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Books on the topic 'Blood components'

Author: Grafiati

Published: 4 June 2021

Last updated: 30 May 2022

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1

H, Smit Sibinga Th. Blood transfusion and blood components. Alexandria, Egypt: World Health Organization, Regional Office for the Eastern Mediterranean, 1995.

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2

Hawker, Robert John. Studies on blood components. Birmingham: University of Birmingham, 2000.

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3

Norris, Jane. Regulation and licensure of whole blood, blood components, and source plasma. Bethesda, MD: AABB, 2009.

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4

Melanaphy, Raymond F. Automatic blood collection mixers: An evaluation of the resultant blood components. [S.l: The Author], 1994.

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5

Norris, Jane. Regulation and licensure of whole blood, blood components, and source plasma. Bethesda, MD: AABB, 2009.

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6

Constantinidou, Chrystala. Blood components that interact with serum-sensitive gonococci. Birmingham: University of Birmingham, 1993.

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7

WHO/ACP, U. B. T. S. Workshop (1991 Kampala Uganda). WHO/ACP U.B.T.S. Workshop: Blood components in Uganda and recommendations. [Kampala?: s.n., 1991.

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8

Richard, Roger, Connie M. Westhoff, Monique Mohammed, and Lynne Uhl. Guidelines for pneumatic tube delivery systems: Validation and use to transport blood components. Bethesda, Md: AABB, 2004.

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9

Beck, Sarah. Prestorage filtration of blood components for patients who are chronically transfusion dependent. Bristol: R&D Directorate, NHS Executive South and West, 1996.

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10

Bergamo Spring Conferences on Haematology (1st 1987). Cellular blood components in haemostasis and thrombosis: Implications from myeloproliferative disorders : proceedings of the Conference held in Bergamo on May 7-8, 1987. London: Libbey, 1988.

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11

Europe, Council of. Guide to the preparation, use and quality assurance of blood components: Recommendation no. R (95) 15. Luxembourg: Council of Europe, 2004.

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12

Blajchman, Morris A., Miguel Lozano, and Joan Cid. Blood component preparation: From benchtop to bedside. Bethesda, Md: AABB Press, 2011.

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13

Noiri, E., and Norio Hanafusa. The concise manual of apheresis therapy. Tokyo: Springer, 2014.

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14

Mead Johnson Symposium on Perinatal and Developmental Medicine (28th 1986 Vail, Colo.). Blood component therapy of neonatal disease. [Ithaca, N.Y., U.S.A: Perinatology Press], 1986.

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15

Williams, Lance A. Quick guide to transfusion medicine. Washington, DC: American Association for Clinical Chemistry, 2014.

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16

McLeod, Bruce C. Apheresis: Principles and practice. Edited by AABB. 3rd ed. Bethesda, Md: AABB Press, 2010.

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17

Directorate, Canada Drugs. Blood collection and blood component manufacturing =: Collecte de sang et préparation des composés sanguins. Ottawa, Ont: Health and Welfare Canada = Santé et bien-être social Canada, 1992.

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18

G, Rock, ed. Apheresis: Proceedings of the 2nd International Congress of the World Apheresis Association, held in Ottawa, Ontario, Canada, May 18-20, 1988. New York, NY: Wiley-Liss, 1990.

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19

McKeown, Giselle Caroline. Evaluation of the optisystem R as a semi-automated method of blood component preparation. [S.l: TheAuthor], 1994.

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20

L, Baldwin Michael, Jefferies Leigh C, and American Association of Blood Banks., eds. Irradiation of blood components. Bethesda, Md: American Association of Blood Banks, 1992.

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21

F, Högman Claes, International Society of Blood Transfusion. Congress, and International Workshop on the Role of Leucocyte Depletion in Blood Transfusion Practice (2nd : 1994 : Amsterdam, Netherlands)., eds. Leucocyte depletion of blood components. Amsterdam: VU University Press, 1994.

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22

Mukherjee, Bibekananda. Technical Manual of Blood Components Preparation. Jaypee Brothers Medical Publishers (P) Ltd., 2016. http://dx.doi.org/10.5005/jp/books/12650.

