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WorksheetsCh. 18 - BC
Total questions: 42
Worksheet time: 21mins
Blood contains this element which takes up 55% of it and is clear and light-yellow fluid.
Blood plasma
White blood cells
Red blood crlls
Blood contains this element which takes up 41%
Blood plasma
White blood cells and platelets
Red blood cells
Blood contains this element which takes up 4%
least abundant formed element
protect against infectious microorganisms and other pathogens
Blood plasma
White blood cells and platelets
Red blood cells
Blood plasma contains plasma proteins which one is this:
smallest and most abundant
Contribute to viscosity and osmolarity; influence blood pressure, flow, and fluid balance
Albumins
Globulins
Fibrinogen
Blood plasma contains plasma proteins which one is this:
antibodies
immune system functions
Albumins
Globulins
Fibrinogen
Blood plasma contains plasma proteins which one is this:
Precursor of fibrin (blood clots)
Albumins
Globulins
Fibrinogen
Which plasma protein deficiency is this:
Low level of protein in blood
Draws water out of blood
Causes edema
Hypoproteinemia
Kwashiorkor
Which plasma protein deficiency is this:
Children with severe protein deficiency
once weaned, eat only cereals
Thin arms and legs
Swollen abdomen/enlarged liver
Edema (ankles/feet)
Hypoproteinemia
Kwashiorkor
Which erythrocyte disorder is this:
An excess of RBCs
Dangers: Increased blood volume, pressure, viscosity, Can lead to embolism, stroke, or heart failure
Polycythemia
Anemia
Sickle-cell disease
Malaria
Which erythrocyte disorder is this:
a low level of red blood cells (or dysfunctional red blood cells)- leads to reduced oxygen flow to the body's organs
Consequences: Tissue hypoxia and necrosis, Blood osmolarity is reduced, producing tissue edema, Blood viscosity is low
Polycythemia
Anemia
Sickle-cell disease
Malaria
Which erythrocyte disorder is this:
a low level of red blood cells (or dysfunctional red blood cells)- leads to reduced oxygen flow to the body's organs
Consequences: Tissue hypoxia and necrosis, Blood osmolarity is reduced, producing tissue edema, Blood viscosity is low
Polycythemia
Anemia
Sickle-cell disease
Malaria
Which erythrocyte disorder is this:
•Hereditary defect that occur mostly among people of recent African descent
•Caused by recessive allele that changes structure of normal Hb into mutated HbS
Polycythemia
Anemia
Sickle-cell disease
Malaria
Which erythrocyte disorder is this:
•parasitic disease spread to humans through the bites of infected mosquitoes
Those with Sickle Cell Trait (carriers) are resistant to this
Polycythemia
Anemia
Sickle-cell disease
Malaria
•Cancer of red bone marrow
hematocrit > 80% (normal ~ 45-50)
Primary polycythemia
Secondary polycythemia
Inadequate erythropoiesis (hemoglobin synthesis)
Hemorrhagic anemia
•From dehydration, emphysema, high altitude, or physical conditioning
RBC count up to 8 million RBCs/μL
Primary polycythemia
Secondary polycythemia
Inadequate erythropoiesis (hemoglobin synthesis)
Hemorrhagic anemia
–Kidney failure (low erythropoietin)
–Iron-deficiency anemia
Pernicious anemia - autoimmune attack of stomach tissue leads to inadequate vitamin B12 absorption
Primary polycythemia
Secondary polycythemia
Inadequate erythropoiesis (hemoglobin synthesis)
Hemorrhagic anemia
From excessive bleeding
Secondary polycythemia
Inadequate erythropoiesis (hemoglobin synthesis)
Hemorrhagic anemia
Hemolytic anemia
From RBC destruction
Secondary polycythemia
Inadequate erythropoiesis (hemoglobin synthesis)
Hemorrhagic anemia
Hemolytic anemia
Which blood type is this:
A antigens/Anti-B antibodies
type A
type B
type AB
type O
Which blood type is this:
B antigens/Anti-A antibodies
type A
type B
type AB
type O
Which blood type is this:
