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    Transfusion Medicine and Hemostasis: Clinical and Laboratory Aspects

    Transfusion Medicine and Hemostasis by Shaz, Beth H.; Hillyer, Christopher D.; Schwartz, Joseph (Yossi);

    Clinical and Laboratory Aspects

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    Beszerezhetőség

    Megrendelésre a kiadó utánnyomja a könyvet. Rendelhető, de a szokásosnál kicsit lassabban érkezik meg.

    Why don't you give exact delivery time?

    A beszerzés időigényét az eddigi tapasztalatokra alapozva adjuk meg. Azért becsült, mert a terméket külföldről hozzuk be, így a kiadó kiszolgálásának pillanatnyi gyorsaságától is függ. A megadottnál gyorsabb és lassabb szállítás is elképzelhető, de mindent megteszünk, hogy Ön a lehető leghamarabb jusson hozzá a termékhez.

    A termék adatai:

    • Kiadás sorszáma 4
    • Kiadó Elsevier Science
    • Megjelenés dátuma 2024. november 20.

    • ISBN 9780323960144
    • Kötéstípus Puhakötés
    • Terjedelem922 oldal
    • Méret 276x215 mm
    • Súly 2490 g
    • Nyelv angol
    • 664

    Kategóriák

    Hosszú leírás:

    Transfusion Medicine and Hemostasis: Clinical and Laboratory Aspects, Fourth Edition continues to be the only "pocket-size" quick reference for pathology and transfusion medicine for residents and fellows. It is helpful to all physicians and allied health professionals who order and administer blood components, cellular therapies, specialized factors for hemostatic abnormalities, coagulation testing, and those who consult and care for these often very ill patients. This book is ideal for pathology, medicine, surgery, and anesthesia residents, transfusion, hematology, and anesthesia fellows, and certified and specialized practitioners, as well as medical technologist in transfusion, cellular therapy, hematology, and coagulation. This new edition covers the many new developments that have occurred since the previous edition to include new blood products, new indications, or clinical conditions in which blood products are used. Similarly, new hemostasis testing is introduced as well as new clinical scenarios due the COVID-19 pandemic that area relevant to hemostasis and transfusion medicine. This includes COVID coagulopathy, Vaccine Induced Thrombotic Immune Thrombocytopenia, Pediatric reference range in coagulation testing, Platelet rich plasma and MNC products - CAR-T cells.

    Több

    Tartalomjegyzék:

