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| Name | Class |
|---|---|
| Albert Einstein College of Medicine | OTHER |
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The goal of this research is to investigate the impact of changing opioid analgesic prescribing defaults on the quantity of opioids prescribed for acute non-cancer pain in adult primary care and emergency department settings. We will change prescribing defaults for select short-acting opioid analgesics including immediate release oxycodone and hydrocodone as well as codeine and tramadol, including their co-formulations with acetaminophen. In a cluster-randomized trial of matched pairs of Montefiore Medical Center clinical sites, stratified by specialty and teaching status, we will evaluate the impact of this intervention on patient-level outcomes using 18 months of data (6 months pre-intervention and 12 months post-intervention).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention | Experimental | The intervention condition consists of a change to the electronic health record so that new opioid analgesic prescriptions automatically default to 10 pills (i.e., the "quantity dispensed" field is pre-populated). This value is modifiable by providers who can tailor the prescription based on clinical factors. |
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| Standard of care | No Intervention | The control condition will be the usual electronic health record interface. The default number of pills varies by medication, most medications currently have either a blank default or a default of 30 pills. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Change in electronic health record default for new opioid analgesic prescriptions | Other |
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| Measure | Description | Time Frame |
|---|---|---|
| Initial prescription <= 10 pills (y/n) | Extracted from the electronic medical record | Through study completion (18 months) |
| Measure | Description | Time Frame |
|---|---|---|
| Initial prescription number of pills | Extracted from the electronic medical record | Through study completion (18 months) |
| Initial prescription morphine milligram equivalents | Extracted from the electronic medical record |
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Clinical Site Inclusion Criteria:
Patient Inclusion Criteria:
Patient Exclusion Criteria:
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 33885773 | Derived | Bachhuber MA, Nash D, Southern WN, Heo M, Berger M, Schepis M, Thakral M, Cunningham CO. Effect of Changing Electronic Health Record Opioid Analgesic Dispense Quantity Defaults on the Quantity Prescribed: A Cluster Randomized Clinical Trial. JAMA Netw Open. 2021 Apr 1;4(4):e217481. doi: 10.1001/jamanetworkopen.2021.7481. | |
| 29678969 |
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| ID | Term |
|---|---|
| D059787 | Acute Pain |
| ID | Term |
|---|---|
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| Through study completion (18 months) |
| Opioid analgesic re-order (y/n) | Extracted from the electronic medical record | Within 30 days after the initial prescription |
| Total opioid analgesic pills prescribed, including re-orders | Extracted from the electronic medical record | Within 30 days after the initial prescription |
| Total morphine milligram equivalents prescribed, including re-orders | Extracted from the electronic medical record | Within 30 days after the initial prescription |
| Outpatient visits | Extracted from the electronic medical record | Within 30 days after the initial prescription |
| Emergency department visits | Extracted from the electronic medical record | Within 30 days after the initial prescription |
| Hospitalizations | Extracted from the electronic medical record | Within 30 days after the initial prescription |
| Bachhuber MA, Nash D, Southern WN, Heo M, Berger M, Schepis M, Cunningham CO. Reducing the default dispense quantity for new opioid analgesic prescriptions: study protocol for a cluster randomised controlled trial. BMJ Open. 2018 Apr 20;8(4):e019559. doi: 10.1136/bmjopen-2017-019559. |