Cardiovascular System Flashcards

1
Q

Tetralogy of fallout

A

Congenital heart disease.
Most common cyanotic congenital heart defect is 50-70%.
Cause unclear.
Associated chromosome 22 deletion.
4 heart abnormalities:
- Stenosis of the right ventricular outflow tract
- Right ventricular hypertrophy (boot-shaped heart on x-ray)
- Ventricular septal defect (shunting of blood between the ventricles going from the right ventricle to the left ventricle and then through the aorta)
dextroposed aorta overriding pulmonic stenosis, RV hypertrophy
Babies:
Cyanosis
Clubbing in fingers and toes
Feeding difficulty
Failure to gain weight

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2
Q

What are the phases of the heart?

A

Atrial Systole
Ventricular Systole
Atrial and Ventricular Diastole

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3
Q

LUB-DUB

A

Atrioventricular valves closing
Mitral valve and tricuspid valve

Semilunar valves closing

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4
Q

Bacterial endocarditis

A
Streptococcus gallolyticus
Staph aureus
Heart valve dysfunction in 85% of patients.
This may lead to congestive heart failure in 30-40% of patients
Symptoms:
- chest pain when you breath
- fatigue
- fever
- chills
- night sweats
- fast heart rate
- SOB
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5
Q

Rheumatic heart disease

A

secondary myocarditis
children following group A hemolytic strep infection
autoimmune, Aschoff bodies, endocarditis esp left valves
mitral stenosis, migratory polyarthritis

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6
Q

Mitral valve prolapse

A

Most common valve disease

Valve leaflets prolapse into atria during systole.

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7
Q

Calcific aortic stenosis

A

Aortic semilunar valve becomes calcified creating decreased aortic flow and increased left ventricular pressure
Most commonly due to calcification of a congenital bicuspid (instead of tricuspid) aortic valve

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8
Q

Ischemic heart disease

A

Reduced coronary flow due to atherosclerotic narrowing of coronary vessels and or thrombosis
Also maybe due to coronary artery spasm
Cause: angina pectoris, sudden cardiac death
COmplications: LCHF, arrhythmias, MI

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9
Q

Infectious Myocarditis

A

Inflammation of the muscle of the heart
Myo = muscle
cardiac = heart
itis = inflammation
Can lead to heart failure as the contractility of the heart decreases due to inflammation
Viral infections:
- due to coxsackie B is the main cause of myocarditis
- due to trypanosomacruzi - chagas disease
- trichinella - roundworm that moves from intestines to parts of the body. It causes myocarditis
- Lyme disease

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10
Q

Non-infectious myocarditis

A
SLE (lupus)
Polymyositis
Drug associated
giant-cell
Symptoms:
- chest pain depending on the position
- Arrythimias 
- Fatigue
- Fever
- SOB
In severe cases, heart failure can occur
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11
Q

What is the main cause of B1 deficiency?

A

Alcoholism

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12
Q

Just know

A

The internal carotid arteries do not “feed” any tissue until they get to the brain
The external carotid feds the face

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13
Q

Organs that get direct branching from the aorta

A

Lungs through the bronchioarteries
Adrenals from the super renal arteries
Gonads from the gonadal arteries

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14
Q

Just know

A

Most abdominal drainage of venous blood is going to go through the liver (portal vein) with the exception of gonadal veins and the renal veins.

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15
Q

Thromboangitis Obliterans/Buerger’s disease

A
thrombo = clot
-angitis = inflammation of arteries
obliterans = blockage
Men > women
Heavy smokers
Inflammation of arteries of extremities.
Gangrene = death of tissue due to lack of blood supply.
Nodular phlebitis
Instep claudication
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16
Q

Claudication

A

Claudication is a pain in the legs or arms that comes on with walking or using the arms.

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17
Q

Gangrene

A

Gangrene is a serious condition where a loss of blood supply causes body tissue to die. It can affect any part of the body but typically starts in the toes, feet, fingers, and hands.

