GI Flashcards

1
Q

How does functional dyspepsia present

A

Recurrent pain in the upper abdomen or periumbilical area that cannot be relieved with change in stool patterns and there is no organic cause

Symptoms must be present once a week for at least 2 months

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2
Q

Tx for functional dyspepsia

A

Eliminate nsaid, spicy foods and soda

Meds - h2 blockers or PPI also low dose antidepressants

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3
Q

How does IBS present

A

Abdominal discomfort improved with defecation, changes in stool frequency or changes in stool consistency

Could also have bowel urgency with feeling of incomplete evacuation. Passage of mucus, bloating, and abdominal distention.

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4
Q

Tx for IBS

A

Dietary changes (reduce sorbitol, fructose and gas forming foods) and address psychological issues

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5
Q

What should you consider in a pt that presents with recurrent abdominal pain and urinary retention, tachycardia, blurred vision, dry mouth

A

Anticholinergic meds that were inappropriately prescribed

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6
Q

What should be the diet for a child who has moderate to severe dehydration due to diarrhea

A

Avoid fatty foods and foods high in simple sugars

Oral rehydration solution should be 2% glucose and 90meq of sodium chloride

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7
Q

What are the different ecoli that cause diarrhea and which ones cause bloody stools

A

Enteropathogenic - non bloody (neonates and kids < 2)

Enterotoxigenic - non- bloody (travelers diarrhea)

Shiga toxin producing/enterohemorrhagic - bloody after 3-4 days (can cause HUS antibiotics contraindicated)

Enteroaggregative - non bloody

Enteroinvasive - bloody with tenesmus

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8
Q

XRAY findings for volvulus

A

Gastric and duodenal dilatation

Decreased intestinal air and cork screw appearance of the duodenum

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9
Q

Lab findings in pyloric stenosis

A

Hypochloremic metabolic alkalosis with severe hypokalemia

Elevated indirect bill

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10
Q

Diagnostic criteria on ultrasound for pyloric stenosis

A

Pyloric length > 14mm

Pyloric muscle thickness > 4mm

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11
Q

How does ectodermal hypoplasia present and how is it diagnosed

A

Absent teeth. X linked

Diagnosed by skin biopsy which shows lack of sweat pores

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12
Q

How does hallermann Strieff syndrome present

A

Underdeveloped small teeth

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13
Q

What are risk factors for h. Pylori

A

Low socioeconomic status and immigration from a developing country

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14
Q

Next step if h. Pylori serologic testing is positive

A

Another study to confirm such as fecal antigen or urea breath test

Limit testing to those at risk

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15
Q

Tx for h. Pylori

A

PPI + 2 antibiotics

Clarithromycin and amox or clarithromycin and metronidazole

7-14 day course

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16
Q

How do you diagnose celiac disease

A

Biopsy

Antibodies are only for screening

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17
Q

Tx for irritable bowel syndrome

A

High fiber diet, attention to emotional factors. Amitryptyline.

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18
Q

How does gardners syndrome present

A

Extra teeth, polyps (premalignant), ostromas

Autosomal dominant

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19
Q

How does peutz-jeghers syndrome present

A

Pigmentation of lips and gums along with a lot of colonic polyps (premalignant)

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20
Q

Tx for UC when disease is a medical emergency

A

Fluids, blood transfusion and steroids

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21
Q

Tx for UC when infection

A

Metronidazole

22
Q

First line medical tx for UC

A

5 ASA (aminosalycylate)

23
Q

Second line medical tx for UC

A

Corticosteroids, 6 mercaptopurine or azarhioprine or methotrexate, cyclosporine or tacrolimus

24
Q

Descriptions for chron’s

A

Skip lesions on XRAY, cobblestone appearance on endoscopy. Transmural lesions and noncaseating granulomas

25
What should you rule out in a child older than 6 that presents with intussusception
Lymphosarcoma
26
Tx for intussusception
Air contrast enema as it's diagnostic and therapeutic
27
Dx and tx for hirschsprung disease
Rectal biopsy / surgical excision Proximal aganglionic segment is distended with stool
28
Tx of peptic ulcer disease
H2 blocker, sucralfate, prostaglandin analogues (misoprostol), PPI
29
What are the rules of 2 for meckel diverticulum
Presents around the age of 2 or bf 2 types of tissue (gastric and intestinal) 2 feet from ileocecal valve 2 inch in length 2% of newborns affected (Painless rectal bleeding)
30
How does cholestatic jaundice present Stasis!
Elevated direct bili and elevated alkaline phosphatase and elevated GGT Liver dz vs anatomic/obstructive hepatobiliary scintigraphy first step for dx Most common cause is TPN
31
How does biliary atresia present
Elevated direct bili in newborn usually at 3 wks of age and less than 2 months old Clay colored stools
32
How does choledochal cyst present
Neonatal jaundice, fever, acholic stool, RUQ pain, palpable mass Dx with ultrasound
33
What is the deficiency in GILBERT syndrome
Glucuronyl transferase deficiency
34
Presentation of GILBERT syndrome
Teenager who is jaundiced after a URI or fasting! Intermittently elevated unconjugated bili w illness or other stressors. Recognized after puberty. Familial condition
35
Lab findings in GILBERT syndrome
Elevated indirect bili and normal LFTs
36
Lab findings in Wilson disease
Low serum Cooper and ceruloplasmin level Elevated tissue Cooper (liver) and urine
37
Tx of Wilson disease
D-Penicillamine
38
Lab finding in liver failure
Elevated serum ammonia level and mental status change Think of reye when you give aspirin to someone with varicella or flu
39
Most specific test in diagnosing pancreatitis
Abdominal ultrasound
40
What can pancreatitis be associated with
Pulmonary edema and pleural effusion
41
Causes of recurrent or chronic pancreatitis
Familial dyslipidemia Hypercalcemia (hx of hyperparathyroidism or kidney stones) Infection, autoimmune, inherited conditions, medications
42
Presentation of cholecystitis
fever, pain radiating to the right scapula, palpable mass in the right upper quadrant Jaundice not common
43
Conditions that predispose kids to cholecystitis
Hemolytic disease, TPN, small intestinal disease, obesity, pregnancy
44
Risk factors for gallstones
CF, ileal resection, treatment with ceftriaxone, TPN
45
Presentation of cholelithiasis
Jaundice, hepatosplenomegaly
46
How do you dx biliary atresia
Biopsy! First test is ultrasound followed by HIDA ultimately a biopsy
47
Tx for biliary atresia
Kasai procedure to act as a bile duct. Where you join liver to intestines
48
What markers will you see during acute Hep b infection
HBsAg HBeAg HBV-DNA
49
What markers are present during recovery of Hep b
Anti-HBs Anti- HBc Anti- HBe
50
What is Hep C associated with
Hepatocellular carcinoma and cirrhosis
51
Most common cause of chronic viral hepatitis
Hep C