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243 CH 21 - 24

243 EXAM 3

TermDefinition
hemoglobin oxygen carrying cappacity
erthropoiesis reticulocytes produced in bone marrow in response to erythropoietin
erythropoeitin released by kidney in response to hypoxemia
requirements for RBC production iron, folate, vitamin B12, erythropoietin, stem cells
hgba adult, 2 a and 2 beta
hgbf child, 2 a and 2 gamma - absorbs oxygen at lower tension
hemoglobin 12 - 16
hematocrit 37 - 50%
mean corpuscular volume size of RBC
macrocytic big, low B12, low folate
microcytic small, iron deficiency anemia, hemoglobinopathy, chronic disease, lead poisoning
normocytic normal, acute bleeding, aplastic anemia, hemolytic anemia, low erythropoietin, malignancy
mean corpuscular hemoglobin average amount of hemoglobin per RBC, color
hypochromic low
normochromic normal
sickle cell hemoglobin hgbs, defect in beta chain, 6th ring
catabolism hemoglobin - heme - biliverdin - bilirubin
bilirubin bile (liver)
globin recycled amino acid
leukopenia reduction in number of all white blood cells
neutropenia reduction in number of neutrophils (1000 - 1500)
group A antibodies in plasma: anti B, A antigen
group B antibodies in plasma: anti A, B antigen
group AB no antibodies in plasma, A and B antigens
group O antibodies in plasma: anti A and Anti B, no antigens
thrombocytopenia decreased number of platelets
leukemia decreased platelet production in bone marrow
excess pooling of platelets in spleen normally holds 1/3 of platelets
idiopathic thrombocytopenic purpura ITP bruising, micro bleeds
clotting factor disorders impaired synthesis of clotting factors due to decreased liver or Vitamin K
Rh incompatibility communication between mother and baby
thalassemia group of inherited disorders of hemoglobin synthesis of alpha or beta chains
polycythemia vera absolute increase in total red blood cell mass
secondary polycythemia due to another disorder
relative polycythemia plasma circulating blood volume, dehydrated of DI (more RBC compared to plasma
polycythemia can lead to stroke
hyperslpenism overactive spleen
neutropenia decreased number of neutrophils 1500
neutropenia etiology chemo, leukemia. infection, sepsis, aplastic anemia, nutritional deficiencies
tranfusion reaction immune response to incompatible blood transfusion
normal hemostasis platelets, clotting factors, vessel endothelium
vascular damage constriction of vessels, slower blood flow with thromboxane hormone
platelet plug platelets aggregate and attach to sub endothelial wall, release granules, von Willebrand factor involved
von willebrand factor measures clotting
blood coagulation intrinsic or extrinsic pathway, different factors become activated throughout
clot retraction fibrin seals site
fibrinolysis heparin stops clotting, clotting factors absorbed or inactivated, fibrin clot split
hemolytic disease of newborn lead to stillbirth or jaundice in an Rh negative mother, can be prevented by injection of RhoGAM
platelet dysfunction thrombocytopathia, diagnose by bleeding time
decrease clotting factors decreased liver stimulation, vitamin K deficiency, decreased calcium intake
inherited coagulation defect hemophilia A - insufficient or defective Factor VIII
signs and symptom's Hemophilia A excessive and spontaneous bleeding, swelling, pain, muscle wasting, difficulty moving
abnormal consumption coagulation defect hemorrhage caused by endothelial layer damage (burns, sepsis, trauma)
sickle cell crisis moves from normal hemoglobin to sickle cell hemoglobin forming long inflexible chains
sickle cell very painful, ischemia everywhere - obstruction of blood flow
anemia decrease in oxygen carrying capacity of blood due to quality and quantity of RBCs, amount of HgB
etiology of anemia decreased RBC production, iron deficiency, blood loss, erythrocyte destruction
iron deficiency anemia most common, iron necessary for hemoglobin synthesis, due to poor intake, poor absorption, inadequate utilization
iron deficiency anemia morphology microcytic, hypo chromic RBC (less iron, less color)
anemia due to hemmorrhage acute blood loss (trauma), orthostatic hypotension, volume depletion 'change of position'
iron deficiency anemia seen chronic kidney disease due to less EPO, low iron
anemia due to hemorrhage changes increased reticulocyte count, no evidence of hemolysis
aplastic anemia toxic, radiologic or immunologic injury to bone marrow (unable to produce cells), low platelets/ RBC
aplastic anemia signs bleeding infections, treated with bone marrow transplant
megoblastic anemia pernicious anemia, folic acid deficiency
vitamin B12 deficiency lack of intrinsic factor
pernicious anemia lack of intrinsic factor, macrocytic (megoblastic), peripheral nerve degeneration
folic acid deficiency pregnant women, neural tube defects
hemolytic anemia causes sickle cell disease, ABO or Rh incompatibility, drug induced
hemolytic anemia signs jaundice, normocytic or normochromic
sickle cell disease inherited disorder in which the presence of hemoglobin S causes erythrocytes to sickle when deoxygenated
hemoglobin S hbS genes; damage to spleen
hemostasis arrest of bleeding
systole ventricles contracting, more pressure
diastole ventricles relaxing, heart is filling
preload stretch, volume before conraction
conditions affecting preload clot blocking blood, dehydration
afterload volume, pressure the heart needs to overcome to pump everything out (resistance)
contractility ability of heart muscle to squeeze and contract
disseminated intravascular clotting damage to endothelial layer, clot formation products consumed, increased hemorrhage
megaloblastic anemia morphology macrocytic
Created by: ahommel
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