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251 Cards in this Set
- Front
- Back
falciform ligament connects ___ and ___
it contains ___ it is derived from ___ |
liver
anterior abdominal wall ligamentum teres fetal umbilical vein |
|
hepatoduodenal ligament connects ___ and ___
it contains ___ it connects the spaces ___ (2) |
liver
duodenum portal triad greater sac lesser sac |
|
portal triad
|
hepartic a.
portal v. CBD |
|
gastrohepatic ligament connects ___ and ___
it contains ___ |
liver
lesser curvature of stomach gastric a.s |
|
gastrocolic ligament connects ___ and ___
it contains ___ |
greater curvature of stomach
transverse colon gastroepiploic a.s |
|
gastrosplenic ligament connects ___ and ___
it contains ___ |
greater curvature of stomach
spleen short gastric a.s |
|
splenorenal ligament connects ___ and ___
it contains ___ (2) |
spleen
posterior abdominal wall splenic a. splenic v. |
|
esophagus has ___ epithelium
|
nonkeratinized stratified squamous
|
|
4 layers of gut wall
|
mucosa
submucosa muscularis serosa |
|
3 parts of mucosa
|
epithelium
lamina propria muscularis mucosae |
|
2 features of submucosa
|
Brunner's glands
Meissner's plexus |
|
Brunner's glands are located in ___ and do ___
they become hypertrophic in ___ |
duodenum (proximal to sphincter of Oddi)
secrete HCO3- + mucus to neutralize chyme pH peptic ulcer disease |
|
Meissner's plexus does ___ (3)
|
regulation of secretion
regulation of blood flow regulation of absorption |
|
3 features of muscularis
|
circular muscle layer
Auerbach's plexus longitudinal muscle layer |
|
longitudinal muscle layer is on ___
circular layer is on ___ |
outside
inside |
|
crypts of Lierberkuhn are located in ___ and do ___ (2)
|
whole small intestine
enzyme secretion epithelial regeneration (stem cells) |
|
3 enzymes secreted from crypts of Lieberkuhn
|
maltase
sucrase enteropeptidase |
|
___ has greatest absorptive surface area
___ has most goblet cells |
duodenum (then j, then i)
jejunum |
|
Peyer's patches are located in ___ (2) layers of ___
|
lamina propria
submucosa ileum |
|
celiac trunk is located at level ___
|
T12
|
|
SMA orifice is located at level ___
|
L1
|
|
L renal a. orifice is located at level ___
|
L1
|
|
gonadal a. orifices are located at level ___
|
L2
|
|
IMA orifice is located at level ___
|
L3
|
|
AA bifurcation is at level
|
L4
|
|
foregut derivatives are ___
they are perfused by ___ they have PARA innervation by ___ |
stomach + proximal duodenum
celiac trunk vagus |
|
midgut derivatives are ___ (5)
they are perfused by ___ they have PARA innervation by ___ |
distal duodenum
jejunum ileum ascending colon proximal 2/3 of transverse colon SMA vagus |
|
hindgut derivatives are ___ (4)
they are perfused by ___ they have PARA innervation by ___ |
distal 1/3 of transverse colon
descending colon sigmoid proximal rectum IMA pelvic nerves |
|
3 branches of celiac in CW order
|
L gastric
splenic common hepatic |
|
common hepatic a. gives ___ (2) to become ___
|
gastroduodenal a.
R gastric hepatic a. proper |
|
R. gastric a. anastomoses with ___
both perfuse ___ |
L gastric a.
lesser curvature of stomach |
|
2nd part of duodenum is perfused by ___ from the ___
|
superior pancreaticoduodenal a.
gastroduodenal a. |
|
greater curvature of stomach is perfused by ___ (2) from ___ on L
and ___ from ___ on R |
L gastroepiploic a.
