Gi2 Flashcards
Tests for active H pylori
Fecal antigen test
Urea breath test
Urease
Chemical secreted by H pylori which allows it to neutralize stomach acid.
Presence is used as a bio marker to indicate the presence of H pylori
Causes of odynophagia
Infection in immunosupprest patients- CMV, herpes, candida
Pill esophagitis
Reflux esophagitis
Upper GI crohns
Innervation of the esophagus
Vagus
Also enteric
If the vagus is cut, there will still be peristalsis, it will just be more disorganized
Esophageal adenocarcinoma
Distal esophageal cancer
Old fat white men with reflux- barrets esohpogas
Squamous cell carcinoma
Non westerners
Risk favored: smoking, nitrates in food, alcohol, underlying achalagia
Causes of benign esophageal strictures
Radiation
Reflux causes scarring with leads to a stricture
Swallowing something alkali
Stuctural dysphasia
Will first have trouble swallowing solids, and later if the obstruction continues to grow liquids
Functional dysphasia
Trouble swallowing solids and liquids
Schatzki’s rings
Narrowing rings near the EGJ that are thought to occur due to reflux
Plummer-Vinson syndrome
Esophageal webs plus an iron deficiency
Possible triggers of achalagia
Association with class 2 human leukocyte antigen DQw1
Molecular mimicry: papilloma virus, polio virus, varicella zoster
Higher prevalence of neural autoantibodies
Diffuse esophageal spasm
Abnormal non peristaltic contractions of the smooth muscle-
Barium swallow looks like a corkscrew
Cholic acid
Neutral pathway- 80% of bile acids go through this pathway
Rate limiting enzyme is CYP2A1
Broken down in the colon into deoxycholic acid which can be reaborbed
Chenodeoxycholic acid
Acid bile pathway
20% of the bile acids move through this pathway
Rate limiting enzyme is CYP27A1
Broken down to lithocholic acid in the colon and very little of these are reaborbed- major way bile acids are lost
Normal platelet levels
150k
pump used to move conjugated bile into the cannilcus
BSEBP
requires ATP
Absorption of conjugated bile acids from the portal system to the hepatocyte
NTCP
Absorption of unconjugated bile acids from the portal system to the hepatocyte
OATP
Absorption of bile from the terminal ilium
ASBT
Na dependent cotransporter
Conjugating enzyme of bilirubin in the liver
UGT
Normal direct bilirubin lab
Values
0-.3 mg/dL
Normal total bilirubin lab values
0.3-1.9 mg/dL
Gilbert’s syndrome
UDT GT deficiency - very common
benign elevations of bilirubin
Worsens with fasting
Crigler- Najjar
UDT-gt complete deifiancty
Not compatible with life - neonate death
Conjugated bilirubin diseases
Dubin Johnson and rotors syndrome
Impaired secretin of conjugated bilirubin into the canalicculius