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Functions of the Blood Transportation
Gases – oxygen and CO2
Nutrients – electrolytes, digestion
Waste – transports to organs that expel waste products
Hormones – travel to target organs in the blood
Functions of the Blood Regulation
pH balance
Fluid balance – maintain proper osmotic pressure
Heat – generated from muscles
Functions of the Blood Protection
Disease – carries cells and antibodies from immune system
Blood loss – clotting mechanism
Constituents
Plasma – fluid portion
Formed elements
Erythrocytes erythr/o (red)
Leukocytes leuk/o (white)
Platelets AKA Thrombocytes thromb/o (clotting) -cytes (cells)
Plasma
55% total blood volume is plasma
91% of plasma is water
8% is proteins (albumin, clotting factors, antibodies, and antibody complements)
1% nutrients, electrolytes, hormones, vitamins, drugs, etc
Formed Elements
Produced in the red bone marrow
Hematopoietic Stem Cells – ancestors of all blood cells able to form into any of the blood cell types
hemat/o (blood)
Erythrocytes
RBC (Red Blood Cells)
Anuclear
few organelles
must be replaced constantly
Protein of 4 amino acid chains with an oxygen- binding heme group
Lives approx. 120 days
Production stimulated by erythropoietin (EPO)
Hemoglobin
O2 carrier, and iron (Fe), and buffer
Gives blood it’s color
Most numerous blood cell
Able to carry H+ ions and act as a buffer
Able to carry CO2 to lungs for elimination
Ability to carry O2 is blocked by CO
Requires nutrients: electrolytes, iron, copper, Vit C
Gases, nutrients, waste, hormones
What are some substances transported in the blood?
7.35 to 7.45
What is the pH range of the blood?
Plasma and formed elements
What are the two main components of the blood?
Protein
Next to water, what is the most abundant type of substance in plasma?
Red bone marrow
Where do blood cells form?
Hematopoietic stem cells
What type of cell gives rise to all blood cells?
Carry oxygen to the tissues
What is the main function of hemoglobin?
Formed Elements Leukocytes
Prominent nuclei of varying sizes
Colorless
Identified by their size and appearance of the cytoplasmic granules
Main function is immunity
Leukocytes: Granulocytes
Show visible granules when stained
Segmented nuclei
Neutrophils
Neutrophils – (55%) phagocytosis
Nuclei have various shapes, segmented
Polymorphs; polymorphonucle ar neutrophils (PMN’s)
morph/o (shape)
Immature cells
have a thick curved band nucleus (Band Cell)
Eosinophils
(2%) allergic reactions; defense against parasites
Basophils
(<1%) allergic reactions; inflammatory response
Agranulocytes: Lymphocytes
No granules
Nuclei are not segmented
Second most numerous of white cells
Mature in lymph tissue
Lymph/o (lymph)
Agranulocytes: Monocytes
Largest in size
Phagocytosis
mon/o (one)
Functions of Leukocytes
Clear the body of foreign materials
Phagocytosis
eat bacteria, seek and destroy phag/o (eat, ingest) (neutrophils and monocytes)
Pus
combination of living and dead bacteria and leukocytes
Abscess
collection of pus in a localized area
Macrophages
large white cells active in disposal macr/o (large) ; born of monocytes
Platelets
Thrombocytes
Smallest of formed elements
Fragments released from megakaryocytes (giant bone marrow cells) kary/o (nucleus)
Enzymes and mitochondria, no nuclei or DNA
Clotting and coagulation
Life span of 10 days
Neutrophils, eosinophils, basophils
What are the three types of granular leukocytes?
Lymphocytes, monocytes
What are the two types of agranular leukocytes?
Clear the body of foreign material and cellular debris.
What is the most important function of leukocytes?
Clotting the blood
What is the function of blood platelets?
Hemostasis
prevention of blood loss hem/o (blood)
Contraction
vasoconstriction
Platelet plug
platelets become sticky and form a temporary plug
Blood clot
coagulation at the site and prevents any further bleeding
Procoagulants
promote clotting
Anticoagulants
prevent clotting
12 Factors
series of well-controlled events to start the clotting process
Fibrinogen
final step converting plasma protein (fibrinogen) into fibrin (solid threads) that forms the clot-gen (producing, originating)
Prothrombinase
enzyme that triggers final clotting mechanism pro- (before, in front of
Prothrombin
is converted into thrombin with the help of Ca++
Thrombin
converts fibrinogen into fibrin
Serum
fluid remaining after the clot formation without the clotting factors
Hemostasis
What is the general term for the process that stops blood loss?
Fibrin
What substance in the blood forms a clot?
Serum does not contain clotting factors
How does serum differ from blood plasma?
