USMLE GI Flashcards

(189 cards)

1
Q

What cells are involved in carcinoid syndrome?

A

Neuroendocrine cells from carcinoid tumors

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2
Q

Symptoms of carcinoid syndrome?

A

Recurrent diarrhea, cutaneous flushing, asthmatic wheezing and R sided valvular heart disease

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3
Q

What would you see in the urine of carcinoid syndrome?

A

Increased 5-hydroxyindoleacetic (5-HIAA) urine

There is increased amount of serotonin being released

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4
Q

Tx of carcinoid syndrome?

A

Surgical resection, somatostatin analogue (octreotide)

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5
Q

Veins implicated in esophageal varices? Caput medusae? Anorectal varices?

A

Esophageal - L gastric to azygos
Caput - paraumbilical to small epigastric veins of anterior abd wall
Anorectal - superior rectal to middle and inferior rectal

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6
Q

Honey in those younger than 1 is implicated in which bacteria?

A

C. botulinum and its spores

Can cause “floppy” head

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7
Q

Symptoms of botulism

A

Four D’s = diplopia, dysarthria, dysphagia and dyspnea

Tx: human botulinum immunoglobulin

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8
Q

Difference between C botulinum and C tetani?

A

C botulinum - toxin inhibits Ach release at NMJ

C tetani - produces tetanospasmin, an exotoxin causing tetanus; blocks release of inhibitory release of inhibitor NTs such as GABA and glycine from Renshaw cells in spinal cord

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9
Q

Arteries, veins and lymphatics above and below dentate line?

A

Artery/vein/lymph above:
superior rectal artery (from IMA), inferior mesenteric vein, internal iliac LN

Artery/vein/lymph below: inferior rectal artery (from internal pudendal a), internal pudendal vein, superficial inguinal LN

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10
Q

ABCDs of C. difficile

A

Toxin A (enterotoxin) - binds to brush border of gut and alters fluid secretion

Abx use

Toxin B (cytotoxin) - disrupts cytoskeleton via actin depolymerization

Colitis (pseudomembranous)

Difficile/diarrhea

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11
Q

Tx of C diff

A

Metronidazole or vanco

Fidaxomicin for recurrent cases

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12
Q

Food aversion, wt loss, postprandial epigastric pain

A

Chronic mesenteric ischemia 2/2 atherosclerosis

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13
Q

Abd pain out of proportion with red “currant jelly” stools

A

Acute mesenteric ischemia

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14
Q

Crampy abd pain followed by hematochezia

A

Colonic ischemia

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15
Q

1 gram of protein yields how many calories?

A

4 calories of energy

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16
Q

Presentation of intestinal atresia

A

Bilious vomiting, abdominal distention within first 1-2 days of life

Duodenal = failure to recanalize; double bubble sign; associated with Down
Jejunal and ileal = disruption of mesenteric vessels, leading to ischemic necrosis, causing segmental resorption (bowel discontinuity or “apple peel”)

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17
Q

Hyperbilirubinemias (AR)

Gilbert syndrome
Crigler-Najjar, type 1
Dubin-Johnson

A

Gilbert = mild decreased UDP-glucuronosyltransferase conjugation and impaired bilirubin uptake; asymptomatic or mild jaundice with stress, illness or fasting

Crigler-Najjar = absent UDP-glucuronosyltransferase; pt die within a few years; jaundice, kernicterus (bilirubin deposition in the brain)

Dubin-Johnson = conjugated hyperbilirubinemia due to defective liver excretion of bilirubin glucuronioids; grossly black/dark liver

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18
Q

Thin curvilinear areas of lucency in premature infants

A

Necrotizing enterocolitis

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19
Q

Where does H pylori preferentially like to colonize?

A

Gastric antrum

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20
Q

Triple positive of H pylori

A

Gram negative rod that is catalase +, oxidase + and urease +

Amoxicillin + Clairthromycin + PPI

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21
Q

Gastric ulcers are associated with which part of the stomach? Duodenal ulcers?

