Gastrointestinal Exam 2 Flashcards

(215 cards)

1
Q

Sphincter of Odi

A

Between pancreas and duodenum

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2
Q

3 exoxrin pancreatic enzymes

A

Protease (trypsin and chymotrypsin)
Lipase
Amylase

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3
Q

Pancreatic delta cells

A

Secrete somatostatin
Endocrine cells more in the tail

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4
Q

Parts of pancreas damaged more with chronic versus acute pancreatitis

A

Acute - exocrine
Chronic - endocrine

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5
Q

MCC of acute pancreatitis

A

Gallstones, Alcohol, Idiopathic 20%

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6
Q

Alcoholic pancreatitis

A

May be due to acinar cell injury or stimulated contraction of sphincter of Oti

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7
Q

Presentation of acute pancreatitis

A

Epigastric pain radiating to the back
Improves leaning forward, worse lying down
N/V, sweating

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8
Q

PE findings for acute pancreatitis- 4

A

May have absent bowel sounds, epigastric tenderness, Jaundice, Mass

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9
Q

Cullen’s sign

A

Bruising around the umbilicus d/t acute pancreatitis

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10
Q

Gray Turner sign

A

Flank bruising d/t pancreatitis

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11
Q

Acute interstitial edematous pancreatitis

A

More common acute pancreatitis - intact blood flow

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12
Q

Necrotizing acute pancreatitis

A

Blood flow not intact - more severe

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13
Q

Labs for acute pancreatitis

A

Amylase and Lipase (more sensitive) 3x upper limit is diagnostic

Leukocytosis on CBC

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14
Q

Imaging for acute pancreatitis

A

Sentinel loop or colon cutoff sign on plain X-ray
US not useful
CT may show enlarged pancreas

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15
Q

Ranson’s Criteria- 5 At Admission and 6 after 48 Hours

A

Pancreatitis Prognosis
Admission:
Age >55
BG > 200mg/dL
Serum LDH >350
AST >250
WBC >16,000

Within 48 hours
HCT decrease >10%
BUN increase >5mg/dL
Serum calcium <8mg/dL
PaO2 <60mmHg
Base deficit >4mEq/L
Estimated fluid sequestration >6L

3+ predict a severe course

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16
Q

Mortality rate for Ranson’s Criteria

A

0-2 - 1%
3-4 - 16%
5-6 - 40%
7-8 - 100%

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17
Q

BISAP criteria for acute pancreatitis

A

BUN >25mg/dL
Impaired Mental Status
Systemic inflammatory response
Age >60
Pleural effusion

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18
Q

Treatment for acute pancreatitis

A

Admit
Rest Pancreas - NPO
IV fluids - early and aggressive
NO MORPHINE, Demerol for pain
Bed rest

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19
Q

Mild acute pancreatitis treatment as symptoms improve

A

Clear liquids and low fat first
Cholecystectomy if gallstone
Monitor for return of bowel sounds

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20
Q

Tx for severe acute pancreatitis

A

ICU, Treat complication, ABX if abcess - imepenem, Fluid resicitation, CT if not improving

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21
Q

Acute pancreatic fluid collection

A

Resolves spontaneously in 7 days

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22
Q

Chronic pancreatitis presentation

A

Slow irreversible loss
MCC = Alcoholism, smoking, autoimmune
Steady pain, worse after eating, DM and steatorrhea d/t enzyme loss
Can have an acute attack

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23
Q

Labs for chronic pancreatitis

A

Slightly elevated lipase and amylase could be normal
Check of autoimmune cause

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24
Q

Imaging for chronic pancreatitis

A

Calcifications on X-ray
CT is preferred
Ultrasound - honeycombing of the pancreas