short gastric a.s splenic a. R gastroepiploic a. gastroduodenal a. |
|
a.s perfusing stomach which lack good anastomosis
|
short gastrics (if splenic a. is blocked)
|
|
4 anastomoses which compensate for AA
|
internal thoracic
sup. pancreaticoduodenal middle colic sup. rectal |
|
internal thoracic , a branch of ___, anastomoses with ___, a branch of ___,
which anastomoses with ___, a branch of ___ |
subclavian
sup. epigastric int. thoracic inf. epigastric ext. iliac |
|
sup. pancreaticoduodenal, a branch of ___,
anastomoses with ___, a branch of ___. |
gastroduodenal
inf. pancreaticoduodenal SMA |
|
middle colic, a branch of ___,
anastomoses with ___, a branch of ___ |
SMA
L colic IMA |
|
4 (first order) portal vein tributaries
|
L gastric
splenic SMV paraumbilical |
|
in addition to the first order portal vein tributaries, ___ feeds the SMV
|
IMV
|
|
___ drains the rectum to the portal circulation___ (2) drains the rectum to the systemic circulation
|
sup. rectal v.
middle rectal v. inf. rectal v. |
|
in portal HTN, L. gastric v. anastomoses with ___
|
esophageal v.
|
|
in portal HTN, paraumbilical v. anastomoses with ___ (2)
|
inferior epigastric v. (from common iliac)
superficial epigastric v. (from int. iliac) |
|
in portal HTN, sup. rectal v. anastomoses with ___ (2)
|
middle rectal v.
inf. rectal v. |
|
internal hemorrhoids are above ___
they are/aren't painful they are perfused by ___ from ___ they are drained by ___ |
pectinate line
aren't sup. rectal a. IMA sup. rectal v. |
|
external hemorrhoids are below ___
they are/aren't painful they are perfused by ___ from ___ they are drained by ___ |
pectinate line
are inf. rectal a. internal pudendal a. inf. rectal v. |
|
internal/external hemorrhoids are associated with portal HTN
|
internal
|
|
zone I of liver is near ___
it is the first to be affected by ___ zone III of liver is near ___ it is the first to be affected by ___ (3) |
portal triad
viral hepatitis central vein ischemia toxins alcoholic hepatitis |
|
CYP is expressed in zone ___
|
III
|
|
liver capillaries are called ___
they don't have ___ the endothelial cells lining them have ___ |
sinusoids
basement membrane fenestrations (100-200 nm) |
|
fenestrations in sinusoid epithelium allow ___ (2) to enter ___
|
plasma
macromolecules space of Disse |
|
space of Disse separates ___ and ___
|
sinusoid endothelium
basolateral side of hepatocytes |
|
apical side of hepatocytes faces ___
|
bile canaliculi
|
|
Kupffer cells are ___s located in liver ___s
|
MQ
sinudoids |
|
Ito cells are aka ___ cells
they live in ___ they do ___ (2) |
stellate
space of Disse fat storage vitamin A storage |
|
___ is associated with pathological Ito cell behavior; in this state,
___ decreases ___ (3) increases |
cirrhosis
vitamin A storage proliferation chemotaxis collagen synthesis |
|
borders of femoral triangle
|
sartorius (lateral)
adductor longus (medial) inguinal ligament (superior) |
|
2 contents of femoral triangle (lateral to medial)
|
femoral n.
femoral sheath |
|
3 contents of femoral sheath (lateral to medial)
|
femoral a.
