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
iivalue. By default this is24.
Details
This sequences 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)
} # }
