Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This pilot study will attempt to apply an electronic chart intervention to improve safety for patients on chronic opioid medications.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Electronic Intervention | Experimental | Individualized opioid taper and safety recommendations will be communicated to prescribers via an electronic medical record encrypted message. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| opioid prescribing | Other | Individualized taper and safety recommendations will be communicated to prescribers via an electronic medical record encrypted message. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in the number of patients who receives naloxone prescription | Change in the number of patients who receives naloxone prescription | baseline, 1, 3- and 6-months and 12 months |
| change of number of documentation about safety discussions | change of number of documentation about safety discussions | baseline, 1, 3- and 6-months and 12 months |
| change of number of order for urine toxicology screening | change of number of order for urine toxicology screening | 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 documentation of prescription drug monitoring program (CURES) results | baseline, 1, 3- and 6-months and 12 months |
| change of number of signed opioid informed consent forms | change of number of signed opioid informed consent forms | baseline, 1, 3- and 6-months and 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Change in number of patients on long-term high risk doses of opioid pain medications | decreases in daily dose of opioids and number of patients on opioids ≥ 90mg MEDD | baseline, 1, 3- and 6-months and 12 months |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Huiqiong Deng, MD, PHD | Stanford Univeristy | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Stanford University | Stanford | California | 94305 | United States |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided