Gastroenterology Flashcards

1
Q

Treatment options for Opioid-induced constipation

A

1) SQ methylnaltrexone
2) oral naloxegol
3) oral naldemedine

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2
Q

What are the four phases of HBV infection?

A

1) Immune tolerant
2) Immune active - evidence of hepatic inflammation
3) Immune control (inactive)
4) Reactivation

Treatment is indicated in the immune active phase

Routine screening for HCC indicated (AFP, U/S)

  • SE asian patients >40 y/o (male), >50 y/o (female)
  • sub-saharan Africa > 20 y/o
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3
Q

What are the criteria for cholecystecomy with regard to asymptomatic gallbladder polyps?

A

1) Polyp >1 cm
2) Polyp of any size in the presence of gallstones
3) Polyp >8 mm in size with coexsting PSC

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4
Q

Indications for SBP prophylaxis in new ascites

A

1) Ascitic fluid protein <1.5 g/dL AND
2) Hyponatremia (<130) OR
3) Kidney dysfunction (serum Cr >1.2) OR
4) CTP Class B or C Cirrhosis

Choose fluoroquinolones for prophylaxis (norfloxacin or ciprofloxacin)

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5
Q

Indications for resection of pancreatic cyst

A

1) Symptoms related to the cyst (pancreatitis, jaundice)
2) Cyst size >3 cm
3) Dilated main pancreatic duct
4) Solid component of the cyst

Surveillance: annual MRI abdomen

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6
Q

Etiologies of secretory diarrhea (occurs despite fasting)

A

1) Medications - colchicine, NSAIDs
2) VIPoma, Carcinoid, Gastrinoma
3) SIBO
4) Short bowel syndrome (bile acid malabsorption)
5) Villous adenoma

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7
Q

Biopsy findings in Crohn’s Disease

A

1) Distorted and branching colonic crypts
2) Neutrophilic and lymphocytic infiltration
3) Skip lesions

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8
Q

What test helps diagnose SIBO?

A

Glucose hydrogen breath testing

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9
Q

Positive anitmitochondrial antibodies are associated with what disease?

A

Primary Biliary Cholangitis (PBC)

~10% may test negative for antimitochondrial Abs

Think about PBC in a middle-aged woman (40-60) with a cholestatic picture +/- symptoms of jaundice, pruritis, and fatigue

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10
Q

Criteria for Lynch Syndrome

A

1) Three family members affected with Lynch-syndrome associated cancers
2) Two successive generations affected
3) One affected family member is a first-degree relative of the other two affected members
4) One cancer was diagnosed <50 years
5) FAP has been ruled out

Lynch-Syndrome associated cancers:

  • Colorectal
  • endometrial
  • Others: stomach, ovary, hepatobiliary, urinary tract, small bowel brain, pancreas, and sebaceous skin adenoma/cancer
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11
Q

Where is colorectal cancer as part of Lynch Syndrome likely to occur? What are the histologic characteristics?

A

1) Proximal colon

2) Tumor-infiltrating lymphocytes, medullary growth

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12
Q

Genes implicated in Lynch Syndrome

A

1) MLH1, MSH2, MSH6, PMS2 - mismatch repair genes

2) EPCAM - epithelia cell adhesion molecule

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13
Q

Treatment for pyogenic vs amebic liver abscess

A

Pyogenic - usually polymicrobial, via gut translocation (most common in US). Tx is often antimicrobials plus surgery. Surgical indications:

  • > 5 cm in size
  • complex abscess
  • presence of gas-formation
  • hemodynamic instability
  • biliary fistulization
  • presence of foreign body

Amebic abscess - usually Entamoeba histolytica, from an endemic area (South/Central America, India, Africa). Symptom onset 3-5 months after infection, which is indicative of hepatic necrosis. Treatment:

  • metronidazole
  • luminal agent (paromomycin)
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14
Q

Treatment of Wilson’s Disease

A

Trientine is preferred to penicillamine due to a lower rate of adverse effects.

Consider zinc supplements to decrease intestinal absorption of copper.

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15
Q

GI bleed with hypotension in patient with prior aortic grafting

A

Aortoenteric fistula

  • evaluate with CT + contrast
  • mortality rate 50% (even with surgical intervention)
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16
Q

What is alosetron used for?

A

IBD-D in women whose symptoms have not responded to conventional therapy

Risk for ischemic colitis and severe constipation
Drug monitoring program enrollment is required

17
Q

What is the Meltzer Triad? What does it indicate?