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25
Management of chronic pancreatitis
Low fat, stop smoking, alcohol Pain management - careful with opioids Treat complications
26
Puestow procedure
Pain relief for dilated duct - attach intestines to pancreas
27
Whipple procedure
Resection of part of the pancreas
28
Part of pancreas easier to resect
Head of the pancreas
29
Risk factors for pancreatic cancers (4)
Over 45 Late onset diabetes Smoking BRACA gene
30
Clinical presentation of pancreatic cancer
Gnawing insidious pain like gastritis Painless jaundice with nontender palpable gallbladder = Courvasier's sign Sister Mary Joseph Nodule
31
Tumor marker for pancreas
CA-19-9
32
Imaging for pancreatic cancer
CT = First line ERCP if uncertain CT
33
Pancrease staging
T1 and T2 confined to pancreas, others not
34
Surgery for pancreatic cancer
Exploratory laparoscopy followed by whipple procedure is suitable
35
Screening for pancreatic cancer
If 1st degree relative - get a CT 10 years before onset in the relative
36
ERCP
More invasive with sedation Diagnostic AND therapeutic
37
MRCP
Like an MRI, less invasive Only diagnostic
38
Triangle of Calot
Medial common hepatic duct Inferior cystic duct Superior-inferior surface of the liver Landmark in cholecystectomy allowing for ligation of cystic duct and artery - need to protect common bile duct
39
CCK
Cholecystokinin - Stimulates gall bladder contraction and sphincter of Oti relaxation
40
Causes of gallstone formation
High cholesterol High Billirubin Sedentary Gall Bladder
41
Lifestyle changes to prevent cholelithiasis
Low carb or mediterranean diet Caffeinated coffee
42
Asymptomatic cholelithiasis
Stones stay in the bottom of gall bladder and do not cause pain by blocking the duct
43
Presentation of cholelithiasis- Pain, Timing, Appearance
RUQ pain to right shoulder blade After fatty meals Dull with nausea and sweating Not ill-appearing
44
Lab results for cholelithiasis
WNL
45
Abd exam with cholelithiasis
No peritoneal sx, no rebounds tenderness Pretty benign
46
Imaging for cholelithiasis
Abd US is procedure of choice - RUQ Could also use CT or XR
47
Treatment for cholelithiasis
NSAIDS for pain Laparoscopic cholecystectomy Don't need to treat if asymptomatic
48
3 reasons for a prophylactic cholecystectomy
Calcified gall bladder 3cm or greater stones Native American
49
Pregnancy and cholecystectomy
Try to wait until 2nd trimester Need labor and delivery and NICU there
50
Intraoperative choleangiogram
Xray with catheter in bile duct to help with surgeon visualization - used to check for nicking of common bile duct
51
Treatment for cholelithiasys in those not candidates for surgery- 2 Pharm options
Urosodiol - Ursodeoxycholic acid Bile salt PO
52
3 types of cholecystitis
Acute Calculus - due to gallstones and MC Acute acalculous - Gallbladder stasis ischemia - major surgeries Chronic cholecystitis - Episodic billiary cholic
53
Presentation of cholecystitis
Appear Ill - Unlike cholic Pain with fatty meal lasting over 6 hours!!! Peritoneal signs
54
Murphys sign
Cholecystitis - Inspiration stops with pressing down in RUQ
55
Lab findings in cholecystitis
Leukocytosis w/ Left shift No elevation of liver enzymes
56
Imaging for acute cholecystitis
Thickening of gallbladder wall Stones Use an US HIDA scan if inconclusive
57
HIDA scan
IV contrast that travels into bile ducts - look for transit time Non-visualized gallbladder = Cholecystitis
58
Other diagnostic test for cholecystitis
CCK injection Ejection fraction of gallbladder under 35
59
Complications of acute cholecystitis
Gangrene of gallbladder Gallbladder perforation Hydrops of gallbladder - distended Mirizzi syndrome - Jaundice from common hepatic duct compression Percelain gallbladder - calcified
60
Management of acute cholecystitis- 4
Abx for E coli - Pip and Taz or 2nd or 3rd gen chep or cipro and metro NPO w/ NG tube Demerol or NSAID for pain Cholecystectomy w/in 24-48 hours
61
New treatment for acute cholecystitis
Cholecystotomy for drainage Alternative if they can't handle a cholecystecomy
62
-choledo-
Common bile duct
63
Choledocholithiasis presentation and cause
Gallstone in common bile duct - uncomplicated RUQ pain up to scapula Jaundice Epigastric tenderness
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Diagnosis for choledocholithiasis
Elevated liver enzymes with bilirubinemia
65
Treatment for choledocholithiasis
ERCP with spincterotomy and stent placement with Cholecystectomy after MRCP used first for low risk - just cholecytectomy if no stone
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Cholangitis
Bacterial infection with stone in common bile duct
67
Triad of acute cholangitis
Charcot triad RUQ pain Fever Jaundice Reynolds Pentad Add - Hypotension and Mental status changes
68
Labs and imaging for acute cholangitis
CBC leukocytosis Liver enzymes Prolonged PT ERCP is the most accurate imaging - Diagnostic procedure of choice, will likely do an US first
69
Treatment for cholangitis
NPO, prep for surgery, IV fluids, Pain control ERCP for stone extraction
70
ABX for cholangitis
Mild/Mod - Cipro and flagyl Severe - Zosyn(Pip and Taz) and Flagyl
71
First line imaging for most billiary diseases
US
72
Primary sclerosing cholangitis
Related to UC and IBD No cure Leads to obstructive symptoms - fibrosis
73
Presentation of PSC
Jaundice Pruritis Hepatosplenomegaly
74
Lab finding for PSCA
Elevated LFTs Increased P-ANCA antibodies (specific to injuries of billiary tree)
75
Imaging for PSCA
MRCP - ERCP if inconclusive Beads on a string seen is indicative - Segmental fibrosis Liver biopsy with "onion skinning" if those are inconclusive
76
Treatment for PSCA
No cure Cipro for episodes Immune suppressants and Ursodeoxycholic acid are being studied ERCP with stent Liver transplant Resection of carcinoma - complication
77
Most deadly gallbladder cancer
Choleangiocarcinoma
78
3 common coexisting conditions with gallbladder carcinoma
Chronic infection - Salmonella Gallbladder polyp Calcification of gallbladder Often invades liver
79
MC location of choleangiocarcinoma
Confluence of R/L hepatic ducts
80
PE findings of biliary tract cancer
RUQ tenderness Courvoisier sign Ascites
81
Diagnostic for Carcinoma of biliary tract
ERCP w/ biopsy or US guided biopsy
82
Tx for biliary tree cancer
Resect Roux en Y if non-resectable to bypass bile duct -bile drains fromthe liver to the duodenum
83
Porta hepatis
Hepatic artery, Portal vein, and hepatic duct - between the four lobes
84
Unconjugated billirubin
Indirect bilirubin that has NOT been processed by the liver. made from protoporphyrin Binds to albumin, lipid soluble
85
Conjugated bilirubin
Made by uridine glucuronyl transferase Water soluble - has been processed by the liver Goes to bile ducts
86
Fates of conjugated bilirubin
Goes to SI, urobilinogen sent to urine, cobilin sent to feces
87
Conjugated hyperbilirubinemia
Pale urine and stools as opposed to unconjugated hyperbilirubinemia Post hepatic jaundice
88
3 factors not made in liver for clotting
III,IV, and VIII - not effected by liver disease
89
Gold standard to diagnose portal hypertension
Insert catheter to get pressure
90
ABCDE of portal hypertension
Ascites Bleeding Caput Medusae Diminished liver function Enlarged spleen
91
Hepatorenal syndrome
Liver failure leads to kidney failure - portal hypertension causes poor perfusion of kidneys
92
Hepatic encephalopathy
Due to ammonia buildup - ammonia can't be made to urea
93
3 enzymes that assess for hepatic tissue damage
AST, ALT, LDH ALT is the most specific to the liver
94
Elevated aminotranseferases indicating acute liver trauma
8-25x normal range AST>ALT (ratio over two - chronic alcohol, under two non-alcoholic) ALT>AST - Acute Liver Trauma
95
2 Liver enxymes to measure obstruction of the billiary tre
