General Surgery/GI Flashcards

1
Q

What diameter of abdominal aorta is considered abnormal - aneurysmal?

A

greater than 3cm

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2
Q

What are some risk factors for the development of abdominal aortic aneurysms?

A

male
higher age
smoking
hypertension
familial history
existing CV disease

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3
Q

How can patients with AAA (abdominal aortic aneurysm) present?

A

asymptomatic
non-specific abdo pain
pulsatile and expansive mass in the abdomen
incidental finding

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4
Q

What investigations are used to diagnose AAA?

A

ultrasound - imaging of choice
CT angiogram - useful for elective surgery

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5
Q

What is the screening programme for AAA?

A

men over 65 y.o. are offered abdominal ultrasound

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6
Q

What diameter would be a small AAA?

A

3 - 4.4 cm

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7
Q

What action is required in small AAA?

A

re-scan every 12 months

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8
Q

What diameter would be a medium AAA?

A

4.5 - 5.4 cm

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9
Q

What action is required in medium AAA?

A

re-scan every 3 months

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10
Q

What diameter would be a large AAA?

A

greater than 5.5 cm

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11
Q

What action is recommended in large AAA?

A

refer to vascular surgery within 2 weeks

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12
Q

What are some non-surgical management options for AAA?

A

treating reversible risk factors:
quitting smoking
hypertension management
healthy lifestyle (diet, exercise)

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13
Q

When is elective repair for AAA recommended?

A
  • if symptomatic
  • if > 5.5 cm
  • if growing >1cm per year
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14
Q

What is the surgical management of AAA?

A

open laparotomy
EVAR - endovascular aneurysm repair

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15
Q

How does ruptured AAA present?

A

severe abdominal pain radiating to back or groin
haemodynamic instability - hypotension, tachycardia
pulsatile and expansive mass in the abdomen
collapse
loss of consciousness

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16
Q

What is the management for haemodynamically unstable patients with ruptured AAA?

A

taken to the theatre immediately
clinical diagnosis only - no imaging

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17
Q

lWhat is the management for frail patients with ruptured AAA?

A

consider palliative approach

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18
Q

What is the management for haemodynamically stable patients with ruptured AAA?

A

CT angiogram to confirm
then surgical repair

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19
Q

What are the risk factors for appendicitis?

A

male
in 20s

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20
Q

What is the typical pain in appendicitis?

A

central abdominal pain that moves to the R iliac fossa in the first 24hrs
then localised to the RIF

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21
Q

What is the McBurney’s point?

A

specific area one third of the distance from the anterior superior iliac spine (ASIS) to the umbilicus

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22
Q

What is the typical presentation of appendicitis?

A

abdominal pain (central -> RIF)
loss of appetite
nausea and vomiting
low-grade fever
Rovsing’s sign
guarding on palpation
RIF rebound tenderness
percussion tenderness

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23
Q

What is Rovsing’s sign?

A

palpation of the left iliac fossa causes pain in the RIF

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24
Q

What are some signs of peritonitis?

