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Scientific Article   |    
Erythrocyte Viability in Blood Salvaged During Total Joint Arthroplasty with Cement
Clifford W. ColwellJr., MD; Ernest Beutler, MD; Carol West; Mary E. Hardwick, RN, MSN; Beverly A. Morris, RN, CNP
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Investigation performed at the Scripps Clinic, La Jolla, California

Clifford W. Colwell Jr., MD
Ernest Beutler, MD
Carol West
Mary E. Hardwick, RN, MSN
Beverly A. Morris, RN, CNP
Scripps Clinic, 10666 North Torrey Pines Road, La Jolla, CA 92037. E-mail address for C.W. Colwell Jr.: colwell@scripps.edu

No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article. Funds were received in total or partial support of the research or clinical study presented in this article. The funding source was The Scholl Foundation.

The Journal of Bone & Joint Surgery.  2002; 84:23-25 
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Abstract

Background: Erythrocyte salvage, the collection of a patient’s blood shed from the surgical wound, is one aspect of blood management. Previous investigators have examined salvaged blood for content; however, to our knowledge, none have examined the viability of erythrocytes after exposure to the chemical and thermal reactions produced by motorized instruments and polymethylmethacrylate during surgery. The purpose of this study was to determine the viability of salvaged erythrocytes from patients undergoing primary total joint arthroplasty with cement.

Methods: Erythrocyte viability studies were performed on specimens from three subjects with use of a double isotope-labeling technique employing chromium-51 and technetium-99m. With use of a fresh blood specimen obtained prior to surgery and a specimen of salvaged blood that had been recycled, washed, and filtered with use of the Cell Saver, the viability of the Cell-Saver-processed erythrocytes, labeled with chromium-51, was calculated on the basis of the technetium-99m-labeled red blood-cell mass.

Results: The mean erythrocyte viability (and standard deviation) in blood salvaged with use of the Cell Saver was 88.0% ± 3.8%. The standard of the American Association of Blood Banks for minimum erythrocyte viability in adequately cross-matched allogeneic blood or predeposited autologous blood is 70%.

Conclusions: The high rate of viability of the erythrocytes in this study shows that the Cell Saver is a valuable adjunct to other blood management techniques for patients having total joint arthroplasty. We believe that the very high mean rate of erythrocyte viability and the extremely small standard deviation in our three subjects, as compared with the standards of the American Association of Blood Banks, made additional study subjects unnecessary.

Figures in this Article
    The concept of autologous transfusion of blood shed during surgery was first proposed in the 1800s but did not become feasible until the mid-1970s. Blood salvage techniques are utilized during both elective orthopaedic operations and those for traumatic injury. Techniques have been developed to use salvaged, reinfused erythrocytes after cell washing and filtering or after filtering alone1-7.
    The survival and/or viability of erythrocytes has been reported by various authors. Ansell et al., using a double isotope-labeling technique, stated that there was no difference between the erythrocyte survival in nonprocessed venous blood and that in venous blood processed with use of the Cell Saver (Haemonetics, Braintree, Massachusetts) during cardiovascular surgery8. Jones et al. used a single isotope-labeling technique and reported a half-life of 22.4 days for erythrocytes in undefined orthopaedic procedures9. Erythrocyte survival of twenty-four days in blood salvaged during spinal surgery was reported by Ray et al.10. In 1993, Umlas et al. reported a twenty-four-hour survival rate of 82.8% and a half-life of nineteen days for erythrocytes in shed, unwashed salvaged blood from seven patients undergoing hip or knee arthroplasty11. Gronborg et al. reported a half-life of twenty-one days for erythrocytes in shed, unwashed blood salvaged with use of a filtering system after cementless total knee arthroplasty12.
    With total hip and knee arthroplasty, there is concern that erythrocytes may be damaged from exposure to motorized instruments or polymethylmethacrylate and the high temperatures that they create. This study was undertaken to determine the viability of erythrocytes exposed to the trauma associated with total joint arthroplasty and then washed and filtered with use of a salvaging system.
     
    Anchor for JumpAnchor for Jump
    +Fig. 1:Estimated blood loss and red blood-cell (RBC) volume for the three subjects at twenty-four hours after surgery.
     
