ArticleThe annals of applied statistics2023
BAYESIAN LEARNING OF COVID-19 VACCINE SAFETY WHILE INCORPORATING ADVERSE EVENTS ONTOLOGY.
Article in The annals of applied statistics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Mathematical modeling and mechanisms of HIV latency for personalized anti latency therapies.NPJ systems biology and applications · 2025Review
- BAYESIAN LEARNING OF COVID-19 VACCINE SAFETY WHILE INCORPORATING ADVERSE EVENTS ONTOLOGY.The annals of applied statistics · 2023Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
While vaccines are crucial to end the COVID-19 pandemic, public confidence in vaccine safety has always been vulnerable. Many statistical methods have been applied to VAERS (Vaccine Adverse Event Reporting System) database to study the safety of COVID-19 vaccines. However, none of these methods considered the adverse event (AE) ontology. AEs are naturally related; for example, events of retching, dysphagia, and reflux are all related to an abnormal digestive system. Explicitly bringing AE relationships into the model can aid in the detection of true AE signals amid the noise while reducing false positives. We propose a Bayesian graph-assisted signal selection (BGrass) model to simultaneously estimate all AEs while incorporating the network of dependence between AEs. Under a fully Bayesian inference framework, we also propose a negative control approach to mitigate the reporting bias and an enrichment approach to detecting AE groups of concern. For posterior computation we construct an equivalent model representation and develop an efficient Gibbs sampler. We evaluate the performance of BGrass via extensive simulations. To study the safety of COVID-19 vaccines, we apply BGrass to analyze approximately one million VAERS reports (01/01/2016-12/24/2021) involving more than 800 AEs. In particular, we found that blood clots (including deep vein thrombosis, thrombosis, and pulmonary embolism) are more likely to be reported after COVID-19 vaccination, compared to influenza vaccines. They are also reported more often for Johnson & Johnson-Janssen vaccine, compared to mRNA-based COVID-19 vaccines. A user-friendly R package BGrass that implements the proposed methods to assess vaccine safety is included in the Supplementary Material and is publicly available at https://github.com/BangyaoZhao/BGrass.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.