Publicly available HIV clinical data from the Women's Interagency HIV cohort Study (WIHS). The entire study enrolled 1164 women. Inclusion criteria of the study are: women at enrolment must be (i) alive, (ii) HIV-1 infected, and (iii) free of clinical AIDS symptoms. Women were followed until the first of the following occurred: (i) treatment initiation (HAART), (ii) AIDS diagnosis, (iii) death, or administrative censoring. The studied outcomes were the competing risks "AIDS/Death (before HAART)" and "Treatment Initiation (HAART)". However, for simplification purposes, only the first of the two competing events (i.e. the time to AIDS/Death), was used. Likewise, for simplification in this clinical dataset example, only complete cases were used. Variables included history of Injection Drug Use ("IDU") at enrollment, African American ethnicity ('Race'), age ('Age'), and baseline CD4 count ('CD4') for a total of \(p=4\) clinical covariates. The question in this dataset example was whether it is possible to achieve a prognostication of patients for AIDS and HAART. See Bacon et al. (2005) and the WIHS website for more details.
Real.1
Dataset consists of a numeric
data.frame
containing \(n=485\) complete observations (samples)
by rows and \(p=4\) clinical covariates by columns, not including the censoring indicator and (censored) time-to-event variables.
It comes as a compressed Rda data file.
This work made use of the High Performance Computing Resource in the Core Facility for Advanced Research Computing at Case Western Reserve University. This project was partially funded by the National Institutes of Health NIH - National Cancer Institute (R01-CA160593) to J-E. Dazard and J.S. Rao.
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Bacon M.C., von Wyl V., Alden C. et al. (2005). "The Women's Interagency HIV Study: an observational cohort brings clinical sciences to the bench." Clin. Diagn. Lab. Immunol., 12(9):1013-1019.
Women's Interagency HIV cohort Study website: https://statepi.jhsph.edu/wihs/wordpress/