Pain control measures in sickle cell diseases are not uniform. Most clinici
ans use parenteral morphine or meperidine for severe pain. Reports of seizu
res associated with meperidine have led to a growing reliance on intravenou
s morphine, usually with patient-controlled devices. Acceptance of morphine
has been poor among patients, and many prefer meperidine. The aim of this
retrospective study was to determine the incidence of meperidine-associated
seizures in a large, mostly pediatric population with sickling disorders.
The results suggest that the incidence of seizures with meperidine is extre
mely small (0.4% of patients; 0.06% of admissions). The risk of seizures sh
ould not dissuade clinicians from using this drug.