Alkaline phosphatase (4x elevation is cholestasis) AND Gamma-glutamyl transpeptidase BOTH is indicative of obstruction Also 5'-nucleotidase specific to the liver
96
Tests of hpatic synthetic function
Albumin levels If other LFTs are normal consider malnutrition PT time See above note
97
Autoimmune hepatitis
Insidious onset to sudden attack presentation Precipitated by viral illness, pregnancy, drug exposure May have a history of autoimmune - Positive ANA, pANCA, anti-SLA Liver biopsy for diagnosis
98
Treatment for autoimmune hepatitis
Prednisone long term Azathioprine - second line Liver transplant if they fail therapy
99
Drugs that can induce hepatitis
Acetominophe Isoniazid Tetracyclines
100
Labs and treatment for drug induced hepatitis
ALT > AST May require a liver transplant
101
Acetominophen toxic doses for kids and adults
Adults - 4g (4000mg) Kids - 80mg/kg
102
Stage one of acetominophen induced hepatitis
.5-24 hours - N/V, diaphoresis, pallor lethargy w/ normal labs
103
Stage two of acetominophen induced hepatitis
24-72 hours Symptoms resolve but labs get worse RUQ pain PT and billirubin elevated
104
Stage three of acetominophen induced hepatitis
72-96 Jaundice, confusion Elevated enzymes Many die
105
Stage 4 of acetominopheni induced hepatitis
4 days to 2 weeks Recovery May have AKI Symptoms and lab values begin to normalize
106
Diagnosis and treatment for acetominphen induced hepatitis
Measure acetominophen level with the blood N-acetylcysteine (activated charcoal) if possible within 1-2 hours of ingestion - give if we don't know when they took it
107
RiskFactors for Alcoholic liver disease
2 drinks per day for men, 1 per day for women Fatty liver to alcoholic hepatitis to cirrhosis 50g daily for 10 years is the threshold Often an incidental finding of labs in the fatty liver stage
108
ALT AST ratio of alcoholic liver disease
2:1 or greater AST to ALT ratio
109
Treatment for alcoholic liver disease
Abstinence from alcohol Folic acid, zinc, thiamine Prednisone for about a month
110
Glasgow alcoholic hepatitis score
Greater than 9 is an indication for steroid treatment
111
Non-alcoholic steatohepatitis
Fatty liver w/o alcohol us Can still lead to cirrhosis Fatty liver is without inflammation RUQ discomfort - vague symptoms Biopsy to diagnose
112
Treatment for non-alcoholic fatty liver disease- 5
Lifestyle modification Hepatitis vaccines Vitamin E, Thiazolidenediones, Metformin
113
Percent of NASH patients who progress to cirrhosis
20%
114
PE findings with cirrhosis- 7
Portal hypertension Pruritis Spider angiomas ED, Gyencomastia Palmar erythemia Jaundice - later in the disease
115
Labs and diagnostics for liver cirrhosis
Minimal elevations in liver enzymes early in the disease cours DDx - Liver biopsy FL - US of Liver
116
Treatment for cirrhosis- 6
TRANSPLANT Avoid alcohol Hepatitis vaccination Spironolactose and Furosemide TIPS - Shunt Paracentesis
117
Bacterial peritonitis related to cirrhosis Agent and Drug of Choice
MC w/ E. coli Treat with cefotaxime
118
Treatment for hepatic encephalopathy
Reduce protein intake Give lactulose ABX - Rifamixin and Flagyl to reduce ammonia producing bacteria
119
Tx for cirrhosis clotting factor deficiencies
Give FFP, Ferrou sulfate for anemia
120
Tx for esophageal varices
Band, Ballon, Tamponade Octreotide for bleeding Beta blocker for maintainence
121
MELD score
Assesses for appropriateness for liver transplant 14 or higher qualifies for a liver transplant
122
Primary billiary cirrhosis
Chronic autoimmune destruction of the bile ducts Common in women 40-60 Fatigue and itchiness are MC symptoms Fat deposits in the fingers Positive ANAD
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Diagnosis- 2 and Tx - 3 for primary billiary cirrhosis
Elevated ALP and cholesterol Baseline US biopsy not needed Ursodeoxycholic acid is tx CHolestyramine for itching Liver transplant is definitive
124
