Ge. Schumacher et Jt. Barr, BAYESIAN AND THRESHOLD PROBABILITIES IN THERAPEUTIC DRAG MONITORING -WHEN CAN SERUM DRUG CONCENTRATIONS ALTER CLINICAL DECISIONS, American journal of hospital pharmacy, 51(3), 1994, pp. 321-327
The use of Bayesian and threshold probabilities is examined with respe
ct to the range of probabilities of toxicity for which obtaining a pat
ient's serum drug concentration leads to information that is potential
ly useful in altering a clinical decision. For the situation of potent
ial drug-induced toxicity, three threshold probabilities are needed to
characterize the decision process: the decision threshold for decidin
g between continuing and discontinuing the drug regimen, the testing t
hreshold that separates the decision to continue the regimen without t
esting the serum drug concentration from the decision to test before d
eciding, and the companion testing threshold that separates the decisi
on to discontinue the regimen without testing from the decision to tes
t before deciding. For digoxin, theophylline, aminoglycosides, vancomy
cin, and phenytoin, three prototypical decision threshold probabilitie
s, 0.33, 0.2, and 0.1, are used, along with published true-positive an
d false-positive rates, to calculate serum concentration testing thres
holds for each drug. Practitioners can be more effective in their use
of serum drug concentration data when a Bayesian approach to probabili
ty assessment is used in conjunction with testing thresholds.