Knowledge assessment of a donor adverse reaction severity grading tool by the National Blood Donor Vigilance Programme of India

Author:

Bisht Akanksha1,Arora Satyam2ORCID,Patidar Gopal3ORCID,Marwaha Neelam4

Affiliation:

1. Haemovigilance Programme of India (HvPI) National Institute of Biologicals, Ministry of Health and Family Welfare, Government of India Noida Uttar Pradesh India

2. Department of Transfusion Medicine Post Graduate Institute of Child Health (PGICH) Noida Uttar Pradesh India

3. Department of Transfusion Medicine All India Institute of Medical Science New Delhi India

4. Department of Transfusion Medicine Post Graduate Institute of Medical Education and Research (PGIMER) Chandigarh India

Abstract

AbstractBackground and ObjectivesThe severity grading tool (SGT) was recently designed by the Association for Advancement of Blood and Biotherapies (AABB) to have more objectivity in severity assignment for an adverse donor reaction after blood donation. A study was performed in India to assess the knowledge (post‐training) and determine the degree of agreement of the SGT between participating centres and the subject expert group.Materials and MethodsThis prospective cross‐sectional survey‐based study was conducted by the National Coordinating Centre (NCC) of the National Blood Donor Vigilance Programme (NBDVP) of India. Thirty‐five real‐world case scenarios, validated by seven national and two international experts, were sent to the participating centres, and their responses received (diagnosis and severity grade) were compared and analysed.ResultsA total of 50 blood centres participated in the study. The overall agreement between the participating centres and the expert group was 66.4%, with a fair Kendall's coefficient of concordance (W) of 0.271 (p‐value < 0.05). The degree of agreement was observed to be more than 80% for 12 centres, 60%–80% for 27 centres and <60% for 11 centres. The overall degree/percentage of agreement for cases with single and multiple types of donor adverse reaction was 71.3% and 42.6%, respectively.ConclusionThe SGT will be an efficient mode to have uniform objective reporting of the adverse donor reactions and may be implemented in the NBDVP of India. This study also highlights the need for training of the blood centres on the basic definitions and categorization of the donor's adverse reaction.

Publisher

Wiley

Subject

Hematology,General Medicine

Reference6 articles.

1. National blood donor vigilance programme of India: Analysis of donor adverse reactions reported during initial 2 years of implementation (2016 and 2017)

2. Standard for Surveillance of Complications Related to Blood Donation.ISBT working party on haemovigilance in collaboration with the International Haemovigilance Network and the AABB Donor Haemovigilance Working Group.2021. [cited 2021 Mar 3]. Available fromhttp://www.isbtweb.org/fileadmin/user_upload/Donor_Standard_Definitions_Final_2014.pdf.

3. Complications of blood donation reported to haemovigilance systems: analysis of eleven years of international surveillance

4. International validation of harmonized definitions for complications of blood donations

5. Grading Severity of Blood Donor Adverse Events Tool.User Brochure AABB.2021. [cited 2021 Mar 6]. Available fromhttps://www.aabb.org/docs/default‐source/default‐document‐library/resources/severity‐grading‐tool‐for‐donor‐adverse‐events.pdf?sfvrsn=ff563263_4.

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