GI Flashcards
commonest cause of LBO
colorectal carcinoma
commonest cause of SBO
adhesions
most common site of a carcinoid tumour
appendix
what does free air on abdo film suggest
perforation
when to refer for 2 wk wait suspected gastro cancer
(urgent endoscopy)
all px 55+ w weight loss + either:
- upper abdo pain
- reflux
- dyspepsia
ix + mx of perianal abscess
urgent MRI to see extent + to see if fistula
drainage via EUA (rectal exam under anaesthesia)
started on intravenous antibiotics e.g. ceftriaxone + metronidazole.
draining seton if complex
Familial adenomatous polyposis (FAP) features
Mutation in the adenomatous polyposis coli (APC) gene
AD
Px dev hundreds of adenomatous polyps in their teens - develop colorectal cancer by their 20s -> prophylactic proctocolectomy
High risk of developing duodenal cancer -> regular endoscopic surveillance.
Hereditary non-polyposis colorectal cancer (HNPCC)/Lynch syndrome features
mutation in the mismatch repair genes MLH1/MSH2
AD
80% risk of developing colorectal cancer by their 30s. Polyps turning to carcinoma occurs more rapidly.
There is increased risk of gastric, endometrial, breast, and prostate cancer.
Regular endoscopic surveillance.
triad of acute mesenteric ischaemia
severe abdo pain
unremarkable abdo exam
shock
what is achalasia
Failure of oesophageal peristalsis and of relaxation of the lower oesophageal sphincter (LOS) due to degenerative loss of ganglia from Auerbach’s plexus
i.e. LOS contracted, oesophagus above dilated.
Achalasia typically presents in middle-age and is equally common in men and women.
clinical presentation of achalasia
dysphagia of BOTH liquids and solids
typically variation in severity of symptoms
heartburn
regurgitation of food
may lead to cough, aspiration pneumonia etc
malignant change in small number of patients
ix for achalasia
oesophageal manometry
- excessive LOS tone which doesn’t relax on swallowing
- most important diagnostic test
barium swallow
- shows grossly expanded oesophagus, fluid level , tapers at the lower oesophageal sphincter
- ‘bird’s beak’ appearance
chest x-ray
- wide mediastinum
- fluid level
tx of achalasia
pneumatic (balloon) dilation is increasingly the preferred first-line option
surgical intervention with a Heller cardiomyotomy should be considered if recurrent or persistent symptoms
intra-sphincteric injection of botulinum toxin is sometimes used in patients who are a high surgical risk
drug therapy (e.g. nitrates, calcium channel blockers) has a role but is limited by side-effects
what can c diff infection cause
pseudomembranous colitis
mx of c diff infection
first-line therapy is oral vancomycin for 10 days
second-line therapy: oral fidaxomicin
third-line therapy: oral vancomycin +/- IV metronidazole
ix c diff
is made by detecting C. difficile toxin (CDT) in the stool
C. difficile antigen positivity only shows exposure to the bacteria, rather than current infection
most common abx to lead to c diff
cephalosporins
first line diagnostic test for small bowel bacterial overgrowth syndrome
hydrogen breath testing
abx tx for small bowel bacterial overgrowth syndrome
rifaximin
what is the most common cause of infectious intestinal disease in the uk (give me a bacteria)
campylobacter jejuni
(gram -ve bacillus)
features of campylobacter jejuni
faecal-oral route
incubation period 1-6 days
- prodrome: headache, malaise
- diarrhoea: often bloody
- abdominal pain: may mimic appendicitis
how to differentiate CROHNS from UC
Crohns NESTS
N – No blood or mucus (these are less common in Crohns.)
