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Clinical Trials/NCT00235027
NCT00235027CompletedNot Applicable

Improving Safety By Computerizing Outpatient Prescribing

Agency for Healthcare Research and Quality (AHRQ)3 sites in 1 country701 target enrollmentStarted: August 1, 2000Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
701
Locations
3
Primary Endpoint
Preventable Adverse drug events

Study Overview

Brief Summary

Patient safety is at the forefront of critical issues in health care. Medications are the single most frequent cause of adverse events, and in the inpatient setting adverse drug events (ADEs) are common, expensive, injurious to patients, and often preventable. Relatively little, however, is known about the frequency of ADEs in the ambulatory setting, how to monitor for outpatient ADEs, or on the impact of prevention strategies such as computerization of prescribing supplemented by decision-support.

Detailed Description

Specific Aim 1: Increase routine identification of outpatient adverse drug events (ADEs) through development of a computerized ADE detection monitor.

Specific Aim 2: Use basic computerized outpatient prescribing to reduce preventable ADEs in a diverse array of outpatient settings.

Specific Aim 3: Use advanced decision-support within computerized prescribing to reduce the frequency of preventable ADEs, medication errors, and potential ADEs.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Care Provider)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • At Brigham & Women's Hospital, clinics utilizing the electronic medical record will be included. At Regenstrief, any clinic that has access to their electronic medical record will be utilized.
  • For the impact of basic decision support, clinics were not randomized
  • For impact of advanced decision support, clinics were randomized to receive the intervention

Exclusion Criteria

  • Clinics not using electronic medical records

Outcomes

Primary Outcomes

Preventable Adverse drug events

Time Frame: 8/5/2004 - 1/5/2005

Data were electronically collected each time a physician entered a prescription that triggered an alert related to medication safety.

Secondary Outcomes

  • Total adverse drug events, medication errors(1/15/2001 - 5/15/2001)

Investigators

Sponsor
Agency for Healthcare Research and Quality (AHRQ)
Sponsor Class
Fed
Responsible Party
Principal Investigator
Principal Investigator

david bates

Chief of General Internal Medicine, BWH

Agency for Healthcare Research and Quality (AHRQ)

Study Sites (3)

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