Gastroenterology and Hepatology Flashcards

1
Q

what are the causes of transudative ascites?

A
right sided heart failure
constrictive pericarditis
nephrotic syndrome
IVCO
Budd-Chiari syndrome
veno-occlusive disease
cirrhosis
liver tumour
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2
Q

what are the causes of exudative ascites?

A
peritonitis
TB
SBP
pancreatitis
bile peritonitis
ovarian carcinoma
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3
Q

what is the management of acute hepatitis A?

A

supportive
isolation
contact public health department
avoid alcohol while infected

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4
Q

define serum ascites albumin gradient

A

serum albumin - ascitic fluid albumin

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5
Q

what is the treatment of ascites?

A

salt restriction (2g/day)
spironolactone 100mg/day, increase as required
therapeutic paracentesis
give 1 unit of 4.5% albumin for every 2L drained
treat underlying disorder

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6
Q

describe the method of toxicity in paracetamol overdose

A

a small portion of paracetamol is converted into NABQI then conjugated with glutathione which is converted to mercapturate then excreted (normal)
in overdose, more NABQI is produced and glutathione is exhausted

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7
Q

define acute liver failure

A

hepatocellular jaundice
increased transaminases
increased PT

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8
Q

describe fulminant liver failure

A

acute liver failure complicated by hepatic encephalopathy

may be acute, hyper acute or subacute

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9
Q

describe the clinical features of acute liver failure

A
encephalopathy
cerebral oedema
jaundice
ascites
coagulopathy
hypotension
hepatopulmonary syndrome
renal dysfunction
metabolic and electrolyte disturbances
sepsis
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10
Q

what are the features and treatment of raised intracranial pressure?

A

increased BP
decreased HR
increased tone

avoid venous jugular compression
bed at 20-30o tilt
mannitol 1g/kg of 20% solution rapidly IV
thiopentone
maintain CPP at >60mmHg
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11
Q

what is the treatment of hypoglycaemia?

A

dextrose infusion 5-10% with boluses as required

give thiamine if malnourished/alcoholic

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12
Q

what is the treatment of haemorrhagic diathesis?

A

vitamin K 10mg IV

PPI to cover against upper GI bleeding

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13
Q

describe hepatorenal syndrome

A

uraemia, hyponatraemia, oliguria
no other obvious renal disease
urine sodium <5mmol/L

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14
Q

what is the pathology and treatment of hepatorenal syndrome?

A

sodium retention
possible imbalance of prostaglandins/thromboxane in the kidney

terlipressin

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15
Q

describe the pathology and treatment of hepatopulmonary syndrome

A

intrapulmonary arterio-venous shunting

treat hypoxia
intubation if grade III or IV coma
avoid ventilation with PEEP; increases ICP

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16
Q

what are the symptoms of IBD?

A
diarrhoea
blood/mucous in stools
anaemia
malaise
weight loss
mass +/- RIF
crampy abdominal pain
local peritonitis
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17
Q

what is the treatment of IBD?

A

sulphasalazine/mesalazine
systemic/topical corticosteroids
azathioprine/methotrexate/infliximab

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18
Q

describe ulcerative colitis

A

relapsing and remitting inflammatory disorder of the colonic mucosa
always involves the rectum
involving just the rectum (proctitis) or the whole bowel (pan colitis)
does not spread proximal to the ileocaecal valve
more common in non-smokers

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19
Q

what are the symptoms and signs of ulcerative colitis?

A
episodic/chronic diarrhoea
crampy abdominal pain
urgency
tenesmus
fever
malaise
weight loss
clubbing
aphthous oral ulcers
erythema nodosum
episcleritis/iritis
large joint arthritis
sclerosing cholangitis
pyoderma gangrenosum
amyloidosis
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20
Q

what are the symptoms of an acute severe attack of ulcerative colitis?

A

fever
tachycardia
tender distended abdomen

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21
Q

what are the complications of ulcerative colitis?

A
bleeding
toxic dilatation of colon
iron deficiency anaemia
venous thrombosis
PBC, PSC, chronic active hepatitis
colonic cancer
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22
Q

what is the treatment of ulcerative colitis?

A

steroids, sulphasalazine, mesalazine (mild)

prednisolone 40mg 7 days then reducing course with steroid enemas (moderate)

hospital admission, NBM, IVF, IV hydrocortisone 100mg 6hrly, monitor bloods, daily axr assess (severe)
after improvement prednisolone with a 5-ASA to maintain remission
or rescue therapy with cyclosporin or infliximab

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23
Q

what are the indications for and the types of surgery in ulcerative colitis?

A

perforation
massive haemorrhage
toxic dilatation
failed medical therapy

proctocolectomy + terminal ileostomy; retain ileocaecal valve and reduce fluid loss
colectomy with ileoanal pouch later

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24
Q

what drugs are considered in immunomodulation with ulcerative colitis?