A

rebound tenderness
percussion tenderness
guarding / rigid abdomen

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25
How do you diagnose appendicitis?
clinical presentation raised inflammatory markers - especially neutrophils!
26
What type of WBC is most typically raised in appendicitis?
neutrophils
27
What investigations are useful in appendicitis diagnosis?
bloods - esp. inflammatory markers (CRP, FBC) ultrasound - esp. in females to exclude gynae pathology CT - if suspecting other diagnoses diagnostic laparotomy - if clinical presentation positive, findings negative
28
What are some key differentials of appendicitis?
ectopic pregnancy ovarian cysts Meckel's diverticulum mesenteric adenitis - inflammation of abdo. lymph nodes
29
What is the initial management of appendicitis?
analgesia nil by mouth IV fluids
30
What is the management of appendicitis?
appendicectomy (laparoscopic)
31
What is coeliac disease?
autoimmune condition caused by gluten sensitivity
32
What is the (basic) pathophysiology of coeliac disease?
sensitivity to gluten repeated exposure leads to villous atrophy this leads to malabsorption
33
What conditions are associated with coeliac?
dermatitis herpetiformis other autoimmune conditions - T1DM, autoimmune thyroid disease
34
What are some possible presentations of coeliac?
asymptomatic chronic / intermittent diarrhoea persistent GI symptoms bloating, abdo pain fatigue weight loss mouth ulcers failure to thrive (children) unexplained anaemia - due to malabsorption of B12, iron, folate dermatitis herpetiformis neurological symptoms
35
How is coeliac diagnosed?
while patient continues to consume gluten (at least 6 weeks prior to testing) blood tests - total IgA levels, anti-TTG antibodies endoscopic intestinal biopsy - gold standard for diagnosis
36
What are the first-line blood tests for coeliac?
total IgA levels - to exclude IgA deficiency anti-tissue transglutaminase antibodies (anti-TTG)
37
What is second-line blood test for coeliac?
anti-EMA (anti-endomysial antibodies_
38
Why do you need to check for IgA levels in suspected coeliac?
IgA deficiency would give a false negative result in coeliac
39
What is the gold standard for coeliac diagnosis?
endoscopic intestinal biopsy - duodenum, jejunum
40
What would a positive intestinal biopsy show in coeliac?
villous atrophy crypt hyperplasia increase in intra-epithelial lymphocytes infiltration of lamina propria with lymphocytes
41
What are some possible complications of coeliac?
nutritional deficiencies anaemia osteoporosis hyposplenism EATL - enteropathy-associated T-cell lymphoma subfertility
42
What HLA (human leukocyte antigen) genotypes is coeliac associated with?
HLA-DQ2 HLA-DQ8
43
What is necrotising enterocolitis?
disorder affecting premature neonates, where part of the bowel becomes necrotic one of the leading causes of death among premature infants
44
What is a typical presentation of necrotising enterocolitis?
feeding intolerance green vomiting tender and distended abdomen bloody stools absent bowel sounds can progress to peritonitis -> generally very unwell
45
How is necrotising enterocolitis diagnosed?
abdominal X ray - gold standard FBC CRP capillary blood gas - metabolic acidosis blood culture - sepsis
46
What will abdominal X ray show in necrotising enterocolitis?
dilated bowel loops bowel wall oedema pneumatosis intestinalis - gas in bowel wall pneumoperitoneum - free gas in peritoneal cavitity gas in portal veins
47
How is necrotising enterocolitis managed?
surgical emergency - surgery often required nil by mouth, IV fluids, TPN, ATB
48
What is volvulus?
bowel twisting around itself and the mesentery it's attached to (which provides the blood supply to the bowel) causes closed loop bowel obstruction
49
What are the two main common types of volvulus?
sigmoid volvulus caecal volvulus
50
What is a typical presentation of volvulus?
constipation abdominal pain abdominal distention vomiting (green)
51
What are the risk factors for sigmoid volvulus?
older patients chronic constipation neuropsychiatric conditions (e.g. Parkinson's)
52
What are the risk factors for caecal volvulus?
adhesions pregnancy
53
How is sigmoid volvulus diagnosed? What is the typical sign?
abdominal X-ray - coffee bean sign (sigmoid volvulus) CT with contrast - to confirm the diagnosis
54
How is volvulus managed INITIALLY?
nil by mouth, IV fluids, NG tube
55
What is the conservative management of sigmoid volvulus?
insertion of flexible / rigid sigmoidoscope to correct the volvulus + insertion of rectal tube (kept in place for a couple of days) to decompress the bowel
56
What are the options for surgical management of sigmoid volvulus?