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18
Q

Nodular phlebitis

A

Serious complication.
It is an inflammatory condition.
There is always a clot or thrombus in the superficial vein.
6-40% will have a DVT
Up to 1/3 will have a pulmonary embolism (clot on the lungs) as the emboli might travel to the lungs.
Nearly always occurs in the legs.
Painful, tender, movement makes it worse, there is usually a lump.
Usually occurs in the great saphenous vein.
Diagnosed with ultrasound.

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19
Q

Raynauds Phenomenon

A

Vasoconstriction of arteries near the skin.
Color changes in fingers and toes
Sometimes affects nose, ears, and lips
Numbness, tingling, pain
The fingers turn white then blue then red due to cold weather.

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20
Q

Reynaud’s disease

A
primary Raynaud phenomenon 
Affects fingers and toes symmetrically
Severity stays constant
Arteries remain undamaged
Common triggers:
Stress, cold temperatures, nicotine, caffeine, medications that affect the sympathetic nervous system
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21
Q

Reynaud’s syndrome

A

secondary Raynaud phenomenon

Affects fingers and toes asymmetrically

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22
Q

Hypothalamus

A

Body’s thermostat

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23
Q

Aneurysms

A

Abnormal bulge in vessel due to weakening of the walls of blood vessels.
Usually affects arteries instead of veins due to higher pressure.
1.5x bigger than usual
Usually occur in the area of the aorta (abdominal 60% and thoracic 40%) where BP is higher.
Secondary to atherosclerosis, vasculitis, smoking, congenital.
Lower back pain
Men > women
>60

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24
Q

Marfan syndrome

A

A congenital disease that affects connective tissue
Symptoms:
- Back pain
- Blurred vision
- Bulging or sunken chest
- Fatigue, scoliosis small pupils, stretch marks

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25
Q

Aortic dissection

A

Lumen of aorta dissects due to pressure and loss of patency.
It creates a false lumen
Takes on a double-barrel shape
Part of the tunica intima is torn.
Causes:
- Hypertension, increase in volume.
Secondary to Marfan’s syndrome, Ehlers-Danlos syndrome, aneurysm

Emergency - can lead to hypotension

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26
Q

Arteriosclerosis

A

thickening and loss of elasticity
Arterio = artery
Sclerosis = hardening
Irritants (chemicals) or high BP causes damage to endothelial cells.
Certain proteins come inside and deposit themselves inside the tunica media.
Monocytes follow them and eat them but they die from too much eating.
They release cytokines bringing other cells in which in turn will also die and stay deposited in there…

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27
Q

Atherosclerosis

A

Formation of an atheromatous plaque
… this causes a lesion called fatty streak which is thrombogenic.
Platelets release platelet-derived growth factors encouraging smooth muscle growth.

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28
Q

Arteriolosclerosis

A

hardening of arterioles

olo = arterioles

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29
Q

Vasculitides

A

a group of disorders that cause vasculitis, which is inflammation in the walls of the blood vessels.

Since blood vessels pass through organs - vasculitis damages those organs and mimics a variety of diseases.

There are usually systemic symptoms like fever, fatigue, joint pain, and weight loss; as well as organ-specific symptoms that may literally involve any organ.

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30
Q

Erythrocyte sedimentation rate (ESR or sed rate)

A

a test that indirectly measures the degree of inflammation present in the body. The test actually measures the rate of fall (sedimentation) of erythrocytes (red blood cells) in a sample of blood that has been placed into a tall, thin, vertical tube.

Giant cell arteritis - most common vasculitis in individuals over the age of 50

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31
Q

Polyarteritis nodosa

A
individuals with hepatitis B/C.
Multi-system disease
Can occur anywhere in the body.
in the skin, it can cause livedo reticularis and palpable purpura.
Numbness, pain, burning, muscle weakness
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32
Q

Giant cell arteritis
or
Temporal Arteritis

A

inflammatory artery disease
Vessel giant cell inflammation of blood vessels going to the temporal artery (portion of external carotid artery).
50% of patients have vision loss

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33
Q

Thrombus vs emboli

A

Thrombus - Any coagulum inside the vessel. Clotted blood

Emboli - Anything in the blood that shouldn’t be there

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34
Q

Kaposi’s sarcoma

A
caused by Human Herpesvirus 8
Mostly seen in patients with HIV.
1 of 7 oncoviruses
Risk factors:
- Immunocompromised
- Organ transplant
- Immunosuppressive meds
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35
Q

Latent phase vs lytic phase

A

In the latent stage of the virus life cycle, a limited number of viral gene products are expressed. In contrast, a large number of proteins are expressed during lytic cycle replication.

