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Title: Randomized Trial of an EHR Embedded Risk Calculator vs. Standard VTE Prophylaxis for Medical Patients

Primary Purpose

Venous Thromboembolism

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Risk calculator
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Venous Thromboembolism focused on measuring Venous Thromboembolism Risk Calculator

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All adult patients (age ≥18 years) admitted to a medical service, including intensive care units, between September 1, 2017 and August 31, 2018 will be eligible.

Exclusion Criteria:

  • patients not eligible to receive VTE prophylaxis because they are already receiving anticoagulation for another purpose (e.g. warfarin for atrial fibrillation or LMWH for DVT or PE present on admission),
  • patients admitted with a terminal condition who are receiving comfort care only
  • Surgical patients who are admitted to the medical service temporarily (e.g. hip fracture)

Sites / Locations

  • Cleveland Clinic Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Usual Care

Risk calculator

Arm Description

Control: Standard order set without risk calculator (usual care)

Intervention: VTE risk calculator embedded in the smart order set incorporated into the EHR and activated for all medical patients

Outcomes

Primary Outcome Measures

Appropriate VTE prophylaxis
Proportion of patients at high risk of VTE who receive prophylaxis and the proportion of patients at low risk who do not receive prophylaxis

Secondary Outcome Measures

Total patients receiving prophylaxis
All patients who received any chemoprophylaxis during hospitalization, regardless of risk status.
Rate of VTE among high risk patients
Symptomatic VTE events not present on admission occurring among patients at high risk for VTE according to the risk calculator.
Rate of VTE among high risk patients
Symptomatic VTE events not present on admission occurring among patients at high risk for VTE according to the risk calculator.
Rate of major bleeding among high risk patients
Major bleeding events among patients with risk factors for bleeding.
Average cost of prophylaxis
Total cost of prophylaxis received during hospitalization
Average cost of hospitalization
Cost of hospitalization as determined by the hospital cost accounting system
Average length of stay
Total days in hospital

Full Information

First Posted
July 10, 2017
Last Updated
May 23, 2019
Sponsor
The Cleveland Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT03243708
Brief Title
Title: Randomized Trial of an EHR Embedded Risk Calculator vs. Standard VTE Prophylaxis for Medical Patients
Official Title
Title: EHR Embedded Risk Calculator vs. Standard VTE Prophylaxis for Medical Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
December 4, 2017 (Actual)
Primary Completion Date
April 14, 2019 (Actual)
Study Completion Date
April 14, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Cleveland Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Venous thromboembolism (VTE) is a serious source of hospital morbidity and mortality. Chemoprophylaxis with heparin has been shown to reduce the occurrence of VTE, but it increases the risk of bleeding and it is uncomfortable to receive. For that reason, VTE prophylaxis should be reserved for patients at moderate to high risk of VTE and low risk of bleeding. However, identifying patients at low risk for VTE can be difficult, because most patients have at least one risk factor for VTE and there are no validated risk prediction tools for use in US hospitals. Instead, many hospitals have opted for a one-size-fits-all approach with near-universal prophylaxis, putting many patients at unnecessary risk of bleeding. However, to provide care that is truly patient-centered, US physicians face several challenges. First, there is no accepted risk calculator that they can use to estimate an individual patient's risk. Second, risk calculators are not readily available at the point of care. As a result, prophylaxis rates have remained stubbornly low in some institutions, while in others the rate of prophylaxis is high, but the rate of inappropriate prophylaxis is also high. This study uses a risk prediction tool developed at the Cleveland Clinic to assess an individual patient's risk of VTE. The tool is incorporated into the electronic health record in the form of a smart order set. In this randomized trial, we will assess the effects of the order set on physician behavior and patient outcomes . Examining the effectiveness of an electronic decision aid embedded in an EHR in routine clinical practice will test whether a smart order set can improve patient care by incorporating patient-specific factors into a complex decision process.
Detailed Description
Specific Aim: Assess the effects of a VTE risk calculator embedded in the admission order set vs. usual care on physician behavior and patient outcomes in a randomized trial Research Strategy: Utilizing a Step-Wedge design, this randomized controlled trial (RCT) will be conducted at 10 Cleveland Clinic hospitals in efforts to assess the effects of a VTE (venous thromboembolism) risk calculator embedded in the admission order set vs. usual care on physician behavior and patient outcomes. Hospitals will be randomized to display the risk calculator to physicians admitting patients or to the usual order set that contains only a description of VTE risk factors. The risk calculator will produce a predicted risk of VTE together with a recommendation regarding the use of prophylaxis for an individual patient. Physicians will be free to ignore the calculator or override its results if they so choose.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Thromboembolism
Keywords
Venous Thromboembolism Risk Calculator

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
Step-Wedge Randomized controlled trial (RCT)
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90537 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Control: Standard order set without risk calculator (usual care)
Arm Title
Risk calculator
Arm Type
Active Comparator
Arm Description
Intervention: VTE risk calculator embedded in the smart order set incorporated into the EHR and activated for all medical patients
Intervention Type
Behavioral
Intervention Name(s)
Risk calculator
Intervention Description
Venous thromboembolism (VTE) risk calculator embedded in the admission order set with personalized recommendation for prophylaxis
Primary Outcome Measure Information:
Title
Appropriate VTE prophylaxis
Description
Proportion of patients at high risk of VTE who receive prophylaxis and the proportion of patients at low risk who do not receive prophylaxis
Time Frame
within 48 hours of index hospitalization admission
Secondary Outcome Measure Information:
Title
Total patients receiving prophylaxis
Description
All patients who received any chemoprophylaxis during hospitalization, regardless of risk status.
Time Frame
14 days
Title
Rate of VTE among high risk patients
Description
Symptomatic VTE events not present on admission occurring among patients at high risk for VTE according to the risk calculator.
Time Frame
14 days
Title
Rate of VTE among high risk patients
Description
Symptomatic VTE events not present on admission occurring among patients at high risk for VTE according to the risk calculator.
Time Frame
45 days
Title
Rate of major bleeding among high risk patients
Description
Major bleeding events among patients with risk factors for bleeding.
Time Frame
14 days
Title
Average cost of prophylaxis
Description
Total cost of prophylaxis received during hospitalization
Time Frame
14 days
Title
Average cost of hospitalization
Description
Cost of hospitalization as determined by the hospital cost accounting system
Time Frame
Up to 30 days
Title
Average length of stay
Description
Total days in hospital
Time Frame
Up to 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All adult patients (age ≥18 years) admitted to a medical service, including intensive care units, between September 1, 2017 and August 31, 2018 will be eligible. Exclusion Criteria: patients not eligible to receive VTE prophylaxis because they are already receiving anticoagulation for another purpose (e.g. warfarin for atrial fibrillation or LMWH for DVT or PE present on admission), patients admitted with a terminal condition who are receiving comfort care only Surgical patients who are admitted to the medical service temporarily (e.g. hip fracture)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Rothberg
Organizational Affiliation
The Cleveland Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic Health System
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22041949
Citation
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Results Reference
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PubMed Identifier
20352366
Citation
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Results Reference
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PubMed Identifier
18242412
Citation
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Results Reference
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Citation
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Results Reference
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PubMed Identifier
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Citation
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Title: Randomized Trial of an EHR Embedded Risk Calculator vs. Standard VTE Prophylaxis for Medical Patients

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