laparotomy Hartmann's procedure - removal of rectosigmoid colon and formation of colostomy
57
How is caecal volvulus managed?
ileocaecal resection right hemicolectomy
58
What are the key features of IBS?
I - intestinal discomfort - abdominal pain related to the bowels B - bowel habit abnormalities S - stool abnormalities
59
What are the main symptoms of IBS? (at least 1 required over 6 months before diagnosis)
pain/discomfort relieved by opening bowels bowel habit abnormalities stool abnormalities
60
What are some common symptoms of IBS? (require 2 out of 4 to diagnose)
passing mucus bloating straining, urgent need to open bowels, incomplete emptying worse after eating
61
What tests can be performed when suspecting IBS?
FBC - for anaemia CRP coeliac serology - anti-TTG faecal calprotectin - for IBD CA125 - for ovarian cancer
62
What are the red flags that would suggest a more sinister diagnosis than IBS?
rectal bleeding unexplained weight loss family history of ovarian / bowel cancer onset after 60+ y.o.
63
What are the key differentials in IBS?
bowel cancer IBD coeliac disease ovarian cancer - can present with non-specific symptoms, esp. in 50+ y.o. pancreatic cancer
64
What lifestyle management options are there for IBS?
drinking enough fluids limiting caffeine, alcohol, fat intake eating regular small meals adjusting fibre intake based on symptoms low FODMAP diet regular exercise psychological intervention
65
What is the first line pharmacological treatment for IBS?
pain: antispasmodics (mebeverine) diarrhoea: loperamide constipation: bulk-forming laxatives (ispaghula husk)
66
When is linaclotide considered in IBS?
if patient not responding to conventional laxatives AND constipated for 12+months
67
What is the second line pharmacological treatment for IBS?
low-dose tricyclic antidepressants - e.g. amitriptyline
68
What are the foregut structures?
Oesophagus, stomach, Liver, biliary, pancreas and proximal duodenum
69
What are the midgut structures?
distal duodenum, jejunum, ileum, cecum, appendix, ascending colon, proximal 2/3 of transverse colon
70
What are the hindgut structures?
distal half of the transverse colon, descending colon, sigmoid colon, and the proximal third of the rectum
71
Where is referred pain from foregut structures perceived?
epigastric region
72
Where is referred pain from midgut structures perceived?
umbilical region
73
Where is referred pain from hindgut structures perceived?
suprapubic region
74
What does colicky pain that becomes constant suggest?
partial obstruction of a hollow viscus (e.g. bowel, bile duct, ureter)
75
What are the types of inguinal hernias?
Direct and indirect
76
What is a direct inguinal hernia?
leading area of weakness is the posterior wall of the inguinal canal, where viscera herniates anteriorly through Hesselbach’s triangle and not into scrotum
77
What is an indirect inguinal hernia?
the leading area of weakness is the deep inguinal ring where intra-peritoneal contents herniate into the inguinal canal alongside spermatic cord, and can exit the canal through the superficial inguinal ring and into the scrotum
78
What is a femoral hernia?
Below the inguinal ligament, inferior and lateral to the pubic tubercle
79
What is a reducible hernia?
The hernia can be manually pushed back (or ‘reduced’) into the abdominal cavity
80
What is an Irreducible hernia?
The hernia sac and its content cannot be pushed back into the abdomen
81
Whan is an incarcerated hernia?
The contents are fixed in the sac with adhesions. The hernia is irreducible but the organ within the sac is not compromised, but is at risk of strangulation
82
What is an obstructed hernia?
the bowel loop trapped within the sac causes bowel obstruction. With further oedema it can become strangulated
83
What are the criteria for urgent referral for colorectal cancer?
Any age with a rectal or abdominal mass Age 40+ with unexplained weight loss and abdominal pain Age 50+ with unexplained rectal bleeding Age 60+ with iron deficiency anaemia
84
What are the possible causes of pancreatitis?
I GET SMASHED I – Idiopathic G – Gallstones E – Ethanol (alcohol consumption) T – Trauma S – Steroids M – Mumps A – Autoimmune S – Scorpion sting (the one everyone remembers) H – Hyperlipidaemia, hypercalcaemia, hypothermia (like milk - fatty, full of calcium, and cold) E – ERCP D – Drugs (furosemide, thiazide diuretics and azathioprine)
85
What are the most common causes of pancreatitis?
alcohol gallstones post-ERCP
86
How does acute pancreatitis present?
severe epigastric pain (may radiate to the back) vomiting abdominal tenderness generally unwell (low-grade fever, tachycardia)
87
What two signs are associated with acute pancreatitis?
Grey-Turner's sign Cullen's sign
