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Transfus Apher Sci. 2013 Feb;48(1):95-102. doi: 10.1016/j.transci.2012.07.008. Epub 2012 Sep 3.

Online reporting system for transfusion-related adverse events to enhance recipient haemovigilance in Japan: a pilot study.

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  • 1Department of Safety Research on Blood and Biological Products, National Institute of Infectious Diseases, Tokyo, Japan.

Abstract

BACKGROUND:

A surveillance system for transfusion-related adverse reactions and infectious diseases in Japan was started at a national level in 1993, but current reporting of events in recipients is performed on a voluntary basis. A reporting system which can collect information on all transfusion-related events in recipients is required in Japan.

METHODS:

We have developed an online reporting system for transfusion-related events and performed a pilot study in 12 hospitals from 2007 to 2010.

RESULTS:

The overall incidence of adverse events per transfusion bag was 1.47%. Platelet concentrates gave rise to statistically more adverse events (4.16%) than red blood cells (0.66%) and fresh-frozen plasma (0.93%). In addition, we found that the incidence of adverse events varied between hospitals according to their size and patient characteristics.

CONCLUSION:

This online reporting system is useful for collection and analysis of actual adverse events in recipients of blood transfusions and may contribute to enhancement of the existing surveillance system for recipients in Japan.

Copyright © 2012. Published by Elsevier Ltd.

PMID:
22954634
[PubMed - indexed for MEDLINE]
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