Gastro Flashcards

1
Q

Virchows triad

A

Inflammation
Endothelial injury
Hypercoagulability

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2
Q

Position of splenic vein in relation to pancreas

A

Posterosuperior border of pancreas

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3
Q

causes of raised amylase

A

Acute pancreatitis
Pancreatic psuedocyst
Mesenteric infract
DKA
Perforated viscus
Acute cholecystitis

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4
Q

Factors indicating severe pancreatitis

A

age >55 years
Hyperglycemia
Hyperlipidemia
Hypoxia
Hypocalcemia
elevated LDH and AST
Neutrophilia

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5
Q

Viruses causing pancreatitis

A

Mumps
Coxsacki B virus

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6
Q

Autoimmune cause of pancreatitis

A

PAN

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7
Q

Metabolic causes ofpancreatitis

A

hyperglycemia
Hypertriglycridemia
Hypothermia(by inducing SIRS and reducing blood flow to pancreas and initiating inflammatory response)
Hypercalcemia

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8
Q

Drugs causing pancreatitis

A

azathioprine, mesalazine*, didanosine, bendroflumethiazide, furosemide, pentamidine, steroids, sodium valproate
Pt taking mesalazine are 7 times more prone to disease than on sulfasalazine

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9
Q

how pancreatitis causes ARDS

A

The inflammatory process in acute pancreatitis leads to the release of pro-inflammatory cytokines such as TNF-alpha, IL-1, and IL-6 into the systemic circulation. These cytokines induce a systemic inflammatory response syndrome (SIRS), which increases vascular permeability and results in pulmonary oedema. Additionally, activated pancreatic enzymes can cause direct injury to alveolar-capillary membranes, exacerbating inflammation and leading to diffuse alveolar damage characteristic of ARDS. Management follows UK guidelines which include supportive care with mechanical ventilation using lung-protective strategies, fluid management to avoid volume overload, and addressing the underlying cause of pancreatitis.

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10
Q

Investigations for pseudocyst of pancreas

A

Investigation is with CT, ERCP and MRI or endoscopic USS

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11
Q
A
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12
Q

What is acute pancreatitis?

A

Acute pancreatitis is an inflammatory condition of the pancreas that occurs suddenly and can be severe.

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13
Q

What are the two most common causes of acute pancreatitis?

A

The two most common causes are gallstones and chronic and excessive alcohol consumption.

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14
Q

True or False: Acute pancreatitis can be caused by medications.

A

True

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15
Q

Fill in the blank: The classic presentation of acute pancreatitis includes severe ______ pain.

A

abdominal

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16
Q

What laboratory test is most indicative of acute pancreatitis?

A

Elevated serum amylase and lipase levels.

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17
Q

Which imaging study is preferred for diagnosing acute pancreatitis?

A

Abdominal ultrasound is preferred for detecting gallstones; CT scan is used for assessing complications.

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18
Q

What is the Ranson criteria used for?

A

The Ranson criteria are used to assess the severity and prognosis of acute pancreatitis.

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19
Q

True or False: Patients with acute pancreatitis should be given oral food intake immediately.

A

False

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20
Q

What is the initial management step in acute pancreatitis?

A

The initial management step is supportive care, including fluid resuscitation and pain management.

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21
Q

What is the role of antibiotics in the management of acute pancreatitis?

A

Antibiotics are not routinely used unless there is evidence of infected pancreatic necrosis.

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22
Q

Which complication is associated with severe acute pancreatitis?

A

Pancreatic necrosis, abscess formation, and systemic inflammatory response syndrome (SIRS).

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23
Q

What is the significance of a patient’s age in acute pancreatitis prognosis?

A

Older age is associated with a higher risk of complications and poorer prognosis.

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24
Q

Fill in the blank: The presence of ______ in the blood can indicate a severe case of acute pancreatitis.

A

elevated CRP levels

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25
Q

What lifestyle change can help prevent recurrent acute pancreatitis?

A

Avoiding alcohol consumption.

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26
Q

True or False: Surgical intervention is often the first line of treatment in acute pancreatitis.

A

False

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27
Q

What is the ‘pancreatic rest’ approach in the management of acute pancreatitis?