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23

E, Brecher Mark, and American Association of Blood Banks., eds. Bacterial and parasitic contamination of blood components. Bethesda, Md: AABB Press, 2003.

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24

J, McCarthy Leo, Baldwin Michael L, and American Association of Blood Banks., eds. Controversies of leukocyte-poor blood and components. Arlington, Va: American Association of Blood Banks, 1989.

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25

Blood Components Therapy: A Physician's Handbook (Op1760). 3rd ed. Amer Assn of Blood Banks, 1989.

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26

M, Shin Linda, and Bellenir Karen, eds. Blood and circulatory disorders sourcebook: Basic information about blood and its components ... Detroit, MI: Omnigraphics, Inc., 1999.

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27

Albert, Tyler J., and Erik R. Swenson. The blood cells and blood count. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0265.

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Blood is a dynamic fluid consisting of cellular and plasma components undergoing constant regeneration and recycling. Like most physiological systems, the concentrations of these components are tightly regulated within narrow limits under normal conditions. In the critically-ill population, however, haematological abnormalities frequently occur and are largely due to non-haematological single- or multiple-organ pathology. Haematopoiesis originates from the pluripotent stem cell, which undergoes replication, proliferation, and differentiation, giving rise to cells of the erythroid, myeloid, and lymphoid series, as well as megakaryocytes, the precursors to platelets. The haemostatic system is responsible for maintaining blood fluidity and, at the same time, prevents blood loss by initiating rapid, localized, and appropriate blood clotting at sites of vascular damage. This system is complex, comprising both cellular and plasma elements, i.e. platelets, coagulation and fibrinolytic cascades, the natural intrinsic and extrinsic pathways of anticoagulation, and the vascular endothelium. A rapid, reliable, and inexpensive method of examining haematological disorders is the peripheral blood smear, which allows practitioners to assess the functional status of the bone marrow during cytopenic states. Red blood cells, which are primarily concerned with oxygen and carbon dioxide transport, have a normal lifespan of only 120 days and require constant erythropoiesis. White blood cells represent a summation of several circulating cell types, each deriving from the hematopoietic stem cell, together forming the critical components of both the innate and adaptive immune systems. Platelets are integral to haemostasis, and also aid our inflammatory and immune responses, help maintain vascular integrity, and contribute to wound healing.

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28

Devlin, Hugh, and Rebecca Craven. Blood. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198759782.003.0010.

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The blood in relation to dentistry is the topic of this chapter. Components of blood are described, including the blood cell types, their development and functions. Anaemias are discussed and their dental implications. Haemostasis and the coagulation pathway are described, followed by the bleeding disorders, how they are detected in blood tests and managed so as to avoid complications arising from dental treatment. The main malignancies of white blood cells are described in relation to dental care. The final section deals with blood and tissue types and their relevance to blood transfusion and tissue transplantation.

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29

Leucocyte Depletion of Blood Components: Present Trends and the Future. Vu University Press, 1994.

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30

(Editor), Linda M. Shin, and Karen Bellenir (Editor), eds. Blood and Circulatory Disorders Sourcebook: Basic Information About Blood and Its Components (Health Reference Series). Omnigraphics, 1998.

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31

Europe, Council of, ed. Guide to the preparation, use and quality assurance of blood components: Recommendation No. R (95) 15. 3rd ed. Strasbourg: Council of Europe Pub., 1997.

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32

Guide to the Preparation, Use and Quality Assurance of Blood Components: Recommendation No. R (95) 15. 3rd ed. Manhattan Pub. Co., 1996.

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33

Guide to the Preparation, Use and Quality Assurance of Blood Components. Council of Europe, 2005.

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34

Europe, Council of, ed. Guide to the preparation, use and quality assurance of blood components. 6th ed. Strasbourg: Council of Europe, 2000.

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35

Europe, Council of, ed. Guide to the preparation, use and quality assurance of blood components. 3rd ed. Strasbourg: Council of Europe, 1995.

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36

Europe, Council of. Guide to the preparation, use and quality assurance of blood components. 7th ed. MANHATTAN PUBLISHING COMPANY, 2001.

