Blood and Anemia Flashcards

1
Q

What is the composition of blood?

A

plasma (55%):
-water (92%)
-proteins (7%)
-salts
-lipids (cholesterol)
-carbohydrates (glucose)
-gases (O2, CO2)
cells (45%):
-RBC (4.5million/mcL)
-WBC (5000-10000/mcL)
-granulocytes
-neutrophils (60-70%)
-eosinophils (1-3%)
-basophils (1%)
-monocytes (4-8%)
-lymphocytes (20-40%)
-platelets (150,000-400,000/mcL)

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2
Q

What is the hematocrit?

A

volume fraction that is cells after centrifugation

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3
Q

What are the sites of hematopoiesis in adults? Children? Fetus?

A

adult: calvarium, vertebrae, ribs, sternum, pelvis
child: bones
fetus: bones, liver, spleen

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4
Q

What is the basic cell of the eight major hematopoietic lineages? What can this cell differentiate into?

A

stem cells
stem cells can become CLP or CMP
CLP–>T cell or B cell
CMP–>RBC, platelets, basophil, eosinophil, neutrophil, monocyte, osteoclast

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5
Q

Describe the intrinsic pathway of the coagulation cascade.

A

starts with vessel damage
XII–>XIIa
XI–>XIa (via XIIa)
IX–>IXa (via XIa)
X–>Xa (via XIa)
II–>IIa (via Xa)
fibrinogen–>fibrin (via Xa)

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6
Q

Describe the extrinsic pathway of the coagulation cascade.

A

starts with trauma
VII–>VIIa
X–>Xa (via VIIa)
II–>IIa (via Xa)
fibrinogen–>fibrin (via IIa)

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7
Q

What makes up the common pathway of the coagulation cascade?

A

Xa

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8
Q

What is the role of anticoagulants?

A

reduce the risk of blood clots which can cause stroke, pulmonary embolism or MI in patients with AF, VTE, ACS, orthopedic surgery

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9
Q

What is the MOA of warfarin?

A

blocks the vitamin-K dependent processes of producing factors II, IX, VII, X
INR monitoring is essential

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10
Q

Which clotting factor is prothrombin?

A

II

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11
Q

What is the MOA of apixaban, rivaroxaban, and edoxaban?

A

factor Xa inhibitors

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12
Q

What is the MOA of heparin?

A

binds to and activates antithrombin, inactivating factor Xa and IIa
may be used during acute DVT and MI management

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13
Q

What is the MOA of enoxaparin and LMWH?

A

reduced anti-factor IIa activity relative to anti-factor Xa activity
more favourable benefit-risk ratios
better PK
less microvascular bleeding and bleeding risk compared to UFH

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14
Q

What is the MOA of dabigatran?

A

direct thrombin inhibitor

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15
Q

True or false: ASA is an anticoagulant

A

false
its an antiplatelet, sometimes used in combo with DOACs

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16
Q

What are examples of antiplatelet drugs?

A

platelet aggregation inhibitors:
-ASA and COX-inhibitors
oral thienopyridines:
-clopidogrel, prasugrel, ticagrelor, ticlopidine
glycoprotein platelet inhibitors:
-abciximab, eptifibatide, tirofiban
protease-activated receptor-1 antagonists
-vorapaxar
miscellaneous:
-dipyridamole (nucleoside transport inhibitor and PDE3 inhibitor)
-cilostazol (PDE3 inhibitor)

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17
Q

What is the function of erythrocytes?

A

transport of oxygen from lungs into peripheral tissues

18
Q

What is the structure of hemoglobin?

A

four heme groups and four globins
-adult: two alpha, two beta
-fetal: two alpha, two gamma

19
Q

What is anemia?

A

reduction of hemoglobin in the blood to below-normal levels
-<13g/dL in males
-<11.5g/dL in females

20
Q

What might anemia be associated with?

A

abnormal hemoglobin: abnormal hematopoiesis
reduced # of RBC: decreased hematopoiesis
structural abnormalities of RBC: abnormal hematopoiesis
may be a consequence of increased loss or destruction of RBC

21
Q

Which vitamins, minerals, and macronutrients could be associated with decreased hematopoiesis?