A

Duodenal ulcers = gastric antrum

Gastric ulcers = gastric corpus/body

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22
Q

Lactose intolerance - what enzyme, histology and stool pH

A

Lactase deficiency
Normal appearing villi
Osmotic diarrhea with decreased stool pH

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23
Q

Tissue type of pancreatic pseudocyst

A

Fibrous and granulation tissue

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24
Q

Where does lipid absorption take place? Bile absorption?

A

Lipid - jejenum

Bile acid - terminal ileum

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25
Bile acid resins
Cholestyramine Colestipol Colesevelam Retains bile acids, prevent reabsorption and more is excreted in stool
26
Three roles of bile
1) digestion and absorption of lipids and fat-soluble vitamins 2) cholesterol excretion 3) antimicrobial activity (via membrane disruption)
27
Lab findings in cholestasis
Direct/conjugated hyperbilirubinemia Elevated alk phos
28
What are markers of biliary disease?
Alk phos, gamma-glutamyl transpeptidase
29
Name of enzyme involved in conjugation of bilirubin?
UDP-glucuronosyl-transferase Adding glucuronic acid to make it soluble
30
Name of molecule that makes your stool dark? Name of molecule that makes your urine yellow?
Stercobilin Urobilin
31
Wilson disease characteristics
Movement abnormalities and psych symptoms
32
Hemachromatosis
Liver disease, skin pigmentation, DM and cardiac enlargement
33
Four general causes of hyperbilirubinemia
Hemolysis, biliary obstruction, liver disease, special causes or HOT Liver = hemolysis, obstruction, tumor and liver dz
34
Lab findings of hemolysis
Increased indirect bilirubin, normal urine bilirubin and increased urobilinogen
35
Lab findings of obstruction
Increased direct bilirubin, increased urine bilirubin and absent urobilinogen
36
Two drugs that can cause hyperbilirubinemia
Rifampin (abx for tx of TB) Probenecid (gout) Both compete with bilirubin for uptake by liver Increase in unconjugated bilirubin
37
Cause of death in Crigler-Najjar syndrome
Kernicterus (bilirubin deposition in brain) Unconjugated bilirubin is soluble in fats and can easily cross BBB or enter placenta
38
Drug tx for Crigler-Najjar, type 2
Phenobarbital, clofibrate
39
Cause of Dubin-Johnson syndrome and characteristic finding
Defective liver excretion Dark liver
40
Lab findings of physiologic neonatal jaundice
Increased unconjugated hyperbilirubinemia 2/2 immature UDP-glucuronosyltransferase
41
Where does bilirubin accumulate in the brain in kernicterus?
Basal ganglia
42
Tx of neonatal jaundice
Phototherapy which converts bilirubin to lumirubin (more H2O soluble)
43
Which type of cell in the stomach secretes gastric acid?
Parietal cells found in gastric glands
44
Three stimuli for acid secretion
Gastrin (direct) binding to CCKb receptor on parietal cells Gastrin (indirect) activates ECL cells to release histamine, which causes stimulation Vagus nerve - activates G cells by using gastrin releasing peptide
45
Role of IF and what releases it?
Necessary for vitamin B12 absorption Released by parietal cells
46
Vomiting causes what kind of acid-base physio?
Metabolic alkalosis due to loss of HCl This causes an increase in HCl production and HCO3 is also generated Urinary Cl is low
47
Urinary chloride is useful in?
Determining metabolic alkalosis of unknown cause Low (<10-20) in vomiting (loss of Cl in gastric secretions) High (>20) in diuretic use (diuretics block NaCl reabsorption)
48
Histamine H2 blockers
Cimetidine, ranitidine, famotidine, nizatidine
49
What activates parietal cell secretion? What deactivates it?
