Hepatic and Biliary Systems Flashcards

1
Q

The Following are the functions for what organ?

  • Synthesize glucose
  • stores glucose
  • synthesizes cholesterol and proteins into hormones and vitamins
  • metabolizes fat, proteins and carbs
  • metabolizes drugs via CYP-540
  • Detoxifies blood
  • involved in acute phase of immune support
  • Processs HGB and stores iron
  • synthesizes coagulations factors
  • Aids in volume control as a blood resevoir
A

Liver

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2
Q

What organ/system is impacted by liver function?

A
  • All
  • Liver dysfunction can lead to multi-organ failure
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3
Q

How many segments are in the liver?

A
  • 8 segments
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4
Q

What seperates the Rt and Lt lobes of the Liver?

A
  • Falciform Ligmament
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5
Q

The _____ vein and _____ artery branch into each segment of the Liver?

A
  • Portal Vein
  • Hepatic Artery
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6
Q

Name (3) Hepatic veins that empty into IVC

A
  • Right Hepatic V
  • Middle Hepatic V
  • Left Hepatic V
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7
Q

The____ _____ of the liver travels along portal veins?

A

Bile ducts

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8
Q

Bile drains through the Hepatic Duct into the ________ and ______ Bile Duct.

A
  • Gallbladder (GB)
  • Common Bile Duct (CBD)
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9
Q

Bile enters duodenum via ______ ______ _________.

A
  • Ampulla of Vater
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10
Q

The liver receives _% of CO, or _-__ L/min.

A
  • 25%
  • 1.25 - 1.5 L/min
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11
Q

Which organ receives the highest CO of all the organs?

A
  • Liver
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12
Q

What vein arises from the splenic vein and superior mesenteric vein?

A

Portal Vein

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13
Q

The _______ vein provides 75% of Hepatic blood and is _________________ by the GI organs, pancreas and spleen.

A
  • Portal Vein
  • deoxygenated
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14
Q

The __________ artery provides 25% of Hepatic blood flow and branches off the _________.

A
  • Hepatic artery
  • Branches off the aorta
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15
Q

Liver O2 delivery

A
  • 50% Portal Vein (deoxygenated)
  • 50% via Hepatic artery
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16
Q

Hepatic Artery blood flow is ________ r/t portal venous blood flow.

A

inversely

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17
Q

hepatic blood flow is _________ and hepatic artery dilates in reponse to ____ portal venous flow.

A
  • Autoregulated
  • low
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18
Q

Portal Venous pressure reflects _______ _______ tone and _______ pressure

A
  • splanchnic arterial tone
  • intrahepatic pressure
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19
Q

Portal Hypertension (↑Portal venous pressure) causes blood to back up into _________ circulation and causes ________ and _________ varices

A
  • systemic
  • esophageal and gastric varices
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20
Q

Hepatic Venous Pressure Gradient (HVPG) 1-5 mmHg

A
  • Normal portal venous pressure
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21
Q

Hepatic Venous Pressure Gradient (HVPG) >10

A
  • Portal HTN
  • cirrhosis, esophageal varices
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22
Q

Hepatic Venous Pressure Gradient (HVPG) >12

A
  • Variceal Rupture
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23
Q

Below are Risk Factors for _______________.
* Family hx
* Heavy ETOH
* Lifestyles
* DM
* Obesisty
* Illicit Drug use
* Multiple Partners
* Tattoos
* Transfusions

A

Liver Dysfunction

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24
Q

These Physical Exam findings indicate__________.
* Pruritis
* jaundice
* Ascites
* Asterixis (flapping tremor)
* Hepatomegaly
* Splenomegaly
* Spider nevi

