63 research outputs found

    Pooling multiple imputations when the sample happens to be the population

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    Current pooling rules for multiply imputed data assume infinite populations. In some situations this assumption is not feasible as every unit in the population has been observed, potentially leading to over-covered population estimates. We simplify the existing pooling rules for situations where the sampling variance is not of interest. We compare these rules to the conventional pooling rules and demonstrate their use in a situation where there is no sampling variance. Using the standard pooling rules in situations where sampling variance should not be considered, leads to overestimation of the variance of the estimates of interest, especially when the amount of missingness is not very large. As a result, populations estimates are over-covered, which may lead to a loss of statistical power. We conclude that the theory of multiple imputation can be extended to the situation where the sample happens to be the population. The simplified pooling rules can be easily implemented to obtain valid inference in cases where we have observed essentially all units and in simulation studies addressing the missingness mechanism only.Comment: 6 pages, 1 figure, 1 tabl

    A note on imputing squares via polynomial combination approach

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    The polynomial combination (PC) method, proposed by Vink and Van Buuren, is a hot-deck multiple imputation method for imputation models containing squared terms. The method yields unbiased regression estimates and preserves the quadratic relationships in the imputed data for both MCAR and MAR mechanisms. However, Vink and Van Buuren never studied the coverage rate of the PC method. This paper investigates the coverage of the nominal 95% confidence intervals for the polynomial combination method and improves the algorithm to avoid the perfect prediction issue. We also compare the original and the improved PC method to the substantive model compatible fully conditional specification method proposed by Bartlett et al. and elucidate the two imputation methods’ characters

    Toward a standardized evaluation of imputation methodology

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    Developing new imputation methodology has become a very active field. Unfortunately, there is no consensus on how to perform simulation studies to evaluate the properties of imputation methods. In part, this may be due to different aims between fields and studies. For example, when evaluating imputation techniques aimed at prediction, different aims may be formulated than when statistical inference is of interest. The lack of consensus may also stem from different personal preferences or scientific backgrounds. All in all, the lack of common ground in evaluating imputation methodology may lead to suboptimal use in practice. In this paper, we propose a move toward a standardized evaluation of imputation methodology. To demonstrate the need for standardization, we highlight a set of possible pitfalls that bring forth a chain of potential problems in the objective assessment of the performance of imputation routines. Additionally, we suggest a course of action for simulating and evaluating missing data problems. Our suggested course of action is by no means meant to serve as a complete cookbook, but rather meant to incite critical thinking and a move to objective and fair evaluations of imputation methodology. We invite the readers of this paper to contribute to the suggested course of action

    How to relate potential outcomes: Estimating individual treatment effects under a given specified partial correlation

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    In most medical research, the average treatment effect is used to evaluate a treatment’s performance. However, precision medicine requires knowledge of individual treatment effects: What is the difference between a unit’s measurement under treatment and control conditions? In most treatment effect studies, such answers are not possible because the outcomes under both experimental conditions are not jointly observed. This makes the problem of causal inference a missing data problem. We propose to solve this problem by 

    Graphical and numerical diagnostic tools to assess multiple imputation models by posterior predictive checking

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    Missing data are often dealt with multiple imputation. A crucial part of the multiple imputation process is selecting sensible models to generate plausible values for incomplete data. A method based on posterior predictive checking is proposed to diagnose imputation models based on posterior predictive checking. To assess the congeniality of imputation models, the proposed diagnostic method compares the observed data with their replicates generated under corresponding posterior predictive distributions. If the imputation model is congenial with the substantive model, the observed data are expected to be located in the centre of corresponding predictive posterior distributions. Simulation and application are designed to investigate the proposed diagnostic method for parametric and semi-parametric imputation approaches, continuous and discrete incomplete variables, univariate and multivariate missingness patterns. The results show the validity of the proposed diagnostic method

    A blended distance to define "people-like-me"