ACh (Gq), gastrin (Gq) and histamine (Gs/i) PG (Gs/i) and somatostatin (Gs/i)
50
Where are G cells found? Parietal cells?
Antrum of stomach Mucosa of body (parietal cells)
51
Zollinger-Ellison syndrome
Gastrin secreting tumor Occurs in duodenum or pancreas (G cells in pancreas) Excessive acid secretion AP, chronic diarrhea, ulcers
52
Tx of gastrinoma
High dose PPI, octeotride (somatostatin)
53
Pernicious anemia
Autoimmune gastritis, causing loss of parietal cells therefore loss of IF Cannot absorb vit B12 High gastrin levels
54
Gastrin stimulates what kind of cells? Dz associated with this?
Parietal cells Pernicious anemia (loss of parietal cells, high gastrin levels)
55
Cholecystokinin
Hormone for gall bladder contraction Released by I cells (small intestines, D and J)
56
Secretin
Released by S cells of duodenum Raises pH in small intestine by pancreatic duct cells!!!
57
Somatostain
Inhibits most GI hormones Released by D cells throughout GI tract
58
Tx of variceal bleeding
Octreotide (used to tx acromegaly, carcinoid syndrome and variceal bleeding)
59
Glucose-dependent insulinotropic peptide
Released by K cells (duodenum, jejenum) Oral glucose is metabolized faster than IV glucose If you administer oral glucose on a pt, GIP will be released
60
VIPomas
VIP secreting tumor in the pancreas (islet cells) WDHA (watery diarrhea), hypokalemia, achlorhydria Tx is octreotide (somatostatin)
61
How does erythromycin play a role in motility?
Erythromycin binds to motilin receptors. Motilin is released by cells in the stomach, intestines and colon. Used to tx gastroparesis
62
What enzyme converts trypsinogen to trypsin?
Enterokinase/enteropeptidase Brush-border enzyme on duodenal and jejunal mucosa
63
What types of cells can you see in reflux esophagitis?
Eosinophils
64
This commonly leads to esophageal stricture formation
Consumption of lye (alkali substances), causing liquefactive necrosis that can later cause strictures
65
Cause of esophagitis
GERD Candida - white pseudomembrane HSV-1 - punched out ulcers CMV - linear ulcers
66
Pathophys of achalasia (primary and secondary)
Primary: loss of ganglion cells in Auerbach's plexus (myenteric) in muscularis therefore dysphagia to solids and liquids Secondary: Chronic Chagas dz
67
Diagnostic testing of achalasia
Increased LES tone in esophageal manometry Barium swallow
68
Which layer of esophagus is involved in Mallory Weiss?
Mucosa at GE junction Painful hematemesis
69
Which layer of esophagus is involved in BoerHaave syndrome?
Transmural rupture Air exits esophagus -> air in mediastinum and under skin in neck
70
Findings in Plummer-Vinson syndrome
Iron deficiency anemia Beefy red tongue Esophageal web Common in middle-age, white women Triad of dysphasia, iron deficiency and esophageal webs (DIE)
71
Which muscle is implicated in Zenker's diverticulum?
Cricopharyngeal muscle (which allows food to pass) Classic location: Killian's triangle between thyropharyngeus muscle and cricopharyngeus muscle
72
What causes high GGT?
Alcohol use
73
Which zone is affected first in alcoholic liver dz? (Where does fatty infiltration occur?)
Zone III (near hepatic vein)
74
Viral hepatitis affects which zone first?
Zone I
75
When do you see ALT > AST?
Nonalcoholic fatty liver dz
76
What is associated with non-alcoholic fatty liver dz?
Obesity
77
Histology of alcoholic hepatitis
Mallory bodies (intracytoplasmic eosinophilic inclusions of damaged keratin/intermediate filaments)
78
Nutmeg liver
Budd-Chiari syndrome RHF
79
Reye syndrome
Children with viral infections who take ASA Chicken pox and influenza B These pts have rapid, severe liver failure, as ASA inhibits beta oxidation, damaging mitochondria
80
Alpha1 anti-trypsin deficiency