    Anchor for JumpAnchor for Jump
    +Fig. 2:Erythrocyte viability for the three subjects at twenty-four hours after surgery.
    Consecutive patients, without a history of coronary artery disease or cerebrovascular disease, who were scheduled for elective total hip or knee arthroplasty with cement were approached to participate in this study, originally designed for eight subjects.
    Four patients agreed to participate and signed a consent form approved by the Scripps Human Subjects Committee, but one subject could not be included in the study because we could not obtain venous access in the contralateral arm to draw post-labeling specimens. Two patients having a total hip arthroplasty and one patient having a total knee arthroplasty completed the study.
    A fresh blood specimen was obtained prior to surgery. During surgery, blood and debris were aspirated by low-pressure suction (£180 cm H2O) from the surgical site into the Cell Saver Reservoir. After closure of the wound, the patient was moved to the Post-Anesthesia Care Unit and drainage was aspirated by low-wall suction (23 mm Hg), through a drain that had been placed in the wound, and was collected in the reservoir. When 400 to 600 mL of drainage had accumulated in the reservoir, the blood and drainage was washed with normal saline solution and centrifuged before reinfusion into the patient.
    Viability studies of erythrocytes collected with use of the Cell Saver were performed with a double isotope-labeling technique using chromium-51 and technetium-99m13 (see Appendix). The red blood-cell viability was corrected for the change in the red blood-cell mass due to bleeding between the time of surgery and the first postoperative day.
    The total amount of salvaged blood transfused was 660 mL. Twenty-four hours postoperatively, the mean total red blood-cell volume was 1657 mL and the mean estimated blood loss was 1117 mL (Fig. 1). The twenty-four-hour mean erythrocyte viability of blood salvaged perioperatively with use of the Cell Saver was 88.0% ± 3.8% (Fig. 2). This value is well above the standard of the American Association of Blood Banks for minimum erythrocyte viability.
    The minimum blood bank requirement for erythrocyte viability in homologous or predeposited autologous blood is 70%14. In this study, the erythrocyte viability of 88.0% ± 3.8% in blood salvaged with use of the Cell Saver was much higher than that value. The viability of the salvaged cells that had been exposed to the trauma associated with motorized instruments and polymethylmethacrylate as well as the suction and solutions involved in the blood salvage process in this study was similar to that in venous blood (mean, 83.7%; range, 69% to 93%), reported by Umlas et al. in their study of six patients, two of whom had a hip arthroplasty and four, a knee arthroplasty11.
    The hematological and coagulation factors of perioperative salvaged blood have been examined in clinical studies. According to Dalen et al., erythrocyte, leukocyte, and platelet counts were significantly (p < 0.001) decreased in unwashed salvaged blood compared with those counts in venous blood at two hours after surgery; however, by six to eight hours after surgery, the erythrocyte count in salvaged blood was similar to that in venous blood, while the leukocyte and platelet counts continued to decline15,16. Another study indicated that unwashed blood allowed initiation of clot formation in normal plasma and contained more fibrin degradation products, including D-dimer, than did washed blood17. Although the use of salvaged blood in total joint arthroplasty has been promoted18, some have discouraged its use from an economic standpoint19. However, the use of salvaged blood is still recommended if >1000 mL of blood loss, which may occur in hip revision and trauma20,21, is anticipated. Perioperative transfusion of salvaged autologous blood has been demonstrated to be an effective adjunct to hemodilution and the use of predeposited autologous blood in blood management22,23.
    In the design of this study, we had planned to enroll eight subjects and anticipated a small standard deviation. After we completed the study of only three subjects, the mean erythrocyte viability was quite high (88.0%) and the standard deviation was extremely low (3.8%), with a coefficient of variation of 4.3%. Given this initial data, the expected conditional power of rejecting the null hypothesis that erythrocyte viability would be 70% was calculated. If the additional five patients had been enrolled, the probability of the mean viability being significantly greater than 70% would have been in excess of 0.9524. Hence, we sought no further enrollment of subjects.
    The erythrocyte viability that was shown in this study confirms that the use of salvaged, reinfused autologous blood is an excellent adjunct to other methods of blood management for patients undergoing total joint arthroplasty.
    The specific technique of the erythrocyte viability studies is presented in detail in the electronic versions of this article, on our web site at www.jbjs.org (go to the article citation and click on "Supplementary Material"), and on our quarterly CD-ROM (call our subscription department, at 781-449-9780, to order the CD-ROM).
    Faris PM, Ritter MA, Keating EM,Valeri CR. Unwashed filtered shed blood collected after knee and hip arthroplasties. A source of autologous blood cells. J Bone Joint Surg Am,1991;73: 1169-78. 731169  1991  [PubMed]
     