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36
Q

Hemangioma

A

Capillary and cavernous types
Capillary type is benign.
Cavernous type is typically found on the skin of the head and neck, and are larger/ If associated with Lindau von Hipple disease = large hemangiomas of brain/eye and internal organs.

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37
Q

Where does the largest decrease in pressure occur?

A

Across the arterioles, because they are the site of highest resistance.

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38
Q

Hypertension

A

BP over 140/90 in anyone over 18 years of age.
120/80-139/89 considered pre-hypertension.
Most are asymptomatic
Need three readings to diagnose
Divided into essential and secondary

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39
Q

Essential hypertention

A

95% of cases
Mainly lifestyle causes
Leads to increased stroke and CHF, renal fibrosis, and coronary artery disease.

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40
Q

Secondary hypertension

A

5% of the cases

Secondary to renal/adrenal/thyroid/toxemia/aortic/CNS disease, also cocaine, descongestant, and ETOH abuse/use

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41
Q

Blood proteins

A

Plasma is the fluid portion of the blood. If the whole blood is allowed to clot and the clot is removed, the remaining fluid is called serum. Plasma proteins can be separated by size by electrophoresis.

42
Q

Prealbumin

A

thyroxine, vitamin A

43
Q

Albumin

A

Oncotic pressure

Binds hormones, drugs

44
Q

Where are the LDLs, IDLs, and VLDLs formed?

A

From the free cholesterol pool in the liver and they are transported out of the liver.

45
Q

What are the binding sites?

A

Chylomicrons - ApoE
LDL - ApoB 100
ApoA1 - HDL

46
Q

Myeloid stem

A

Make megakaryocyte cells (then PLT), proerythroblast cells (retic’s then RBC’s), and monoblast (then myeloblast and then WBC’s)

47
Q

Remember

A

We do not want free iron running around that is going to cause oxidation.

48
Q

Where is iron stored?

A

Ferritin in the liver

49
Q

Heme iron

A

Through diet from meat - unregulated uptake - put into plasma - used for erythropoiesis

50
Q

Non-heme iron

A

From plants - regulated uptake - bound to transferrin - exported to the plasma - goes to cells or into the liver to bind with ferritin.

51
Q

What does heme do?

A

Holds on to oxygen

52
Q

What is the life span of hemoglobulin?

A

120 days

53
Q

Where in the body do I find reticuloendothelial cells?

A

Liver, spleen, and bone marrow.

54
Q

What are reticuloendothelial cells coupled with?

A

Leakest capillaries

55
Q

Bilirubin has two states

A

pre-state or unconjugated or indirect and conjugated bilirubin or direct

56
Q

Heme synthesis

A

?????

57
Q

Hemoglobin

A

Heme - iron
globin - protein
Hb is a tetramer with 4 O2 binding sites

58
Q

Myoglobin

A

Oxygen storage site in muscle. It is similar to Hb, but binds the O2 more tightly, and will only let it go under low O2 situations.

59
Q

What is more acidic: arterial or venous blood?

A

Venous due to CO2

60
Q

What happens when you have vitamin B12 deficiency?

A

Megaloblastic anemia

61
Q

Role of glutathione

A

It reduces peroxide to water so my RBC’s are stable

62
Q

What operates the NADH system?

A

Glucose-6-phosphate dehydrogenase. It converts NADP to NADPH to form oxidized glutathione so it can reduce peroxide into water.
If there is a deficiency of glutathione, I will end up having too much peroxide in RBC damaging it

63
Q

Anemia

A

Anemia is a condition in which you lack enough healthy red blood cells to carry adequate oxygen to your body’s tissues

64
Q

Sickle cell anemia

A

Autosomal recessive
A genetic disease where RBC takes shape of a sickle.
They are easily destroyed causing anemia.
Defective hemoglobin cause.
Life span of RBCs is 20 days
Chronic hemolytic anemia, vasoocclusive complications > leg ulcers, strokes, bone infarcts, pain, 1/2 survive to age 40.