femoral v. femoral canal |
|
7 layers of abdominal wall from external to internal
|
skin
subcutaneous tissue external oblique internal oblique transversus abdominis transversalis fascia parietal peritoneum |
|
5 layers of spermatic cord from outside to in
|
skin
external spermatic fascia cremaster muscle + fascia internal spermatic fascia vestige of processus vaginalis |
|
___ in abdominal wall becomes external spermatic fascia
|
superficial + deep fascia of external oblique
|
|
___ in abdominal wall becomes cremaster muscle
|
superficial + deep fascia of internal oblique
|
|
___ in abdominal wall becomes internal spermatic fascia
|
transversalis fascia
|
|
___ in abdominal wall becomes vestige of processus vaginalis
|
parietal peritoneum
|
|
rectus abdominis muscle is enclosed by ___
|
rectus sheath
|
|
rectus sheath receive fibers from ____ (3)
|
external oblique
internal oblique transversus abdominis |
|
___ is a smaller muscle which runs alongside rectus abdominis
|
pyramidalis
|
|
diaphragmatic hernias can occur in ___ due to malformation of ___
|
babies
pleuroperitoneal membrane |
|
2 kinds of hiatus hernias
___ is more common |
sliding (GE junction moves)
paraesophageal (stomach moves up but GEJ stays) sliding |
|
barium XR finding in hiatus hernia
|
hourglass stomach
|
|
gastrin is made by ___ cells in ___
it does ___ (3) release is triggered by ___ (3) and inhibited by ___ |
G
antrum parietal cell H+ pumping gastric mucosal proliferation gastric motility stomach distention AAs in stomach (esp F, W) vagal tone gastric pH<1.5 |
|
CCK is made by ___ cells in ___ (2)
it does ___ (3) release is triggered by ___ |
I
duodenum jejunum increased pancreatic secretion increased gallbladder contraction reduced gastric emptying fatty content in duodenum |
|
secretin is made by ___ cells in ___
it does ___ (3) release is triggered by ___ |
S
duodenum pancreatic HCO3- secretion reduced gastric H+ increased bile secretion acidic chyme in duodenum |
|
somatostatin is made by ___ cells in ___ (2)
it does ___ (5) release is triggered by ___ and inhibited by ___ |
D
islets of langerhans GI mucosa reduced GH release reduced gastric H+ reduced gastric enzymes reduced pancreatic exocrine secretion reduced pancreatic endocrine secretion (insulin + glucagon) acidic chyme vagal stimulation |
|
gastric inhibitory peptide is made by ___ cells in ___ (2)
it does ___ (2) release is triggered by ___ (3) |
K
duodenum jejunum reduced gastric H+ increased insulin release FFA AA Glc |
|
GIP is aka ___
|
Glc-dependent insulinotropic peptide
|
|
vasoactive intestinal polypeptide is made by ___ (3)
it does ___ (3) release is triggered by ___ (2) and inhibited by ___ |
PARA ganglia in sphincters
PARA ganglia in gallbladder PARA ganglia in small intestine increased intestinal water secretion increased intestinal electrolyte secretion relaxation of sphincters distention vagal tone SYM tone |
|
NO effect on GI
|
smooth muscle relaxation
|
|
motilin is made by ___
it does ___ release is triggered by ___ |
small intestine
migrating motor complexes fasting |
|
ghrelin is made by ___ cells in ___
it does ___ (3) release is triggered by ___ and inhibited by ___ |
P/D1
gastric fundus GH release ACTH release PRL release preprandial postprandial |
|
intrinsic factor is made by ___ cells in ___
it does ___ |
parietal cells
gastric body/fundus B12 binding |
|
H+ is made by ___ cells in ___
release is triggered by ___ (3) and inhibited by ___ (4) |
parietal
gastric body/fundus HA ACh gastrin somatostatin GIP PGs secretin |
|
pepsinogen is made by ___ cells in ___
it does ___ release is triggered by ___ (2) |