E – Entire GI tract
S – “Skip lesions” on endoscopy
T – Terminal ileum most affected and Transmural (full thickness) inflammation
S – Smoking is a risk factor
Crohn’s is also associated with weight loss, strictures and fistulas.
get increased goblet cells
how to differentiate UC from CROHNS
U… C… CLOSE UP
C – Continuous inflammation
L – Limited to colon and rectum
O – Only superficial mucosa affected
S – Smoking is protective
E – Excrete blood and mucus
U – Use aminosalicylates
P – Primary sclerosing cholangitis
get crypt abscesses
mx of UC mild/moderate
First line: aminosalicylate (e.g. mesalazine oral or rectal)
Second line: corticosteroids (e.g. prednisolone)
mx of UC severe disease
First line: IV corticosteroids (e.g. hydrocortisone)
Second line: IV ciclosporin
maintaining remission of UC
Aminosalicylate (e.g. mesalazine oral or rectal) - topical is better if dis limited to rectum
Azathioprine
Mercaptopurine
inducing remission in crohns
First line are steroids (e.g. oral prednisolone or IV hydrocortisone).
If steroids alone don’t work, consider adding immunosuppressant medication under specialist guidance:
Azathioprine
Mercaptopurine
Methotrexate
Infliximab
Adalimumab
maintaining remission in crohns
1st line:
Azathioprine
Mercaptopurine
Alternatives:
Methotrexate
Infliximab
Adalimumab
electrolyte abnormalities in refeeding syndrome
Hypophosphataemia
hypokalaemia
hypomagnesaemia
what is haemochromatosis + what is its inheritance
AR disorder of iron absorption + metabolism -> iron accumulation
what is haemochromatosis inheritance like
AR
inheritance of mutations in the HFE gene on both copies of chromosome 6.
testing for haemochromatosis
ferritin (not as sensitive)
transferrin saturation
genetic testing for family members
mx of haemochromatosis 1st + 2nd line
venesection (try and keep transferrin sat , 50% + serum ferritin conc < 50 ug/l
Deferoxamine 2nd line
haemochromatosis presentation
iron overload usually becomes sx after 40yrs
presents later in females as menstruation eliminates some iron
Chronic tiredness
Joint pain
Pigmentation (bronze skin)
Testicular atrophy
Erectile dysfunction
Amenorrhoea (absence of periods in women)
Cognitive symptoms (memory and mood disturbance)
Hepatomegaly
comps of haemochromatosis
Secondary diabetes (iron affects the functioning of the pancreas)
Liver cirrhosis
Endocrine and sexual problems (hypogonadism, erectile dysfunction, amenorrhea and reduced fertility)
Cardiomyopathy (iron deposits in the heart)
Hepatocellular carcinoma
Hypothyroidism (iron deposits in the thyroid)
Chondrocalcinosis (calcium pyrophosphate deposits in joints) causes arthritis
what is wilson’s disease
copper build up
how to screen for Wilson’s disease
caeruloplasmin
first-line test for screening coeliac disease
tissue transglutaminase (TTG) antibodies (IgA)
endomyseal antibody (IgA) - needed to look for selective IgA deficiency, which would give a false negative coeliac result
test recommended for H. pylori post-eradication therapy
urea breath test
RFs that disrupt the mucus barrier -> peptic ulcers
Helicobacter pylori
Non-steroidal anti-inflammatory drugs (NSAIDs)
RFs that increase stomach acid -> peptic ulcer
Stress
Alcohol
Caffeine
Smoking
Spicy foods
risk of bleeding from a peptic ulcer is increased by what meds?
Non-steroidal anti-inflammatory drugs (NSAIDs)
Aspirin
Anticoagulants (e.g., DOACs)
Steroids
SSRI antidepressants
signs of upper GI bleeding
Haematemesis (vomiting blood)
Coffee ground vomiting
Melaena (black, tarry stools)
Fall in haemoglobin on a full blood count
peptic ulcer presentation
Epigastric discomfort or pain
Nausea and vomiting
Dyspepsia
upper GI bleeding
iron def anaemia
how does eating affect ulcers
worsens the pain of gastric ulcers
the pain of duodenal ulcers improves immediately after eating but is worse 2-3 hrs later (when it gets to duo)
dx of peptic ulcers
endoscopy
During endoscopy, a rapid urease test (CLO test) can be performed to check for H. pylori. A biopsy is considered during endoscopy to exclude malignancy.
