Ra. Schoenenberger et al., APPROPRIATENESS OF ANTIEPILEPTIC DRUG LEVEL MONITORING, JAMA, the journal of the American Medical Association, 274(20), 1995, pp. 1622-1626
Objectives.-To develop explicit, reliable appropriateness criteria for
antiepileptic drug level monitoring and to assess the appropriateness
of monitoring in one tertiary care institution. Design.-Appropriatene
ss criteria derived from the literature and through expert opinion wer
e used to evaluate a stratified random sample of antiepileptic drug le
vel determinations obtained from chart review. Setting.-Tertiary care
center performing more than 10 000 antiepileptic drug level determinat
ions per year. Patients.-A total of 330 inpatients in whom antiepilept
ic drug levels were measured a total of 855 times. Methods.-Drug level
s were assessed at least 200 times for each of four antiepileptic drug
s (phenytoin, carbamazepine, phenobarbital, and valproic acid). Main O
utcome Measures.-The proportion of antiepileptic drug levels with an a
ppropriate indication and, of those, the proportion sampled appropriat
ely. Results.-Overall, 27% (95% confidence interval, 24% to 30%) of le
vels had an appropriate indication. Interrater agreement for appropria
teness was substantial (kappa=0.61). There was no significant differen
ce in the appropriateness rate among the four drugs (range, 25% to 29%
), Of the 624 antiepileptic drug level determinations considered inapp
ropriate (73%), only four (0.6%) were more than 20% higher than the up
per limit of normal, and none of the four patients had clinical signs
of drug toxicity, A median of six levels (range, one through 69) was d
etermined per patient, and the median interval between level determina
tions was 24 hours. Of the 27% of level determinations with an appropr
iate indication, 51% were sampled correctly, resulting in an overall a
ppropriateness rate of 14%. Conclusions.-Only 27% of antiepileptic dru
g level determinations had an appropriate indication, and half of thes
e were not sampled correctly. Routine daily monitoring without pharmac
ological justification accounted for most of the inappropriate drug le
vel determinations. Efforts to decrease inappropriate monitoring may r
esult in substantial cost reductions without missing important clinica
l results.