Abstract
Background
Migraine headaches are a common reason for pediatric emergency department (ED) visits.
Small studies suggest the potential efficacy of sub-anesthetic doses of propofol for
migraine with a favorable side effect profile and potentially decreased length of
stay (LOS).
Objective
The objective of this study was to compare the efficacy of low-dose propofol (LDP)
to standard therapy (ST) in pediatric migraine treatment.
Methods
We conducted a prospective, pragmatic randomized controlled trial from April 2014
through June 2016 in the ED at two pediatric hospitals. Patients aged 7–19 years were
eligible if they were diagnosed with migraine by the emergency physician and had a
presenting visual analog pain score (VAS) of 6–10. Primary outcome was the percent
of pain reduction. Secondary outcomes were ED LOS, 24-h rebound headache, return visits
to the ED, and adverse reactions.
Results
Seventy-four patients were enrolled, but 8 were excluded, leaving 66 patients in the
final analysis (36 ST, 30 LDP). Pain reduction was 59% for ST and 51% for LDP (p = 0.34) with 72.2% vs. 73.3% achieving a VAS ≤ 4 with initial therapy (p = 0.92). There was a nonsignificant trend toward shorter median LOS from drug administration
to final disposition favoring propofol (79 min vs. 111 min; p = 0.09). Rebound headache was significantly more common in the ST vs. LDP group (66.7%
vs. 25.0%; p = 0.01).
Conclusions
LDP did not achieve better pain reduction than ST, however, LDP was associated with
significantly fewer rebound headaches and a nonsignificant trend toward shorter median
LOS from drug administration to disposition.
Keywords
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Article info
Publication history
Published online: February 15, 2018
Accepted:
January 6,
2018
Received in revised form:
January 3,
2018
Received:
October 23,
2017
Footnotes
This was partially supported by an American Academy of Pediatrics resident research award.
Identification
Copyright
© 2018 Elsevier Inc. All rights reserved.