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37

The effects of marathon running on blood components and pulmonary function. 1988.

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38

Europe, Council of, ed. Guide to the preparation, use and quality assurance of blood components. 5th ed. Strasbourg: Council of Europe Publishing, 1999.

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39

The effects of marathon running on blood components and pulmonary function. 1985.

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40

Guide To The Preparation, Use And Quality Assurance Of Blood Components. Stationery Office, 2004.

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41

The effects of marathon running on blood components and pulmonary function. 1988.

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42

Europe, Council of. Guide to the Preparation, Use and Quality Assurance of Blood Components. 8th ed. Council of Europe, 2003.

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43

Europe, Council of, ed. Guide to the preparation, use and quality assurance of blood components. 3rd ed. Strasbourg: Council of Europe, 1995.

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44

The effects of marathon running on blood components and pulmonary function. 1988.

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45

El Kenz, Hanane, and Philippe Van der Linden. The physiology of blood in anaesthetic practice. Edited by Jonathan G. Hardman. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0011.

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Following the discovery of the ABO blood groups by Landsteiner in 1901, Albert Hustin described the first transfusion of a whole blood unit in 1914. The modern transfusion era really begins in 1916 with the discovery of sodium citrate as an anticoagulant by the same physician, allowing blood conservation in dedicated packs. Since that time, many advances have been made especially over the past two decades in the storage, the conservation, and the laboratory testing of blood components and in transfusion medicine practice. Transfusion of whole blood has been replaced by blood component therapy, which consists of the administration of packed red blood cells, fresh frozen plasma, or platelets. Although blood transfusion is safer than ever, the risk of complications will never reach zero. The risk of infectious transfusion-transmitted diseases has been markedly reduced by the implementation of extensive infectious disease testing, donor selection, and pathogen-inactivation procedures. In countries with a high human development index, the leading causes of allogeneic blood transfusion-related deaths actually resulted from immunological and septic complications. The first section of this chapter describes the structure, function, and immunological aspects of the different blood components that are routinely transfused today. The second section details the composition of the different blood components, their indications, the pre-transfusion compatibility tests, and the main adverse effects associated with their transfusion.

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46

Blood Components and Pharmacologic Agents in the Treatment of Congenital and Acquired Bleeding Disorders. American Association of Blood Banks, 2000.

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47

Thomas, Dafydd, and Katy Beard. Blood conservation and transfusion in anaesthesia. Edited by Michel M. R. F. Struys. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0051.

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Over the last three decades, avoidance of allogeneic transfusion in order to decrease adverse events within the recipient has become a part of clinical care. Although the main driver was an avoidance of transfusion-transmitted disease, other immunological consequences have been noted, and it is widely regarded as desirable to avoid the use of allogeneic component transfusion unless there is an essential physiological need. Of course this attempt at decreasing allogeneic blood component use has a potentially beneficial effect of blood component supply, leading to decreased use within the surgical specialties, while allowing increased use in clinical cases where there is currently no alternative to the transfusion of allogeneic components, such as those cases who have received chemotherapy and marrow suppression. The development of an array of techniques and treatments to decrease dependence of blood component transfusion has led to a care pathway that attempts to treat preoperative anaemia, minimize operative blood loss, and withhold allogeneic transfusion in the postoperative period according to clinical need. Many questions remain about the appropriate level of haemoglobin depending upon the comorbidities suffered by the patient, which is why patient blood management has gained popularity, as each patient deserves an individual care plan according to need.

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48

Europe, Council of. Guide to the Preparation, Use and Quality Assurance of Blood Components (Health). Council of Europe, 2007.

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49

(Editor), J. Desmyter, B. Van Weemen (Editor), and S. Seidl (Editor), eds. Current (Safety) Issues in the Screening of Donor Blood and the Preparation of Pure Blood Components (Vox Sanguinis,). S. Karger AG (Switzerland), 1986.

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50

Compact Regs Part 606: CFR 21 Part 606 Current Good Manufacturing Practice for Blood and Blood Components (10 Pack). 2nd ed. Informa Healthcare, 2003.

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