A

The ‘pancreatic rest’ approach involves nil per os (NPO) status to minimize pancreatic stimulation.

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28
Q

Which scoring system is used to predict mortality in acute pancreatitis?

A

APACHE II scoring system.

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29
Q

Fill in the blank: Patients with acute pancreatitis should be monitored for ______ failure.

A

respiratory

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30
Q

What is the term for the collection of fluid surrounding the pancreas after acute pancreatitis?

A

Pancreatic pseudocyst.

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31
Q

What dietary changes are recommended after recovery from acute pancreatitis?

A

A low-fat diet and avoidance of alcohol.

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32
Q

True or False: Acute pancreatitis can resolve on its own without treatment.

A

True, in mild cases.

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33
Q

What is the role of ERCP in acute pancreatitis management?

A

ERCP is used to remove stones from the bile duct if they are causing pancreatitis.

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34
Q

What is a common symptom that may indicate a complication of acute pancreatitis?

A

Persistent fever or increasing abdominal pain.

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35
Q

What is the ‘3-day rule’ in the context of acute pancreatitis management?

A

If a patient does not improve within 3 days, further investigation is warranted.

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36
Q

Fill in the blank: The ______ sign is a physical exam finding associated with acute pancreatitis.

A

Cullen’s

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37
Q

What does GERD stand for?

A

Gastroesophageal reflux disease

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38
Q

True or False: GERD is characterized by the retrograde flow of gastric contents into the esophagus.

A

True

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39
Q

What is a common symptom of GERD?

A

Heartburn

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40
Q

Which diagnostic test is often used to confirm GERD?

A

24-hour pH monitoring

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41
Q

Name a lifestyle modification that can help manage GERD symptoms.

A

Avoiding large meals

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42
Q

What class of medication is typically used first-line for GERD treatment?

A

Proton pump inhibitors (PPIs)

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43
Q

What is the primary cause of peptic ulcers?

A

Helicobacter pylori infection

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44
Q

Fill in the blank: The most common complication of peptic ulcers is __________.

A

Hemorrhage

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45
Q

True or False: Nonsteroidal anti-inflammatory drugs (NSAIDs) can contribute to the development of peptic ulcers.

A

True

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46
Q

What is the hallmark symptom of a duodenal ulcer?

A

Epigastric pain that improves with food

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47
Q

What imaging study is typically used to evaluate peptic ulcers?

A

Upper gastrointestinal endoscopy

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48
Q

What is the treatment regimen for H. pylori eradication?

A

Triple therapy: PPI, amoxicillin, and clarithromycin

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49
Q

What condition is characterized by the presence of multiple gastric ulcers?

A

Zollinger-Ellison syndrome

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50
Q

Name one risk factor for developing gastric cancer.

A

Chronic gastritis

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51
Q

What is the primary symptom of gastric cancer?

A

Weight loss

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52
Q

True or False: Linitis plastica is a type of gastric cancer that presents with a thickened gastric wall.

A

True

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53
Q

What type of imaging is preferred for staging gastric cancer?

A

CT scan of the abdomen

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54
Q

What is the role of endoscopic ultrasound in gastric cancer?

A

To assess the depth of invasion and lymph node involvement

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55
Q

What is the most common type of esophageal cancer?

A

Adenocarcinoma

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56
Q

Fill in the blank: Achalasia is characterized by __________ of the lower esophageal sphincter.

A

Increased tone

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57
Q

What is a common symptom of achalasia?

A

Dysphagia for solids and liquids

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58
Q

What diagnostic test is used to confirm achalasia?

A

Esophageal manometry

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59
Q

True or False: Surgical myotomy is a treatment option for achalasia.

A

True

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60
Q

What is the most common cause of esophagitis?

A

Reflux disease

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61
Q

What is a potential complication of severe esophagitis?

A

Stricture formation

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62
Q

What is the mainstay treatment for esophagitis caused by reflux?

A

Proton pump inhibitors (PPIs)

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63
Q

Name one infectious cause of esophagitis.

A

Candida infection

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64
Q

True or False: Eosinophilic esophagitis is associated with food allergies.

A

True

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65
Q

What is the primary treatment for eosinophilic esophagitis?

A

Elimination diet or topical corticosteroids

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66
Q

What is the main symptom of a hiatal hernia?

