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Clinical Trials/NCT00952471
NCT00952471CompletedPhase 3

Reduction in Clinical Variance Using Targeted Design Changes in Computerized Provider Order Entry Order (CPOE) Sets

Brian Jacobs1 site in 1 country458 target enrollmentStarted: September 1, 2004Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor
Enrollment
458
Locations
1
Primary Endpoint
Reduced variation from in evidence-based care through integrating evidence into the clinician workflow in the EMR system.

Study Overview

Brief Summary

Selective redesign of order sets using different ways to frame the order and physician decision-making in a computerized provider order entry system could increase adherence to evidence-based care and reduce population-specific variance.

Detailed Description

Variance in ordering of care can be characterized as the lack of uniform use of specific treatments by clinicians for a given medical condition. Unwarranted variance in healthcare has been associated with prolonged length of stay, diminished health and increased cost. Practice variation in the management of asthma can be significant and few investigators have evaluated strategies to reduce this variation. We hypothesized that selective redesign of order sets using different ways to frame the order and physician decision-making in a computerized provider order entry system could increase adherence to evidence-based care and reduce population-specific variance.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Factorial
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •All patients admitted using an acute asthma exacerbation order set.

Exclusion Criteria

  • •Patients who did not have either an admission or discharge diagnosis of asthma exacerbation.
  • •In addition, patients admitted to the intensive care unit directly or transferred to the intensive care unit within 24-hours were excluded from analysis.
  • •Finally, patients were excluded from analysis if asthma was not the presenting problem.

Arms & Interventions

Baseline Period

No Intervention

Patients in the baseline period were cared for using the standard historical electronic order set.

Post Intervention Period

Active Comparator

Patients in the Post intervention period were cared for with evidence-bsed modified order set changes

Intervention: Evidence Based Intervention to order set (Other)

Outcomes

Primary Outcomes

Reduced variation from in evidence-based care through integrating evidence into the clinician workflow in the EMR system.

Time Frame: 2 years

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Brian Jacobs
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Brian Jacobs

MD

Children's National Research Institute

Study Sites (1)

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