Hello!
I am initializing a tissue simulation using the "prepacing" method, whereby a cell model is run prior to the tissue simulation and state parameters are assigned to the tissue based on LAT sequence.
The problem I am having is that the cell model requires a small timestep ~0.05 in order for the states to reach equilibrium (otherwise, every other stimulus fails to produce a proper depolarization, and equilibrium with the same APD per beat is never achieved; this is for a particular set of parameters in the mMS model at bcl of 300. I would imagine, by looking at the trace, that after a few beats of this small dt, that the cell model could probably be run successfully at a much larger dt, but 'getting it going' is the problem).
Is it the case that the timestep used for prepacing a tissue simulation is restricted to being the same timestep used for the tissue simulation itself? Otherwise, how might I use a small timestep in the prepacing simulation to achieve equilibrium, followed by a larger timestep in the tissue simulation?
(note: I am specifically using the 'prepace' method so that states can be assigned based on LATs from a file, as assigning the same states to every tissue region, using the "im_sv_init" method, does not seem to be sufficient).
(I have considered running a few microseconds of simulation with prepacing at a very small timestep, saving the state, and then continuing the simulation with a larger timestep. However, keeping track of every activation, in order to ensure that there was a depolarization and repolarization on every beat, then becomes trickier).
Thanks!
Sam