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Blood
Blood
• Essential Life Supportive Fluid• Transported in Closed System
Throughout Body Through Blood Vessels
Physical Characteristics
• Viscous• pH 7.35 – 7.45• Temperature: 38 degrees C; 100.4
degrees F• 7% - 8% of total body weight• Males: 5 – 6 liters• Females: 4 – 5 liters
Functions of Blood
• Transportation– What is transported?
• Regulation– What does it help regulate?
• Protection– How does it protect?
Four Components
• Plasma
• Erythrocytes: (RBCs)
• Leukocytes (WBCs)
• Platelets
Plasma
• Liquid portion: 90-92% water with fibrous proteins (fibrin)
• Straw colored, sticky fluid
• Carries electrolytes, hormones, gases, and organic compounds
Erythrocytes
• Shape: biconcave disc• flexibility to change shape• Mature anucleate• Lifespan: 100 – 120 days• 97% is hemoglobin
• Transports O2
Leukocytes/WBCs
Surveillance, Fighters, Protectors
5 Types of WBCs• Neutrophils: granululocyte
(bacterial and some fungal infections)
• Lymphocyte: agranulocyte (T&B cells)
• Monocyte: agranulocyte• Eosinophil: granulocyte (allergic
reactions, parasitic infections)• Basophil: granulocyte
Platelets
• Thrombocytes
• Involved in blood clotting
• Lifespan: live only 10 days
• Aspirin inactivates the platelets
Red Blood Cell Disorders
• Iron-deficiency anemia– Insufficient Fe
– Affects ______
– Results in_____
– Patient is _____
– Most commontype of anemia
– Looks?
Red Blood Cell Disorders
• Aplastic anemia– Failure of ____ to
produce enough blood cells
• Pernicious anemia– Lack of intrinsic factor
– Inability to absorb vitamin _____
Sickle Cell Anemia
• History– Observed in 1910
– 1917 found sickled in blood smear
– 1949 discovered Hemoglobin S during electrophoresis
• Different amino acid
– Sickle Cell Trait
Sickle Cell Trait
Sickle Cell Trait
• Hemoglobin AS
• Heterozygous State
• ~ 8% of American Blacks
• Helps against malaria
• What causes a reaction?
Sickle Cell
• Hemoglobin SS
• Homozygous State
• No cure
• Clinical features: bone and joint abnormalities, enlarged heart, heart murmurs, retinal hemorrhage
Red Blood Cell Disorder
• Diamond Blackfan Anemia – Rare, 5-7 per million– bone marrow fails to
make RBC, severely anemic
– Associated with birth defects (most common head and face, arms and hands, heart, genitourinary
White Blood Cell Disorder• Leukemia
– White blood cell or bone marrow cancer
– Two main categories: • Acute
• Chronic
– Subcategorized• Myelogenous
• Lymphocytic
Cateogories
• Acute: immature WBC
• Chronic: mature, abnormal WBC
• Lymphocytic: affects bone marrow that makes WBC lymphocytes
• Myelogenous: bone marrow cells that make RBC, Platelets, WBC other than lymphocytes
White Blood Cell DisordersAcute Lymphoblastic Leukemia (ALL)
• Most common type in young children
• Affects adults, usually over 65
• Bone cancer where immature blood cells are made
• Treatments: good chance for cure in children
Chronic Lymphocytic Leukemia
• Most often affects adults over 55
• Sometimes younger adults, almost never children
• Bone marrow cancer, progresses slowly
• Treatments: help control disease
White Blood Cell Disorders
Acute Myelogenous Leukemia (AML)
• Most common in adults
• More common in men
• Affects myeloid cells: that make mature RCB, WBC, platelets
• Rapid forming
Chronic Myelogenous Leukemia (CML)
• Mainly in adults (rare for children)
• Progresses slowly
http://ww2.cancercenter.com/leukemia/types/
Platelet/Thrombocytes
• Thrombocytes: nuclear fragments borne from megakaryoblast
• Activated by clotting proteins in plasma make a plug to stop bleeding
Diseases
Thromobocytopenia
• Abnormally low platelet count
Clotting disorders
• Petechiae, brusing, deep vein thrombosis
• DVT- blood clot in deep vein. Usually in lower leg, thigh, or pelvis. – What happens if the clot
breaks off and gets to the lung?
Clotting Disorders
Other Blood Disorders• Hemochromatosis
– Absorbs too much Fe from food and vitamins
– Fe builds up=Fe overload
– Build up can build up over time and damage organs (liver, heart, pancreas)
– Causes: heart arrhythmias, cirrhosis
• Bleeding & Clotting Disorders– Important problem for
women because disorders to reproductive issues
– Heavy menstrual bleeding (menorrhagia)
– Bleeding & clotting complications of pregnancy
– Recurrent fetal loss
Hemophilia• Inherited bleeding disorder
• Blood does not clot
• Clotting factors are low or none
• Problems???
Hemolytic disease of the newborn
• In fetus is Rh+ and mother was Rh-
• Must have previous Rh+ pregnancy– Antibodies cross the placenta and destroy the
RBC– Results in decreased RBC for fetus = death or
jaundice
• Mother has to receive Rhogam injection after every Rh+ pregnancy
Jaundice
Mononucleosis
• Mono
• Kissing Disease
• Noncancerous leukocyte disorder from virus called Epstein-Barr virus
• Lymphocytes
• Signs and Symptoms?
• Resolves itself in 4-6 weeks.
Mononucleosis
Mono: aboveLeukemia: belowDifference is the Auer rods in lymphocyte