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Serious Medication Errors in Pediatrics: Evaluation of Prevention Strategies - Article


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Clinical Trial: Serious Medication Errors in Pediatrics: Evaluation of Prevention Strategies

This study is currently recruiting patients.
Verified by Brigham and Women''''s Hospital July 2005

Sponsors and Collaborators: Brigham and Women''''s Hospital
National Patient Safety Foundation
Children''''s Hospital Boston
Information provided by: Brigham and Women''''s Hospital
ClinicalTrials.gov Identifier: NCT00153205

Purpose

The purpose of this study is to determine how effective ward based clinical pharmacists and computerized physician order entry are in reducing serious medication errors in pediatric inpatients.
Condition Intervention
medication errors
medical records systems, computerized
patient safety
 Device: computerized physician order entry

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Historical Control, Single Group Assignment, Safety Study

Further Study Details: 
Primary Outcomes: serious medication errors
Expected Total Enrollment:  1000

Study start: February 2000;  Expected completion: June 2006
Last follow-up: April 2006;  Data entry closure: April 2006

This is a prospective cohort study at Children’s Hospital and Brigham and Women''''s Hospital, before and after the introduction of two distinct interventions. The first intervention at Children''''s Hospital was the introduction of clinical pharmacists on inpatient pediatric wards to target errors at the stages of physician ordering and nurse. The second intervention is technological: the introduction of physician computer order entry at BWH neonatal intensive care unit. This intervention will most effectively target errors at the stage of physician ordering, and secondarily address errors at the stage of pharmacy dispensing and nurse transcription. Data on serious medication errors will be collected pre and post each intervention.

Eligibility

Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Patients in the BWH NICU in the study pods during the study period

Exclusion Criteria:

  • Patients in other units, non-study pods, or outside of the study period

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00153205

Rainu Kaushal      212 746 1703    rkaushal@partners.org

Massachusetts
      Brigham and Women''''s Hospital, Boston,  Massachusetts,  02120,  United States; Recruiting
Rainu Kaushal  212-746-1703    rkaushal@partners.org 

Study chairs or principal investigators

Rainu Kaushal,  Principal Investigator,  BWH   

More Information

Study ID Numbers:  2005-P-000322/1; BWH
Last Updated:  September 9, 2005
Record first received:  September 8, 2005
ClinicalTrials.gov Identifier:  NCT00153205
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-13


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