Engaging primary care patients at risk for suicide in mental health treatment: user insights to inform implementation strategy design.

IF 2 Q2 MEDICINE, GENERAL & INTERNAL
Courtney Benjamin Wolk, Matteo Pieri, Samantha E Weiss, Joseph Harrison, Gabriela Kattan Khazanov, Molly Candon, David W Oslin, Matthew J Press, Eleanor Anderson, Emilie Famiglio, Alison Buttenheim, Shari Jager-Hyman
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Abstract

Background: Given that the majority of suicide decedents visit primary care in the year preceding death, primary care has been identified as a key setting in which to engage patients at risk for suicide in mental health services. The objective of this research was to identify barriers and facilitators to engagement in mental health services among primary care patients at risk for suicide to inform the development of strategies to increase engagement.

Methods: Seventy-four semi-structured qualitative interviews were conducted with primary care patients (n = 20), primary care (n = 18) and behavioral health (n = 12) clinicians, mental health intake coordinators (n = 4), and health system and clinic leaders (n = 20). Patients who had been referred for mental health services from primary care and reported an elevated score (≥ 1) on item 9 on the Patient Health Questionnaire at the time of referral were eligible to participate. Eligible clinicians and leaders were employed in a primary care or behavioral health setting in a single large health system with an integrated mental health program. Interviews typically lasted 30-60 min, were completed over video conference or phone, and were coded by members of the research team using a rapid qualitative analysis procedure.

Results: Participants were primarily female (64.9%), white (70.3%) and non-Hispanic/Latine (91.9%). The most identified barriers to mental health care engagement were waitlists, capacity limits, insurance, patient characteristics, communication, collaboration, and/or difficulties surrounding travel. The most commonly cited facilitators of engagement included telehealth, integrated care models, reminders, case management support, psychoeducation, motivational enhancement, and scheduling flexibility. Concrete suggestions for improving engagement in mental health services included increasing communication between providers, streamlining referral and intake processes, providing reminders and follow ups, and advocacy for increased reimbursement for suicide risk assessment.

Conclusions: Results underscore the myriad barriers patients at risk for suicide encounter when attempting to engage in mental health care in a primary care setting. Facilitators of engagement and suggestions for improving connections to care were also identified, which can inform the design of implementation strategies to improve engagement in mental health services among primary care patients at risk for suicide.

Trial registration: ClinicalTrials.gov Identifier: NCT05021224 (Registered August 19, 2021).

让有自杀风险的初级保健患者参与心理健康治疗:用户洞察力为实施策略设计提供参考。
背景:鉴于大多数自杀死者都是在死前一年到基层医疗机构就诊的,因此基层医疗机构被认为是让有自杀风险的患者参与心理健康服务的关键场所。本研究的目的是找出有自杀风险的初级医疗患者参与心理健康服务的障碍和促进因素,为制定提高参与度的策略提供参考:我们对初级医疗患者(20 人)、初级医疗(18 人)和行为健康(12 人)临床医生、心理健康接收协调员(4 人)以及医疗系统和诊所领导(20 人)进行了 74 次半结构化定性访谈。由初级医疗机构转介到心理健康服务机构并在转介时报告患者健康问卷第 9 项得分升高(≥ 1 分)的患者有资格参与。符合条件的临床医生和领导均受雇于一个拥有综合心理健康项目的大型医疗系统中的初级保健或行为健康机构。访谈一般持续 30-60 分钟,通过视频会议或电话完成,由研究小组成员使用快速定性分析程序进行编码:参与者主要为女性(64.9%)、白人(70.3%)和非西班牙裔/拉丁裔(91.9%)。参与心理健康医疗服务最常见的障碍是候诊名单、医疗能力限制、保险、患者特征、沟通、合作和/或出行困难。最常被提及的促进参与的因素包括远程医疗、综合护理模式、提醒、个案管理支持、心理教育、动机强化和时间安排的灵活性。提高心理健康服务参与度的具体建议包括:加强医疗服务提供者之间的沟通、简化转介和接收流程、提供提醒和跟进服务,以及倡导增加自杀风险评估的报销额度:结论:研究结果表明,有自杀风险的患者在尝试接受初级医疗机构的心理健康服务时会遇到各种各样的障碍。此外,还发现了促进参与的因素以及改善与医疗服务联系的建议,这些都可以为设计实施策略提供参考,从而改善有自杀风险的初级医疗患者参与心理健康服务的情况:试验注册:ClinicalTrials.gov Identifier:NCT05021224(2021年8月19日注册)。
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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