COMMONLY REQUESTED INFORMATION
SAMPLE COLLECTION PROCESS
Note: Delay of service may result from the omission of required information on the patient’s specimen label or specimen. Patients having Blood Bank testing with the possibility of receiving a transfusion must have a properly labeled (patient’s name and date of birth) Blood Bank wristband placed on them prior to the venipuncture. The Blood Bank wristband has a unique barcode with specific letters/numbers for patient/specimen identification. This special BBID wristband has extra barcode stickers for future use. One of these unique barcode stickers from the BBID wristband MUST be placed on the specimen label after collection. Specimens with handwritten information and/or BBID wristbands that are handwritten MUST be accompanied by a Certification Form or they will be rejected by the Blood Bank.
TRANSFUSION SERVICE ORDERS
TRANSFUSION SERVICE REQUESTS
SPECIAL SERVICES
Adams Infusion Center (717) 339-2666, located at 40 V-Twin Drive in Gettysburg. Exceptions are weekends, holidays, weekdays after 5:00 p.m. or urgent transfusions. In these cases, a call should be placed to the WellSpan Gettysburg Hospital Blood Bank for assistance (717) 339-2317.
Apple Hill Infusion Center (717) 741-8637, located at the Apple Hill Medical Center, Suite #120. The Apple Hill Infusion Center also schedules transfusions for the York Hospital (YH) 5 Main Infusion room. Exceptions are weekends, holidays, weekdays after 5:00 p.m. or urgent transfusions. In these cases, a call should be placed to the YH 5 Main Infusion room for assistance (717) 851-4070. If assistance is needed after hours and you are unable to reach the 5 Main infusion room, a call should be made to the nursing station on 7 South (717) 851-2625.
Ephrata Cancer Center (717) 721-4840, located at 460 N. Reading Road in Ephrata.
The GSH Blood Donor Center is located at 750 Norman Drive, Lebanon, and can be reached at 270-8960. To make a donation, drop in during the hours shown below, or schedule an appointment by calling the Donor Center.
Blood Donor HoursFriday: 7:00 am to 2:00 pm
Both outpatient facilities must be advised if the patient currently has or has ever had MRSA or VRE.
Pre-transfusion testing should be done the day before the scheduled transfusion. It may take longer to get the blood ready for patients with a history of an antibody, so drawing the sample in advance will provide the best customer service.
These are referral tests that will be sent to the American Red Cross (ARC) or Grifols Reference Laboratory. Call the Blood Bank at (717) 851-2520 for special instructions and requirements.
SPECIAL PRODUCT REQUESTS
ADMINISTRATION OF BLOOD COMPONENTS
Component/Products and Their Indication
Testing Requirements | Component/ Product | Composition | Indications | Turn-Around Time |
Product-Order RBCs | Red Blood Cells* | RBC (approx Hct 75%); reduced plasma; WBCs; plasma | Increase red cell mass in symptomatic anemia | Crossmatched: < 45 minutes; Uncrossmatched: 15 minutes. |
Red Blood Cells* -Leukocytes reduced, prepared by filtration. | >85% of the original volume of RBC; <5x106 WBC; few platelets and minimal plasma | Increase red cell mass in symptomatic anemia; <5x106 WBC to decrease the likelihood of febrile reactions; immunization to leukocytes (HLA Ags) or CMV transmission. | ||
Red Blood Cells -Washed | RBC (approx Hct 75%); <5x108 WBC; no plasma | Increase red cell mass in symptomatic anemia; reduce risk of allergic reaction to plasma proteins. | Requires an additional 45 minutes for washing the unit. | |
Type & Rh | Platelets* | Platelets (>5.5x1010/unit); RBC’s; WBC; plasma | Bleeding due to thrombo-cytopenia or thrombo-cytopathy | Distributed as a pre-pooled platelet pool; 15 minutes. |
Platelet Pheresis* | Platelets (>3.0x1011/unit); RBC’s; WBC; plasma | Bleeding due to thrombo-cytopenia or thrombo-cytopathy | 15-20 minutes. Reservations preferred. | |
Fresh Frozen Plasma | Source of non-labile factors | Treatment of some coagulation disorders | 1-3 units/30 minutes; >4 units/45 minutes. | |
Cryoprecipitate AHF | Fibrinogen, Factors VIII & XIII; Von Willebrand Factor | Deficiency in Fibrinogen, Factor XIII, Second choice in treatment of Hemophilia A, Von Willebrand Disease; can be used to make topical Fibrin Glue. | Distributed as a 5-6 unit pre-pooled cryoprecipitate pool. 30 minutes | |
Type & Antibody Screen | Rh Immune Globulin (RIG) | IgG Anti-D; Preparations of IM use | Prevention of Hemolytic Disease of the Newborn due to the D antigen; prevention of alloimmunization of Anti-D in an Rh negative patient who receives Rh positive red cell products. | 1 vial/45 minutes |
*These products can be requested as irradiated. Irradiation of the product with 25 Gy should be used to reduce the risk of Transfusion Associated-Graft versus Host Disease (TA-GVHD) in susceptible patients such as; immuno compromised recipients (Hematopoietic Progenitor Transplant patients, Congenital Immune Deficiency), a fetus receiving transfusions, recipients of donor units from relatives, recipients of HLA-matched platelets, etc.