A

Heartburn

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67
Q

What type of hiatal hernia is most common?

A

Sliding hiatal hernia

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68
Q

Fill in the blank: A __________ is a protrusion of the stomach through the diaphragm.

A

Hiatal hernia

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69
Q

What is the primary treatment for symptomatic hiatal hernia?

A

Lifestyle modifications and PPIs

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70
Q

What is the name of the procedure to correct a hiatal hernia?

A

Nissen fundoplication

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71
Q

True or False: Barrett’s esophagus is a precancerous condition associated with chronic GERD.

A

True

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72
Q

What is the primary method for diagnosing Barrett’s esophagus?

A

Endoscopy with biopsy

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73
Q

What is the risk associated with Barrett’s esophagus?

A

Increased risk of esophageal adenocarcinoma

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74
Q

What is the initial management for Barrett’s esophagus?

A

Regular surveillance endoscopies

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75
Q

What is the common name for the condition characterized by esophageal webs?

A

Plummer-Vinson syndrome

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76
Q

Fill in the blank: The classic triad of Plummer-Vinson syndrome includes dysphagia, iron deficiency anemia, and __________.

A

Esophageal webs

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77
Q

What is the treatment for Plummer-Vinson syndrome?

A

Iron supplementation and dilation of esophageal webs

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78
Q

What is the primary cause of esophageal varices?

A

Portal hypertension

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79
Q

True or False: Esophageal varices can lead to life-threatening hemorrhage.

A

True

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80
Q

What is the first-line treatment for acute variceal hemorrhage?

A

Endoscopic variceal band ligation

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81
Q

What medication is used to reduce portal pressure in variceal hemorrhage?

A

Vasopressin or octreotide

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82
Q

What is a common complication of untreated varices?

A

Rebleeding

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83
Q

Fill in the blank: The __________ is a muscular tube that connects the throat to the stomach.

A

Esophagus

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84
Q

Genetic causes of chronic pancreatitis

A

cystic fibrosis
hemochromatosis

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85
Q

can we rely on enzyme assay in chronic pancretitis?

A

No because cells producing those enzymes are destroyed and there is fibrosis that obstructs

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86
Q

Diagnostics for chronic pancreatitis

A

we use a combination of patient history (including symptoms like recurrent abdominal pain), imaging studies such as CT or MRI scans which can show structural changes in the pancreas, and sometimes more advanced tests like endoscopic ultrasound or ERCP. In some cases, functional testing using secretin stimulation test may also be used.

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87
Q

Chronic pancreatitis complications

A

Osteoporosis
PUD
Diabetes (type 3c)
Steatorrhea

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88
Q

Common location for pancreatic cancer

A

Head of pancreas

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89
Q

Investigation of choice for pancreatic cancer

A

HRCT
(double duct sign)

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90
Q

Association of pancreatic cancer

A

increasing age
smoking
diabetes
chronic pancreatitis (alcohol does not appear an independent risk factor though)
hereditary non-polyposis colorectal carcinoma
multiple endocrine neoplasia
BRCA2 gene
KRAS gene mutation

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91
Q
A
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92
Q

Complications of c.diff

A

Toxic megacolon
Bowel perfortaion
Sepsis
Pseudomembranous colitis

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93
Q

Amtibiotics causing c.diff infection

A

Clindamycin
Cephalosporin
Ceftriaxone
Mero

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94
Q

First line antibiotic for c.diff

A

Vanco
2nd: Febuxostat

(Supportive care, isolation for 48hr)

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95
Q
A
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96
Q

Colon cancer commonly metastasize to

A

Liver

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97
Q

Rectal cancer metastasize commonly to

A

Lungs

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98
Q

Apple core sign on barium enema

A

Colorectal cancer

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99
Q

Difference between FAP and HNPCC

A

FAP on left side and full of polyps
HNPCC on right side (proximal colon) and no polyps and remain asymptomatic until last stage bcs no polyps found and only occult bleeding
Colonoscopy doesnt really help with HNPCC

