Medication Errors and Adverse Drug Events (ADEs) in Ambulatory Pediatrics
Recruitment status was: Recruiting
Pediatric Patients With a Variety of Medical Conditions.
Device: Computerized Physician Order Entry
|Study Design:||Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
|Official Title:||Ambulatory Medication Errors and Adverse Drug Events (ADEs) in Pediatrics|
- Medication Errors
- Adverse Drug Events
|Study Start Date:||September 2001|
|Estimated Study Completion Date:||July 2005|
This study has the following 2 goals:
Aim 1: To determine the rates, types, and predictors of medication errors and ADEs.
Aim 2: To perform a trial assessing the effectiveness of an intervention (CPOE) on reducing serious medication errors.
We hypothesize that:
- Medication errors and ADEs are frequent in ambulatory pediatrics.
- Presence of the following predictors will be associated with higher error rates: cultural, racial, socioeconomic, educational, and linguistic barriers to communication, understanding, and successful completion of prescribed therapies; complex medical or chronic medical conditions; complex medication regimens; non-physician providers with limited clinical experience; high provider workloads; and complex prescription refill systems.
- Prevention strategies, including both technology-based and behavioral/ human factors-based interventions, will be effective and cost-effective in reducing rates of serious medication errors (defined as preventable ADEs and non-intercepted potential ADEs).
Please refer to this study by its ClinicalTrials.gov identifier: NCT00229671
|United States, Massachusetts|
|Brigham and Women's Hospital|
|Boston, Massachusetts, United States, 02120|
|Principal Investigator:||Rainu Kaushal||Brigham and Women's Hospital|