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Hello,
I was working on compartmental modeling and I was wondering what the clinical issues are for
considering two compartmental model data/drug as one compartmental model data/drug.
Thanks,
Joe DePasquale
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Joe,
There are no "clinical issues" with one or two compartment models. You
have a set of data from your study and you are applying a mathematical
model to describe the data. Your data dictates what model to choose,
i.e., what model describes your data best. In other words, you don't
choose a one or two compartment model based on "clinical issues", the
data drives your choice of the model.
Toufigh
--
Toufigh Gordi, PhD
www.tgordi.com
E-mail: tg.at.tgordi.com
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Joe,
The issue you are interested in is discussed in details by John G. Wagner in 'Fundamentals of
Clinical Pharmacokinetics', pp. 154-155, 2nd ed, 1975.
We observed in clinical setting collapsing of 2-COM to 1-COM (Terziivanov,D. et al. Pharmacokinetics
and quantitative characterization of Cefotiam excretion ways after i.v. administartion in patinets
after cholecystectomy. Eur J Clin Pharmacol., 1986, 30, 439-444). In the paper we have described a
patient with PK characteristics determining a 'collapse' of 2-COM to 1-COM. I hope it will be
helpful to you.
Greetings,
Dimiter
Dimiter Terziivanov, MD,PhD,DSc, Professor
Head, Dept. of Pharmacology and Clinical Pharmacology
SOFIA UNIVERSITY
“ST. KLIMENT OHRIDSKI”
FACULTY OF MEDICINE
FACULTY OF CHEMISTRY AND PHARMACY
UNIV HOSP "LOZENETZ"
1 Koziak str.
1407 Sofia, BULGARIA
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Hi,
One of the effect could be underestimation of the Cmax, which can be a problem if either safety or
efficacy are deemed related to it.
Best regards,
Nathalie
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Thank you all for the input. I know the data dictates the model, but I wanted to talk about the
consequences or pitfalls of choosing a 1CM when a 2CM should have been used instead.
Underestimation of the Cmax is very helpful and I will be sure to refer to the text mentioned as
well. All of your answers have been very helpful. I appreciate the help!
Thanks,
Joe
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