针对重症精神病患者的协作护理干预:PARTNERS2 计划,包括复杂干预措施的开发和分组研究试验

H. Plappert, R. Byng, S. Reilly, Charley Hobson-Merrett, Jon Allard, Elina Baker, N. Britten, M. Calvert, Mike Clark, S. Creanor, Linda M Davies, Rebecca Denyer, Julia Frost, Linda Gask, Bliss Gibbons, John Gibson, Laura Gill, Ruth Gwernan-Jones, Joanne Hosking, Peter Huxley, Alison Jeffery, Benjamin Jones, T. Keeley, R. Laugharne, S. Marwaha, C. Planner, T. Rawcliffe, A. Retzer, Debra Richards, Ruth Sayers, Lynsey Williams, V. Pinfold, Maximillian Birchwood
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In phase 2 we conducted a cluster randomised controlled trial measuring quality of life using the Manchester Short Assessment of Quality of Life and secondary outcomes including time use, recovery and mental well-being; a cost-effectiveness study; and a mixed-methods process evaluation. Public involvement underpinned all of the workstream activity through the study Lived Experience Advisory Panel and the employment of service user researchers in the project team.\n\n\nThe study of records showed that care for individuals under secondary care is variable and substantial and that people are seen every 2 weeks on average. The updated Cochrane review showed that collaborative care interventions were highly variable, and no reliable conclusions can be drawn about effectiveness. The PARTNERS model incorporated change at organisational, practitioner and individual levels. Coaching was selected as the main form of support for individuals’ personal goals. 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引用次数: 0