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100
Q

HbsAg positive
Anti- Hbc positive

A

Carrier

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101
Q

HbsAg positive

A

Acute hepatitis

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102
Q

Diagnosis of carcinoidd ssydrome

A

Octreotide scan
Urinary 5HIAA
Nicain levels

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103
Q

Gene involved in hemochromatosis

A

HFE gene on both copies of chromosome 6

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104
Q

Iron profile in hemochromatosis

A

transferrin saturation > 55% in men or > 50% in women
raised ferritin (e.g. > 500 ug/l) and iron
low TIBC

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105
Q
A
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106
Q

HbsAg negative
Anti-Hbs positive

A

Immunized

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107
Q

Anti-Hbc positive
HbsAg negative

A

Previous hep B positive and not a carrier

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108
Q

Bronze skin pigmentation

A

Hemochromatosis

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109
Q
A
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110
Q

HbsAg +
HbeAg +
Anti-HbC igG +

A

Chronic hepatitis

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111
Q
A
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112
Q

Causes of UC flares

A

Stress
NsAIDS
STEROIDS
Cessation of smoking

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113
Q
A
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114
Q

Watershed areas

A

Splenic flexure
Rectosigmoid junction

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115
Q

Griffith’s point

A

Splenic flexure

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116
Q

Why watershed areas are prone to ischemia

A

Due to their location at furthest point from arterial supply

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117
Q

Thumbprinting is a sign of

A

Ischemic colitis

118
Q

Ischemic colitiss affect what area

A

Watershed areas

119
Q

Ischmic colitis leads to

A

Infoammation
Ulceration
Haemorrhage

120
Q

Why thumbprinting is seen

A

Due to mucosal edema and haemorrhage

121
Q

10-25 years
Neurological symptoms (basal gqmglia)
Sp3eeech disturbance
KF rings
RTA
Blue nails
Excessive salivation
Family hx of liver disease

A

Wilson’s disease

123
Q

Management for wilsons

A

Penicillamine
Trinetine hydrochloride
Tetrathiomolybdate

125
Q

Wjich antiviral is contraindicated in pregnancy

126
Q

Antiviral that can be given in preg hepatitis

A

Lamivudine
Tenofovir

129
Q

Glasgow-Blatchford score at first assessment

A

helps clinicians decide whether patients can be managed as outpatients or not

130
Q

Rockall score is used after endoscopy

A

provides a percentage risk of rebleeding and mortality
includes age, features of shock, co-morbidities, aetiology of bleeding and endoscopic stigmata of recent haemorrhage

132
Q

Painless bleeding
Old age
Do not cause pain on defecation
O/E reveal lesion on proctoscopy

A

Rectal polyp

133
Q

A triad of abd pain, hepatomegaly and ascites

A

Budd chiari syndrome

134
Q

Initial radiological investigation for budd chiari syndrome

A

U/S WITH DOPPLER

135
Q

Causes of budd chiari syndrome

A

polycythaemia rubra vera
thrombophilia: activated protein C resistance, antithrombin III deficiency, protein C & S deficiencies
pregnancy
combined oral contraceptive pill: accounts for around 20% of cases

136
Q

Differentiate between cholestatic and hepatic cuase on labs

A

proportionate rise in ALT > proportionate rise in ALP = hepatitic
proportionate rise in ALT < proportionate rise in ALP = obstructive/cholestatic

137
Q

Whats a cholestatic picture on the LFTs

A

cholestatic: initially raised ALP and GGT, then raised serum direct bilirubin as it spills over into blood and urine.

138
Q

biliary disease in patients with HIV is sclerosing cholangitis due to which infections

A

CMV, Cryptosporidium and Microsporidia

139
Q

cholestasis
jaundice, pruritus
raised bilirubin + ALP
right upper quadrant pain
fatigue
ANA and pANCA positive
HIV related

140
Q

Type of cells in gastric adenocarcinoma

A

Signet ring cells

141
Q

Risk factors for gastric cancer

A

Helicobacer pylori
triggers inflammation of the mucosa → atrophy and intestinal metaplasia → dysplasia
pernicious anaemia, atrophic gastritis
diet
salt and salt-preserved foods
nitrates
ethnicity: Japan, China
smoking
blood group A

142
Q

lymphatic spread of gastric cancer

A

left supraclavicular lymph node (Virchow’s node)
periumbilical nodule (Sister Mary Joseph’s node)

