Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-8bhkd Total loading time: 0 Render date: 2024-11-19T13:03:29.325Z Has data issue: false hasContentIssue false

20 - Blood transfusion/preoperative considerations and complications

Published online by Cambridge University Press:  12 January 2010

Cassandra D. Josephson
Affiliation:
Emory University, Transfusion Medicine, Atlanta, GA
Krista L. Hillyer
Affiliation:
Emory University, Transfusion Medicine, Atlanta, GA
Christopher D. Hillyer
Affiliation:
Emory University, Transfusion Medicine, Atlanta, GA
Michael F. Lubin
Affiliation:
Emory University, Atlanta
Robert B. Smith
Affiliation:
Emory University, Atlanta
Thomas F. Dodson
Affiliation:
Emory University, Atlanta
Nathan O. Spell
Affiliation:
Emory University, Atlanta
H. Kenneth Walker
Affiliation:
Emory University, Atlanta
Get access

Summary

Introduction

This chapter is a guide for the physicians who selects, orders, or administers blood components. Blood component descriptions, alternative therapies, and general and specific product indications and contraindications are specifically addressed. Special surgical situations requiring blood components are covered, such as emergency release of blood units and massive transfusion. Technical considerations including pretransfusion evaluation, blood bank component inventory, and general aspects of transfusion are also discussed. Finally, adverse infectious and non-infectious complications are described in detail.

Whole blood and packed red blood cells

Description

Whole blood (WB) is the starting point for the manufacture of most of the components used in transfusion. Whole blood contains red blood cells, plasma, clotting factors, platelets, and approximately 109 white blood cells. However, packed red blood cells (pRBCs) are the most commonly transfused blood component. pRBCs are made from whole blood collections by centrifugation or by apheresis techniques. In the USA, over 12 million units of pRBCs are transfused each year. Table 20.1 provides important information on WB and pRBC products including approximate volumes, compositions, and storage periods.

Indications

Historically, WB was used to replace volume and red cell mass, usually during resuscitation of a patient when masssive transfusion was required. Availability of WB is dependent upon each institution and blood center. Its use is discouraged, however, as the use of specific blood components may be best tailored to the individual and unique needs of each patient.