88
What is the Grey-Turner's sign?
flank discolouration in acute pancreatitis (Turner - "turn around" - flank)
89
What is Cullen's sign?
periumbilical discolouration in acute pancreatitis (Cullen - "central" - periumbilical)
90
What investigations are needed to calculate the Glasgow score in acute pancreatitis?
FBC (for white cell count) U&E (for urea) LFT (for transaminases and albumin) Calcium ABG (for PaO2 and blood glucose)
91
What is the Glasgow score for acute pancreatitis?
PANCREAS: P – Pa02 < 8 KPa A – Age > 55 N – Neutrophils (WBC > 15) C – Calcium < 2 R – uRea >16 E – Enzymes (LDH > 600 or AST/ALT >200) A – Albumin < 32 S – Sugar (Glucose >10)
92
What investigations, other than the ones required for Glasgow score, do you need in acute pancreatitis?
amylase / lipase - if 3x the upper limit CRP USS abdomen - initial investigation of choice to assess for gallstones CT abdomen - good to assess for complications; usually not required
93
How is acute pancreatitis staged, according to the Glasgow score?
0 or 1 – mild pancreatitis 2 – moderate pancreatitis 3 or more – severe pancreatitis
94
How is acute pancreatitis managed?
if moderate/severe - consider HDU/ICU admission Initial resuscitation (ABCDE approach) IV fluids Analgesia Nutritional support (by mouth wherever possible, with parenteral nutrition if oral intake is not possible) Careful monitoring Treatment of gallstones in gallstone pancreatitis (ERCP / cholecystectomy) Antibiotics if there is evidence of a specific infection (e.g., abscess or infected necrotic area) Treatment of complications (e.g., endoscopic or percutaneous drainage of large collections)
95
What are the possible complications of acute pancreatitis?
Necrosis of the pancreas Infection in a necrotic area Abscess formation Acute peripancreatic fluid collections Pseudocysts (collections of pancreatic juice) can develop 4 weeks after acute pancreatitis Chronic pancreatitis ARDS (acute respiratory distress syndrome) - systemic complication
96
What is chronic pancreatitis?
chronic inflammation of the pancreas leads to fibrosis and reduced function
97
What is the most common cause of chronic pancreatitis?
alcohol
98
What are the features of chronic pancreatisis?
similar to acute, but longer-lasting and less intense pain worse after a meal diabetes steatorrhoea - fatty stools fat malabsorption fat-soluble vitamin deficiency
99
What are the possible complications of acute pancreatitis?
Chronic epigastric pain Loss of exocrine function, resulting in a lack of pancreatic enzymes (particularly lipase) secreted into the GI tract Loss of endocrine function, resulting in a lack of insulin, leading to diabetes Damage and strictures to the duct system, resulting in obstruction in the excretion of pancreatic juice and bile Formation of pseudocysts or abscesses
100
How is chronic pancreatitis managed?
Abstinence from alcohol and smoking Analgesia Replacement pancreatic enzymes (Creon) - if loss of pancreatic enzymes (i.e. lipase) lack of enzymes leads to malabsorption of fat, greasy stools (steatorrhoea), and deficiency in fat-soluble vitamins Subcutaneous insulin - to treat diabetes ERCP with stenting - to treat strictures and obstruction to the biliary system and pancreatic duct
101
How is chronic pancreatitis investigated?
abdominal x-ray - pancreatic calcification CT - pancreatic calcification functional tests - faecal elastase to assess exocrine function if imaging inconclusive
102
What is Charcot's triad?
RUQ pain Fever Jaundice (raised bilirubin)
103
What is Charcot's triad sign of?
acute cholangitis
104
What is acute cholangitis?
infection and inflammation in the bile ducts it's a surgical emergency
105
What are the main causes of acute cholangitis?
obstruction in the bile ducts (e.g. gallstones in the common bile duct) infection introduced during ERCP benign or malignant stricture sclerosing cholangitis
106
What is sclerosing cholangitis?
chronic liver disease causing inflammation and scarring of bile ducts
107
What is Reynold's pentad?
jaundice RUQ pain fever hypotension confusion (Charcot's triad + hypotension + confusion)
108
What are the most common infective organisms responsible for acute cholangitis?
Escherichia coli Klebsiella species Enterococcus species
109
How is acute cholangitis initially managed?
Nil by mouth IV fluids Blood cultures IV antibiotics (as per local guidelines) analgesia Involvement of seniors and potentially HDU or ICU
110
How is acute cholangitis diagnosed?
Abdominal ultrasound scan (least sensitive) - first line imaging CT scan Magnetic resonance cholangio-pancreatography (MRCP) Endoscopic ultrasound (most sensitive)
111
How is acute cholangitis managed?