A

Active Liver Problems

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25
Hepato-biliary Functions Tests Labs
* BMP, CBC * PT/INR * AST * ALT * Bilirubin * Alkaline Phosphatase * GGT
26
What is the most liver specific enzyme test?
ALT
27
Imaging to Evaluate hepato-biliary Function
* Ultrasound * Doppler U/S * CT * MRI
27
Acute Liver Failure, Alcoholic Liver Disease and Non-Alcoholic Liver Disease are all causes of ____________.
Hepatocellular Injury
27
Labs that indicate Hepatocellular Injury
↑AST/ALT
28
AST/ALT will be elevated ____ x in Acute Liver Failure (ALF)
* 25x
29
In Alcoholic Liver dz, ___:___ ration is 2:1
* AST: ALT ratio is 2:1
30
Hepatobiliary disease: Reduced Synthetic Function labs
* ↓Albumin * ↑PT/INR
31
Hepatobiliary disease: Cholestasis labs
* ↑Alk Phosphatase * ↑GGT * ↑bilirubin
32
_________________ is caused by hepatocytes secreting bile through ducts, into common hepatic duct and into Gallbladder and Common bile duct
Cholelithiases "Gallstones"
33
The _________ stores bile to deliver during meals ____________ duct secretes bile directly into duodenum.
* Gallbladder * Common Bile Duct
34
Obesity, high cholesterol, DM, pregnancy, female, and family history are all common risk factors of ______________.
Cholethiasis
35
Symptoms of Cholelithiasis
* RUQ pain -- referred to shoulders * N/V, indigestion * Fever (acute obstructon)
36
IVF, antibiotics, pain management and Lap Cholecystectomy are treatment for _______________.
Choleliathiasis
37
________________ is a stone obstructions ofthe common bile duct that can lead to biliary colic.
* Choledocolithiasis
38
_____________ is inflammation of bile duct system.
Cholangitis
38
Initial Symptoms of Choledocolithiasis
* N/V * Cramping * RUQ pain
39
Symptoms of Cholangitis
* Fever * rigors * jaundice
40
Cholangitis Treatment
* Endoscopic removal of stone via ERCP
41
Below is the surgical overview for what procedure? * Endoscopist threads guidewire through Sphincter of Oddi, into Ampulla of Vater to retrieve stone from pancreatic duct or CBD * GA, usually prone w/left tilt (tape ETT to left) * Glucagon may be required in the event of Oddi Spasm
* Endoscopic Retrograde Cholangiopancreatography
42
ERCP patient and ETT postioning
* pt is proned, head to the right * Tape ETT to left
43
Name (3) types of Hyperbilirubinemia
* Bilirubin * Unconjugated (indirect) hyperbilirubinemia * Conjugated (direct) hyperbilirubinemia
44
_________ is the end product of heme-breakdown
* Bilirubin
45
_____________ hyperbilirubinemia is the imbalance between bilirubin synthesis and conjugation. _____________ hyperbilirubinemia is caused by an obstruction, causing reflux of conjugated bilirubin into the circulation
Unconjugated (indirect) Conjugated (direct)
46
Name (5) types of Viral Hepatitis
* A * B * C * D * E
47
Name the (2) Viral Hepatitis that are more chronic
* B * C
48
Name the most common viral hepatitis requiring liver tranplant in the US.
* HCV
49
Name the Top indicator for liver transplants in US
Alcoholic Liver Disease (ALD)
50
Cirrhosis: Alcohol Liver Disease
* Most common cause of cirrhosis * underreported d/t stigma * intiatlly asymptomatic
51
Treatment of Alcoholic Liver Disease includes ________ , management of symptoms, transfusion for platelets < ___________ and a liver ________.
* Abstinence * < 50,000 * Liver transplant
52
Symptoms of _____________ Liver Disease include: * Malnutrition * muscle wasting * Parotid gland hypertrophy * Jaundice * thrombocytopenia * ascites * Hepatosplenomegaly * Pedal Edema
Alcoholic
53
When can ETOH withdrawal after someone stops drinking?
* 24-72 hr after stopping
54
Alcoholic Liver Disease: Lab Values
* ↑Mean corpuscular volume (MCV) * ↑Liver enzymes * ↑ɣ-glutamyl-transferase (GGT) * ↑Bilirubin * Blood ethanol (acute intox)
55
____________ Fatty Liver Disease is on the rise in the US and is diagnosied when hepatocytes contain > ___% fat
*Non-Alcoholic * > 5% fat
56
Name (3) disease processes that Non-Alcoholic Fatty Liver Disease progresses to
* NASH * Cirrhosis * Hepatocellular carcinoma
57
Besides Alcohol Liver Disese, what (2) disease processes are becoming additional causes of liver transplants in the US?