摘要

精神分裂症和躁郁症等严重精神疾病患者在情绪、认知、身体和社交方面都会面临巨大挑战。在英国,大多数患有严重精神疾病的人都没有接受过专业的精神健康护理。协作护理是一种支持系统,它将临床和组织部分结合起来,提供以人为本的综合护理。在英国,该系统还未针对重性精神病进行过测试。我们的目标是开发并评估一种基于初级护理的协作护理模式(PARTNERS),与常规护理模式相比,该模式旨在改善精神分裂症、双相情感障碍或其他精神病患者的生活质量。第一阶段的研究包括:(1) 了解背景:对初级和二级护理医疗记录的观察性回顾研究,以及对 Cochrane 综述 "重性精神病患者的协作护理方法 "的更新;(2) 开发和形成性评估 PARTNERS 干预方案:综述协作护理和康复方面的文献,采访协作护理和康复方面的主要领导者,与服务使用者进行焦点小组讨论,以及对原型干预模式进行形成性评估;(3) 开发该领域的试验科学工作:双相情感核心结果集和招募方法。在第二阶段,我们开展了一项群组随机对照试验,使用曼彻斯特生活质量短期评估来衡量生活质量,以及包括时间利用、康复和心理健康在内的次要结果;一项成本效益研究;以及一项混合方法过程评估。公众参与是所有工作流程活动的基础,为此成立了生活体验咨询小组,并在项目团队中聘用了服务使用者研究人员。最新的 Cochrane 综述报告显示,合作护理干预措施差异很大,无法就其有效性得出可靠的结论。PARTNERS 模式包括组织、从业人员和个人层面的变革。辅导被选为支持个人实现个人目标的主要形式。在形成性评估中,我们发现需要更多的强化督导和 "补充 "培训,才能实现预期的实践转变。我们为躁郁症制定了一套核心结果,并为试验选择了衡量标准。我们制定了一个阶梯式的招募方法,包括初步接洽和预约。总共从 39 家诊所随机招募了 198 名参与者。参与者接受了 PARTNERS 干预或常规护理。9-12 个月的随访率为 86%。干预组与对照组的曼彻斯特生活质量短期评估总分的平均变化没有差异[干预组为 0.25(标准差 0.73),对照组为 0.21(标准差 0.86)]。我们还发现任何次要测量指标均无差异。接受干预和未接受干预的人群在安全结果(如危机)方面没有差异。虽然干预和常规护理的成本相似,但没有足够的证据就 PARTNERS 的整体成本效益得出结论。混合方法过程评估表明,有相当一部分人没有接受完整的干预。部分原因是护理伙伴缺席和参与者的选择。深入的现实主义案例研究表明,参与者普遍对支持表示赞赏,一些人认为有一个 "专业朋友 "非常重要。有证据表明,对一些人来说,干预措施的实施带来了具体的个人变化。第一阶段的记录研究提供了以前没有记录的对常规护理的见解。现实主义的复杂干预发展既有理论依据,又很实用。在 COVID-19 大流行期间,该试验一直在进行,随访率很高。过程评估深入探讨了参与者对干预措施反应的个体变化。试验方法的不足之处包括:实施效果不理想,结果测量可能对患者最欣赏的变化不敏感,以及收集某些结果存在困难等。虽然没有证明 PARTNERS 优于常规护理,但也没有证明改用 PARTNERS 护理不安全。全面实施干预措施具有挑战性,但这在包括精神病患者在内的护理研究中是意料之中的。当以个体化目标设定的形式提供心理支持时,一些人对干预措施反应良好,有证据表明,与 "专业朋友 "接触对一些人特别有帮助。
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Collaborative care intervention for individuals with severe mental illness: the PARTNERS2 programme including complex intervention development and cluster RCT
Individuals living with severe mental illness such as schizophrenia and bipolar can have significant emotional, cognitive, physical and social challenges. Most people with severe mental illness in the United Kingdom do not receive specialist mental health care. Collaborative care is a system of support that combines clinical and organisational components to provide integrated and person-centred care. It has not been tested for severe mental illness in the United Kingdom. We aimed to develop and evaluate a primary care-based collaborative care model (PARTNERS) designed to improve quality of life for people with diagnoses of schizophrenia, bipolar or other psychoses when compared with usual care. Phase 1 included studies to (1) understand context: an observational retrospective study of primary and secondary care medical records and an update of the Cochrane review ‘Collaborative care approaches for people with severe mental illness’; (2) develop and formatively evaluate the PARTNERS intervention: a review of literature on collaborative care and recovery, interviews with key leaders in collaborative care and recovery, focus groups with service users and a formative evaluation of a prototype intervention model; and (3) develop trial science work in this area: a core outcome set for bipolar and recruitment methods. In phase 2 we conducted a cluster randomised controlled trial measuring quality of life using the Manchester Short Assessment of Quality of Life and secondary outcomes including time use, recovery and mental well-being; a cost-effectiveness study; and a mixed-methods process evaluation. Public involvement underpinned all of the workstream activity through the study Lived Experience Advisory Panel and the employment of service user researchers in the project team. The study of records showed that care for individuals under secondary care is variable and substantial and that people are seen every 2 weeks on average. The updated Cochrane review showed that collaborative care interventions were highly variable, and no reliable conclusions can be drawn about effectiveness. The PARTNERS model incorporated change at organisational, practitioner and individual levels. Coaching was selected as the main form of support for individuals’ personal goals. In the formative evaluation, we showed that more intensive supervision and ‘top-up’ training were needed to achieve the desired shifts in practice. A core outcome set was developed for bipolar, and measures were selected for the trial. We developed a stepped approach to recruitment including initial approach and appointment. The trial was conducted in four areas. In total, 198 participants were recruited from 39 practices randomised. Participants received either the PARTNERS intervention or usual care. The follow-up rate was 86% at 9–12 months. The mean change in overall Manchester Short Assessment Quality of Life score did not differ between the groups [0.25 (standard deviation 0.73) for intervention vs. 0.21 (standard deviation 0.86) for control]. We also found no difference for any secondary measures. Safety outcomes (e.g. crises) did not differ between those receiving and those not receiving the intervention. Although the costs of intervention and usual care were similar, there is insufficient evidence to draw conclusions about the overall cost-effectiveness of PARTNERS. The mixed-methods process evaluation demonstrated that a significant proportion of individuals did not receive the full intervention. This was partly due to care partner absence and participant choice. The in-depth realist informed case studies showed that participants generally appreciated the support, with some describing having a ‘professional friend’ as very important. For some people there was evidence that delivery of the intervention had led to specific personal changes. The phase 1 records study provided insights into usual care that had not been previously documented. The realist informed complex intervention development was both theoretical and pragmatic. The trial continued through the COVID-19 pandemic with high levels of follow-up. The process evaluation had the depth to explore individual changes in participants’ response to the intervention. Weaknesses in the trial methodology included suboptimal implementation, outcome measures that may not have been sensitive to changes patients most appreciated and difficulties collecting some outcomes. While PARTNERS was not shown to be superior to usual care, the change to PARTNERS care was not shown to be unsafe. Full intervention implementation was challenging, but this is to be expected in studies of care that include those with psychosis. Some individuals responded well to the intervention when psychological support in the form of individualised goal setting was flexibly deployed, with evidence that having access to a ‘professional friend’ was experienced as particularly helpful for some individuals. Key components of the PARTNERS model could be developed further and tested, along with improved supervision in the context of ongoing community mental health care change. This trial is registered as ISRCTN95702682. This award was funded by the National Institute for Health and Care Research (NIHR) Programme Grants for Applied Research programme (NIHR award ref: NIHR200625) and is published in full in Programme Grants for Applied Research; Vol. 12, No. 6. See the NIHR Funding and Awards website for further award information.
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
9
审稿时长
53 weeks
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