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Donor Hemovigilance

AABB's donor hemovigilance efforts focus primarily on education, collaboration with other international organizations, and projects undertaken by the AABB Donor Hemovigilance Working Group. Donor hemovigilance resources can be found at the links below.

Donor Severity Validation Study – Participants Needed

In January 2018, a sub-group of the AABB Donor Hemovigilance Working Group undertook the task of developing the Donor Adverse Reaction Severity Grading Tool to enhance objective assignment of severity. The severity assignment tool is designed to be used with the Standard for Surveillance of Complications Related to Blood Donation by ISBT/AABB/IHN. The tool aims to avoid terms such as mild, moderate and severe that could set a blood collector up for legal action if a donor has an adverse event that is considered "severe." It is patterned after an established clinical severity scale, Common Terminology Criteria for Adverse Events (CTCAE1) v 5.0, which rates severity by Grades 1-5 with 1 through 5 being roughly associated with mild, moderate, severe, life-threatening and death.

A validation study to assess the validity of the proposed blood donor adverse event grading tool for hemovigilance surveillance purpose is being conducted through February 28, 2019. Participants will classify the severity grading of the 32 donor adverse reaction case reports provided in the study utilizing 2014 Standard for Surveillance of Complications Related to Blood Donation together with the associated Donor Adverse Reaction Severity Grading Tool. To participate in the study please complete the survey at the link provided below by February 28, 2019:

Participate in the Study 


Resources

AABB Donor Hemovigilance Reports

Questions? Contact Hemovigilance@aabb.org or +1.301.215.6588.