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      Intermediate and advanced topics in multilevel logistic regression analysis

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          Abstract

          Multilevel data occur frequently in health services, population and public health, and epidemiologic research. In such research, binary outcomes are common. Multilevel logistic regression models allow one to account for the clustering of subjects within clusters of higher‐level units when estimating the effect of subject and cluster characteristics on subject outcomes. A search of the PubMed database demonstrated that the use of multilevel or hierarchical regression models is increasing rapidly. However, our impression is that many analysts simply use multilevel regression models to account for the nuisance of within‐cluster homogeneity that is induced by clustering. In this article, we describe a suite of analyses that can complement the fitting of multilevel logistic regression models. These ancillary analyses permit analysts to estimate the marginal or population‐average effect of covariates measured at the subject and cluster level, in contrast to the within‐cluster or cluster‐specific effects arising from the original multilevel logistic regression model. We describe the interval odds ratio and the proportion of opposed odds ratios, which are summary measures of effect for cluster‐level covariates. We describe the variance partition coefficient and the median odds ratio which are measures of components of variance and heterogeneity in outcomes. These measures allow one to quantify the magnitude of the general contextual effect. We describe an R 2 measure that allows analysts to quantify the proportion of variation explained by different multilevel logistic regression models. We illustrate the application and interpretation of these measures by analyzing mortality in patients hospitalized with a diagnosis of acute myocardial infarction. © 2017 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd.

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          An Original Stepwise Multilevel Logistic Regression Analysis of Discriminatory Accuracy: The Case of Neighbourhoods and Health

          Background and Aim Many multilevel logistic regression analyses of “neighbourhood and health” focus on interpreting measures of associations (e.g., odds ratio, OR). In contrast, multilevel analysis of variance is rarely considered. We propose an original stepwise analytical approach that distinguishes between “specific” (measures of association) and “general” (measures of variance) contextual effects. Performing two empirical examples we illustrate the methodology, interpret the results and discuss the implications of this kind of analysis in public health. Methods We analyse 43,291 individuals residing in 218 neighbourhoods in the city of Malmö, Sweden in 2006. We study two individual outcomes (psychotropic drug use and choice of private vs. public general practitioner, GP) for which the relative importance of neighbourhood as a source of individual variation differs substantially. In Step 1 of the analysis, we evaluate the OR and the area under the receiver operating characteristic (AUC) curve for individual-level covariates (i.e., age, sex and individual low income). In Step 2, we assess general contextual effects using the AUC. Finally, in Step 3 the OR for a specific neighbourhood characteristic (i.e., neighbourhood income) is interpreted jointly with the proportional change in variance (i.e., PCV) and the proportion of ORs in the opposite direction (POOR) statistics. Results For both outcomes, information on individual characteristics (Step 1) provide a low discriminatory accuracy (AUC = 0.616 for psychotropic drugs; = 0.600 for choosing a private GP). Accounting for neighbourhood of residence (Step 2) only improved the AUC for choosing a private GP (+0.295 units). High neighbourhood income (Step 3) was strongly associated to choosing a private GP (OR = 3.50) but the PCV was only 11% and the POOR 33%. Conclusion Applying an innovative stepwise multilevel analysis, we observed that, in Malmö, the neighbourhood context per se had a negligible influence on individual use of psychotropic drugs, but appears to strongly condition individual choice of a private GP. However, the latter was only modestly explained by the socioeconomic circumstances of the neighbourhoods. Our analyses are based on real data and provide useful information for understanding neighbourhood level influences in general and on individual use of psychotropic drugs and choice of GP in particular. However, our primary aim is to illustrate how to perform and interpret a multilevel analysis of individual heterogeneity in social epidemiology and public health. Our study shows that neighbourhood “effects” are not properly quantified by reporting differences between neighbourhood averages but rather by measuring the share of the individual heterogeneity that exists at the neighbourhood level.
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            Explained variation for logistic regression.

            Different measures of the proportion of variation in a dependent variable explained by covariates are reported by different standard programs for logistic regression. We review twelve measures that have been suggested or might be useful to measure explained variation in logistic regression models. The definitions and properties of these measures are discussed and their performance is compared in an empirical study. Two of the measures (squared Pearson correlation between the binary outcome and the predictor, and the proportional reduction of squared Pearson residuals by the use of covariates) give almost identical results, agree very well with the multiple R2 of the general linear model, have an intuitively clear interpretation and perform satisfactorily in our study. For all measures the explained variation for the given sample and also the one expected in future samples can be obtained easily. For small samples an adjustment analogous to Radj2 in the general linear model is suggested. We discuss some aspects of application and recommend the routine use of a suitable measure of explained variation for logistic models.
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              A Comparison of Cluster-Specific and Population-Averaged Approaches for Analyzing Correlated Binary Data

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                Author and article information

                Contributors
                peter.austin@ices.on.ca
                Journal
                Stat Med
                Stat Med
                10.1002/(ISSN)1097-0258
                SIM
                Statistics in Medicine
                John Wiley and Sons Inc. (Hoboken )
                0277-6715
                1097-0258
                23 May 2017
                10 September 2017
                : 36
                : 20 ( doiID: 10.1002/sim.v36.20 )
                : 3257-3277
                Affiliations
                [ 1 ] Institute for Clinical Evaluative Sciences Toronto Ontario Canada
                [ 2 ] Institute of Health Management, Policy, and Evaluation University of Toronto Toronto Ontario Canada
                [ 3 ] Schulich Heart Research Program, Sunnybrook Research Institute Toronto Ontario Canada
                [ 4 ] Unit for Social Epidemiology, Faculty of Medicine Lund University Malmö Sweden
                [ 5 ] Center for Primary Health Care Research Region Skåne Malmö Sweden
                Author notes
                [*] [* ] Correspondence to: Peter Austin, Institute for Clinical Evaluative Sciences, G106, 2075 Bayview Avenue, Toronto, Ontario M4N 3M5, Canada.

                E‐mail: peter.austin@ 123456ices.on.ca

                Author information
                http://orcid.org/0000-0003-3337-233X
                Article
                SIM7336 SIM-16-0830.R3
                10.1002/sim.7336
                5575471
                28543517
                becfd042-f44d-4d11-aa25-ac579ccec2bb
                © 2017 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 15 November 2016
                : 21 April 2017
                Page count
                Figures: 1, Tables: 2, Pages: 21, Words: 11122
                Funding
                Funded by: Canadian Institutes of Health Research
                Award ID: MOP 86508
                Funded by: Heart and Stroke Foundation of Canada
                Funded by: Swedish Research Council
                Award ID: VR #2013‐2484
                Award ID: 2013‐2484
                Funded by: Canadian Institutes of Health Research (CIHR)
                Award ID: MOP
                Funded by: Ontario Ministry of Health and Long‐Term Care (MOHLTC)
                Categories
                Tutorial in Biostatistics
                Tutorial in Biostatistics
                Custom metadata
                2.0
                sim7336
                10 September 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.1.8 mode:remove_FC converted:30.08.2017

                Biostatistics
                multilevel analysis,hierarchical models,logistic regression,multilevel models,clustered data

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