Gen Surg - Others Flashcards

haemorrhoids anal fissures anal fistula upper GIB dysphagia & odynophagia GERD barrett's oesophagus hiatal hernia

1
Q

what are haemorrhoids

A

normal vascular and CT columns that exist in the anal canal — there are 3 in total

split into internal and external haemorrhoids — internal = above dentate line; external = below dentate line
internal = can bleed or prolapse
external = can thrombose

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2
Q

what causes haemorrhoids

A

poor dietary habits
constipation — prolonged straining
increased intra-abdominal P

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3
Q

what are the 4 degree of internal haemorrhoids

A

1st degree: bleeds only
2nd degree: prolapses BUT reduces spontaneously
3rd degree: prolapses BUT has to be manually reduced
4th degree: permanently prolapsed — may strangulate

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4
Q

how does thrombosed external haemorrhoids present + how to manage

A

presentation : acute excruciating pain

Tx: surgical evacuation of haemorrhoid + excision of skin overlying

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5
Q

how would u manage internal haemorrhoids that is bleeding/prolapsed

A

conservative Tx
secondary prevention
only evacuate when the natural desire to do so arises
minimise straining or lingering
increased dietary fibre
increased physical activity
sitz baths — warm water + 3x a day
(to clean perineum)

medical Tx
laxatives — stool softeners or bulking agents
topical analgesia + steroids
injection sclerotherapy —- for 1st or 2nd degree
rubber band ligation —- for 2nd degree
trans-anal haemorrhoidal dearterialisation — for 2nd & 3rd degree

surgical Tx = haemorrhoidectomy

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6
Q

what are anal fissures

A

longitudinal split of the anoderm in the distal anal canal — extending from the anal verge proximally — towards (but not extending beyond) the dentate line

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7
Q

what causes anal fissures

A

primary causes = local trauma
passage of hard stool
prolonged diarrhoea
vaginal delivery
anal sex

secondary causes
IBD — eg. CD
granulomatous diseases — eg. extrapulmonary TB, sarcoidosis
malignancy — eg. squamous cell anal ca, leukaemia
communicable diseases — eg. HIV, syphillis, chlamydia

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8
Q

what defines acute or chronic anal fissure

A

acute = <6 wks of onset
chronic = >6wks of onset OR certain features
eg. fibrosis, fibrotic edges, perianal skin tag

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9
Q

how do anal fissures present

A

pain — exacerbated by defecation
+/- bleeding
+/- perianal skin tags
+/- puritus ani

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10
Q

how to manage anal fissures

A

conservative Tx = prevention
healthy bowel habits
high fibre diet
adequate fluids

medical Tx
laxatives
warm sitz baths — ie local wound care
analgesia

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11
Q

what is an anal fistula

A

fistula: chronic abnormal connection between 2 epithelial-lined surfaces
anal fistula is when a fistula forms between the anus and an adjacent structure

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12
Q

what can cause anal fistulas

A

anorectal abscess —- ruptures or is drained
CD
lymphogranuloma venereum
radiation proctitis
rectal foreign bodies
primary perianal actinomycosis

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13
Q

how would an anal fistula present

A

symptoms (Hx)
intermittent rectal pain
chronic purulent discharge
pustule-like lesion in the peri-anal or buttock area
intermittent + malodorous perianal drainage & pruritus

signs (exam)
perianal skin — excoriated + inflamed
induration just below skin
proctosigmoidoscopy

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14
Q

what classification used for anal fistulas

A

park’s classification
intersphincteric
trans-sphincteric
extrasphincteric
suprasphincteric

