Medicine:Intraoperative blood salvage
| Intraoperative blood salvage | |
|---|---|
| ICD-9 | 99.00 |
| MeSH | D057725 |
Intraoperative blood salvage (IOS), also known as cell salvage, is a specific type of autologous blood transfusion. Specifically IOS is a medical procedure involving recovering blood lost during surgery and re-infusing it into the patient. It is a major form of autotransfusion.
It has been used for many years and gained greater attention over time as risks associated with allogenic (separate-donor) blood transfusion have seen greater publicity and become more fully appreciated. Several medical devices have been developed to assist in salvaging the patient's own blood in the perioperative setting. The procedure is frequently used in cardiothoracic and vascular surgery, during which blood usage has traditionally been high. A greater effort to avoid adverse events due to transfusion has also increased the emphasis on blood conservation (see bloodless surgery).
Background
Providing safe blood for transfusion remains a challenge despite advances in preventing transmission of hepatitis B virus (HBV), hepatitis C virus (HCV), AIDS/HIV, HTLV-I/II, West Nile virus (WNV), syphilis, Chagas disease, Zika virus, and transfusion-transmitted bacterial infection. Human errors such as misidentifying patients and drawing blood samples from the wrong person (i.e., wrong blood in tube or WBIT) is more of a risk than transmissible diseases in many developed nations.[citation needed]
Much more common risks of allogeneic transfusion include allergic transfusion reactions as well as febrile non-hemolytic transfusion reactions. Additional risks include transfusion related acute lung injury (TRALI), transfusion associated circulatory overload (TACO) and transfusion-associated immunomodulation. TRALI is a potentially life-threatening condition with symptoms such as dyspnea, fever, and hypotension occurring within hours of transfusion. TACO is a much more common (even with cases being underreported) potentially life-threatening condition involving respiratory compromise within hours of a transfusion. TACO must be suspected when there is respiratory distress with other signs, including pulmonary edema, unanticipated cardiovascular system changes, and evidence of fluid overload (including improvement after diuresis), during or up to 24 hours after transfusion.[1] Transfusion-associated immunomodulation, which may suppress the immune response and cause adverse effects such as a small increase in the risk of postoperative infection.[citation needed]
Other risks such as classic or variant Creutzfeldt–Jakob disease (vCJD), an invariably fatal disease, remain worrisome as there are currently no approved tests for which to screen blood donors for this disease. Blood centers worldwide have instituted criteria to reject donors who may have been exposed to classic CJD and vCJD. Screening for transmissible diseases and deferral policies for classic CJD and vCJD designed to improve safety have unfortunately contributed to shrinking the donor pool. Blood shortages exist in the United States and worldwide. In many industrialized countries 5% or less of the eligible population are blood donors.[citation needed]
As a result, some in the global medical community have moved from allogeneic blood (blood collected from another person) towards autologous transfusion, in which patients receive their own blood. Another impetus for autologous transfusion is the position of Jehovah's Witnesses on blood transfusions. For religious reasons, Jehovah's Witnesses may choose not to accept any allogeneic transfusions from a volunteer's blood donation but may accept the use of autologous blood salvaged during surgery to restore their blood volume and homeostasis during the course of an operation, although not autologous blood donated beforehand. Each Jehovah's Witness patient must be individually counselled as to all the possible blood products that are available as they may choose to accept some and not others (i.e., while not accepting whole blood nor any of the four main components of blood, [plasma; platelets; red cells; white cells] some may accept fractions derived from those components, or medications containing such minor fractions); it is an individual choice for each patient. There are other religious/ non-religious individuals besides Jehovah's Witnesses that would refuse allogeneic blood products but may choose to accept intraoperative blood salvage.[citation needed]
Bloodless options
Ways to avoid the adverse events associated with allogenic transfusion are often grouped under the umbrella phrase bloodless surgery. There are several so-called bloodless options. These include:
- Minimally invasive surgical techniques
- Erythropoietin (a hormone that stimulates peripheral stem cells in the bone marrow to produce red blood cells)
- Blood salvage procedures
- Blood substitutes such as blood volume expanders and oxygen carriers (the latter as yet unlicensed in North America)
Blood salvage procedures
Cell processing
Regardless of manufacturer, there are many types of cell processors. Cell processors are red cell washing devices that collect anticoagulated shed or recovered blood, wash and separate the red blood cells (RBC) by centrifugation or filtration such as the HemoClear filter. After, the washed RBCs can be returned to the same patient by reinfusion. RBC washing devices can help remove byproducts in salvaged blood such as activated cytokines, anaphylatoxins, and other waste substances that may have been collected in the reservoir suctioned from the surgical field. However, they also remove viable platelets, clotting factors, and other plasma proteins essential to whole blood and homeostasis. The various RBC-savers also yield RBC concentrates with different characteristics and quality.[citation needed]
Direct transfusion
Direct transfusion is a blood salvaging method associated with cardiopulmonary bypass (CPB) circuits or other extracorporeal circuits (ECC) that are used in surgery such as coronary artery bypass grafts (CABG), valve replacement, or surgical repair of the great vessels. Following bypass surgery, the ECC circuit contains a significant volume of diluted whole blood that can be harvested in transfer bags and re-infused into patients. Residual CPB blood is fairly dilute ([Hb] = 6–9 g/dL; 60–90 g/L) compared to normal values (12–18 g/dL; 120–180 g/L) and can also contain potentially harmful contaminants such as activated cytokines, anaphylatoxins, and other waste substances that have been linked to organ edema and organ dysfunction and need a diuretic to reverse.
