This combines a sequence of event tables.
Arguments
- ...
The event tables and optionally time between event tables, called waiting times in this help document.
- samples
How to handle samples when repeating an event table. The options are:
"clear"
Clear sampling records before combining the datasets"use"
Use the sampling records when combining the datasets
- waitII
This determines how waiting times between events are handled. The options are:
"smart"
This "smart" handling of waiting times is the default option. In this case, if the waiting time is above the last observed inter-dose interval in the first combined event table, then the actual time between doses is given by the wait time. If it is smaller than the last observed inter-dose interval, the time between event tables is given by the inter-dose interval + the waiting time between event tables."+ii"
In this case, the wait time is added to the inter-dose interval no matter the length of the wait time or inter-dose interval
- ii
If there was no inter-dose intervals found in the event table, assume that the interdose interval is given by this
ii
value. By default this is24
.
Details
This seq
uences all the event tables in added in the
argument list ...
. By default when combining the event
tables the offset is at least by the last inter-dose interval in
the prior event table (or ii
). If you separate any of the
event tables by a number, the event tables will be separated at
least the wait time defined by that number or the last inter-dose
interval.
References
Wang W, Hallow K, James D (2015). "A Tutorial on rxode2: Simulating Differential Equation Pharmacometric Models in R." CPT: Pharmacometrics and Systems Pharmacology, 5(1), 3-10. ISSN 2163-8306
Examples
if (FALSE) { # \dontrun{
library(rxode2)
library(units)
# Model from rxode2 tutorial
# Using a nlmixr2 style function
mod1 <-function(){
ini({
KA <- 2.94E-01
CL <- 1.86E+01
V2 <- 4.02E+01
Q <- 1.05E+01
V3 <- 2.97E+02
Kin <- 1
Kout <- 1
EC50 <- 200
})
model({
C2 <- centr/V2
C3 <- peri/V3
d/dt(depot) <- -KA*depot
d/dt(centr) <- KA*depot - CL*C2 - Q*C2 + Q*C3
d/dt(peri) <- Q*C2 - Q*C3
d/dt(eff) <- Kin - Kout*(1-C2/(EC50+C2))*eff
})
}
## These are making the more complex regimens of the rxode2 tutorial
## bid for 5 days
bid <- et(timeUnits="hr") |>
et(amt=10000,ii=12,until=set_units(5, "days"))
## qd for 5 days
qd <- et(timeUnits="hr") |>
et(amt=20000,ii=24,until=set_units(5, "days"))
## bid for 5 days followed by qd for 5 days
et <- seq(bid,qd) |>
et(seq(0,11*24,length.out=100))
bidQd <- rxSolve(mod1, et)
plot(bidQd, C2)
## Now Infusion for 5 days followed by oral for 5 days
## note you can dose to a named compartment instead of using the compartment number
infusion <- et(timeUnits = "hr") |>
et(amt=10000, rate=5000, ii=24, until=set_units(5, "days"), cmt="centr")
qd <- et(timeUnits = "hr") |>
et(amt=10000, ii=24, until=set_units(5, "days"), cmt="depot")
et <- seq(infusion,qd)
infusionQd <- rxSolve(mod1, et)
plot(infusionQd, C2)
## 2wk-on, 1wk-off
qd <- et(timeUnits = "hr") |>
et(amt=10000, ii=24, until=set_units(2, "weeks"), cmt="depot")
et <- seq(qd, set_units(1,"weeks"), qd) |>
add.sampling(set_units(seq(0, 5.5,by=0.005),weeks))
wkOnOff <- rxSolve(mod1, et)
plot(wkOnOff, C2)
## You can also repeat the cycle easily with the rep function
qd <-et(timeUnits = "hr") |>
et(amt=10000, ii=24, until=set_units(2, "weeks"), cmt="depot")
et <- etRep(qd, times=4, wait=set_units(1,"weeks")) |>
add.sampling(set_units(seq(0, 12.5,by=0.005),weeks))
repCycle4 <- rxSolve(mod1, et)
plot(repCycle4, C2)
} # }