A
azathioprine
methotrexate
infliximab
adalimumab
calcineurin inhibitors
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25
describe Crohn's disease and its risk factors
transmural granulomatous inflammation commonly affects terminal ileum and proximal colon NOD2/CARD15 mutation smoking NSAIDs
26
describe the histology of Crohn's disease
``` granulomas containing multinucleate giant cells transmural inflammation neutrophil infiltrates skip lesion wall thickening discrete deep ulcers cobblestone mucosa ```
27
what are the symptoms and signs of Crohn's disease?
``` diarrhoea urgency abdominal pain weight loss fever PR blood malaise ``` ``` anal/perianal/oral lesions skin tags fissure fistula anal disease adhesions strictures perforation fatty liver renal stones malnutrition ```
28
what are the complications of Crohn's disease?
``` small bowel obstruction toxic dilatation abscess formation fistula rectal haemorrhage colonic carcinoma B12 deficiency iron deficiency anaemia venous thromboembolism ```
29
what is the treatment of Crohn's disease?
reducing course prednisolone (mild) hospital admission, NBM, IVF, hydrocortisone 100mg IV 6hrly (severe) antibiotics daily bloods and axr after improvement start oral prednisolone if no improvement consider infliximab/adalimumab perianal disease - local surgery with seton insertion
30
what is the long-term treatment of Crohn's disease?
PENTASA reduces recurrent disease post-op azathioprine methotrexate TNF alpha inhibitors
31
describe the pathology of oesophageal cancer
squamous tumours - mid thoracic portion | adenocarcinomas - lower oesophagus or on a background of barrett's oesophagus
32
what are the risk factors for oesophageal cancer?
``` smoking alcohol barrett's oesophagus chronic reflux obesity Chinese/russian ethnicity achalasia tylosis ```
33
what are the symptoms of oesophageal cancer?
``` asymptomatic dyspepsia progressive dysphagia vomiting weight loss ```
34
what is the treatment of oesophageal cancer?
surgery oesophageal stenting radical radiotherapy chemotherapy
35
what are the risk factors for gastric cancer?
``` Japanese hypo/achlorydia male high salts and nitrates gastric polyps ```
36
what are the symptoms of gastric cancer?
``` dyspepsia epigastric pain anorexia early satiety iron deficiency anaemia haematemesis melaena ```
37
what are the risk factors for colorectal cancer?
``` male FHx IBD (especially ulcerative colitis) familial polyposis coli diet low in fibre, fruit and vegetables diet high in red meat and fat obesity cholecystectomy ```
38
what are the signs of a right-sided colon cancer?
iron deficiency anaemia abdominal pain abdominal mass
39
what are the signs of a left-sided colon cancer?
blood per rectum altered bowel habit abdominal mass
40
what are the signs of a rectal cancer?
tenesmus obstruction blood per rectum
41
what is the treatment of colorectal cancer?
adjuvant chemotherapy and radiotherapy serial monitoring of CEA marker to detect recurrence isolated hepatic metastases of a single liver lobe can be resected
42
what are the signs, symptoms and risk factors of pancreatic cancer?
``` abdominal pain radiating through to the back obstructive jaundice weight loss pruritus double duct sign at ERCP small bowel obstruction CA19-9 ``` increased risk in diabetes and smokers
43
what are the risk factors for hepatocellular cancer?
``` africa, asia and japan hepatitis B and C cirrhosis long-term OCP use aflatoxin ```
44
what is the treatment of hepatocellular cancer?
resection transplant chemo/ethanol injection not tumour/embolisation (palliative)
45
what are the signs, risk factors and treatment of cholangiocarcinoma?
obstructive jaundice PSC liver fluke infection choledochal cyst caroli's disease transplant resection
46
what are the symptoms and risk factors for benign hepatic adenoma?
OCP >5 years anabolic steroids asymptomatic intraperitoneal bleeding RUQ pain
47
what are the causes of changes in the bowel habit?
``` coeliac Crohn's diverticulitis IBS IBD thyroid disorders antibiotics laxatives cancers nerve damage (stroke) spinal cord injury ```
48
what are the specific investigations for suspected IBD?
``` faecal calprotectin stool O&S barium enema sigmoidoscopy serum iron, B12, folate, albumin AXR colonoscopy & biopsy CT small bowel ```
49
define significant weight loss
5% over 3-6 months
50
what are the causes of intentional weight loss?
exercise/dieting bariatric surgery anorexia nervosa/eating disorder
51
what are the causes of unintentional weight loss with normal intake?
hyperthyroidism increased exercise (marathon runner) malabsorption (pancreatic, bowel) DM
52
what are the causes of unintentional weight loss with decreased intake?
malignancy GI disease psychological endocrine
53
what features of weight loss suggest malignancy?
nocturnal symptoms progressive symptoms FHx
54
what are the consequences of sepsis?
increased BMR negative nitrogen balance increased gluconeogenesis increased production of acute phase proteins
