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| Name | Class |
|---|---|
| UMass Memorial Health | OTHER |
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This is a study of emergency physicians' prescribing patterns related to opioid (narcotic) medications. We are trying to determine whether giving providers access to their own prescribing data influences their prescribing patterns.
Opioid misuse is a known public safety threat and public health problem, both nationwide and in the Commonwealth of Massachusetts. As a part of these efforts, Emergency Department (ED) outpatient prescriptions have been identified as a potential area for improvement. The Massachusetts Hospital Association (MHA), in conjunction with other stakeholders, developed a set of recommendations to address opioid management and prescribing within the ED setting.
This study is timed to coincide with the rollout by UMassMemorial Health Care of a system-wide opioid prescribing practice guideline/policy which mirrors the Massachusetts Hospital Association's guideline. This rollout provides a unique opportunity for a natural experiment related to provider prescribing practices.
This is a quality improvement project with two primary objectives:
There are two corresponding specific aims:
This project is timed to coincide with the separately planned implementation of a system-wide opioid prescribing guideline. The guideline implementation is an independent event, but we feel that it presents a unique opportunity for a simultaneous experimental intervention to assess whether providing clinicians with their individual data alters their prescribing practices beyond any effect achieved simply by being subject to the new guideline. Data collected from the electronic medical record and clinician self-reported data about their perceptions of their prescribing practices will be used to evaluate both the effect of the guideline implementation (i.e. comparison of prescribing patterns for all clinicians before and after guideline implementation) and the combined effect of guideline implementation plus individual profile intervention (i.e. comparisons across intervention versus control groups).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control | No Intervention | Providers who are subject only to the routine implementation of clinical practice guidelines without additional experimental intervention | |
| Intervention | Experimental | Providers who are subject to routine clinical practice guideline implementation AND receive provider's own individual prescribing data profile intervention ("Individual prescribing data profile and self-assessment") |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Individual prescribing data profile and self-assessment | Behavioral | Prior to receiving his or her individual data profile, each provider in the intervention group will be asked to identify his or her self-assessment of his or her own opioid prescribing practices. Immediately after providing self-perception data, providers will be provided with their true profile data with a visual display of where they fall within the distribution of their peers. All peer data are de-identified. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in number of opioid prescriptions per hundred patients seen | Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Change in percentage of total prescriptions written that are opioids | Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention | |
| Change in median quantity of pills dispensed per opioid prescription | Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Self-assessment of decile for number of opioid prescriptions per hundred patients seen | The provider's self-assessment of their decile of number of opioid prescriptions per hundred patients seen, compared to their peers | Once, at time of enrollment |
| Self-assessment of decile for percentage of total prescriptions written that are opioids |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Sean Michael, MD | UMass Memorial Health | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UMass Clinton Hospital | Clinton | Massachusetts | United States | |||
| UMass Memorial Marlborough Hospital |
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| Change in number of prescriptions for long-acting opioid formulations | Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention |
The provider's self-assessment of their decile of their percentage of total prescriptions written that are opioids, compared to their peers |
| Once, at time of enrollment |
| Self-assessment of decile for median quantity of pills dispensed per opioid prescription | The provider's self-assessment of their decile of their median quantity of pills dispensed per opioid prescription, compared to their peers | Once, at time of enrollment |
| Self-assessment of decile for number of prescriptions for long-acting opioid formulations | The provider's self-assessment of their decile of their number of prescriptions for long-acting opioid formulations, compared to their peers | Once, at time of enrollment |
| Marlborough |
| Massachusetts |
| United States |
| UMass Memorial Medical Center | Worcester | Massachusetts | United States |
| ID | Term |
|---|---|
| D059026 | Diagnostic Self Evaluation |
| ID | Term |
|---|---|
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
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