Hemorrhage
excessive bleeding
Transfusion
administering blood to one person from another
Agglutinins
antibodies that may cause the RBCs of the donor’s blood to undergo agglutination (clumping)
Hemolysis
RBC’s have ruptured due to the agglutination -lysis (loosening, dissolving, separation)
Blood Type Testing
4 blood types: A, B, AB, and O
Anti-A serum, Anti-B serum
Antigens
proteins that live on the surface of blood cells that stimulate antibody production
Type O
is universal DONOR
Type AB
is universal RECEIVER
Rh Factor
Rhesus monkey
D antigen
Positive or negative
Hemolytic Disease of the Newborn (HDN) (erthroblastosis fetalis) – RhoGAM
Rh negative mother with Rh positive baby first pregnancy
Uses of Blood Components
Treated with anticoagulant
May be stored for up to 35 days
Autologous blood transfusion
donate own blood prior to surgery
Whole Blood Transfusions
⚫ Massive hemorrhage
⚫ Internal bleeding
⚫ During surgery or post-op
⚫ Replacement for hemolytic disease of newborn
Use of Blood Components
Components separated by centrifuge
Packed cells refers to RBC’s
Platelets
Leukocytes (T-cells and T-cell helpers)
Use of Plasma
Used during emergencies when blood type has not been determined
May be frozen and saved (FFP)
When thawed, may have cryoprecipitate that is rich in fibrinogen and clotting factors cry/o (frozen)
Increases osmotic pressure to get more fluid into circulation
Contains all the factors for clotting
Contains antibodies left by lymphocytes
A, B, AB, O
What are the four ABO blood type groups?
A antigen, B antigen, Rh factor (D antigen)
What are the blood antigens most often involved in incompatibility reactions?
Centrifuge
How is blood commonly separated into its component parts?
Blood Disorders
Three groups:
⚫ Anemia -emia (blood)
⚫ Leukemia
⚫ Clotting disorders
Anemia
Results from loss of RBCs
Impaired delivery of oxygen to tissues
Hemorrhagic anemia
sudden (acute) or gradual (chronic) loss of RBC’s due to bleeding
Hemolytic anemia
excessive destruction of RBC’s, overactive spleen, infections, parasites, HDN
Sickle Cell Anemia
Type of hemolytic anemia
Hemoglobin is abnormal
Change shape after O2 is released
Very fragile cells, become tangled masses that block vessels
Joint swelling and pain, abdominal pain
Sickle Cell trait – from one paren
Iron-Deficiency Anemia
not enough iron intake to meet needs, especially children and young women
Pernicious Anemia
Vitamin B-12 deficiency due to a lack of intrinsic factor; deterioration of nervous system
Thalassemia
Hereditary condition; Mediterrean descent
Not enough RBC’s produced, destroyed in bone marrow before matured
Have excess iron in the blood and bone marrow; absorb too much iron from the digestive trac
Aplastic anemia
caused by chemical or physical agents such as drugs, toxic substances, x-ray, injury
Bone Marrow Suppression
Aplastic anemia – caused by chemical or physical agents such as drugs, toxic substances, x-ray, injury
Chronic disorders of the liver or kidney, cancer, RA
Bone marrow will not produce red or white blood cells, leading to leukopenia -penia (lack of)
Leukemia
Neoplastic disease, increased number of WBC’s that crowd out other cells
Incompetent, cannot perform immune properties
Myelogenous leukemia
starts in bone marrow
Lymphocytic leukemia
arises in lymphoid tissue
Leukemia: Symptoms
General symptoms of anemia (low RBC’s)
Bleeds easily (low platelet count)
Frequent infections
Enlarged spleen and other organs possible
Leukemia: Treatments
Chemotherapy and x-ray therapy
Bone marrow transplant
Long recovery
Prognosis is poor
Clotting Disorders- Hemophilia
hereditary bleeding disorder, missing Factor VIII
Symptoms are, easily bruised
and bleeding, internal hemorrhage,
bleeding into joints causing pain
Clotting Disorders- Von Willebrand disease
missing von Willebrand factor that makes platelets sticky
Symptoms are, easily bruised
and bleeding, internal hemorrhage,
bleeding into joints causing pain
Clotting Disorders- Thrombocytopenia
deficiency of circulating platelets; hemorrhage in the skin and mucous membranes
Clotting Disorders- Disseminated intravascular coagulation
excessive coagulation; platelets are used up faster than they can reproduce; burns, trauma, infections, drugs
Decrease in RBCs that hinder O2 circulation to tissues
What is anemia?
Increase of incompetent WBCs compromising the immune system
What is leukemia?
Platelets
What blood components are low in cases of thrombocytopenia?
Standard Blood Tests- Complete Blood Count (CBC)
cells counts with differential
Standard Blood Tests- Blood Chemistries (SMA)
covers all of the systems
Hematocrit
Percentage of RBC’s in whole blood
% per unit volume (38%/dL)
Men: 42 to 54%/dL
Women: 36 to 46%/dL
Determining if anemia exists
Or bleeding post op
Hemoglobin
Determine oxygen delivery to tissues
Grams/dL or percentage of a given standard
Men: 14 to 17g/dL
Women: 12 to 15g/dL
Anemia
Blood Cell Counts: RBCs
RBC – 4.5 to 5.5 million/mcL
Polycythemia
increased RBC count, high altitudes
Polycythemia Vera
bone marrow disorder
Blood Cell Counts: WBCs
WBC – 5,000 to 10,000/mcL
Leukopenia
below 5,000; depressed bone marrow or bone marrow tumor
Leukocytosis
above 10,000; infection
Blood Cell Counts: Platelets
Normal range 150,000 to 400,000/mcL
Very low count may cause bleeding problems, requiring platelet transfusion
Blood Slide Smears
Drop of blood spread on a slide and examined under a microscope
Reticulocytes
immature RBCs