55
what are the consequences of starvation and sepsis?
``` increased glucose demand glycogen stores rapidly used increased gluconeogenesis protein oxidation muscle loss increasingly negative nitrogen balance less oral intake ```
56
describe the mechanism of acute phase protein production in sepsis
``` increased proteolysis and increased protein synthesis -> increased free amino acid pool -> increased acute phase protein ```
57
describe nitrogen balance
the equilibrium between protein intake and losses
58
describe cachexia
``` general muscle wasting from famine reduced oral intake malabsorption increased catabolism ```
59
how do you assess a patient's nutritional status?
``` reported recent weight loss food diary behavioural patterns BMI biochemical markers MUST assessment ```
60
what are the requirements for maintaining adequate nutrition?
intact GI tract ability to absorb nutrients adequate diet
61
what are the signs and symptoms of diabetes?
``` polyuria polydipsia genital thrush unexplained weight loss (mostly T1DM) visual blurring lethargy ```
62
how does weight loss occur in diabetes?
glucose cannot get into the cells due to a lack of insulin and so the body breaks down fat and muscle to use for energy the glucose remains in the blood and the kidneys excrete it, causing frequent urination and weight loss due to dehydration and loss of calories
63
what are the symptoms of thyrotoxicosis?
``` diarrhoea weight loss increased appetite sweating heat intolerance palpitations tremor irritability oligomenorrhoea ```
64
what are the signs of thyrotoxicosis?
``` tachycardia goitre warm moist skin tremor lid lag and retraction thin hair palmar erythema ```
65
what are the signs of Grave's disease?
``` exopthalmos ophthalmoplegia oedematous swellings above lateral malleolus clubbing painful finger and toe swelling periosteal reaction in limb bones ```
66
what will investigations show in thyrotoxicosis?
``` TSH suppressed increased T3 and T4 mild normocytic anaemia mild neutropenia increased ESR, Ca, LFT thyroid autoantibodies isotope scan eye exam ```
67
describe the pathology of Grave's disease
circulating IgG autoantibodies binding to and activating G-protein-coupled TSH receptors, causing smooth thyroid enlargement and increased hormone production
68
what are the causes of thyrotoxicosis?
``` Grave's disease toxic multi nodular goitre toxic adenoma ectopic thyroid tissue iodine excess levothyroxine excess contrast media ```
69
what is the treatment of thyrotoxicosis?
beta blockers (symptomatic) titration Carbimazole 20-40mg/24hr for 4 weeks Carbimazole and thyroxine simultaneously (block & replace) radioiodine (contraindicated in pregnancy and worsens eye disease) thyroidectomy (risk of recurrent laryngeal nerve damage and hypoparathyroidism)
70
what are the side effects of Carbimazole?
agranulocytosis | must stop if suspected infection
71
what are the complications of thyrotoxicosis?
``` HF (thyrotoxic cardiomyopathy) angina AF osteoporosis ophthalmopathy gynaecomastia thyroid storm ```
72
what are the symptoms and signs of malabsorption?
``` diarrhoea weight loss steatorrhoea bloating lethargy anaemia (B12, folate, iron) bleeding disorders (low vitamin K) oedema (low protein) metabolic bone disease (low vitamin D) neuropathy ```
73
describe coeliac disease
T cell mediated protamine intolerance causes villous atrophy and malabsorption HLA DQ2
74
what are the symptoms and complications of coeliac disease?
``` diarrhoea weight loss anaemia bloating abdominal pain mouth ulcers steatorrhoea ``` GI T-cell lymphoma malignancy osteoporosis neuropathy
75
what are the symptoms and causes of chronic pancreatitis?
``` epigastric pain that radiates to the back relieved by sitting forward steatorrhoea weight loss bloating brittle diabetes ``` alcohol cystic fibrosis haemochromatosis duct obstruction
76
what is the treatment and complications of chronic pancreatitis?
``` analgesia lipase fat soluble vitamins insulin surgery ``` pseudocyst diabetes biliary obstruction pancreatic cancer
77
what are the symptoms of Crohn's disease?
``` diarrhoea urgency PR bleeding weight loss aphthous ulcers perianal abscess/fistulae/strictures clubbing skin/joint/eye involvement ```
78
what is the treatment and complications of Crohn's disease?
DMARDs immunosuppression surgery in severe cases ``` SBO toxic dilatation abscess fistulae colon cancer rectal haemorrhage PSC ```
79
what are the signs and symptoms of malignancy?
``` nausea vomiting change in bowel habit melena dysphagia odynophagia abdominal pain jaundice masses/raised lymph nodes ```
80
describe refeeding syndrome
must be considered in feeding with inadequate oral intake for >5 days surges in insulin large intracellular shifts in potassium, phosphate and magnesium resulting in low plasma levels
81
what are the consequences of refeeding syndrome?
