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Effect of Introducing the Mucosal Atomization Device for Fentanyl Use in Out-of-Hospital Pediatric Trauma Patients

Published online by Cambridge University Press:  24 May 2013

Daniel P. O'Donnell*
Affiliation:
Department of Emergency Medicine, Indiana University School of Medicine, Indianapolis, Indiana USA
Luke C. Schafer
Affiliation:
Department of Emergency Medicine, Indiana University School of Medicine, Indianapolis, Indiana USA
Andrew C. Stevens
Affiliation:
Department of Emergency Medicine, Indiana University School of Medicine, Indianapolis, Indiana USA
Elizabeth Weinstein
Affiliation:
Department of Emergency Medicine, Indiana University School of Medicine, Indianapolis, Indiana USA
Charles M. Miramonti
Affiliation:
Department of Emergency Medicine, Indiana University School of Medicine, Indianapolis, Indiana USA
Mary Ann Kozak
Affiliation:
Department of Emergency Medicine, Indiana University School of Medicine, Indianapolis, Indiana USA
*
Correspondence: Daniel P. O'Donnell, MD Department of Emergency Medicine Indiana University School of Medicine 3930 Georgetown Rd. Indianapolis, Indiana 46254 USA E-mail [email protected]

Abstract

Background

Pain associated with pediatric trauma is often under-assessed and under-treated in the out-of-hospital setting. Administering an opioid such as fentanyl via the intranasal route is a safe and efficacious alternative to traditional routes of analgesic delivery and could potentially improve pain management in pediatric trauma patients.

Objective

The study sought to examine the effect of introducing the mucosal atomization device (MAD) on analgesia administration as an alternative to intravenous fentanyl delivery in pediatric trauma patients. The hypothesis for the study is that the introduction of the MAD would increase the administration of fentanyl in pediatric trauma patients.

Methods

The research utilized a 2-group design (pre-MAD and post-MAD) to study 946 pediatric trauma patients (age <16) transported by a large, urban EMS agency to one of eight hospitals in Marion County, which is located in Indianapolis Indiana. Two emergency medicine physicians independently determined whether the patient met criteria for pain medication receipt and a third reviewer resolved any disagreements. A comparison of the rates of fentanyl administration in both groups was then conducted.

Results

There was no statistically significant difference in the rate of fentanyl administration between the pre-MAD (30.4%) and post-MAD groups (37.8%) (P = .238). A subgroup analysis showed that age and mechanism of injury were stronger predictors of fentanyl administration.

Conclusion

Contrary to the hypothesis, the addition of the MAD device did not increase fentanyl administration rates in pediatric trauma patients. Future research is needed to address the barriers to analgesia administration in pediatric trauma patients.

O'DonnellDP, SchaferLC, StevensAC, WeinsteinE, MiramontiCM, KozakMA. Effect of Introducing the Mucosal Atomization Device for Fentanyl Use in Out-of-Hospital Pediatric Trauma Patients. Prehosp Disaster Med. 2013;28(4):1-3.

Type
Brief Report
Copyright
Copyright © World Association for Disaster and Emergency Medicine 2013 

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References

1.American Academy of Pediatrics. Committee on Psychosocial Aspects of Child and Family Health; Task Force on Pain in Infants, Children, and Adolescents. The assessment and management of acute pain in infants, children, and adolescents. Pediatrics. 2001;108(3):793-797.Google Scholar
2.Swor, R, McEachin, CM, Seguin, D, Grall, KH. Prehospital pain management in children suffering traumatic injury. Prehosp Emerg Care. 2005;9(1):40-43.CrossRefGoogle ScholarPubMed
3.Alexander, J, Manno, M. Underuse of analgesia in very young pediatric patients with isolated painful injuries. Ann Emerg Med. 2003;41(5):617-622.CrossRefGoogle ScholarPubMed
4.Garrison, HG, Maio, RF, Spaite, D, et al. Emergency Medical Services Outcomes Project (EMSOP) IV: pain measurement in out-of-hospital outcomes research. Ann Emerg Med. 2002;40(2):172-179.CrossRefGoogle Scholar
5.Zempsky, WT, Cravero, JP. American Academy of Pediatrics Committee on Pediatric Emergency Medicine and Section on Anesthesiology and Pain Medicine. Relief of pain and anxiety in pediatric patients in emergency medical systems. Pediatrics. 2004;114(5):1348-1356.CrossRefGoogle Scholar
6.Borland, ML, Jacobs, I, King, B, O'Brien, D. A randomized controlled trial comparing intranasal fentanyl to intravenous morphine for managing acute pain in children in the emergency department. Ann Emerg Med. 2007;49(3):335-340.CrossRefGoogle ScholarPubMed
7.Borland, ML, Jacobs, I, Geelhoed, G. Intranasal fentanyl reduces acute pain in children in the emergency department: a safety and efficacy study. Emerg Med (Fremantle). 2002;14(3):275-280.CrossRefGoogle ScholarPubMed
8.Fleiss, JL. Statistical Methods for Rates and Proportions. New York: John Wiley & Sons; 1981.Google Scholar
9.Hennes, H, Kim, MK, Pirrallo, RG. Prehospital pain management: a comparison of providers’ perceptions and practices. Prehosp Emerg Care. 2005;9(1):32-39.CrossRefGoogle ScholarPubMed
10.Izsak, E, Moore, JL, Stringfellow, K, Oswanski, MF, Lindstrom, DA, Stombaugh, HA. Prehospital pain assessment in pediatric trauma. Prehosp Emerg Care. 2008;12(2):182-186.CrossRefGoogle ScholarPubMed