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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

机译:新型笔设备用于自我管理重组人类生长激素的验证和易用性:来自两中心可用性研究的结果

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Abstract: 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?.
机译:摘要:尽管不坚持治疗很常见,但严格遵守推荐的治疗方案对于重组人生长激素治疗的成功至关重要。使用/存储期间的易用性和安全性是设计用于长期使用的生长激素注射装置的几个重要因素之一。进行这项研究是为了验证可用性并评估新笔设备(SurePal?)的易用性,该笔设备已开发用于支持日常使用的重组人类生长激素产品Omnitrope?。 (生长激素)。这项研究的主要目的是评估代表临床实践中笔的预定使用者的研究参与者是否能够有效,安全地在注射垫中进行注射程序,并能够在不遭受针刺伤害的情况下拆卸笔。共有106名参与者(61名成人和45名儿童/青少年)在两个学习中心(一个在美国,一个在德国)入学。两项主要可用性任务的结果均符合预定义的接受标准,> 85%的参与者成功执行了每个任务。大多数参与者还成功地执行了所有其他评估的任务/处理步骤,成功率高反映在将每个任务归类为“非常容易”或“容易”的参与者中。第二次使用该设备后,87%–97%的参与者将其评为“非常容易”或“容易”使用。总而言之,这种新型笔装置对于成人和儿童都是安全且易于使用的,并且将有助于支持对重组人类生长激素产品Omnitrope?的有效,长期每日给药。

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