Medical Abdomen Flashcards

(58 cards)

1
Q

Causes of splenomegaly

A
Infections 
Haemolysis 
Portal hypertension
Malignancy
Felty's syndrome
Infective endocarditis
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2
Q

Signs of decompensated liver disease

A
 Jaundice
 Encephalopathy: asterixis, confusion
 Foetor hepaticus: ammonia and ketones 
 Hypoalbuminaemia: oedema and ascites 
 Coagulopathy: bruising
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3
Q

Causes of CLD

A

Common
 EtOH
 Viral
 NASH

Rare
 Genetic: HH
 AI: AH
 Drugs: methotrexate

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4
Q

Drug for pruritus

A

Cholestyramine

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5
Q

Mx of Hepatitis C

A

interferon-α + ribavarin

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6
Q

Mx of encephalopathy

A

Nurse in well lit, calm environment
Correct any precipitants
Avoid sedatives
Give Lactulose + rifaximin

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7
Q

How to treat hepatorenal syndrome?

A

IV albumin + terlipressin

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8
Q

Mx ascites?

A

Conservative: fluid and salt restrict, daily weight
Medical: Spironolactone/ Furosemide
Surgical: Ascitic Tap, TIPS

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9
Q

Complications of chronic liver disease

A
  1. Liver failure/decompensation
  2. SBP
  3. Portal HTN: SAVE
  4. HCC
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10
Q

How is Cirrhosis graded?

A

Child Pugh Score

Graded A-C using severity of 5 factors (ABCDE)

 Albumin
 Bilirubin
 Clotting
 Distension: ascites 
 Encephalopathy
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11
Q

Precipitants of Encephalopathy

A

DIGS

Diuretics
Infection
GI bleed
Sepsis/ stroke

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12
Q

How would you manage decompensated liver disease?

A
General Mx
 HDU or ITU
 Rx any precipitant
 Good nutrition: e.g. via NGT with high carbs
 Thiamine supplements
 Prophylactic PPIs vs. stress ulcers

Monitoring
 Fluids: urinary and central venous catheters
 Bloods: daily FBC, U+E, LFT, INR
 Glucose: 1-4hrly + 10% dextrose IV 1L/12h

Mx Complications
 Ascites: daily wt, fluid and Na restrict, diuretics, tap
 Coagulopathy: Vit K, FFP, platelets
 Encephalopathy: avoid sedatives, lactulose, rifaximin
 Sepsis / SBP: tazocin or cefotaxime
 Hypoglycaemia: dextrose
 Hepatorenal syndrome: IV albumin + terlipressin

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13
Q

Pathophysiology of encephalopathy

A

 ↓ hepatic metabolic function
 Diversion of toxins from liver directly into systemic
system.
 Ammonia accumulates and passes to brain where
astrocytes clear it causing glutamate → glutamine
 ↑ glutamine → osmotic imbalance → cerebral oedema.

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14
Q

Presentation of encephalopathy

A
 Asterixis, Ataxia
 Confusion
 Constructional apraxia 
 Dysarthria
 Seizures
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15
Q

What is Hepatorenal syndrome?

A

Cirrhosis → splanchnic arterial vasodilatation → effective circulatory volume → RAS activation → renal arterial vasoconstriction.

Persistent underfilling of renal circulation → failure

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16
Q

What makes up the portal triad?

A

Hepatic artery
Portal vein
Bile duct

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17
Q

Mx of SBP

A

Tazocin or cefotaxime until sensitivities known

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18
Q

Causes of ascites

A
 Cirrhosis
 CCF
 Carcinomatosis
 Budd Chiari
 TB
 Pancreatitis
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19
Q

SAAG interpretation

A

Serum Ascites Albumin Gradient
SAAG = Se albumin – Ascites Albumin

SAAG ≥1.1g/dL = Portal HTN (97% accuracy)
 Cirrhosis in 80%

SAAG <1.1g/dL
 Neoplasia: e.g. peritoneal mets or ovarian Ca
 Inflammation: pancreatitis
 Nephrotic syndrome
 Infection: TB peritonitis
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20
Q