ERCP (endoscopic retrograde cholangio-pancreatography) PTC (percutaneous transhepatic cholangiogram) - for patients unsuitable for ERCP
112
What is ERCP?
Endoscopic retrograde cholangio-pancreatography insertion of endoscope to the sphincter of Oddi retrograde injection of contrast into the duct through the sphincter of Oddi and x-ray images to visualise biliary system
113
What procedures can be performed during an ERCP?
Cholangio-pancreatography: retrograde injection of contrast into the duct through the sphincter of Oddi and x-ray images to visualise biliary system Sphincterotomy: making a cut in the sphincter to dilate it and allow stone removal Stone removal: a basket can be inserted and pulled through the common bile duct to remove stones Balloon dilatation: a balloon can be inserted and inflated to treat strictures Biliary stenting: a stent can be inserted to maintain a patent bile duct (for strictures or tumours) Biopsy: a small biopsy can be taken to diagnose obstructing lesions
114
What risks are associated with ERCP?
bleeding acute pancreatitis gastric / duodenal perforation cholangitis
115
What is PTC?
Percutaneous transhepatic cholangiogram radiologically guided insertion of a drain through the skin and liver, into the bile ducts to relieve immediate obstruction stent can be inserted as a long-term solution suitable for patient who are unsuitable for ERCP
116
What is cholecystitis?
inflammation of the gallbladder caused by a blockage of the cystic duct preventing the gallbladder from draining
117
What are the main types of acute cholecystitis?
calculous cholecystitis - secondary to gallstones acalculous cholecystitis - after long period of fasting, TPN etc. (gallbladder not regularly stimulated)
118
How does acute cholecystitis typically present?
RUQ pain (may radiate to right shoulder) nausea + vomiting Fever Tachycardia (fast heart rate) and tachypnoea (raised respiratory rate) Murphy’s sign Raised inflammatory markers and white blood cells LFTs usually normal
119
What is Murphy's sign?
sign of acute cholecystitis inspiratory arrest upon palpation of the right upper quadrant
120
What imaging can be used to diagnose acute cholecystitis?
abdominal USS - first line imaging MRCP (magnetic resonance cholangio-pancreatography)
121
What will abdominal USS show in acute cholecystitis?
Thickened gallbladder wall Stones or sludge in gallbladder Fluid around the gallbladder
122
What is the immediate (conservative) management of acute cholecystitis?
emergency admission nil by mouth analgesia IV fluids IV antibiotics NG tube / antiemetics
123
What is the ultimate management for cholecystitis?
ERCP - to remove the stones cholecystectomy - ideally within 1 week of diagnosis
124
What are some possible complications of cholecystitis?
sepsis gallbladder empyema gangrenous gallbladder perforation
125
What is gallbladder empyema?
infected tissue and pus collecting in the gallbladder
126
How is gallbladder empyema treated?
IV antibiotics and cholecystectomy OR cholecystostomy - drain into the gallbladder to drain the infected contents
127
What are the risk factors for developing gallstones?
Fat Fair Forties Female
128
What is biliary colic?
severe pain in RUQ/epigastrium caused by stones temporarily obstructing the drainage of the gallbladder often triggered by eating
129
How do patients with gallstones typically present?
asymptomatic biliary colic complications of gallstones (cholecystitis, cholangitis, pancreatitis, obstructive jaundice)
130
What causes elevated bilirubin?
obstruction in the biliary system may be caused by - gallstone in the bile duct - mass pressing on the bile ducts (e.g. cholangicarcinoma, head of pancreas tumour)
131
What can raised alkaline phosphatase (ALP) suggest?
liver / bone problems (incl. malignancy) pregnancy biliary obstruction (if RUQ pain/jaundice as well)
132
What is the first-line imaging when you suspect gallstones?
USS abdomen
132
What can raised alanine aminotransferase (ALT) and aspartate aminotransferase (AST) suggest?
obstructive picture - slightly raised ALT and AST in patients with cholestasis hepatic picture - if AST and ALT significantly higher compared to ALP -> suggests hepatocellular injury
133
What diameter should the bile duct normally be?
less than 6mm
134
What is MRCP and what is it used for?
MRI for the biliary system useful for biliary tree disease
135
How are asymptomatic gallstones managed?
conservatively
136
How are symptomatic gallstones managed?
cholecystectomy
137
What are some possible complications of cholecystectomy?
bleeding infection damage to bile duct damage to bowel and other organs VTE post-cholecystectomy syndrome
138
What is post-cholecystectomy syndrome?
