Analysis of Longitudinal Data, Second Edition by Peter Diggle, Patrick Heagerty, Kung-Yee Liang, Scott Zeger

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By Peter Diggle, Patrick Heagerty, Kung-Yee Liang, Scott Zeger

The hot variation of this significant textual content has been thoroughly revised and extended to develop into the main updated and thorough expert reference textual content during this fast-moving and significant zone of biostatistics. new chapters were extra on absolutely parametric versions for discrete repeated measures facts and on statistical versions for time-dependent predictors the place there is suggestions among the predictor and reaction variables. It additionally includes the numerous beneficial positive factors of the former variation akin to, layout matters, exploratory equipment of study, linear versions for non-stop information, and versions and strategies for dealing with facts and lacking values.

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With data tory variables, x2 3 , to obtain residuals, collected at a fixed number of equally spaced time points, correlation can be studied using a scatterplot matrix in which r 23 is plotted against r1k for all j < k =- 1, . , rt. 5. CD4+ cell numbers To illustrate the idea of a scatterplot matrix, we have rounded the CD4+ observation times to the nearest year, so that there are a maximum of seven observations between —2 and 4 for each individual. 13 shows each of the 7 choose 2 scatterplots of responses from a person at different times.

M. In group B, the same equation holds but with different coefficients, NB and of subjects, m; each person has n repeated observations. 2 p for all j k. In and Corr(Yii, Yk) addition, we assume of explanatory variables so that xij = that each person has the same set xj. A typical example of such xj is 01B• Both groups have the same number SAMPLE SIZE CALCULATIONS 29 the duration between the first and the jth visit. in which case 3 ) A and 3 1 0 are the rates of change in Y for groups A and 13 respectively.

4. Consider a response variable that both changes over time and varies among subjects. Examples include age, blood pressure, or weight. 3, we begin with a model of + fi j 1, , n; i 1, . r 1 on the right-hand side. This assumption is rather a st rong one and doomed to fail in many studies. The model can be modified by allowing each person to have their own intercept. Ow , that is, by replacing + with so that + 0(ri j — x21) + 2 j . 3) represent extreme cases for modelling the crosssectional variation in the response variable at baseline.

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