Acute normovolemic hemodilution (ANH) is a form of autologous transfusion where whole blood is collected from a patient at the start of surgery into a standard blood collection bag with anticoagulant with the simultaneous replacement of intracellular volume using acellular fluids (such as normal saline). The patient's own blood is re-infused at the end of the surgical case (presumably when any bleeding has stopped).[2]
Ultrafiltration
Hemofiltration or ultrafiltration devices constitute the third major type of blood salvage in operating rooms. In general, ultrafiltration devices filter the patient's anticoagulated whole blood. The filter process removes unwanted excess non-cellular plasma water, low molecular weight solutes, platelet inhibitors and some particulate matter through hemoconcentration, including activated cytokines, anaphylatoxins, and other waste substances making concentrated whole blood available for reinfusion. Hemofilter devices return the patient's whole blood with all the blood elements and fractions including platelets, clotting factors, and plasma proteins with a substantial Hb level. Presently, the only whole blood ultrafiltration device in clinical use is the Hemobag.[3][4] These devices do not totally remove potentially harmful contaminants that can be washed away by most RBC-savers. However, the contaminants that are potentially reduced by using RBC-savers, as shown by data from in vitro laboratory tests, are transient and reversible in vivo with hemostatic profiles returning to baselines within hours. The key is that coagulation and homeostasis are immediately improved with the return of concentrated autologous whole blood.
Over the years numerous studies have been done to compare these methods of blood salvage in terms of safety, patient outcomes, and cost effectiveness, often with equivocal or contradictory results.[5][6][7][8][9]
See also
References
- ↑ Bolton-Maggs, Paula (2017). The 2016 Annual SHOT Report (2017). Serious Hazards of Transfusion (SHOT).. ISBN 978-0-9558648-9-6.
- ↑ Standards for Perioperative Autologous Blood Collection and Administration, 5th edition. Bethesda, MD: AABB. 2013. pp. 47. ISBN 978-1-56395-840-3.
- ↑ Hemobag
- ↑ "Archived copy". http://www.noblood.org/forum/content/209-Intraoperative_blood_salvage.[full citation needed]
- ↑ "Six different hemofiltration devices for blood conservation in cardiac surgery". Ann Thorac Surg 51 (5): 747–53. May 1991. doi:10.1016/0003-4975(91)90116-8. PMID 2025077.
- ↑ "Comparison of three blood-processing techniques during and after cardiopulmonary bypass". Ann Thorac Surg 56 (4): 938–43. October 1993. doi:10.1016/0003-4975(93)90360-T. PMID 8215672.
- ↑ "Cell saver, ultrafiltration and direct transfusion: comparative study of three blood processing techniques". Thorac Cardiovasc Surg 49 (3): 149–52. June 2001. doi:10.1055/s-2001-14291. PMID 11432472.
- ↑ Freischlag, Julie Ann (2004). "Intraoperative blood salvage in vascular surgery - worth the effort?". Crit Care 8 (Suppl 2): S53–S56. doi:10.1186/cc2409. PMID 15196326. PMC 3226144. http://ccforum.com/content/8/S2/S53. Retrieved 2006-03-13.
- ↑ "Improved coagulation and blood conservation in the golden hours after cardiopulmonary bypass". J Extra Corpor Technol 39 (2): 105–8. June 2007. PMID 17672193.
Further reading
- "Improved coagulation and blood conservation in the golden hours after cardiopulmonary bypass". The Journal of Extra-corporeal Technology 39 (2): 103–8. June 2007. PMID 17672193.
- "Evaluation of coagulation factors and platelet function from an off-line modified ultrafiltration technique for post-cardiopulmonary bypass circuit blood recovery". Perfusion 28 (3): 214–22. May 2013. doi:10.1177/0267659112470710. PMID 23271047.
- "The Hemobag: the modern ultrafiltration system for patients undergoing cardiopulmonary by pass". Journal of Cardiothoracic Surgery 7: 55. 2012. doi:10.1186/1749-8090-7-55. PMID 22697396.
- "An in-vitro comparison between Hemobag and non-Hemobag ultrafiltration methods of salvaging circuit blood following cardiopulmonary bypass". The Journal of Extra-corporeal Technology 42 (2): 128–33. June 2010. PMID 20648897.
- "Changes in mechanical fragility and free hemoglobin levels after processing salvaged cardiopulmonary bypass circuit blood with a modified ultrafiltration device". The Journal of Extra-corporeal Technology 44 (1): 21–5. March 2012. PMID 22730860.
- "Outcomes and biochemical parameters following cardiac surgery: effects of transfusion of residual blood using centrifugation and multiple-pass hemoconcentration". Journal of Cardiothoracic and Vascular Anesthesia 27 (6): 1174–80. December 2013. doi:10.1053/j.jvca.2013.03.011. PMID 23988781.
- "Use of the Hemobag for modified ultrafiltration in a Jehovah's Witness patient undergoing cardiac surgery". The Journal of Extra-corporeal Technology 38 (3): 265–70. September 2006. PMID 17089515.
- "A new practical technique to reduce allogeneic blood exposure and hospital costs while preserving clotting factors after cardiopulmonary bypass: the Hemobag". Perfusion 20 (6): 343–9. October 2005. doi:10.1191/0267659105pf831oa. PMID 16363320. http://prf.sagepub.com/cgi/pmidlookup?view=long&pmid=16363320.
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