A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department
NCT ID: NCT02665429
Last Updated: 2017-06-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
109 participants
INTERVENTIONAL
2016-02-01
2017-03-01
Brief Summary
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Detailed Description
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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:
* Improve understanding of physician practice patterns related to emergency department (ED) opioid prescribing
* Evaluate the effectiveness of providing individual clinician profile data in influencing behavior change among ED providers, as it relates to their opioid prescribing patterns
There are two corresponding specific aims:
* Quantitatively describe the current state of opioid prescribing by ED clinicians at four UMass Memorial EDs (using prescriptions generated within the ED electronic health information system between February 2014 and the study implementation date). Descriptive statistics being considered for feasibility of study include:
* Number of opioid prescriptions per hundred patients seen
* Percentage of total prescriptions written that are opioids
* Mean or median quantity of pills dispensed per opioid prescription
* Number of prescriptions for long-acting opioid formulations
* Evaluate the effect on prescribing practices of providing individual clinicians with their profile data to illustrate their personal opioid prescribing patterns, relative to the de-identified distribution for all other clinicians in the ED group
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).
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Control
Providers who are subject only to the routine implementation of clinical practice guidelines without additional experimental intervention
No interventions assigned to this group
Intervention
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")
Individual prescribing data profile and self-assessment
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.
Interventions
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Individual prescribing data profile and self-assessment
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.
Eligibility Criteria
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Inclusion Criteria
* Have placed at least one electronic prescription for a medication of interest (namely opioids) in the PulseCheck electronic medical record system during the 12 months prior to the implementation of the opioid guidelines
* Be actively practicing in a UMass-affiliated ED at time of implementation of the guidelines
Exclusion Criteria
ALL
No
Sponsors
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UMass Memorial Health
OTHER
University of Massachusetts, Worcester
OTHER
Responsible Party
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Sean Michael
Emergency Medicine Administrative Leadership Fellow
Principal Investigators
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Sean Michael, MD
Role: PRINCIPAL_INVESTIGATOR
UMass Memorial Health
Locations
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UMass Clinton Hospital
Clinton, Massachusetts, United States
UMass Memorial Marlborough Hospital
Marlborough, Massachusetts, United States
UMass Memorial Medical Center
Worcester, Massachusetts, United States
Countries
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Other Identifiers
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H00009241
Identifier Type: -
Identifier Source: org_study_id
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