both A and B antigens/No antibodies
type A
type B
type AB
type O
Which blood type is this:
neither antigens/both antibodies
type A
type B
type AB
type O
Universal donor
most common blood type
no surface antigens
type O
type AB
Universal recipient
rarest blood type
no plasma antibodies
type O
type AB
which granulocyte leukocyte is this:
60-70%
polymorphonuclear leukocytes
Barely visible granules in cytoplasm; three- to five-lobed nucleus
neutrophils
eosinophils
basophils
lymphocytes
monocytes
which granulocyte leukocyte is this:
2-4%
large rosy-orange granules; bilobed nucleus
neutrophils
eosinophils
basophils
lymphocytes
monocytes
which granulocyte leukocyte is this:
less than 1%
large, abundant, violet granules (obscure a large S-shaped nucleus)
neutrophils
eosinophils
basophils
lymphocytes
monocytes
which agranulocyte leukocyte is this:
25-33%
variable amounts of bluish cytoplasm (scanty to abundant); ovoid/round, uniform dark violet nucleus
neutrophils
eosinophils
basophils
lymphocytes
monocytes
which agranulocyte leukocyte is this:
3-8%
usually largest WBC; ovoid, kidney or horseshoe-shaped nucleus
neutrophils
eosinophils
basophils
lymphocytes
monocytes
stoppage of bleeding
hemostasis
hemorrhage
excessive bleeding
hemostasis
hemorrhage
which hemostasis step is this:
Vascular spasm—prompt constriction of a broken vessel
First protection against blood loss
Causes: Some Pain receptors cause blood vessels to constrict, Smooth muscle injury, Platelets release serotonin (vasoconstrictor)
step 3
step 1
step 2
which hemostasis step is this:
Platelet plug formation
Intact vessels are coated with prostacyclin—a platelet repellant
Broken vessel exposes collagen, platelets stick to damaged vessel and other platelets
Positive feedback cycle (+ chemotaxis) is active until break in small vessel is sealed
step 3
step 1
step 2
which hemostasis step is this:
Coagulation (clotting)—last and most effective defense against bleeding
Conversion of plasma protein fibrinogen into insoluble FIBRIN threads to form framework of clot
Procoagulants (clotting factors) are present in plasma
Activate one factor and it will activate the next to form a reaction cascade…
step 3
step 1
step 2
dissolution of a clot
kallikrein converts plasminogen into plasmin,a fibrin-dissolving enzyme that breaks up the clot
fibrinolysis
patelet repulsion
thrombin dilution
natural anticoagulants
Platelets do not adhere to prostacyclin-coated endothelium
fibrinolysis
patelet repulsion
thrombin dilution
natural anticoagulants
By rapidly flowing blood
Heart slowing in shock can result in clot formation
fibrinolysis
patelet repulsion
thrombin dilution
natural anticoagulants
Heparin (from basophils and mast cells) interferes with formation of prothrombin activator
Antithrombin (from liver) deactivates thrombin before it can act on fibrinogen
fibrinolysis
patelet repulsion
thrombin dilution
natural anticoagulants
which clotting disorder is this:
family of hereditary diseases characterized by deficiencies of one or more clotting factors
more common in males
Frequent hematomas—masses of clotted blood in the tissues
Tx - transfusion of plasma or purified clotting factors
hemophilia
thrombosis
embolus
infarction
which clotting disorder is this:
abnormal clotting in unbroken vessel
Most likely to occur in leg veins of inactive people (DVT)
hemophilia
thrombosis
embolus
infarction
which clotting disorder is this:
anything that can travel in the blood and block blood vessels
Pulmonary embolism: clot may break free, travel to lungs
hemophilia
thrombosis
embolus
infarction
which clotting disorder is this:
(tissue death) may occur if clot blocks blood supply to an organ (MI or stroke)
650,000 Americans die annually
hemophilia
thrombosis
embolus
infarction
