Guidelines for the Transfusion of Packed Red Blood Cells, Fresh Frozen
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Guidelines for Transfusions
Guidelines for Transfu- sion Prepared by: Community Transfusion Committee Lincoln, Nebraska CHAIR: Aina Silenieks, MD MEMBERS: L. Bausch, M.D. R. Burton, M.D. S. Dunder, M.D. D. Voigt, M.D. B. J. Wilson, M.D. COMMUNITY Becky Croner REPRESENTATIVES: Ellen DiSalvo Christa Engel Phyllis Ericson Kelly Gillaspie Pat Gilles Vic Grdina Jessica Henrichs Kelly Jensen Laurel McReynolds Christina Nickel Angela Novotny Kelley Thiemann Janet Wachter Jodi Wikoff Guidelines For Transfusion Community Transfusion Committee INTRODUCTION The Community Transfusion Committee is a multidisciplinary group that meets to monitor blood utilization practices, establish guidelines for transfusion and discuss relevant transfusion related topics. It is comprised of physicians from local hospitals, invited guests, and community representatives from the hospitals’ transfusion services, nursing services, perfusion services, health information management, and the Nebraska Community Blood Bank. These Guidelines for Transfusion are reviewed and revised biannually by the Community Trans- fusion Committee to ensure that the industry’s most current practices are promoted. The Guidelines are the standard by which utilization practices are evaluated. They are also de- signed to provide helpful information to assist physicians to provide appropriate blood compo- nent therapy to patients. Appendices have been added for informational purposes and are not to be used as guidance for clinical decision making. ADULT RED CELLS A. Indications 1. One of the following a. Hypovolemia and hypoxia (signs/symptoms: syncope, dyspnea, postural hypoten- sion, tachycardia, angina, or TIA) secondary to surgery, trauma, GI tract bleeding, or intravascular hemolysis, OR b. Evidence of acute loss of 15% of total blood volume or >750 mL blood loss, OR c. -
27. Clinical Indications for Cryoprecipitate And
27. CLINICAL INDICATIONS FOR CRYOPRECIPITATE AND FIBRINOGEN CONCENTRATE Cryoprecipitate is indicated in the treatment of fibrinogen deficiency or dysfibrinogenaemia.1 Fibrinogen concentrate is licenced for the treatment of acute bleeding episodes in patients with congenital fibrinogen deficiency, including afibrinogenaemia and hypofibrinogenaemia,2 and is currently funded under the National Blood Agreement. Key messages y Fibrinogen is an essential component of the coagulation system, due to its role in initial platelet aggregation and formation of a stable fibrin clot.3 y The decision to transfuse cryoprecipitate or fibrinogen concentrate to an individual patient should take into account the relative risks and benefits.3 y The routine use of cryoprecipitate or fibrinogen concentrate is not advised in medical or critically ill patients.2,4 y Cryoprecipitate or fibrinogen concentrate may be indicated in critical bleeding if fibrinogen levels are not maintained using FFP. In the setting of major obstetric haemorrhage, early administration of cryoprecipitate or fibrinogen concentrate may be necessary.3 Clinical implications y The routine use of cryoprecipitate or fibrinogen concentrate in medical or critically ill patients with coagulopathy is not advised. The underlying causes of coagulopathy should be identified; where transfusion is considered necessary, the risks and benefits should be considered for each patient. Specialist opinion is advised for the management of disseminated intravascular coagulopathy (MED-PP18, CC-PP7).2,4 y Cryoprecipitate or fibrinogen concentrate may be indicated in critical bleeding if fibrinogen levels are not maintained using FFP. In patients with critical bleeding requiring massive transfusion, suggested doses of blood components is 3-4g (CBMT-PP10)3 in adults or as per the local Massive Transfusion Protocol. -
Blood, Lymph, and Immunity Joann Colville
