Gastroenterology Flashcards

1
Q

Is IBD associated with any autoimmune disease, if so which ones

A

Yes

SLE
AS
Hashimotos thyroiditis

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2
Q

How would IBD typically present

A

Intermittent bloody diarrhoea with mucous
weight loss
abdo pain
perianal pain & abscess

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3
Q

What are the extra-intestinal manifestations of IBD?

A

Skin
Erythema nodosum
Pyoderma gangrenosum

Joint arthropathy
Peripheral large joint arthritis
Ankylosis spondylitis
Sacroilitis

Mouth
Aphthous ulcers

Eye
Iritis
Uveitis
Episcleritis

Chronic liver disease
Cirrhosis
Chronic active hepatitis
Fatty liver PSC
Cholangiocarcinoma
Metastatic CRC
Amyloid CLD

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4
Q

What investigations would u order if a patient comes in with bloody diarrhoea + what results might u see

A

Bloods
FBC
Low hb — sec to iron deficiency anaemia
Low platelets — bleeding diasthesis sec to CLD
Elevated haematocrit — sec to dehydration

U&E
Elevated urea&raquo_space; Cr = dehydration
Electrolyte abnormalities sec to diarrhoea — hypoK + metabolic acidosis

LFTs
Low albumin — sec to protein losing enteropathy
Deranged LFTs due to CLD or PSC

PT/APTT
ESR/CRP
Blood cultures

Stool studies
Gram stain
C&s
Microscopy — check for ova, cysts, leukocytes
C.difficile toxin

Imaging
Plain film abdo — if UC = toxic megacolon, mucosal orders (ie thumb printing), perforation

Colonoscopy & biopsy
If UC
Confluent lesions — most severe in rectum & distal colon
No strictures

If CD
Strictures — string sign
Skip lesions
Cobble stoning of mucous
Deep fissured ulcerations
Fistula
Loss of haustra

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5
Q

what are some red flags for diarrhoea?

A

weight loss
intractable vomiting
severe dehydration
bloody stool
temp >38.1
incontinence
urgency
nocturnal symptoms

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6
Q

PUD is most common in which part of the GIT

A

duodenal is most common
gastric is 2nd most common

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7
Q

what causes PUD

A

helicobacter pylori infection

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8
Q

how does PUD present

A

epigastric pain — dull
worsened by food = gastric ulcer
worsened when hungry + relieved by meals = duodenal ulcer
heartburn

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9
Q

risk factors for PUD

A

chronic NSAID use
polypharmacy in elderly —- esp SSRIs, steroids, aspirin, anticoagulants, alendronate
prev PUD
h.pylori infection
age >60 y/o
chronic kiney or liver disease
smoking
alcohol
stress (cushing’s ulcers)
burns (curling’s ulcers)

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10
Q

what Ix would u order for suspected PUD

A

bloods
FBC — ?microcytic anaemia

OGD — visualise ulcer

to test for h.pylori
CLO Campylobacter-like test — requires OGD to be done + biopsy
UBT urea breath test

if possible compications
erect CXR — ?pneumoperitoneum

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11
Q

how would u Tx PUD

A

acute phase
if active bleeding = blablabla

if symptomatic but not bleeding
PPI
+/- H2 antagonists —- if persistent symptoms or C/I to PPI
antacids

if H.pylori +ve triple therapy — 2 Abx + PPI BD for 14/7
eg. esomeprazole + amoxicillin +clarithromycin
if penicillin allergic = metronidazole

long term

conservative Tx
dont smoke
avoid alcohol
weight loss
stop NSAIDs + medication rationalisation

medical Tx = as with acute phase

monitoring: repeat OGD after PPI — ensure gastric ulcer healing

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12
Q

DDx for epigastric pain

A

PUD
malignant ulcer — sec to gastric ca
oesophagitis
GERD
pancreatits
ACS —- inferior MI
AAA
acute cholecystitis
biliary colic

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13
Q

what is coeliac disease?

A

small bowel autoimmune disorder — characterised by mucosal inflammation + villous atrophy + crypt hyperplasia upon exposure to dietary gluten — improves upon withdrawal of gluten from diet

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14
Q

risk factors for coeliac disease

A

1st degree relative — 15%risk
HLA-DQ2 & HLA-DQ8
IgA deficiency
dermatitis herpetiformis
other autoimmune conditions
IBD
T1DM

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15
Q

how would coeliac disease present

A

symptoms (Hx)
diarrhoea — steatorrhoea sec to fat malabsorption
abdo bloating + excessive flatus
weight loss
fatigue
+/- vesicular rash (dermatitis herpetiformis)
faltering growth

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16
Q

Ix for suspected coeliac disease

A

bloods
FBC —— microcytic/macrocytic anaemia sec to iron & B12 deficiency
iron studies
folate & B12 levels
CRP/ESR
anti-tTG IgA & IgA levels
anti-EMA Ab (endomysial)

OGD & D2 biopsy
findings
macroscopic villous atroophy
scalloping
loss of mucosal folds

r/o other causes
stool
c&s, microscopy (ova & parasites)
faecal calprotectin
faecal elastase —- ?pancreatic insufficiency
chloride sweat test —- ?CF

17
Q

how do u classify coeliac disease

A

classic
refractory —– persistent symptoms & villous atrophy despite strict adherence to gluten free diet for 6 months
asymptomatic

18
Q

histology & endoscopy findings of CD Crohn’s disease vs UC ulcerative colitis

A

histology:

CD:
transmural inflammation
presence of granulomas

UC:
mucosal & submucosal inflammation
polymorphonuclear cells aggregate

endoscopy

CD:
skip lesions
cobble stoning of mucous
deep fissured ulcerations
fistulas
loss of haustra
strictures – string sign

UC:
continuous lesions
presence of crypts
formation of residual mucosal tissue

19
Q

Tx of IBD inflammatory bowel disease

A

severe acute phase

according to UC: true love and witts criteria or CD: CD activity index
admit to hospital
NPO + maintenance fluids
IV hydrocortisone + rectal steroids

monitor
vitals
physical exam — distension, bowel sounds, tenderness
Ix daily: FBC, ESR, CRP, U&E +/- PFA

if by day 3 CRP >45 or >5 stools/day = action required
colectomy OR
rescue therapy: cyclosporin/infliximab

Tx CD:

inducing remission = steroids +/- purines
steroids
if left-sided colon disease = prednisolone
if right-sided colon = budesonide (ileal release)
add ons (to step up)
azothioprine/mercaptopurine
methotrexate
infliximab/adalimumab

maintaining remission = purines
1st line = azothioprine, mercaptopurine
2nd line = methotrexate

surgical Tx = colectomy
doesnt cure – aim: remove worst affected areas + rest distal bowel

Tx UC:

mild UC:
5-ASA (sulphasalazine, mesalazine)
prednisolone 20mg OD
+/- steroid foams (colifoam) BD

moderate UC
5-ASA
prednisolone 40mg/wk –> 30mg/wk –> 20mg/wk 4 wks
steroid enema BD