Liebe Besucherinnen und Besucher,
aufgrund unseres Sommerfestes sind wir am 03. September 2026 bis 14 Uhr erreichbar. Am 04. September 2026 sind wir wieder wie gewohnt für Sie da. Vielen Dank für Ihr Verständnis.
Ihr Team von Sack Fachmedien
Buch, Englisch, 200 Seiten, Format (B × H): 191 mm x 235 mm, Gewicht: 450 g
Buch, Englisch, 200 Seiten, Format (B × H): 191 mm x 235 mm, Gewicht: 450 g
ISBN: 978-0-443-13780-8
Verlag: Elsevier Science
Quick Guide to Hemostasis and Transfusion Medicine is a patient reference that recommends indication-based laboratory test selection and interpretation to diagnose and treat hemorrhagic and thrombotic disorders using blood components, biologics, and synthetic therapeutics. The book introduces hemostasis and transfusion medicine for students, residents, and fellows, supplementing standard texts. It uses headings, bulletpoints, telegraphic syntax, tables, figures, and speedy lookup features and is an essential quick reference for health care providers who order, perform, and interpret hemostasis and immunohematology assays and administer hemostasis therapy.
Autoren/Hrsg.
Weitere Infos & Material
1. Approach to bleeding patients
1.1. Patient history, bleeding assessment test protocol
1.2. Acquired versus congenital, isolated versus coagulopathy, systemic versus anatomic
2. Approach to thrombosis patient
2.1. Patient history
2.2. Acquired versus congenital thrombosis
2.3. Arterial versus venous thrombosis
3. Blood specimen management
4. Test utilization and indications
5. Antithrombotic therapy
5.1. Oral anticoagulants: warfarin and DOACs
5.2. Parenteral anticoagulants: heparin types
5.3. Direct thrombin inhibitors
5.4. Antiplatelet therapeutics
6. Platelets
6.1. Normal platelet function
6.2. Platelet disorders: thrombocytopenia and functional disorders
6.3. Immune and thrombotic thrombocytopenic purpura
6.4. Platelet function testing
6.5. Viscoelastometry
7. Coagulation
7.1. Normal coagulation cascade
7.2. Clot-based and chromogenic testing
8. Bleeding disorders: diagnosis and management
8.1. Acquired coagulopathies: liver disease, dietary deficiencies, kidney disease
8.2. Trauma-induced coagulopathy
8.3. Hemophilia: congenital single factor deficiencies
8.4. Von Willebrand disease
8.5. Disseminated intravascular coagulation
8.6. Laboratory protocols
8.7. Viscoelastometry
9. Thrombophilia
9.1. Congenital thrombosis risk factors
9.2. Antiphospholipid syndrome
9.3. Heparin-induced thrombocytopenia with thrombosis
9.4. Thromboinflammation
9.5. Laboratory protocols
10. Transfusion safety
11. Blood donation, processing, management
11.1. Donor qualification, whole blood, plateletpheresis, plasmapheresis
11.2. Directed donations
12. Blood components: Red blood cells, leukocyte-reduction, CMV-negative products, irradiated products, plasma, cryoprecipitate, platelet concentrate, whole blood, coagulation factor concentrates
13. Patient blood management: medical transfusion decisions, transfusion refusal
13.1. Urgent blood need, group O whole blood
13.2. Massive transfusion protocol
13.3. Transfusion of neonates and neonatal immune thrombocytopenia
13.4. Platelet concentrates
13.5. Transfusion in autoimmune hemolytic anemia, sickle cell disease, IgA deficiency, etc
13.6. Progenitor cell transplant
14. Managing adverse transfusion effects: signs and symptoms—immediate and delayed, laboratory investigation, care
15. Therapeutic apheresis: indications, types, technical and clinical considerations
16. Features
16.1. Glossary and abbreviations
16.2. Table of tables
16.3. Table of figures
16.4. Table of equations
16.5. Reference intervals and therapeutic targets
16.6. Index
16.7. References