``` cardiac instability/arrhythmias seizures delirium parasthesia myopathy haemolysis paralysis oedema respiratory and cardiac failure ```
82
what symptoms require a red flag referral for GORD?
``` dysphagia weight loss haematemesis melena persistent vomiting iron deficiency anaemia epigastric mass ```
83
what is the treatment of GORD?
PPI full-dose for 4-8 weeks (lansoprazole 30mg OD) oesophageal stricture dilatation; remain on full-dose long-term therapy (lansoprazole 30mg OD) continuous/recurring symptoms - lowest dose PPI or H2RA therapy (ranitidine)
84
what is the management of Barrett's oesophagus?
offer laparoscopic fundoplication for those who respond to PPI but do not want to continue long-term antacid and/or alginate therapy
85
what are the features of oropharyngeal dysphagia?
delay in swallow initiation postnasal regurgitation when swallowing cough when swallowing repetitive swallowing required
86
what are the causes of oropharyngeal dysphagia?
``` CVA Parkinson's MS MND ALS MG pharyngeal pouch head and neck malignancies enlarged thyroid anticholinergics opiates ```
87
what are the causes of oesophageal dysphagia?
``` foreign body (acute) tumour peptic stricture oesophageal rings and webs eosinophilic oesophagitis chemical injury radiation infectious oesophagi's (herpes, candida) achalasia dysmotility disorders scleroderma mixed CT diseases ```
88
what are the causes of oesophageal dysphagia with solid food?
``` stricture oesophagitis cancer oesophageal rings, webs eosinophilic oesophagitis ```
89
what are the causes of oesophageal dysphagia with liquids?
scleroderma absent contractility achalasia distal oesophageal spasm
90
what is the treatment of a benign stricture?
``` high dose PPI inject steroid and dilate stents self-dilatation surgery ```
91
how is eosinophilic oesophagitis diagnosed?
food impaction >15 eosinophils per HPF lack of response to high dose PPI normal pH monitoring
92
what is the treatment of eosinophilic oesophagitis?
topical steroids dilatation elimination diet (paeds)
93
what is the treatment of achalasia?
botox balloon dilatation heller myotomy
94
describe functional dysphagia
sense of food sticking or passing abnormally through the oesophagus no oesophageal, mucosal or structural abnormality no GORD or EoE no major oesophageal motor disorders
95
what is the treatment of oesophageal hypersensitivity?
high dose PPI | SSRI (fluoxetine) or TCA (amitriptyline)
96
what are the symptoms and signs of anaemia?
``` dyspnoea lethargy chest pain tinnitus headache palpitations pallor tachycardia flow murmur ESM cardiac enlargement ankle swelling (CF) ```
97
what are the causes of microcytic anaemia?
``` haematological defect IDA sideroblastic; lead poisoning globin defect thalassaemia ```
98
what are the causes of normocytic anaemia?
blood loss bone marrow failure renal failure pregnancy (increased plasma volume)
99
what are the causes of macrocytic megaloblastic anaemia?
vitamin B12 or folate deficiency anti-folate drugs (phenytoin, methotrexate) cytotoxic (hydroxycarbamide)
100
what are the causes of macrocytic non-megaloblastic anaemia?
reticulocytosis alcohol or liver disease hypothyroidism myelodysplasia
101
what are the signs of haemolytic anaemia?
``` reticulocytosis mild macrocytosis haptoglobin reduced increased bilirubin increased urobilinogen mild jaundice ```
102
what are the causes of haemosiderosis?
endocrine, liver and cardiac damage
103
what are the causes and treatment of sideroblastic anaemia?
``` congenital acquired myelodysplastic/proliferative disease chemotherapy anti-TB drugs lead ``` remove cause pyridoxine transfusion for severe anaemia
104
what is the pathophysiology of thalassemia?
unbalanced production of globin chains haemolytic while still in the bone marrow and removal by the spleen autosomal recessive inheritance
105
what are the features of beta thalassemia major?
``` severe anaemia jaundice failure to thrive extra medullary erythropoiesis frontal bossing maxillary overgrowth hepatosplenomegaly haemochromatosis >10yrs ```
106
what are the causes of iron deficiency anaemia?
``` menorrhagia GI bleeding poor diet coeliac disease Crohn's disease ```
107
what is the treatment of iron deficiency anaemia?
oral or IV iron
108
what are the causes of haematemesis?
``` varices oesophago-gastro-duodenitis PUD/DU oesophageal or gastric cancer mallory-weiss tear mucosal tear angiodysplasia HHT large arteriole rupture in stomach or bowel warfarin thrombolytics epistaxis ```
109
what are the causes of rectal bleeding?
``` diverticular disease rectal haemorrhoids camplyobacter shigella E. coli C. diff amoebic dysentery polyps UC Crohn's neoplasia gastric/upper bowel bleeding ischaemic colitis HHT angiodysplasia ```
110
what are the signs of an upper GI bleed?
``` tachycardia chronic liver disease melena PR hypotension/postural hypotension reduced urine output reduced GCS ```
111
what are the causes of upper GI bleeding?
