Hematology Flashcards

(46 cards)

1
Q

Thrombosis

Thrombotic event

A

Formation of an inappropriate clot

Reason for forming a clot other than something from intravascular space moving to extra vascular space

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2
Q

Hypoxia vs ischemia

A

Hypoxia is decreased o2 tension in tissue

Ischemia is decreased o2 tension in vessel

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3
Q

Half of blood is what

A

Plasma

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4
Q

Plasma mostly what

7% is what

1% what

A

Water

Plasma proteins

Solutes

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5
Q

Plasma proteins

60%-

35%- and kinds/what they do

4%-

1%

A

Albumin (oncotic pressure)

Globulins (IGG, IGM, IGA), transfer ions/hormones/lipids/immunity

Fibrinogen, essential clotting factor (I)

Regulatory proteins

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6
Q

How much of blood sample is actually blood

What is in Buffy coat/percent

A

45%

1%, platelets and WBC

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7
Q

RBC

__-___ million
____ day life cycle
Shape

A

4.2-6.2
120
Non-uncleared cytoplasmic disc

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8
Q

Leukocytes

Have ___ unlike red cells
___-___ mm3
___ ___ ___ are ___ in structure even though they are immunocytes

A

Nucleus 5-10,000

Natural killer cells, granular

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9
Q

Growth factor that controls process of differentiation

A

G-CSF

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10
Q

PSC releases what for self renewal

Allows it to what

A

SCF, not rely on environment

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11
Q

Where hematopoiesis and lymphopoiesis occurs in

Adults

Embryo

A

Red marrow in bone marrow

Spleen and liver

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12
Q

Multi lineage cytokines 3

Single lineage cytokines 3

A

SCF
GM-CSF
IL-6

G/M-CSF
EPO
TPO

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13
Q

Treating with SCF, GM CSF, IL 3, or IL 6 makes a PSC ___ or ___

A

Myeloid or lymphoid

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14
Q

GM CSF, IL 6, IL 3 lead to 3 kinds of stem cells

A

Granulocytes-macrophage stem cells

Megakaryocytic stem cells

Erythropoietic stem cells

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15
Q

GM CSF, G CSF, M CSF lead to 2

A

Granulocyte stem cells

Monocytic stem cells

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16
Q

GM CSF and g CSF LEAD TO 4

A

Neutrophil
Eosinophils
Basophils/mast cells

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17
Q

GM CSF and M CSF lead to 2

A

Monocytes and macrophages

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18
Q

TPO leads to 2

A

Megakaryocytes and platelets

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19
Q

IL 3 and IL 6 lead to 1

20
Q

PSC to erythrocyte

  1. PSC
  2. Add ___
  3. Committed proeryhtrocyte
  4. Normoblast: ___shrinks/reabsorbed
  5. ____: leaves marrow and enters blood. No ___
  6. Erythrocyte
A

EPO

Nucleus

Reticulocyte, nucleus

21
Q

Increase in hemoglobin= decrease in ____

22
Q

Increased reticulocyte % could mean

A

Destroying cells to quickly

23
Q

Which vitamin plays role in DNA synthesis and maturation. What deficiency leads to

A

B12, non functional red cells

24
Q

___ ___ needed to make HGB

25
O blood has what on it Create antibodies against what
H antigen Blood type that you don't have
26
Which blood type doesn't make antibodies
AB
27
RH - means what | Rh + means what
No d protein | D protein
28
Granulocytes mature where Agranulocyte mature where Kinds of a granulocytes: ___ leads to ___. ___ leads to __ and __ cells
Bone marrow Blood stream Monocytes, macrophages Lymphocytes, b and T cells
29
Thrombocytes 7-10 ___ life span __-___ mm/3 ___ can be used to make them, but ___ essential
Day 140,000-340,000 IL6, TPO
30
Platelets have ___ occurring in cell. Why ___ needed Has ___ granules and ___ granules Granules contain functional units for __ ___, active units, and ___ factors
Functions, mitochondria Alpha, dense Growth factors, clotting factors
31
___ granule release has to occur to form a clot What layer is called to prevent platelet activation
Alpha Calyx
32
____ used as indicator in anemia
MCV
33
Aspiration Doesn't indicate ___ of ___ Can dx 4
Efficiency of activity Anemia, leukemia, platelet disorders, immunoglobulin disorders
34
Biopsy Maintains ___ ___ When ___ suggested, ___ marrow, more than 1 __ __ reduced
Cell structure Tumors, fibrotic, cell type
35
Pets Blood cell count compared to adults __ml/kg full term neonate vs ___ml/kg adult
Higher 85 vs 75
36
Aged RBC Life span: Replaced more ___ because of ___ WBC ___ function decreases with age, due to 2 Platelets are more ____
Normal Slowly, iron depletion/less absorp/less binding capacity Lymphocyte, less T cell function and less responsive humoral system Sticky
37
Exposure to ___ ___ activates ___
Basement membrane, platelets
38
___ stick to ___, how we get adhesions (platelets sticking to ___)
GP, VWF, wall
39
VWF released from where
Subendothelial matrix
40
Primary hemostasis 2 steps
Platelet plug and vasoconstriction
41
Secondary hemostasis Why goes on here, ___ activated
Coagulation cascade, Roman numerals/clotting factors
42
___ __ formed at end of secondary hemostasis Tertiary hemostasis What happens
Blood clot Fibrinolysis to break down clot
43
Thrombin starts as ____ | Which form in secondary hemostasis, because it is __ by an enzyme
Prothrombin, thrombin, cleaved
44
Need __ __ to make clotting factors What affects this What heparin does
Vitamin k Warfarin Blocks factor 10, needed to form clots
45
Intrinsic arm 4 Extrinsic arm
Endothelium and subendothelial matrix, platelets, clotting factors Anything released out of this system. Smooth muscle cell damage
46
___ breaks down ___. Makes ___ which breaks down clot ___ is product of breaking down clot, can be inhibited by ___-1 What shuts down process of plasmin
Tpa, fibrin. Plasmin FDP, PAI-1 Anti plasmin