Emphysema and cirrhosis are seen Imbalance b/w elastase and elastase inhibitor AAT (which protects elastin) - emphysema Abnormal alpha1 builds up in liver, pathologic polymerization of AAT - cirrhosis Stain purple with PAS
81
Two bacteria involved in liver abscess
Entamoeba histolytica (protozoa) Echinococcus (helminth)
82
Tx of Tylenol (acetaminophen) OD
N-acetylcysteine
83
Tx of hyperammonemia
Low protein diet Lactulose (synthetic disaccharide and laxative) - it gets broken down to FAs, which decrease pH, favoring ammonium levels than ammonia
84
Portal vein thrombosis
Acute onset abd pain Splenomegaly Liver biopsy will be normal
85
Spontaneous bacterial peritonitis
E. coli and Klebsiella Tx: cefotaxime
86
Which cells are implicated in cirrhosis?
Stellate cells = perisinusoidal cell. Secretes TGF-beta, proliferates and produce fibrous tissue Major contributor to cirrhosis
87
Which bacteria is implicated in HCC?
Aspergillus. It is a fungus that produces aflatoxin
88
Lab findings for HCC?
Increased alpha-fetal protein
89
Common site of metastasis of HCC?
Lung
90
Associated RF for hepatic adenoma
Contraceptive use, anabolic steroids
91
Vinyl chloride and arsenic can cause what liver pathology?
Hepatic angiosarcoma
92
ATP7B gene for Wilson's dz is found on which chr?
Chr 13
93
If you suspect someone with Wilson's dz, what do you do?
Order slit lamp exam
94
Tx of Wilson's dz?
Pencillamine
95
HFE gene in hemochromatosis?
Chr 6 | Most commonly due to homozygous C282Y mutation
96
Cause of secondary hemochromatosis
Chronic transfusion therapy for beta-thal major
97
What should pts with hemochromatosis NOT consume?
Alcohol, vitamin C
98
Lab tests for hemochromatosis (iron, ferritin, transferrin, % saturation transferrin)
Increased iron Increased ferritin Decreased/normal transferrin/TIBC % saturation transferrin
99
Tx of hemochromatosis
phlebotomy
100
Four RFs of gallstones?
4 F's = female, forty, fat, fertile (multiparity) If an elderly pt has gallstone symptoms, think CA
101
Other RFs for gallstones?
Excess estrogen Altered lipid metabolism Loss of bile salts
102
What causes the pain seen in biliary colic?
Pain after eating, esp fatty meals CCK stimulates gallbladder contraction
103
Choledocholithiasis
Presence of gallstone common bile duct, often leading to elevated ALP, GGT, direct bilirubin and/or AST/ALT
104
Porcelain gallbladder
Calcified gallbladder Increased rate of gallbladder CA
105
Charcot's triad Reynolds pentad
Fever, abd pain, jaundice (part of ascending cholangitis) Charcot + confusion + hypotension
106
Bacterial causes of ascending cholangitis
E. coli, Klebsiella, Enterobacter Rare cause: Clonorchis sinensis (will see peripheral eosinophilia)
107
Air in the biliary tree
Gallstone ileus, where massive gallstone erodes through gallbladder wall Creation of a fistula with small intestine
108
Common bacteria that causes gallbladder carcinoma
Salmonella typhi
109
Primary biliary cirrhosis
Autoimmune disorder with T cell attacking the small intralobular bile ducts Granulomatous inflammation
110
Dx of primary biliary cirrhosis
Anti-mitochondrial antibodies, markedly elevated alk phos
111
What condition is associated with primary biliary cirrhosis?
Sjogren
112
What condition is associated with primary sclerosing cholangitis?
Ulcerative colitis
113
Lab findings (dx) of primary sclerosing cholangitis
Elevated IgM, positive p-ANCA
114
Pathology of primary sclerosing cholangitis
Periductal fibrosis Alternating strictures Beading of intra- and extra-hepatic bile ducts
115
What can cause cholangiocarcinoma?
Primary sclerosing cholangitis (UC) Clonorchis sinensis (Chinese liver fluke)
116
Curling ulcer