143
Q

HFE on chromosome 6 autosomal recessive

A

Haemochromatosis

144
Q

ATP7B on chromosome 13 -

A

Wilson’s disease
autosomal recessive

145
Q

HFE gene responsible for what

A

iron storage in body

146
Q

why serum ferritin is unreliable in diagnosis of hemochromatosis

A

because it is an acute phase reactant and can be raised in any other inflammation in body

147
Q

Typical iron study profile in patient with haemochromatosis

A

transferrin saturation > 55% in men or > 50% in women
raised ferritin (e.g. > 500 ug/l) and iron
low TIBC

148
Q

to confirm diagnosis of hemochromatosis

A

molecular genetic testing for the C282Y and H63D mutations
MRI is generally used to quantify liver and/or cardiac iron
liver biopsy is now generally only used if suspected hepatic cirrhosis

149
Q

Management for severe colitis

A

should be treated in hospital
IV steroids are usually given first-line
IV ciclosporin may be used if steroids are contraindicated
if after 72 hours there has been no improvement, consider adding IV ciclosporin to IV corticosteroids or consider surgery

150
Q

if the patient has abdominal pain relieved by defecation or associated with altered bowel frequency stool form, in addition to 2 of the following 4 symptoms:
altered stool passage (straining, urgency, incomplete evacuation)
abdominal bloating (more common in women than men), distension, tension or hardness
symptoms made worse by eating
passage of mucus

151
Q

Redflags for IBS

A

rectal bleeding
unexplained/unintentional weight loss
family history of bowel or ovarian cancer
onset after 60 years of age

152
Q

investigations for IBS

A

CBC
ESR/CRP
coeliac disease screen (tissue transglutaminase antibodies)

153
Q

Extra intestinal manifestaion of IBD

A

Arthritis
skin lesions
Gall stones
PSC (uc)
Oral ulcers

154
Q

ASCA positive in

155
Q

pANCA positive in

156
Q

Riskfactor for barrets

A

gastro-oesophageal reflux disease (GORD) is the single strongest risk factor
male gender (7:1 ratio)
smoking
central obesity

157
Q

Test to assess exocrine function of pancreas

A

fecal elastase

158
Q

Risk factors for HCC

A

liver cirrhosis, for example secondary* to hepatitis B & C, alcohol, haemochromatosis and primary biliary cirrhosis
alpha-1 antitrypsin deficiency
hereditary tyrosinosis
glycogen storage disease
aflatoxin
drugs: oral contraceptive pill, anabolic steroids
porphyria cutanea tarda
male sex
diabetes mellitus, metabolic syndrome

159
Q

wilson is not a risk factor for which cancer

160
Q

symptomatic relief of pruritis

A

Cholestyramine

161
Q

It may be considered in patients who do not adequately respond to ursodeoxycholic acid for PBC , or in those with advanced disease, but is not used as a first-line treatment option.

A

Prednisolone

162
Q

Diarrhoea + hypokalaemia →

A

villous adenoma

163
Q

Adenoma, metabolic acidosis and hypokalemia

A

Villous adenoma

164
Q

On sigmoidoscopy or colonoscopy, villous adenomas appear as

A

cauliflower like growth

165
Q

Metabolic ketoacidosis with normal or low glucose:

A

think alcohol

166
Q

3 causes of raised ketones

A

Diabetes
starvation
Alcohol

167
Q

glucose > 11mmol/L (or known diabetes), pH < 7.3, bicarbonate < 15mmol/L and ketones > 3mmol/L. This patient does not have a history of diabetes and is not taking drugs that could cause euglycaemic diabetic ketoacidosis

168
Q

Metabolic acidosis
Elevated anion gap
Elevated serum ketone levels
Normal or low glucose concentration

A

Alcoholic diabetic ketoacidosis

169
Q

treatment for alcoholic ketoacidosis

A

infusion of saline & thiamine. Thiamine is required to avoid Wernicke encephalopathy or Korsakoff psychosis.

170
Q

Charcots triad

A

RUQ pain
Jaundice
Fever high hrade with rigor and chills

171
Q

Reynold Pentad

A

RUQ pain
hypotension
Jaundice
Confusion
Fever

172
Q

complication of ileocecal resection

A

bile acid malabsorption

173
Q

diagnosis for bacterial gastroenteritis

A

stool culture positive

174
Q

confirmed NAFLD and an ELF score >10.51 diagnosis

A

liver fibrosis.