A

1) Aesthenia (weakness)
2) Arthralgias
3) Palpable purpura

Classic presentation of Type II cryoglobulinemia
Hep C a common cause, treat the virus

18
Q

How do you calculate the stool osmolar gap?

A

290 - 2[stool Na + stool K]

> 100 is consistent with osmotic
< 50 is consistent with secretory (think high stool Na and high stool K)

19
Q

Fever, diarrhea, weight loss in an AIDS patient: etiologies

A

1) Cryptosporidium
2) E. histolytica
3) Giardia
4) isospora
5) Strongyloides
6) AIDS enteropathy

20
Q

Rarer causes of chronic diarrhea

A

1) Diabetes
2) Amyloidosis - visceral autonomic neuropathy, gastroparesis, postural hypotension
3) Carcinoid syndrome
4) Lactase deficiency
5) IBS-D

21
Q

How to diagnose Carcinoid Syndrome

A

1) 24hr urine 5-HIAA (positive if >25 mg/day)
2) CT may show metastases in liver
3) MRI and octreoscan (many carcinoid tumors express somatostatin receptors, which are bound by the radiolabeled somatostatin analogue octerotide)

A 24 hour fast will improve osmolar diarrhea, but not secretory diarrhea

22
Q

Malabsorption (chronic diarrhea) can cause which 6 major deficiencies?

A

Think “PIC ACC”

P: PT/INR - Vitamin K deficiency
I: Iron deficiency
C: Calcium deficiency
A: Albumin
C: Cholesterol
C: Carotene (Vitamin A) deficiency
23
Q

Which ARB has been associated with enteropathy/malabsorption?

A

Olmesartan: causes sprue-like enteropathy

24
Q

Whipple’s Triad:

A

1) Arthraligas
2) Abdominal pain
3) Diarrhea/malabsorption leading to weight loss

Caused by gram + bacillus T. whipplei
Can see Neuro sx (depression, paranoia, dementia)
Biopsy: Foamy macrophages, +PAS staining
Tx: Ceftriaxone or PCN IV x14 days, then TMP/SMX x1 year

25
Q

Medications for IBS-C

A

1) Linaclotide
2) Lubiprostone

Both stimulate intestinal secretion

26
Q

What are the inherited polyposis syndromes

A

1) FAP: AD, APC gene, 100s to 1000s of adenomas, 100% CA risk, proctocolectomy needed, screen for duodenal CA
2) Attenuated FAP: AD, APC gene, 10s-100s of polyps, delayed-onset CRC
3) MUTYH polyposis - AR, phenotype is similar to attenuated FAP, screen for duodenal CA as well
4) Gardner Syndrome: Variant of FAP with tumors outside of the colon (osteomas, thyroid cancer, desmoids)
5) Peutz-Jeghers syndrome: harmartomatous polyps, small bowel, stomach and colon. Freckles on lips/buccal mucosa, intussusception is common, increased CA risk (CRC, stomach, breast, pancreatic)
6) Juvenile Polyposis: consider if 3-5 juvenile polyps of the colon

7) Serrated Polyposis Syndrome
- Five or more serrated polyps proximal to the sigmoid colon, with two or more greater than 10 mm in size
- Any number of serrated polyps in patients with first-degree relatives with serrated polyposis syndrome
- More than 20 serrated polyps throughout the colon

27
Q

Non-polyposis Colorectal Syndromes

A

1) Lynch

2) PTEN Hamartoma (Cowden Syndrome)

28
Q

Colonoscopy follow up interval for one or two tubular adenomas (<1 cm)?

A

5 years

29
Q

Colonoscopy follow up interval for 3-10 adenomas?

A

3 years

30
Q

Colonoscopy follow up interval for an adenoma >1 cm?

A

3 years

31
Q

Colonoscopy follow up interval for small rectal hyperplastic polyps?

A

10 years

32
Q

Colonoscopy follow up interval for adenoma with high-grade dysplasia or villous features?

A

3 years

33
Q

Colonoscopy follow up interval for >10 adenomas?

A

<3 years, consider familial polyposis syndrome

34
Q

Colonoscopy follow up interval for large (>2 cm) sessile polyp removed in piecemeal fashion?

A

2-6 months

35
Q

Colonoscopy follow up interval for polyp with adenocarcinoma (minimal invasion, >2 mm margin)?

A

2-3 months

36
Q

Treatment for HBV

A

Tenofovir
Entecavir
Pegylated interferon