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15
Q

management of anal fistulas

A

EUA examination under anaesthesia

options
fistulotomy
fistulectomy
seton insertion
advancement flap
plus and glues

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16
Q

causes of upper GIB

A

peptic ulcers 36%
oesophagitis 24%
gastritis 22%
varices 11%

17
Q

risk factors for upper GIB

A

chronic liver disease
alcohol
smoking
NSAIDs
vomiting
steroids
PUD

18
Q

Ix for upper GIB

A

bloods
FBC
U&E
GXM if severe
coag profile
ABG + lactate

OGD

CT angiogram

19
Q

scoring system for upper GIB

A

Glasgow Blatchford scoring system
predicts need for intervention in upper GIB

20
Q

management of upper GIB

A

IV PPI bolus/transfusion

if stable = GI endoscopy in 24 hrs

if unstable = urgent endoscopy
stop haemorrhage via haemostatic clips, adrenaline injections, haemostatic powder

if massive haemorrhage = ABCDs
2 large bore 14-16G IV cannulas
transfuse IV crystalloids, if severe = unmatched O -ve blood initially —- matched blood once available
activate massive transfusion protocol
balanced transfusion — 1:1:1 RCC, FFP, platelets
reverse any anticoags + correct any underlying coag deficits

if suspected variceal bleeding = IV terlipression + octreotide
+/- Sengstaken-Blakemore tube (in ED setting)
OGD for variceal banding
+/- TIPS Transjugular intrahepatic portosystemic shunt

21
Q

what is dysphagia and odynophagia and what are their DDx

A

dysphagia: difficulty swallowing
odynophagia: painful swallowing

DDx

intraluminal
foreign body
food bolus
oesophageal webs

intramural
lump — benign vs malignant
GERD
oesophagitis
dysmotility disorders
scleroderma
stricture
eosinophilic oesophagitis
neuro
hiatal hernia
volvulus

extraluminal
lymphadenopathy
goitre
pharyngeal pouch
haematoma

others
oesophageal rupture
Mallory-Weiss tear
oesophageal ulcers

22
Q

what is GERD

A

it is a condition that develops when reflux of stomach contents causes troublesome symptoms and/or complications

23
Q

risk factors of GERD

A

causes of increased intra-abdominal P
obesity
pregnancy

causes of loss of anti-reflux mechanisms
alcohol
smoking
fam Hx
DM
hiatal hernia
oesophageal dysmotility
gastric dysfunction
meds

24
Q

Ix for GERD

A

urease breath test — for H.pylori

Upper GI Endoscopy

contrast swallow

ambulatory pH and impedence monitoring

oesophageal manometry

25
Q

management of GERD

A

conservative Tx
lifestyle — reduce alcohol, smoking cessation, weight loss
review meds causing dyspepsia – eg. NSAIDs

medical Tx
PPIs —- if ineffective = add H2 antagonist
metoclopramide/domperidone —prokinetic agent
Tx of H.pylori if present

surgical Tx = laparoscopic Nissen (360 degrees) fundoplication

26
Q

what is Barrett’s oesophagus

A

when the normal squamous epithelial lining of the distal oesophagus changes to metaplastic columnar epithelium

27
Q

risk factors of barrett’s oesophagus

A

smoking
alcohol
obesity
white
male
>50 y/o

28
Q

management of barrett’s oesophagus

A

high dose PPI — symptom control
aspirin – reduces progression to high grade dysplasia

monitoring: surveillance endoscopy

29
Q

what is a hiatal hernia

A

the displacement of part or all of the stomach through the oesophageal hiatus

30
Q

what types of upper GI hernias are there

A

type 1: sliding hiatal hernia
2-3: para-oesophageal hernia — incl rolling hernia
4: intrathoracic herniation of abdominal viscera

31
Q

presentation of hiatal hernia

A

asymptomatic 50%

symptomatic (Hx)
epigastric or chest pain
heartburn, regurgitation
post-prandial fullness
dysphagia

iron deficiency anaemia

32
Q

Ix for suspected hiatal hernia

A

CXR
contrast swallow
CT TAP
oesophageal manometry — to guide choice of fundoplication

note: NO OGD!!!

33
Q

management of hiatal hernias

A

conservative Tx = weight loss, smoking cessation, alcohol reduction

medical Tx
PPIs
domperidone — prokinetic agent

surgical Tx
indication: symptomatic
most common = laparoscopic transabdominal repair

if emergency presentation of gastric volvulus =NG tube decompression
failure = urgent surgical repair

34
Q

complications of hiatal hernia

A

GERD
anaemia
gastric outlet obstruction
gastric volvulus
gastric ischaemia