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Major transport system of the body that moves oxygen, glucose, nutrients, hormones, electrolytes, and cell wastes.
Blood
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Body's defense that carries white blood cells and antibodies.
Blood
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Mechanism for controlling body temperature and distributes heat to peripheral tissues.
Blood
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Medium through which body fluid levels and blood pressure are measured and adjusted.
Blood
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Number of liters of blood in an adult?
5 Liters
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55% Component of blood.
Water and dissolved solutes.
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45% Component of blood.
Cells or formed elements such as arythrocytes, leukocytes, thrombocytes/platelets.
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Proportion of red blood cells in blood.
Hematocrit
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Percent of hematocrit in males and females.
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Clear yellowish fluid - cells have been removed.
Plasma
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Fluid and solutes - cells and fibrinogen have been removed.
Serum
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Maintain osmotic pressure in the blood. Albumin, globulins, fibrinogen, antibodies.
Plasma Proteins
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Where all blood cells originate from?
Red bone marrow. That is found in flat, irregular bones, ribs, vertebrae, sternum, pelvis.
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Red Blood Cells
Erythrocytes
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Shape and Structure of Erythrocyte
- Biconcave, flexible discs.
- Non-nucleated when mature.
- Contain hemoglobin.
- Size and structure essential for easy passage through small blood vessels.
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Hormone from kidney.
Stimulates erythrocyte production.
Response to tissue hypoxia.
Erythropoietin
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Red Blood Cell Production Raw Materials
Amino acids, iron, vitamin B12, vitamin B6, and folic acid.
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Parts that make up hemoglobin.
Globin + 2 pairs of amino acid chians + 4 heme groups.
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Fully saturated with oxygen in the lungs.
Oxyhemeglobin is bright red (arterial)
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As blood circulates, oxygen dissociates from hemeglobin.
Deoxygemeglobin - blueish - red (venous)
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When a RBC dies, globin is broken down into...
Amino acids which get recycled and iron that is recycled by the liver or bone marrow.
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When a RBC dies, heme is broken down it is...
Converted into bilirubin and transported to the liver and excreted in bile.
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Leukopoiesis
Production of white blood cells. Stimulated by CSFs produced by macrophages and T-lymphocytes.
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When WBCs leave capillaries and enter tissues by...
Diapedesis
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50-60% of WBC
Survive only 4 days
First to respond to tissue damage
Neutrophils
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Migrate from blood to tissue to become mast cells
Release heparin and histamine
Basophils
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Combat effects of histamine
Increased by allergic reactions and parasitic infections
Eosinophils
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B and T
30-40% of WBCs
Lymphocytes
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Enter tissues to become macrophages
Monocytes
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Another name for platelets
Thrombocytes
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Part of blood that is essential for blood clotting.
Made of megakaryocytes.
Stick to damaged tissue and each other to form plug.
Initiate the coagulation process.
Thrombocytes
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Another name for blood clotting.
Hemostasis
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Blood clotting steps (3)
Vasoconstriction. Thrombocytes adhere to injured tissue. Coagulation.
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Breaking up of clot.
Fibrinolysis
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Coagulation
Clot formation
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No antigens
Anti-A and Anti-B antibodies
Can recieve only same blood
O
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A antigen
Anti-B antibodies
Can recieve O and A
A
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B antigen
Anti-A antibodies
Can recieve O and B
B
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A and B antigens
No antibodies
Receive all blood types
AB
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Functions of Lymphatic System
- Return to excess interstitial fluid and protein to the blood.
- Filter and destroy unwated material from body fluids.
- Initiate immune response.
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Component of Lymphatic System that remove foreign or unwanted material from lymph fluid before it enters general circulation.
Lymph Nodes and Lymphoid Tissue
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Essential to immune response and sensitization of B and T lymphocytes.
Lymph Nodes
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Reduction in oxygen transport in the blood due to a decrease in hemoglobin.
Anemia
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Low hemoglobin or anemia results of...
- Declining production
- Decrease in erythrocytes
- Combination
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Decrease energy produced in all cells; cell metabolism and reproduction decreases
Effect of anemia
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Tachycardia and vasoconstriction
Effect of anemia to compensate to oxygenate tissues
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Deficiency of a required nutrient
Bone function impaired
Blood loss
Excessive desruction of erythrocytes
Causes of anemia
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In small, less color erythrocytes
Iron Deficiency Anemia results
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Low dietary intake
Chronic blood loss
Impaired absorption
Severe liver disease
Iron Deficiency Anemia causes
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Cold intolerance
Irriability
Brittle hair, concave nails
Delayed healing
Tachycardia, dypnea, and synoscope
Iron Deficiency Anemia signs and symptoms
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Another name for pernicious anemia
Megaloblastic anemia
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Very large, immature, nucleated erythrocyes
Megaloblasic
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Type of anemia that usually results from a deficit of folic acid or vitamin B12, pregnancy.
Pernicious Anemia Results from...
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Cause of pernicious anemia
Malabsorption or result of gastrectomy
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Decreased gastric juices leads to GI discomfort, nausea and diarrhea
Enlarged tongue
Pernicious Anemia signs and symptoms
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Bone marrow is hyperactive
Vit B12 is low
Diagnostic Test of pernicious anemia
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Impairment of failure of bone marrow function from radiation, chemicals, drugs, hep c, autoimmune disease.
