Effects of Performance Feedback on Imaging Use in the Emergency Department
Primary Purpose
Pulmonary Embolism
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Physician Feedback Reporting
Sponsored by
About this trial
This is an interventional health services research trial for Pulmonary Embolism focused on measuring Quality Improvement, Physician Feedback
Eligibility Criteria
Inclusion Criteria:
- All attending physicians in the emergency department
Exclusion Criteria:
- None
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control
Intervention
Arm Description
The intervention consisted of quarterly performance feedback reports sent via e-mail.
Outcomes
Primary Outcome Measures
Adherence to Evidence-Based Guidelines
Percentage of CTPE orders that adhere to evidence-based guidelines for the ordering of CTs for PE
Secondary Outcome Measures
Use of Computed Tomography for Pulmonary Embolism
#CTPEs/1,000 ED visits for each physician
Yield of Computed Tomography for Pulmonary Embolism
Percentage of CTPE orders that are positive for acute PE
Full Information
NCT ID
NCT02283086
First Posted
November 2, 2014
Last Updated
November 4, 2014
Sponsor
Brigham and Women's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02283086
Brief Title
Effects of Performance Feedback on Imaging Use in the Emergency Department
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
DESIGN: An IRB-approved, HIPAA-compliant prospective randomized controlled trial conducted from January 1, 2012-December 31, 2013.
SETTING: The ED of an urban Level-I adult trauma center with existing CDS for CTPE.
PARTICIPANTS: All attending physicians were stratified into quartiles by 2012 CTPE use and randomized to receive feedback reporting or not.
INTERVENTION: Quarterly performance feedback reports consisting of individual and anonymized group data on EBG adherence (using the Wells criteria), CTPE use (CTPEs per 1,000 patients), and yield (percentage of CTPEs positive for PE) beginning January 2013.
Detailed Description
Setting and Subjects This IRB-approved and HIPAA-compliant prospective randomized controlled trial was conducted from January 1, 2012 to December 31, 2013 in the ED of an urban Level-I adult trauma center. Imaging CDS was deployed for all CTPE requests throughout the study period as previously reported. Ordering providers could ignore the evidence presented in CDS and proceed with CTPE requests deviating from evidence-based guidelines without interference. The investigators included all attending emergency physicians and, prior to randomization, stratified them into quartiles by 2012 CTPE use. Physicians were randomized by quartile into two groups using a random number generator: the intervention group received individualized feedback reports on CTPE adherence to EBG, use (defined as number of CTPEs per 1,000 patients), and yield (percentage of CTPEs positive for PE), and the control group did not.
Data Collection Use of CTPEs for each physician was calculated using the number of completed CTPE examinations and the total number of patients seen during the quarter. Yield of CTPEs for acute PE was determined using a previously validated natural language processing tool and reported as a percentage of total CTPEs completed. Adherence to EBG was determined by applying the Wells Criteria and reviewing the serum D-dimer levels (if obtained). The discrete criteria making up the Wells Criteria were prospectively documented in the investigators computerized order entry (CPOE) system at the time of order entry, as previously reported.
In order to determine whether any differences observed in guideline adherence were the result of "gaming" (erroneous data entry to either avoid potentially onerous CDS interactions or to enhancing the physician's apparent performance on feedback reports) the investigators performed manual chart reviews of 100 randomly chosen charts from each of the two groups. These chart reviews were performed by an attending physician to assess concordance between adherence to EBG calculated from the CDS data, and adherence to EBG calculated from data documented in the ED visit clinical note. The sample size was determined using a baseline concordance of 90% as previously reported, and chosen to detect a difference in concordance of 15% between groups with a power of 80% and an alpha error rate of 5%. Demographic data (including gender and both age and years since residency training as measured at the beginning of the study period) was also captured for all the attending physicians in the study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Embolism
Keywords
Quality Improvement, Physician Feedback
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
43 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
No Intervention
Arm Title
Intervention
Arm Type
Experimental
Arm Description
The intervention consisted of quarterly performance feedback reports sent via e-mail.
Intervention Type
Behavioral
Intervention Name(s)
Physician Feedback Reporting
Intervention Description
The performance feedback reports displayed both individual physicians' statistics as well as their performance compared to anonymized results for the entire group of emergency physicians.
Primary Outcome Measure Information:
Title
Adherence to Evidence-Based Guidelines
Description
Percentage of CTPE orders that adhere to evidence-based guidelines for the ordering of CTs for PE
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Use of Computed Tomography for Pulmonary Embolism
Description
#CTPEs/1,000 ED visits for each physician
Time Frame
2 years
Title
Yield of Computed Tomography for Pulmonary Embolism
Description
Percentage of CTPE orders that are positive for acute PE
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
All attending physicians in the emergency department
Exclusion Criteria:
None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ramin Khorasani, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Effects of Performance Feedback on Imaging Use in the Emergency Department
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