Bj. Zarowitz, BIOELECTRICAL-IMPEDANCE ANALYSIS MEASUREMENTS FOR DRUG PHARMACOKINETICS, The American journal of clinical nutrition, 64(3), 1996, pp. 519-523
I review the rationale, methods, and existing data for using bioelectr
ical impedance to determine drug pharmacokinetics. Because drugs distr
ibute into body compartments after absorption, it is expected that bio
electrical impedance measurements may correlate with drug pharmacokine
tics (absorption, distribution, metabolism, and excretion). Authors ha
ve examined correlations between total body water, extracellular fluid
, and body cell mass and the drug volume of distribution or clearance
and the elimination rate constant. Multiple-regression models with the
all-subsets technique provided the most accurate equations with the l
owest prediction errors and the highest correlation coefficients. Appl
ication of bioelectrical impedance-derived equations to a different se
t of patients allows prediction of pharmacokinetics. However, bioelect
rical impedance equations do not yield more accurate dosing estimates
than do standard dosing methods, and large dosing errors are possible
in patients with aberrant physiology. Therefore, until multicenter tri
als in large subject populations can provide stable, accurate equation
s applicable to a wide variety of patient populations, bioelectrical i
mpedance offers no advantage over standard pharmacokinetic dosing meth
ods for the drugs studied.