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ISBT 128 Blood Product Labeling for Transfusionists Americas Technical Advisory Group ICCBBA iccbba

ISBT 128 Blood Product Labeling for Transfusionists Americas Technical Advisory Group ICCBBA www.iccbba.org. Objectives. Describe the major differences between Codabar and ISBT 128 of blood product labels

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ISBT 128 Blood Product Labeling for Transfusionists Americas Technical Advisory Group ICCBBA iccbba

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  1. ISBT 128 Blood Product Labeling for TransfusionistsAmericas Technical Advisory GroupICCBBAwww.iccbba.org

  2. Objectives • Describe the major differences between Codabar and ISBT 128 of blood product labels • Correctly verify unit identification number, blood type, and product attributes and expiration date • List 3 advantages of ISBT 128 labeling as to the safety of blood usage

  3. Current Label

  4. New Label

  5. Differences • Black and White Only • Longer, but unique, Unit Identification Number • Product Code Includes Codes for Divisions • Expiration Date Location Changed and Time Now Included • Autologous and Directed Units May Look Different

  6. Unit Identification Number • Unit Identification number Must use entire number • W1234 06 123456 • The 00 and 1 are codes for laboratory process control E1234V00 E1234V00

  7. Product Description Product Code Includes Division Information Product Description

  8. Divided Unit Product Description • Product Code Includes Information for Divided Unit • Undivided unit is always 00 at end of the ISBT 128 Product Code • Divided Parts Are Represented by A0, B0, C0, etc. • If Part A0 is Subdivided, it would be Aa, Ab, etc.

  9. Divided Unit Product Description

  10. Expiration Date • New Location • New Format • DDMMMYYYY • Time Displayed if other than Midnight • If midnight, no time is displayed

  11. Blood Type Label • ABO/Rh Group

  12. Biohazard Autologous Label

  13. Autologous Units- Blood Types

  14. Special Testing CMV and Sickle Testing • Special Testing • Antigens • ie, K, Jka, Fya, E • CMV • Sickle

  15. Advantages of the New Labeling • Complies with new drug regulations for Barcodes and labeling of blood components effective April 26, 2006 [ 21 CFR 606.121(c)(13)(ii-iii) ] • Provides a unique unit number • Enhances patient safety • Facilitates point of care documentation of treatment when scanning barcodes • Standardizes blood labels across the world

  16. Important Note • This does not replace your institutional policies for identifying patients and blood components at the bedside • The intention of this presentation is to assist you in identifying information vital to this task

  17. Questions?

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