Urology/nephrology Flashcards
(122 cards)
What are the 2 types of peritoneal dialysis?
CAPD=Continuous ambulatory peritoneal dialysis
APD= Automated peritoneal dialysis
Types of bladder outlet obstruction
Posterior urethral valve, prostatic hypertrophy, fucntional eg. nruogenic bladder- spina bifida, transverse myseltiis, trauma etc. Prune belly syndrome
Posterior urethral valve
Commonest congenital cause of bladder obstruction in male infants. Presents with antenatal hydropnephrosis, UTI, poor urinary stream, renal dysfunction. Management- valve resection, antibiotic prophylaxis, CKD care.
PKD1 and 2 gene mutaitons
Genes code for polycystin 1 and 2. Polycystins are located in renal tubular epithelia. Overexpressed in cyst cell.
How does VUR present?
Antenatal hydro-uretero-nephrosis. UTI and pyelonephritis. VUR in 30-40%. UTI + VUR= 30% renal scarring.
Pathology of bladder cancer
- 90% is transitional cell carcinoma
- 5% squamous cell carcinoma
- 2% adenocarcinoma
- other secondaries
What can you use to diagnose prostate cancer?
- Digital rectal examination
- Prostate specific antigen
- Transrectal ultrasound guided needle biopsy
What causes membranous glomerulonephritis?
Immune complex deposition, which results in complement activation against glomerular basement membrane proteins. Prognosis follows rule of thirds.
What patients are not suitable for peritoneal dialysis?
Grossly obese, intra-abdominal adhesions, frail, home not suitable.
What is Henoch-Schonlein purpura?
A systemic vasculitis- leads to deposition of IgA in skin and kidneys. A cause of nephritic syndrome.
What problems are not helped by dialysis?
Anaemia, renal bone disease, neuropathy, endocrine disturbances.
Why do you get oedema in nephrotic syndrome?
Hypoalbuminaemia results in decreased intravascular oncotic pressure. As a result, fluid moves out of the intravascular compartment and into the surrounding tissues causing oedema.
Adult polycystic kidney disease
Commonest inherited kidney disorder- autosomal dominant. In 5-10% of patients with end stage renal failure. PKD1 gene mutation 85%. PKD2 mutation 15%.
What is a complicated UTI?
Upper urinary tract infection +/- systemic signs and symptoms. Catheter-associated UTI.
How do you slow the progression of chronic kidney disease?
Aggressive BP control, good diabetic control, diet, smoking cessation, lowering cholesterol, treat acidosis.
What is Glomerulonephritis?
A renal disease characterised by inflammation and damage to the glomeruli. This allows protein (+/- blood) to leak out into the urine.
What is the treatment of metastatic bladder cancer?
Chemo: M-VAC: Methotrexate Vinblastine Doxorubicin Cisplatin
How do you diagnose UTI?
Multistix (leucoyctes and nitrites- positive for L+F= UTI in 90%) , microscopy/flow cytometry (negative for pus cells and bacteria= no UTI), urine culture.
What is involved in being ‘clinically uraemic’?
Anorexia, vomiting, itch, restless less, weight loss, metallic taste and more. It is an indication in CKD patients that we need to start dialysis.
What is acute bacterial prostatitis?
An acute infection of the prostate gland that causes pelvic pain and urinary tract symptoms, such as dysuria, urinary frequency, and urinary retention, and may lead to systemic symptoms, such as fevers, chills, nausea, emesis, and malaise.
What is TURP?
Transurethral resection of the prostate.
Minimal change disease
Commonest form of GN in children. Podocytes fuse together- leads to leakage of protein. Acute presentation, may follow URTI. Idiopathic but may be secondary to malignancy.
When might you have multiple organisms causing UTI?
-Long term catheters
-Recurrent infection
-Structural/ neurological abnormalities
>95% caused by single organism.
What are the paraneoplastic syndromes associated with renal cancer?
Polycythaemia (increased Epo), hypercalcaemia, hypertension (renin secretion), deranged LTFs.