Type
Chapter
Information
Medical Management of the Surgical Patient
A Textbook of Perioperative Medicine
, pp. 269 - 284
Publisher: Cambridge University Press
Print publication year: 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Anonymous. Practice guidelines for blood component therapy: a report from the American Society of Anesthesiologists Task Force on Blood Component Therapy. Anesthesiology 1996; 84: 732–747.CrossRef
Carson, J. L., Hill, S., Carless, P.et al. Transfusion triggers: a systematic review of the literature. Transfus. Med. Rev. 2002; 16(3): 187–199.CrossRefGoogle ScholarPubMed
Wall, M. H. & Prielipp, R.Transfusion in the operating room and the intensive care unit: current practice and future directions. Int. Anesth. Clin. 2000; 38(4): 149–169.CrossRefGoogle ScholarPubMed
Roback, J. D., Bray, R. A., & Hillyer, C. D.Longitudinal monitoring of WBC subsets in packed RBC units after filtration: implications for transfusion transmission of infections. Transfusion 2000; 40: 500–506.CrossRefGoogle ScholarPubMed
Akahoshi, M., Takanashi, M., & Masuda, M.A case of transfusion-associated graft-versus host disease not prevented by leukocyte depletion filters. Transfusion 1992; 32: 169–172.CrossRefGoogle ScholarPubMed
Goodnough, L. T. & Brecher, M. E.Autologous blood transfusion. Intern. Med. 1998; 37: 238–245.CrossRefGoogle ScholarPubMed
Brecher, M. (ed.) Technical Manual, 14th edn. American Association of Blood Banks, 2002: Bethesda, MD: 106.
Henry, D. A., Carless, P. A., Moxey, A. J.et al. Pre-operative autologous donation for minimising perioperative allogeneic blood transfusion [Review]. Cochrane Database Syst. Rev. 2002; 3.Google Scholar
Goodnough, L. T., Monk, T. G., Sicard, G.et al. Intraoperative salvage in patients undergoing elective abdominal aortic aneurysm repair: an analysis of cost and benefit. J. Vasc. Surg. 1996; 24: 213–218.CrossRefGoogle ScholarPubMed
Goodnough, L. T., Brecher, M. E., & Monk, T. G.Acute normovolemic hemodilution in surgery. Hematology 1992; 2: 413–420.CrossRefGoogle Scholar
Manucci, P. M.Drug therapy: hemostatic drugs. N. Engl. J. Med. 1998; 339: 245–253.CrossRefGoogle Scholar
Henry, D. A., Moxey, A. J., Carless, P. A.et al. Anti-fibrinolytic use for minimising perioperative allogeneic blood transfusion [Review]. Cochrane Database Syst. Rev. 2002; 3.Google Scholar
Samama, C. M., Langeron, O., Rosencher, N.et al. Aprotinin versus placebo in major orthopedic surgery: a randomized, double-blinded, dose-ranging study. Anesth. Analg. 2002; 95: 287–93.CrossRefGoogle ScholarPubMed
Peters, D. C. & Noble, S.Aprotinin: An update of its pharmacology and therapeutic use in open heart surgery and coronary artery bypass surgery. Drugs 1999; 57: 233–260.CrossRefGoogle ScholarPubMed
Donovan, J. F.Microscopic vasovasotomy: current practice and future trends. Microsurgery 1995; 16: 325–332.CrossRefGoogle Scholar
Kollias, S. L. & Fox, J. M.Meniscal repair. Where do we go from here? Clin. Sports Med. 1996; 15: 621–630.Google Scholar
Martinowitz, U., Schulman, S., Horoszowski, H.et al. Role of fibrin sealants in surgical procedures on patients with hemostatic disorders. Clin. Orthop. Related Res. 1996; 328: 65–75.CrossRefGoogle Scholar
Mccarthy, P. M.Fibrin glue in cardiothoracic surgery. Transfus. Med. Rev. 1993; 7: 173–229.CrossRefGoogle ScholarPubMed
Rousou, J., Levitsky, S., Gonzalez-Lavin, L.et al. Randomized clinical trials of fibrin sealant in patients undergoing resternotomy or reoperation after cardiac operations. A multicenter study. J. Thorac. Cardiovasc. Surg. 1989; 97: 194–203.Google ScholarPubMed
Schlag, G. Immuno's fibrin sealant: The European experience. Abstract from Symposium on Fibrin Sealant: Characteristics and Clinical Uses. Uniformed Services University of the Health Sciences, Bethesda, MD, 1994. Dec. 8–9.
Bucur, S. Z. & Hillyer, C. D. Cryoprecipitate and related products. In Hillyer, C. D., Hillyer, K. L., Strobel, F. J.et al. Handbook of Transfusion Medicine, 1/e. California: Academic Press, 2001: 50.Google Scholar
Goodnough, L. T., Monk, T. G., & Andriole, G. L.Current concepts: erythropoietin therapy. N. Engl. J. Med. 1997; 336: 933–938.CrossRefGoogle Scholar
Gmur, J., Burger, J., Schanz, U.et al. Safety of stringent prophylactic platelet transfusion policy for patients with acute leukemia. Lancet 1991; 338: 1223–1226.CrossRefGoogle Scholar
Pisciotto, P. T., Benson, K., Hume, H.et al. Prophylactic versus therapeutic platelet transfusion practices in hematology and/or oncology patients. Transfusion 1995; 35: 498–502.CrossRefGoogle ScholarPubMed
