An Electronic Chart Intervention to Improve Safety for Patients on Chronic Opioid Therapy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 43
- 试验地点
- 2
- 主要终点
- Change in the number of patients who receives naloxone prescription
研究概览
简要总结
This pilot study will attempt to apply an electronic chart intervention to improve safety for patients on chronic opioid medications.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients prescribed long-term opioid therapy of doses greater than 90 morphine equivalent daily dose (MEDD)
排除标准
- •Patients prescribed short-term opioid medications for acute pain (less than a 90-day supply over the past 120 days), sublingual buprenorphine, methadone maintenance for opioid use disorder or with oncology or palliative care diagnoses will be excluded.
结局指标
主要结局
Change in the number of patients who receives naloxone prescription
时间窗: baseline, 1, 3- and 6-months and 12 months
Change in the number of patients who receives naloxone prescription
change of number of documentation about safety discussions
时间窗: baseline, 1, 3- and 6-months and 12 months
change of number of documentation about safety discussions
change of number of order for urine toxicology screening
时间窗: baseline, 1, 3- and 6-months and 12 months
change of number of order for urine toxicology screening
change of number of documentation of prescription drug monitoring program (CURES) results
时间窗: baseline, 1, 3- and 6-months and 12 months
change of number of documentation of prescription drug monitoring program (CURES) results
change of number of signed opioid informed consent forms
时间窗: baseline, 1, 3- and 6-months and 12 months
change of number of signed opioid informed consent forms
次要结局
- Change in number of patients on long-term high risk doses of opioid pain medications(baseline, 1, 3- and 6-months and 12 months)
研究者
Huiqiong Deng
Clinical Assistant Professor
Stanford University