non-specific symptoms after a cholecystectomy diarrhoea indigestion epigastric / RUQ pain nausea intolerance of fatty foods flatulence
139
What are some presenting features of colorectal cancer?
change in bowel habits - usually more loose and frequent rectal bleeding - bright red/melena abdominal pain/discomfort unexplained weight loss iron deficiency anaemia - microcytic, low ferritin -> SoB, fatigue bowel obstruction - if tumour obstructs the lumen -> severe pain, nausea, vomiting rectal/abdominal mass on examination
140
What are some risk factors for colorectal cancer?
FH of bowel cancer FAP - familial adenomatous polyposis HNPCC (Lynch syndrome) - hereditary nonpolyposis colorectal cancer IBD higher age diet low in fibre and high in red/processed meat obesity, sedentery lifestyle smoking alcohol
141
What is FAP (familial adenomatous polyposis)?
autosomal dominant condition mutation of tumour suppressor gene APC (adenomatous polyposis coli gene) formation of hundreds of polyps by 30-40 y.o. usually become cancerous by 40 y.o. prophylactic panproctocolectomy
142
What is HNPCC / Lynch syndrome?
hereditary non-polyposis colorectal cancer autosomal dominant most common form of inherited colorectal cancer mutations in DNA mismatch repair genes MLH1/MLH2 tumours in proximal colon, poorly differentiated and aggressive
143
What is FIT test?
faecal immunochemical test - type of faecal occult blood test which uses antibodies that specifically recognise human Hb
144
When is FIT test offered to patients?
as a part of bowel cancer screening programme: - every 2 years from 60-74 y.o. - if abnormal - colonoscopy test in GP for patients who do not meet the criteria for 2 week referral (e.g. only change in bowel habit, only weight loss etc.)
145
What are some criteria for the 2-week wait referral for colonoscopy?
positive FIT test and - abdominal mass - change in bowel habits - iron-deficiency anaemia - 40+ and unexplained weight loss and abdo pain - <50 with rectal bleeding and abdo pain/weight loss - 50+ and rectal bleeding/abdo pain/weight loss - 60+ and anaemia
146
How is bowel cancer investigated?
colonoscopy / sigmoidoscopy CT colonography - CT scan with bowel prep and contrast; if patient not fit for colonoscopy staging CT scan - CT TAP carcinoembryonic antigen (CEA) - tumour marker
147
How is tumour invasiveness staged?
T1 - submucosa involvement T2 - involvement of muscularis propria T3 - involvement of subserosa and serosa T4 - spread through the serosa
148
What surgical procedures are performed in bowel cancer?
right hemicolectomy left hemicolectomy high anterior resection low anterior resection abdomino-perineal resection Hartmann's procedure
149
What is right hemicolectomy?
removal of caecum, ascending colon, proximal transverse colon
150
What is left hemicolectomy?
removal of distal transverse and descending colon
151
What is high anterior resection?
removal of sigmoid colon
152
What is low anterior resection?
removal of sigmoid colon and upper rectum
153
What is abdomino-perineal resection?
removal of rectum and anus -> permanent colostomy
154
What is Hartmann's procedure?
usually emergency procedure removal of rectosigmoid colon (rectal stump sutured closed) can be reversed
155
What is low anterior resection syndrome?
after low anterior resection urgency and frequency of bowel movements faecal incontinence difficulty controlling flatulence
156
What treatments (other than surgery) can be used in bowel cancer?
radiation therapy chemotherapy targeted therapies - e.g. bevacizumab, cetuximab
157
What is constipation?
infrequent stools (<3x per week) difficult stool passage (straining, discomfort) incomplete defecation
158
How is constipation managed?
investigate and exclude any secondary causes, red flag symptoms exclude faecal impaction (faeces stuck in the rectum) lifestyle advice - increase fibre, ensure adequate liquid intake, ensure adequate activity levels laxatives - first-line: bulk-forming laxatives - e.g. ispaghula husk - second-line: osmotic laxatives - e.g. macrogol
159
What are the possible complications of constipation?
overflow diarrhoea acute urinary retention haemorrhoids
160
What are red flag symptoms in constipation?
neurological signs and symptoms, esp. in LL (spinal cord lesion) vomiting (obstruction) ribbon stool (anal stenosis) abnormal anus (anal stenosis, IBD) abnormal lower back, buttocks (spina bifida, spinal cord lesions) acute severe abdominal pain and bloating (obstruction)
161
What are diverticula?
blood vessels supplying the colon penetrate the circular muscle of the colon - areas of weakness if increased pressure - gaps form in these areas of circular muscle mucosa herniates through these gaps - formation of pouches (diverticula) they do NOT form in the rectum
