1. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Human Anatomy & Physiology SEVENTH EDITION Elaine N. Marieb Katja Hoehn PowerPoint ® Lecture Slides prepared by Vince Austin, Bluegrass Technical and Community College C H A P T E R 17 Blood

2. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Hemostasis Disorders: Thromboembolytic Conditions  Thrombus – a clot that develops and persists in an unbroken blood vessel  Thrombi can block circulation, resulting in tissue death  Coronary thrombosis – thrombus in blood vessel of the heart

3. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Hemostasis Disorders: Thromboembolytic Conditions  Embolus – a thrombus freely floating in the blood stream  Pulmonary emboli can impair the ability of the body to obtain oxygen  Cerebral emboli can cause strokes

4. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  Substances used to prevent undesirable clots:  Aspirin – an antiprostaglandin that inhibits thromboxane A 2  Heparin – an anticoagulant used clinically for pre- and postoperative cardiac care  Warfarin – used for those prone to atrial fibrillation Prevention of Undesirable Clots

5. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  Disseminated Intravascular Coagulation (DIC): widespread clotting in intact blood vessels  Residual blood cannot clot  Blockage of blood flow and severe bleeding follows  Most common as:  A complication of pregnancy  A result of septicemia or incompatible blood transfusions Hemostasis Disorders

6. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  Thrombocytopenia – condition where the number of circulating platelets is deficient  Patients show petechiae due to spontaneous, widespread hemorrhage  Caused by suppression or destruction of bone marrow (e.g., malignancy, radiation)  Platelet counts less than 50,000/mm 3 is diagnostic for this condition  Treated with whole blood transfusions Hemostasis Disorders: Bleeding Disorders

7. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  Inability to synthesize procoagulants by the liver results in severe bleeding disorders  Causes can range from vitamin K deficiency to hepatitis and cirrhosis  Inability to absorb fat can lead to vitamin K deficiencies as it is a fat-soluble substance and is absorbed along with fat  Liver disease can also prevent the liver from producing bile, which is required for fat and vitamin K absorption Hemostasis Disorders: Bleeding Disorders

8. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  Hemophilias – hereditary bleeding disorders caused by lack of clotting factors  Hemophilia A – most common type (83% of all cases) due to a deficiency of factor VIII  Hemophilia B – due to a deficiency of factor IX  Hemophilia C – mild type, due to a deficiency of factor XI Hemostasis Disorders: Bleeding Disorders

9. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Hemostasis Disorders: Bleeding Disorders  Symptoms include prolonged bleeding and painful and disabled joints  Treatment is with blood transfusions and the injection of missing factors

10. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Blood Transfusions  Whole blood transfusions are used:  When blood loss is substantial  In treating thrombocytopenia  Packed red cells (cells with plasma removed) are used to treat anemia

11. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  RBC membranes have glycoprotein antigens on their external surfaces  These antigens are:  Unique to the individual  Recognized as foreign if transfused into another individual  Promoters of agglutination and are referred to as agglutinogens  Presence or absence of these antigens is used to classify blood groups Human Blood Groups

12. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  Humans have 30 varieties of naturally occurring RBC antigens  The antigens of the ABO and Rh blood groups cause vigorous transfusion reactions when they are improperly transfused  Other blood groups (M, N, Dufy, Kell, and Lewis) are mainly used for legalities Blood Groups

13. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  The ABO blood groups consists of:  Two antigens (A and B) on the surface of the RBCs  Two antibodies in the plasma (anti-A and anti-B)  ABO blood groups may have various types of antigens and preformed antibodies  Agglutinogens and their corresponding antibodies cannot be mixed without serious hemolytic reactions ABO Blood Groups

14. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings ABO Blood Groups Table 17.4

15. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  There are eight different Rh agglutinogens, three of which (C, D, and E) are common  Presence of the Rh agglutinogens on RBCs is indicated as Rh +  Anti-Rh antibodies are not spontaneously formed in Rh – individuals  However, if an Rh – individual receives Rh + blood, anti-Rh antibodies form  A second exposure to Rh + blood will result in a typical transfusion reaction Rh Blood Groups

16. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Hemolytic Disease of the Newborn  Hemolytic disease of the newborn – Rh + antibodies of a sensitized Rh – mother cross the placenta and attack and destroy the RBCs of an Rh + baby  Rh – mother becomes sensitized when exposure to Rh + blood causes her body to synthesize Rh + antibodies

17. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Hemolytic Disease of the Newborn  The drug RhoGAM can prevent the Rh – mother from becoming sensitized  Treatment of hemolytic disease of the newborn involves pre-birth transfusions and exchange transfusions after birth

18. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings  Transfusion reactions occur when mismatched blood is infused  Donor’s cells are attacked by the recipient’s plasma agglutinins causing:  Diminished oxygen-carrying capacity  Clumped cells that impede blood flow  Ruptured RBCs that release free hemoglobin into the bloodstream Transfusion Reactions

19. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Transfusion Reactions  Circulating hemoglobin precipitates in the kidneys and causes renal failure

20. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Blood Typing  When serum containing anti-A or anti-B agglutinins is added to blood, agglutination will occur between the agglutinin and the corresponding agglutinogens  Positive reactions indicate agglutination

21. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Blood type being testedRBC agglutinogensSerum Reaction Anti-AAnti-B ABA and B++ BB–+ AA+– ONone–– Blood Typing

22. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Plasma Volume Expanders  When shock is imminent from low blood volume, volume must be replaced  Plasma or plasma expanders can be administered

23. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Plasma Volume Expanders  Plasma expanders  Have osmotic properties that directly increase fluid volume  Are used when plasma is not available  Examples: purified human serum albumin, plasminate, and dextran  Isotonic saline can also be used to replace lost blood volume

24. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Diagnostic Blood Tests  Laboratory examination of blood can assess an individual’s state of health  Microscopic examination:  Variations in size and shape of RBCs – predictions of anemias  Type and number of WBCs – diagnostic of various diseases  Chemical analysis can provide a comprehensive picture of one’s general health status in relation to normal values

25. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Developmental Aspects  Before birth, blood cell formation takes place in the fetal yolk sac, liver, and spleen  By the seventh month, red bone marrow is the primary hematopoietic area  Blood cells develop from mesenchymal cells called blood islands  The fetus forms HbF, which has a higher affinity for oxygen than adult hemoglobin

26. Copyright © 2006 Pearson Education, Inc., publishing as Benjamin Cummings Developmental Aspects  Age-related blood problems result from disorders of the heart, blood vessels, and the immune system  Increased leukemias are thought to be due to the waning deficiency of the immune system  Abnormal thrombus and embolus formation reflects the progress of atherosclerosis