    Gannon DM, Lombardi AV Jr, Mallory TH, Vaughn BK, Finney CR,Niemcryk S. An evaluation of the efficacy of postoperative blood salvage after total joint arthroplasty. A prospective randomized trial. J Arthroplasty,1991;6: 109-14. 6109  1991  [PubMed]
     
    Goulet JA, Bray TJ, Timmerman LA, Benson DR,Bargar WL. Intraoperative autologous transfusion in orthopaedic patients. J Bone Joint Surg Am,1989;71: 3-8. 713  1989  [PubMed]
     
    Healy WL, Pfeifer BA, Kurtz SR, Johnson C, Johnson W, Johnston R, Sanders D, Karpman R, Hallack GN,Valeri CR. Evaluation of autologous shed blood for autotransfusion after orthopaedic surgery. Clin Orthop,1994;299: 53-9. 29953  1994  [PubMed]
     
    Semkiw LB, Schurman DJ, Goodman SB,Woolson ST. Postoperative blood salvage using the Cell Saver after total joint arthroplasty. J Bone Joint Surg Am,1989;71: 823-7. 71823  1989  [PubMed]
     
    Slagis SV, Benjamin JB, Volz RG,Giordano GF. Postoperative blood salvage in total hip and knee arthroplasty. A randomised controlled trial. J Bone Joint Surg Br,1991;73: 591-4. 73591  1991  [PubMed]
     
    Weinstein IM,Beutler E. The use of 51 Cr and 59 Fe in a combined procedure to study erythrocyte production in normal human subjects and in patients with hemolytic or aplastic anemia. J Lab Clin Med,1955;45: 616-22. 45616  1955  [PubMed]
     
    Ansell J, Parrilla N, King M, Fournier L, Szymanski I, Doherty P, Vander Salm T,Cutler B. Survival of autotransfused red blood cells recovered from the surgical field during cardiovascular operations. J Thorac Cardiovasc Surg,1982;84: 387-91. 84387  1982  [PubMed]
     
    Jones RB, Propst-Proctor SL, McDougall IR, Yhap EO, Bleck EE,Rinsky LA.. Erythrocyte survival following intraoperative autotransfusion in orthopaedic surgery. Orthop Trans,1984;8: 381. 8381  1984 
     
    Ray JM, Flynn JC,Bierman AH. Erythrocyte survival following intraoperative autotransfusion in spinal surgery: an in vivo comparative study and 5-year update. Spine,1986;11: 879-82. 11879  1986  [PubMed]
     
    Umlas J, Jacobson MS,Kevy SV. Survival and half-life of red cells salvaged after hip and knee replacement surgery. Transfusion,1993;33: 591-3. 33591  1993  [PubMed]
     
    Gronborg H, Otte KS, Jensen TT, Marving J, Solgaard S,Rechnagel K. Survival of autotransfused red cells. 51 Cr studies in 10 knee arthroplasty patients. Acta Orthop Scand,1996;67: 439-42. 67439  1996  [PubMed]
     
    Beutler E,West C. Measurement of the viability of stored red cells by the single-isotope technique using 51 Cr. Analysis of validity. Transfusion,1984;24: 100-4.. 24100  1984  [PubMed]
     
    American Association of Blood Banks. Standards for blood banks and transfusion services. 16th ed. Bethesda, MD: American Association of Blood Banks; 1993. p 9-11 
     
    Dalen T, Brostrom LA,Engstrom KG. Autotransfusion after total knee arthroplasty. Effects on blood cells, plasma chemistry and whole blood rheology. J Arthroplasty,1997;12: 517-25. 12517  1997  [PubMed]
     
