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Clinical Trials/NCT01304108
NCT01304108CompletedPhase 4

Spreading and Improving DVT Prophylaxis at Mayo Clinic (DVT-P-Spread)

Mayo Clinic1 site in 1 country3,000 target enrollmentStarted: January 1, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
3,000
Locations
1
Primary Endpoint
% of in patients with an appropriate VTE prophylaxis plan

Study Overview

Brief Summary

Preventing the formation of blood clots in the veins so they do not injure leg veins or travel to the lungs, also called venous thromboembolism prophylaxis (VTE-P) is an essential component of safe in-patient care, yet it is deployed sub-optimally in many hospitals, including The investigators own. Two prior VTE-P improvement projects were completed at Mayo Clinic hospitals, one in the Department of Medicine, and the other in selected divisions of the Department of Surgery. Both projects resulted in marked improvement in the percentage of patients receiving appropriate VTE-P. This project seeks to utilize the lessons learned from these two pilots along with known best practices for "spreading" to deploy methods that enhance VTE-P to the entire hospitalized population. The investigators seek appropriate VTE-P rates exceeding 95%.

Detailed Description

Venous thromboembolism prophylaxis (VTE-P) is an essential component of safe in-patient care, yet it is deployed sub-optimally in many hospitals, including our own. Two prior VTE-P improvement projects were completed at Mayo Clinic hospitals, one in the Department of Medicine, and the other in selected divisions of the Department of Surgery. Both projects resulted in marked improvement in the percentage of patients receiving appropriate VTE-P. This project seeks to utilize the lessons learned from these two pilots along with known best practices for "spreading" to deploy methods that enhance VTE-P to the entire hospitalized population. The investigators seek appropriate VTE-P rates exceeding 95%. This began as a quality improvement project. The investigators have taken baseline measures of VTE-P rates in our hospitals, intervened with various electronic prompts to use appropriate VTE-P, and have and will re-measure VTE-P rates. The investigators intend to present and publish our methods and results so that lessons learned may be shared and applied elsewhere.

Study Design

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

Eligibility Criteria

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

Inclusion Criteria

  • Inpatients with age > 17 years old

Exclusion Criteria

  • Outpatients
  • Inpatients with age less than or equal to 17 years old

Arms & Interventions

Order Set

Experimental

Insertion of VTE-P Order Set "tollgate" in all active admission and transfer orders.

Intervention: VTE-P Tollgate (Other)

Clinical Decision Support Pop-up

Experimental

Deploy rules-based pop-up that reminds ordering clinicians when patients do not have an active VTE-P plan.

Intervention: BLAZE Pop up (Other)

Usual Care

Active Comparator

Usual care, without the experimental additions

Intervention: Usual Care (Other)

Outcomes

Primary Outcomes

% of in patients with an appropriate VTE prophylaxis plan

Time Frame: Baseline to 1 month

The investigators will measure the number of patients in a statistically valid random sample of hospitalized patients who have a VTE-prophylaxis plan consistent with current recommendations.

Secondary Outcomes

  • Clinically significant complications of VTE-P anticoagulant therapy(baseline to 1 month)

Investigators

Sponsor Class
Other

Study Sites (1)

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