``` PUD/DU mallory-weiss tear acute erosions/gastritis varices oesophagitis stomach/oesophageal cancer ```
112
what are the components of the Rockall score?
``` age shock (BP, HR, co-morbidities) final diagnosis evidence of recent haemorrhage active bleeding visible vessel adhered clot ```
113
what is the treatment of oesophageal varices?
``` variceal banding Sengstaken-Blakemore tube beta blockers broad spectrum antibiotics IV terlipressin repeat endoscopic banding TIPSS ```
114
what are the signs of lower GI bleeding?
``` pale and cold extremities sweating pulse volume bruises mouth and nose bleeding abdominal tenderness +/- peritonism masses signs of chronic liver disease blood, melon, palpable mass, haemorrhoids (PR) ```
115
what are the causes of lower GI bleeding?
``` diverticular bleeds angiodysplasia colorectal cancer ischaemic colitis Meckel's diverticulum infectious colitis IBD haemorrhoids radiation proctitis aorta-enteric fistula ```
116
what is the treatment of lower GI bleeding?
surgical resection colonoscopic haemostasis radiological embolisation may be upper GI
117
what is the treatment of GI bleeding?
``` resuscitate and stabilise IV fluids group and crossmatch ABG and bloods correct clotting factors oxygen if hypoxic IV PPI urgent endoscopy inform surgeons incase need for surgery/embolisation ```
118
what are the causes of folate deficiency?
``` reduced intake increased demand (pregnancy, haemolytic, malignancy) coeliac Crohn's phenytoin methotrexate trimethoprim ```
119
what are the causes of B12 deficiency?
``` decreased meat, fish and dairy intake decreased intrinsic factor pernicious anaemia post-gastrectomy ileal resection bacterial overgrow congenital metabolic errors ```
120
what are the symptoms of B12 deficiency?
``` anaemia pallor and mild jaundice glossitis parasthesia peripheral neuropathy depression dementia optic atrophy subacute combined degeneration of the cord ```
121
describe pernicious anaemia
most common cause of macrocytic anaemia autoimmune attack against gastric parietal cells that secrete intrinsic factor and acid = achlorhydria and lack of gastric intrinsic factor secretion >40yrs associated with thyroid disease, vitiligo and addison's
122
describe the diagnosis and treatment of pernicious anaemia
presence of intrinsic factor and parietal cell antibodies in serum lifelong quarterly hydroxocobalamin B12 injections
123
define delirium
an acute mental disturbance characterised by confused thinking and disrupted attention usually accompanied by disordered speech and hallucinations usually develops over 1-2 days
124
describe hyperactive delirium
heightened arousal, restless, agitated and aggressive
125
describe hypoactive delirium
withdrawn, quiet and sleepy | can be more difficult to recognise
126
what are the signs of delirium?
``` disordered thinking euphoric, fearful, depressed, or angry language impaired delusions reversal of sleep/awake cycle inattention disorientated memory deficits ```
127
what are the risk factors for delirium?
``` >65yrs dementia severe illness surgery infection impaired hearing/vision poly pharmacy (including alcohol) dislocation to an unfamiliar environment sleep deprivation immbolisation CNS damage previous CVA ```
128
what are the warning signs in delirium?
head injury + warfarin focal neurology reduced GCS high NEWS score
129
what is the treatment of delirium?
``` reduce distress encourage family to sit with patient moderately lit quiet room improve orientation to time and place verbal de-escalation hearing aids and glasses avoid physical restraints ``` ``` haloperidol lorazepam (alternative in Parkinson's or QTC prolongation) ```
130
define stroke
rapid onset, focal neurological deficit due to a vascular lesion lasting >24hrs infarction due to ischaemia (80%) or intracerebral haemorrhage (20%)
131
what are the risk factors for stroke?
``` smoking hypertension diabetes high lipids FHx AF cardiac valve disease peripheral vascular disease Hx ethnicity OCP ```
132
what are the symptoms of a stroke?
``` facial drop weakness in arms or legs dysarthria/dysphagia sudden loss/blurring of vision dizziness confusion balance and co-ordination problems sudden/severe headache loss of consciousness ```
133
describe a total anterior circulation stroke
``` hemiplegia (contralateral) homonymous hemianopia (contralateral) higher cortical dysfunction ```
134
describe an anterior cerebral artery stroke
contralateral motor/sensory loss in the legs>arms | face is spared
135
describe a middle cerebral artery stroke
contralateral motor/sensory loss in face and arms>legs contralateral homonymous hemianopia cognitive changes
136
describe a posterior cerebral artery stroke
contralateral homonymous hemianopia with macula sparing
137
describe locked-in syndrome
patient aware and cognitively intact but completely paralysed except for the eye muscles ventral pons infarction (basilar artery) central pontine myelinolysis rapid correction of hyponatraemia
138