Causes of portal HT

A
Pre-hepatic:
 Portal vein thrombosis 
 PV, ET
 PNH
 Nephrotic syndrome

Hepatic:
 Cirrhosis

Post-hepatic
 Cardiac: RHF, TR, constrictive pericarditis
 Budd-Chiari (hepatic vein thrombosis)

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21
Q

Symptoms of SBP

A

Fever, abdo pain and ascites

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22
Q

Management of refractory ascites

A

TIPSS

Transplant

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23
Q

Causes of Jaundice

A

Pre-hepatic (haemolysis - unconjugated)

  • AIHA
  • HS
  • SCD

Hepatic (conjugated/ unconjugated)

  • CLD
  • Hepatitis
  • Drugs

Post Hepatic (conjugated)

  • Gallstones
  • Ca Head Panc
  • LN enlargement
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24
Q

Mercedes Benz scar ddx

A

 Liver transplant
 Segmental resection
 Whipples’: pancreaticoduodenectomy

25
Causes of Hepatomegaly
``` Malignancy Cirrhosis (ALD, NASH, PBC) Congestion Infections (Viral, Toxo, Abscess) Infiltration (amyloid, sarcoid) Vasc (Budd-chiari, Sickle Cell) ```
26
Imaging you would consider for hepatomegaly
Abdo US PV + Hepatic duplex CT MRI (enhanced with gadolinium)
27
How do you treat HH?
Venesection + desferrioxamine
28
How do you treat Wilson's?
Penicillamine
29
How can you tell you are palpating the spleen?
```  Can’t get above it  Moves inferiorly toward RIF on respiration  Notch  Dull PN  Not ballotable ```
30
Function of the spleen
```  Phagocytosis of old RBCs, WBCs  Phagocytosis of opsonised bugs: esp. encapsulates  Antibody production  Sequestration of formed blood elements  Platelets, lymphocytes and monocytes  Haematopoiesis ```
31
Causes of hyposplenism
 Splenectomy  Coeliac disease  IBD  SCD
32
Indications of a splenectomy
```  Trauma - uncontrollable splenic bleeding, hilar vascular injuries, devascularised spleen  Rupture: e.g. secondary to EBV  AIHA  ITP  HS  Hypersplenism ```
33
Complications of splenectomy
 Redistributive thrombocytosis → early VTE  Temporary post-op aspirin prophylaxis  Gastric dilatation: transient ileus  May disturb gastro-omental vessel ligatures  Prophylactic NGT post-op  Left lower lobe atelectasis  Pancreatitis: tail shares blood supply ̄c spleen  ↑ susceptibility to infections  Encapsulates: haemophilus, pneumo, meningo
34
Causes of enlarged kidneys
``` Bilateral  ADPKD  Diabetes  HIV  Bilateral RCC (5%)  Bilateral cysts: e.g. in VHL  Amyloidosis ``` ``` Unilateral  Simple renal cyst  RCC  Compensatory hypertrophy  + contralateral nephrectomy: ADPKD ```
35
Mx of ADPKD
General  ↑ water intake, ↓ Na, ↓ caffeine (may ↓ cyst formation) Monitor U+E and BP Genetic counselling  50% chance of transmission  10% are de novo mutations  MRA screen for berry aneurysms Medical  Rx HTN aggressively: <130/80 (ACEi best)  Rx infections Surgical: Nephrectomy  Recurrent bleeds or infections  Abdominal discomfort
36
Risk factors for RCC
```  Smoking  Obesity  HTN  Dialysis: 15% of pts. develop RCC  4% heritable: e.g. VHL syndrome ```
37
Presentation of RCC
Haematuria Loin pain Loin mass Invasion of L renal vein → varicocele
38
Mx of RCC
