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120 Cards in this Set
- Front
- Back
When blood is centrifuged is separates because of their different densities with ___________ on top and RBCs on the bottom. |
plasma |
|
"Buffy coat" |
white cells between the plasma and RBCs |
|
Plasma makes up ___% of the blood volume |
55 |
|
Erythrocytes makes up ___% of the blood volume |
44 |
|
Leukocytes makes up ___% of the blood volume |
<1 |
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Platelets makes up ___% of the blood volume |
<1 |
|
Plasma functions |
solvent, osmotic balance, clotting, defense, absorbs heat, pH buffering |
|
Erythrocytes are ____ blood cells |
red |
|
Women Erythrocyte count is usually a bit ______ than mens |
lower |
|
Erythrocytes function |
carries O2 |
|
Leukocytes function |
defense and immunity |
|
platelets function |
clotting |
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Plasma is ___% water |
92 |
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Plasma is ___% salt |
1 |
|
Plasma is ___% proteins, nutrients, wastes, gases, hormones |
7 |
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Serum is plasma without the __________ proteins |
clotting |
|
Normal pH of blood |
7.35-7.45 |
|
The chemical reactions that occur in our body and run our body can not happen if our blood ___ is wonky. |
pH |
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A Normal blood volume for non-pregnant women is _____L. |
4-5 |
|
A Normal blood volume for pregnant women is _____L. |
6-7 |
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A Normal blood volume for man is _____L. |
5-6 |
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Hematocrit is the % of total blood volume that is _____. |
RBCs |
|
Why do we check the hematocrit? |
For things like anemia; it helps us know how much O2 the blood can trasnport |
|
Hemoglobin is the ____ carrying component of the RBCs. |
O2 |
|
How much hemoglobin is normally in a men's blood? |
13.8-18.2 g/dL |
|
How much hemoglobin is normally in a women's blood? |
12/1-15.1 g/dL |
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How much hemoglobin is normally in a child's blood? |
11-16 g/dL |
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How much hemoglobin is normally in a pregnant women's blood? |
11-13 g/dL |
|
The color of _______ indicates the amount of O2 it is carrying. |
blood |
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Erythrocytes carry O2, are anucleate, have few organelles, are sacs of __________, make ATP anerobically. |
hemoglobin |
|
anucleate |
no nucleus |
|
Hematopoiesis takes place in the bone __________ and vertebrae and proximal ends of femur and humerus. |
marrow |
|
hemocytoblast |
stem cell |
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Hematopoiesis need _____, _________ and ______ to make RBCs. |
B12, folic acid, iron |
|
Hematopoiesis are released into the bloodstream as __________. |
reticulocytes |
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Reticulocytes take ___ days to mature. |
2 |
|
RBCs only live ____ days. |
120 |
|
Ruptured RBCs are removed from circulation as they pass through the _______ and liver, where the products of their breakdown are recycled and re-used during erythropoiesis. |
spleen |
|
erythropoiesis |
formation of new RBCs |
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Damaged RBCs are phagocytized in the spleen, liver and bone marrow are broken down. During this process, hemoglobin is split into the ____ and ______ for recycling later. |
heme, globin |
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The _______ part of hemoglobin breaks down further into amino acids. |
globin |
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The ____ part of hemoglobin is split into iron (Fe3+) and non-iron parts. |
heme |
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The ______ part of the heme is stored for subsequent use. |
iron |
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The non-iron part of heme is converted to biliverdin which is then further converted into a pigment called _________ which is released into the bloodstream and travels to the liver. |
bilirubin |
|
When bilirubin reaches the liver, it is excreted in _____ into the small intestine and from there travels to the large intestine. |
bile |
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Reticulocytes are _________ ______. |
immature RBCs |
|
Rtc |
Reticulocytes |
|
Reticulocytes circulate in the bloodstream for ___ days before they mature. |
2 |
|
Anemia |
decrease in O2 carrying ability of the blood. |
|
types of anemia |
iron deficiency, pernicious, folic acid deficiency |
|
Iron Deficiency is caused by |
iron deficiency in diet or poor absorption |
|
Iron deficiency's effect on blood |
decreased hgb in RBCs |
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pernicious is caused by |
B12 deficiency |
|
pernicious anemia's effect on the blood |