Occurs in burn pts Loss of skin -> loss of fluids -> dehydration -> hypotension to stomach -> mucosal damage Result: acute gastritis and ulcers
117
Cushing ulcer
Increased vagal stimulation Increased ACh Increased H production
118
Autoimmune gastritis vs H pylori gastritis
Autoimmune - destruction of gastric parietal cells, therefore body/fundus is affected first H pylori -
119
Where does H pylori affect first?
Antrum of stomach
120
Which CA is associated with H pylori?
MALT lymphoma (B-cell CA)
121
Which enzyme is more specific for pancreatic damage?
Lipase
122
If you see ulcers in duodenum or jejenum, what should you suspect?
Zollinger-Ellison syndrome
123
Brunner's glands
Found in duodenum in submucosa Produces alkaline (basic) fluid; thick in peptic ulcer dz
124
Odd RFs of intestinal gastric CA?
Type A blood | Nitrosamines found in smoked meats
125
Histology of diffuse gastric CA?
Signet ring cells and linitis plastica (stomach thickened like leather)
126
Which CA is acanthosis nigricans associated with?
Gastric carcinoma
127
Menetrier disease
Hyperplasia of gastric mucosa; excessive gastric mucous secretions and loss of acid Protein loss, hypoalbuminemia Can lead to gastric adenocarcinoma
128
Celiac sprue is what type of HS?
Type IV Associated with HLA-DQ2, HLA-DQ8
129
Histology of celiac dz
Blunting of villi Crypt hyperplasia Lymphocytes in lamina propria
130
Antibody for celiac dz
IgA anti-tissue transglutaminase IgA anti-endomysial Anti-gliadin
131
Most commonly affected area in celiac dz
Duodenum
132
What CA is associated with celiac dz?
T-cell lymphoma
133
Skin condition associated with celiac dz?
Dermatitis herpetiformis
134
Bacteria that causes Whipple dz
Tropheryma whipplei
135
Four cardinal features of Whipple dz
Diarrhea Abd pain Wt loss Joint pain
136
Marker for autoimmune pancreatitis
IgG4 positive plasma cells
137
One of the main complications of acute pancreatitis
Pseudocyst (lined by granulation tissue, not epithelium)
138
Fat necrosis can lead to?
Hypocalcemia/hypomg
139
Two common causes of chronic pancreatitis
Alcohol abuse in adults | CF in kids
140
Trousseau syndrome
Migratory thrombophlebitis in pancreatic CA
141
Appendicitis pathogenesis
Fecaliths in adults | Lymphoid hyperplasia in kids
142
Where does a false diverticulum usually occur?
Where the vasa recta perforate muscularis externa
143
Where does diverticulosis occur? What typically causes it?
Sigmoid colon Straining to pass stool (wall stress); low fiber diet
144
Most common cause of SBO
Adhesions
145
Currant jelly findings
Intussusception Medical injury, near the ileocecal junction
146
Common lead point (intussusception) in kids and adults?
Kids - Meckel diverticulum Adults - intraluminal mass/tumor KNOW: adenovirus (STRONG association) Peyer patch hypertrophy
147
Which volvulus is more common in elderly? Kids?
Sigmoid in adults Midgut volvulus in kids
148
SBO common causes vs LBO
Adhesion Bulge CA LBO; CA, adhesions, volvulus
149
Pathophys of Hirschsprung's dz
Absent ganglion cells (derived from neural crest cells) Nerve cells of Meissner's plexus and Auerbach's pleux Failure to migrate
150
Ogilvie syndrome
Acute "pseudo-obstruction" of intestines; dilated colon in asbence if a lesion Usually hospitalized or nursing home pts Often severe illness or recent surgery Often associated with narcotics
151
Major RF for necrotizing enterocolitis
Prematurity
152
Classic XR finding of necrotizing enterocolitis
Pneumatosis intestinalis
153
Angiodysplasia is common where?
Cecum and R sided colon Caused hy high wall stress Leads to lower GI bleeding
154
Osler-Weber-Rendu syndrome
aka hereditary hemorrhagic telangiectasia AD Telangiectasias throughout GI tract Rarely leads to AVMs Common clinical features: nose bleeds, GI bleeding, Fe deficiency