Hepatitis A Etiology and Incubation
Fecal Oral route Incubates for TWO weeks No chronic carrier state
125
Hepatitis A presentation - 6
More severe in adults Distaste for smoking N/V/D RUQ pain gets worse with movement Jaundice and acholic stools Hepatomegaly
126
Diagnosis of HAV
Jaundice with known risk for Hep A Established by IgM anti HAV antibodies - peak during symptoms ALT>AST Imaging not indicated
127
Treatment for HAV
Symptomatic treatment - fluids and rest Avoid alcohol Prevent via handwashing and vaccination
128
3 antigens of Hepatitis B
HBcAg - Core antigen HBeAg - Secreted BY the core HBsAg - HBV surface antigen
129
Risk factors for HBV
Bloodborne Sexual activity, mother to baby, healthcare workers, IVDU, incarceration, previous STD
130
Clinical presentationand incubation of Acute HBV
6 week to 6 month incubation Recurrent fever RUQ pain Jaundice Subsides in a few weeks
131
HBsAg
First to elevate - persists throughout clinical illness - presence for >6 months indicates chronic illness
132
anti-HBs
Indicates recovery when coupled with decline of HBsAg Indicates vaccine response and immunity when no HBsAG is present
133
IgM anti HBc
One month after HBsAG is detected Indicates declining acute hepatitis B 3-6 month persistence Acute flares of chronic disease
134
IgG anti-HBC
Persists indefinitely With Anti-HBs = recovery With HBsAG = Chronic disease
135
HBeAG
Elevated with infectivity - helps us know how infectious it is Appearance of antibody indicates reduction in infectivity Parallelled by HBV DNA
136
Labs of acute hepatitis
ALT greater than AST - more marked than HAV
137
Txand Prophylaxis for HBV
Avoid alcohol and activity Antiviral therapy only if chronic HBIG for prophylaxis within 7 days of exposure and newborns with HBV positive mothers
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Tx for chronic HBV
Can lead to hepatocellular carcinoma and cirrhosis Nucleoside and nucleotide analogs - 1st line Interferon treatment - 2nd line
139
Hepatitis C
IVDU, Sexually transmitted, Healthcare, often co-infected with HIV
140
Presentation and course of HCV
6-7 week incubation period Often a mild presentation Often becomes chronic Anti-HCV antibodies - RNA indicates a CURRENT infection, only Ab's indicate a past infection
141
Prevention for hepatitis C
No vaccine Safe sex and needle use
142
Management for HCV
Harvoni - combo drug of ledipasvir/sofosbusir
143
HCV protease inhibitors and polymerase inhibitos for HCV
8 week course Prevent viral replication
144
Hepatitis D
Only associated with Hepatitis B infection!! Mainly in IVDU Anti-HDV antibodies in serum
145
Hepatitis E
In non-US contries more often - fecal-oral Most severe among young pregnant women May be spread by swine Test for IgM anti-HEV in serum Treat with oral ribovirin to treat
146
Hemochromatosis
Autosomal recessive Increased iron absorption from the duodenum and storage in the liver Usually don't present until older than 50 "bronze diabetes"
147
Diagnosis of hemochromatosis
Mild LFT elevationElevated serum Iron and serum ferritin Test first degree family members Genetic testing available
148
Treatment for hemocrhomatosis
Weekly phlebotomy for 2-3 years Chelating agents if unable to tolerate phlebotomy - Defaroxamin Liver transplant for cirrhosis
149
WIlson disease
Autosomal recessive disorder Presents before age 40 Excessive absorption of copper and decreased excretion by the liver leading to low ceruloplasmin Deposition of copper in liver and brain
150
Presentation of Wilson disease
Kayser Fleischer copper rings around iris - pathognomic Parkinsonianism, Dysphagia Personality changes
151
Labs for Wilson disease
Urine copper Low serum ceruloplasmin levels Liver biopsy to assess chronic hepatitis/cirrhosis
152
Five Treatments for Wilson disease
Restrict copper - nuts chocolate shellfish Penicillamin - Drug of choice - Chelating agent and increases urinary excretion B6 - antimetabolite of copper Zinc promotes fecal copper excretion Liver transplant if not caught early