    1. Blood banking and transfusion medicine - the field, the discipline and the industry
    2. Quality principles in Transfusion medicine
    3. Regulatory issues in transfusion medicine
    4. Role of the physician in the blood center
    5. Blood donor, donation process and technical aspects of blood collection
    6. Apheresis blood component collections
    7. Recipient-specific blood donations
    8. Adverse donor reactions (iron)
    9. Component preparation and manufacturing
    10. Serologic testing of donor products
    11. Overview of infectious disease testing
    12. HIV screening
    13. Hepatitis B screening
    14. Hepatitis C screening
    15. WNV screening
    16. Zika screening
    17. Babesia screening
    18. Syphilis, HTLV and Chagas screening
    19. Bacterial mitigation of platelets
    20. Role of the transfusion service physician
    21. Pretransfusion testing
    22. Antibody identification
    23. Direct antiglobulin test
    24. Molecular DNA based blood group typing
    25. ABO and H blood group systems
    26. RH and RhAg blood group system
    27. KELL and KIDD blood group systems
    28. MNS AND DUFFY blood group systems
    29. LEWIS, I P1Pk and Glob blood group systems
    30. Other blood group systems, collections, and antigens
    31. Human platelet and neutrophil antigens
    32. HLA Antigens
    33. Red blood cells products
    34. Plasma products
    35. Platelet products (to include PAS if not previously mentioned; was mentioned In the 2nd edition)
    36. Cryoprecipitate and fibrinogen concentrates
    37. Granulocyte products
    38. Albumin and related products
    39. Human immunoglobuin preparations
    40. Rh immune globulin
    41. Coagulation Factor products
    42. Platelet rich plasma
    43. Convalescent plasma, including COVID convalescent plasma
    42. Nonfactor therapies for bleeding disorders
    44. Blood Pharming and alternative blood production methods
    45. Irradiation of blood products
    44. Leukoreduction of blood products
    46. CMV-safe blood products
    47. Frozen blood products
    48. Washed blood products
    49. Volume reduced blood products
    50. Pathogen reduction technologies
    51. Intrauterine, Neonatal and pediatric transfusion medicine
    52. Perinatal transfusion medicine
    53. AutoImmune hemolytic anemias
    54. Transfusion management in patients with hemoglobinopathies
    55. Transfusion of Patients Undergoing Hematopoietic Stem Cell Transplantation
    56. Transfusion of Patients Undergoing Solid Organ Transplantation
    57. Transfusion support and hemostatic monitoring in patients connected to extracorporeal devices
    58. Transfusion of patients receiving antithrombotic therapy
    59. Blood transfusion in economically restricted and developing countries
    60. Management of Patients Who Refuse Blood Transfusion
    61. Platelet transfusion refractory patients
    62. Massive transfusion
    63. Patient blood management
    64. Overview of adverse events and outcomes following transfusion
    65. Febrile non-hemolytic transfusion reactions
    66. Allergic transfusion reactions
    67. Acute hemolytic transfusion reactions
    68. Delayed hemolytic transfusion reactions
    69. Transfusion-Associated Circulatory Overload
    70. Transfusion-Related Acute Lung Injury
    71. Septic transfusion reactions
    72. Metabolic, hypotensive and other acute reactions and complications
    73. Post transfusion purpura
    74. Transfusion associated graft versus host disease
    75. Transfusion related immunomodulation
    76. Iron Overload
    77. Transfusion transmitted diseases
    78. Overview to therapeutic apheresis
    79. Therapeutic plasma exchange
    80. Therapeutic erythrocytapheresis
    81. Therapeutic thrombocytapheresis
    82. Therapeutic leukocytapheresis and adsorptive cytapheresis
    83. Extracorporeal photopheresis
    84. LDL apheresis
    85. Immunoabsorption
    86. COVID-19 & Apheresis
    87. Therapeutic phlebotomy
    88. Overview of cellular therapy
    89. HPC products derived from bone marrow and peripheral blood
    90. Cord blood banking (expansion)
    91. Regenerative medicine (iPS)
    92. Immunotherpy (T cells): CAR-T, TILs, gene therapy and more
    93. Adverse events associated with HPC product infusion
    94. Quality and regulatory issues in cellular therapy
    95. Tissue banking in the hospital setting
    96. Overview of the coagulation system
    97. Approach to the patient with a bleeding disorder
    98. Congenital thrombocytopenia
    99. fetal and Neonatal alloimmune thrombocytopenia
