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Adverse reactions following transfusion of blood components, with a focus on some rare reactions: Reports to the International Haemovigilance Network Database (ISTARE) in 2012–2016 - 18/08/22

Doi : 10.1016/j.tracli.2022.03.005 
C. Politis a, , J. Wiersum-Osselton b, C. Richardson c, E. Grouzi d, I. Sandid e, G. Marano f, N. Goto g, J. Condeço h, K. Boudjedir e, M. Asariotou a, L. Politi i, K. Land j
a Coordinating Centre for Haemovigilance and Surveillance of Transfusion, Hellenic National Public Health Organization, Attika, Greece 
b TRIP Hemovigilance and Biovigilance Office, Leiden, The Netherlands 
c Panteion University of Social and Political Sciences, Athens, Greece 
d Transfusion Service and Clinical Hemostasis, Saint Savvas Oncology Hospital of Athens, Athens, Greece 
e French National Agency for Medicines and Health Products Safety (ANSM), France 
f National Blood Centre, Instituto Superiore di Sanita, Rome, Italy 
g Safety Vigilance Division, Technical Department, Blood Service Headquarters, Japanese Red Cross Society, Tokyo, Japan 
h Transplantacao, Instituto Portugues do Sangue e da Transplantacao, Port, Portugal 
i Directorate of Surveillance and Prevention of Infectious Diseases, Hellenic National Public Health Organization 
j Clinical Services at Vitalant San Antonio, Texas, United States 

Corresponding author. Coordinating Centre for Haemovigilance and Surveillance of Transfusion, Hellenic National Public Health Organization, Agrafon 3-5, 15123 Attika, Greece.Coordinating Centre for Haemovigilance and Surveillance of Transfusion, Hellenic National Public Health Organization, Agrafon 3-5Attika15123Greece

Abstract

Objectives

The International Haemovigilance Network's (IHN) ISTARE database collects surveillance data on all adverse reactions (AR) associated with transfusion of blood and blood components, facilitating the sharing of best practice and benchmarking for improving blood safety and quality. Up to 2012, no publications discussed certain rare AR. The aim of this study is to examine ISTARE data on AR from 2012 to 2016, focusing on hypotensive reactions, post-transfusion purpura (PTP), transfusion-associated graft versus host disease (TA-GvHD), hyperkalemia and hypocalcemia.

Materials and methods

National Haemovigilance Systems (HVS), provided aggregate annual data on AR by type of reaction, severity, imputability to transfusion, and blood component implicated. Twenty-nine HVS provided 104 annual reports covering 107,778,290 blood units issued.

Results

Among AR reported, 25% were serious, including 368 deaths. The 284 transfusion-transmitted infections included 187 bacterial infections, 84 viral and 13 parasitic or fungal; nine deaths resulted. AR related to the respiratory system transfusion-associated circulatory overload, transfusion-related acute lung injury and transfusion-associated dyspnoea accounted for 8.3% of all AR, 20.1% of serious, and 52.2% of deaths. Of 1634 rare AR, 1565 were hypotensive, 38 PTP, 17 GvHD, 9 hyperkalemia and 5 hypercalcemia. Half were serious and 16 fatalities were recorded (13 hypotensive, 2 GvHD, one PTP). Among 14 countries that reported any hypotensive AR, incidences diverged widely.

Conclusions

ARs in this group are frequently severe or life-threatening. Hypotensive AR are the most common, but may have been overlooked and counted under allergic and other AR presenting with hypotension. Compliance with the ISBT definition may be suboptimal, thus its real incidence may be higher. Data on GvHD may contribute to clarifying the role of leukodepletion with or without irradiation. ISTARE continues to be a useful surveillance tool for all transfusion AR and provides relevant insights into overlooked and rare AR, thus offering important contributions towards maximising transfusion safety.

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Keywords : Haemovigilance, Adverse reactions, Surveillance, Transfusion, Benchmarking


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© 2022  Société française de transfusion sanguine (SFTS). Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 29 - N° 3

P. 243-249 - août 2022 Retour au numéro
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