784 research outputs found

    The impact of deniers on epidemics: A temporal network model

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    We propose a novel network epidemic model to elucidate the impact of deniers on the spread of epidemic diseases. Specifically, we study the spread of a recurrent epidemic disease, whose progression is captured by a susceptible–infected–susceptible model, in a population partitioned into two groups: cautious individuals and deniers. Cautious individuals may adopt self-protective behaviors, possibly incentivized by information campaigns implemented by public authorities; on the contrary, deniers reject their adoption. Through a mean-field approach, we analytically derive the epidemic threshold for large-scale homogeneous networks, shedding light onto the role of deniers in shaping the course of an epidemic outbreak. Specifically, our analytical insight suggests that even a small minority of deniers may jeopardize the effort of public health authorities when the population is highly polarized. Numerical results extend our analytical findings to heterogeneous networks

    Consensus over activity-driven networks

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    The problem of self-coordination of a network of dynamical systems toward a common state is often referred to as the consensus problem. In view of its wide range of applications, the consensus problem has been extensively studied in the past few decades. However, most of the available results focus on static networks, challenging our mathematical understanding of coordination in temporal networks. In this article, we study discrete-time stochastic consensus over temporal networks, modeled as activity-driven networks. In this paradigm, each node has a specific tendency to create links in the network, measured through an activity potential. Differences in the activity potential of nodes favor the evolution of heterogeneous networks, in which some nodes are more involved in the process of information sharing than others. Through stochastic stability theory, we characterize the expected consensus state, which is found to be dominated by low-activity nodes. By further leveraging eigenvalue perturbation techniques, we derive a closed-form expression for the convergence rate in a mean-square sense, which points at a detrimental effect of moderate levels of heterogeneity for large networks. Simulations are conducted to support and illustrate our analytical findings

    Modeling memory effects in activity-driven networks

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    Activity-driven networks (ADNs) have recently emerged as a powerful paradigm to study the temporal evolution of stochastic networked systems. All the information on the time-varying nature of the system is encapsulated into a constant activity parameter, which represents the propensity to generate connections. This formulation has enabled the scientific community to perform effective analytical studies on temporal networks. However, the hypothesis that the whole dynamics of the system is summarized by constant parameters might be excessively restrictive. Empirical studies suggest that activity evolves in time, intertwined with the system evolution, causing burstiness and clustering phenomena. In this paper, we propose a novel model for temporal networks, in which a self-excitement mechanism governs the temporal evolution of the activity, linking it to the evolution of the networked system. We investigate the effect of self-excitement on the epidemic inception by comparing the epidemic threshold of a Susceptible-Infected-Susceptible model in the presence and in the absence of the self-excitement mechanism. Our results suggest that the temporal nature of the activity favors the epidemic inception. Hence, neglecting self-excitement mechanisms might lead to harmful underestimation of the risk of an epidemic outbreak. Extensive numerical simulations are presented to support and extend our analysis, exploring parameter heterogeneities and noise, transient dynamics, and immunization processes. Our results constitute a first, necessary step toward a theory of ADNs that accounts for memory effects in the network evolution

    On Assessing Control Actions for Epidemic Models on Temporal Networks

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    In this letter, we propose an epidemic model over temporal networks that explicitly encapsulates two different control actions. We develop our model within the theoretical framework of activity driven networks (ADNs), which have emerged as a valuable tool to capture the complexity of dynamical processes on networks, coevolving at a comparable time scale to the temporal network formation. Specifically, we complement a susceptible-infected-susceptible epidemic model with features that are typical of nonpharmaceutical interventions in public health policies: i) actions to promote awareness, which induce people to adopt self-protective behaviors, and ii) confinement policies to reduce the social activity of infected individuals. In the thermodynamic limit of large-scale populations, we use a mean-field approach to analytically derive the epidemic threshold, which offers viable insight to devise containment actions at the early stages of the outbreak. Through the proposed model, it is possible to devise an optimal epidemic control policy as the combination of the two strategies, arising from the solution of an optimization problem. Finally, the analytical computation of the epidemic prevalence in endemic diseases on homogeneous ADNs is used to optimally calibrate control actions toward mitigating an endemic disease. Simulations are provided to support our theoretical results

    A novel framework for community modeling and characterization in directed temporal networks

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    Abstract We deal with the problem of modeling and characterizing the community structure of complex systems. First, we propose a mathematical model for directed temporal networks based on the paradigm of activity driven networks. Many features of real-world systems are encapsulated in our model, such as hierarchical and overlapping community structures, heterogeneous attitude of nodes in behaving as sources or drains for connections, and the existence of a backbone of links that model dyadic relationships between nodes. Second, we develop a method for parameter identification of temporal networks based on the analysis of the integrated network of connections. Starting from any existing community detection algorithm, our method enriches the obtained solution by providing an in-depth characterization of the very nature of the role of nodes and communities in generating the temporal link structure. The proposed modeling and characterization framework is validated on three synthetic benchmarks and two real-world case studies

    Managing patients taking novel oral anticoagulants (NOAs) in dentistry: A discussion paper on clinical implications

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    Background The aim of this paper is to contribute to the discussion on how to approach patients taking new orally administered anticoagulants (NOAs) dabigatran etexilate (a direct thrombin inhibitor), rivaroxaban and apixaban (factor Xa inhibitors), before, during and after dental treatment in light of the more recent knowledges. Discussion In dentistry and oral surgery, the major concerns in treatment of patients taking direct thrombin inhibitors and factor Xa inhibitors is the risk of haemorrhage and the absence of a specific reversal agent. The degree of renal function, the complexity of the surgical procedure and the patient\u2019s risk of bleeding due to other concomitant causes, are the most important factors to consider during surgical dental treatment of patients taking NOAs. For patients requiring simple dental extraction or minor oral surgery procedures, interruption of NOA is not generally necessary, while an higher control of bleeding and discontinuation of the drug (at least 24 h) should be requested before invasive surgical procedures, depending on renal functionality. Summary The clinician has to consider that the number of patients taking NOAs is rapidly increasing. Since available data are not sufficient to establish an evidence-based dental management, the dentist must use caution and attention when treating patients taking dabigatran, rivaroxaban and apixaban
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