* Non-Alcoholic Fatty Liver Disease (NAFLD) * Non-Alcoholic Steatohepatitis (NASH)
58
______ _______ is the gold standard of diagnosis of Non-Alcoholic Fatty Liver Disease, in addition to imaging and histology.
* Liver Biopsy (gold standard)
59
Treatment for Non-Alcoholic Fatty Liver Disease
* Diet * Exercise * Liver transplant
60
Who does Autoimmune Hepatitis predominantly affect?
Women
61
Postive autoantibodies, hypergammaglobulinemia and AST/ALT 10-20 x normal can diagnose ____________ Hepatitis.
Autoimmune
62
Treatment for Autoimmune Hepatitis
* steroids * azathioprine
63
Transplant indicated for ____________ Hepatitis when treatments fail and acute liver failure ensues.
Autoimmune
64
Most common cause of Drug Induced Liver Injury
* acetaminophen OD
65
Is Drug Induced Liver Injury reversable?
* Yes * normally reversible after drug is removed
66
_____________________________________ is a group of rare, genetically inherited disorderes that lead to a defect in the enzymes that breakdown and store protein, carbohydrates and fatty acids.
Inborn Error of Metabolism
67
How prevalent is inborn Errors of Metabolism?
* Occurs in 1:2,500 births
68
The most severe form of Inborn Error of Metabolism Occur in the _______ period cause a ______ degree of mortality.
* neonatal * mortality.
69
Name (3) Specific Inborn Errors of Metabolism
* Wilson's Disease * Alpha-1 Antitrypsin Deficiency * Hemochromatosis
70
____________________________________ is an autosomal recessive disease characterized by impaired copper metabolism. The excessive copper buildup leads to oxidative stress in the liver, basal ganglia and cornea.
Wilsons Disease "hepatolenticular degeneration"
71
Wilsons Disease "hepatolenticular degeneration" symptoms can be asymptomatic to sudden onset of liver _____ and has ________ and psychiatric manifestations.
* failure * neurologic
72
____________________ is diagnosed with: * serum ceruloplasmin * amiotransferase * urine copper level * Liver biopsy for copper level
*Wilsons Disease "hepatolenticular degeneration"
73
Wilsons Disease "hepatolenticular degeneration"is treated with Copper - ______ therapy and oral ________ to bind copper in GI tract.
* chelation * zinc
74
Define Alpha-1 Antitrypsin Deficiency
* genetic disorder resultsing in a defective a-1 antitrypsin protein
75
Alpha-1 antitrypsin protects the _____ and ______ from neutrophil elastase.
* liver * lungs
76
Name the #1 genetic cause of liver transplants in children
* Alpha-1 antitrypsin Deficiency
77
Alpha-1 Antitrypsin Deficiency Treatments
* pooled a-1 antitrypsin effective for pulmonary symptoms * No treatment for liver.
78
______________ is excess iron in the body that leads to multi-organ dysfunction. It may be genetic.
* Hemochromatosis
79
Hemochromatosisis caused by genetics, repetative ________ transfusions and high-dose _________ infusions.
* blood * iron infusions
80
Cirrhosis, heart failure, diabetes, adrenal insufficiency and polyarthropathy are all presentations of ________________ .
Hemochromatosis
81
How can you diagnose Hemichromatosis?
* elevated AST/ALT * elevated transferrin saturation * elevated ferritin * genetic mutation testing * Echocardiogream and MRI * liver biopsy
82
Hemochromatosisis treated with _________ phlebotomy, iron-______ drugs and liver transplant.
* weekly phlebotomy * iron-chelating drugs
83
_____ ______ cholangitis aka biliary cirrhosis is an autoimmune, progressive destruction of bile ducts with periportal inflammation and cholestasis.
Primary Biliary Cholangitis (PBC)
84
Primary Biliary Cholangitis (PBC) aka biliary cirrhosis can lead to
* liver scarring * fibrosis * cirrhosis
85
Primary Biliary Cholangitis (PBC) aka biliary cirrhosis primarily affect ______, is diagnosed in _________ age, and caused by exposure to _______ toxins.
* Females > Males * diagnosis in middle age * caused by exposure to enviromental toxins
86
Symptoms of Primary Biliary Cholangitis (PBC) aka biliary cirrhosis
* Jaundice * fatigue * itching
87
How can you diagnosis Primary Biliary Cholangitis (PBC) aka biliary cirrhosis
* Labs: ↑Alk Phos,↑GGT, + **Antimitochondrial antibodies** * Imaging: CT, MRI, MRCP * Liver biopsy
88
