Advertisement
Journal Home
Search for

Volume 27, Issue 4, Pages 475-480 (May 2009)


View previous. 21 of 44 View next.

Slower infusion of metoclopramide decreases the rate of akathisia

Linda A. Regan, MDabCorresponding Author Informationemail address, Robert S. Hoffman, MDbc, Lewis S. Nelson, MDbc

Received 5 March 2008; accepted 31 March 2008.

Abstract 

Objective

We investigated the difference in incidence of acute akathisia related to the rate of infusion in patients receiving metoclopramide for acute nausea, vomiting, or migraine headache in the emergency department (ED).

Methods

Randomized, prospective, double-blind clinical trial of patients aged 18 years and older who were to receive intravenous metoclopramide for the treatment of nausea, vomiting, or headache were eligible. Patients were excluded if they were taking medications that might mimic or mask akathisia, had a movement disorder, renal insufficiency, or were unable or unwilling to consent. Pregnant women and prisoners were also excluded. Subjects were randomized to receive 1 of 2 accepted metoclopramide administration regimens. The regimens included 10 mg of metoclopramide administered either as a 2-minute bolus (BG) or as a slow infusion for 15 minutes (IG). All patients received a normal saline placebo at the opposite rate to maintain blinding. The main outcome was development of akathisia noted at 60 minutes after drug administration as measured either with The Prince Henry Hospital akathisia rating scale or by sudden unexplained departure from the ED during treatment.

Results

One hundred twenty-seven patients were eligible for the study. Fifty-nine patients met exclusion criteria. Of the remaining 68 patients, 36 were randomized to the BG and 32 were randomized to the IG. In the BG, 11.1% of patients developed akathisia compared with 0% in the IG (P = .026). Four patients developed akathisia based on the scale and 2 departed suddenly from the ED.

Conclusions

Slower infusion of metoclopramide reduces the incidence of akathisia.

a Department of Emergency Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA

b Department of Emergency Medicine, NYU Medical Center/Bellevue Hospital Center, New York, NY 10016, USA

c New York City Poison Control Center, New York, NY 10016, USA

Corresponding Author InformationCorresponding author. Tel.: +1 410 955 5107; fax: +1 410 502 5146.

PII: S0735-6757(08)00277-5

doi:10.1016/j.ajem.2008.03.044


View previous. 21 of 44 View next.

Advertisement