Cause of aplastic anemia
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Leukopenia and thrombocytopenia
Signs and symptoms of aplastic anemia
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CBC and bone marrow biopsy
Diagnostic tests for aplastic anemia
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Blood transfusion or bone marrow transplant
Treatment for aplastic anemia
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Result of excessive destruction of RBCs
Leads to low erythrocyte count and low total hemoglobin
Causes genetic disorders, immune reactions, blood incompatibility
Hemolytic Anemias
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Inherited characteristic leads to abnormal hemoglobin
Sickle Cell
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Hbs is deoxygenated and crystalilized and changes shape
Sickle Cell
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Pain caused from occluded blood vessels
Sickle Cell
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Homozygotes
Most normal hemoglobin replaced by HbS, creates clinical signs of sickle cell. ss
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Heterozyotes
1/2 hemeglobin is replaced by HbS. Ss
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Reduce crisis with drugs
Avoidance of strenous activity
Prevent dehydration, acidosis, infection, and exposure to cold
Sickle Cell Treatment
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Genetic defect in which one or more genes for hemoglobin are missing or variant
Thalassemia
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Interferes with the production of globin chains
Thalassemia
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Decrease or lack of alpha or beta chains
Thalassemia Types
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Hemolysis
Normal skeletal development is impaired
Child growth impaired
Thalassemia Signs and Symptoms
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Iron Overload
Thalassemia Diagnositc Test
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Blood transfusions
Iron chelation
Splenectomy
Treatment of Thalassemia
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Increased production of erythrocytes and other cells in bone marrow
Increased blood volume
Blood vessels distended and blood flow is sluggish
Primary Polycythemia
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Increase in RBCs that occurs in response to prolonged hypoxia and increased erythropoietin secretion
Secondary Polycythemia
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Neoplastic disorder of unknown origin
Develops btwn age 40 and 60
Primary Polycemia
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A compensatory mechanism
Secondary Polycemia
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Cyanosis
Pruritus
Increased bp, full bounding pulse
CHF develops
Polycythemia Signs and Symptoms
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Hemoglobin and hematocrit levels are increased
Bone marrow is hypercellular
Diagnostic Test Polycythemia
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Drugs or radiation to supress bone marrow
Periodic phlebotomy to remove blood
Treatment of Polycythemia
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Persistent bleeding
Blood in feces
Feeling faint and anxious, low bp, rapid pulse
Warning signs of blood clotting disorders
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Chemotherapy, radiation
Vit K deficiency
Liver Disease
Hemorrhagic fever
Anticoagulant drugs
Causes of excessive bleeding in a blood clotting disorder
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Most common inherited clotting disorder
Hemophilia A
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Deficit or abnormality of clotting factor IX
Hemophilia B (Christmas disease)
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Deficit or abnomality of clotting factor XI
Hemophilia C (Rosenthal's)
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70% have severe form
Prolonged hemorrhage
Persistent oozing
Hematomas
Blood in urine
Hemophilia A
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PTT and coagulation are prolonged
Diagnostic Test Hemophilia A
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Precautions to prevent injury
Replacement therapy for factor VIII
Treatment for Hemophilia A
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Excessive bleeding and clotting
Disseminated Intravascular Coagulation - DIC
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Obstetric complications
Infection
Cancer
Major trauma
Initate.....
Disseminated Intravascular Coagulation - DIC
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Multiple Bleeding Sites
Respiratory Impairment
Seizures
Acute Renal Failure
- Disseminated Intravascular Coagulation - DIC
- Signs and Symptoms
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One or more of the leukocyte types are present as undifferentiated, immature, nonfuctional that multiply uncontrollably in the bone marrow
Leukemias
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High proportion of very immatue, nonfuctional cells (blast cells) in bone marrow and peripheral circulations
Acute Leukemia
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Higher proportion of mature cells (have reduced function)
Chronic Leukemia
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Onset marked by infection unresponsive to treatment or excessive bleeding
Bone pain
Weight loss and fatigue
Fever
Enlarged spleen
Leukemia Signs and Symptoms
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Blood smear shoes immature leukocytes and altered numbers of WBCs
RBCs and platelets are decreased
Leukemia Diagnostic Test
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Chemotherapy only treatment
Leukemia
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Lymphomas disorders
Hodgkins and Non-Hodgkins Lymphoma
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Malignant neoplasm involving lymphocyte proliferation in the lymph nodes
Lymphomas
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Occurs in age 20-40
Equal in men and women
Prognosis early is excellent
Initially involves one lymph node (neck) then spreads in orderly fashion.
Hodgkins Disease
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Reed-Sternberg cells (giant cell)
Hodgkins Disease
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Hodgkins - Stage I
Single lymph node or region affected
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Hodgkins - Stage II
Two or more lymph nodes or regions affected on same side of diaphragm
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Hodgkins - Stage III
Nodes on both sides of the diaphragm and the spleen
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Hodgkins - Stage IV
diffuse extralymphatic involvement
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Lymph node large, painless, nontender
Recurrent infection
Weight loss, anemia, low grade fever, night sweats, faituge
Hodgkins Signs and Symtoms
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Radiation, chemo, surgery treatments
Hodgkins
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Associated with HIV infection
Involve B lymphocytes
Widespread metastases
Non-Hodgkins
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Multiple tumors with bone destruction develop in vertebrae, ribs, pelvis, and skull
Hypercalcemia
Tumor cells spread throughout body
Older adults
Multiple Myeloma
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Malignancy well advance before diagnosis
Pain
Ademia
Fractures
Kidney failure
Multiple Myeloma
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Median survival is 3 years
Analgesics for bone pain
Multiple Myeloma
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