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Both individually and cluster randomized study designs have been used for vaccine trials to assess the effects of vaccine on reducing the risk of disease or infection. The choice between individually and cluster randomized designs is often driven by the target estimand of interest (eg, direct versus total), statistical power, and, importantly, logistic feasibility. To combat emerging infectious disease threats, especially when the number of events from one single trial may not be adequate to obtain vaccine effect estimates with a desired level of precision, it may be necessary to combine information across multiple trials. In this article, we propose a model formulation to estimate the direct, indirect, total, and overall vaccine effects combining data from trials with two types of study designs: individual‐randomization and cluster‐randomization, based on a Cox proportional hazards model, where the hazard of infection depends on both vaccine status of the individual as well as the vaccine status of the other individuals in the same cluster. We illustrate the use of the proposed model and assess the potential efficiency gain from combining data from multiple trials, compared to using data from each individual trial alone, through two simulation studies, one of which is designed based on a cholera vaccine trial previously carried out in Matlab, Bangladesh. [ABSTRACT FROM AUTHOR]

The COVID-19 epidemic has required countries to implement different containment strategies to limit its spread, like strict or weakened national lockdown rules and the application of age-stratified vaccine prioritization strategies. These interventions have in turn modified the age-dependent patterns of social contacts. In our recent paper, starting from the available age-structured real data at the national level, we identified, for the Italian case, specific virulence parameters for a two-age-structured COVID-19 epidemic compartmental model (under 60, and 60 years and over) in six different diseases transmission scenarios under concurrently adopted feedback interventions. An interpretation of how each external scenario modifies the age-dependent patterns of social contacts and the spread of COVID-19 disease has been accordingly provided. In this paper, which can be viewed as a sequel to the previous one, we mainly apply the same general methodology therein (involving the same dynamic model) to new data covering the three subsequent additional scenarios: (i) a mitigated coordinated intermittent regional action in conjunction with the II vaccination phase; (ii) a super-attenuated coordinated intermittent regional action in conjunction with the II vaccination phase; and (iii) a last step towards normality in conjunction with the start of the III vaccination phase. As a new contribution, we show how meaningful updated information can be drawn out, once the identification of virulence parameters, characterizing the two age groups within the latest three different phases, is successfully carried out. Nevertheless, differently from our previous paper, the global optimization procedure is carried out here with the number of susceptible individuals in each scenario being left free to change, to account for reinfection and immunity due to vaccination. Not only do the slightly different estimates we obtain for the previous scenarios not impact any of the previous considerations (and thus illustrate the robustness of the procedure), but also, and mainly, the new results provide a meaningful picture of the evolution of social behaviors, along with the goodness of strategic interventions. [ABSTRACT FROM AUTHOR]

BACKGROUND: Pfizer-BioNTech vaccine was one of the first vaccines developed for COVID-19 to be used in Iraq. While the benefits of the vaccine outweigh the risks, potential side effects remain major concerns for people and can increase vaccine hesitancy despite usually being short-lasting and mild. This study aimed to evaluate the side effects of Pfizer -BioNTech vaccination among vaccinated adults in Erbil city, Iraq. METHODS: A cross-sectional study was carried out with a convenience sample of 401 subjects who received the Pfizer vaccine in nine public healthcare centres in Erbil, Iraq, on February 20th, 2022, and April 17th 2022. Data were collected through interviews with the patients using a questionnaire designed by the researchers. A p-value = 0.05 was considered statistically significant. RESULTS: The prevalence of side effects was 84.4%. Among participants who experienced side effects, the most common was pain at the injection site (93.1% for the first dose and 88% for the second dose). For the first dose, the onset of side effects on the vaccination day (day zero) was reported by 78.9% of those experiencing side effects, and the duration was one day for 45.4% of participants. Severity was rated as mild by 54.3%, and similar results were found for the second dose. Analgesics were used following the first dose by 47% of participants, which resulted in good relief for 96.6% of patients using them, and similar results were found for the second dose. CONCLUSIONS: Most participants who received the Pfizer-BioNTech vaccine experienced side effects, the most common of which was pain at the injection site, which was reported for both the first and second doses. [ABSTRACT FROM AUTHOR]