    100. Acquired neonatal thrombocytopenia
    101. Bernard Soulier syndrome and other GPIb-IX-V related receptor defects
    102. Glanzmann's thrombocytopenia
    103. Other platelet glycoprotein disorders
    104. Platelet storage-granule defects
    105. Failure to release and aspirin-like defects
    106. Other Platelet abnormalities
    107. Acquired platelet disorders
    108. Acute (childhood) ITP
    109. Chronic ITP
    110. Drug induced thrombocytopenia
    111. Heparin induced thrombocytopenia
    112. Vaccine Induced Thrombotic Immune Thrombocytopenia
    113. Autoimmune lymphoproliferative syndrome
    114. Hemolytic uremic syndrome
    115. Thrombotic thrombocytopenic purpura
    116. Antiphospholipid syndrome
    117. Von Willebrand Disease
    118. Hemophilia A
    119. Hemophilia B
    120. Congenital disorders of fibrinogen
    121. Factor XIII, D ?2-Antiplasmin, and Plasminogen Activator Inhibitor-1 deficiencies
    122. Factor XI deficiency
    123. Factor VII deficiency
    124. Factor II, factor V, and factor X deficiencies
    125. Bleeding disorders in pregnancy
    126. Vascular bleeding disorders
    127. Hemostasis in Liver Disease
    128. Bleeding risks with Vitamin K deficiency
    129. Bleeding risks with cardiac disease
    130. Bleeding risks with renal disease
    131. Bleeding risks with cancer
    132. Disseminated intravascular coagulopathy
    133. coagulopathy in sickle cell disease and other hemoglobiniopathies
    134. COVID coagulopathy
    135. Thrombosis in COVID Coagulopathy---Anticoagulation guidelines
    136. Bleeding in COVID coagulopathy
    137. Acquired coagulation factor inhibitors
    138. Overview of purposes of hemostasis testing and common sources of error
    139. Pediatric reference ranges in coagulation testing?
    140. Prothrombin Time
    141. Activated Partial Thrombolplastin Time
    142. Mixing studies
    143. Coagulation Factor Testing
    144. Testing of Nonfactor therapies: emicizumab
    145: Testing of Nonfactor therapies: inhibitors of anticoagulant pathways (fitusiran and concizumab)
    146. Specific Factor Inhibitor Testing
    147. Thrombin time and Fibrinogen Evaluation
    148. laboratory diagnosis of inherited von Willebrand Disease
    149. Laboratory Diagnosis of Acquired von Willebrand's Syndrome
    150. Laboratory Assessment of Treatment of von Willebrand's Disease
    151. Measurement of platelet count, mean platelet volume, and reticulated platelets
    152. Platelet Function Analyzer
    153. thromboelastography/thromboelastometry
    154. Platelet Aggregation Studies
    155. Laboratory Diagnosis of Platelet Functional Defects
    156. Confirmatory testing for diagnosis of platelet disorders
    157. Platelets in COVID coagulopathy
    158. Anti-platelet Therapy Monitoring
    159. Laboratory evaluation of factor XIII deficiency
    160. Fibrinolytic testing
    161. Age-adjusted D-Dimer cut offs to rule out PE/ VTE 162. Laboratory techniques in fibrinolysis testing
    163. Laboratory evaluation of long-term thrombophilic disorders
    164. Thrombophilia testing in children
    165. Antithrombin Testing
    166. Protein C deficiency evaluation
    167. Protein S deficiency evaluation
    168. testing for Activated Protein C Resistance
    169. Molecular Testing for Factor V Leiden and Prothrombin Gene Mutations in inherited thrombophilia
    170. Chronic elevated levels of?Factor VIII?and other coagulation factors
    171. Laboratory Monitoring for Heparins, fondaparinux, direct thrombin inhibitors, and oral anti-Xa medications
    172: DOAC interferences in coagulation testing
    173. Laboratory testing in patients receiving DOAC antidotes
    174. Laboratory support for warfarin monitoring
    175. Molecular testing in Coagulation
    176. Acquired prothrombotic conditions
    177: Ventricular assist device: anticoagulation monitoring
    178. Laboratory Evaluation of Heparin-Induced Thrombocytopenia
    179. Laboratory Evaluation of Thrombotic Thromcytopenic Purpura
    180. D-Dimer testing in COVID coagulopathy
    181. Other coagulation tests in COVID coagulopathy
    182. Laboratory diagnosis of lupus anticoagulant and anti-phopholipid antibodies
    183. Lupus anticoagulant testing in COVID-19
    184. Circulating microparticles
    185. Thrombin Generation Assays
    186. Laboratory testing of contact factors
    187. Contact factors and complements
    188. Monitoring of new anticoagulants---inhibitors of contact factors
    189. Reference ranges in transgender

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