Developing feasible person-centred care alternatives to emergency department responses for adults with epilepsy: a discrete choice analysis mixed-methods study.

Adam J Noble, Pete Dixon, Amy Mathieson, Leone Ridsdale, Myfanwy Morgan, Alison McKinlay, Jon Dickson, Steve Goodacre, Mike Jackson, Beth Morris, Dyfrig Hughes, Anthony Marson, Emily Holmes
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引用次数: 0

Abstract

Background: Calls have been made for paramedics to have some form of care pathway that they could use to safely divert adults with epilepsy away from emergency departments and instigate ambulatory care improvements. Different configurations are possible. To know which to prioritise for implementation/evaluation, there is a need to determine which are acceptable to service users and likely National Health Service-feasible.

Objective(s): (1) Identify configurations being considered, (2) understand service users' views of them and current provision, (3) identify what sort of care service users want and (4) determine which configuration(s) is considered to achieve optimal balance in meeting users' preference and being National Health Service-feasible.

Design: Service providers were surveyed to address objective 1. Interviews with service users addressed objective 2. Objective 3 was addressed by completing discrete choice experiments. These determined users' care preferences for different seizure scenarios. Objective 4 was addressed by completing 'knowledge exchange' workshops. At these, stakeholders considered the findings on users' stated preferences and judged different pathway configurations against Michie's 'acceptability, practicability, effectiveness, affordability, side-effects and equity' feasibility criteria.

Setting: This project took place in England. The survey recruited representatives from neurology and neuroscience centres and from urgent and emergency care providers. For the interviews, recruitment occurred via third-sector support groups. Recruitment for discrete choice experiments occurred via the North West Ambulance Service NHS Trust and public advert. Workshop participants were recruited from neurology and neuroscience centres, urgent and emergency care providers, support groups and commissioning networks.

Participants: Seventy-two services completed the survey. Interviews were conducted with 25 adults with epilepsy (and 5 relatives) who had emergency service contact in the prior 12 months. Discrete choice experiments were completed by 427 adults with epilepsy (and 167 relatives) who had ambulance service contact in the prior 12 months. Workshops were completed with 27 stakeholders.

Results: The survey identified a range of pathway configurations. They differed in where they would take the patient and their potential to instigate ambulatory care improvements. Users had been rarely consulted in designing them. The discrete choice experiments found that users want a configuration of care markedly different to that offered. Across the seizure scenarios, users wanted their paramedic to have access to their medical records; for an epilepsy specialist (e.g. an epilepsy nurse, neurologist) to be available to advise; for their general practitioner to receive a report; for the incident to generate an appointment with an epilepsy specialist; for the care episode to last < 6 hours; and there was a pattern of preference to avoid conveyance to emergency departments and stay where they were. Stakeholders judged this configuration to be National Health Service-feasible within 5-10 years, with some elements being immediately deployable.

Limitations: The discrete choice experiment sample was broadly representative, but those reporting recent contact with an epilepsy specialist were over-represented.

Conclusions: Users state they want a configuration of care that is markedly different to current provision. The configuration they prefer was, with support and investment, judged to likely be National Health Service-feasible. The preferred configuration should now be developed and evaluated to determine its actual deliverability and efficacy.

Study registration: The study is registered as researchregistry4723.

Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme (NIHR award ref: 17/05/62) and is published in full in Health and Social Care Delivery Research; Vol. 12, No. 24. See the NIHR Funding and Awards website for further award information.

为成人癫痫患者开发可行的以人为本的护理方案,以取代急诊科的应对措施:离散选择分析混合方法研究。
背景:人们呼吁辅助医务人员制定某种形式的护理路径,用于将成年癫痫患者从急诊科安全地分流出来,并促进非住院护理的改善。可以有不同的配置。目标:(1) 确定正在考虑的配置,(2) 了解服务使用者对这些配置的看法和目前的提供情况,(3) 确定服务使用者想要什么样的护理,(4) 确定哪种配置可在满足使用者偏好和国民健康服务可行性之间实现最佳平衡:设计:针对目标 1,对服务提供者进行了调查;针对目标 2,对服务使用者进行了访谈。目标 3 通过离散选择实验来实现。这些实验确定了用户在不同癫痫发作情况下的护理偏好。目标 4 通过完成 "知识交流 "研讨会来实现。在这些研讨会上,利益相关者审议了关于用户偏好的调查结果,并根据 Michie 的 "可接受性、实用性、有效性、经济性、副作用和公平性 "可行性标准对不同的治疗路径配置进行了评判:该项目在英格兰进行。调查招募了来自神经内科和神经科学中心以及急诊护理提供商的代表。访谈则通过第三部门支持团体进行招募。离散选择实验通过西北救护车服务 NHS 信托公司和公共广告进行招募。研讨会的参与者则来自神经病学和神经科学中心、紧急医疗服务提供者、支持团体和委托网络:72家服务机构完成了调查。对 25 名在过去 12 个月中接触过急诊服务的成年癫痫患者(和 5 名亲属)进行了访谈。427 名在过去 12 个月中接触过救护车服务的成人癫痫患者(和 167 名亲属)完成了离散选择实验。与 27 名利益相关者举行了研讨会:调查确定了一系列路径配置。结果:调查发现了一系列路径配置,这些路径配置在将患者送往何处以及改善非卧床护理的潜力方面存在差异。在设计过程中,很少征求用户的意见。离散选择实验发现,用户想要的护理配置与所提供的护理配置明显不同。在所有的癫痫发作情景中,用户都希望他们的护理人员能够访问他们的医疗记录;希望癫痫专家(如癫痫护士、神经科医生)能够提供建议;希望他们的全科医生能够收到一份报告;希望该事件能够促成与癫痫专家的预约;希望护理持续时间小于 6 小时;还有一种模式是希望避免被送往急诊科,而是留在原地。利益相关者认为这种配置在 5-10 年内对国民健康服务是可行的,其中一些要素可以立即部署:局限性:离散选择实验的样本具有广泛的代表性,但报告最近接触过癫痫专科医生的人所占比例过高:用户表示,他们想要一种与当前服务明显不同的护理配置。他们所希望的配置在得到支持和投资的情况下,被认为很可能在国民健康服务中是可行的。现在应该对首选配置进行开发和评估,以确定其实际可实现性和有效性:研究注册:研究注册号为 Researchregistry4723:该奖项由国家健康与护理研究所(NIHR)的健康与社会护理服务研究项目(NIHR奖项编号:17/05/62)资助,全文发表于《健康与社会护理服务研究》(Health and Social Care Delivery Research)第12卷第24期。更多奖项信息,请参阅 NIHR Funding and Awards 网站。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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