decrease in RBC number, RBCs look large and immature |
|
folic acid deficiency is caused by |
folic acid deficiency in diet |
|
folic acid's effect on blood |
decrease in RBC number, large, immature |
|
hemorrhagic anemia is caused by |
loss of blood |
|
hemorrhagic anema's effect on blood |
decrease in RBCs |
|
hemolytic anemia is caused by |
blood incompatibility, destruction of RBCs |
|
hemolytic anemia's effect on blood |
decrease in RBCs |
|
sickle cell anemia is caused by |
genetic malformation of RBCs |
|
sickle cell anemia's effect on blood |
destruction of RBCs |
|
aplastic anemia is caused by |
destruction of bone marrow by cancer, radiation, medication |
|
aplastic anemia's effect on blood |
decrease in RBCs |
|
thalasemia anemia |
genetic malformation of RBCs |
|
polycythemia |
too many RBCs |
|
Possible negative effects of too many RBCs |
could crowd out other things, look flushed, sludgy blood, can't move through vessels well, can't circulate well, hard on heart |
|
White blood cells participate in the body's _______. |
defense |
|
Normal range for WBCs |
4-11,000 per mm3 of blood |
|
WBCs __________ in number when activated by pathogens. |
increase |
|
neutrophils's function |
phagocytes (short term) |
|
eosinophils's function |
increase during allergy attacks |
|
basophil's function |
contain histamine, heparin. may prevent clotting in body |
|
lymphocytes's function |
B&T cells immune system |
|
monocytes's function |
phagophcytes (macrophages) (chronic) |
|
phagocytes |
engulf pathogens |
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neutrophils make up ____% of our WBCs |
40-70 |
|
eosinophils make up ____% of our WBCs |
1-4 |
|
basophils make up ____% of our WBCs |
1 |
|
lymphocytes make up ____% of our WBCs |
20-45 |
|
monocytes make up ____% of our WBCs |
4-8 |
|
types of WBCs |
neutrophils, eosinophils, basophils, lymphocytes, monocytes |
|
WBCs are _______ than RBCs. |
larger |
|
Leukemia |
form of cancer where WBCs multiply wildly in bone marrow and crowd out RBCs and platelets. |
|
hemostasis |
stoppage of blood flow, it's fast and localized |
|
three components of hemostasis |
1.vasoconstriction 2.platelet plug 3.coagulation |
|
Why is vasoconstriction helpful? |
It helps minimize the open field |
|
_________ release chemicals when they stick to the wound |
platelets |
|
coagulation |
when blood becomes gelatinous |
|
During __________ an invisible net of fibers are being formed which traps RBCs. |
coagulation |
|
Injury > _____________ > platelet plug > thromboplastin released by damaged cells > _______ ________ > coagulation |
vasoconstriction, clotting cascade |
|
There are ____ clotting factors that we need to coagulate our blood properly. |
12 |
|
Our clotting factors are synthesized in the _______. |
liver |
|
fibrin |
fibrous netting that is the end result of the clotting process |
|
clotting disorders |
Vit K Deficiency Disease, Hemophilia, DIC |
|
DIC |
Disseminated Intravascular Coagulation |
|
Vit K Deficiency Disease cause |
prothrombin is not being produced in the liver |
|
Hemophilia cause |
one clotting factor is missing due to genetic mutation |
|
DIC cause |
clotting gone awry. Factors get used up, leading to internal bleeding |
|
Thrombus |
clot in an unbroken blood vessel |
|
The danger of a thrombus is |
that it may break off and get lodged some where in the circulatory system |
|
If a thrombus dislodges it's most likely to get lodged in the ________ or _______. |
lung, brain |
|
a thrombus in the heart |
pulmonary embolism, "heart attack" |
|
Possible etiologies for a bleeding disorder |
platelet deficiency (thrombocytopenia), lack of clotting factors (b/c liver is impaired), hemophilia, Vit K deficiency, bone marrow cancer, radition |
|
etiologies |
cause |
|
There are over ____ RBC antigens in humans - but there are only a few cause severe transfusion reactions. |
30 |
|
The ABO ______ ______ were defined to avoid transfusion reactions. |
blood groups |
|
ABO blood groups |
A B AB O |
|
antigen |
a substance that the body recognizes as foreign (usually a protein) |
|
antibody |
recognizes antigen and attachs to the surface antigens foreign cells |
|
agglutination |
clumping of RBCs |
|
Agglutination occurs because ______ rupture. |
RBCs |
|
Rh positive means their RBCs carry the Rh _________. |
antigen |
|
When Rh+ blood is given to a Rh- person, the person's immune system produces antibodies to the Rh__ blood. |
positive |
|
Rh factor |
the (+) or (-) aspect of the ABO blood cells |
|
Rh incompatibility during pregnancy is only possible if the woman is Rh__ and their partner is Rh ___. |
(-), (+) |
|
Rh incompatibility destroys _____ in the infant |
RBCs |
|
Fetal hemoglobin has an increased ability to pick up _____. |
O2 |
|
Fetal hemoglobin helps to compensate for lower __ ___________ of maternal blood as copmared to air. |
O2 saturation |
|
_______ ___________ can be in part caused by the replacement of fetal RBCs with ones that contain adult hemoglobin. |
infant jaundice |