The COVID-19 epidemic has required countries to implement different containment strategies to limit its spread, like strict or weakened national lockdown rules and the application of age-stratified vaccine prioritization strategies. These interventions have in turn modified the age-dependent patterns of social contacts. In our recent paper, starting from the available age-structured real data at the national level, we identified, for the Italian case, specific virulence parameters for a two-age-structured COVID-19 epidemic compartmental model (under 60, and 60 years and over) in six different diseases transmission scenarios under concurrently adopted feedback interventions. An interpretation of how each external scenario modifies the age-dependent patterns of social contacts and the spread of COVID-19 disease has been accordingly provided. In this paper, which can be viewed as a sequel to the previous one, we mainly apply the same general methodology therein (involving the same dynamic model) to new data covering the three subsequent additional scenarios: (i) a mitigated coordinated intermittent regional action in conjunction with the II vaccination phase; (ii) a super-attenuated coordinated intermittent regional action in conjunction with the II vaccination phase; and (iii) a last step towards normality in conjunction with the start of the III vaccination phase. As a new contribution, we show how meaningful updated information can be drawn out, once the identification of virulence parameters, characterizing the two age groups within the latest three different phases, is successfully carried out. Nevertheless, differently from our previous paper, the global optimization procedure is carried out here with the number of susceptible individuals in each scenario being left free to change, to account for reinfection and immunity due to vaccination. Not only do the slightly different estimates we obtain for the previous scenarios not impact any of the previous considerations (and thus illustrate the robustness of the procedure), but also, and mainly, the new results provide a meaningful picture of the evolution of social behaviors, along with the goodness of strategic interventions.

Results from randomized controlled trials (RCTs) help determine vaccination strategies and related public health policies. However, defining and identifying estimands that can guide policies in infectious disease settings is difficult, even in an RCT. The effects of vaccination critically depend on characteristics of the population of interest, such as the prevalence of infection, the number of vaccinated, and social behaviors. To mitigate the dependence on such characteristics, estimands, and study designs, that require conditioning or intervening on exposure to the infectious agent have been advocated. But a fundamental problem for both RCTs and observational studies is that exposure status is often unavailable or difficult to measure, which has made it impossible to apply existing methodology to study vaccine effects that account for exposure status. In this study, we present new results on this type of vaccine effects. Under plausible conditions, we show that point identification of certain relative effects is possible even when the exposure status is unknown. Furthermore, we derive sharp bounds on the corresponding absolute effects. We apply these results to estimate the effects of the ChAdOx1 nCoV-19 vaccine on SARS-CoV-2 disease (COVID-19) conditional on postvaccine exposure to the virus, using data from a large RCT. [ABSTRACT FROM AUTHOR]

To estimate causal effects of vaccine on post-infection outcomes, Hudgens and Halloran (2006) defined a post-infection causal vaccine efficacy estimand VEI based on the principal stratification framework. They also derived closed forms for the maximum likelihood estimators of the causal estimand under some assumptions. Extending their research, we propose a Bayesian approach to estimating the causal vaccine effects on binary post-infection outcomes. The identifiability of the causal vaccine effect VEI is discussed under different assumptions on selection bias. The performance of the proposed Bayesian method is compared with the maximum likelihood method through simulation studies and two case studies - a clinical trial of a rotavirus vaccine candidate and a field study of pertussis vaccination. For both case studies, the Bayesian approach provided similar inference as the frequentist analysis. However, simulation studies with small sample sizes suggest that the Bayesian approach provides smaller bias and shorter confidence interval length. [ABSTRACT FROM AUTHOR]

Highlights: [•] We explore the population impact of partially effective dengue vaccines (PEV). [•] We consider scenarios of heterogeneity between serotypes. [•] We use an age-stratified compartmental dengue transmission model. [•] We show that PEV could be important tools for dengue control. [•] We examine direct vs. indirect effects of vaccination. [ABSTRACT FROM AUTHOR]