Renal Failures Flashcards

1
Q

What is the definition of renal failure?

A

A condition where the kidneys fail to maintain hydroelectrolytic and acid-base balance, leading to accumulation of metabolic waste (urea, creatinine, uric acid).

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2
Q

What are the two types of renal failure?

A
  • Acute Kidney Injury (AKI) – Sudden onset, potentially reversible.
    • Chronic Kidney Disease (CKD) – Progressive and irreversible kidney dysfunction.
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3
Q

What is acute kidney injury (AKI)?

A

A sudden loss of kidney function over hours to days, leading to electrolyte imbalances and waste accumulation.

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4
Q

What is oligoanuria, and how is it related to AKI?

A
  • Oliguria: Urine output < 400 mL/24h
    • Anuria: No urine output
    • Important in AKI diagnosis!
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5
Q

What are the three main types of AKI?

A
  • Prerenal (Functional) – Due to decreased kidney perfusion.
    • Intrinsic (Renal/Parenchymal) – Due to direct kidney damage.
    • Postrenal (Obstructive) – Due to urinary obstruction.
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6
Q

What are common causes of prerenal AKI?

A

Hypoperfusion due to dehydration, heart failure, shock, nephrotic syndrome, cirrhosis.

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7
Q

Can prerenal AKI be reversed?

A

Yes, if fluid balance is restored in time.
Intrinsic AKI (Renal)

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8
Q

What are common causes of intrinsic AKI?

A

Glomerulonephritis, infections, toxins, autoimmune diseases (ANCA, Anti-GBM), multiple myeloma, ischemia.

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9
Q

What investigations help diagnose intrinsic AKI?

A
  • Hemolysis markers (LDH, haptoglobin).
    • Autoimmune markers (ANCA, Anti-GBM, ANA).
    • Renal biopsy (definitive test).
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10
Q

What are the main causes of postrenal AKI?

A

Urinary stones, prostate hypertrophy, bladder tumors, retroperitoneal fibrosis.

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11
Q

What are the main biochemical markers of AKI?

A
  • Elevated creatinine (>50% increase).
    • Increased blood urea nitrogen (BUN).
    • Hyperkalemia, metabolic acidosis.
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12
Q

What electrolyte imbalances occur in AKI?

A

Hyperkalemia, hyponatremia, hyperchloremia.

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13
Q

What are the acid-base disturbances in AKI?

A

Metabolic acidosis (pH < 7.38).

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14
Q

What is the definition of chronic kidney disease (CKD)?

A

GFR < 60 mL/min/1.73m² for >3 months due to irreversible structural kidney damage.

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15
Q

What are the most common causes of CKD?

A
  • Hypertension
    • Diabetes (Diabetic Nephropathy)
    • Glomerulonephritis
    • Polycystic Kidney Disease (PKD)
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16
Q

Why is CKD a major public health issue?


A

Requires long-term management and can progress to dialysis or kidney transplant.

17
Q

What are the key biochemical markers in CKD?

A
  • Elevated serum creatinine.
    • Reduced GFR (<60 mL/min).
    • Proteinuria.
    • Hyperkalemia, metabolic acidosis.
18
Q

What is the best method for estimating GFR?

A

CKD-EPI formula (more accurate than MDRD).

19
Q

What is the role of Cystatin C in CKD diagnosis?

A

Proposed as a better GFR marker but less commonly used than creatinine.

20
Q

What is nephrotic syndrome?

A

A glomerular disease causing protein loss in urine due to increased glomerular permeability.

21
Q

What are the four key biochemical features of nephrotic syndrome?

A
  • Heavy proteinuria (>3g/24h).
    • Hypoalbuminemia (<30 g/L).
    • Hyperlipoproteinemia (high cholesterol & triglycerides).
    • Edema (due to low oncotic pressure).
22
Q

What are the key urinary findings in nephrotic syndrome?

A

Massive proteinuria (>3g/24h in adults, >50 mg/kg/day in children).

23
Q

What are common blood findings in nephrotic syndrome?

A
  • Hypoalbuminemia (<30 g/L).
    • Hyperlipidemia.
    • Hypercoagulability (high fibrinogen).
24
Q

What are the most common symptoms of nephrotic syndrome?

A
  • Generalized edema (soft, pitting).
    • Fluid effusions (ascites, pleural effusion).
    • Weight gain & oliguria.
25
Q

Why do nephrotic patients have a high risk of thrombosis?

A

Increased fibrinogen and loss of anticoagulants in urine.

26
Q

Why do nephrotic patients develop infections?

A

Loss of immunoglobulins in urine leads to immunodeficiency.

27
Q

What are the key characteristics of pure nephrotic syndrome?

A
  • Affects children (+).
    • Selective proteinuria (Albumin >85%).
    • Highly corticosteroid-sensitive (+++).
    • No hypertension, hematuria, or renal failure.
28
Q

What are the key characteristics of mixed nephrotic syndrome? (Glomerulonephritis, Systemic Disease)

A
  • Corticosteroid-resistant.
    • Non-selective proteinuria (includes albumin & other proteins).
    • Associated with hypertension & renal insufficiency.
29
Q

What systemic diseases can cause mixed nephrotic syndrome?

A

Diabetes, Lupus, Amyloidosis, Rheumatoid Purpura.

30
Q

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?

A

Diagnosis: Pure nephrotic syndrome (Minimal Change Disease).
Next step: Start corticosteroids. If resistant, consider renal biopsy.