Blood, Lymph, and Immunity Joann Colville CHAPTER OUTLINE .»: BLOOD Function Introduction Lymphatic Structures Plasma THE IMMUNE SYSTEM Cellular Components of Blood Function Red Blood Cells Immune Reactions Platelets Immunization: Protection Against Disease White Blood Cells THE LYMPHATICSYSTEM Lymph Formation Characteristics LEARNING OBJECTIVES • List and describe the functions of blood • List the functions of the lymphatic system • Describe the composition of blood plasma • Describe the structure and functions of the lymph nodes, • Describe the characteristics of mature erythrocytes spleen, thymus, tonsils, and GALT Describe the structure of the hemoglobin molecule and • List the functions of the immune system explain the fate of hemoglobin following intravascular and • Differentiate between specific and nonspecific immune extravascular hemolysis reactions • Give the origin of thrombocytes and describe their • Differentiate between cell-mediated and humoral immunity characteristics and functions • List the components involved in cell-mediated immunity • Listthe types of leukocytes and describe the functions of each and explain the role of each • Describe the formation of lymph fluid and its circulation List and describe the classes of immunoglobulins through the lymphatic system • Differentiate between active and passive immunity BLOOD vessels of the cardiovascular system. It has three main func- tions: transportation, regulation, and defense. INTRODUCTION Blood. Say the word, and some people cringe, others faint, Function and if you believe authors Bram Stoker, Stephen King, and 1. Blood is a transport system. Christopher Moore (all authors of vampire books), others • It carries oxygen, nutrients, and other essential com- drool. But no matter what you think about blood, animals pounds to every living cell in the body. -
Transfusion Service Introduction Blood/Blood Products Requests and Turnaround Time Expectations
Transfusion Service Introduction All blood products and blood components are supplied to UnityPoint Health-Meriter Hospital by the American Red Cross Blood Services. Pathology consultation is available regarding blood and/or components and dosages. ABO and Rho(D)—specific type is used whenever possible for leuko-poor packed cell transfusions. ABO-compatible blood is used for all plasma and platelet components whenever possible. For any orders involving HLA-matched components, the patient must have been HLA typed (sent to the American Red Cross) a minimum of 48 hours prior to intended infusion of the component. HLA typing is only required once. Blood components that are thawed, pooled, washed, volume-reduced, or deglycerolized for a patient will be charged to the patient even if not transfused. The charge is done because these components may not be suitable for another patient. Examples include: Autologous or directed donations Pooled cryoprecipitate 4-hour expiration Thawed fresh frozen plasma 24-hour expiration Thawed cryoprecipitate 6-hour expiration Deglycerolized red cells 24-hour expiration Washed red cells 24-hour expiration All blood components must be completely infused within 4 hours of release from UnityPoint Health-Meriter Laboratories Blood Bank, or be infused within the expiration time. Refer to UnityPoint Health -Meriter’s Blood and Blood Products Transfusion Policy #123 for additional information located on MyMeriter. Blood/Blood Products Requests and Turnaround Time Expectations Requests from UnityPoint Health-Meriter Hospital are entered in the hospital computer system and print in the UnityPoint Health- Meriter Laboratories Blood Bank. For the comfort of the patient, it is important to coordinate collection for other tests with Blood Bank specimens. -
The Diagnosis of Paroxysmal Nocturnal Hemoglobinuria: Role of Flow Cytometry
THE DIAGNOSIS OF PAROXYSMAL NOCTURNAL HEMOGLOBINURIA: ROLE OF FLOW CYTOMETRY Alberto Orfao Department of Medicine, Cancer Research Centre (IBMCC-CSIC/USAL), University of Salamanca, Salamanca, Spain Paroxysmal nocturnal hemoglobinuria (PNH) on one or multiple populations of peripheral blood is an acquired clonal disorder typically affecting red cells and/or leucocytes of PNH patients, this young adults, which involves the phosphatidylino- translating into a new diagnostic test. Because sitol glycan anchor biosynthesis class A gene of this flow cytometry became an essential tool (PIGA) coded in chromosome X, in virtually every in the diagnosis of PNH. In turn, it could be also case. The altered gene encodes for a defective pro- demonstrated that investigation of the presence of tein product, the pig-a enzyme which is involved GPI-deficient cells among circulating mature neu- in the early steps of the synthesis of glycosylphos- trophils and monocytes, increases the sensitivity phatidylinositol (GPI). This later molecule (GPI) of red blood cell screening because of the shorter acts as an anchor of a wide range of proteins to lifetime of both populations of leucocytes. Despite the cell surface. At present a large number of GPI- all the above, routine assessment of CD55 and anchor associated proteins have been described CD59 is also associated with several limitations which are expressed by one or multiple distinct due to distinct patterns of expression among dif- compartments of hematopoietic cells. The altered ferent cell populations, dim and heterogeneous PIGA gene leads to an altered GPI anchor which expression among normal individuals and the lack leads to defective expression of GPI-AP on the of experience in many labs as regards the normal cytoplasmic membrane, on the cell surface. -
