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Equity in Diagnostic Imaging Trial (EDIT)

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Mount Sinai Health System

Status

Completed

Conditions

Headache

Treatments

Other: Clinical Decision Support
Other: Audit-feedback

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01611714
3P60MD000270-09S1 (U.S. NIH Grant/Contract)
GCO 02-0515(3)

Details and patient eligibility

About

This study will 1) Develop two interventions: a) an audit-feedback email intervention that provides clinicians with data on CT scan ordering practices by patient race; and b) a clinical decision support (CDS) message in the electronic medical record headache template; and 2) Compare the effectiveness of these 2 interventions in eliminating a previously observed Black-White disparity in CT scanning rates to rule out subarachnoid hemorrhage (SAH).

Full description

Investigators at our institution (Hwang & Richardson)* documented a racial disparity in the use of CT scans to diagnose subarachnoid hemorrhage, (SAH) a life-threatening form of stroke. Subsequent analyses found a similar finding in NHAMCS, a national ED Visit database*. The investigators will compare the effectiveness of 1) an audit-feedback intervention that provides data on race-specific CT rates and 2) a clinical decision support (CDS) message in the electronic "headache" charting template in eliminating the previously observed Black-White disparity in CT rates to rule out SAH.

Study Setting: The adult section of the Mount Sinai Emergency Department, an urban academic department with an annual volume of over 70,000 adult visits and a patient population representing a diverse cross-section of race and socioeconomic groups. The adult patients are cared for by a staff that includes: attending physicians, physician assistants, emergency medicine resident physicians, and rotating resident physicians from other specialties. The department has a dedicated CT scanner that is readily available around the clock. Epic Production is used for all physician and nurse documentation and for all order entry (including CT scans).

Over a 24-month period the investigators will compare the intervention and control groups' rates of testing for SAH across races, controlling for patient acuity, age and co-morbidities. Because the close working relationships among the attending and resident physicians in our department may lead to knowledge diffusion, the intervention may change the behavior of the control group as well as the intervention group, thus leading to an underestimation of the intervention effect as measured by the between- groups difference. The investigators will use a time series design to allow us to evaluate this effect. 10 months after the implementation of the first intervention, the clinical decision support message will be implemented. The impact of each intervention will be evaluated using a repeated measures design using a mixed linear model.

Enrollment

181 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Attending Physicians, Emergency Room Resident Physicians, and PA's will be included if:

  • they provide care to adult patients in the emergency department of Mount Sinai Hospital.

Patients will be enrolled for medical record review if

  • they present with a complaint of headache and charted on the headache template in the period between four years pre-intervention and the end of the study period.

Exclusion criteria

  • anyone who does not meet the inclusion criteria will be excluded from the study

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

181 participants in 4 patient groups

Audit-feedback
Experimental group
Description:
Arm 1: Audit-feedback only
Treatment:
Other: Audit-feedback
CDS message
Experimental group
Description:
Arm 2: CDS message only
Treatment:
Other: Clinical Decision Support
Both Interventions
Experimental group
Description:
Arm 3: Audit-feedback and CDS message
Treatment:
Other: Clinical Decision Support
Other: Audit-feedback
Control
No Intervention group
Description:
Arm 4: Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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