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The Effects of a Results Management System on Physician Awareness of Post-Discharge Test Results

The Effects of a Results Management System on Physician Awareness of Post-Discharge Laboratory and Radiology Results

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00146354
Enrollment
Unknown
Registered
2005-09-07
Start date
Unknown
Completion date
Unknown
Last updated
2007-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy, Medical Record Systems, Computerized

Keywords

Electronic Medical Record, Electronic Results Tracking, Patient Safety, Post-Discharge Test Results

Brief summary

This project aims to define the problem of results that return after patient discharge and to study the implementation of an Electronic Medical Record (EMR)-based system for tracking these results.

Detailed description

The transfer of care at hospital discharge is complex and requires the transmission of large amounts of data between inpatient physicians (hospitalists) and outpatient physicians (PCPs), including information about pending tests. Frequently, laboratory and radiology tests are not finalized until after a patient is discharged, and when the responsibility for these pending results is not clearly defined, they can be missed. Our project aims to define the problem of these post-discharge results and to study the implementation of an EMR-based system (Hospitalist Results Manager, HRM) for tracking these results on the hospitalist services at Brigham and Women's Hospital (BWH) and Massachusetts General Hospital (MGH). The project consists of two phases: a cross-sectional study before intervention to define the epidemiology of post-discharge results, and a randomized trial of HRM to determine its effect on physician awareness of these results.

Interventions

BEHAVIORALHospitalists Results Manager

Sponsors

Harvard Risk Management Foundation
CollaboratorOTHER
Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
ECT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Admitted under enrolled study Attendings at the two study locations * Patient had test result finalized after discharge and prior to subsequent admission

Exclusion criteria

* Test result noted in discharge summary * Test result not clinically actionable

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026