Gastroenterology Flashcards
(32 cards)
Transplanted kidney - reasons
UK - DM, glomerulonephritis, PKD
Kidney transplant - barriers
Donor matching
Malignancy
Ongoing deep seated infection or vasculitis
Obesity
Renal transplant - medication complications
Steroids - thin skin, easy bruising, cushingoid
Ciclosporin - hirsuitism, gingival hyperplasia
Tacrolimus - tremor
Glucose intolerance
HTN
Increased infection, haematological and skin malignancy
Chronic liver disease - causes
UK commonest - ALD, NAFLD
Globally - viral hepatitis
Others:
- AI - AIH, PBC, PSC
- Haemochromatosis, alpha-1 antirypsin
- Drugs
Cirrhosis - ix
Hx - drugs, ETOH, travel + family
Bloods -
Synthetic - coag, albumin, glucose
BBV, ferritin, caeruloplasmin
ANA, AMA, smooth muscle, anti-LKM1
AFP
USS + doppler + ascitic tap
Fibroscan / CT
+/- biopsy
Ascites tests
SAAG - if high (>1.1 = portal hypertension)
- If low - malignancy, cancer, pancreatitis
MC+S
Amylase / lipase
Cytology
Causes high albumin ascites
Cirrhosis
CCF
Budd-Chiari
Nephrotic
Meig’s
Low albumin ascites causes
TB
Malignancy
Pancreatitis
Ascites causes
Portal hypertension
Vascular - budd-chiari, CCF, constrictive pericarditis
Low albumin, protein losing enteropathy, malnutrition
Peritoneal disease - Meig’s, TB, malignancy
Other - Pancreatic leak, advanced hypothyroidism
PBC antibody and complications, and treatment
AMA +ve
Cirrhosis + associated complications
HCC
Ursodeoxycholic acid
Cholestyramine - pruritus
Transplant
Hepatosplenomegaly
Hepatomegaly
Splenomegaly - causes
Mild
Myelofroliferative, portal HTN, haemolytic anaemia, infections (EBV, endocarditis, hepatitis)
Mod
Myelo / lymphoproliferative. Gauchers and amyloidosis
Massive
Myeloproliferative - CML and myelofibrosis
Tropical infections - malaria, visceral leishmaniasis)
Splenomegaly ix
Blood film. LDH.
Autoimmune screen
Thin and thick films. Blood cultures.
Osmotic fragility tests
HIV screen.
USS abdomen
? CT CAP - if ? malignant
+/- bone marrow trephine
Splenectomy indications
Rupture
ITP
Hereditary spherocytosis
Splenomegaly mx
Treat cause
Vaccination - encapsulated organisms (pneumococcus, meningococcus, haemophilus influenzae)
Lifelong penicillin
Transplanted liver indications
Acute - paracetamol overdose, Hep A / B
Cirrhosis causes
HCC
Liver signs which do not resolve post transplant
Duptyrens contracture
Splenomegaly
Gynaecomastia
Polycystic kidney disease - extra renal issues
HTN
Renal failure
Proteinurea or haematuria
Liver or pancreatic cysts
Cerebral aneurysms
PKD genetics
AD
80% Type 1 - chromosome 16
Type 2 - chromosome 4 - later onset, less severe, slower progression
Infantile PKD - autosomal recessive, less common
ADPKD management
BP control - ACEi
Lipid control
High fluid, low salt diet
Tolvaptan - vasopressin receptor antagonist
RRT / transplant
ADPKD nephrectomy indications
Make room for transplant kidney
RCC
Chronic infection + pain
Significant haematuria
Why no peritoneal dialysis in ADPKD?
Bulk + volume of fluid
Increases cyst infection rate
Ascites - causes
I