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Complete the associated blood transfusion form: Include all relevant patient details (e.g. name, date of birth, unique identification number). Document any special requirements for blood transfusion (e.g. CMV-negative blood or irradiated blood). Document the number of units of blood required if a crossmatch is needed.
Although the health-care provider making the decision to transfuse is usually responsible for carrying out the process of informing the patient and obtaining consent, this task may be delegated to a member of the health-care team who is working on behalf of that health-care provider, such as a nurse practitioner or a
Fresh whole blood has always been thought of as the standard for transfusion; however, medical advancement has allowed the efficient use of the different components, such as packed red blood cells (PRBCs), individual factor concentrates, fresh frozen plasma (FFP), platelet concentrates, and cryoprecipitate.
Before administering the transfusion, document that you matched the label on the blood bag to the patients name, patients medical record number, patients blood ABO group and Rh factor, donors blood ABO group and Rh factor, crossmatch data, blood bank ID number, and expiration date of the product.
Informed consent should be obtained prior to all blood and blood product transfusions, except in emergency situations. Informed consent for blood transfusion is a requirement of The Joint Commission as well as AABB (formerly the American Association of Blood Banks).
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Someone could also give non-verbal consent, as long as they understand the treatment or examination about to take place for example, holding out an arm for a blood test. Consent should be given to the healthcare professional responsible for the persons treatment. This could be a: nurse arranging a blood test.
Valid consent for blood transfusion should be obtained and documented in the patients clinical record by the healthcare professional.
Before administering the transfusion, document that you matched the label on the blood bag to the patients name, patients medical record number, patients blood ABO group and Rh factor, donors blood ABO group and Rh factor, crossmatch data, blood bank ID number, and expiration date of the product.

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