chief
gastric body/fundus peptide cleavage vagal tone H+ |
|
HCO3- is made by ___ cells in ___ (4) and ___ in duodenum
it does ___ release is triggered by ___ |
mucosal
salivary glands stomach duodenum pancreas Brunner's glands H+ neutralization secretin |
|
GI hormone elevated in Prader-Willi
|
Ghrelin
|
|
GI hormone deficiency associated with achalasia
|
NO
|
|
GI hormone elevation causing copious diarrhea
|
VIP
|
|
GI hormone used to treat VIPoma
another tumor it's used for is ___ |
somatostatin
carcinoid |
|
GI hormone elevated in Zollinger-Ellison syndrome
|
gastrin
|
|
3 kinds of salivary gland
|
parotid
submaxillary sublingual |
|
___ glands are most serous
___ glands are most mucinous |
parotid
sublingual |
|
salivary secretion has SYM stimulation from ___ and PARA stimulation from ___ (2)
|
superior cervical ganglion
CN7 CN9 |
|
low salivary flow makes ___ saliva
high flow makes ___ saliva |
hypotonic
isotonic |
|
ACh acts on stomach via ___R
this and the ___R are linked to ___ |
M3
CCK_B (gastrin) G_q |
|
gastric G_q does ___ to cause H+ secretion
|
activates H+ ATPase
|
|
H+ in parietal cells is produced by ___ and is exchanged by ___ for ___
|
CA
ATPase K+ |
|
HA acts on parietal cells via ___R
this is linked to ___ it causes gastric H+ secretion by ___ing |
H2
G_s activating ATPase |
|
pancreatic zymogens are activated by ___, which is activated by ___ released by ___
|
trypsin
enterokinase/enteropeptidase duodenal mucosa |
|
gut absorption of glucose is via ___
gut absorption of galactose is via ___ gut absorption of fructose is via ___ |
SGLT1
SGLT1 GLUT5 |
|
absoprtion through SGLT requires ___
|
Na+
|
|
bile acids are absorbed in ___
B12 is absorbed in ___ Fe is abosrbed as ___ in ___ folate is absorbed in ___ |
ileum
ileum Fe2+ duodenum jejunum |
|
salivary gland tumors are most commonly in ___
|
parotid
|
|
most common salivary gland tumor
|
pleomorphic adenoma
|
|
pleomorphic adenoma is a painful/painless mass
it is mobile/fixed |
painless
mobile |
|
most common salivary malignancy
|
mucoepidermoid carcinoma
|
|
3 causes of esophagitis
|
GERD
infection chemical ingestion |
|
3 infections causing esophagitis
|
HSV1
CMV candida |
|
Plummer-Vinson syndrome pw ___ (3)
|
dysphagia
glossitis Fe deficiency anemia |
|
dysphagia in Plummer-Vinson is 2/2
|
esophageal webs
|
|
2 structural defects associated with esophageal ca
|
Zenker's diverticulum
esophageal webs |
|
___ is most common esophageal ca worldwide
___ is most common in US |
SCC
none- SCC=adeno |
|
esophageal SCC happens in ___ of esophagus
esophageal adenoca happens in ___ of esophagus |
upper 2/3
lower 1/3 |
|
celiac has Abs to ___ (2)
___ is used for screening |
gliadin
TTG anti-TTG |
|
skin abnormality associated with celiac
|
dermatitis herpetiformis
|
|
malignancy associated with celiac
|
T cell Ly (moderately increased risk)
|
|
2 kinds of acute gastritis
|
Curling ulcer (burn patient)
Cushing ulcer |
|
in Cushing ulcer ___ causes ___ which causes ___
|
brain injury
high vagal tone H+ hypersecretion |
|
2 kinds of chronic gastritis
___ is more common |
A
B B |
|
type A chronic gastritis affects ___
it is caused by ___ and causes ___ (2) |
body/fundus
autoimmunity pernicious anemia achlorhydria |
|
type B chronic gastritis affects ___
it is caused by ___ |
antrum
HP |
|
menetrier's disease pw ___ (4)
it is a RF for ___ |
gastric hypertrophy
parietal cell atrophy increased mucous cells protein loss stomach cancer |
|
in menetrier's disease ___ are hypertrophied
|
stomach rugae
|
|
4 RFs for gastric adenoca
|
dietary nitrosamine
achlorhydria chronic gastritis type A blood |
|