153
Gilbert syndrome
Mild unconjugated hyperbilirubinemia Familial Reduced activity of glucuronyl transferase Random outbreaks of jaundice Bilirubin above 3mg/dL Benign, educate about flare-ups
154
Crigler Najjar syndrome
Infantile jaundice Glucuronyl transferase deficiency Autosomal recessive Rapid and severe Does not go away after 2-3 weeks
155
Crigler Najjar Types
Type I - 20-50mg/dL Type II <20mg/dL High levels definitive for diagnosis
156
Treatment for crigler najjar syndrome
Phototherapy under fluorescent light Plasmapheresis Liver transplant - curative Phenobarbital for type II
157
Dubin Johnson syndrome
Genetic Conjugated bilirubin not sent to bile ducts Intermittent jaundice and fatigue Elevated conjugated bilirubin Black liver Benign - can be exacerbated by illlness or pregnancy
158
Rotor syndrome
Rare genetic disorder Stored bilirubin leaks back into the blood stream Inject dye for a transport study to differentiate from Dubin Johnson Benign
159
Budd-Chiari syndrome
Hereditary or acquire hepatic venous outflow obstruction, RUQ Pain, jaundice, ascites
160
Budd-Chiari diagnosis
Doppler US Can move on to an MRI
161
Tx for BC syndrome
Lovenox if clotting problem TIPS - shunt Pericentesis
162
Kernicterus
Crigler Najjar syndrome Brain damage from high bilirubin levels in a baby's blood
163
MC Hepatocellular carcinoma
Parenchymal cell carcinoma d/t cirrhosis
164
Lab findings for hepatocellular carcinoma
Alpha fetoprotein CT/MRI for mass Liver biopsy
165
Screening for hepatocellular cancer
Liver US Q 6 months
166
Carnett's sign
If a patient's pain on palpation worsens when flexing the abdominal muscles the pain is located in the abdomenal wall rather than the abdomen itself
167
Murphy's sign
Inspiratory arrest during deep palpation of the RUQ - good indicator for Gallbladder inflammation
168
Rovsing sign
Indirect tenderness RLQ pain with LLQ palpation - indicates appendicitis
169
Psoas sign
Patient flexes the thigh against resistance of the examiner's hand - on left side - Pain is indicative of appendicitis
170
Obturator sign
Flexion and internal and then external rotation of the thigh causes pain - appendicitis, diverticulitis, PID
171
Cough test
Indicative of peritoneal irritation
172
Volvulus
Torsion of segment of bowel MC - sigmoid Obstruction and strangulation - often in older adults 70+ Chronic constipation is a risk factor
173
Presentation of volvulus
Insidious onset of abdominal pain Abdominal distension Severe and colicky Tympany on exam w/ tenderness Fever and tachycardia after perforation
174
Diagnosis of volvulus
CT to establish diagnosis Whirl pattern and bird beak appearance Abdominal X-ray can also be performed
175
Treatment of volvulus
IV fluids Endoscopic detorsion - advance scope through twisted segment Elective resection if there is a risk of recurrence or major necrosis
176
177
Cecal volvulus
More rare than Sigmoid volvulus Can be caused by violent coughing, tumor, or pregnancy
178
Presentation of cecal volvulus
Highly variable Gradual onset of pain with N/V
179
Diagnosis of cecal colvulus
CT - first line Whirlwind and birds beak Coffee bean and comma sign with Abdominal X ray
180
Treatment for cecal volvulus
Can't do endoscopic - must do open Ileocecal detorsion if possible - if not possible cecopexy to anchor cecum to the wall
181
Intussusception
Bowel folds back into itself 6 months-3 years more common in males and in the ileocolic area Mostly idiopathic
182
Presentation of instussusception
Intermittent severe abdominal pain, 15-20 minute attacks Current jelly stools Sausage shaped mass in the right side of the abdomen Tender and distended abdomen
183
Diagnosis and tx of instussusception
Utrasound is number 1 - coiled spring Barium enema confirmatory- can be CURATIVE Sonogrophy guided non-surgical reduction with saline or pneumatic reduction - air is less dangerous
