Renal Vascular Disease Flashcards
What is the link between HTN and renal disease?
HTN causes renal disease, and renal disease often causes HTN
What are the typical and rarer causes of renovascular disease?
Typical:
- Atherosclerosis - in 80% if these they are >50yrs, arteriopaths often with co-existant, IHD, stroke, PVD)
- Fibromuscular dysplasia - around 10%. tend to be younger women
Rarer:
- Takayasu’s arteritis, anti-phospholipid syndrome, post renal transplant, thromboembolism, external compression.
What are the signs of renovascular disease?
- Increased BP resistant to treatment
- worsening renal function after ACE-i or ARB in bilateral renal artery stenosis.
- ‘Flash’ pulmonary oedema (sudden, no LV impairment)
- Abdominal +/- carotid or femoral bruits may be found, weak leg pulses
What tests would you do for suspected renovascular disease?
- USS - asymmetry of size (affected smaller) + disturbance of renal blood flow on doppler
- CT/MR angiography more sensitive
- renal angiography is ‘gold-standard’ but invasive so do after CT/MR
How do you treat renovascular disease?
- Comprehensive antihypertensive regimes
- Transluminal angioplasty +/- stent or renovascular surgery
What is HUS? What are its common features?
Haemolytic uraemic syndrome - characterised by Microangiopathic Haemolytic Anaemia (MAHA, a process of intravascular haemolysis + red cell fragmentation)
- Endothelial damage triggers thrombosis, platelet consumption and fibrin strand deposition i the renal microvasculature
- The strands cause mechanical destruction of passing red cells.
- Thrombocytopenia and AKI results
What causes HUS?
- 90% from E. Coli strain O157
- produces a toxin that attacks endothelial cells.
- outbreaks tend to occur in children, undercooked meat
What are the signs of HUS?
- Abdominal pain
- Bloody diarrhoea
- AKI
What tests do you carry out for suspected HUS?
- Check urine for blood + protein
- Blood film - fragmented blood cells
- Low platelets and Hb
How do you treat HUS?
- Seek help,
- Dialysis for AKI might be needed
- Plasma exchange used in sever persistent disease
What is TTP? What are its common features?
Thrombotic Thrombocytopenic Purpura - overlaps with HUS
- Many clinicians consider them a spectrum of disease
- MAHA present, with jaundice and low platelets
- Can also include AKI, fluctuating CNS signs and fever.
What causes TTP?
- Genetic susceptibility - deficiency of a protease that normally cleaves multimers of Von Wilebrand Factor.
- Large VWF multimers form, causing platelt aggregation and fibrin deposition in smal vessels, leading to micro thrombi.
- 40% idiopathic
- autoimmunity (SLE)
- cancer
- pregnancy
- drug associated
Is TTP serious? How do you test for it?
HAEMATOLOGICAL EMERGENCY
Test as in HUS.
How do yo treat TTP?
- Plasma exchange may be life-saving
- Non-responders try steroids
Is a rare disease, but treatment needs to be prompt so diagnosis must be made early.
If thrombocytopenia and anaemia due to unexplained causes, think TTP and refer immediately.
Urgent peripheral blood smear should show MAHA.
What is important to remember with diabetes and renal vascular disease.
Diabetes should really be thought of as a vascular disease.
Both type 1 + 2 can lead to renal vascular disease (2 more than 1)
!! SCREEN DIABETICS EVERY YEAR FOR MICROALBUMINAEMIA !!
Microalbuminaemia - 30-300mg albumin/24hr.
Gives an early warning sign of impending renal problems. Also a strong independent risk factor for cardiovascular disease.
- STANDARD DIPSTICKS DO NOT DETECT THIS, so use special ones or use albumin: creatinine ratio ( >2.5 men, >3.5 women)