Rossom Rebecca C, Crain A Lauren, Bart Gavin, Richards Julie E, Boggs Jennifer M, O'Connor Patrick J, Borgert-Spaniol Caitlin, Kane Sheryl, Hooker Stephanie A
HealthPartners Institute, Minneapolis, Minnesota.
Hennepin Healthcare Research Institute, Minneapolis, Minnesota.
AJPM Focus. 2024 Oct 2;3(6):100280. doi: 10.1016/j.focus.2024.100280. eCollection 2024 Dec.
Individuals with opioid use disorder are at elevated suicide risk, but systematic screening in this population is rarely done. This study assessed the effects of targeted clinical decision support prompts on structured suicide risk assessment completion.
The study used a cluster-randomized controlled pragmatic pilot design. Adult primary care patients (aged 18-75 years) with or at risk for opioid use disorder or opioid overdose and suicide were eligible. Patients sought care from 15 Midwestern primary care clinics between July, 31, 2021 and July, 31, 2022. Data were analyzed between March and June 2023. Clinicians in intervention and control clinics received a printout from rooming staff, prompted by a clinical decision support-generated electronic health record alert, suggesting clinicians talk with patients about opioid risks. Intervention clinician handouts also alerted them to patients estimated to be at increased suicide risk and recommended completion of a Columbia Suicide Severity Rating Scale to further evaluate suicide risk. The handouts for control clinicians did not include suicide risk alerts. The main outcome measured the completion of the Columbia Suicide Severity Rating Scale in the 14 days following a visit.
A total of 115 eligible patients (69 intervention, 46 control) made at least 1 visit to a randomized clinic. Patients mean age was 39 years, and 57% were women; 48% of patients had a high risk of opioid use disorder or opioid overdose, 39% had an opioid use disorder diagnosis, 12% had an opioid use disorder in remission diagnosis, and 5% had a recent opioid overdose. Over a mean follow-up of 249 days, 20.3% of intervention patients and 17.4% of control patients had at least 1 Columbia Suicide Severity Rating Scale completed in the next 14 days (=0.70). Most (71%-75%) Columbia Suicide Severity Rating Scale scores were 0, indicating no risk.
This pilot study did not increase the uptake of structured suicide risk assessments in primary care for patients at elevated risk for opioid use disorder and suicide. More robust interventions are likely needed to promote suicide risk assessment in primary care.
患有阿片类药物使用障碍的个体自杀风险升高,但在该人群中进行系统筛查的情况很少见。本研究评估了针对性临床决策支持提示对结构化自杀风险评估完成情况的影响。
本研究采用整群随机对照实用试点设计。符合条件的是患有阿片类药物使用障碍或有阿片类药物过量及自杀风险的成年初级保健患者(年龄在18 - 75岁之间)。患者于2021年7月31日至2022年7月31日期间在15家中西部初级保健诊所寻求治疗。数据于2023年3月至6月进行分析。干预诊所和对照诊所的临床医生收到一份由病房工作人员打印的资料,该资料由临床决策支持生成的电子健康记录警报提示,建议临床医生与患者谈论阿片类药物风险。干预临床医生的资料还提醒他们注意估计自杀风险增加的患者,并建议完成哥伦比亚自杀严重程度评定量表以进一步评估自杀风险。对照临床医生的资料不包括自杀风险警报。主要结局指标是就诊后14天内哥伦比亚自杀严重程度评定量表的完成情况。
共有115名符合条件的患者(69名干预组,46名对照组)至少到一家随机分配的诊所就诊过。患者的平均年龄为39岁,57%为女性;48%的患者有阿片类药物使用障碍或阿片类药物过量的高风险,39%有阿片类药物使用障碍诊断,12%有阿片类药物使用障碍缓解期诊断,5%近期有阿片类药物过量。在平均249天的随访中,20.3%的干预组患者和17.4%的对照组患者在接下来的14天内至少完成了1次哥伦比亚自杀严重程度评定量表( = 0.70)。大多数(71% - 75%)哥伦比亚自杀严重程度评定量表得分是0,表明无风险。
这项试点研究并未提高在初级保健中对阿片类药物使用障碍和自杀风险升高患者进行结构化自杀风险评估的接受度。可能需要更有力的干预措施来促进初级保健中的自杀风险评估。