184
Tx for intussusception if you suspect a perforation
Pneumatic reduction is better than barium
185
Presentation of appendicitis
MC between 10-30 MCC is a fecalith Vague, colicky pain localizing the the RLQ within 12 hours Pt can localize pain upon coughing Rebound tenderness McBurney's point tenderness
186
Diagnosis of appendicitis
Mostly clinical CT to confirm diagnosis US can confirm but not exclude diagnosis
187
Management for appendicitis
Laparoscopic appendectomy Hydration Cefoxitin or Ampacillin-Sulbactam
188
Toxic megacolon
Complication of IBD or Crohns Non-obstructive dilation of 6+ cm with systemic symptoms
189
Presentation of toxic megacolon
ABdominal pain and distension Severe bloody diarrhea Toxic appearing Dehydrated Recent travel, abx use, use of antimotility agents
190
Diagnosis of toxic megacolon
Radiographic evidence of colonic distension on CT or XR - CT preferred PLUS 3 of: Fever 100.4+ HR 120+ Leukocytosis over 10,500 Anemia PLUS 1 of: Dehydration Altered mental status Electrolyte disturbances Hypotension
191
Most effected area in toxic megacolon
Transverse colon
192
Treatment for toxic megacolon
NG tube to decompress colon Stop medications PPI for stress ulcer prevention Bowel rest - NPO Serial CMP, BMP, Radiograph
193
Indications for surgery in toxic megacolon- 5
Surgery for perforation, necrosis, ischemia, hypertension, or compartment syndrome
194
Pharm for toxic megacolon
Amp, gent, metronidazole OR 3rd Gen Ceph w/ metronidazole Corticosteroids
195
Acute mesenteric ischemia
Ischemia of the SMALL bowel Occlusive or non-occlusive MC in the SMA
196
Presentation of acute mesenteric ischemia
Abdominal pain out of proportion to findings Severe, sudden, perumbilical Fecalant breath odor
197
Labs and Dx for diagnosis for acute mesenteric ischemia
Metabolic acidosis - is indicative until proven otherwise Mesenteric arteriography - dx of choice CT/MRI are nonspecific
198
Tx for acute mesenteric ischemia
Opioids for pain control Broad spectrum abx and NG tube Anticoagulation and Nitroglycerin Abdominal exploration d/t intestinal ischemia
199
MCC of upper GI bleeding
Peptic ulcer disease
200
MCC of lower GI bleed
Bleeding diverticulum
201
Presentation of GI bleed
Melena Hematochezia Coffee ground emesis Blood y emesis Weight loss suggests malignancy Jaundice suggests liver problem
202
Things that can mimic GI bleeding
Iron or Bismuth - Melena Beets - Hematochezia Cefdinir - Red Stools
203
Division between upper and lower GI
Ligament of treitz
204
Risk factors for umbilical hernea
Pregnancies Ascites Obesity Intra-abdominal hernia
205
Treatment for umbilical hernia
Surgical repair Open or Mesh depending on size (open if larger)
206
Features of hernia associated with strangulation
Firm Severe tenderness Abdominal distension
207
Treatment of ventral hernia
Any hernia in abdominal area Does not require surgery or is a poor surgical candidate or hernia is not emergent - can use an abdominal binder
208
X ray colors
Bone - White Tissue - gray Air - Black
209
Indication of air in the peritoneal cavity
Air UNDER the diaphragm - may be a bowel perforation or air expansion from laparoscopy
210
Feces on X ray
Soft tissue with opacities
211
Colors on US
Hypoechoic - Dense muscle and connective tissue Hyperechoic - Bright - Air fat and gas Anechoic - Fluid and blood filled structures appear more black
212
Contrast use for abdominal CT
IV - best for tumors, vascular abnormalities, urinary tract Oral - Best for visualizing the bowel lumen, esophagus, stomach Non-contrast - Best for evaluating stones
213
Pros/Cons of CT
Helps enhance and delineate between organs Takes a while, renal failure can cause an allergic reaction or flushing
214
Barium swallow
Used with X ray Continue images as it passes through the small bowel Can also do a barium enema
215
MC complication of ERCP
Pancreatitis