what is the treatment of a stroke?
``` ensure patent airway NBM until swallowing assessed don't over hydrate monitoring (glucose 4-11, BP <185/110) urgent CT/MRI thrombolysis with tPA clot retrieval if large vessel occluded antiplatelets refer to stroke unit DVT prophylaxis surgery carotid endarterectomy ```
139
what is the secondary prevention of a stroke?
start statin after 48hr aspirin/clopidogrel 300mg 2weeks after then reduce dose warfarin for cardiac thromboembolism 2 weeks post-stroke
140
define transient ischaemic attack
sudden onset focal neurology lasting <24hr due to temporary occlusion of part of the cerebral circulation
141
what are the causes of a TIA?
atherothromboembolism from carotids cardioembolism (post-MI, AF, valve disease) hyper viscosity (polycythaemia, myeloma)
142
what are the signs of a TIA?
carotid bruits murmur AF HTN
143
what is the treatment of a TIA?
aspirin or clopidogrel 300mg OD 2 weeks then 75mg after BP, lipids, smoking, DM, exercise, diet control ABCD2 score (assess risk) score >4, refer within 24hrs score <4, refer within 7 days
144
what are the components of the ABCD2 score?
age >60 BP >140/90 clinical features (unilateral weakness, speech disturbance without weakness) duration of symptoms (>1hr, 10-59 minutes) diabetes
145
what are the symptoms of a sagittal sinus thrombosis?
``` headache vomiting seizures reduced vision papilloedema ```
146
what are the symptoms of a transverse sinus thrombosis?
headache +/- mastoid pain focal neuro seizures papilloedema
147
what are the symptoms of a sigmoid sinus thrombosis?
cerebellar signs | lower CN palsies
148
what are the symptoms of an inferior petrosal sinus thrombosis?
5th and 6th CN palsies
149
what are the symptoms of a cavernous sinus thrombosis?
``` spread from facial pustules or folliculitis headache chemosis eyelid oedema proptosis painful ophthalmoplegia fever ```
150
what are the symptoms of a cortical vein thrombosis?
venous infarcts with stroke-like focal symptoms | evolve over days
151
what are the causes of intracranial venous sinus thrombosis?
``` pregnancy/puerperium OCP head injury dehydration intra/extracranial malignancy thrombophilia ```
152
what are the treatment of intracranial venous sinus thrombosis?
LMWH -> warfarin (INR 2-3) | fibrinolytics (streptokinase)
153
describe the spinal cord
extends from the cranio-cervical junction at the top of C1 to the conus medullaris opposite the bottom of L1
154
describe the motor and sensory pathways of the spinal cord
the principle descending motor pathway is the corticospinal tract that crosses in the midbrain the two principal ascending sensory pathways are the dorsal columns (carry vibration and joint position sense ) and spinothalamic tracts (carries pain and temperature)
155
describe a complete transection of the cord
due to trauma or severe inflammation complete loss of all modalities distal to the transection including motor, sensory and sphincter function
156
describe a hemisection of the cord
brown-sequard syndrome due to trauma, glioma, MS loss of motor function and dorsal column sensation ipsilateral to the hemisection contralateral loss of pain and temperature
157
describe a central cord lesion
due to syringomyelia, intramedullary tumour, trauma, central necrosis syringomyelia - cervical and thoracic region leading to dissociated sensory loss (preserved dorsal column function) and LMN weakness, atrophy and fasciculations
158
what are the symptoms and causes of cord compression?
back pain lower limb; weakness, numbness, sensory changes, reflex loss ``` metastases in spine abscess haematoma disc prolapse intrinsic cord tumour ```
159
what is the treatment of cord compression?
``` treat the cause dexamethasone 8mg IV BD radiotherapy chemotherapy surgical drainage of abscess and antibiotics decompressive laminectomy ```
160
what are the symptoms of conus medullaris lesions?
mixed UMN/LMN weakness early constipation and retention back pain sacral sensory disturbance
161
what are the symptoms of caudal equina lesions?
``` saddle anaesthesia back pain radicular pain down legs bilaterally flaccid, areflexic lower limb weakness incontinence/faeces/urine retention poor anal tone ```
162
what are the symptoms of cervical spondylitis?
usually asymptomatic neck stiffness +/- crepitus stabbing/dull arm pain (brachialgia) upper limb motor and sensory disturbances according to compression levels (often C7) myelopathy with quadraparesis and sphincter dysfunction
163
what are the treatment of cervical spondylitis?
``` stiff collar analgesia transforaminal steroid injection decompression laminectomy or laminoplasty ```
164
what are the symptoms and signs of lumbar spondylitis?
``` most commonly compression by L4/5, L5/S1 discs severe pain on sneezing/coughing lumbago sciatica limited spinal flexion pain on straight-leg raise ```
165
what is the treatment of lumbar spondylitis?