Blood Product Replacement: Obstetric Hemorrhage
CMQCC OBSTETRIC HEMORRHAGE TOOLKIT Version 2.0 3/24/15 BLOOD PRODUCT REPLACEMENT: OBSTETRIC HEMORRHAGE Richard Lee, MD, Los Angeles County and University of Southern California Medical Center Laurence Shields, MD, Marian Regional Medical Center/Dignity Health Holli Mason, MD, Cedars-Sinai Medical Center Mark Rollins, MD, PhD, University of California, San Francisco Jed Gorlin, MD, Innovative Blood Resources/Memorial Blood Center, St. Paul, Minnesota Maurice Druzin, MD, Lucile Packard Children’s Hospital Stanford University Jennifer McNulty, MD, Long Beach Memorial Medical Center EXECUTIVE SUMMARY • Outcomes are improved with early and aggressive intervention. • Both emergency blood release and massive transfusion protocols should be in place. • In the setting of significant obstetric hemorrhage, resuscitation transfusion should be based on vital signs and blood loss and should not be delayed by waiting for laboratory results. • Calcium replacement will often be necessary with massive transfusion due to the citrate used for anticoagulation in blood products. • During massive transfusion resuscitation, the patient’s arterial blood gas, electrolytes, and core temperature should be monitored to guide clinical management and all transfused fluids should be warmed; direct warming of the patient should be initiated as needed to maintain euthermia and to avoid added coagulopathy. BACKGROUND AND LITERATURE REVIEW After the first several units of packed red blood cells (PRBCs) and in the face of continuing or worsening hemorrhage, aggressive transfusion therapy becomes critical. This report covers the experience with massive transfusion protocols. Lessons from military trauma units as well as civilian experience with motor vehicle accidents and massive obstetric hemorrhage have identified new principles such as earlier use of plasma (FFP/thawed plasma/plasma frozen within 24 hours/liquid plasma) and resuscitation transfusion while laboratory results are pending. -
Platelet Transfusion
Lab Dept: Transfusion Services Test Name: PLATELET TRANSFUSION General Information Lab Order Codes: TPLT Special charges: HLA Matched-MHLA, AHLA PLA1 Negative – PLAT, APLA1 Platelet Crossmatching PLTX – CPLT Synonyms: Leukocyte Reduced Platelets; Random Platelets; Platelet Rich Plasma; Platelet concentrate; Leukocyte Reduced Platelet Pheresis; Single- Donor Platelets; SDP Platelet pheresis; Apheresis Platelets; LRPH CPT Codes: P9035 – Platelet pheresis, Leukocyte reduced 86806 – Lymphocytotoxicity assay, visual crossmatch, without titration 86813 – HLA Matched 86945 – Irradiation 86985 – Volume Reduction 86965 – Pooling 86903 – Platelet Antigen typing 86999 – Washing 86022 – Platelet Crossmatch Test Includes: Leukocyte Reduced Platelet Pheresis consists of platelets suspended in 200-300 mL of plasma collected by cytapheresis. Each unit contains at least 3 x 1011 platelets, and ≤5.0 x 106 leukocytes. One pheresis unit equals 5-6 random unit platelet concentrate. Logistics Test Indications: Refer to Guidelines for the Transfusion of Blood Components. Platelet Crossmatching or HLA-Matched Platelets may be useful for patients receiving repeated platelet transfusions who have become refractile, and for patients who repeatedly develop febrile non-hemolytic transfusion reactions after platelet transfusions. Volume Reduced Platelets are indicated in the event that ABO - incompatible platelets must be transfused due to availability or in patients with severe fluid restrictions. Refer to Blood Component Compatibility Chart Lab Testing Sections: Transfusion Services Phone Numbers: MIN Lab: 612-813-6824 STP Lab: 651-220-6558 Test Availability: Daily, 24 hours Turnaround Time: 1 - 2 hours Standard Dose/Volume: <10 kg: 10 – 15 mL/kg up to one unit or 50 mL maximum 10 – 15 kg: 1/3 pheresis unit 15 – 25 kg: 1/2 pheresis unit >25 kg: 1 pheresis unit Rate of Infusion: 10 minutes/unit, <4 hours Administration: Must be administered through a blood component administration filter. -