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    Curve matching is a prediction technique that relies on predictive mean matching, which matches donors that are most similar to a target based on the predictive distance. Even though this approach leads to high prediction accuracy, the predictive distance may make matches look unconvincing, as the profiles of the matched donors can substantially differ from the profile of the target. To counterbalance this, similarity between the curves of the donors and the target can be taken into account by combining the predictive distance with the Mahalanobis distance into a `blended distance' measure. The properties of this measure are evaluated in two simulation studies. Simulation study I evaluates the performance of the blended distance under different data-generating conditions. The results show that blending towards the Mahalanobis distance leads to worse performance in terms of bias, coverage, and predictive power. Simulation study II evaluates the blended metric in a setting where a single value is imputed. The results show that a property of blending is the bias-variance trade off. Giving more weight to the Mahalanobis distance leads to less variance in the imputations, but less accuracy as well. The main conclusion is that the high prediction accuracy achieved with the predictive distance necessitates the variability in the profiles of donors

    Prevalence of questionable research practices, research misconduct and their potential explanatory factors:A survey among academic researchers in The Netherlands

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    Prevalence of research misconduct, questionable research practices (QRPs) and their associations with a range of explanatory factors has not been studied sufficiently among academic researchers. The National Survey on Research Integrity targeted all disciplinary fields and academic ranks in the Netherlands. It included questions about engagement in fabrication, falsification and 11 QRPs over the previous three years, and 12 explanatory factor scales. We ensured strict identity protection and used the randomized response method for questions on research misconduct. 6,813 respondents completed the survey. Prevalence of fabrication was 4.3% (95% CI: 2.9, 5.7) and of falsification 4.2% (95% CI: 2.8, 5.6). Prevalence of QRPs ranged from 0.6% (95% CI: 0.5, 0.9) to 17.5% (95% CI: 16.4, 18.7) with 51.3% (95% CI: 50.1, 52.5) of respondents engaging frequently in at least one QRP. Being a PhD candidate or junior researcher increased the odds of frequently engaging in at least one QRP, as did being male. Scientific norm subscription (odds ratio (OR) 0.79; 95% CI: 0.63, 1.00) and perceived likelihood of detection by reviewers (OR 0.62, 95% CI: 0.44, 0.88) were associated with engaging in less research misconduct. Publication pressure was associated with more often engaging in one or more QRPs frequently (OR 1.22, 95% CI: 1.14, 1.30). We found higher prevalence of misconduct than earlier surveys. Our results suggest that greater emphasis on scientific norm subscription, strengthening reviewers in their role as gatekeepers of research quality and curbing the “publish or perish” incentive system promotes research integrity

    Nationwide epidemiological approach to identify associations between keratoconus and immune-mediated diseases

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    Background: The aetiology of keratoconus (KC) remains poorly understood. KC has typically been described as a non-inflammatory disorder of the cornea. Nonetheless, there is increasing presumptive evidence for the role of the immune system in the pathogenesis of KC. Aim: To evaluate the association between KC and immune-mediated diseases on a population level. We hypothesise that KC is immune-mediated rather than a predominantly degenerative disease. Methods: Data were obtained from the largest health insurance provider in the Netherlands. Dutch residents are obligatorily insured. The data contained all medical claims and sociodemographic characteristics from all KC patients plus all those data from a 1:6 age-matched and sex-matched control group. The primary outcome was the association between KC and immune-mediated diseases, as assessed by conditional logistic regression. Results: Based on our analysis of 2051 KC cases and 12 306 matched controls, we identified novel associations between KC and Hashimoto's thyroiditis (OR=2.89; 95% CI: 1.41 to 5.94) and inflammatory skin conditions (OR=2.20; 95% CI: 1.37 to 3.53). We confirmed known associations between KC and atopic conditions, including allergic rash (OR=3.00; 95% CI: 1.03 to 8.79), asthma and bronchial hyperresponsiveness (OR=2.51; 95% CI: 1.63 to 3.84), and allergic rhinitis (OR=2.20; 95% CI: 1.39 to 3.49). Conclusion: Keratoconus appears positively associated with multiple immune-mediated diseases, which provides a population-based argument that systemic inflammatory responses may influence its onset. The identification of these particular diseases might shed light on potential comparable pathways through which this proinflammatory state is achieved, paving the way for pharmacological treatment strategies
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