Automated Versus Conventional Hospital Discharge Summaries and Prescriptions

April 15, 2010 updated by: Unity Health Toronto

Automated Versus Conventional Hospital Discharge Summaries and Prescriptions: A Randomized Controlled Trial

The purpose of this study is to determine whether a semi-automated electronic patient discharge summary program leads to increased community physician and housestaff satisfaction and patient outcomes as compared to conventional discharge reports.

Study Overview

Detailed Description

For patients hospitalized with an acute illness, the days following discharge constitute a critical period. Patients must adjust to changes in their medications, follow up with family doctors and other specialists and know what symptoms should prompt a return to hospital. The community physicians who follow them rely on information from their hospitalization to facilitate this transition, and provide continuity of care.

Communication between hospital and community physicians is essential to this process, and has traditionally been accomplished by a dictated discharge summary. Previous studies have shown that while dictated discharge summaries can be inaccurate, incomplete, or untimely, computer generated summaries are produced more quickly and accurately. Moreover, database-generated discharge summaries are preferred by physicians in the community.

We have designed a web-based computer program with quality assurance features that automatically generates timely discharge summaries. We aim to study this program over a 2 month period on our general medicine unit by means of a randomized controlled trial. Our hypothesis is that community physicians will prefer the computer generated summaries, over the standard dictated summaries. If effective, our system could be implemented more widely, and would stand to improve communication with community physicians, continuity of care, and patient safety.

Study Type

Interventional

Enrollment (Actual)

209

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ontario
      • Toronto, Ontario, Canada, M5B 1W8
        • St. Michael's Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Hospitalization on General Internal Medicine ward at St. Michael's Hospital

Exclusion Criteria:

  • Transfer to another service
  • Death during admission
  • Remains in hospital past dates specified in study protocol

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: eDischarge
The eDischarge arm will consist of two teams on the General Internal Medicine ward at St. Michael's Hospital who have been randomly assigned to use the electronic discharge summary program.
The customized electronic discharge summary program will be used to generate patient discharge summaries.
No Intervention: Traditional
The traditional arm will consist of two teams on the General Internal Medicine ward at St. Michael's Hospital who have been randomly assigned to use "traditional," dictated discharge summaries.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Primary care physician satisfaction from satisfaction score assessment form with 100-mm visual analogue scale
Time Frame: Satisfaction score assessment form to be sent one week after patient's discharge from hospital. If form is not returned in 14 days, a reminder and second form will be sent.
Satisfaction score assessment form to be sent one week after patient's discharge from hospital. If form is not returned in 14 days, a reminder and second form will be sent.

Secondary Outcome Measures

Outcome Measure
Time Frame
St. Michael's Hospital housestaff satisfaction from satisfaction score assessment form with 100-mm visual analogue scale
Time Frame: Housestaff will fill out form upon completion of the rotation during which the study has been performed
Housestaff will fill out form upon completion of the rotation during which the study has been performed
Completion of specialist outpatient workups at St. Michael's Hospital recommended during course of hospitalization
Time Frame: Within the first 30 days of patient's discharge from hospital
Within the first 30 days of patient's discharge from hospital
Patient visits to Emergency Room at St. Michael's Hospital
Time Frame: Within the first 30 days after patient's discharge from hospital
Within the first 30 days after patient's discharge from hospital
Patient/proxy care transition assessment through the use of the CTM-3.
Time Frame: Phone call made to patient or proxy one week after discharge. If patient/proxy is not reached, follow up calls will be made daily until patient/proxy is reached.
Phone call made to patient or proxy one week after discharge. If patient/proxy is not reached, follow up calls will be made daily until patient/proxy is reached.
Prescribing errors as assessed by comparing discharge summary to inpatient record
Time Frame: Upon discharge
Upon discharge
Patient readmissions to St. Michael's Hospital
Time Frame: Within 30 days of discharge
Within 30 days of discharge

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: David M Maslove, MD, Unity Health Toronto
  • Principal Investigator: Chaim M Bell, MD, PhD, FRCPC, St. Michael's Hospital; University of Toronto

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2008

Primary Completion (Actual)

June 1, 2008

Study Completion (Actual)

July 1, 2008

Study Registration Dates

First Submitted

April 7, 2008

First Submitted That Met QC Criteria

April 30, 2008

First Posted (Estimate)

May 2, 2008

Study Record Updates

Last Update Posted (Estimate)

April 16, 2010

Last Update Submitted That Met QC Criteria

April 15, 2010

Last Verified

April 1, 2010

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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