Patient's Guide to Blood Transfusions
Health Information For Patients and the Community A Patient’s Guide to Blood Transfusions Your doctor may order a blood transfusion as part of your therapy. This brochure will focus on frequently asked questions about blood products, transfusions, and the risks and benefits of the blood transfusion. PLEASE NOTE: This information is not intended to replace the medical advice of your doctor or health care provider and is intended for educational purposes only. Individual circumstances will affect your individual risks and benefits. Please discuss any questions or concerns with your doctor. What is a blood transfusion? A blood transfusion is donated blood given to patients with abnormal blood levels. The patient may have abnormal blood levels due to blood loss from trauma or surgery, or as a result of certain medical problems. The transfusion is done with one or more of the following parts of blood: red blood cells, platelets, plasma, or cryoprecipitate. What are the potential benefits of a blood transfusion? If your body does not have enough of one of the components of blood, you may develop serious life-threatening complications. • Red blood cells carry oxygen through your body to your heart and brain. Adequate oxygen is very important to maintain life. • Platelets and cryoprecipitate help to prevent or control bleeding. • Plasma replaces blood volume and also may help to prevent or control bleeding. How safe are blood transfusions? Blood donors are asked many questions about their health, behavior, and travel history in order to ensure that the blood supply is as safe as it can be. Only people who pass the survey are allowed to donate. -
Patient Information Leaflet – Plasma Exchange Procedure
Therapeutic Apheresis Services Patient Information Leaflet – Plasma Exchange Procedure Introduction Antibodies, which normally help to protect you from infection, can begin to attack your own This leaflet has been written to give patients healthy cells, or an over production of proteins can information about plasma exchange (sometimes cause your blood to become thicker and slow down called plasmapheresis). If you would like any more the blood flow throughout your body. A plasma information or have any questions, please ask the exchange can help improve your symptoms, doctors and nurses involved in your treatment at although this may not happen immediately. the NHS Blood and Transplant (NHSBT) Therapeutic Apheresis Services Unit. Although plasma exchange may help with symptoms, it will not normally cure your condition When you have considered the information given as it does not switch off the production of the in this leaflet, and after we have discussed the harmful antibodies or proteins. It is likely that procedure and its possible risks with you, we will this procedure will form only one part of your ask you to sign a consent form to indicate that you treatment. are happy for the procedure to go ahead. Before any further procedures we will again check that you are happy to proceed. How do we perform Plasma Exchange? What is a plasma exchange? Plasma exchange is performed using a machine Blood is made up of red cells, white cells and called a Blood Cell Separator which can separate platelets which are carried around in fluid called blood into its various parts. The machine separates plasma. -
Red Blood Cells, Leukocyte Reduced Covenant and AHS Sites
This document applies to all Red Blood Cells, Leukocyte Reduced Covenant and AHS sites. Class: Human blood component, derived from OTHER NAMES: Packed red blood cells, Packed whole blood cells INTRAVENOUS OTHER ROUTES DIRECT IV Intermittent Continuous Infusion Infusion SC IM OTHER Acceptable No Yes No No No No Routes* * Professionals performing these restricted activities have received authorization from their regulatory college and have the knowledge and skill to perform the skill competently. DESCRIPTION OF PRODUCT: Red Blood Cell (RBC) concentrates are prepared from approximately 480mL whole blood usually collected in 70mL of anticoagulant. The unit is plasma reduced by centrifugation, platelet reduced by either centrifugation or filtration and leukocyte reduced by filtration. RBCs are typically resuspended in approximately 110mL of nutrient. Collected from volunteer donors by the Canadian Blood Services (CBS). Donor is screened and blood is tested for: