A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department

Analgesics, Opioid Clinical Trial

Official title:

A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02665429
• Other study ID #: H00009241
• Status: Completed
• Phase: N/A
• First received: January 20, 2016
• Last updated: June 23, 2017
• Start date: February 1, 2016
• Est. completion date: March 1, 2017

Study information

• Verified date: June 2017
• Source: University of Massachusetts, Worcester
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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:

• 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).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 109
• Est. completion date: March 1, 2017
• Est. primary completion date: March 1, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Provider who practices Emergency Medicine in one or more of four UMass-affiliated EDs (UMassMemorial Medical Center, Marlborough Hospital, and Clinton Hospital), including attending physicians, resident physicians, and advanced practice providers (PAs and NPs).

• 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:

Related Conditions & MeSH terms

• Analgesics, Opioid
• Delivery of Health Care
• Drug Prescribing
• Emergencies
• Over Prescribing
• Practice Guidelines as Topic
• Practice Management, Medical
• Prescribing Patterns, Physician

Intervention

Behavioral:
• 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.

Locations

Country	Name	City	State
United States	UMass Clinton Hospital	Clinton	Massachusetts
United States	UMass Memorial Marlborough Hospital	Marlborough	Massachusetts
United States	UMass Memorial Medical Center	Worcester	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
University of Massachusetts, Worcester	UMass Memorial Health Care

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	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
Other	Self-assessment of decile for percentage of total prescriptions written that are opioids	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
Other	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
Other	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
Primary	Change in number of opioid prescriptions per hundred patients seen		Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention
Secondary	Change in percentage of total prescriptions written that are opioids		Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention
Secondary	Change in median quantity of pills dispensed per opioid prescription		Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention
Secondary	Change in number of prescriptions for long-acting opioid formulations		Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention