DMlate | R Documentation |
These two datasets each contain a random sample of 10,000 persons from
the Danish National Diabetes Register. DMrand
is a random sample
from the register, whereas DMlate
is a random sample among those
with date of diagnosis after 1.1.1995. All dates are radomly jittered by
adding a U(-7,7) (days).
data(DMrand)
data(DMlate)
A data frame with 10000 observations on the following 7 variables.
sex
Sex, a factor with levels M
F
dobth
Date of birth
dodm
Date of inclusion in the register
dodth
Date of death
dooad
Date of 2nd prescription of OAD
doins
Date of 2nd insulin prescription
dox
Date of exit from follow-up.
All dates are given in fractions of years, so 1998.000 corresponds to 1 January 1998 and 1998.997 to 31 December 1998.
All dates are randomly perturbed by a small amount, so no real persons have any of the combinations of the 6 dates in the dataset. But results derived from the data will be quite close to those that would be obtained if the entire 'real' diabetes register were used.
Danish National Board of Health.
B Carstensen, JK Kristensen, P Ottosen and K Borch-Johnsen: The Danish National Diabetes Register: Trends in incidence, prevalence and mortality, Diabetologia, 51, pp 2187–2196, 2008.
In partucular see the appendix at the end of the paper.
data(DMlate)
str(DMlate)
dml <- Lexis( entry=list(Per=dodm, Age=dodm-dobth, DMdur=0 ),
exit=list(Per=dox),
exit.status=factor(!is.na(dodth),labels=c("DM","Dead")),
data=DMlate )
# Cut the follow-up at insulin start, and introduce a new timescale,
# and split non-precursor states
system.time(
dmi <- cutLexis( dml, cut = dml$doins,
pre = "DM",
new.state = "Ins",
new.scale = "t.Ins",
split.states = TRUE ) )
summary( dmi )
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