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Samenvatting

With authoritative coverage of rare and common hemostatic disorders, Consultative Hemostasis and Thrombosis, 4th Edition, keeps you both up to date with all that’s new in this fast-moving field as well as reviewing background and development and citing pertinent classical literature. Broad differential diagnoses are provided, underscoring the editors’ position that correct treatment begins with correct diagnosis. This trusted resource by Drs. Craig S. Kitchens, Craig M. Kessler, Barbara A. Konkle, Michael B. Streiff, and David A. Garcia is designed for rapid reference and critical decision making at the point of care. Emphasizes real-world problems and solutions, with quick access to concise descriptions of each condition, associated symptoms, laboratory findings, differential diagnosis, and treatment. Features a user-friendly design, full-color format, abundant laboratory protocols, and at-a-glance tables and charts throughout. Provides thorough updates on core information on hemostasis and thrombosis, including deep venous thrombosis (DVT), pulmonary embolisms, hypercoagulability, thrombocytopenia, von Willenbrand disease, and more.

Covers new treatment information on hemophilia A and B.

Contains new chapters on hereditary hemorrhagic telangiectasia, hemolytic uremic syndrome, and paroxymal nocturnal hemoglobinuria.

Two new editors, Dr. Michael B. Streiff and Dr. David A. Garcia, offer fresh perspectives and valuable experience. Expert Consult™ eBook version included with purchase. This enhanced eBook experience allows you to search all of the text, figures, and references from the book on a variety of devices.

Specificaties

ISBN13:9780323462020
Taal:Engels
Bindwijze:Gebonden

Inhoudsopgave

<p>Kitchens: CONSULTATIVE HEMOSTASIS & THROMBOSIS</p> <p>TOC</p> <p>PART 1: Hemorrhagic Processes</p> <p>1. Consultative Process</p> <p>2. An Approach to the Bleeding Patient: Correlation of Clinical Symptoms and Signs with Laboratory Testing</p> <p>3. Hemophilia A and B</p> <p>4. Less Common Congenital Disorders of Hemostasis</p> <p>5. Acquired Coagulation Disorders Due to Inhibitors</p> <p>6. von Willebrand Disease</p> <p>7. General Aspects of Thrombocytopenia, Platelet Transfusions, and Thrombopoietic Growth Factors</p> <p>8. Primary Immune Thrombocytopenia</p> <p>9. Congenital and Acquired Disorders of Platelet Function and Number</p> <p>10. Purpura and Other Hematovascular Disorders</p> <p>11. HHT</p> <p>12. Disseminated Intravascular Coagulation </p> <p>13. The Cross-Talk of Inflammation and Coagulation in Infectious Disease and Their Roles in Disseminated Intravascular Coagulation</p> <p>PART 2: Thrombotic Processes</p> <p>14. Thrombophilia: Clinical and Laboratory Assessment and Management</p> <p>15. Pediatric Aspects of Thrombophilia</p> <p>16. Deep Vein Thrombosis, Pulmonary Embolism and Primary Pulmonary Hypertension</p> <p>17. Venous Thromboses at Unusual Sites</p> <p>18. The Post Thrombotic Syndrome</p> <p>19. Thrombocytosis: Essential Thrombocytemia and Reactive Causes</p> <p>20. Antiphospholipid Syndrome</p> <p>21. Antiplatelet Treatment in Cardiovascular Medicine</p> <p>22. Non-Arteriosclerotic Arterial Occlusive Disease</p> <p>23. Thrombosis and Cancer</p> <p>24. Thrombotic Thrombocytopenic Purpura</p> <p>25. Hemostatic Disorders of Complement Activation (PNH and aHUS) - New Chapter</p> <p>26. Heparin-Induced Thrombocytopenia</p> <p>PART 3: Therapeutic Agents</p> <p>27. Antithrombotic Agents</p> <p>28. Blood Component and Pharmacological Agents</p> <p>29. Therapeutic Apheresis – Applications for Hemorrhagic & Thrombotic Disorders </p> <p>30. Vena Caval Filters</p> <p>PART 4: Issues Specific to Women </p> <p>31. Thrombotic Risk of Contraceptives and other Hormnal Therapies</p> <p>32. Bleeding and the Management of Hemorrhagic Disorders in Pregnancy</p> <p>33. Thrombophilia in Pregnancy</p> <p>PART 5: Special Issues</p> <p>34. Surgery and Hemostasis</p> <p>35. Anticoagulation in the Perioperative Period</p> <p>36. Understanding and Managing the Coagulopathy of Liver Disease</p> <p>37. Outpatient Anticoagulant Therapy38. Hematologic Interventions for Acute Central Nervous System Disease</p> <p>39. Pending: Atrial Septal Abnormalties and Cryptogenic Stroke</p> <p>40. Hemorrhage Control and Thrombosis Following Severe Injury</p> <p>41. Hemostatic Aspects of Sickle Cell Disease</p>
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        Consultative Hemostasis and Thrombosis