gastric/duodenal ulcers have worse pains with meals
|
gastric
|
|
___% of gastric ulcers have HP infection
___% of duodenal ulcers do |
70
almost 100 |
|
3 complications of duodenal ulcer
|
bleeding
penetration of pancreas perforation |
|
inflammation in ulcerative colitis involves ___ layers
|
mucosa
submucosa |
|
gross histopath in UC (2)
|
pseudopolyps
loss of haustra |
|
3 UC complications
|
malnutrition
toxic megacolon CRC |
|
diarrhea in UC is always ___
|
bloody
|
|
2 extra-GI UC manifestations
|
pyoderma gangrenosum
PSC |
|
2 UC drugs
|
sulfasalazine
infliximab |
|
sulfasalazine is related to ___
|
aminosalicylic acid
|
|
4 extra-GI manifestations of Crohn's
|
migratory polyarthritis
erythema nodosum ankylosing spondylitis uveitis |
|
2 Crohn's drugs
|
CS
infliximab |
|
irritable bowel syndrome has ___ with at least 2 of ___ (3)
|
recurrent abdominal pain
pain improves with defecation change in stool frequency change in stool appearance |
|
IBS pw ___ or ___ or ___
|
diarrhea
constipation alternating diarrhea + constipation |
|
tx for IBS
|
symptomatic
|
|
diverticulitis can cause ___ bleeding
complication of diverticulitis |
bright red rectal
colovesical fistula (pneumaturia) |
|
colonic polyps are most commonly in ___
___% are non-neoplastic ____ polyps are precancerous |
rectosigmoid
90 adenomatous |
|
most common non-neoplastic polyp
|
hyperplastic
|
|
T/F: juvenile polyposis syndrome has elevated CRC risk
|
true
|
|
Peutz-Jeghers polpys are ___s
|
hamartoma
|
|
3 extra-GI manifestation of Peutz-Jeghers
|
hyperpigmentation of lips
hyperpigmentation of hands hyperpigmentation of genitals |
|
Peutz-Jeghers has elevated risk of ___
|
CRC
|
|
CRC is ___th most common cancer in US
|
3
|
|
Gardner's syndrome is FAP + ___ (3)
|
osseous tumors
soft tissue tumors retinal hyperplasia |
|
Turcot's syndrome is FAP + ___
|
malignant CNS tumor
|
|
CRC in proximal colon pw ___ (3)
|
dull pain
Fe deficiency anemia fatigue |
|
CRC in distal colon pw ___ (3)
|
obstruction
colicy pain hematochezia |
|
tumor marker for CRC
|
CEA
|
|
without risk factors, screening for CRC starts at age ___ with ___ (2)
|
50
occult blood colonoscopy |
|
___% of FAP progress to CRC
___% of Lynch syndrome population progresses to CRC |
100
80 |
|
FAP is a ___ trait
it always involves ___ |
AD
rectum |
|
Lynch syndrome is a ___ trait
|
AD
|
|
3 stages of adenoma-ca sequence
|
polyp development
polyp growth transformation |
|
gene linked to polyp development in adenoma-ca sequence
|
APC
|
|
gene linked to polyp growth in adenoma-ca sequence
|
K-Ras
|
|
gene linked to transformation in adenoma-ca sequence
|
p53
|
|
carcinoid is most commonly in ___
only ___ carcinoid tumors have carcinoid syndrome |
small intestine
metastatic |
|
micronodular cirrhosis is associated with ___ (3)
nodules are ___ mm |
EtOH
Wilson's disease hemochromatosis <3 |
|
macronodular cirrhosis is associated with ___ (2)
nodules are ___ mm |
infectious hepatitis
drug-induced hepatitis >3 |
|
___ cirrhosis is associated with HCC
|
macronodular
|
|
aminotransferase pattern for viral hepatitis
|
ALT>AST
|
|
aminotransferase pattern for alcoholic hepatitis
|
AST>ALT
|
|
aminotransferase pattern for MI
|
high AST
|
|
liver enzyme for alcoholism
|
GGT
|
|
ALP is elevated in ___ (3)
|
obstructive liver disease
bile duct disease bone disease |
|
amylase is elevated in ___ (2)
|
acute pancreatitis
mumps |
|
lipase is elevated in ___
|
acute pancreatitis
|
|
Reye's syndrome is a reaction to ___ in context of ___ occurring in ___
|
aspirin
viral disease children |
|
Reye's syndrome pw ___ (3)
|
hepatoencephalopathy
hypoglycemia coma |
|
