hematology i. cvs= heart + blood + vessels (integrated with immune system) both = circulatory system

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Hematology I. CVS= heart + blood + vessels (integrated with immune system) both = circulatory system

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Hematology

I. CVS= heart + blood + vessels

(integrated with immune system)

both = circulatory system

II. Functions of blood;

1. transport gases, nutrients, hormones, metab. wastes

2. reg. pH + ion conc. of interstitial fluid (electrolytes)

3. restricts fluid loss at injury

4. defends against toxins and pathogens

5. stabilizes body temp.

III. Characteristics of blood

• temp= 100 degrees F• pH= 7.35-7.45 (narrow range)• viscosity= 5 times more than

water• amount= 7% of body weight in

kg

IV. Composition; fluid CT

• fluid is called plasma• cells (formed elements) are;

– RBC- erythrocytes– WBC- leukocytes– Platelets – cell fragments

• Hematocrit- shows % of solid elements• Centrifuged tube shows parts• (refer to plate)

V. Plasma characteristics;• straw colored• 46-63% of whole blood• 92% water• contains electrolytes and metabolites• contains 3 types of proteins

1. albumins- 60% of proteins; combines w/ and transports fatty acids and hormones, contributes to osmotic pressure

2. globulins- 35%; ex. Immunoglobulins(antibodies), transport globulins

3. fibrinogen- 4%; involved in clotting, blood w/o it is called serum

VI. Erythrocytes;• - made in red bone marrow• -1/3 of all cells in body• very specialized• shape is biconcave disc (p. 629)• 1. increases SA:V• 2. stackable to form rouleaux• 3. flexible due to spectrin• enucleated, no mitosis• no mitochondria or ribosomes• don’t use O2 (use anaerobic resp.)• packed with hemoglobin (Hb)• Life span 120 days

VII. Hemoglobin (p. 630)• 4 aa chains –2 alpha + 2 beta • each chain wraps around a

heme pigment• heme will chem. comb. w/

oxygen• Hb + O2 HbO2• Oxyhemoglobin makes bl.

bright red• O2 can disassociate making

deoxyhemoglobin and bl. becomes burgundy

VIII. Recyclying RBCs –p. 6321. RBCs become become engulfed by phagocytes of

liver, spleen and bone marrow.- alpha and beta chains broken down into amino

acids and metabolized or released into bl. -heme stripped of its iron and becomes biliverdin

(green)2 . biliverdin becomes bilirubin (yellow) 3. Bilirubin transported to liver to be excreted in bile.

-.Jaundice develops when bile can’t be secreted.

2. Fe carried via transferrin to marrow to be recycled 3. . Excess Fe stored in ferritin in liver

IX. Hematopoiesis- production of cells

-• refer to p. 643

• erythropoiesis- RBC formation

X. WBC’s

• – most work outside the bl. stream inside tissues or in lymph organs

• -2 groups- see plateA. Granular- (-phil)

neutrophil- 50-70%eosinophil- 2-4% (stain red)basophil- <1% (stain blue)

B. Agranular- (-cyte)lymphocyte- 20-30%monocyte- 2-8%

XI. WBC characteristics;

• Ameboid movement

• Diapedesis

• Chemotaxis

• Phagocytosis

Functions of WBC’ (refer to chart p. 642)

Monocytes

• largest WBC

• spherical

• tissue macrophage

• largest component of pus

Neutrophils• lobed nucleus,polymorphs

• pale colored granules

• very mobile, fast

• first to injury site

• 10 hour life span

• “eat” bacteria – form pus

• die and release chemicals to attract more cells

Basophils

• granules filled with heparin and histamine

• respond in inflammation

XII. Platelets- thrombocytes

• (not complete cells) p. 643

• -produced by megakaryocyte in bone marrow

• -responsible for hemostasis (clotting

XIII. Hemostasis- p. 6471. Vascular phase – immediate contraction of bl.v2. Platelet phase 0-30 secs

a. damaged cells release chemicalsb. damaged cells become sticky and contractc. platelets arrive at wound site and stick to damaged areas forming a “plug”

3. Coagulation phase 30 secs-8 min a. coagulation begins involving blood proteins called clotting factors (30 sec after(work in a chain reaction and need Ca+and K+ to work) refer to p. 648b. prothrombin forms thrombin enables fibrinogen to form fibrinc. prostaglandins released form tissues attract more platelets and clot forms(aspirin inhibits prostaglandin production)d. clot dries on surface and forms scab which pulls wounded tissue together

hemolytic anemia in the newborn

• Occurs when a fetus is Rh+ and mother is Rh− • the mother will produce antibodies against the fetal

antigen when blood is exchanged during birth.• complicates future pregnancies, because her antibodies

will enter the fetal circulation system and react with fetal blood, causing hemolysis.

• Treatment= Anti-Rh+ antibody is injected into the mother after her first delivery.

-destroys the fetal Rh+ cells in the mother's circulation preventing Rh +antibody production in the mother

-next child will not be at risk for hemolytic anemia.