i. Hepatitis B Surface Antigen (HBsAg) ii. Syphilis iii. Antibodies to Hepatitis B core antigen (HBcore), Hepatitis C Virus (HCV), Human T-cell Lymphotropic Virus (HTLV-1 and 2), Human Immune Deficiency Virus (HIV-1 and 2) iv. Nucleic Acid Testing (NAT) for presence of HCV RNA, HIV-1 RNA and West Nile Virus (WNV) RNA . CBS also tests blood for ABO/Rh and clinically significant antibodies. Some donors are tested for CMV status. RBCs do NOT contain any coagulation factors or platelets. AVAILABILITY: . Contact your local transfusion service/laboratory for ABO and Rh types stocked at your site. ABO compatible (not always identical) may be required if the transfusion service cannot provide sufficient quantities of the patient’s blood group (See ABO compatibility chart at: http://www.albertahealthservices.ca/assets/wf/lab/wf-lab-clin-tm-abo-compatability.pdf). -
Important Information for Female Platelet Donors
Important Information for Female Platelet Donors We are grateful for the support you provide our community blood program and especially appreciate your willingness to help save lives as a volunteer platelet donor. We also take our responsibility to provide a safe and adequate blood supply very seriously and need to share the following information regarding a change to our donor eligibility criteria for female platelet donors. We recently began performing a Human Leukocyte Antigen (HLA) antibody test on each of our current female platelet donors who have ever been pregnant. In addition, we modified our Medical History Questionnaire to ask donors whether they have been pregnant since their last donation. Platelet donors who respond yes to that question will be screened for HLA antibodies. Platelet donors will also be retested after every subsequent pregnancy. These adjustments are being made as part of our effort to reduce occurrences of Transfusion-Related Acute Lung Injury (TRALI). TRALI is a rare but serious complication of blood transfusions most commonly thought to be caused by a reaction to HLA antibodies present in the donor’s plasma. When transfused, these antibodies can sometimes cause plasma to leak into the patient’s lungs, creating fluid accumulation — a condition referred to as acute pulmonary edema. Female donors who have been pregnant are more likely than others to have these HLA antibodies in their plasma. Once the antibodies develop, they are present forever. The antibodies could be harmful if transfused into certain patients. The antibodies are present in plasma — and platelet donations contain a high volume of plasma, so our current efforts are directed at screening blood samples from female platelet donors to test for the HLA antibody. -
Transfusion Guidelines Updated February, 2005
Transfusion Guidelines Updated February, 2005 I. Whole Blood The use of whole blood is not recommended and is not available from the Blood Center. Blood components should be selected according to the patient’s needs. II. Red Blood Cells (RBCs) Transfusion must be completed within 4 hours of issue from the Blood Bank. If transfusion is not begun immediately the RBCs must be stored at 1-6° C or returned to the Blood Bank. (Storage is only allowed in preapproved areas, such as the operating room and several of the critical care areas). The effectiveness of each transfusion should be documented in the medical record. Single unit transfusions of RBCs are often effective. In adult patients, one unit of RBCs will increase the hemoglobin level by approximately 1 g/dl (hematocrit by 3%). A. Acceptable Usage 1. Acute Blood loss exceeding 30-40% of blood volume (pediatric patients - 10-15 ml/Kg) and/or not responding to appropriate volume resuscitation, and/or with ongoing blood loss. 2. Patient is normovolemic and there is evidence to support a need for increased oxygen carrying capacity by the following : a. Hypotension not corrected by adequate volume replacement alone. b. PVO2<25 torr, when SaO2 completely saturated; extraction ratio>50%, VO2<50% of baseline. c. Neonates and young infants less than 56 weeks postmenstrual age with hematocrit < 0.30 and frequent and/or severe apnea/bradycardia, poor weight gain, sustained tachycardia and/or tachypnea or mild respiratory distress. d. Neonates and young infants less than 56 weeks postmenstrual age with hematocrit < 0.35 and moderate respiratory distress or with hematocrit < 0.40 and severe respiratory distress, cyanotic congenital heart disease or receiving extracorporeal membrane oxygenation.