Whole blood: Difference between revisions
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==Medical use== |
==Medical use== |
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Whole blood has similar risks to a transfusion of red blood cells and must be [[cross-match]]ed to avoid hemolytic [[transfusion reaction]]s. Most of the indications for use are identical to those for RBCs, and whole blood is not used{{clarify}} because the extra plasma can contribute to [[transfusion associated circulatory overload]] (TACO), a potentially dangerous complication. |
Whole blood has similar risks to a transfusion of red blood cells and must be [[cross-match]]ed to avoid hemolytic [[transfusion reaction]]s. Most of the indications for use are identical to those for RBCs, and whole blood is not used{{clarify|date=October 2017}} because the extra plasma can contribute to [[transfusion associated circulatory overload]] (TACO), a potentially dangerous complication. |
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Whole blood is sometimes "recreated" from stored red blood cells and [[fresh frozen plasma]] (FFP) for neonatal transfusions. This is done to provide a final product with a very specific hematocrit (percentage of red cells) with [[ABO|type O]] red cells and [[ABO|type AB]] plasma to minimize the chance of complications. |
Whole blood is sometimes "recreated" from stored red blood cells and [[fresh frozen plasma]] (FFP) for neonatal transfusions. This is done to provide a final product with a very specific hematocrit (percentage of red cells) with [[ABO|type O]] red cells and [[ABO|type AB]] plasma to minimize the chance of complications. |
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Revision as of 18:07, 27 October 2017
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Whole blood (WB) is human blood from a standard blood donation.[1] It is used in the treatment of massive bleeding, in exchange transfusion, and when people donate blood to themselves.[2][1] One unit brings up hemoglobin levels by about 10 g/L.[3] Cross matching is typically done before the blood is given.[2][4] It is given by injection into a vein.[5]
Side effects include allergic reactions such as anaphylaxis, red blood cell breakdown, high blood potassium, infection, volume overload, and lung injury.[2][3] Whole blood is made up of red blood cells, white blood cells, platelets, and blood plasma.[3] It is best within a day of collection; however, can be used for up to three weeks.[4][3][6] The blood is typically combined with an anticoagulant and preservative during the collection process.[7]
The first transfusion of whole blood was in 1818; however, common use did not begin until the First and Second World War.[4][8] It is on the World Health Organization's List of Essential Medicines, the most effective and safe medicines needed in a health system.[9] In the 1980s the cost of whole blood was about 50 USD per unit in the United States.[10] Whole blood is no longer commonly used outside of the developing world and military.[2] It is used to make a number of blood products including packed red blood cells, platelet concentrate, cryoprecipitate, and fresh frozen plasma.[1]
Medical use
Whole blood has similar risks to a transfusion of red blood cells and must be cross-matched to avoid hemolytic transfusion reactions. Most of the indications for use are identical to those for RBCs, and whole blood is not used[clarification needed] because the extra plasma can contribute to transfusion associated circulatory overload (TACO), a potentially dangerous complication.
Whole blood is sometimes "recreated" from stored red blood cells and fresh frozen plasma (FFP) for neonatal transfusions. This is done to provide a final product with a very specific hematocrit (percentage of red cells) with type O red cells and type AB plasma to minimize the chance of complications.
Processing
Historically, blood was transfused as whole blood without further processing. Most blood banks now split the whole blood into two or more components,[11] typically red blood cells and a plasma component such as fresh frozen plasma. Platelets for transfusion can also be prepared from a unit of whole blood. Some blood banks have replaced this with platelets collected by plateletpheresis because whole blood platelets, sometimes called "random" platelets, must be pooled from multiple donors to get enough for a therapeutic dose.
The collected blood is generally separated into components by one of three methods. A centrifuge can be used in a "hard spin" which separates whole blood into plasma and red cells or for a "soft spin" which separates it into plasma, buffy coat (used to make platelets), and red blood cells. The third method is sedimentation: the blood simply sits overnight and the red cells and plasma are separated by gravitational interactions.
Storage
Whole blood is typically stored under the same conditions as red blood cells and can be kept up to 35 days if collected with CPDA-1 storage solution or 21 days with other common storage solutions such as CPD.
If the blood will be used to make platelets, it is kept at room temperature until the process is complete. This must be done quickly to minimize the warm storage of RBCs in the unit.
Name
In the US, the capitalized "Whole Blood" means a specific standardized product for transfusion or further processing, where "whole blood" is any unmodified collected blood.
References
- ^ a b c Hillyer, Christopher D. (2007). Blood Banking and Transfusion Medicine: Basic Principles & Practice. Elsevier Health Sciences. p. 190. ISBN 0443069816. Archived from the original on 2017-01-12.
{{cite book}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ a b c d Connell, NT (December 2016). "Transfusion Medicine". Primary care. 43 (4): 651–659. PMID 27866583.
- ^ a b c d Plumer, Ada Lawrence (2007). Plumer's Principles and Practice of Intravenous Therapy. Lippincott Williams & Wilkins. p. 422. ISBN 9780781759441. Archived from the original on 2017-01-12.
{{cite book}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ a b c Bahr, MP; Yazer, MH; Triulzi, DJ; Collins, RA (December 2016). "Whole blood for the acutely haemorrhaging civilian trauma patient: a novel idea or rediscovery?". Transfusion medicine (Oxford, England). 26 (6): 406–414. PMID 27357229.
- ^ Linton, Adrianne Dill (2015). Introduction to Medical-Surgical Nursing. Elsevier Health Sciences. p. 287. ISBN 9781455776412. Archived from the original on 2017-09-14.
{{cite book}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ Marini, John J.; Wheeler, Arthur P. (2012). Critical Care Medicine: The Essentials (4 ed.). Lippincott Williams & Wilkins. p. 267. ISBN 9781451152845. Archived from the original on 2017-01-11.
{{cite book}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ Rudmann, Sally V. (2005). Textbook of Blood Banking and Transfusion Medicine. Elsevier Health Sciences. p. 205. ISBN 072160384X. Archived from the original on 2017-01-12.
{{cite book}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ Hemmings, Hugh C.; Egan, Talmage D. (2012). Pharmacology and Physiology for Anesthesia: Foundations and Clinical Application. Elsevier Health Sciences. p. 628. ISBN 1455737933. Archived from the original on 2017-01-11.
{{cite book}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ "WHO Model List of Essential Medicines (19th List)" (PDF). World Health Organization. April 2015. Archived from the original (PDF) on 13 December 2016. Retrieved 8 December 2016.
{{cite web}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ Blood policy & technology. DIANE Publishing. 1985. p. 8. ISBN 9781428923331. Archived from the original on 2017-01-12.
{{cite book}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ Christopher D. Hillyer; Beth H. Shaz; James C. Zimring; Thomas C. Abshire (17 June 2009). Transfusion Medicine and Hemostasis: Clinical and Laboratory Aspects. Elsevier. pp. 45–. ISBN 978-0-12-374432-6. Archived from the original on 23 September 2017. Retrieved 16 November 2010.
{{cite book}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help)