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Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study
Close adherence to the recommended treatment regimen is important for the success of recombinant human growth hormone therapy, although nonadherence can be common. Ease of use and safety during use/storage are among several important factors in the design of a growth hormone injection device intende...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770891/ https://www.ncbi.nlm.nih.gov/pubmed/24039458 http://dx.doi.org/10.2147/MDER.S50088 |
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author | Rapaport, Robert Saenger, Paul Schmidt, Heinrich Hasegawa, Yukihiro Colle, Michel Loche, Sandro Marcantonio, Sandra Bonfig, Walter Zabransky, Markus Lifshitz, Fima |
author_facet | Rapaport, Robert Saenger, Paul Schmidt, Heinrich Hasegawa, Yukihiro Colle, Michel Loche, Sandro Marcantonio, Sandra Bonfig, Walter Zabransky, Markus Lifshitz, Fima |
author_sort | Rapaport, Robert |
collection | PubMed |
description | Close adherence to the recommended treatment regimen is important for the success of recombinant human growth hormone therapy, although nonadherence can be common. Ease of use and safety during use/storage are among several important factors in the design of a growth hormone injection device intended for long-term use. This study was performed to validate the usability and assess the ease of use of a new pen device (SurePal™) that has been developed to support daily administration of the recombinant human growth hormone product, Omnitrope® (somatropin). The primary objectives of the study were to assess if study participants, representing intended users of the pen in clinical practice, were able to perform an injection procedure into an injection pad effectively and safely and disassemble the pen without receiving a needlestick injury. A total of 106 participants (61 adults and 45 children/adolescents) were enrolled at two study centers (one in the US, one in Germany). Results for both primary usability tasks met the predefined acceptance criteria, with >85% of participants successfully performing each task. All of the other tasks/handling steps assessed were also successfully performed by most participants, with high success rates reflected in the high proportion of participants who classified each task as “very easy” or “easy”. After a second use of the device, 87%–97% of participants rated it as “very easy” or “easy” to use. In summary, the new pen device is safe and easy to use for both adults and children, and will help to support effective, long-term daily administration of the recombinant human growth hormone product, Omnitrope®. |
format | Online Article Text |
id | pubmed-3770891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37708912013-09-13 Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study Rapaport, Robert Saenger, Paul Schmidt, Heinrich Hasegawa, Yukihiro Colle, Michel Loche, Sandro Marcantonio, Sandra Bonfig, Walter Zabransky, Markus Lifshitz, Fima Med Devices (Auckl) Original Research Close adherence to the recommended treatment regimen is important for the success of recombinant human growth hormone therapy, although nonadherence can be common. Ease of use and safety during use/storage are among several important factors in the design of a growth hormone injection device intended for long-term use. This study was performed to validate the usability and assess the ease of use of a new pen device (SurePal™) that has been developed to support daily administration of the recombinant human growth hormone product, Omnitrope® (somatropin). The primary objectives of the study were to assess if study participants, representing intended users of the pen in clinical practice, were able to perform an injection procedure into an injection pad effectively and safely and disassemble the pen without receiving a needlestick injury. A total of 106 participants (61 adults and 45 children/adolescents) were enrolled at two study centers (one in the US, one in Germany). Results for both primary usability tasks met the predefined acceptance criteria, with >85% of participants successfully performing each task. All of the other tasks/handling steps assessed were also successfully performed by most participants, with high success rates reflected in the high proportion of participants who classified each task as “very easy” or “easy”. After a second use of the device, 87%–97% of participants rated it as “very easy” or “easy” to use. In summary, the new pen device is safe and easy to use for both adults and children, and will help to support effective, long-term daily administration of the recombinant human growth hormone product, Omnitrope®. Dove Medical Press 2013-09-02 /pmc/articles/PMC3770891/ /pubmed/24039458 http://dx.doi.org/10.2147/MDER.S50088 Text en © 2013 Rapaport et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed. |
spellingShingle | Original Research Rapaport, Robert Saenger, Paul Schmidt, Heinrich Hasegawa, Yukihiro Colle, Michel Loche, Sandro Marcantonio, Sandra Bonfig, Walter Zabransky, Markus Lifshitz, Fima Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study |
title | Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study |
title_full | Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study |
title_fullStr | Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study |
title_full_unstemmed | Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study |
title_short | Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study |
title_sort | validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770891/ https://www.ncbi.nlm.nih.gov/pubmed/24039458 http://dx.doi.org/10.2147/MDER.S50088 |
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