Outlines requirements for donor qualification, blood collection, processing, storage, and transfusion.

Current edition: 31st edition
Effective date: April 1, 2018
Revision cycle: 24 months (April of even numbered years)

Acquiring Standards

The print version, portal version and bundle package of the 31st edition of Standards for Blood Banks and Transfusion Services is available for purchase.

Standards Development

• Summary of significant changes to the 29th edition.
• Response to Comments - Standards for Blood Banks and Transfusion Services, 30th edition. For a complete look at the significant changes that have been made to the 30th edition, please refer to the Guidance within the Standards Portal.
• Response to Comments - Standards for Blood Banks and Transfusion Services, 31st edition. For a complete look at the significant changes that have been made to the 31st edition, please refer to the Guidance within the Standards Portal.
  

Outlines requirements for the donor eligibility and collection, processing, storage, and administration of any type of cellular therapy product.

Current edition: 8th edition
Effective date: July 1, 2017
Revision cycle: 24 months (July of odd numbered years)

Acquiring Standards

The print and Portal versions of the 8th edition of Standards for Cellular Therapy Services, are available for purchase on the Standards Resources webpage.

Related Information   

• Responses to Public Comments to the 8th edition of CT Standards.
  For a complete look at the significant changes that have been made to the 8th edition, please refer to the Guidance within the Standards Portal.

Outlines requirements for highly specialized laboratories that provide an essential service to patients who have specific serologic complexities and/or need rare blood components.

Current edition: 10th edition
Effective date: January 1, 2018
Revision cycle: 24 months (January of even numbered years)

Acquiring Standards

The print version, Portal versions, and bundle packages of the 10th edition of Standards for Immunohematology Reference Laboratories, are available for purchase on the Standards Resources webpage.

Standards Development

• Immunohematology Reference Laboratories – Inventory Resources, Reference Standards 2.2.A and B.
• Response to Comments Received to the 9th edition of Standards for Immunohematology Reference Laboratories.
• Response to Comments Received to the 10th edition of Standards for Immunohematology Reference Laboratories.
  For a complete look at the significant changes that have been made to the 9th edition, please refer to the Guidance within the Standards Portal.
• Errata sheet for reference standards 2.2A and 2.2B in the Standards for Immunohematology Reference Laboratories, 9th edition.

Outlines requirements for identifying and predicting red cell, platelet, and neutrophil antigens by molecular methods.

Current edition: 3rd edition
Effective date: October 1, 2016
Revision cycle: 24 months (October of even numbered years)

Acquiring Standards

The print and Standards Portal versions of the 3rd edition of Standards for Molecular Testing for Red Cell, Platelet, and Neutrophil Antigens, are available for purchase on the Standards Resources webpage.

Standards Development

• Response to Comments to the 4th edition
• Response to Comments to the 3rd edition

The Standards for Out of Hospital Transfusion Service (OHTAS Standards) was prepared by the AABB Board of Directors, AABB staff and key volunteers from AABB’s Blood Banks/Transfusion Services Standards Committee. The goal of the OHTAS Standards is to maintain and enhance the quality and safety of services provided by out of hospital transfusion services (infusion centers, long term care facilities, hospice or home care settings) and to provide a basis for the accreditation by AABB.

Current edition: 1st edition
Effective date: July 1, 2018
Revision cycle: 24 months (July of even numbered years)

Acquiring Standards

The print version, Portal versions and bundle packages of the 1st edition of Standards for Out-of-Hospital Transfusion Administrative Services is available for purchase on the Standards Resources webpage.

Outlines requirements for essential activities of a patient blood management program surrounding patient evaluation and clinical management of those who may or may not require a transfusion. Specific topics include the use of appropriate indications for transfusion, minimization of blood loss, and optimization of patient red cell mass. In recognition of the range of clinical services offered at different hospitals, the Patient Blood Management Standards Program Unit created three program activity levels (Levels 1, 2 and 3). While a small hospital’s program may perform activities described as Level 3, a hospital with a large trauma center might incorporate all activities encompassed by Level 1. The levels do not reflect a hierarchy; they simply acknowledge differences in the structure of the hospital in which the PBM program is located.

Current edition: 2nd edition
Effective date: January 1, 2018
Revision cycle: 24 months (January of even numbered years)

Acquiring Standards

The print version, Portal versions, and bundle packages of the 2nd edition of Standards for a Patient Blood Management Program, are available for purchase on the Standards Resources webpage.

Standards Development

• Response to Comments Received to the 2nd edition of Standards for Patient Blood Management.

Related Information

• The Joint Commission and AABB are now offering  Patient Blood Management Certification. 
• Learn more about AABB’s Patient Blood Management initiatives, including webinars, education modules and digital downloads.  

Outlines requirements for the delivery of perioperative services by a facility’s anesthesiologists, perfusionists, surgeons, transfusionists, and other relevant professionals.

Current edition: 7th edition
Effective date: January 1, 2017
Revision cycle: 24 months (January of odd numbered years)

Acquiring Standards

The print version of the 7th edition of Standards for Perioperative Autologous Blood Collection and Administration, is available for purchase on the Standards Resources webpage.

Standards Development

• Summary of significant changes to the 6th edition.
• Response to Comments to the 8th edition
  

Outlines requirements for laboratories performing parentage testing and complex relationship testing.

Current edition: 13th edition
Effective date: January 1, 2018
Revision cycle: 24 months (January of even numbered years)

Acquiring Standards

The print version, Portal versions, and bundle packages of the 13th edition of Standards for Relationship Testing Laboratories, are available for purchase on the Standards Resources webpage.

Standards Development

• Responses to Public Comments to the 12th edition of RT Standards are available.
  For a complete look at the significant changes that have been made to the 12th edition, please refer to the Guidance within the Standards Portal.
• Responses to Public Comments to the 13th edition of RT Standards are available.