162
What are the symptoms of diverticular disease?
altered bowel habit rectal bleeding abdominal pain
163
What are some complications of diverticular disease?
diverticulitis - inflammation of diverticula haemorrhage formation of fistula perforation + faecal peritonitis perforation + formation of abscess development of diverticular phlegmon
164
How is diverticular disease diagnosed?
colonoscopy / CT cologram / barium enema
165
How is diverticulitis classified based on the severity?
Hinchey severity classification: 1 - para-colonic abscess 2 - pelvic abscess 3 - purulent peritonitis 4 - faecal peritonitis
166
How is diverticular disease treated?
increase fibre intake ATB - if mild diverticulitis if more severe - draining of abscess / segmental resection
167
What is diarrhoea?
3+ loose/watery stools per day acute diarrhoea < 14 days Persistent diarrhoea 2-4 weeks chronic diarrhoea > 4 weeks
168
What are the common causes of acute diarrhoea?
gastroenteritis - abdo pain, nausea, vomiting diverticulitis - LQ pain, fever ATB therapy - more common in broad spectrum ATBs constipation causing overflow - alternating diarrhoea and constipation Medications - laxative overuse, metformin (esp. at the start of the treatment)
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What are the common causes of chronic diarrhoea?
IBS - abdo pain, bloating, change in bowel habit, fatigue ulcerative colitis - bloody diarrhoea, cramping abdo pain, weight loss, faecal urgency, tenesmus Crohn's - cramping abdo pain, mouth ulcers, obstruction colorectal cancer - rectal bleeding, anaemia, constitutional symptoms coeliac - lethargy, anaemia, weigh loss
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How is diarrhoea investigated?
stool sample if - patient systemically unwell and needs ATB / hospital admission - blood / pus in stool - immunocompromised - recent ATB, PPI, hospital admission - recent foreign travel - public health indication bloods - not routinely done - AKI, hypokalaemia, hyponatraemia if severe
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What are the features of small bowel obstruction?
vomiting first, then constipation diffuse central abdominal pain N+V (typically bilious vomiting) constipation lack of flatulence abdominal distention tinkling bowel sounds focal tenderness, guarding, rebound tenderness
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How is small bowel obstruction investigated?
abdo XR - distended small bowel loops (>3cm in diameter) with fluid levels CT with contrast - definitive investigation
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How is small bowel obstruction managed?
NBM IV fluids nasogastric tube with free drainage surgery
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What are the most common mechanical causes of small bowel obstruction?
- extramural - adhesions, hernias, neoplasm - mural - inflammatory strictures, Meckel's diverticulum - intraluminal - gallstone ileus, ingested foreign body
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What are the most common mechanical causes of large bowel obstruction?
extramural - diverticular disease, volvulus mural - colorectal adenocarcinoma intraluminal - faecal impaction
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What are the clinical features of large bowel obstruction?
constipation first, then vomiting absence of passing flatus / stool abdominal pain abdominal distention nausea and vomiting (feculent) peritonism (if also perforation)
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How is large bowel perforation investigated?
abdo XR CT with contrast
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How is large bowel perforation managed?
NBM IV fluids nasogastric tube with free drainage surgery - if symptoms after 72hrs of conservative management IV ATB - if perforation / surgery
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What are the 3 main categories of bowel ischaemia?
acute mesenteric ischaemia chronic mesenteric ischaemia ischaemic colitis
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What are the typical features of bowel ischaemia?
abdominal pain - often sudden onset, severe rectal bleeding diarrhoea fever elevated WBC - lactic acidosis
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How is bowel ischaemia investigated?
CT
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What is acute mesenteric ischaemia?
typically caused by an embolism -> occlusion of artery supplying the small bowel typically Hx of AF sudden onset severe pain
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How is acute mesenteric ischaemia managed?
