension & renal insufficiency.
What systemic diseases can cause mixed nephrotic syndrome?
Diabetes, Lupus, Amyloidosis, Rheumatoid Purpura.
A 45-year-old male presents with severe edema, proteinuria (6 g/24h), and hypoalbuminemia (20 g/L). He has no hematuria or hypertension.
* What is the most likely diagnosis?
* What is the next step?
Diagnosis: Pure nephrotic syndrome (Minimal Change Disease). Next step: Start corticosteroids. If resistant, consider renal biopsy.