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1.
Epidemiol Prev ; 44(5-6 Suppl 2): 297-306, 2020.
Article in English | MEDLINE | ID: covidwho-2252225

ABSTRACT

BACKGROUND: the first confirmed cases of COVID-19 in WHO European Region was reported at the end of January 2020 and, from that moment, the epidemic has been speeding up and rapidly spreading across Europe. The health, social, and economic consequences of the pandemic are difficult to evaluate, since there are many scientific uncertainties and unknowns. OBJECTIVES: the main focus of this paper is on statistical methods for profiling municipalities by excess mortality, directly or indirectly caused by COVID-19. METHODS: the use of excess mortality for all causes has been advocated as a measure of impact less vulnerable to biases. In this paper, observed mortality for all causes at municipality level in Italy in the period January-April 2020 was compared to the mortality observed in the corresponding period in the previous 5 years (2015-2019). Mortality data were made available by the Ministry of Internal Affairs Italian National Resident Population Demographic Archive and the Italian National Institute of Statistics (Istat). For each municipality, the posterior predictive distribution under a hierarchical null model was obtained. From the posterior predictive distribution, we obtained excess death counts, attributable community rates and q-values. Full Bayesian models implemented via MCMC simulations were used. RESULTS: absolute number of excess deaths highlights the burden paid by major cities to the pandemic. The Attributable Community Rate provides a detailed picture of the spread of the pandemic among the municipalities of Lombardy, Piedmont, and Emilia-Romagna Regions. Using Q-values, it is clearly recognizable evidence of an excess of mortality from late February to April 2020 in a very geographically scattered number of municipalities. A trade-off between false discoveries and false non-discoveries shows the different values of public health actions. CONCLUSIONS: despite the variety of approaches to calculate excess mortality, this study provides an original methodological approach to profile municipalities with excess deaths accounting for spatial and temporal uncertainty.


Subject(s)
COVID-19/epidemiology , Models, Theoretical , Mortality/trends , Pandemics , SARS-CoV-2 , Urban Population/statistics & numerical data , Adolescent , Adult , Aged , Aged, 80 and over , Bayes Theorem , COVID-19/mortality , Cities , Female , Geography, Medical , Humans , Italy/epidemiology , Male , Middle Aged , Risk , Young Adult
2.
Annals of Data Science ; 2023.
Article in English | Scopus | ID: covidwho-2231676

ABSTRACT

This research aimed to investigate the spatial autocorrelation and heterogeneity throughout Bangladesh's 64 districts. Moran I and Geary C are used to measure spatial autocorrelation. Different conventional models, such as Poisson-Gamma and Poisson-Lognormal, and spatial models, such as Conditional Autoregressive (CAR) Model, Convolution Model, and modified CAR Model, have been employed to detect the spatial heterogeneity. Bayesian hierarchical methods via Gibbs sampling are used to implement these models. The best model is selected using the Deviance Information Criterion. Results revealed Dhaka has the highest relative risk due to the city's high population density and growth rate. This study identifies which district has the highest relative risk and which districts adjacent to that district also have a high risk, which allows for the appropriate actions to be taken by the government agencies and communities to mitigate the risk effect. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

3.
BMC Med Res Methodol ; 23(1): 25, 2023 01 25.
Article in English | MEDLINE | ID: covidwho-2214531

ABSTRACT

BACKGROUND: Numerous clinical trials have been initiated to find effective treatments for COVID-19. These trials have often been initiated in regions where the pandemic has already peaked. Consequently, achieving full enrollment in a single trial might require additional COVID-19 surges in the same location over several years. This has inspired us to pool individual patient data (IPD) from ongoing, paused, prematurely-terminated, or completed randomized controlled trials (RCTs) in real-time, to find an effective treatment as quickly as possible in light of the pandemic crisis. However, pooling across trials introduces enormous uncertainties in study design (e.g., the number of RCTs and sample sizes might be unknown in advance). We sought to develop a versatile treatment efficacy assessment model that accounts for these uncertainties while allowing for continuous monitoring throughout the study using Bayesian monitoring techniques. METHODS: We provide a detailed look at the challenges and solutions for model development, describing the process that used extensive simulations to enable us to finalize the analysis plan. This includes establishing prior distribution assumptions, assessing and improving model convergence under different study composition scenarios, and assessing whether we can extend the model to accommodate multi-site RCTs and evaluate heterogeneous treatment effects. In addition, we recognized that we would need to assess our model for goodness-of-fit, so we explored an approach that used posterior predictive checking. Lastly, given the urgency of the research in the context of evolving pandemic, we were committed to frequent monitoring of the data to assess efficacy, and we set Bayesian monitoring rules calibrated for type 1 error rate and power. RESULTS: The primary outcome is an 11-point ordinal scale. We present the operating characteristics of the proposed cumulative proportional odds model for estimating treatment effectiveness. The model can estimate the treatment's effect under enormous uncertainties in study design. We investigate to what degree the proportional odds assumption has to be violated to render the model inaccurate. We demonstrate the flexibility of a Bayesian monitoring approach by performing frequent interim analyses without increasing the probability of erroneous conclusions. CONCLUSION: This paper describes a translatable framework using simulation to support the design of prospective IPD meta-analyses.