histopath of Reye's syndrome
|
microvesicular fatty change
|
|
2 viruses associated with Reye's syndrome
|
VZV
influenza B |
|
mechanism of Reye's syndrome
|
impaired beta oxidation
|
|
microscopic finding in alcoholic hepatitis
|
Mallory bodies
|
|
Mallory bodies are ___
|
eosinophilic cytoplasmic inclusions
|
|
in cirrhosis, fibrosis occurs near ___
|
central vein
|
|
marker for HCC
|
AFP
|
|
because of ___, HCC can cause ___
|
hematogenous spread
Budd-Chiari syndrome |
|
microscopic finding in a1AT deficiency
|
PAS+ globules in liver
|
|
3 kinds of jaundice
|
prehepatic (hemolytic)
intrahepatic posthepatic (obstructive) |
|
prehepatic jaundice has ___ hyperbilirubinemia,
___ urine bilirubin, and ___ urine urobilinogen |
indirect
no high |
|
intrahepatic jaundice has ___ hyperbilirubinemia,
___ urine bilirubin, and ___ urine urobilinogen |
mixed
high normal/low |
|
posthepatic jaundice has ___ hyperbilirubinemia,
___ urine bilirubin, and ___ urine urobilinogen |
direct
high low |
|
3 steps of post-conjugation bilirubin metabolism
these are done by ___ ___ is colorless ___ is colored |
unconjugation
bilirubin -> urobilinogen uroblinogen -> urobilin gut bacteria urobilinogen urobilin |
|
T/F: AST is present in cytosol
T/F: AST is present in mitochondria |
true
true |
|
T/F: ALT is present in cytosol
T/F: ALT is present in mitochondria |
true
false |
|
patients with renal failure have low ___ activity
|
ALT
|
|
in general ___ is higher than ___ in liver disease. 3 exceptions are
|
ALT
AST alcohol fatty liver cirrhosis |
|
4 illicit drugs which cause abnormal AST/ALT
|
PCP
ecstasy anabolic steroids cocaine |
|
6 viruses which can cause severe ALT, AST elevation
|
hep A-E
HSV |
|
ALP is increased in ___ (2 populations)
|
pregnant women
children |
|
in bone ALP is expressed by ___
|
osteoblasts
|
|
3 kinds of infiltrating diseases which cause elevated ALP
|
granulomatous disease
amyloidosis malignancy |
|
deficient enzyme in Gilbert's is ___, which causes deficient ___.
this causes elevated ___. jaundice can be corrected with ___. |
UDPGT
bilirubin conjugation indirect bilirubin phenobarbital |
|
deficient enzyme in Crigler-Najjar is ___. difference from Gilbert's is ___.
|
UDPGT
zero enzyme expression in Crigler |
|
Crigler-Najjar type ___ is the most severe. it causes ___
|
1
death in infancy |
|
Crigler-Najjar type 2 can be treated with ___
|
phenobarbital
|
|
___ is deficient in Dubin-Johnson and Rotor's syndromes
enzyme is ___ |
secretion of conjugated bilirubin into canaliculi
OAT (organic anion transporter) |
|
gross histopath of Dubin-Johnson (but not Rotor's)
|
black liver
|
|
defective enzyme in Wilson's disease
it does ___ |
APT7B
attachment of Cu to ceruloplasmin |
|
defective ATP7B in Wilson's disease causes ____ inside hepatocytes and
____ (2) in blood stream |
Cu accumulation
release of ceruloplasmin without Cu (apoceruloplasmin) rapid degradation of ceruloplasmin |
|
4 abnormal lab tests in Wilson's disease
|
LFTs
serum ceruloplasmin serum Cu urine Cu |
|
in Wilson's,
serum ceruloplasmin is ___ serum Cu is ___ urine Cu is ___ |
low
low high |
|
Keyser-Fleischer ring is located in ___
|
cornea
|
|
blood abnormality in Wilson's disease
|
hemolytic anemia
|
|
tx for Wilson's
|
penicillamine
|
|
main gene linked to primary hemochromatosis
|
HFE
|
|
normally, HFE does ___ in ___ cells
this allows the cells to ___ by ___ing |
complexes with TfR
duodenal crypt epithelial sense serum Fe levels endocytosing circulating Fe-Tf |
|
mutant HFE causes defective ___
which causes ___ |
Fe level sensing
upregulation of Fe-absorption proteins (including ferroportin) |
|