Management of Transfusion Reactions
send as much information as you can – all vital signs related to each transfusion (if using downtime procedure, send a copy of the completed Blood Issue Forms), and each blood bag/administration set(s) from each transfusion(s).
TRANSFUSION REACTION INFORMATION
Assessment: |
Description: |
Usual Cause: |
Recommendation: |
Allergic Transfusion Reaction Mild-Moderate |
Any of: Hives, itching, wheezing, throat tightening, hypotension. |
Antibodies to plasma proteins (fairly common). |
Recommend pretreatment with an antihistamine such as diphenhydramine. Consider combined H1 and H2 blocker pretreatment or steroids for recurrent allergic reactions. Administer blood slowly, with nursing supervision. |
Allergic Transfusion Reaction Severe |
Anaphylaxis, anaphylactoid shock or laryngeal edema requiring intubation and/or epinephrine administration. |
Antibodies to plasma proteins (fairly common). Antibodies to IgA in IgA deficient individuals (rare). |
Recommend administering washed RBC’s and pretreating with antihistamines and steroids prior to transfusions. Administer blood products slowly, under close nursing supervision. Consider testing the patient’s (pretransfusion) IgA level. |
Hypotensive Transfusion Reaction |
Hypotension, tachycardia, facial flushing, and abdominal pain. |
Bradykinin generation, may be exacerbated by ACE inhibitors. |
Recommend using pre-storage leuko-reduced products, and giving future transfusions slowly with close nursing supervision. Stop the transfusion immediately during a hypotensive episode, place patient in the Trendelenburg position, and administer fluids. |
Unrelated (Patient's symptoms are unrelated to the transfusion) |
Any. May mimic a true transfusion reaction. Always is appropriate for the nurse to stop the transfusion and initiate a work-up. |
Underlying disease process of patient / side effect of medication. Commonly: Neutropenia, infection, cardiac failure. |
No specific recommendations at this time. |
Febrile Non-hemolytic Transfusion Reaction |
Within 2 hours of transfusion: Fever (temperature increase of 1 ºC or 1.8 ºF), chills, shakes, rigors. |
Antibodies to leukocytes, platelets or plasma proteins stimulate endogenous pyogen release; passive cytokine infusion. Case is complicated by other reasons for fever (neutropenia or infection). |
Recommend administering leukoreduced blood components and pretreating with an antipyretic such as acetaminophen. |
Possible Febrile Non-hemolytic Transfusion Reaction |
Within 2 hours of transfusion: Fever (temperature increase of 1 ºC or 1.8 ºF), chills, shakes, rigors. |
Antibodies to leuko-cytes, platelets or plasma proteins stimulate endogenous pyogen release; passive cytokine infusion. Case is complicated by other reasons for fever (neutropenia or infection). |
Consider administering leukoreduced blood components and pretreating with an antipyretic such as acetaminophen. |
Probable Febrile Non-hemolytic Transfusion Reaction |
Within 2 hours of transfusion: Fever (temperature increase of 1 ºC or 1.8 ºF), chills, shakes, rigors. |
Antibodies to leukocytes or plasma proteins; passive cytokine infusion. Case is complicated by other reasons for fever (neutropenia or infection). |
Recommend administering leukoreduced blood components and pretreating with an antipyretic such as acetaminophen. |
Possible Septic Transfusion Reaction, Pending Cultures |
Fever (usually a rise ≥ 2 ºC or 3.6 ºF or a rapid increase in temperature), rigors, chills, shock, potential death. May develop quickly or several hours after transfusion. Culture transfusion bag AND patient; compare results to confirm. If clinicians culture the patient, culture the bag. If clinicians refuse to culture the patient, do NOT culture the bag. Associated products should be recalled. |
Contaminated blood product, usually donor venipuncture site contamination or occult bacteremia. Skin flora contaminants: Staph, Propionibacteria. Gram Negative's implicated in clinical reactions and capable of causing death: Acinetobacter, Klebsiellla, Serratia, Enterobacter, Escherichia. Less common, Gram Positive Cocci implicated in clinical reactions:Staphylococcus, Streptococcus. Likes to grow in RBCs: Yersina, Pseudomonas |
Provide supportive care and appropriate antibiotic coverage. Follow patient's blood cultures. |
Septic Transfusion Reaction |
Provide supportive care and appropriate antibiotic coverage. Follow patient's blood cultures. |
Transfusion Related Acute Lung Injury (TRALI) |
Within 6 hours of transfusion: Dyspnea, fever, hypoxia, pulmonary edema, hypotension, normal pulmonary capillary wedge pressure. "White-out" on post-transfusion chest x-ray. May require intubation. Differential diagnosis: Volume Overload. For TRALI: BNP should remain normal, no left atrial hypertension, non-responsive to diuresis. |
