GI Flashcards

1
Q

hemochromatosis diagnosis

treat with

A

elevated transferrin sat, ferritin>1000

phlebotomy

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2
Q

chronic diarrhea 2/2 malabsorption of artificial sweeteners

A

diarrhea, bloating, elevated osmotic gap

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3
Q

SAAG 1.1 or greater+ ascitic protein of 2.5 or greater

cirrhosis/portal htn

A

cardiac cause of ascites

ascitic protein <2.5

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4
Q

SBP treatment

A

3rd gen cephalosporin and albumin (1.5g/kg on day of diagnosis, 1g/kg on day 3)

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5
Q

dyspepsia + alarm features

A

age>50 yo, anemia, dysphagia, odynophagia, vomiting, weight loss, family history of cancer, PUD, gastric surgery->scope

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6
Q

No alarm features, endemic h. pylori

not endemic h. pylori
partial response to PPI
if still refractory with normal scope

A

test for h. pylori, treat

PPI
increase dose to twice daily
ph monitoring->fundoplication

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7
Q

AKI in the setting of cirrhosis

A

25% albumin challenge, then midodrine and octreotide (rule out ATN with urinalysis first)

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8
Q

ulcer with arterial spurting or a nonbleeding visible vessel

A

clips, thermal therapy or sclerosants

clean based ulcers don’t need to be treated

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9
Q

primary sclerosing cholangitis
diagnosis

look for

A

ANA, anti-smooth muscle
MRCP-beads on a string

ulcerative colitis (colonoscopy)

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10
Q

chronic NSAID use

A

start omeprazole 20mg or misoprostol

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11
Q

chronic pancreatitis

A

clinical features (pain, recurrent attacks of pancreatitis, weight loss) with objective findings of steatorrhea and pancreatic calcifications

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12
Q

chronic diarrhea, abdominal pain, and malabsorption

confirm with

A

test for celiac with tissue transglutaminase antibodies
small bowel biopsy: intraepithelial lymphocytosis, crypt hyperplasia, and villous blunting
also elevated LFTs

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13
Q

irritable bowel syndrome studies

A

no testing/imaging/procedures

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14
Q

unexplained liver disease in patient <40 yo (+hemolytic anemia)
screen
diagnosis

A

consider Wilson disease
low alk phos, elevated ASTs
low ceruloplasmin , elevated urine copper excretion
liver biopsy

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15
Q

Budd-chiari

A

ascites

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16
Q

gallbladder polyp> 1cm

any polyp+ symptomatic OR PSC OR gallstones

A

cholecystectomy

chole

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17
Q

pancreatitis + presence of gallstones (obstructing or not, cholecystitis or not)

A

chole

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18
Q

Crohns flare while preggo

A

certolizumab (preferred), infliximab, adalimumab (anti-TNF agents)
5-aminosalicylates for UC, not Crohns

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19
Q

functional dyspepsia

treatment

A

epigastric pain/discomfort, postprandial fullness, and/or early satiety in the absence of a structural explanation

treat h. pylori/ ppi/ ranitidine->TCA

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20
Q

nonalcoholic fatty liver disease treatment

A

weight loss

surveillance is necessary only when cirrhosis is present

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21
Q

IBD (UC/Crohns) surveillance colonoscopy

PSC+ IBD

A

every 1 to 2 years beginning after 8 to 10 years of disease.

as soon as PSC diagnosis is made

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22
Q

large (≥10 mm) or dysplastic sessile serrated polyps or traditional serrated adenomas, repeat colonoscopy in

an adenoma 10 mm or larger, (2) three to ten adenomas, (3) an adenoma with a villous component or high grade dysplasia

> 20mm polyp/ removed in pieces

A

3 years

3 years

3-6 months

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23
Q

calcified asymptomatic incidental gallstones

A

observe

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24
Q

chronic diarrhea+ exposure to young kids/ water

A

giardia (O &P)