65
Q

Hemolytic anemia

A

Increase RBC hemolysis due to own antibodies target RBCs for destruction.
Idiopathic.
Medication side effect
Extrinsic because our immune system cells believe our RBCs are foreign.

66
Q

Hemolytic anemia

A

Increase RBC hemolysis due to own antibodies target RBCs for destruction.
Idiopathic.
Medication side effect
Extrinsic because our immune system cells believe our RBCs are foreign.
Intravascular or extravascular (spleen), increased total body iron, jaundice, splenomegaly
G6PD: MOST common. Bite cell anemia, Heinz bodies

67
Q

Pernicious anemia

A

atrophiic gastritis with loss of parietal cells and IF, B12 def.
Megaloblastic anemia = macrocytic

68
Q

Pernicious anemia

A

atrophic gastritis with loss of parietal cells and IF, B12 def.
Megaloblastic anemia = macrocytic

69
Q

Alpha thalassemia

A

4 genes for alpha chain, 1 hurt = silent killer, 2 hurt = AT minor/trait, 3 hurt hemolytic throughout life, 4 genes hurt = fetal death

70
Q

Beta thalassemia

A

2 genes for beta chain heterozygotes = minor/trait, minimal or no anemia, homozygotes = severe anemia
Both thalassemias: teardrop cells, basophilic stippling, target cells.
Hypochromic, microcytic; small cells with bigger Hgb than in iron def.

71
Q

Aplastic anemia

A

pancytopenia, failure/suppression of myeloid stem cells after exposure to drug, infection, idiopathic

72
Q

Polycythemia Vera

A

Myeloproliferative disease, high HgB, middle age, viscous blood, tx phlebotomy, survive 10 years

73
Q

Multiple myeloma

A

Cancer that arises from the bone marrow, from malignant transformation of plasma cells.
Myeloma = cancerous plasma cells
Myeloma cells produce unwanted substances such as paraprotein that can damage other organs.
Bone eating type of lesion
Bone pain
Plasma cells overproduce Ig’s.

74
Q

Hairy Cell Leukemia

A
B cells with hair-like projections
Virus related, pancytopenia 
Middle-aged men most common
Most survive > 10
Rare
75
Q

Leukemia

A

Leukemia is a cancer of white blood cells. White blood cells (also called leukocytes or WBCs) fight infections and other diseases. In leukemia, the bone marrow (spongy material inside the bones) makes many white blood cells that aren’t normal. These abnormal WBCs crowd the bone marrow and get into the bloodstream.

76
Q

ALL or Acute Lymphocytic Anemia

A

Most common type of cancer in children.
Associated with virus, down’s, radiation exposure.
Remission or cure with tx. Fever/ bone pain

77
Q

ALL or Acute Lymphocytic Anemia

A

Most common type of cancer in children.
Associated with virus, down’s, radiation exposure.
Remission or cure with tx. Fever/ bone pain
Survivable

78
Q

Acute Myoblastic Leukemia

A

Most common type of leukemia in adults.
This type of cancer gets worse if not treated fast.
Risk factors: chemotherapy, smokers
Symptoms: fever, SOB, easy bruising or bleeding, fatigue, weight loss or loss of appetite.
Not survivable

79
Q

Chronic Myelogenous Leukemia

A

well-differentiated granulocytic, Philadelphia chromosome
25-60 slow for 3 years, then blast crisis when 85% die (accelerated phase)
May include any cell line. Hepatosplenomegaly, generalized

80
Q

Chronic lymphocytic leukemia

Leukemia of retirement

A

Most common overall Leukemia and most common after 60
Well-differentiated B-cell lymphocytic
More males/ Never Asian.
Acute state RARE unlike CML

81
Q

Extrinsic

A

I cut myself and I need to clot on the outside of my body
Creates thromboembolic phenomenon and creates strokes, MI
Factors 2 7 9 10 - vitamin K dependent

82
Q

Intrinsic

A

Not cut myself, I will clot inside my blood vessels

Factor 10 like in intrinsic

83
Q

What does the prothrombin activator going to do?