Subject(s)
COVID-19 , Humans , COVID-19/epidemiology , Computer Simulation , Research Design , Sample Size , Bayes Theorem
4.
AIMS Public Health ; 9(4): 703-717, 2022.
Article in English | MEDLINE | ID: covidwho-2110358

ABSTRACT

The dynamic mechanism of the COVID-19 pandemic has been studied for disease prevention and health protection through areal unit-based log-linear Poisson processes to understand the outbreak of the virus with confirmed daily empirical cases. The predictor of the evolution is structured as a function of a short-term dependence and a long-term trend to identify the pattern of exponential growth in the main epicenters of the virus. The study provides insight into the possible pandemic path of each areal unit and a guide to drive policymaking on preventive measures that can be applied or relaxed to mitigate the spread of the virus. It is significant that knowing the trend of the virus is very helpful for institutions and organizations in terms of instituting resources and measures to help provide a safe working environment and support for all workers/staff/students.

5.
Spat Stat ; 50: 100593, 2022 Aug.
Article in English | MEDLINE | ID: covidwho-1628848

ABSTRACT

On the occasion of the Spatial Statistics' 10th Anniversary, I reflect on the past and present of Bayesian disease mapping and look into its future. I focus on some key developments of models, and on recent evolution of multivariate and adaptive Gaussian Markov random fields and their impact and importance in disease mapping. I reflect on Bayesian disease mapping as a subject of spatial statistics that has advanced to date, and continues to grow, in scope and complexity alongside increasing needs of analytic tools for contemporary health science research, such as spatial epidemiology, population and public health, and medicine. I illustrate (potential) utility and impact of some of the disease mapping models and methods for analysing and monitoring communicable disease such as the COVID-19 infection risks during an ongoing pandemic.

6.
Front Public Health ; 10: 927658, 2022.
Article in English | MEDLINE | ID: covidwho-1974694

ABSTRACT

Background: Area deprivation has been shown to be associated with various adverse health outcomes including communicable as well as non-communicable diseases. Our objective was to assess potential associations between area deprivation and COVID-19 standardized incidence and mortality ratios in Bavaria over a period of nearly 2 years. Bavaria is the federal state with the highest infection dynamics in Germany and demographically comparable to several other European countries. Methods: In this retrospective, observational ecological study, we estimated the strength of associations between area deprivation and standardized COVID-19 incidence and mortality ratios (SIR and SMR) in Bavaria, Germany. We used official SARS-CoV-2 reporting data aggregated in monthly periods between March 1, 2020 and December 31, 2021. Area deprivation was assessed using the quintiles of the 2015 version of the Bavarian Index of Multiple Deprivation (BIMD 2015) at district level, analyzing the overall index as well as its single domains. Results: Deprived districts showed higher SIR and SMR than less deprived districts. Aggregated over the whole period, the SIR increased by 1.04 (95% confidence interval (95% CI): 1.01 to 1.07, p = 0.002), and the SMR by 1.11 (95% CI: 1.07 to 1.16, p < 0.001) per BIMD quintile. This represents a maximum difference of 41% between districts in the most and least deprived quintiles in the SIR and 110% in the SMR. Looking at individual months revealed clear linear association between the BIMD quintiles and the SIR and SMR in the first, second and last quarter of 2021. In the summers of 2020 and 2021, infection activity was low. Conclusions: In more deprived areas in Bavaria, Germany, higher incidence and mortality ratios were observed during the COVID-19 pandemic with particularly strong associations during infection waves 3 and 4 in 2020/2021. Only high infection levels reveal the effect of risk factors and socioeconomic inequalities. There may be confounding between the highly deprived areas and border regions in the north and east of Bavaria, making the relationship between area deprivation and infection burden more complex. Vaccination appeared to balance incidence and mortality rates between the most and least deprived districts. Vaccination makes an important contribution to health equality.


Subject(s)
COVID-19 , Bayes Theorem , COVID-19/epidemiology , Germany/epidemiology , Humans , Incidence , Pandemics , Poverty Areas , Retrospective Studies , SARS-CoV-2
7.
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz ; 64(9): 1146-1156, 2021 Sep.
Article in German | MEDLINE | ID: covidwho-1353690

ABSTRACT

BACKGROUND: Maps of the temporal evolution of the regional distribution of a health-related measure enable public health-relevant assessments of health outcomes. OBJECTIVES: The paper introduces the concept of standardized case fatality rate (sCFR). It describes the ratio of the regional variation in mortality to the regional variation in the documented infection process. The regional sCFR values are presented in maps and the time-varying regional heterogeneity observed in them is interpreted. MATERIALS AND METHODS: The regional sCFR is the quotient of the regional standardized mortality and case rate. It is estimated using a bivariate model. The sCFR values presented in maps are based on SARS-CoV­2 reporting data from Bavaria since the beginning of April 2020 until the end of March 2021. Four quarters (Q2/20, Q3/20, Q4/20, and Q1/21) are considered. RESULTS: In the quarters considered, the naïve CFR values in Bavaria are 5.0%, 0.5%, 2.5%, and 2.8%. In Q2/20, regional sCFR values are irregularly distributed across the state. This heterogeneity weakens in the second wave of the epidemic. In Q1/21, only isolated regions with elevated sCFR (> 1.25) appear in southern Bavaria. Clusters of regions with sCFR > 1.25 form in northern Bavaria, with Oberallgäu being the region with the lowest sCFR (0.39, 95% credibility interval: 0.25-0.55). CONCLUSIONS: In Bavaria, heterogeneous regional SARS-CoV-2-specific sCFR values are shown to change over time. They estimate the relative risk of dying from or with COVID-19 as a documented case. Strong small-scale variability in sCFR suggests a preference for regional over higher-level measures to manage the incidence of infection.


Subject(s)
COVID-19 , COVID-19/mortality , Germany/epidemiology , Humans , Incidence , Risk , SARS-CoV-2
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