175
Q

metabolic syndrome

A

HTN
DM
Obesity

176
Q

Hepatic steatosis on u/s seen as

A

Echogenicity

177
Q

normal AST:ALT

A

less than 1 if elevated indicate liver fibrosis

178
Q

diagnosis and monitoring of NAFLD. It made the following suggestions if the ELF blood test was not available:

A

FIB4 score or NALFD fibrosis score
these scores may be used in combination with a FibroScan (liver stiffness measurement assessed with transient elastography)

179
Q

effect of vipoma

A

WDHA (Watery diarrhea, Hypokalemia, Achlorhydria) also called Verner-Morrison

180
Q

triad of ovarian fibroma, ascites, and pleural effusions.

A

Meigs syndrome

181
Q

Ascitic fluid analysis in a patient with spontaneous bacterial peritonitis would reveal

A

a raised white cell count with predominantly neutrophils.

182
Q

Diarrhoea - biospy shows pigment laden macrophages =

A

laxative abuse

183
Q

Treatment for eosinophilic esophagitis

A

Diet (elemental diet)
Drugs (PPI+ steroids i.e fluticasone or budesonide)
Dilatation

184
Q

somatostatin secreted from

185
Q

CCK secreted from

A

I cells of upeer small intestine

186
Q

S cells

A

These cells secrete secretin a bicarbonate-rich fluid from the pancreas and hepatic cells and are stimulated by fatty acids.

187
Q

Internal hemorrhoids are located above dentate line and are supplied by

A

splanchnic nerves

188
Q

external hemorrhoids by

A

pudendal nerve (s2-s4) hence are painful.

189
Q

CXR findings of achalasia

A

widened mediastinum or an air-fluid level in the oesophagus

190
Q

squamous cell carcinoma of esophagus

A

sensitive to radiotherapy

191
Q

Raised IgG
Raised transaminases
With mild change in ALP

A

Autoimmune hepatitis

193
Q

Drugs that should not be given in pt with IBS

195
Q

First line treatment for hepatorenal syndrome

A

Terlipressin

196
Q

Lab findings for AIH

A

Raised AsT AlT but ALP almost normal
Raised IgG
Antibodies positive
Hypergammaglobulinemia

198
Q

: Histopathological findings in autoimmune hepatitis include

A

interface hepatitis with lymphoplasmacytic infiltrate and rosette formation of hepatocytes

199
Q

Causes of SCC of esophagus (ASAP)

A

Alcohol
Smoking
Achalasia
Plummer winson

200
Q

Drugs causing liver cirrhosis (MMA)

A

Methotrexate
Methyldopa
Amiadrone

201
Q

Nitrofurantoin

A

can work against gram-positive and gram-negative antibiotics and is often the first-line treatment for uncomplicated urinary tract infections. Unfortunately, a potential side effect is an acute hepatitis and hepatic failure, rather than cholestasis.

202
Q

imaging modality of choice for chronic pancreatitis.

A

CT pancreas. will show calcification in pancreas

203
Q

is a rare systemic auto-inflammatory disease characterised by the classic triad of fevers, joint pain, and a distinctive salmon-coloured bumpy rash.

A

Adult-onset Still’s disease

204
Q

best investigation to differentiate hydatid cysts from amoebic and pyogenic cysts

205
Q

classical triad of; biliary colic, jaundice, and urticaria

A

Biliary rupture of hydatid cyst

206
Q

Serology test for hydatid cyst

A

ELISA
(combined with imaging studies such as ultrasound, CT or MRI scans for a more accurate diagnosis according to UK management guidelines.)

207
Q

pre- and post-operatively for hydatid disease

A

Albendazole and definitive is surgery

208
Q

drug of choice for amoebic abscesses.