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25
type 1 autoimmune pancreatitis treatment
``` imaging features (focal pancreatic enlargement with a featureless rim and a nondilated pancreatic duct), increased serum IgG4 level, and extrapancreatic organ involvement (sclerosing cholangitis or IgG4-associated cholangitis) steroids ```
26
GI bleed with neg EGD/colonoscopy OR pos capsule | endoscopy
push enteroscopy
27
IBS with constipation treatment | IBS diarrhea
fiber->polyethylene glycol->linaclotide, Lubiprostone | rifaximin
28
primary biliary cholangitis/cirrhosis treatment
cholestatic liver enzyme profile in the setting of a positive antimitochondrial antibody test fatigue, dry mouth/eyes, itching ursodiol
29
complicated pancreatitis management
enteral feeding
30
hepatocellular adenoma >5 cm or β-catenin nuclear reactivity positive otherwise
resection CT q6months-1 year
31
CMV esophagitis treatment
ganciclovir
32
GI bleeding + pain
some sort of colitis
33
suspected esophageal cancer
scope
34
Type I (not assoc with MEN or Zollinger-Elinson) gastric neuroendocrine tumor that's <1cm, <5 of them
endoscopic removal, no further management
35
Roux en Y + diarrhea, bloating, flatulence, and weight loss
treat for SIBO (abx)
36
comm acquired diarrhea <72 hours
supportive care, no cultures
37
sporadic (no fam hx) solitary juvenile polyp
no future health risk once the polyp is removed and do not require surveillance endoscopy
38
oropharyngeal dysphagia diagnosis
videofluoroscopy
39
maintaining remission in ulcerative colitis
taper steroid, azathioprine, 6-mercaptopurine (only in high TPMT) , or an anti−tumor necrosis factor agent (infliximab)
40
African, >20 yo with chronic Hep B infection | Asian men > 40 yo, women >50 yo
u/s of liver q 6months
41
Peptic ulcers at low risk for bleeding (clean based or with a nonprotuberant pigmented spot)
oral PPI, early d/c
42
Barrett with high grade dysplasia no dysplasia
radiofrequency ablation, photodynamic therapy, or endoscopic mucosal resection repeat endoscopy in 3-5 years
43
insulinoma imaging when CT fails | workup
endoscopic u/s | 72 hour fast, then imaging
44
microscopic collagenous colitis | treatment
may be drug induced loperamide or diphenoxylate for mild persistent disease, bismuth subsalicylate for moderate disease, or budesonide for severe disease
45
cirrhotic HCC up to three hepatocellular carcinoma tumors ≤3 cm or one tumor ≤5 cm angiolymphatic or extrahepatic involvement, doesn't meet Milan criteria
no need for biopsy, lesions larger than 1 cm that enhance in the arterial phase and have washout of contrast in the venous phase transplant sorafenib
46
MYH-associated polyposis inheritance pattern
AR
47
Variceal hemorrhage+ cirrhosis
antibiotics (fluoroquinolones)
48
sphincter of oddi dysfunction vs choledocholithiasis
nothing vs h/o stones
49
non–acetaminophen-related acute liver failure causes treatment LFTs in multiple thousands + low bilirubin
drug induced : augmentin among others N-acetylcysteine and transplant eval herpes hepatitis
50
young man with solid-food dysphagia that requires endoscopy for removal endoscopy findings treatment
eosinophilic esophagitis rings, longitudinal furrows, and sometimes strictures swallowed aerosolized topical glucocorticoids (fluticasone or budesonide)
51
FAP surveillance s/p total colectomy and ileorectal anastomosis.
upper endoscopy q1-5 years
52
Acute hep B
self-resolves in 90% of adults serial monitoring of LFTs if protracted (>6 months) or fulminant (marked dysfunction)->lamivudine, entecavir, or tenofovir
53
chronic pancreatitis pain
Tylenol, ibuprofen->tramadol->pregabalin | Extracorporeal shock wave lithotripsy for pancreatic duct stones
54
``` refractory UC (to steroids) mild to moderate disease ```
IV steroids or anti-TNF (-mabs) | 5-aminosalicylate
55
UGI bleed and CVD aspirin
resume before d/c+ daily PPI
56
serrated polyposis syndrome
(1) five or more serrated polyps proximal to the sigmoid colon, two or more of which are 10 mm in diameter or greater, (2) any number of serrated polyps proximal to the sigmoid colon in an individual with a first-degree relative who has SPS, or (3) more than 20 serrated polyps distributed throughout the colon. (can be found over multiple scopes) ANNUAL SCOPE
57
H. pylori primary therapy | salvage therapy
omeprazole, clarithromycin, amoxicillin | 10 days of replace clarithromycin OR BIMT
58
unconjugated hyperbilirubinemia + normal rec count
gilbert syndrome
59
history of colorectal cancer screening
1 year post op, 3 years post op, q5 years after
60
painless watery diarrhea without bleeding
microscopic colitis lymphocytic colitis: intraepithelial lymphocytosis (>20 intraepithelial lymphocytes per 100 epithelial cells) collagenous: subepithelial collagen thickening
61
Nonocclusive mesenteric ischemia
jejunal wall thickening and dilation, ongoing hypotension, fever, and abdominal pain in low flow state
62
cirrhosis + MELD >15
transplant eval
63
Most common cause of UGIB
PUD
64
Acalculous cholecystitis
percutaneous cholecystostomy (draining tube), abx
65
sporadic fundic gland polyps (1-5 mm, <10) without dysplasia
associated with PPI | no excision/ surveillance
66
lynch syndrome colonoscopy
25 yo : q1-2 years | OR 2-5 years earlier than family member if he/she was <25 yo
67
treat chronic hep b if
HBV DNA or LFTs are elevated
68
IBS diarrhea, test for
celiac
69
chest pain eval
rule out cardiac causes before evaluating GERD