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NURS 319: Hematology

Chapter Chapters 12-14 Hematology

QuestionAnswer
Red blood cells carry oxygen, male: 4.5 to 5.5 million and female: 4.0 to 5.5 million, life span 120 days, biconcave disc, red, found in bone marrow
white blood cells fight infection, 4,000 to 10,000 cells/mcL, 12-20 days, round shape, colorless/ light purple, found in blood and lymph tissue
platelets blood clotting, 90,000 to 450,000, 7-10 days, discoid shape, gold, found in blood and spleen
hematopoiesis process of blood cell production
a pluripotent cell can differentiate into myeloid stem cell or lymphoid stem cell
a myeloid stem cell can differentiate into erythroblasts, megakaryoblasts, myeloblasts, monoblasts
a lymphoid stem cell can differentiate into lymphoblasts
a erythroblast can differentiate into reticulocyte
a megakaryoblast can differentiate into megakaryocyte
a myeloblast can differentiate into basophils, eosinophils, neutrophils
a lymphoblast can differentiate into b-lymphocyte or t-lymphocyte
a reticulocyte can differentiate into erythrocyte
a megakaryocyte can differentiate into thrombocyte
function of basophils elevate during parasitic infections and allergies
function of eosinophils elevate during infection and inflammation
function of neutrophils release enzymes to destroy microorganisms, releasing free radicals
functions of monocytes phagocytosis, cytokine synthesis
what measures the numbers of RBCs, WBCs, and platelets and their indices composition of blood
protein on the red blood cell that carries oxygen to the body's cells and CO2 from organs to the lungs hemoglobin
how is hemoglobin measured mean corpuscular hemoglobin level
volume or proportion of RBCs in the blood MCHC level
Mean corpuscular volume measures the size of RBCs tells you the type of anemia present in the blood
MCHC measures the amount of Hemoglobin a single RBC has related to the volume of the cell
mean corpuscular hemoglobin (MHC) is the measure of the average amount of _____ contained in each RBC mass
low MCHC anemia
high MCHC hemoglobin elevation
low MCH iron-deficient anemia
high MCH RBCs too big from pernicious anemia
arrest of bleeding hemostasis
3 things that play a role in hemostasis 1. vasoconstriction 2. platelet plug formation 3. blood coagulation
when hemostasis goes wrong 1. primary hemostasis 2. secondary hemostasis
primary hemostasis blockage of blood flow
secondary hemostasis loss of blood
steps of hemostasis bleeding constrict vessels to minimize blood flow platelets go to injury to try and plug the bleed fibrin formation blood clots
when vessel tissue is damaged platelets are "called" to the area of damage by the release of von Willebrand factor
3 steps to platelet plug formation (clot formation) 1. endothelial injury exposes collagen and releases vWF 2. Glycoprotein binds fibrinogen- enhances platelet buildup 3. platelets release thromboxane a2, brings more platelets over
what is the intrinsic pathway responsible for forming a clot when superficial damage occurs to the epithelial tissue
intrinsic pathway stimulating factor 12
the intrinsic pathway has less clotting factors than the common pathway
the final/ common pathway where intrinsic and extrinsic join together
lab values that determine how long it takes for pathways to respond calcium and potassium
pathway responsible for forming a clot when damage occurs through the wall of the blood vessel extrinsic pathway
extrinsic pathway starts with the release of what factor 7
common pathway starts actual production of tissue
factor x stimulates factor Va, which stimulates prothrombin to become thrombin
thrombin stimulates the production of fibrinogen
fibrinogen converts to fibrin
fibrin does what combines with platelets and collagen to form a clot
if clots do not break down, they will continue to grow and block a blood vessel, this is called deep vein thrombosis
a clot can also break off and travel elsewhere in the body. this is called pulmonary embolism (in lungs)
fibrinolysis dissolution of a clot
what is released to begin fibrinolysis fibrin
if the clot is an extravascular clot, then what is released to start the breakdown process tissue plasminogen activator
fibrin and tissue plasminogen activator activate plasminogen
plasminogen activates conversion to plasmin
plasmin along with fibrin degradation products break down clots
test that checks for blood clots D-dimer
two causes of clotting disorders platelet number and coagulation activity
erythropoiesis formation of RBCs
where does erythropoiesis occur? bone marrow
why does erythropoiesis occur? replace RBCs as they're filtered
what condition would cause erythropoiesis to occur? hypoxia
what is bilirubin? yellow pigment that is leftover from bile and supposed to be excreted
which organ gets rid of bilirubin liver
conjugated bilirubin soluble in water, can be excreted in urine
unconjugated bilirubin water insoluble
yellowing of the skin and whites of the eyes jaundice
jaundice indicates dysfunction of the liver
abnormally low number of circulating RBCs or hemoglobin (or both) anemia
anemia causes diminished oxygen carrying capacity
anemia symptoms GI tract blood loss, heavy periods, tachycardia, jaundice, splenomegaly
leukopenia decreased leukocytes
neutropenia decreased neutrophils
agranulocytosis neutrophil count is less than 100 neutrophils per mcL of blood
neutropenia symptoms fever, chills, sore throat, abdominal pain, pain near the anus
what is hodgkin's disease? b cell malignancy
what age group do you see hodgkin's disease most? 15-20 years old and over 55
hodgkin's disease symptoms enlarged lymph nodes
what makes hodgkin's disease stand out? owl eye B cell appearance
what is non-hodgkin's disease B. T or NK cell malignancy
which is more common? hodgkins or non-hodgkins? non-hodgkins
symptoms of non-hodgkins disease enlarged, painless lymph nodes, chromosomal translocation of 14 and 18
chronic myelogenous leukemia overproduction of mature myeloid cells anemia, increased infection, increased bleeding, high WBC
acute myelogenous leukemia proliferation of undifferentiated myeloid blast cells symptoms typical of leukemia
chronic lymphocytic leukemia B-cell malignancy leukemia symptoms
acute lymphocytic leukemia immature T or B cells and chromosomal/ genetic alterations anemia, increased bleeding, enlarged lymph nodes. splenomegaly, increased infection risk, bone pain
leukemia symptoms fever/chills, fatigue/ weakness, frequent/ severe infections, weight loss, swollen lymph nodes, enlarged liver, enlarged spleen, easy bleeding/ bruising, recurrent nosebleeds, petechiae
Created by: lcorlew1
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