Book contents
- Frontmatter
- Contents
- List of contributors
- Preface
- Glossary
- 1 The structure and production of blood platelets
- 2 Platelet immunology: structure, functions, and polymorphisms of membrane glycoproteins
- 3 Mechanisms of platelet activation
- 4 Platelet priming
- 5 Platelets and coagulation
- 6 Vessel wall-derived substances affecting platelets
- 7 Platelet–leukocyte–endothelium cross talk
- 8 Laboratory investigation of platelets
- 9 Clinical approach to the bleeding patient
- 10 Thrombocytopenia
- 11 Reactive and clonal thrombocytosis
- 12 Congenital disorders of platelet function
- 13 Acquired disorders of platelet function
- 14 Platelet transfusion therapy
- 15 Clinical approach to the patient with thrombosis
- 16 Pathophysiology of arterial thrombosis
- 17 Platelets and atherosclerosis
- 18 Platelets in other thrombotic conditions
- 19 Platelets in respiratory disorders and inflammatory conditions
- 20 Platelet pharmacology
- 21 Antiplatelet therapy versus other antithrombotic strategies
- 22 Laboratory monitoring of antiplatelet therapy
- 23 Antiplatelet therapies in cardiology
- 24 Antithrombotic therapy in cerebrovascular disease
- 25 Antiplatelet treatment in peripheral arterial disease
- 26 Antiplatelet treatment of venous thromboembolism
- Index
14 - Platelet transfusion therapy
Published online by Cambridge University Press: 15 October 2009
- Frontmatter
- Contents
- List of contributors
- Preface
- Glossary
- 1 The structure and production of blood platelets
- 2 Platelet immunology: structure, functions, and polymorphisms of membrane glycoproteins
- 3 Mechanisms of platelet activation
- 4 Platelet priming
- 5 Platelets and coagulation
- 6 Vessel wall-derived substances affecting platelets
- 7 Platelet–leukocyte–endothelium cross talk
- 8 Laboratory investigation of platelets
- 9 Clinical approach to the bleeding patient
- 10 Thrombocytopenia
- 11 Reactive and clonal thrombocytosis
- 12 Congenital disorders of platelet function
- 13 Acquired disorders of platelet function
- 14 Platelet transfusion therapy
- 15 Clinical approach to the patient with thrombosis
- 16 Pathophysiology of arterial thrombosis
- 17 Platelets and atherosclerosis
- 18 Platelets in other thrombotic conditions
- 19 Platelets in respiratory disorders and inflammatory conditions
- 20 Platelet pharmacology
- 21 Antiplatelet therapy versus other antithrombotic strategies
- 22 Laboratory monitoring of antiplatelet therapy
- 23 Antiplatelet therapies in cardiology
- 24 Antithrombotic therapy in cerebrovascular disease
- 25 Antiplatelet treatment in peripheral arterial disease
- 26 Antiplatelet treatment of venous thromboembolism
- Index
Summary
INTRODUCTION
Platelet transfusions were first introduced in the 1960s as a separate component for transfusion. Since then, the use of platelet transfusions has continued to increase, with current concerns focused on the appropriate use of this therapy for thrombocytopenic patients or those with platelet dysfunction.
PLATELET PRODUCTS AVAILABLE FOR TRANSFUSION
Whole blood-derived platelet concentrates or apheresis platelets
Platelets are obtained from either donated whole blood or by apheresis procedures. Two methods of preparing platelets from whole blood are illustrated in Figure 14.1. Almost all of Europe uses the buffy-coat method of platelet preparation from whole blood, and Canada is converting to this method of platelet preparation. Only the United States continues to use the platelet-rich plasma (PRP) method of platelet preparation. Comparative studies have shown no differences in the quality of these platelet concentrates, with storage times up to 5 days. However, there are several advantages to the buffy-coat platelet preparation system: (1) preparation can be fully automated; (2) platelets can be prepared from whole blood up to 24 h from collection rather than requiring platelet preparation within 6 h, as mandated for PRP platelet concentrates; (3) platelets are routinely pre-storage pooled, allowing rapid platelet release from the production facility; (4) the residual WBC count is less than that of PRP platelets; (5) pooled platelets are usually stored in additive solution rather than plasma, making more plasma available for other purposes as well as reducing the risk of transfusion-related acute lung injury (TRALI); and (6) with storage of platelets beyond the current 5 days, platelet viability may be better maintained in the buffy-coat form rather than in PRP concentrates.
- Type
- Chapter
- Information
- Platelets in Hematologic and Cardiovascular DisordersA Clinical Handbook, pp. 242 - 260Publisher: Cambridge University PressPrint publication year: 2007