155
Feared complication of UC
Toxic megacolon | Evidence of nitric oxide that inhibits smooth muscle tone; can cause perforation
156
Antibody tests for UC and Crohn
UC - p-ANCA Crohn - anti-saccharomyces cerevisiae antibodies (ASCA)
157
Common location of Crohn
Terminal ileum Therefore malabsorption, vit B12 deficiency, malabsorption of bile salts RLQ
158
Immunology of Crohn and UC
Th1 for Crohn Th2 for UC
159
Tx's of UC
Sulfasalazine (gets broken down into 5-aminosalicylic acid 5-ASA) Mesalamine (5-ASA)
160
Common side effect of sulfasalazine
Oligospermia in men
161
Benign and most common polyps
Hyperplastic
162
Peutz-Jeghers syndrome
AD, multiple hamartomas throughout GI tract Pigmented spots on lips and buccal mucosa Risk of gastric, small intestinal and colon CA
163
Three genetics of colon CA
1) two genetic pathways (chromosomal instability, and microsatellite) 2) cyclooxygenase-2 expression increased in colon CA 3) DCC gene mutated in advanced colorectal CA
164
Chromosomal instability pathway of colorectal CA
Loss of APC gene KRAS mutation Loss of tumor suppressor gene (p53) AK-53
165
Gardner syndrome
FAP + osseous and soft tissue tumors, congenital hypertrophy of retinal pigment epithelium and impacted/supernumerary teeth
166
Turcot syndrome
FAP + brain tumor (medulloblastoma)
167
Microsatellite instability
Mismatch of microsatellites (short repeating segments of DNA)
168
Lynch syndrome
Hereditary nonpolyposis colorectal CA (HNPCC) Inherited mutation of DNA mismatch repair enzymes; leads to colon CA via microsatellite instability
169
Most common non-colon malignancy in Lynch syndrome
Endometrial CA
170
Gene implicated in colorectal CA
DCC gene | Defect in colorectal gene
171
S bovis endocarditis is identified. What test is next?
Colonoscopy to screen for colorectal CA
172
Tumor marker for colorectal CA
Carcinoembryonic antigen | CEA
173
Vitamin B3 is derived from what aa?
Tryptophan Can see pellagra in carcinoid syndrome since tryptophan is used to make serotonin
174
Clinical manifestations of carcinoid syndrome
Recurrent diarrhea, cutaneous flushing, asthmatic wheezing, R sided valvular heart dz
175
Tx of carcinoid syndrome
Octreotide
176
Milk alkali syndrome
High intake of calcium carbonate (ulcers) Triad: hypercalcemia, metabolic alkalosis and renal failure
177
Side effects of aluminum hydroxide
Constipation, phosphate binder therefore hypophosphatemia
178
Side effects of Mg hydroxide
Diarrhea, hyporeflexia, hypotension, cardiac arrest
179
Antacids can affect the drug absorption of which drug?
Tetracycline Fluorquinolones Isoniazid Fe supplements
180
Common side effect of histamine (H2) blockers
Confusion, esp among elderly
181
Side effects of cimetidine
1st H2 blocker Potent P450 inhibitor Antiandrogen (gynecomastia, impotence, PRL release) Crosses BBB (dizziness, confusion, HA) Reduces creatinine excretion
182
Side effects of PPIs
C diff infection (loss of protection from H) Pneumonia (more pathogens) Malabsorption therefore low Mg and Ca therefore hip fractures
183
Mechanism of ondansetron What is it good for?
5-HT3 antagonist For those undergoing CA chemotherapy
184
Mechanism of metoclopramide
D2 receptor antagonists Dopamine blocks ACh effects, therefore causing increased esophagus and gastric motility Used in gastroparesis
185
AEs of metoclopramide
Drowsiness Parkinsonian effects
186
CI of meteoclopramide
Known sz disorders Parkinson's dz BO
187
Which enzyme is absent in galactosemia?
Galactose-1-phosphate uridyltransferase
188
Which gene is implicated in familial adenomatous polyposis?
APC gene
189
Most common benign liver tumor
Cavernous hemangioma