Thrombosis patterns and clinical outcome of COVID-19 vaccine-induced immune thrombotic thrombocytopenia: A Systematic Review and Meta-Analysis

•The incidence of COVID-19 vaccine-related venous thrombosis was 28 per 100,000 doses•Common sites of thrombosis: cerebral vein (54%), deep vein/pulmonary thromboembolism (36%), splanchnic vein (19%)•Thrombosis after COVID-19 vaccination occurred more in women and in those aged <50•The pooled ant...

Full description

Saved in:
Bibliographic Details
Published inInternational journal of infectious diseases Vol. 119; pp. 130 - 139
Main Authors Kim, Ah Young, Woo, Wongi, Yon, Dong Keon, Lee, Seung Won, Yang, Jae Won, Kim, Ji Hong, Park, Seoyeon, Koyanagi, Ai, Kim, Min Seo, Lee, Sungsoo, Shin, Jae Il, Smith, Lee
Format Journal Article
LanguageEnglish
Published Canada Elsevier Ltd 01.06.2022
The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases
Elsevier
Subjects
Online AccessGet full text
ISSN1201-9712
1878-3511
1878-3511
DOI10.1016/j.ijid.2022.03.034

Cover

Loading…
More Information
Summary:•The incidence of COVID-19 vaccine-related venous thrombosis was 28 per 100,000 doses•Common sites of thrombosis: cerebral vein (54%), deep vein/pulmonary thromboembolism (36%), splanchnic vein (19%)•Thrombosis after COVID-19 vaccination occurred more in women and in those aged <50•The pooled antiplatelet factor 4 antibody positivity rate was 91%•Without the benefit of non-heparin anticoagulation, the mortality rate was 32% To meta-analyse the clinical manifestations, diagnosis, treatment, and mortality of vaccine-induced immune thrombotic thrombocytopenia (VITT) after adenoviral vector vaccination. Eighteen studies of VITT after ChAdOx1 nCoV-19 or Ad26.COV2.S vaccine administration were reviewed from PubMed, Scopus, Embase, and Web of Science. The meta-analysis estimated the summary effects and between-study heterogeneity regarding the incidence, manifestations, sites of thrombosis, diagnostic findings, and clinical outcomes. The incidence of total venous thrombosis after ChAdOx1 nCoV-19 vaccination was 28 (95% CI 12-52, I2=100%) per 100,000 doses administered. Of 664 patients included in the quantitative analysis (10 studies), the mean age of patients with VITT was 45.6 years (95% CI 43.8-47.4, I2=57%), with a female predominance (70%). Cerebral venous thrombosis (CVT), deep vein thrombosis (DVT)/pulmonary thromboembolism (PE), and splanchnic vein thrombosis occurred in 54%, 36%, and 19% of patients with VITT, respectively. The pooled incidence rate of CVT after ChAdOx1 nCoV-19 vaccination (23 per 100,000 person-years) was higher than that reported in the pre-pandemic general population (0.9 per 100,000 person-years). Intracranial haemorrhage and extracranial thrombosis accompanied 47% and 33% of all patients with CVT, respectively. The antiplatelet factor 4 antibody positivity rate was 91% (95% CI 88-94, I2=0%) and the overall mortality was 32% (95% CI 24-41, I2=69%), and no significant difference was observed between heparin- and non-heparin-based anticoagulation treatments (risk ratio 0.84, 95% CI 0.47-1.50, I2=0%). Patients with VITT after SARS-CoV-2 vaccination most frequently presented with CVT following DVT/PE and splanchnic vein thrombosis, and about one-third of patients had a fatal outcome. This meta-analysis should provide a better understanding of VITT and assist clinicians in identifying VITT early to improve outcomes and optimise management. [Display omitted]
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Undefined-3
Co-first authors.
ISSN:1201-9712
1878-3511
1878-3511
DOI:10.1016/j.ijid.2022.03.034