A

Metronidazole

209
Q

Pyogenic liver abscesses treatment

A

require drainage and antibiotics, often a combination of metronidazole with a cephalosporin or quinolone

210
Q

hallmark symptom of refeeding syndrome

A

Refeeding syndrome

211
Q

Wernicke enceph triad

A

Ataxia
“Mental confusion
Ophthalmoplegia

212
Q

Korsakoff syndrome

A

Ante and retrograde amnesia
Confabulations
Amnesia

213
Q

ECG changes for refeeding syndrome

A

Torsades-des-pointes secondary to hypomagnesaemia can result as a consequence of refeeding syndrome
Uwaves and flattening of T waves as a result of hypokalemia

214
Q

common complication
of TIPSS

A

exacerbation of hepatic encephalopathy

215
Q

Drug used in exacerbation of UC

A

Oral azathioprine
Oral mercaptopurine

216
Q

During Endoscopy for H pylori.

217
Q

only test recommended for H. pylori post-eradication therapy

A

Urea breath test

218
Q

STK11/LKB1 mutation

219
Q

Risk factors for SBP

A

Varices
Advanced cirrhosis
Use of PPI
Previous episode of SBP
Malnutrition

220
Q

Organism causing SBP

A

E.coli
Gram negative ones commonly

221
Q

________ is more common than vitamin B12 deficiency in coeliac disease)

A

Folate def:

222
Q

Serology of coeliac

A

tissue transglutaminase (TTG) antibodies (IgA) are first-choice according to NICE
endomyseal antibody (IgA)
needed to look for selective IgA deficiency, which would give a false negative coeliac result

223
Q

Gold standard for diagnosis of coeliac

A

Endoscopic intestinal biopsy that shows
villous atrophy
crypt hyperplasia
increase in intraepithelial lymphocytes
lamina propria infiltration with lymphocytes

224
Q

is the investigation of choice for suspected carcinoid tumours

A

Urinary 5-HIAA

225
Q

Gilberts syndrome

A

Mutation of UDGT1A1

226
Q

Raised level of unconjugated bilirubin(17- 100) with normal LFTs

A

Gilberts syndrome

227
Q

s jaundice, which can be intermittent and often precipitated by factors such as fasting, dehydration, stress, physical exertion or illness. Associated symptoms can include mild abdominal discomfort and fatigue but many individuals are asymptomatic.

A

Gilbert syndrome
(Autosomal recessive)

228
Q

Test to evaluate RTA

A

Ammonium chloride acidification test

229
Q

Flushing, diarrhoea, bronchospasm, tricuspid stenosis, pellagra →

A

carcinoid with liver mets - diagnosis: urinary 5-HIAA

230
Q

secondary prophylaxis of hepatic encephalopathy

A

Lactulose
Rifaximin

231
Q

melanosis coli which is characterised by a brown-black discolouration of the colon due to lipofuscin deposition in macrophages within the lamina propria.

A

Laxative abuse

232
Q

Diagnostic test small bowel bacterial overgrowth syndrome

A

Hydrogen breathe test

233
Q

Management for SBBOS

A

Rifaximin
Coamoxiclav
Metronidazole

234
Q

neonates with congenital gastrointestinal abnormalities
scleroderma
diabetes mellitus

A

Risk factors for SBBOS

235
Q

Infertility is sulphasalazine or mesalazine

A

Sulphasalazine
(S for Sperm and S for Sulphasalazine)

236
Q

Neurological causes of dysphagia

A

CVA
Parkinson’s disease
Multiple Sclerosis
Brainstem pathology
Myasthenia Gravis

237
Q

Dysphagia for both solids and liquids
Ptosis
Extraocular m/s weakness

A

Myasthenia Gravis

238
Q

biomarker for neutrophilic infiltration and inflammation within the colon. Elevated levels are often seen in inflammatory bowel disease;

A

Fecal calprotectin

239
Q

Organisms which may colonise CF patients

A

Staphylococcus aureus
Pseudomonas aeruginosa
Burkholderia cepacia*
Aspergillus

240
Q

Diarrhoea, weight, arthralgia, lymphadenopathy, ophthalmoplegia ?

