Intravenous administration of prochlorperazine by 15-minute infusion versus 2-minute bolus does not affect the incidence of akathisia: A prospective,randomized, controlled trial
Rw. Collins et al., Intravenous administration of prochlorperazine by 15-minute infusion versus 2-minute bolus does not affect the incidence of akathisia: A prospective,randomized, controlled trial, ANN EMERG M, 38(5), 2001, pp. 491-496
Study objective: We sought to compare the rate of akathisia after administr
ation of intravenous prochlorperazine as a 2-minute bolus or 15-minute infu
sion.
Methods: We conducted a prospective, randomized, double-blind study in the
emergency department of a central-city teaching hospital. Patients aged 18
years or older treated with prochlorperazine for headache, nausea, or vomit
ing were eligible for inclusion. Study participants were randomized to rece
ive 10 mg of prochlorperazine administered intravenously by means of 2-minu
te push (bolus group) or 10 mg diluted in 50 mL of normal saline solution a
dministered by means of intravenous infusion during a 15-minute period (inf
usion group). The main outcome was the number of study participants experie
ncing akathisia within 60 minutes of administration. Akathisia was defined
as either a spontaneous report of restlessness or agitation or a change of
2 or more in the patient-reported akathisia rating scale and a change of at
least I in the investigator-observed akathisia rating scale. The intensity
of headache and nausea was measured with a 100-mm visual analog scale.
Results: One hundred patients were enrolled. One study participant was excl
uded after protocol violation. Seventy-three percent (73/99) of the study p
articipants were treated for headache and 70% (70/99) for nausea. In the bo
lus group, 26.0% (13/50) had akathisia compared with 32.7% (16/49) in the i
nfusion group (Delta=-6.7%; 95% confidence interval [Cl] -24.6% to 11.2%).
The difference between the bolus and infusion groups in the percentage of p
articipants who saw a 50% reduction in their headache intensity within 30 m
inutes was 11.8% (95% Cl -9.6% to 33.3%). The difference in the percentage
of patients with a 50% reduction in their nausea was 12.6% (95% Cl -4.6% to
29.8%).
Conclusion: A 50% reduction in the incidence of akathisia when prochlorpera
zine was administered by means of 15-minute intravenous infusion versus a 2
-minute intravenous push was not detected. The efficacy of prochlorperazine
in the treatment of headache and nausea likewise did not appear to be affe
cted by the rate of administration, although no formal statistical comparis
ons were made.