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Improvised traction splints: a wilderness medicine tool or hindrance?

Abstract

OBJECTIVES
To investigate whether a traction splint made from improvised materials is as efficacious as commercially available devices in terms of traction provided and perceived comfort and stability.
METHODS
This was a prospective randomized crossover study utilizing 10 healthy, uninjured volunteers. The subjects were randomized to be placed in 4 different traction devices, in differing order, each for 30 minutes. Three of the traction splints are commercially available: The HARE, Sager, and Faretech CT-EMS. The fourth traction device was an improvised splint made as described in Medicine for the Backcountry: A Practical Guide to Wilderness First Aid. At the end of 30 minutes the pounds of force created by each device was measured. The volunteers were also asked at that time to subjectively report the comfort and stability of the splint separately on a scale from 1 to 10.
RESULTS
All traction splints performed similarly with regard to the primary outcome measure of mean pounds of traction created at the end of 30 minutes of application with results ranging from 10.4 to 13.3 pounds. There was little difference reported by participants in regard to stability or comfort between the 4 traction devices.
CONCLUSIONS
In this small pilot study, an improvised traction splint was not inferior to commercially available devices. Further research in needed in this area.

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  • Publisher Full Text
  • Authors

    Weichenthal L, Spano S, Horan B, Miss J

    Institution

    Department of Emergency Medicine, UCSF-Fresno Medical Education Program, Fresno, CA 93701, USA. lweichenthal@fresno.ucsf.edu

    Source

    Wilderness & environmental medicine 23:1 2012 Mar pg 61-4

    MeSH

    Adult
    Cross-Over Studies
    Emergency Treatment
    Female
    Fractures, Bone
    Humans
    Male
    Patient Satisfaction
    Pilot Projects
    Prospective Studies
    Splints
    Traction
    Wilderness Medicine

    Pub Type(s)

    Journal Article
    Randomized Controlled Trial

    Language

    eng

    PubMed ID

    22441092