A

Whipple’s disease

241
Q

Previous hepatitis B infection, not a carrier, would be indicated by a

A

positive Anti-HBs and Anti-HBc, and negative HBs antigen

243
Q

HNPCC screening started when

A

At 25years of age
Or 5 years prior the last member was diagnosed

244
Q

increases secretion of bicarbonate-rich fluid from pancreas and hepatic duct cells

245
Q

inhibits gastric acid secretion and absorption from the intestine while promoting smooth muscle relaxation and blood flow

246
Q

Causes of hypoalbuminemia

A

Liver disease
Renal disease
Malnutrition
Sepsis
Burns

247
Q

For assessing mural invasion what test to be done

A

Endoscopic ultrasound

249
Q

Complication of patients on clindamycin for cellulitis that they must be warned about

252
Q

Chief cells secrete what

A

pepsin, a proteolytic enzyme

253
Q

Red flag features in IBS

FOUR

A

F - Family history of bowel or ovarian cancer

O - Onset after 60 years of age

U - Unintentional/unexplained weight loss

R - Rectal bleeding

254
Q

Angiodyssplasia associated with what heart condition

A

Aortic stenosis

255
Q

Heydes syndrome

A

Angiodysplasia
Aortic stenosis

257
Q

Cause of heyde syndrome

A

Aquifer vwF def

258
Q

Management of angiodysplasia

A

endoscopic cautery or argon plasma coagulation
antifibrinolytics e.g. Tranexamic acid
oestrogens may also be used

259
Q

Diagnosis of angiodysplasia by

A

Colonoscopy
Mesenteric angiography if acute bleeding

260
Q

Microscopic colitis presents with what on histology

A

Intraepithelial lymphocytes >20 per 100 epithelial cells

261
Q

Adverse effects of PPI

A

Hypomagnesemia
Hyponatremia
Osteoporosis
Microscopic colitis
Increased risk of c.diff infection

262
Q

_______ are used to monitor treatment in haemochromatosis

A

Ferritin and transferrin saturation

266
Q

Antibiotics having known interaction wwith alcohol

A

Metronidazole
Tinidazole

267
Q

In suspected SBP- diagnosis is by paracentesis.

A

Confirmed by neutrophil count >250 cells/ul

268
Q

used in the management of Crohn’s disease and ulcerative colitis by mitigating the inflammation process.

A

5- aminosalicylic acid

269
Q

Recurrent episode of c.diff toxin

A

With 12wks: oral fidaxomicin
After 12 wks: oral vanco or fidaxo

272
Q

perianal itching, particularly at night
girls may have vulval symptoms

A

Threadworms

273
Q

Threadworm management

A

CKS recommend a combination of anthelmintic with hygiene measures for all members of the household
mebendazole is used first-line for children > 6 months old. A single dose is given unless infestation persists

274
Q

Palpable gall bladder with painless jaundice

A

Courvosiers sign
Positive in cholangiocarcinoma

275
Q

Other than antibiotics what is the risk factor for CDI

276
Q

Chronic anal fissure - treatment

A

topical glyceryl trinitrate

277
Q

How does topical glyceryl trinitrate work

A

It works by relaxing the internal anal sphincter, which reduces pressure and increases blood flow to promote healing of the fissure. Its side effects can include headaches or dizziness due to systemic absorption.

278
Q

it is essential for these patients to receive regular immunisations for coeliac patient

A

because they develop hyposplenism which increases their risk to develop infections

279
Q

What clotting factors produced from liver

A

Liver produces clotting factors II, V, VII, IX and X and they are vit K dependent

280
Q

Diarrhoea - biospy shows pigment laden macrophages =

A

laxative abuse

281
Q

Amylase:

A

breaks starch down to sugars

282
Q

NAAT testing for

A

Chlamydia
Herpes

283
Q

type of pneumonia involved in reactivation of type 1 HSV

A

s. pneumonia

284
Q

Investigation of choice for herpes

285
Q

treatment for acyclovir

A

suppressive therapy and oral acyclovir
started after 36wks of gestation
delivery via c section

286
Q

N.gonorrhea is a gram ____

A

negative diplococci

287
Q

Treatment for influenza

A

only in immunocompromised individual
first ine : Oseltamivir
2nd line: Zanamivir

288
Q

Organism involved in hand foot and mouth disease

A

enterovirus
coxsackie A16 virus
highly contagious

289
Q

Helminthic conditions treatment of choice

A

Bendezoles
Ivermectin

290
Q

Treatment for Hep B

A

Interferon alpha 2a
second line: tenofovir, entecavir or telbivudine