GU Flashcards
Define Acute Kidney Injury?
An abrupt and sustained rise in serum urea and creatinine levels due to a rapid decline in eGFR. This leads to failure to maintain fluid, electrolyte and acid base balance
What is the criteria for AKI?
Rise in creatinine level > 26umol/l in 48hours
Rise in creatinine level > 1.5x the baseline
Urine output <0.5ml/Kg/hr for >6 consecutive hours
Give some causes of AKI?
Pre-renal = NSAIDs/ACEis (= hypoperfusion), dehydration, haemorrhage, shock, cardiac failure and cirrhosis Intra-renal = acute tubular necrosis due to toxins, thrombosis/embolism, glomerular damage Post-renal = urinary tract obstruction e.g. malignancy, stones or compression
S&S of AKI
Palpable kidneys/bladder, oliguria, oedema, hypertension, dehydration, fatigue, dysponea, weakness, nausea/vominting, confustion, seizures etc.
S&S depend greatly on cause!
Describe the basic treatment for the 3 types of AKI?
Pre-renal = correct volume depletion with fluids and give antibiotics if septic Intra-renal = refer to nephrology Post-renal = catheterise and consider CT-KUB. Stent if obstruction
How do you treat hyperkalaemia?
Insulin and dextrose
What are the three types of Renal Replacement Therapy?
Heamofiltration - most commonly used (exchange via convection)
Haemodialysis - exchange via diffusion
Peritoneal dialysis - used commonly in CKD (uses the peritoneum as an exchange surface adn can be done from home)
Complications of Renal Replacement Therapy?
Increased risk of cardiovascular disease, infection, malignancy adn amyloidosis
Define chronic kidney disease?
A eGFR <60ml/min/1.73m2 for >3months with or without evidence of kidney damage
Causes of CKD?
T2DM, hypertension, PCKD, amyloidosis, priamry glomerulonephritis, SLE and vasculitis
S&S of CKD ?
Weight loss, anorexia, oliguria, haematuria, nausea/vomiting, insomnia, itching, oedema, anaemia, fatigue, amenorrhoea and erectile dysfunction.
Symptoms occur late in disease
Treatment of CKD?
Reduce BP to <130/80 - ACEis, diuretics and CCBs
Reduce PTH if raised to protect bones - give phosphate binders and calcium supplements
Renal replacement therapy and kidney transplant.
How do you differentiate CKD from AKI?
Normochromic anaemia, small kidneys and osteodystrophy indicate CKD
Complications of CKD?
Anaemia (due to low EPO), bone disease/pain, autonomic dyfunction (e.g. postural hypotension and disturbed GI motility), cardiovascular disease and skin disease.
Decreased cerebral function and seizures in severe disease
ADPKD vs ARPKD
ADPKD = Autosomal dominant mutation in the PKD1/PKD2 genes. It leads to cyst formation and kidney function decline throught life. ARPKD = Autosomal recessive mutation in teh PKHD1 gene. It leads to cyst formation and kidney function decline in infancy.
S&S of ADPKD?
Bilateral kidney enlargement with cysts, hypertension, uric acid renal stone formation, haematuria, nocturia, abdominal pain and reduced kidney function
Diagnostic criteria for ADPKD?
Diagnose if: 15-39 = 3 or more cysts (uni/bilateral) 40-59 = 2 or more cysts on each kidney 60+ = 4 or more cysts on each kidney Diagnosis can not be excluded in under 30s
S&S of ARPKD?
Enlarged polyscystic kindeys, renal cysts/hepatic fibrosis in infancy and reduced renal function
Treatment for PKDs?
No direct treatment, remove cysts/kidneys, ACEis for blood pressure control and analgesics.
SCREEN CLOSE RELATIVES
Causes of Nephritic syndrome?
IgA nephropathy due to streptococcal infection (often of the throat), SLE, ANCA vasculitits, Hep B/C infection, systemic sclerosis and malaria
S&S of nephritic syndrome?
Moderate-large eGFR decrease, haematuria, <2g/24hrs proteinuria, hypertension, oliguria, nausea and anorexia
Causes of Nephrotic syndrome?
Podocyte abnormalities.
Primary = Minimal Change Disease, Membranous Nephropathy, Focal Segmental Glomerulosclerosis
Secondary = DM, amyloid build-up, infections, RA and SLE
S&S of nephrotic syndrome?
Normal - mild decrease in eGFR (does NOT develop into AKI), hypoalbuminaemia, pitting oedema and proteinuria > 3g/24hrs
What is minimal change disease?
Seen commonly in children, kidneys appear normal under light microscope but under electron microscope fusion of foot processes can be seen
What is membranous nephropathy?
IgG deposits in teh basement membrane lead to damage - occurs due to autoimmune disease, infection and drugs
What is focal segmental glomerulosclerosis?
segmental scarring of the glomeruli
What are the main complications of nephrotic syndrome?
Increased susceptibility to infection (Igs lost in urine), increased risk of thromboembolism and hyperlipidaemia (liver goes into overdrive due to low albumin)