Kidney diseas Flashcards
Nephrotic syndrome
‘Leaky kidneys’ which allows filtration of large molecules
Triad of signs:
- Proteinuria
- Oedema
- Low blood albumin
Low blood albumin reduces osmotic pressure and causes salt and water to leak into tissues= oedema.
Low osmotic pressure= activation of RAAS= more fluid retention
Increased clotting tendency due to lack of antithrombin III
Hyperlipidaemia- due to increased hepatic protein synthesis
Clinical features of nephrotic syndrome
Oedema
Proteinuria- more than 3g/day
Low serum albumin
High cholesterol
Nephritic syndrome
Inflamed kidneys
Characterised by:
- Microscopic Haematuria
- Proteinuria- with okay levels of serum albumin
- Hypertension due to fluid retention
- Reduced urine output
Acute kidney injury
Rapid decline in excretory kidney function
Causes:
- Acute tubular necrosis
- Reactions of contrast
- Certain drugs
- Rhabdomyolysis- break down of damaged skeletal muscle
- Interstitial nephritis
- Obstruction
AKI stage I
Serum creatinine criteria:
- Increase of 26micromol/L within 48 hours
- 1.5-1.9x baseline
Urine volume criteria:
- <0.5ml/kg/h for 6-12 hours
AKI stage II
Serum creatinine criteria:
- 2.0-2.9x baseline
Urine volume criteria:
- <0.5ml/kg/h for 12 hours
AKI stage III
Serum creatinine criteria:
- Increase above 354micromol/L within 48 hours
- > 3x baseline
- Patients <18, decrease of eGRF<35ml/min per 1.73m3
Urine volume criteria:
- <0.3ml/kg/h for 24 hours
- Anuria for 12 hours
AKIN and RIFLE limitations for diagnosing AKI
Assumes we know Creatinine baseline
Assumes urinary output is measured
Assumes creatinine kinetics are the same across different stages of CKD
Indications for renal replacement therapy
Uncontrollable:
- Fluid overload
- Metabolic acidosis
- Hyperkalaemia
Uremic pericarditis/ encephalopathy
Poisoning
Chronic kidney disease signs
Nocturia+ Poluria
Oedema
Acidaemia
Anaemia
Hypocalcaemia/ hyperphosphatemia
Multi-system disease that may involve kidney
Small vessel vasculitis
HIV
Sarcoidosis
Myeloma
Systemic lupus erythematosus
Autosomal dominant polycystic disease
Disease inherited in autosomal dominant fashion.
Abnormal tubular structure and growth of multiple cysts.
Diagnosis of CKD
Proteinuria
Reduced GFR
- 3 eGFR<60
- Over a period not less than 60 days.
- Progressive decline