Blood Flashcards

1
Q

What is polycythemia??

A

It is a genetic neoplasia where there is an increase in RBC. Leads to sludgy blood.

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2
Q

PCV

A

Packed cell volume

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3
Q

What is PCV synonymous with??

A

Hematocrit

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4
Q

What are some examples of blood smears?

A

Wright, Giemsa, and diff-quick

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5
Q

What controls erythropoeisis?

A

Erythropoietin

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6
Q

Where does hemopoiesis occur?? `

A

In flat bones and some long bones:
Flat bones: skull, ribs, sternum, vertebrae, pelvis
Long bone: femur

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7
Q

Where does hemopoeisis first occur in the fetus?

A

“Blood islands” in the wall of the yolk sac, during the first trimester.

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8
Q

Where does hempoeisis occur in the second trimester?

A

In the liver, lymphatic tissue, and during the last month of pregnancy it occurs in the bone marrow.

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9
Q

Once the baby is born, where does hemopoeisis occur?

A

It occurs in the marrow cavities

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10
Q

What is the overall trend of erythropoiesis?

A

There is progressive decrease in size, loss of the nucleus and organelles, and an increase in hemoglobin

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11
Q

Follow the stages of erythropoeisis.

A

Preoerythroblast, erythroblast/normoblast, reticulocyte—> mature RBC.

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12
Q

What happens within the cell before the RBC is put into the blood stream?

A

The nucleus is extruded, and the organelles degenerate.

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13
Q

How do RBC’s make ATP?

A

Anaerobic gylcolysis

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14
Q

What is reticulocytosis?

A

Increase in the production of reticulocytes in the circulation. This is reltated to chronic blood loss aka hemolytic anemia. AKA AKA left shift.

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15
Q

What leads to macrocytes??

A

A vitamin B12 and B9 deficiency

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16
Q

What are two characteristics of anemia?

A

Blood loss or the decrease in Iron

17
Q

What is the difference between anemic RBCs and normal?

A

Microcytic (smaller) and hypochromatic (pale staining)

Normocytic and normochromic

18
Q

Describe a megakaryocyte and its role in blood clotting.

A

These cells are what platelets are formed from. These cells develop pleated demarcation channels in the cytoplasms and the platelets tear off.

19
Q

What drug impairs coagulation? Or platelet function? ??

A

Aspirin

20
Q

The intrinsic pathway requires numerous other clotting factors. What are they?

A

Von willebrand’s factor and facto VIII and a longer cascade rxn

21
Q

WHat happens when a blood vessel breaks?

A

Releases thromboplastin which initiates the EXTRINSIC pathway. It also exposes collagen which leads to the INTRINSIC pathway. Platelets adhere to the exposed collagen and release serotonin.

22
Q

What is serotonin?

A

It is a strong vasoconstrictor. Works to prevent blood loss.

23
Q

Where do the intrinsic pathways and the extrinsic pathways converge?

A

At the point where factor X is activated. Here prothrombin is converted into thrombin and fibrinogen is turned into fibrin.

24
Q

What causes a heart attack or stroke?

A

Inapppropriate clot formation!

25
Q

What is hemophilia A?

A

It is a deficiency in clotting factor VIII

26
Q

What is hemophilia B?

A

Factor iX deficiency

27
Q

What is hemophilia C?

A

Factor XI deficiency

28
Q

What is another type of hemophilia?

A

Von wilebrand’s disease.