为苏格兰格拉斯哥近期非致命用药过量的无家可归者提供整体健康和社会关怀外联服务:药剂师和第三部门无家可归者慈善工作者外联参与非医疗独立处方药(PHOENIx)试点随机对照试验

Richard Lowrie, Andrew McPherson, Frances Mair, K. Stock, Donogh Maguire, V. Paudyal, Clare Duncan, Rebecca Blair, C. Lombard, Steven Ross, Fiona Hughes, J. Moir, Ailsa Scott, Frank Reilly, L. Sills, Jennifer Hislop, Stephen Wishart, David Brannan, James Roy Robertson, Rebekah Ramage, Alison Boyle, Nicola Greenlaw, Andrea E Williamson
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引用次数: 0

摘要

目的:研究随机对照试验(RCT)的进展标准,包括急诊室就诊率和非致命性药物过量,以及针对近期出现非致命性街头药物过量的无家可归者的全面、综合医疗和社会护理外展干预措施(PHOENIx)。苏格兰格拉斯哥,128 名在过去 6 个月中至少有过一次非致命性街头吸毒过量经历的成年无家可归者。来自国民健康服务机构的药剂师和第三部门的无家可归者工作者每周提供一次外展服务。PHOENIx 小组发展治疗关系,除 UC 外,还解决健康(身体健康、心理健康和吸毒问题)和社会护理(住房、福利和社会处方)问题。主要标准:进展标准:招募(4 个月内≥100 名参与者);在基线、6 个月和 9 个月收集数据的参与者比例≥80%;在每个随访期(6 个月和 9 个月)保留试验的参与者比例≥60%;每周接受干预的参与者比例≥60%;在 6 个月或 9 个月的随访中,急诊室就诊率和吸毒过量率有所下降。次要指标:参加者的住院情况和住院时间;与健康相关的生活质量(QoL);接受身体和精神健康状况治疗的情况以及问题药物使用情况。与 UC 相比,PHOENIx 的急诊室就诊、用药过量和住院治疗的中位时间似乎有所延迟,但急诊室就诊、用药过量或住院治疗的参与者人数没有增加。在 6 个月和 9 个月时,PHOENIx 的 QoL 和治疗接受率似乎高于 UC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Holistic health and social care outreach for people experiencing homelessness with recent non-fatal overdose in Glasgow, Scotland: the Pharmacist and third sector Homeless charity worker Outreach Engagement Non-medical Independent prescriber Rx (PHOENIx) pilot randomised controlled trial
To examine randomised controlled trial (RCT) progression criteria including emergency department (ED) attendance and non-fatal overdose, from a holistic, integrated health and social care outreach intervention (PHOENIx), for people experiencing homelessness with recent non-fatal street drug overdose.Pilot RCT. 1:1 randomisation to PHOENIx plus usual care (UC) or UC.Glasgow, Scotland.128 adults experiencing homelessness with at least one non-fatal street drug overdose in the preceding 6 months.Pharmacists from the National Health Service and third sector homelessness workers offered weekly outreach. PHOENIx teams develop therapeutic relationships to address health (physical health, mental health and problem drug use) and social care (housing, welfare benefits and social prescribing) in addition to UC. UC comprised building-based primary and secondary health, social and third sector services.Primary: progression criteria: recruitment (≥100 participants in 4 months); ≥80% of participants with data collected at baseline, 6 and 9 months; ≥60% of participants retained in the trial at each follow-up period (6 and 9 months); ≥60% of participants receiving the intervention weekly; any reduction in the rate of presentation to ED and overdoses, at 6- or 9-month follow-up. Secondary: participants with, and time to: hospitalisations; health-related quality of life (QoL); treatment uptake for physical and mental health conditions, and problematic drug use.Progression criteria were exceeded. In PHOENIx compared with UC, there appeared to be a delay in the median time to ED visit, overdose and hospitalisation but no improvement in number of participants with ED visits, overdoses or hospitalisations. QoL and treatment uptake appeared to be higher in PHOENIx versus UC at 6 and 9 months.A definitive RCT is merited, to assess the impact of PHOENIx on people with multiple, severe disadvantages.ISRCTN10585019.
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