Renal Flashcards
What is oedema
Defined as an increase in interstitial fluid
In a clinical setting what causes oedema?
“swelling”, pitting oedema, facial puffiness, ascites, pleural effusions, pulmonary oedema
What are some causes of increased interstitial fluid
- Obstruction of lymphatic drainage
- Obstruction of venous drainage
- Lowered oncotic pressure
- Salt and water retention
Venous obstruction (venous thrombosis)
Lymphoedema - congenital or blockage
What causes of lowered oncotic pressure and what does it cause?
Low albumin/ protein
Malnutrition
Decreased production:
Liver
Increased loss:
Gut
Kidney- nephrotic syndrome
What causes increased Salt and Water retention
Kidney – impaired GFR
Heart failure
3 year old boy referred by GP with a 3 days history facial swelling, abdominal swelling. Treated for allergy. Passing foaming urine. Well in himself. Recent cold 10 days ago. No PMHx. No FHx.
Useful findings
Differential diagnosis
Initial investigation
Initial management
3 Key features of Nephrotic syndrome
Heavy proteinuria
Hypoalbunaemia
Oedema
What do we have in nephrotic syndrome
Podocytes
What does quantitative heavy proteinuria look like?
First morning urine protein:creatinine
Normal < 20 mg/mmol
No definite level that is nephrotic
BUT > 600 mg/mmol likely to produce hypoalbuminaemia BUT occurs at lower levels
Semin- quantitative proteinuria
Negative 0 mg/dL
trace 15-30
1+ 30-100
2+ 100-300
3+ 300-1000
4+ >1000
Hypalbuminaemia features
Normal range ~ 35 – 45 g/l
Fluid retention & oedema usually with albumin < 25 – 30 g/l but not strict cut off
Serum albumin linked to fluid retention
Other protein losses responsible for other complications eg infection, thrombosis
What are the 3 types of nephrotic syndrome?
Congenital NS (<1 year)
Steroid sensitive NS
Steroid resistant NS
Features of steroid sensitive NS
Normal BP
No macroscopic haematuria
Normal renal function
No features to suggest nephritis
Respond to steroids
Histology – “minimal change” usually
Features of steroid resistant NS
Elevated BP
Haematuria
May be impaired renal function
Features may suggest nephritis
Failure to respond to steroids
Histology – various, underlying glomerulopathy, basement membrane abnormality
S + S of Steroid sensitive NS
Peak age of onset 2 – 5 yrs
M > F
Higher incidence in those from Asian sub-continent
? Immunological aetiology
Recurrent relapses
~ 5% continue into adult life
Normal renal function if steroid responsive
Treatment for SSNS
Standard course of prednisolone for first episode:
60mg/m2 for 4 weeks
40mg/m2 on alternate days for 4 weeks
Other considerations:
Na & water moderation
Diuretics
Pen V
Measles & varicella immunity & pneumococcal immunisation
Features of acute glomerulonephritis
Haematuria – often macroscopic
Proteinuria – varying degree
Impaired GFR – rising creatinine, variable degree
Salt and water retention – hypertension, oedema