A

iron deficiency
vitamin B12 deficiency
protein deficiency

22
Q

What is a genetic disorder that can cause abnormal hematopoiesis?

A

sickle cell anemia

23
Q

What are examples of bleeding that can put a person at risk for increased loss or destruction of RBC?

A

prolonged menstrual bleeding
peptic ulcer

24
Q

What is the morphology of a normal RBC?

A

biconcave disk
7mcm

25
Q

Provide morphologies of RBC and an example with each.

A

normocytic, normochromic anemia
-dilutional anemia
microcytic, hypochromic anemia
-iron deficiency
macrocytic, normochromic anemia
-deficiency of B12 and/or folic acid
anemias associated with abnormal RBC shape:
-elliptocytosis, spherocytosis, sickle cell anemia

26
Q

Provide examples of the many different symptoms of anemia.

A

eyes: yellowing
skin: pale, cold, yellowing
respiratory: shortness of breath
muscular: weakness
intestinal: changed stool color
central: fatigue, dizziness, fainting (severe cases)
blood vessels: low bp
heart: palpitations, tachycardia, angina or MI (severe)
spleen: enlargement

27
Q

What might cause decreased hematopoiesis?

A

bone marrow failure
-aplastic anemia
-myelophthisic anemia
deficiency of nutrients:
-B12 and folic acid (megaloblastic anemia)
-protein

28
Q

What usually causes abnormal hematopoiesis?

A

genetic abnormalities
-sickle cell anemia, thalassemia

29
Q

What might cause increased loss and destruction of RBC?

A

bleeding
intrasplenic sequestration
immune hemolysis
infections (malaria)
hemolytic anemia

30
Q

Describe hemolytic anemia.

A

increased RBC destruction
intracorpuscular defects:
-structural abnormalities
-sickle cell anemia, thalassemia, hereditary spherocytosis
extracorpuscular defects:
-antibodies, infectious agents, mechanical factors

31
Q

What is the most common form of anemia?

A

iron deficiency anemia

32
Q

What is the etiology of iron deficiency anemia?

A

increased loss of iron (chronic bleeding)
inadequate iron intake or absorption
increased iron requirements:
-babies, adolescents, adult women, pregnant women

33
Q

True or false: folate is a fat-soluble vitamin

A

false
water-soluble type of vitamin B (B9)

34
Q

What are sources of folic acid?

A

green leafy vegetables
citrus
pulses

35
Q

What is the role of folate?

A

folic acid works with B12 and vitamin C in protein and DNA metabolism
formation of red and white blood cells

36
Q

What are contributors to folate deficiency?

A

diseases in which folic acid is not well absorbed
-Celiac or Crohns
excessive alcohol
overcooked fruits and veg
hemolytic anemia or kidney dialysis
medicines (phenytoin, sulfasalazine, TMP/SMX)

37
Q

True or false: WBC disorders are usually a result of abnormal function

A

false
usually a result of abnormal number

38
Q

What might cause neutrophilia?

A

increased marrow activity:
-bacterial infections
-acute inflammation
-leukemia
release from marrow pool:
-stress
-corticosteroids
-endotoxin exposure
demargination into blood:
-bacterial infections
-hypoxemia
-stress
-corticosteroids
-exercise

39
Q

What might cause neutropenia?

A

decreased marrow activity:
-drugs
-radiation
-megaloblastic anemia
-aplastic anemia
-marrow replacement by tumor
decreased neutrophil survival
-sepsis
-viral or rickettsial infection
-immune destruction via drug
-immune destruction via antibodies

40
Q

What might cause lymphopenia?

A

immunodeficiency (AIDS
corticosteroids
toxic drugs
Cushings

41
Q

What might cause lymphocytosis?

A

medium to large, atypical lymphocytes predominant:
-viral infections
-active immune response
-lymphoma, leukemia
small, mature lymphocytes predominant:
-chronic infections (TB)
-autoimmune diseases (myasthenia gravis)
-metabolic diseases (Addisons disease)
-lymphoma, leukemia
immature cells predominant:
-leukemia, lymphoma