Cargando…

Acceptability of the reusable SurePal™ self-injection device for Omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study

BACKGROUND: SurePal™ is a reusable self-injection system that has been developed to support daily administration of Omnitrope(®) (Sandoz, Kundl, Austria). A questionnaire-based cross-sectional survey was conducted to evaluate acceptability of, and preference for, SurePal™ in pediatric patients who w...

Descripción completa

Detalles Bibliográficos
Autores principales: Partsch, Carl-Joachim, Schnabel, Dirk, Ehtisham, Sarah, Johnstone, Helen C, Zabransky, Markus, Kiess, Wieland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578482/
https://www.ncbi.nlm.nih.gov/pubmed/26405430
http://dx.doi.org/10.2147/MDER.S93209
_version_ 1782391123071729664
author Partsch, Carl-Joachim
Schnabel, Dirk
Ehtisham, Sarah
Johnstone, Helen C
Zabransky, Markus
Kiess, Wieland
author_facet Partsch, Carl-Joachim
Schnabel, Dirk
Ehtisham, Sarah
Johnstone, Helen C
Zabransky, Markus
Kiess, Wieland
author_sort Partsch, Carl-Joachim
collection PubMed
description BACKGROUND: SurePal™ is a reusable self-injection system that has been developed to support daily administration of Omnitrope(®) (Sandoz, Kundl, Austria). A questionnaire-based cross-sectional survey was conducted to evaluate acceptability of, and preference for, SurePal™ in pediatric patients who were prescribed treatment with Omnitrope(®) within routine clinical care. METHODS: This multicenter, observational study was incorporated into the ongoing non-interventional PATRO (PAtients TReated with Omnitrope(®)) Children study. Patients (or caregivers) were provided with a questionnaire that included five main topics; attractiveness of the device, training received, using SurePal™, the low drug wastage system, and experience versus other devices used previously (where applicable). Questions were scored on a 5-point scale, with −2 being the worst possible outcome (eg, very hard/very poor) and 2 being the best possible outcome (eg, very easy/excellent). RESULTS: A total of 186 patients were included in this study (Germany, n=154; UK, n=32). The attractiveness of SurePal™ was rated as excellent/good by 87.1% of patients. Overall, 86.5% of patients found that using their SurePal™ was very easy/easy. Almost all patients (96.2%) found that preparing their SurePal™ for injection was very easy/easy, and 89.2% found that injecting with SurePal™ was very easy/easy. 85.5% of patients recorded that the dose memory function was helpful, and 87.6% that taking their SurePal™ apart after an injection was very easy/easy. Of the 88 patients who recorded that they had used the low drug waste feature, 89.8% found the feature to be helpful. Among pre-treated patients (n=42), 81% recorded that SurePal™ was much better/better than their previously used device. CONCLUSION: This questionnaire-based cross-sectional survey in pediatric patients confirms the ease of use and patient preference for SurePal™, a reusable self-injection system that has been developed to support daily administration of Omnitrope(®).
format Online
Article
Text
id pubmed-4578482
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-45784822015-09-24 Acceptability of the reusable SurePal™ self-injection device for Omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study Partsch, Carl-Joachim Schnabel, Dirk Ehtisham, Sarah Johnstone, Helen C Zabransky, Markus Kiess, Wieland Med Devices (Auckl) Original Research BACKGROUND: SurePal™ is a reusable self-injection system that has been developed to support daily administration of Omnitrope(®) (Sandoz, Kundl, Austria). A questionnaire-based cross-sectional survey was conducted to evaluate acceptability of, and preference for, SurePal™ in pediatric patients who were prescribed treatment with Omnitrope(®) within routine clinical care. METHODS: This multicenter, observational study was incorporated into the ongoing non-interventional PATRO (PAtients TReated with Omnitrope(®)) Children study. Patients (or caregivers) were provided with a questionnaire that included five main topics; attractiveness of the device, training received, using SurePal™, the low drug wastage system, and experience versus other devices used previously (where applicable). Questions were scored on a 5-point scale, with −2 being the worst possible outcome (eg, very hard/very poor) and 2 being the best possible outcome (eg, very easy/excellent). RESULTS: A total of 186 patients were included in this study (Germany, n=154; UK, n=32). The attractiveness of SurePal™ was rated as excellent/good by 87.1% of patients. Overall, 86.5% of patients found that using their SurePal™ was very easy/easy. Almost all patients (96.2%) found that preparing their SurePal™ for injection was very easy/easy, and 89.2% found that injecting with SurePal™ was very easy/easy. 85.5% of patients recorded that the dose memory function was helpful, and 87.6% that taking their SurePal™ apart after an injection was very easy/easy. Of the 88 patients who recorded that they had used the low drug waste feature, 89.8% found the feature to be helpful. Among pre-treated patients (n=42), 81% recorded that SurePal™ was much better/better than their previously used device. CONCLUSION: This questionnaire-based cross-sectional survey in pediatric patients confirms the ease of use and patient preference for SurePal™, a reusable self-injection system that has been developed to support daily administration of Omnitrope(®). Dove Medical Press 2015-09-15 /pmc/articles/PMC4578482/ /pubmed/26405430 http://dx.doi.org/10.2147/MDER.S93209 Text en © 2015 Partsch et al. This work is published by Dove Medical Press Limited, 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 Limited, provided the work is properly attributed.
spellingShingle Original Research
Partsch, Carl-Joachim
Schnabel, Dirk
Ehtisham, Sarah
Johnstone, Helen C
Zabransky, Markus
Kiess, Wieland
Acceptability of the reusable SurePal™ self-injection device for Omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study
title Acceptability of the reusable SurePal™ self-injection device for Omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study
title_full Acceptability of the reusable SurePal™ self-injection device for Omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study
title_fullStr Acceptability of the reusable SurePal™ self-injection device for Omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study
title_full_unstemmed Acceptability of the reusable SurePal™ self-injection device for Omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study
title_short Acceptability of the reusable SurePal™ self-injection device for Omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study
title_sort acceptability of the reusable surepal™ self-injection device for omnitrope(®) among pediatric patients: results from a questionnaire-based, cross-sectional, multicenter observational study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578482/
https://www.ncbi.nlm.nih.gov/pubmed/26405430
http://dx.doi.org/10.2147/MDER.S93209
work_keys_str_mv AT partschcarljoachim acceptabilityofthereusablesurepalselfinjectiondeviceforomnitropeamongpediatricpatientsresultsfromaquestionnairebasedcrosssectionalmulticenterobservationalstudy
AT schnabeldirk acceptabilityofthereusablesurepalselfinjectiondeviceforomnitropeamongpediatricpatientsresultsfromaquestionnairebasedcrosssectionalmulticenterobservationalstudy
AT ehtishamsarah acceptabilityofthereusablesurepalselfinjectiondeviceforomnitropeamongpediatricpatientsresultsfromaquestionnairebasedcrosssectionalmulticenterobservationalstudy
AT johnstonehelenc acceptabilityofthereusablesurepalselfinjectiondeviceforomnitropeamongpediatricpatientsresultsfromaquestionnairebasedcrosssectionalmulticenterobservationalstudy
AT zabranskymarkus acceptabilityofthereusablesurepalselfinjectiondeviceforomnitropeamongpediatricpatientsresultsfromaquestionnairebasedcrosssectionalmulticenterobservationalstudy
AT kiesswieland acceptabilityofthereusablesurepalselfinjectiondeviceforomnitropeamongpediatricpatientsresultsfromaquestionnairebasedcrosssectionalmulticenterobservationalstudy