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Pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes

OBJECTIVE: Pen needles used for subcutaneous injections have gradually become shorter, thinner and more thin walled, and thereby less robust to patient reuse. Thus, different needle sizes, alternative tip designs and needles resembling reuse were tested to explore how needle design influences ease o...

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Autores principales: Præstmark, Kezia A, Jensen, Morten L, Madsen, Nils B, Kildegaard, Jonas, Stallknecht, Bente M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5174793/
https://www.ncbi.nlm.nih.gov/pubmed/28074137
http://dx.doi.org/10.1136/bmjdrc-2016-000266
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author Præstmark, Kezia A
Jensen, Morten L
Madsen, Nils B
Kildegaard, Jonas
Stallknecht, Bente M
author_facet Præstmark, Kezia A
Jensen, Morten L
Madsen, Nils B
Kildegaard, Jonas
Stallknecht, Bente M
author_sort Præstmark, Kezia A
collection PubMed
description OBJECTIVE: Pen needles used for subcutaneous injections have gradually become shorter, thinner and more thin walled, and thereby less robust to patient reuse. Thus, different needle sizes, alternative tip designs and needles resembling reuse were tested to explore how needle design influences ease of insertion, pain and skin trauma. RESEARCH DESIGN AND METHODS: 30 subjects with injection-treated type 2 diabetes and body mass index 25–35 kg/m(2) were included in the single-blinded study. Each subject received abdominal insertions with 18 different types of needles. All needles were tested twice per subject and in random order. Penetration force (PF) through the skin, pain perception on 100 mm visual analog scale, and change in skin blood perfusion (SBP) were quantified after the insertions. RESULTS: Needle diameter was positively related to PF and SBP (p<0.05) and with a positive pain trend relation. Lack of needle lubrication and small ‘needle hooks’ increased PF and SBP (p<0.05) but did not affect pain. Short-tip, obtuse needle grinds affected PF and SBP, but pain was only significantly affected in extreme cases. PF in skin and in polyurethane rubber were linearly related, and pain outcome was dependent of SBP increase. CONCLUSIONS: The shape and design of a needle and the needle tip affect ease of insertion, pain and skin trauma. Relations are seen across different data acquisition methods and across species, enabling needle performance testing outside of clinical trials. TRIAL REGISTRATION NUMBER: NCT02531776; results.
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spelling pubmed-51747932017-01-10 Pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes Præstmark, Kezia A Jensen, Morten L Madsen, Nils B Kildegaard, Jonas Stallknecht, Bente M BMJ Open Diabetes Res Care Technological Advances OBJECTIVE: Pen needles used for subcutaneous injections have gradually become shorter, thinner and more thin walled, and thereby less robust to patient reuse. Thus, different needle sizes, alternative tip designs and needles resembling reuse were tested to explore how needle design influences ease of insertion, pain and skin trauma. RESEARCH DESIGN AND METHODS: 30 subjects with injection-treated type 2 diabetes and body mass index 25–35 kg/m(2) were included in the single-blinded study. Each subject received abdominal insertions with 18 different types of needles. All needles were tested twice per subject and in random order. Penetration force (PF) through the skin, pain perception on 100 mm visual analog scale, and change in skin blood perfusion (SBP) were quantified after the insertions. RESULTS: Needle diameter was positively related to PF and SBP (p<0.05) and with a positive pain trend relation. Lack of needle lubrication and small ‘needle hooks’ increased PF and SBP (p<0.05) but did not affect pain. Short-tip, obtuse needle grinds affected PF and SBP, but pain was only significantly affected in extreme cases. PF in skin and in polyurethane rubber were linearly related, and pain outcome was dependent of SBP increase. CONCLUSIONS: The shape and design of a needle and the needle tip affect ease of insertion, pain and skin trauma. Relations are seen across different data acquisition methods and across species, enabling needle performance testing outside of clinical trials. TRIAL REGISTRATION NUMBER: NCT02531776; results. BMJ Publishing Group 2016-12-15 /pmc/articles/PMC5174793/ /pubmed/28074137 http://dx.doi.org/10.1136/bmjdrc-2016-000266 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Technological Advances
Præstmark, Kezia A
Jensen, Morten L
Madsen, Nils B
Kildegaard, Jonas
Stallknecht, Bente M
Pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes
title Pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes
title_full Pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes
title_fullStr Pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes
title_full_unstemmed Pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes
title_short Pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes
title_sort pen needle design influences ease of insertion, pain, and skin trauma in subjects with type 2 diabetes
topic Technological Advances
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5174793/
https://www.ncbi.nlm.nih.gov/pubmed/28074137
http://dx.doi.org/10.1136/bmjdrc-2016-000266
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