what do you see in bloods if there is an upper GI bleed
raised urea
histology of coeliac disease
villous atrophy
crypt hyperplasia
raised intra-epithelial lymphocytes
histology of crohn’s
inflammation in all layers from mucosa to serosa, goblet cells, granulomas
skip lesions
histology of UC
inflammation doesn’t reach below submucosa, crypt abscesses
continuous
what is the rockall score
used after endoscopy and utilises information such as the patient’s age, observations, comorbidities and the endoscopy result to provide an estimation of rebleeding risk and mortality
what is the Glasgow-Blatchford score
used before endoscopy to help assess patients with suspected upper GI bleeds who are deemed ‘lower risk’ and could be managed as outpatients (assesses likihood of them needing medical intervention)
most common site for UC
rectum
globus (feeling of something stuck in throat), hoarseness + no red flags dx?
+ what might be on endoscopy?
?laryngopharyngeal reflux (ie silent reflux)
erythema being seen on endoscopy
what is Globus hystericus
the sensation of a lump being stuck in the throat, with no physical findings present
how do you categorise mild, moderate and severe UC
mild = < 4 poos + minimal bleeding
moderate = 4-6
severe = 6+ , v bloody + systemic sx
Dukes’ classification
describes the extent of spread of colorectal cancer
A = confined to mucosa
B = invading bowel wall
C = lymph nodes mets
D = distant mets
do CT TAP (thorax, abdomen and pelvis)
Loop ileostomy
to divert stool away from the healing portion post-anterior resection. They are typically used when the intention is to later reverse the stoma and restore bowel continuity
ileostomy for small intestine
they are spouted to keep digested material away from the skin
end ileostomy
the end of the ileum, is brought to the surface of the abdomen to create an artificial opening called a stoma. An end ileostomy is usually undertaken following complete excision of the colon or when an ileocolic anastomosis is not planned
End colostomy
surgical procedure where one end of the colon is brought to the surface of the abdomen to create an artificial opening called a stoma. Colostomies are flush to the skin because the contents of the colon are less irritable to the skin
often permanent and not commonly used if anastomosis is planned.
most common type of colorectal cancer + location
adenocarcinoma
66% arise in colon (more proximal than distal), 30% rectum
what comprises the proximal colon
the ascending colon and the transverse colon
what comprises the distal colon
the descending colon and the sigmoid colon
what is an adenoma
type of polyp
precursor lesion in most cases of colon cancer
benign, dysplastic tumour of columnar cells or glandular tissue
where do colorectal tumours metastisize
LIVER (due to portal vein)
lung
RFs for colorectal carcinoma
Age (>60)
Male
low fibre diet
saturated fat + red meat
sugar
colorectal polyps, adenomas
alcohol + smoking
obesity
UC
FHx
genetic dis
what can reduce risk of colorectal carcinoma
veg
garlic
milk
exercise
low dose aspirin
colorectal carcinoma presentation
change in bowel habit
rectal bleeding
weight loss
abdo pain
iron def anaemia
rectal mass in rectal cancer?
abdo mass
the closer the cancer is to the anus the more visible blood + mucus will be
4 cardinal signs of obstruction
absolute constipation
colicky abdo pain
abdo distension
vomiting (faeculent)
sx + signs of right sided carcinoma (proximal colon)
usually asx until they present with iron def anaemia due to bleeding (so will present at more advanced stage)
palpable mass in right iliac fossa?
sx + signs of left sided carcinoma (distal colon)
change in bowel habit with blood + mucus in stools
alt constipation + diarrhoea
may be palpable mass in left iliac fossa or on PR exam
tenesmus (feeling you need a poo but empty)
when to refer for urgent ix suspected bowel cancer
> 40 unexplained weight loss + abdo pain
50 unexplained rectal bleeding
60 iron def anaemia or change in bowel habit
+ve FIT
what is the Faecal immunochemical tests (FIT)
look very specifically for the amount of human haemoglobin in the stool
when to use a FIT test
GP to help assess for bowel cancer in px who do not meet the criteria for a two week wait referral eg:
Over 50 with unexplained weight loss and no other symptoms
Under 60 with a change in bowel habit
Screening