``` rest analgesia mobilisation/physiotherapy transforaminal steroid injection diseconomy or laminectomy may be considered with continuing pain or muscle weakness ```
166
what are the symptoms of spinal stenosis?
``` spinal claudication aching or heavy buttock and lower limbs pain on walking parathesia/numbness pain eased by leaning forward pain on spine extension ```
167
what is the treatment of spinal stenosis?
NSAIDs epidural steroid injection canal decompression surgery
168
what are the symptoms and causes of subacute combined degeneration of the cord?
``` symmetrical dysaesthesiae loss of posterior column sensory modalities spastic para or quaraparaesis brisk knee jerks absent ankle jerks extensor plantas ``` ``` B12 deficiency (treatment is parenteral B12 replacement) seen alongside pernicious anaemia, severe malnutrition, nitrous oxide abuse ```
169
describe the pathology and causes of Lhermitte's sign
transit short-lasting sensation at the back of the neck, lower back after neck flexion electric-like, tingling, buzzing disappears on normal posture MS spondylosis vitamin B12 adulation myelopathy
170
describe the pathology and treatment of Guillian-Barre syndrome
acute inflammatory demyelinating polyneuropathy post infectious (campylobacter, EBV, zoster) symmetrical ascending weakness antibodies attack nerves can advance quickly and causes paralysis can affect respiratory muscles IV immunoglobulins
171
what is the treatment of a coma?
``` antibiotics with IV acyclovir if CNS infection suspected respiratory support haemodynamic support fluid and electrolyte balance VTE prophylaxis acid-base balance ```
172
what makes up the portal triad?
bile duct branch of the hepatic artery branch of the portal vein
173
what are the causes of transaminase derangement?
``` hepatocyte damage alcohol viral hepatitis paracetamol ischaemia ```
174
what are the causes of ALP/GGT derangement?
``` cholestasis biliary disease primary biliary cholangitis drugs fatty liver ```
175
describe acute liver disease and its causes
<2-3 months paracetamol alcohol viral hepatitis
176
describe chronic liver disease and its causes
>6 months progression to fibrosis ``` caused by fatty liver disease alcohol viral hepatitis autoimmune liver disease metabolic ```
177
what are the causes of jaundice?
prehepatic - haemolysis, thalassemia, haemoglobinpoathies, Gilbert's syndrome hepatic - viral hepatitis, drugs, cirrhosis, tumours post hepatic - gallstones, cancer of bile duct, pancreatic carcinoma, lymph node enlargement in portal vein
178
what are the complications of liver cirrhosis?
``` jaundice hepatic encephalopathy coagulopathy portal hypertension liver cancer ```
179
what are the symptoms and signs of hepatocellular carcinoma?
RUQ pain weight loss decompensated disease AFP predominately in patients with cirrhosis single lesion or diffuse growth
180
what is the treatment of hepatocellular carcinoma?
``` resection transplant (CLT/LDLT) RF/PEI TACE sorafenib supportive care ```
181
what are the signs of chronic liver disease?
``` jaundice ascites hepatomegaly cirrhosis caput medusae gynaecomastica palmar erythema spider naevi bruising leukonychia asterixis finger clubbing fetor hepaticus xanthelasma parotid enlargement xanthoma hepatic flap ```
182
what are the markers of liver inflammation?
AST ALT GGT ALP
183
what are the tests that measure synthetic liver function?
bilirubin albumin PT
184
what causes an increase in AST and ALT?
``` infection (hepatotropic viruses) alcohol autoimmune disease paracetamol statins anaesthetics haemochromatosis Wilson's disease vascular insult ```
185
what can cause AST>ALT and GGT increase?
alcohol
186
what can cause ALT>AST, GGT and ferritin increase?
fatty liver disease
187
what causes an increased GGT and ALP?
biliary obstruction (stones, slide, strictures) primary and secondary biliary cholangitis primary sclerosing cholangitis ischaemia heart failure fibrosis
188
what are the components of the GMAWS?
``` agitation hallucination orientation sweating tremor ```
189
what is the mechanism by which ascites accumulates in liver disease?
portal hypertension -> reduced albumin -> reduced oncotic pressure -> transudation of fluid reduced aldosterone metabolism ->RAAS activation -> reduced renal blood flow -> salt and water retention
190
what is the management of a patient with chronic liver disease?
alcohol withdrawal IV thiamine (pabrinex) twin vials 3x daily oral/IV benzodiazepines determine mortality using GAHS and Maddrey's discriminant function (corticosteroids if >32)
191
describe the mechanism and the components of the Lille score
prediction of mortality in patients with severe alcoholic hepatitis who have been treated with corticosteroids ``` age renal insufficiency albumin PT bilirubin evolution of bilirubin at day 7 ```
192
what is the treatment of alcoholic hepatitis?
``` if infection, treat with antibiotics prednisolone 40mg daily x7 days at day 7 assess using Lille score <0.45 continue for 28 days (responder) >0.56 stop (non-responder) alcohol abstinence nutrition ```
