RESEARCH ARTICLE
Portable Medical Equipment Holder Assists Pediatric Venipuncture
Eugen-Matthias Strehle1, *, Thomas William Needham2
Article Information
Identifiers and Pagination:
Year: 2015Volume: 2
First Page: 1
Last Page: 5
Publisher ID: MEDJ-2-1
DOI: 10.2174/1874220301502010001
Article History:
Received Date: 28/8/2014Revision Received Date: 1/12/2014
Acceptance Date: 2/1/2015
Electronic publication date: 30/1/2015
Collection year: 2015
open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
Abstract
Objectives:
Phlebotomy and venous cannulation are common, technically challenging and potentiallydistressing procedures in pediatrics. The aim of this pilot study was to assess whether a novel medical equipment holdercould be a useful adjunct for venipuncture in children.
Methods:
Doctors and nurses at a district general hospital were asked to analyze the portable medical equipment holderand complete a questionnaire. The questionnaire consisted of twelve questions regarding seniority of the practitioner andtheir opinions of the device.
Results:
Fifty-three questionnaires were completed by a variety of pediatric health professionals. Overall, 98% ofparticipants rated the device as useful, 2% assumed a neutral position and no practitioner described the device as notuseful. A positive first impression was shared by 92% of the participants. A non-disposable device was preferred over thedisposable alternative. The square shape and plain colour of the prototype were considered suitable by the majority ofparticipants. Plastic was the preferred material. The modal price range suggested for a non-disposable device was £5 ($8)or less. Several modifications to the design were suggested.
Conclusion:
The portable medical equipment holder was well received by the pediatric staff. Design modifications putforward by the participants progressed to the development of an improved device. Further clinical research, preferably in amulti-centre study, is required.