    Dalen T, Brostrom LA,Engstrom KG. Cell quality of salvaged blood after total knee arthroplasty. Drain blood compared to venous blood in 32 patients. Acta Orthop Scand,1995;66: 329-33. 66329  1995  [PubMed]
     
    Blaylock RC, Carlson KS, Morgan JM, Tobin GO, Reeder GD,Anstall HB. In vitro analysis of shed blood from patients undergoing total knee replacement surgery. Am J Clin Pathol,1994;101: 365-9. 101365  1994  [PubMed]
     
    Cowell HR. Perioperative red blood-cell transfusion [editorial]. J Bone Joint Surg Am,1989;71: 1-2. 711  1989  [PubMed]
     
    Cone J, Day LJ, Johnson GK, Murray DG,Nelson CL. Blood products: optimal use, conservation, and safety. Instr Course Lect,1990;39: 431-4. 39431  1990  [PubMed]
     
    . Consensus Conference on Autologous Transfusion. Final Consensus Statement. Transfusion,1996;36: 667. 36667  1996 
     
    Sculco TP. Blood management in orthopedic surgery. Am J Surg,1995;170(6ASuppl): 60S-3S. 170(6ASuppl)60  1995 
     
    Oishi CS, D’Lima DD, Morris BA, Hardwick ME, Berkowitz SD,Colwell CW Jr. Hemodilution with other blood reinfusion techniques in total hip arthroplasty. Clin Orthop,1997;339: 132-9. 339132  1997  [PubMed]
     
    Schmied H, Schiferer A, Sessler DI,Meznik C. The effects of red-cell scavenging, hemodilution, and active warming on allogeneic blood requirements in patients undergoing hip or knee arthroplasty. Anesth Analg,1998;86: 387-91. 86387  1998  [PubMed]
     
    Lan KKG, Simon R,Halperin M. Stochastically curtailed tests in long-term clinical trials. Commun Statist Sequential Analysis,1982;1: 207-19. 1207  1982 
     

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    Anchor for JumpAnchor for Jump
    +Fig. 1:Estimated blood loss and red blood-cell (RBC) volume for the three subjects at twenty-four hours after surgery.
    Anchor for JumpAnchor for Jump
    +Fig. 2:Erythrocyte viability for the three subjects at twenty-four hours after surgery.
    Faris PM, Ritter MA, Keating EM,Valeri CR. Unwashed filtered shed blood collected after knee and hip arthroplasties. A source of autologous blood cells. J Bone Joint Surg Am,1991;73: 1169-78. 731169  1991  [PubMed]
     
    Gannon DM, Lombardi AV Jr, Mallory TH, Vaughn BK, Finney CR,Niemcryk S. An evaluation of the efficacy of postoperative blood salvage after total joint arthroplasty. A prospective randomized trial. J Arthroplasty,1991;6: 109-14. 6109  1991  [PubMed]
     
    Goulet JA, Bray TJ, Timmerman LA, Benson DR,Bargar WL. Intraoperative autologous transfusion in orthopaedic patients. J Bone Joint Surg Am,1989;71: 3-8. 713  1989  [PubMed]
     
    Healy WL, Pfeifer BA, Kurtz SR, Johnson C, Johnson W, Johnston R, Sanders D, Karpman R, Hallack GN,Valeri CR. Evaluation of autologous shed blood for autotransfusion after orthopaedic surgery. Clin Orthop,1994;299: 53-9. 29953  1994  [PubMed]
     
    Semkiw LB, Schurman DJ, Goodman SB,Woolson ST. Postoperative blood salvage using the Cell Saver after total joint arthroplasty. J Bone Joint Surg Am,1989;71: 823-7. 71823  1989  [PubMed]
     
    Slagis SV, Benjamin JB, Volz RG,Giordano GF. Postoperative blood salvage in total hip and knee arthroplasty. A randomised controlled trial. J Bone Joint Surg Br,1991;73: 591-4. 73591  1991  [PubMed]
     