There is no ____ for Primary Biliary Cholangitis, but _____ bile acid and slow progression.
* no cure * exogenous
89
_______ _________ _______ is an autoimmune, chronic inflammation of larger bile ducts. Can be Intrahepatic and extrahepatic.
Primary Sclerosing Cholangitis (PCS)
90
This is caused by: * Fibrosis in biliary tree→strictures (beads on string appearance)→ cirrhosis, ESLD * Males > females, onset 40s.
Primary Sclerosing Cholangitis (PSC)
91
Symptoms of Primary sclerosing Cholangitis (PSC) include ______, itching, deficiency of ____ - soluble vitamins and cirrhosis.
* Fatique * fat-soluble vitamins
92
Primary Sclosing Cholangitis (PSC) Labs
* ↑alkaline phosphatase and ɣ-glutamyl-transferase * +auto-antibodies
93
Diagnosis of Primary Sclerosing Cholangitisis done by a ____ or _____ showing biliary stricture w dilated bile ducts and a _____ biopsy.
* MRCP or ERCP * Liver biopsy
94
___________ transplant is the only long term treatment of Primary Sclerosing Cholangitis (PSC). No drug therapy is currently effective.
Liver
95
____________of Primary Sclerosing Cholangitis (PSC) is common after transplant d/t _____________ nature.
*Re-occurrence * autoimmune
96
__________________ is a life-threatening severe liver injury occuring within days to 6 months after insult.
*Acute Liver Failure
97
Acute Liver Failure Lab work will show a _____ ______ in AST/ALT, AMS and coagulopathy.
* Rapid increase in AST/ALT, AMS, coagulopathy
98
The following are all causes of ______________: * 50% cases are drug induced (tylenol OD) * Viral hepatitis * autoimmune * hypoxia * ALF of Pregnancy * HELLP
Acute Liver Failure
99
Symptoms of ______________________: * Jaundice * nausea * RUQ pain * cerebral edema * encephalopathy * multiorgan failure death
Acute Liver Failure
100
Treatment for Acute Liver failure includes treating the ________, and _________ care. If that fails, the only other treatment is a Liver ___________.
* Treat the cause * supportive care * liver transplant
101
______________ is the final stage of liver disease. Normal liver parenchyma replaced with scar tissue.
Cirrhosis
102
Symptoms of _____________: * Asymptomatic in early stages * jaundice * ascites * varices * coagulopathy * encephalopathy
Cirrhosis
103
Alcoholic fatty liver, Non-Alcoholic fatty liver, NCV and HBV are all common causes of ____________.
Cirrhosis
104
Elevated AST/ALT, bilirubin, Alk phopshate, PT/INR, and thrombocytopenia can all indicate_______________.
Cirrhosis
105
Cure/treatment for Cirrhosis
* Transplant is only cure
106
_________________ is increased vascular resistance within the portal venous system with an HVPG > 5.
Portal HTN
107
______________ is the most common complication of cirrhosis.
* Ascites
108
Management of Ascites
* ↓Salt diet * albumin replacement
109
_________________ leads to increased blood volume and peritoneal accumulation of fluid.
Ascites Portal- HTN
110
Transjugular Intrahepatic Portosystemic Shunt (TIPS) is the surgical management of ____________ and reduces _____- HTN
* Ascites * Reduces Portal-HTN
111
Spontaneous Bacterial Peritonitisis the most common infection r/t ___________ and requires antibiotics
* cirrhosis
112
Varices present in ___% of cirrhosis patients. _______ is the most lethal complication.
* 50% * Hemorrage
113
How to prevent hemorrhage due to Varices
* Beta-blockers * prophylactic endoscopic variceal banding and ligation * Refactory bleeding --> balloon tamponade
114
____________________- is the buildup of nitrogenous waste d/t poor liver detoxification and can cause Neuropsychiatric symptoms (cognitive impairment → coma)
Hepatic Encephalopathy
115
Hepatic Encephalopathyis treated with _____ and ______ to ↓ammonia-producing bacteria in gut
* Lactulose * Rifaximin
116
Hepatorenal Syndrome, hepatopulmonary syndrome and portopulmonary HTN are (3) ____________ Complications
Cirrhosis
117
____________________ causes release of endogenous vasodilators (NO, PGs) →↓systemic MAP→↓RBF
Hepatorenal Syndrome
118
Midodrine, Octreotide and albumin are all used to Treat ___________________.
Hepatorenal Syndrome
119
_____________ Syndrome is a triad of chronic liver disease, hypoxemia, intrapulmonary vascular dilation. With platypnea (hypoxemia when upright) d/t Rt to Lt intrapulmonary shunt.
Hepatopulmonary Syndrome