A

Activate prothrombin to thrombin (with calcium and vitamin K).
Then thrombin is going to activate fibrinogen to fibrin

84
Q

clotting

A

positive feedback
factor 10 comes down and activates prothrombin to thrombin
Factor 10 activates factor 8

It activates these two so more thrombin can be produced so there could be more clotting

85
Q

Poiselle’s

A

Thickness and resistance of blood

the only one that has pie

86
Q

Hemophilia A

A

Factor VIII deficiency, sex-linked recessive, males (female carrier), spontaneous bleeding into joints with associated pain and swelling.
Blood in urine or stool.
Bruising
Nosebleeds

87
Q

Hemophilia B/Christmas disease

A

factor IX deficiency, male-only (female carrier)

Same symptoms as A, but less severe

88
Q

Von Willebrand’s

A

Autosomal dominant
Deficiency of factor activator
Not enough working von Willebrand factor to help with platelet adhesion to bind and carry factor VIII to stop bleeding.

89
Q

Hydrostatic pressure

A

Equal to blood pressure

90
Q

Edema

A

Fluid exchange = balance of [Hydrostatic Pressure (drives out) and Oncotic Pressure (keeps in)] (Starling’s laws).
Arterial hydrostatic pressure drives fluid out, Oncotic (Albumen) pressure tries to attract it in. Leftover fluid collected by lymphatics.

91
Q

Anasarca

A

generalized edema

End stage heart failure

92
Q

Lymph

A

Vascular system

One-way flap valves

93
Q

Burkitt Lymphoma

lymph = Lymphocytes
Oma = tumor
A

B lymphocyte tumor
Rapid proliferation of B lymphocytes.
Lump on jaw
Dyspnea and pain
Predominantly affects children and teenagers
EBC (Epstein Barr virus) associates with this disease

94
Q

EBV

A

Human Herpesvirus 4
Spreads through saliva
It can cause mononucleosis
It is associated with Nasopharyngeal carcinoma

95
Q

Hodgkin’s lymphoma

A

Common in people at the age of 20s and after 60.
Painless enlargement of lymph nodes.
Curable, familial, prognosis depends on the stage.
Fever, fatigue, itchy skin, weight loss.
Reed-Sternberg cell

96
Q

Frank-starling

A

The intrinsic ability of the heart to adapt to changing blood volumes.

Basic idea: The greater the Heart is filled during diastole (PRELOAD) the greater the volume of blood that will be pumped into the aoorta.

Within normal limits, changes in arterial pressure (afterload) have little effect on the rate of pumping by the heart.

97
Q

Rules about heart

A

The cause of the failure is generally the place I am pumping to. The symptoms and signs are the places I am draining inside of that heart.
Right-side heart failure is almost caused by pulmonary heart failure or a failed left heart that backs up into the pulmonary circuit.
Pulmonary pressure increase for any reason will cause the right side to fail

98
Q

Right-side heart failure

A
Usually has to do with the pulmonary system or the left heart.
Symptoms are:
- poor drainage of the venous circuit. 
- Jugular venous distention
- Portal hypertension
- Ascites
99
Q

Right-side heart failure

A

Usually has to do with the pulmonary system or the left heart.

  • emphysema, mitral stenosis, left ventricular failure
  • poor drainage of the venous circuit.
  • Jugular venous distention
  • Portal hypertension
  • Ascites
100
Q

Left-side hypertension

A
coronary artery disease 
systemic circulation
Symptoms:
- Lung symptoms such as pulmonary edema
Ischemic heart disease, systemic hypertension
Aortic or mitral valve disease; exertional dyspnea
PND, tachycardia, cardiac asthma
Crackles, cough, cyanosis
101
Q

Cor Pulmonale

A

Right ventricular hypertrophy secondary to pulmonary hypertension