Biomedical subjects

C B Dean

Publications and source records attributed to C B Dean.

7 recordsLinked to original sources

PubMed2002

Spatio-temporal modelling of rates for the construction of disease maps.

There have been significant developments in disease mapping in the past few decades. The continual development of statistical methodology in this area is responsible for the growing popularity of disease mapping because of its potential usefulness in regional health planning, disease surveillance and intervention, and allocating health funding. Here we review the area of disease mapping where relative risks pertain to an event such as incidence or mortality over space and time. In particular we briefly discuss the use of generalized additive mixed models, an additive extension of generalized linear mixed models, for spatio-temporal analysis of disease rates. To illustrate the procedures, we present an in-depth analysis of infant mortality data in the province of British Columbia, Canada. The goals of the analysis are to produce more reliable small-area estimates of mortality rates, assess spatial patterns over time, and examine risk trends at both global (provincial) and local (local health area) levels.

British Columbia↗

PubMed2002

A semiparametric model for the analysis of recurrent-event panel data.

In many longitudinal studies, interest focuses on the occurrence rate of some phenomenon for the subjects in the study. When the phenomenon is nonterminating and possibly recurring, the result is a recurrent-event data set. Examples include epileptic seizures and recurrent cancers. When the recurring event is detectable only by an expensive or invasive examination, only the number of events occurring between follow-up times may be available. This article presents a semiparametric model for such data, based on a multiplicative intensity model paired with a fully flexible nonparametric baseline intensity function. A random subject-specific effect is included in the intensity model to account for the overdispersion frequently displayed in count data. Estimators are determined from quasi-likelihood estimating functions. Because only first- and second-moment assumptions are required for quasi-likelihood, the method is more robust than those based on the specification of a full parametric likelihood. Consistency of the estimators depends only on the assumption of the proportional intensity model. The semiparametric estimators are shown to be highly efficient compared with the usual parametric estimators. As with semiparametric methods in survival analysis, the method provides useful diagnostics for specific parametric models, including a quasi-score statistic for testing specific baseline intensity functions. The techniques are used to analyze cancer recurrences and a pheromone-based mating disruption experiment in moths. A simulation study confirms that, for many practical situations, the estimators possess appropriate small-sample characteristics.

Animals↗

PubMed2001

The use of mixture models for identifying high risks in disease mapping.

Conventional approaches for estimating risks in disease mapping or mortality studies are based on Poisson inference. Frequently, overdispersion is present and this extra variability is modelled by introducing random effects. In this paper we compare two computationally simple approaches for incorporating random effects: one based on a non-parametric mixture model assuming that the population arises from a discrete mixture of Poisson distributions, and the second using a Poisson-normal mixture model which allows for spatial autocorrelation. The comparison is focused on how well each of these methods identify the regions which have high risks. Such identification is important because policy makers may wish to target regions associated with such extreme risks for financial assistance while epidemiologists may wish to target such regions for further study. The Poisson-normal mixture model is presented from both a frequentist, or empirical Bayes, and a fully Bayesian point of view. We compare results obtained with the parametric and non-parametric models specifically in terms of detecting extreme mortality risks, using infant mortality data of British Columbia, Canada, for the period 1981-1985, breast cancer data from Sardinia, for the period 1983-1987, and Scottish lip cancer data for 1975-1980. However, we also investigate the performance of these models in a simulation study. The key finding is that discrete mixture models seem to be able to locate regions which experience high risks; normal mixture models also work well in this regard, and perform substantially better when spatial autocorrelation is present.

Adult↗

PubMed2001

Simultaneous modelling of operative mortality and long-term survival after coronary artery bypass surgery.

Typical analyses of lifetime data treat the time to death or failure as the response variable and use a variety of modelling strategies such as proportional hazards or fully parametric, to investigate the relationship between the response and covariates. In certain circumstances it may be more natural to view the distribution of the response variable as consisting of two or more parts since the survival curve appears segmented. This article addresses such a scenario and we propose a model for simultaneously investigating the effects of covariates over the two segments. The model is an analogue of that proposed by Lambert for zero-inflated Poisson regression. The application is central to the model development and is concerned with survival after coronary artery bypass surgery. Here operative mortality, defined as death within 30 days after surgery, and long-term mortality, are viewed as distinct outcomes. For the application considered, the survivor function displays much steeper descent during the first 30 days after surgery, that is, for operative mortality, than after this period. An investigation of the effects of covariates on operative and long-term mortality after coronary artery bypass surgery illustrates the usefulness of the proposed model.

Age Factors↗

PubMed2001

Detecting interaction between random region and fixed age effects in disease mapping.

The purpose of this article is to draw attention to the possible need for inclusion of interaction effects between regions and age groups in mapping studies. We propose a simple model for including such an interaction in order to develop a test for its significance. The assumption of an absence of such interaction effects is a helpful simplifying one. The measure of relative risk related to a particular region becomes easily and neatly summarized. Indeed, such a test seems warranted because it is anticipated that the simple model, which ignores such interaction, as is in common use, may at times be adequate. The test proposed is a score test and hence only requires fitting the simpler model. We illustrate our approaches using mortality data from British Columbia, Canada, over the 5-year period 1985-1989. For this data, the interaction effect between age groups and regions is quite large and significant.

Age Factors↗

PubMed2001

Autoregressive spatial smoothing and temporal spline smoothing for mapping rates.

This article proposes generalized additive mixed models for the analysis of geographic and temporal variability of mortality rates. This class of models accommodates random spatial effects and fixed and random temporal components. Spatiotemporal models that use autoregressive local smoothing across the spatial dimension and B-spline smoothing over the temporal dimension are developed. The objective is the identification of temporal treads and the production of a series of smoothed maps from which spatial patterns of mortality risks can be monitored over time. Regions with consistently high rate estimates may be followed for further investigation. The methodology is illustrated by analysis of British Columbia infant mortality data.

Biometry↗

PubMedDate not supplied

Parametric bootstrap and penalized quasi-likelihood inference in conditional autoregressive models.

This paper discusses a variety of conditional autoregressive (CAR) models for mapping disease rates, beyond the usual first-order intrinsic CAR model. We illustrate the utility and scope of such models for handling different types of data structures. To encourage their routine use for map production at statistical and health agencies, a simple algorithm for fitting such models is presented. This is derived from penalized quasi-likelihood (PQL) inference which uses an analogue of best-linear unbiased estimation for the regional risk ratios and restricted maximum likelihood for the variance components. We offer the practitioner here the use of the parametric bootstrap for inference. It is more reliable than standard maximum likelihood asymptotics for inference purposes since relevant hypotheses for the mapping of rates lie on the boundary of the parameter space. We illustrate the parametric bootstrap test of the practically relevant and important simplifying hypothesis that there is no spatial autocorrelation. Although the parametric bootstrap requires computational effort, it is straightforward to implement and offers a wealth of information relating to the estimators and their properties. The proposed methodology is illustrated by analysing infant mortality in the province of British Columbia in Canada.

Algorithms↗