Abstract
Background
Gastroparesis associated nausea, vomiting & abdominal pain (GP N/V/AP) are common
presentations to the emergency department (ED). Treatment is often limited to antiemetic,
prokinetic, opioid, & nonopioid agents. Haloperidol (HP) has been shown to have analgesic
& antiemetic properties. We sought to evaluate HP in the ED as an alternative treatment
of GP N/V/AP.
Methods
Using an electronic medical record, 52 patients who presented to the ED w/GP N/V/AP
secondary to diabetes mellitus and were treated w/HP were identified. Patients who
received HP were compared to themselves w/the most recent previous encounter in which
HP was not administered. ED length of stay (LOS), additional antiemetics/prokinetics
administered, hospital LOS, and morphine equivalent doses of analgesia (ME) from each
visit were recorded. Descriptive statistics, categorical (Chi Square Test or Z-Test
for proportion) and continuous (Wilcoxon Signed Rank Test) comparisons were calculated.
Statistical significance was considered for two tail p-values less than 0.05.
Results
A statistically significant reduction in ME (Median 6.75 [IQR 7.93] v 10.75 [IQR12]:
p = 0.001) and reduced admissions for GP (5/52 v 14/52: p = 0.02) when HP was administered was observed. There were no statistically significant
differences in ED or hospital LOS, and additional antiemetics administered between
encounters in which HP was administered and not administered. No complications were
identified in patients who received HP.
Conclusions
The rate of admission and ME was found to be significantly reduced in patients with
GP secondary to diabetes mellitus who received HP. HP may represent an appropriate,
effective, and safe alternative to traditional analgesia and antiemetic therapy in
the ED management of GP associated N/V/AP.
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Article Info
Publication History
Published online: March 12, 2017
Accepted:
March 10,
2017
Received in revised form:
March 10,
2017
Received:
January 18,
2017
Footnotes
☆Meetings: An abstract only version of this article was presented at ACEP 2016.
Identification
Copyright
© 2017 Elsevier Inc. All rights reserved.