urgent surgery poor prognosis tho
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What is ischaemic colitis?
acute but transient compromise in blood flow to the colon may lead to ulceration, inflammation, haemorrhage more likely to occur in "watershed" areas - e.g. splenic flexure
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How is ischaemic colitis investigated?
abdo XR - thumbprinting (due to mucosal oedema/haemorrhage)
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How is ischaemic colitis managed?
supportive management surgery - if conservative management fails or generalised peritonitis / perforation / ongoing haemorrhage
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What is chronic mesenteric ischaemia?
"intestinal angina" narrowing of mesenteric arteries by atherosclerosis intermittent abdominal pain
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What is the classical presentation of chronic mesenteric ischaemia?
central colicky abdominal pain after eating weight loss (due to food avoidance -> pain) abdominal bruit
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What are the risk factors for chronic mesenteric ischaemia?
higher age FH smoking diabetes high cholesterol HTN
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How is chronic mesenteric ischaemia diagnosed?
CT angiography
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How is chronic mesenteric ischaemia managed?
reduce modifiable risk factors secondary prevention (statins, antiplatelets) revascularisation (e.g. percutaneous mesenteric artery stenting, open surgery like bypass grafting)
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What are the most common causative organisms of gastroenteritis?
viruses: rotavirus norovirus adenovirus (also causes respiratory symptoms)
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What signs on general inspection can a patient with colorectal cancer have?
pallor cachexia koilonychia
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What are the features of haemorrhoids?
painless rectal bleeding pruritus - itch pain soiling
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What are the two main types of haemorrhoids?
internal - above dentate line, do not cause pain external - below dentate line, prone to thrombosis, may be painful
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How are internal haemorrhoids graded?
grade 1 - do not prolapse out of the anal canal grade 2 - prolapse on defecation, reduce spontaneously grade 3 - can be manually reduced grade 4 - cannot be manually reduced
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How are haemorrhoids managed?
stool softening - increase fibre and fluid intake topical local anaesthetics and steroids rubber band ligation
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What will DRE show in mechanical bowel obstruction?
collapsed rectum
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What will DRE show in functional bowel obstruction?
distended rectum
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What does neoadjuvant chemotherapy mean?
chemotherapy started before surgery to shrink the tumour
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When do you give ATBs in gastroenteritis?
if high risk: - elderly - immunocompromised - systemically unwell
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What is the most common cause of bacterial gastroenteritis?
campylobacter - bloody diarrhoea -
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How does gastroenteritis typically present?
N+V (bloody) diarrhoea dehydration abdominal pain
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What are the features of bacterial gastroenteritis?
bloody diarrhoea little vomiting fever abdominal pain
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What are the features of viral gastroenteritis?
watery diarrhoea vomiting can have fever can have abdo pain
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What is Peutz-Jeghers syndrome?
autosomal dominant numerous hamartomatous polyps in GI tract pigmented freckles on lips, face, palms, soles often small bowel obstruction conservative management
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How is bowel obstruction initially managed?
Nil-by-mouth (NBM) IV fluids & correct electrolyte disturbances (‘drip’) Nasogastric tube (NG tube) to decompress the bowel (‘suck’) and prevent aspiration Urinary catheter for fluid balance Analgesia as required with suitable anti-emetics VTE prophylaxis (high risk of DVT given cancer diagnosis) Antibiotics
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