Large numbers of specimens (5000-18 000) were screened for amphetamine
s, barbiturates, cocaine, marijuana, opiates, and phencyclidine by RIA
(Roche), Emit II (Syva), and a new immunoassay, CEDIA (cloned enzyme
donor immunoassay, Microgenics). All immunoassays performed equivalent
ly for cocaine, opiates, and phencyclidine. All immunoassays detected
the same amphetamine/methamphetamine-positive specimens, but all also
detected numerous specimens containing cross-reacting sympathomimetic
amines. CEDIA detected 100%, Emit II 93%, and RIA 82% of the barbitura
te-positive specimens. Emit II and CEDIA detected 86-88% of the specim
ens found by RIA to be marijuana positive. A subset of specimens was a
dditionally screened by Online (Roche) and TDx (Abbott) for amphetamin
es, cocaine, and marijuana. Online and TDx also detected all of the am
phetamine-positive specimens and numerous specimens containing cross-r
eacting sympathomimetic amines. All immunoassays performed equivalentl
y for cocaine, and the four nonisotopic tests detected 86-89% of the m
arijuana positives found by RIA. Interfering sympathomimetic amine dru
g compounds can be eliminated by using an oxidizing agent, thus decrea
sing the number of unconfirmable amphetamine presumptive positives. Th
e CEDIAs for all of the major drugs of abuse are reliable and effectiv
e for large-volume urine screening programs.