TY - JOUR
T1 - Addressing vaccine-induced immune thrombotic thrombocytopenia (Vitt) following covid-19 vaccination
T2 - A mini-review of practical strategies
AU - Chen, Po Wei
AU - Tsai, Zong Yun
AU - Chao, Ting Hsing
AU - Li, Yi Heng
AU - Hou, Charles Jia Yin
AU - Liu, Ping Yen
N1 - Funding Information:
The authors would like to thank Vercentrys for providing editing support for the manuscript. This review was supported from the Ministry of Science and Technology of Taiwan, MOST grant MOST 109-2327-B-006-005-and D110-G2512 from Higher Education Sprout Project, Ministry of Education to the Headquarters of University Advancement at National Cheng Kung University.
Publisher Copyright:
© 2021, Republic of China Society of Cardiology. All rights reserved.
PY - 2021/7
Y1 - 2021/7
N2 - In response to the COVID-19 pandemic, several vaccines were developed and rolled out at unprecedented speed, and notwithstanding this rapid pace of development, the results from initial clinical trials involving tens of thousands of adult subjects generally indicated that most vaccines were remarkably effective and safe, with no major safety warningsnoted.However,withmorethan2billionvaccinationdosesadministeredtodate,reportsofrareadverse events following immunization (AEFI) are beginning to emerge. In late February 2021, atypical thrombotic events following immunization with the adenoviral vector-based ChAdOx1 nCov-19 vaccine were first reported, and similar events have also been observed in recipients of the adenoviral vector-based Ad26.COV2.S vaccine and the mRNA based BNT162b2 and mRNA-1273 vaccines. These manifestations of atypical thrombosis and thrombocytopenia following COVID-19 vaccine immunization are now collectively referred to as vaccine-induced immune thrombotic thrombocytopenia (VITT). Although the reported incidence remains very low and does not affect the overall benefit of immunization, it is also true that if left untreated, VITT can be debilitating or even fatal. Therefore, this review seeks to provide a comprehensive overview regarding the incidence, pathogenesis, presentation, diagnosis, and treatment of VITT, as well as considerations for special populations, based on the currently available evidence in the literature. It is hoped that this will enhance awareness of this vaccine side effect, so that cases of VITT may be identified and treated in a timely and appropriate manner.
AB - In response to the COVID-19 pandemic, several vaccines were developed and rolled out at unprecedented speed, and notwithstanding this rapid pace of development, the results from initial clinical trials involving tens of thousands of adult subjects generally indicated that most vaccines were remarkably effective and safe, with no major safety warningsnoted.However,withmorethan2billionvaccinationdosesadministeredtodate,reportsofrareadverse events following immunization (AEFI) are beginning to emerge. In late February 2021, atypical thrombotic events following immunization with the adenoviral vector-based ChAdOx1 nCov-19 vaccine were first reported, and similar events have also been observed in recipients of the adenoviral vector-based Ad26.COV2.S vaccine and the mRNA based BNT162b2 and mRNA-1273 vaccines. These manifestations of atypical thrombosis and thrombocytopenia following COVID-19 vaccine immunization are now collectively referred to as vaccine-induced immune thrombotic thrombocytopenia (VITT). Although the reported incidence remains very low and does not affect the overall benefit of immunization, it is also true that if left untreated, VITT can be debilitating or even fatal. Therefore, this review seeks to provide a comprehensive overview regarding the incidence, pathogenesis, presentation, diagnosis, and treatment of VITT, as well as considerations for special populations, based on the currently available evidence in the literature. It is hoped that this will enhance awareness of this vaccine side effect, so that cases of VITT may be identified and treated in a timely and appropriate manner.
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U2 - 10.6515/ACS.202107_37(4).20210628A
DO - 10.6515/ACS.202107_37(4).20210628A
M3 - Article
AN - SCOPUS:85112412289
SN - 1011-6842
VL - 37
SP - 355
EP - 364
JO - Acta Cardiologica Sinica
JF - Acta Cardiologica Sinica
IS - 4
ER -