Medical  Reserved for pts. ̄c poor prognosis  Temsirolimus (mTOR inhibitor) Surgical  Radical nephrectomy  Consider partial if small tumour or 1 kidney  Prognosis: 45% 5ys
39
Differentials for gum hypertrophy
```  Drugs: ciclosporin, phenytoin, nifedipine  Familial  AML  Scurvy  Pregnancy ```
40
Commonest indications for a renal transplant
 Diabetic nephropathy  GN  Polycystic Kidney Disease  Hypertensive nephropathy
41
Contraindications for a renal transplant
 Active infection  Cancer  Severe co-morbidity  Failed pre-implantation x-match
42
Symptoms of renal transplant rejection
Hyperacute rejection: minutes  Path: ABO incompatibility  Presentation: thrombosis and SIRS ``` Acute Rejection: <6mo  Path: Cell-mediated response  Presentation  Fever and graft pain  ↓ urine output  ↑ Cr  Rx: Responsive to immunosuppression ``` Chronic Rejection: >6mo  Presentation: Gradual ↑ in Cr and proteinuria  Path: Interstitial fibrosis + tubular atrophy  Rx: supportive, not responsive to immunosuppression
43
Complications of dialysis
```  Cardiovascular disease  Malnutrition  Infection  Amyloidosis  β2-microglobulin accumulation  Renal cysts → RCC ```
44
Complications of AV access
```  Bleeding  Aneurysm  Thrombosis and stenosis  Infection  Steal syndrome ```
45
General complications of dialysis
```  Malnutrition  Infection  Cardiovascular disease  Amyloidosis  Renal cysts → RCC ```
46
Complications of haemodialysis
Disequilibration syndrome (leads to cerebral oedema) Fluid balance: BP↓, pulmonary oedema Electrolyte imbalance Aluminium toxicity (in dialysate) → dementia Psychological factors
47
Methods of renal replacement therapy
Haemodialysis Peritoneal dialysis Renal transplant Haemofiltration
48
Catheter used with peritoneal dialysis
Tenchkhoff catheter
49
Types of AV fistula
 Radio-cephalic @ wrist = Cimino-Brescia |  Brachio-cephalic @ the elbow
50
Complications of a tunnelled cuffed catheter
Adverse events @ insertion: e.g. pneumothorax Line or tunnel infection Blockage Retraction
51
The commonest cause of CKD
HT DM RAS GN
52
Complications of CKD
CRF HEALS  Cardiovascular disease  Renal osteodystrophy  Fluid (oedema) ```  HTN  Electrolyte disturbances: K, H  Anaemia  Leg restlessness  Sensory neuropathy ```
53
Signs of IBD
``` General  Often young female pt.  Laparotomy scars  Malnutrition or wt. loss  Cushingoid  Pallor ``` Hands  Clubbing  Leukonychia  Beau’s lines Eyes  Pale conjunctivae  Iritis, episcleritis Mouth  Aphthous ulcers  Gingival hypertrophy (cyclosporin) Legs  Erythema nodosum  Pyoderma gangrenosum
54
Acute Severe Exacerbation or IBD Criteria
True-Love and Witts Criteria Symptoms  BMs>6x/d  Large PR bleed Systemic Signs  ↑HR>90  Pyrexia >37.8 Laboratory Values  ↓ Hb <10.5g/dL  ESR >30mm/Hr
55
Drugs for UC induction
Oral 1: 5-ASAs 2: prednisolone 3: ciclosporin / infliximab Topical: Enemas / foams - 5-ASA - Pred
56
Drugs for CD induction
Oral 1: Ileocaecal: budesonide 1: Colitis: sulfasalazine 2: prednisolone (tapering) 3: methotrexate 4: infliximab / adalimumab
57
Drugs for UC maintenance
1: 5-ASA 2: azathioprine 3: infliximab / adalimumab
58
Drugs for Crohn's maintenance
1: azathioprine/mercaptopurine 2: methotrexate 3: infliximab / adalimumab