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Human factors validation study of 3 mg sumatriptan autoinjector, for migraine patients

机译:偏头痛患者3 mg舒马曲坦自动注射器的人为因素验证研究

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Background: Migraine pain relief is reported by more than 50% of patients who receive low dose (3?mg) of sumatriptan. Currently, there is no two-step autoinjector of low-dose sumatriptan available on the market for acute migraine treatment. To fulfill this need, a fully assembled, single-dose, subcutaneous autoinjector (sumatriptan 3 mg; product-code DFN-11) was developed. The device allows for injection with a simple two-step, push-to-inject process and provides feedback of the injection activation, progress, and completion. Objective: To determine if DFN-11 autoinjector can be used correctly and safely by migraine patients. Methods and participants: A human factors validation study was conducted with 45 migraine patients (30 oral-only medications users; 15 injectable sumatriptan users) who performed one unaided simulated injection. Two days prior, half the oral participants were briefly trained. All others were only given the device to inspect and written instructions to review. No injections were performed during the initial session. All participants received written instructions at the injection session. Results: All participants (45/45; 100%) performed the injection without any errors. Objective measures included device removal from packaging, cap removal, expiration date check, -inspection of fluid in window, identification of allowable injection site, proper device positioning, dose confirmation, and device disposal. All participants (45/45; 100%) reported no difficulty administering the injection and no concerns about using the autoinjector during a severe migraine onset. Conclusion: The results showed that the DFN-11 autoinjector can be used with safe handling without patterns of confusion, failures, high-risk errors, wet injections, or patient safety risks. The DFN-11 autoinjector was validated to be used correctly and safely by migraine patients, whether they were injection experienced, unexperienced, trained, or self-trained.
机译:背景:据报道,超过50%的患者接受低剂量(3毫克)舒马曲坦的偏头痛缓解。当前,市场上没有可用于急性偏头痛治疗的低剂量舒马曲坦两步自动注射器。为了满足这一需求,开发了完全组装的单剂量皮下自动注射器(舒马普坦3毫克;产品代码DFN-11)。该设备允许通过简单的两步推入式注射过程进行注射,并提供注射激活,进展和完成的反馈。目的:确定偏头痛患者是否可以正确安全地使用DFN-11自动注射器。方法和参与者:对45名偏头痛患者(30名仅口服药物使用者; 15名可注射舒马曲坦使用者)进行了一项人为因素验证研究,他们进行了一次独立的模拟注射。前两天,对一半的口语参与者进行了简短的培训。其他所有设备都只提供了检查设备和书面说明进行审查。在初始阶段没有进行注射。所有参与者在注射会议上均收到书面指示。结果:所有参与者(45/45; 100%)进行注射均无任何错误。客观措施包括从包装中取出器械,取下瓶盖,检查保质期,检查窗口中的液体,确定允许的注射部位,正确的器械位置,剂量确认和器械处置。所有参与者(45/45; 100%)报告说,在严重偏头痛发作期间,注射给药没有困难,也没有担心使用自动注射器。结论:结果表明,DFN-11自动注射器可以安全使用,而不会出现混淆,失败,高风险错误,湿式注射或患者安全风险的情况。验证偏头痛患者可以正确,安全地使用DFN-11自动注射器,无论他们是注射经验丰富,经验不足,受过训练的还是自我训练的。

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