193
what is the management of uncomplicated ascites?
dietary restriction of sodium (80-120mmol/day or 4.6-6.9g) anti-mineralocorticoid drugs furosemide (no response to anti-mineralocorticoids or hyperkalaemia develops) torasemide (weak response to furosemide)
194
what are the features of diverticulitis
presents in older ages | pain in the left iliac fossa
195
describe the liver lobules
blood flows from the portal triad to the central vein in the branches of the portal vein and hepatic artery bile flows from the centre to the portal triad in the bile duct surrounded by hepatocytes
196
what are the functions of the liver
``` digestion; bile production coagulation metabolism immune function storage of vitamins, minerals and glucose ```
197
what would the LFTs look like in hepatocyte damage due to alcohol?
AST/ALT GGT (+MCV, IgA, ferritin) approx 2-300
198
what are the causes of transaminases >1000?
viral hepatitis drugs; paracetamol ischaemia
199
what are the causes of deranged ALP/GGT?
``` cholestasis biliary disease; deranged LFTs and pain 90% gallstones primary biliary cholangitis drugs fatty liver ```
200
describe fibroscan
assess liver stiffness non-invasive quick safe
201
what are the complications of liver cirrhosis?
liver dysfunction; jaundice, hepatic encephalopathy, coagulopathy portal hypertension liver cancer
202
describe the indications and components of the child Pugh score
``` shows the estimated 1 and 2 year survival of cirrhosis encephalopathy ascites bilirubin albumin PT; seconds prolonged, INR ```
203
what are the components of portal hypertension?
``` increased hepatic vascular resistance increased portal blood inflow formation of portosystemic collaterals 20-60% mortality pressure = resistance (liver) x blood flow ```
204
what are the surveillance techniques used to detect hepatocellular carcinoma?
6 monthly USS AFP; rises with exacerbation of underlying disease
205
what is the function of AST & ALT?
elevated in response to liver parenchymal injury
206
what is the function of ALP & GGT?
found in cells lining bile ducts and elevated in cholestatic diseases
207
what questions should be asked in a jaundice history?
symptoms; pain, urine colour, stool colour, itch risk factors; alcohol, viral hepatitis, drugs, FHx past medical history; NAFLD, pancreatitis, gallstones, malignancy
208
what investigations should be done to diagnose liver disease?
``` U&E blood glucose coagulation screen liver screening panel CXR USS diagnostic peritoneal tap OGD ```
209
what tests are done in a liver screening pan?
``` hepatitis screen; acute viruses, viruses leading to chronic disease autoimmune coeliac IgG ferritin & % saturation copper & caeruloplasmin A1-anti trypsin levels ```
210
what are the components of the GAHS?
``` age WCC urea PT ratio or INR bilirubin ```
211
define maddrey's discriminant function
a disease specific prognostic score of alcoholic hepatitis 4.6 x bilirubin + (patients PT - control PT) >32; 30-50% mortality in 1 month
212
what is the lifestyle management of liver disease?
alcohol abstinence ascites management nutrition
213
what are the infective causes of liver failure?
viral hepatitis (B, C, CMV) yellow fever leptospirosis
214
what are the drug related causes of liver failure?
paracetamol overdose halothane isonazid
215
what are the vascular causes of liver failure?
Budd Chiari syndrome | veno-occlusive disease
216
what are the other causes of liver failure?
``` AFLD NAFLD PBC haemochromatosis autoimmune hepatitis alpha-1 antitrypsin deficiency Wilsons disease HELLP fatty liver of pregnancy malignancy ```
217
what are the signs of liver failure?
``` jauncide asymptomatic hepatic encephalopathy fetor hepaticus asterixis/flap constructional apraxia ascites ```
218
what are the signs of chronic liver disease?
``` leukonychia malnourishment IVDU finger clubbing palmar erythema hyperdynamic circulation Dupuytren’s spider naevi xanthelasma gynaecomastica atrophic testes reduced body hair parotid swelling hepatomegaly shrunken liver lethargy bruising thin skin ```
219
what are the signs of portal hypertension?
splenomegaly caput medusa oesophageal varices ascites
220
what is the treatment of portal hypertension?
band varices prophylactic beta blockers TIPPS procedure
221
what are the complications of chronic liver disease?
``` portal hypertension upper GI haemorrhage ascites spontaneous bacterial peritonitis hepatic encephalopathy hepatopulmonary syndrome hepatorenal syndrome ```
222
what is the management of chronic liver disease?
``` essential monitoring treat the underlying cause nutrition (thiamine and folate) cholestryamine reduced alcohol intake ``` be mindful of sepsis, GI bleeds/varices, hypoglycaemia, encephalopathy
223
what medications should be reviewed when GORD is diagnosed/suspected?
``` NSAIDs bisphosphonates calcium antagonists nitrates theophylline corticosteroids ```