Hanson, S. R. & Slichter, S. J.Platelet kinetics in patients with bone marrow hypoplasia: evidence for a fixed platelet requirement. Blood 1985; 66: 1105–1109.Google ScholarPubMed
Rebulla, P., Finazzi, G., Marangoni, F.et al. The threshold for prophylactic platelet transfusions in adults with acute myeloid leukemia. Gruppo Italiano Malattie Ematologiche Maligne dell'Adulto. N. Engl. J. Med. 1997; 337: 1870–1875.CrossRefGoogle ScholarPubMed
Wandt, H., Frank, M., Ehninger, G.et al. Safety and cost effectiveness of a 10 × 10(9)/L trigger for prophylactic platelet transfusions compared with the traditional 20 × 10(9)/L trigger: a prospective comparative trial of 105 patients with acute myeloid leukemia. Blood 1998; 91: 3601–3606.Google ScholarPubMed
Takahashi, T., Abe, H., Nakai, K., & Sekiguchi, S.Bradykinin generation during filtration of platelet concentration with a white cell-reduction filter [letter]. Transfusion 1995; 35; 967.CrossRefGoogle Scholar
Friedman, D. F., Lukas, M. B., Jawad, A.et al. Alloimmunization to platelets in heavily transfused patients with sickle cell disease. Blood 1996; 88: 3216–3222.Google ScholarPubMed
TRAP. Leukocyte reduction and ultraviolet B irradiation of platelets to prevent alloimmunization and refractoriness to platelet transfusions. The Trial to Reduce Alloimmunization to Platelets Study Group. N. Engl. J. Med. 1997; 337: 1861–1869.CrossRef
Kutar, D. J., Cebon, J., Harker, L. A.et al. Platelet growth factors: potential impact on transfusion medicine. Transfusion 1999; 39: 321–332.CrossRefGoogle Scholar
Churchwell, K. B., McManus, M. L., Kent, P.et al. Intensive blood and plasma exchange for treatment of coagulopathy in Meningococcemia. J. Clin. Apher. 1995; 10: 171–177.CrossRefGoogle ScholarPubMed
Cohen, H.Avoiding misuse of fresh frozen plasma. Br. Med. J. 1993; 307: 395–396.CrossRefGoogle ScholarPubMed
Crosson, J. T.Massive transfusion. Clin. Lab. Med. 1996; 16: 873–882.Google ScholarPubMed
Linden, J. V., Wagner, K., Voytovich, A. E., & Sheehan, J.Transfusion errors in New York State: an analysis of 10 years' experience. Transfusion 2000; 40: 1207–1213.CrossRefGoogle ScholarPubMed
Myhre, B. A. & McRuer, D.Human error – a significant cause of transfusion mortality. Transfusion 2000; 40: 879–885.CrossRefGoogle ScholarPubMed
Carr, R., Hutton, J. L., Jenkins, J. A.et al. Transfusion of ABO mismatched platelets leads to early platelet refractoriness. Br. J. Haematol. 1990; 75: 408–413.CrossRefGoogle ScholarPubMed
Pierce, R. N., Reich, L. M., & Mayer, K.Hemolysis following platelet transfusions from ABO-incompatible donors. Transfusion 1985; 25: 60–62.CrossRefGoogle ScholarPubMed
Iserson, K. V. & Huestis, D. W.Blood warming: current applications and techniques. Transfusion 1991; 31: 558–571.CrossRefGoogle ScholarPubMed
Kopko, P. M., Marshall, C. S., MacKenzie, M. R.et al. Transfusion-related acute lung injury – report of a clinical look-back investigation. J. Am. Med. Assoc. 2002; 287(15): 1968–1961.CrossRefGoogle ScholarPubMed
Vamvakas, E. C. & Carven, J. H.Allogeneic blood transfusion, hospital charges, and length of hospitalization: a study of 487 consecutive patients undergoing colorectal cancer resection. Arch. Pathol. Lab. Med. 1998; 122: 145–151.Google ScholarPubMed
Hillyer, C. D., Lankford, K. V., Roback, J. D.et al. Transfusion of the HIV seropositive patient: immunomodulation, viral reactivation, and limiting exposure to EBV (HHV-4), CMV (HHV-5), and HHV – 6, 7, and 8. Transfus. Med. Rev. 1999; 13: 1–17.CrossRefGoogle Scholar
Linden, J. V., Tourault, M. A., & Scribner, C. L.Decrease in frequency of transfusion fatalities. Tranfusion 1997; 37: 243–244.CrossRefGoogle ScholarPubMed
Ness, P. M., Shirley, R. S., Thoman, S. K., & Buck, S. A.The differentiation of delayed serologic and delayed hemolytic transfusion reactions: incidence, long-term serologic findings, and clinical significance. Transfusion 1990; 30: 688–693.CrossRefGoogle ScholarPubMed
Dodd, R. Y., Notari, E. P., & Stramer, S. L.Current prevalence and incidence of infectious disease markers and estimated window-period risk in the American Red Cross blood donor population. Transfusion 2002; 42: 975–979.CrossRefGoogle ScholarPubMed
Goodnough, L. T., Brecher, M. E., Kanter, M. H., & AuBuchon, J. P.Transfusion Medicine. First of two parts. Blood Transfus. N. Engl. J. Med. 1999; 340: 438–447.CrossRefGoogle ScholarPubMed
Blajchman, M. A.Bacterial contamination and proliferation during the storage of cellular blood products. Vox Sang. 1998; 74: 155–159.CrossRefGoogle ScholarPubMed
Goldman, M. & Blajchman, M. A.Blood product-associated bacterial sepsis. Transfus. Med. Rev. 1991; 5: 73–83.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×