    Weinstein IM,Beutler E. The use of 51 Cr and 59 Fe in a combined procedure to study erythrocyte production in normal human subjects and in patients with hemolytic or aplastic anemia. J Lab Clin Med,1955;45: 616-22. 45616  1955  [PubMed]
     
    Ansell J, Parrilla N, King M, Fournier L, Szymanski I, Doherty P, Vander Salm T,Cutler B. Survival of autotransfused red blood cells recovered from the surgical field during cardiovascular operations. J Thorac Cardiovasc Surg,1982;84: 387-91. 84387  1982  [PubMed]
     
    Jones RB, Propst-Proctor SL, McDougall IR, Yhap EO, Bleck EE,Rinsky LA.. Erythrocyte survival following intraoperative autotransfusion in orthopaedic surgery. Orthop Trans,1984;8: 381. 8381  1984 
     
    Ray JM, Flynn JC,Bierman AH. Erythrocyte survival following intraoperative autotransfusion in spinal surgery: an in vivo comparative study and 5-year update. Spine,1986;11: 879-82. 11879  1986  [PubMed]
     
    Umlas J, Jacobson MS,Kevy SV. Survival and half-life of red cells salvaged after hip and knee replacement surgery. Transfusion,1993;33: 591-3. 33591  1993  [PubMed]
     
    Gronborg H, Otte KS, Jensen TT, Marving J, Solgaard S,Rechnagel K. Survival of autotransfused red cells. 51 Cr studies in 10 knee arthroplasty patients. Acta Orthop Scand,1996;67: 439-42. 67439  1996  [PubMed]
     
    Beutler E,West C. Measurement of the viability of stored red cells by the single-isotope technique using 51 Cr. Analysis of validity. Transfusion,1984;24: 100-4.. 24100  1984  [PubMed]
     
    American Association of Blood Banks. Standards for blood banks and transfusion services. 16th ed. Bethesda, MD: American Association of Blood Banks; 1993. p 9-11 
     
    Dalen T, Brostrom LA,Engstrom KG. Autotransfusion after total knee arthroplasty. Effects on blood cells, plasma chemistry and whole blood rheology. J Arthroplasty,1997;12: 517-25. 12517  1997  [PubMed]
     
    Dalen T, Brostrom LA,Engstrom KG. Cell quality of salvaged blood after total knee arthroplasty. Drain blood compared to venous blood in 32 patients. Acta Orthop Scand,1995;66: 329-33. 66329  1995  [PubMed]
     
    Blaylock RC, Carlson KS, Morgan JM, Tobin GO, Reeder GD,Anstall HB. In vitro analysis of shed blood from patients undergoing total knee replacement surgery. Am J Clin Pathol,1994;101: 365-9. 101365  1994  [PubMed]
     
    Cowell HR. Perioperative red blood-cell transfusion [editorial]. J Bone Joint Surg Am,1989;71: 1-2. 711  1989  [PubMed]
     
    Cone J, Day LJ, Johnson GK, Murray DG,Nelson CL. Blood products: optimal use, conservation, and safety. Instr Course Lect,1990;39: 431-4. 39431  1990  [PubMed]
     
    . Consensus Conference on Autologous Transfusion. Final Consensus Statement. Transfusion,1996;36: 667. 36667  1996 
     
    Sculco TP. Blood management in orthopedic surgery. Am J Surg,1995;170(6ASuppl): 60S-3S. 170(6ASuppl)60  1995 
     
    Oishi CS, D’Lima DD, Morris BA, Hardwick ME, Berkowitz SD,Colwell CW Jr. Hemodilution with other blood reinfusion techniques in total hip arthroplasty. Clin Orthop,1997;339: 132-9. 339132  1997  [PubMed]
     
    Schmied H, Schiferer A, Sessler DI,Meznik C. The effects of red-cell scavenging, hemodilution, and active warming on allogeneic blood requirements in patients undergoing hip or knee arthroplasty. Anesth Analg,1998;86: 387-91. 86387  1998  [PubMed]
     
    Lan KKG, Simon R,Halperin M. Stochastically curtailed tests in long-term clinical trials. Commun Statist Sequential Analysis,1982;1: 207-19. 1207  1982 
     
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