Lp. James et al., Phenothiazine, butyrophenone, and other psychotropic medication poisoningsin children and adolescents, J TOX-CLIN, 38(6), 2000, pp. 615-623
Objective: To describe the presentation, epidemiology, management, and outc
ome of phenothiazine and butyrophenone ingestions in children requiring hos
pitalization. Method: Retrospective case series in two pediatric hospitals,
Results: Eighty-six cases were identified among 83 patients. The majority
(69.7%) of ingestions occurred in children <6 years of age and there was no
gender predominance, These ingestions mere more common in African American
s (65.1%), They occurred more commonly in the patient's (64.0%) or a relati
ve's (22.1%) home and haloperidol and thioridazine accounted for 58.1% of e
xposures. Depressed levels of consciousness and dystonia were the most comm
on presenting signs, present in 90.7% and 51.2% of patients, respectively.
Miosis occurred in only 13.9% of the patients. Fluid boluses were administe
red to 28.7% of the patients but about a quarter of these had coingested po
tentially cardiotoxic drugs, In addition, 2 of the 12 (13.9%) patients with
abnormal electrocardiograms had also ingested potentially cardiotoxic drug
s. Numerous diagnostic tests were performed in these patients including ele
ctrolyte panels (80.2%), complete blood counts (69.8%), liver function test
s (31.4%), serum osmolality (20.9%), blood cultures (10.5%), lumbar punctur
es (17.4%), head computed tomographies (15.1%), and electroencephalograms (
3.5%). The median length of hospitalization was 1.78 (range 1-9) days and t
here were no deaths. Patients presenting with dystonias were more likely to
have extensive diagnostic testing for neurologic disease than those presen
ting without dystonias, Conclusion: The presentation of phenothiazine and b
utyrophenone ingestions in children and adolescents may be nonspecific and
confounded by coingestants, Patients with dystonias had more extensive neur
ologic testing than patients without dystonias, suggesting that physicians
may not recognize dystonias as a clinical finding characteristic of phenoth
iazine or butyrophenone exposure.