Dias Ana V, Zeidan Ziad, Copp Matt, Eslabra Frances, Hassan Rawan, Middleton Rory
Orthopaedics, Royal College of Surgeons of England, London, GBR.
Orthopaedics and Trauma, Royal Cornwall Hospital, Truro, GBR.
Cureus. 2024 Feb 4;16(2):e53537. doi: 10.7759/cureus.53537. eCollection 2024 Feb.
Background Penthrox is a handheld inhaler that administers methoxyflurane. Its use is approved for analgesia in moderate-to-severe trauma-related pain in adults in the ED. The literature currently lacks methodologically robust qualitative data on individual patient experiences. Using a structured qualitative study, we set out to address this shortcoming. Methods Five patients were selected as a focus group to identify key themes they felt were important to explore, and these were included in the questionnaire design. We retrospectively identified all uses of Penthrox in the ED from June to August 2021. Qualitative data was gathered using the Trickett short interview method, and responses were grouped into positive and negative descriptors. In addition, quantitative data concerning their experience using the 5-point Likert scale was also gathered. Results A total of 101 participants responded to the questionnaire. Penthrox was utilised mainly for the manipulation of fractures, most commonly those of the ankle and wrist. Around 90% reported an overall satisfaction of ≥ good, and 97% reported the ease of use to be ≥ good. Its analgesic effectiveness was rated as excellent by 52%, and ≥ good by 89%. The most reported side effects were drowsiness (13%) and nausea (7%). The majority reported no side effects (74%). About 94% of the participants said they would take it again if required. An NVivo word cloud (Lumivero, Denver, CO, USA) was created visually, confirming an overall positive experience amongst the patients. Conclusions This study shows that Penthrox is a well-tolerated and user-friendly means of alleviating trauma-related pain in the ED. It highlights the importance of taking into consideration the individual patient journey alongside robust evidence-based data on safety and efficacy for the development of a holistic treatment.
喷他佐辛是一种用于吸入甲氟醚的手持吸入器。其已获批用于急诊科成人中度至重度创伤相关疼痛的镇痛。目前的文献缺乏关于个体患者体验的方法学上可靠的定性数据。我们通过一项结构化定性研究来解决这一不足。方法:选取5名患者组成焦点小组,以确定他们认为重要且值得探索的关键主题,并将这些主题纳入问卷设计。我们回顾性确定了2021年6月至8月急诊科所有喷他佐辛的使用情况。使用特里克特简短访谈法收集定性数据,并将回答分为正面和负面描述词。此外,还收集了关于他们使用5点李克特量表体验的定量数据。结果:共有101名参与者回复了问卷。喷他佐辛主要用于骨折处理,最常见的是脚踝和手腕骨折。约90%的人报告总体满意度≥良好,97%的人报告易用性≥良好。其镇痛效果被52%的人评为优秀,89%的人评为≥良好。报告最多的副作用是嗜睡(13%)和恶心(7%)。大多数人(74%)报告无副作用。约94%的参与者表示如果需要会再次使用。通过可视化创建了一个NVivo词云(美国科罗拉多州丹佛市的Lumivero公司),证实患者总体体验良好。结论:本研究表明,喷他佐辛是急诊科缓解创伤相关疼痛的一种耐受性良好且用户友好的方法。它强调了在基于强有力的安全和疗效循证数据的同时,考虑个体患者历程对于制定整体治疗方案的重要性。