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dc.contributor.authorDonoghoe, Mark W
dc.contributor.authorMarschner, Ian C
dc.date.accessioned2017-05-04
dc.date.available2017-05-04
dc.date.issued2016-04-14
dc.identifier.citationDonoghoe MW, Marschner IC. Estimation of adjusted rate differences using additive negative binomial regression. Statistics in Medicine 2016; 35(18): 3166–3178.en
dc.identifier.urihttp://hdl.handle.net/2123/16709
dc.description.abstractRate differences are an important effect measure in biostatistics and provide an alternative perspective to rate ratios. When the data are event counts observed during an exposure period, adjusted rate differences may be estimated using an identity-link Poisson generalised linear model, also known as additive Poisson regression. A problem with this approach is that the assumption of equality of mean and variance rarely holds in real data, which often show overdispersion. An additive negative binomial model is the natural alternative to account for this, however, standard model-fitting methods are often unable to cope with the constrained parameter space arising from the non-negativity restrictions of the additive model. In this paper, we propose a novel solution to this problem using a variant of the ECME algorithm. Our method provides a reliable way to fit an additive negative binomial regression model and also permits flexible generalisations using semi-parametric regression functions. We illustrate the method using a placebo-controlled clinical trial of fenofibrate treatment in patients with type II diabetes, where the outcome is the number of laser therapy courses administered to treat diabetic retinopathy. An R package is available that implements the proposed method. Copyright c 2015 John Wiley & Sons, Ltd.en
dc.publisherWileyen
dc.relationAustralian Research Council (DP110101254)en
dc.rightsOther
dc.subjectECME algorithmen
dc.subjectnegative binomial regressionen
dc.subjectoverdispersionen
dc.subjectrate differenceen
dc.subjectsemi-parametric regressionen
dc.titleEstimation of adjusted rate differences using additive negative binomial regressionen
dc.typeArticleen
dc.type.pubtypePost-printen
usyd.facultyFaculty of Medicine and Health, NHMRC Clinical Trials Centreen


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