Recipient-specific donor HLA or anti-neutrophil antibodies in the plasma component of a transfusion. Other theory - neutrophil priming lipid mediator. Less commonly, recipient antibody to donor WBCs. |
Provide respiratory and blood pressure supportive care. TRALI reaction is donor specific, and therefore, the patient is at no increased risk during future transfusions if needed. However, we recommend administering leuko-reduced blood components and pretreating with an antipyretic, such as acetaminophen, and an antihistamine, such as diphenhydramine, to reduce the risk for febrile or allergic reactions. |
Possible Transfusion Related Acute Lung Injury (TRALI) |
Within 6 hours of transfusion: Dyspnea, fever, hypoxia, pulmonary edema, hypo-tension, normal pulmonary capillary wedge pressure. Post-transfusion chest x-ray shows edema or infiltrates. Patient has complicating factors: myocardial infarction, cardiac failure, volume overload. |
Recipient-specific donor HLA or anti-neutrophil antibodies in the plasma component of a trans-fusion. Other theory - neutrophil priming lipid mediator. Less commonly, recipient antibody to donor WBCs. |
Provide respiratory and blood pressure supportive care. TRALI reaction is donor specific, and therefore, the patient is at no increased risk during future transfusions if needed. However, we recommend administering leukoreduced blood components and pretreating with an antipyretic, such as acetaminophen, and an antihistamine, such as diphen-hydramine, to reduce the risk for febrile or allergic reactions. |
Hypervolemia “TACO” (Transfusion Associated Circulatory Overload) |
Dysnpea, headache, hyper-tension (>50 mmHg rise), pulmonary edema, congestive heart failure, cardiac arrhythmias. Severe cases: Flash pulmonary edema. Responds to diuresis. |
Too rapid and/or excessive fluid and/or blood administration. Check volumes of blood and fluid given prior to "reaction" |
Induce diuresis. Provide cardio-respiratory support as clinically indicated. If future transfusion is necessary, proceed slowly, or in divided doses (call blood bank to have units divided). |
Acute Hyperhemolytic Transfusion Reaction |
Hemoglobinemia (red serum), hemoglobinuria (red urine - not due to RBCs), fever, chills, anxiety, shock, DIC, dyspnea, chest pain, flank pain, oliguria. HCT drops significantly lower than pretransfusion levels. |
Rare - usually seen in chronically transfused hemoglobinopathy patients, with multiple alloantibodies (esp. beta thalassemia, sickle cell disease) |
Do not transfuseadditional blood products. Provide supportive care, including fluid administration and diuresis, blood pressure and respiratory support. Monitor the patient for DIC and shock. |
Acute (Intravascular) Hemolytic Transfusion Reaction |
Hemoglobinemia (red serum), hemoglobinuria (red urine - not due to RBCs), fever, chills, anxiety, shock, DIC, dyspnea, chest pain, flank pain, acute renal failure, cardiac arrest. HCT will drop to Pretrans-fusion levels. Monitor HCT, LDH, bilirubin, haptoglobin levels, BUN, Creatinine, platelets and coags. Repeat compatibility testing. |
ABO incompatibility (clerical error) or unknown/missed red blood cell alloantibody or other complement fixing red cell antibody. |
Do not transfuse additional blood products, until blood bank work up is completed. Provide supportive care, including fluid administration and diuresis, blood pressure and respiratory support. Monitor the patient for DIC and shock. |
Mild (Extravascular) Delayed Hemolytic Transfusion Reaction |
Asymptomatic. May see gradual HCT drop to pre-transfusion levels. May see positive DAT, increased LDH, indirect bilirubin. |
IgG non-complement fixing antibody (often Rh or Kell). Coated RBC's are cleared by reticulo-endothelial system (especially spleen). Time course: Reaction within days: anamnestic response; Reaction after 3 weeks - new antibody |
Monitor the patient's hematocrit, renal and hepatic function, coagulation profile. Acute treatment is generally not required. Because of antibody formation, future antibody screens and cross-matches may take additional time. |
Severe (Extravascular) Delayed Hemolytic Transfusion Reaction |
Fever, malaise, indirect hyperbilirubinemia, increased LDH, urine urobilinogen, falling HCT. DAT may be negative, if all coated RBCs are cleared. |
IgG non-complement fixing antibody (often Rh or Kell). Coated RBC's are cleared by reticulo-endothelial system (especially spleen). Time course: Reaction within days: anamnestic response; Reaction after 3 weeks - new antibody |
Monitor the patient's hematocrit, renal and hepatic function, coagulation profile, and provide supportive care if necessary. Because of antibody formation, future antibody screens and crossmatches may take additional time. |
TRANSMISSION OF INFECTIOUS DISEASES