120
________________________ HTN is accompanied by portal HTN. Systemic vasodilation triggers production of pulmonary vasoconstrictors.
Portopulmonary HTN
121
Treatment of Portopulmonary HTN includes _____ - inhibitors, NO, Prostacycline analogs and endothelium receptors antagonists. __________ is the only cure.
* PDE-i *** Transplant is the only cure**
122
____________ surgery is contraindicated in acute hepatisis, severe chronic hepatitis and ALF.
Elective
123
Name the (2) Scoring systems to determine severity and prognosis of liver disease
* Child-Turcotte Pugh (CTP) * Model for End Stage Liver Disease (MELD)
124
This scoring system of Liver disease has points based on bilirubin, albumin, PT and encephalopathyon.
Child-Turcotte Purge (CTP)
125
This scoring system of Liver disease score is based on bilirubin, INR, creatine and sodium.
Model for End Stage Liver Disease (MELD)
126
Pre-Op considerations for Liver Disease
* Careful history and physical * Standard preop labs: CBC, BMP, Pt/INR * Low threshold for invasive monitoring
127
Increased Risks with Anesthesia in Liver Disease
* ↑Risks aspiration * HoTN * hypoxemia
128
For Anesthesia in Liver Disease, ____ > _____ for fluids and drugs many have a _____ onset/prolonged DoA.
* colloids > crystaloids * slower onset/prolonged DoA
129
Alcoholism does what to the MAC of volatiles
* increases
130
Name (2) NMB that are ideal for Liver Disease
* Succinylcholine * Cisatracurium
131
Plasma cholinesterase amounts ________ in severe liver disease.
* decreased
132
What (2) things do you have to manage in Liver patients to prevent complications
* Bleeding * Coagulations
133
__________________________ procedure is a stent or graft placed btw hepatic veins and portal veins. Shunts portal flow to systemic circulation and reduces portosymstemic pressure gradient.
Transjugular Intrahepatic Portosystemic Shunt (TIPS)
134
Refactory ________ hemorrhage and Refactory _________ are indications for Transugular Intrahepatic Portosystemic Shunt
* Refractory variceal hemorrhage * Refractory ascites
135
Contraindications of TIPS
* Heart Failure * Tricuspid regurgitation * Severe pulmonary HTN
136
________________ is a resection to remove neoplasma, leaving adequate tissue for regeneration.
Partial Hepatectomy
137
Up to ____% removal of the liver is tolerated in pts with normal liver function.
* 75%
138
Anesthestic Considerations for a Partial Hepatectomy
* avoid invasive monitoring * blood products available * adequate vascular acess for blood/pressors
139
In a Partial Hepatectomy, what might the surgeon clamp the_____ and _______ to control blood loss?
* IVC * hepatic artery
140
Standard practice for a Partial Hepatectomy is to maintain ____ CVP by fluid restriction prior to resection to reduce _______ ________.
* low CVP * blood loss
141
What will patient's require after Partial Hepatectomy for adequate pain control?
* PCA pump
142
In a partial Hepatectomy, what determines the tolerable amount of resection?
* preexisting liver disease and function
143
Whare are some post-op complications for Partial Hepatectomy of liver resection?
* Post -Op coagulation disturbances
144
What is the definitive treatment for ESLD?
* Liver transplant
145
Name the most common indicator for a Liver transplant?
* Alcoholic liver disease
146
Living Donor for Liver Transplant considerations....
* surgeries timed together * minimal ischemic time
147
Liver Transplant: Brain Dead Donor considerations
* keep Hemodynamics stable for organ perfusion
148
Intraoperative Management for Liver transplants
* Maintain Hemodynamics * A-line, CVC, PA cath, TEE * Control coagulation
149
Liver Transplant: Preoperative Anesthetic Considerations
* Pre-Op evaluation * vascular access * blood products available
150
Liver Transplant: Dissection Anesthetic Considerations
* hemodynamics compromise from loss of ascites * hemorrhage during dissection
151
Liver Transplant: Anhepatic Anesthetic Considerations
**HD compromise: ** * IVC clamping * metabolic acidosis * hypocalcemia from citrate intoxication * hyperkalemia * hypothermia * hypoglycemia