hemochromatosis pw ___ (3)
|
cirrhosis
DM skin pigmentation |
|
2 complications of hemochromatosis
|
HCC
CHF |
|
PSC is associated with ___
finding on ERCP is ___ serum finding is ___ histopath is ___ complication is ___ |
UC
beading IgM hypergammaglobulinemia bile duct onion skinning fibrosis 2' biliary cirrhosis |
|
1' biliary cirrhosis is associated with ___ (2)
serum finding is ___ |
scleroderma
CREST anti-mitochondrial Abs |
|
PSC and PBC pw ___ (5)
|
severe obstructive jaundice (dark urine, acholic stool)
steatorrhea pruritus hypercholesterolemia hepatosplenomegaly |
|
complication of 2' biliary cirrhosis
|
ascending cholangitis
|
|
in hemochromatosis, TIBC is ___ or ___
|
low
normal |
|
dd of acute pancreatitis (10)
|
Gallstone
EtOH Trauma Steroids Mumps Autoimmune Scorpion sting Hyperlipidemia/hypercalcemia ERCP Drugs (e.g. sulfa) |
|
electrolyte disturbance associated with acute pancreatitis
|
hypocalcemia
|
|
2 life-threatening conditions associated with acute pancreatitis
|
DIC
ARDS |
|
2 markers for pancreatic adenoca
|
CEA
CA 19-9 |
|
2 populations predisposed to pancreatic adenoca
|
Jewish
African-American |
|
T/F: smoking is RF for pancreatic adenoca
|
true
|
|
T/F: EtOH is RF for pancreatic adenoca
|
false (probably)
|
|
H2 blockers end in ___
|
tidine
|
|
4 cimetidine SEs
|
CYP inhibitor
antiandrogenic effects CNS penetration reduced CCT |
|
4 cimetidine antiandrogenic SEs
|
high PRL
gynecomastia low libido impotence |
|
3 cimetidine CNS SEs
|
confusion
dizziness HA |
|
misoprostol is a ___ analog
it does ___ (2) for stomach and ___ (2) in ob-gyn setting |
PGE1
increased gastric mucus production decreased gastric H+ production uterine contractility cervical ripening |
|
misoprostol is indicated for ____ (4)
|
labor induction
abortificant gastroprotection for NSAID tx PDA patency maintenance |
|
2 pathways for gastric H+ secretion
|
direct
indirect |
|
in direct gastric H+ pathways, ___ from ___ cells causes ___ cells to ___
|
ACh
postsynaptic vagal parietal release H+ |
|
in indirect gastric H+ pathways, ___ from ___ cells causes ___ cells to ___.
this causes ___ cells to ___, which causes ___ cells to ___. |
Gastrin-releasing peptide (GRP)
postsynaptic vagal G release gastrin enterochromaffin-like (ECL) release HA parietal release H+ |
|
pirenzepine and ___ are ___s
they are used for ___ (2) |
propantheline
muscarinic blockers decreasing gastric H+ secretion decreasing ECL HA secretion |
|
overdose of aluminum hydroxide antacid causes ___ (4)
|
constipation
hypophosphatemia osteodystrophy neurological sx |
|
2 neurological aluminum hydroxide sx
|
proximal muscle weakness
seizures |
|
4 magnesium hydroxide antacid overdose sx
|
diarrhea
cardiac arrest hypotension hyporeflexia |
|
2 calcium carbonate antacid overdose sx
|
hypercalcemia
rebound H+ hypersecretion |
|
electrolyte disturbance associated with all antacids
|
hypokalemia
|
|
sulfasalazine is activated by ___
|
gut bacteria
|
|
3 sulfasalazine SEs
|
nausea
sulfonamide rxn oligospermia (reversible) |
|
ondansetron is a ___
it is used as ___ |
5-HT3 blocker
anti-emetic |
|
2 ondansetron indications
|
post-op
cancer chemo |
|
2 ondansetron SEs
|
headache
constipation |
|
metoclopramide is a ___
it is indicated for ___ (2) |
D2R blocker
post-op gastroparesis DM gastroparesis |
|
metoclopramide increases GI ___ (4)
but doesn't affect ___ |
resting tone
contractility motility LES tone colon transit time |
|
5 metoclopramide SEs
|
parkinsonism
restlessness drowsiness depression diarrhea |
|
metoclopramide interacts with ___ (2)
|
digoxin
DM drugs |
|
metoclopramide is contraindicated in ___
|
SBO
|