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

Sponsor
University of Massachusetts, Worcester (Other)
Overall Status
Completed
CT.gov ID
NCT02665429
Collaborator
UMass Memorial Health Care (Other)
109
3
2
12.9
36.3
2.8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Individual prescribing data profile and self-assessment
N/A

Detailed 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).

Study Design

Study Type:
Interventional
Actual Enrollment :
109 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
A Quality Improvement Project to Investigate Individual Provider Variation in Opioid Prescribing From the Emergency Department
Actual Study Start Date :
Feb 1, 2016
Actual Primary Completion Date :
Mar 1, 2017
Actual Study Completion Date :
Mar 1, 2017

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control

Providers who are subject only to the routine implementation of clinical practice guidelines without additional experimental intervention

Experimental: 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")

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.

Outcome Measures

Primary Outcome Measures

  1. 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 Outcome Measures

  1. Change in percentage of total prescriptions written that are opioids [Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention]

  2. Change in median quantity of pills dispensed per opioid prescription [Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention]

  3. Change in number of prescriptions for long-acting opioid formulations [Pre-intervention baseline compared to 1, 2, 3, 6, 9, 12 months post-intervention]

Other Outcome Measures

  1. Self-assessment of decile for number of opioid prescriptions per hundred patients seen [Once, at time of enrollment]

    The provider's self-assessment of their decile of number of opioid prescriptions per hundred patients seen, compared to their peers

  2. Self-assessment of decile for percentage of total prescriptions written that are opioids [Once, at time of enrollment]

    The provider's self-assessment of their decile of their percentage of total prescriptions written that are opioids, compared to their peers

  3. Self-assessment of decile for median quantity of pills dispensed per opioid prescription [Once, at time of enrollment]

    The provider's self-assessment of their decile of their median quantity of pills dispensed per opioid prescription, compared to their peers

  4. Self-assessment of decile for number of prescriptions for long-acting opioid formulations [Once, at time of enrollment]

    The provider's self-assessment of their decile of their number of prescriptions for long-acting opioid formulations, compared to their peers

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 UMass Clinton Hospital Clinton Massachusetts United States
2 UMass Memorial Marlborough Hospital Marlborough Massachusetts United States
3 UMass Memorial Medical Center Worcester Massachusetts United States

Sponsors and Collaborators

  • University of Massachusetts, Worcester
  • UMass Memorial Health Care

Investigators

  • Principal Investigator: Sean Michael, MD, UMass Memorial Health Care

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sean Michael, Emergency Medicine Administrative Leadership Fellow, University of Massachusetts, Worcester
ClinicalTrials.gov Identifier:
NCT02665429
Other Study ID Numbers:
  • H00009241
First Posted:
Jan 27, 2016
Last Update Posted:
Jun 27, 2017
Last Verified:
Jun 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Sean Michael, Emergency Medicine Administrative Leadership Fellow, University of Massachusetts, Worcester
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 27, 2017