Rationale and design for a cluster randomized quality-improvement trial to increase the uptake of evidence-based therapies for patients at high cardiovascular risk: The BRIDGE-Cardiovascular Prevention trial.

Journal Article (Journal Article;Pragmatic Clinical Trial)

BACKGROUND: Translating evidence into clinical practice in the management of high cardiovascular risk patients is challenging. Few quality improvement interventions have rigorously evaluated their impact on both patient care and clinical outcomes. OBJECTIVES: The main objectives are to evaluate the impact of a multifaceted educational intervention on adherence to local guidelines for the prescription of statins, antiplatelets and angiotensin converting enzyme inhibitors or angiotensin II receptor blockers for high cardiovascular risk patients, as well as on the incidence of major cardiovascular events. DESIGN: We designed a pragmatic two arm cluster randomized trial involving 40 clusters. Clusters are randomized to receive a multifaceted quality improvement intervention or to routine practice (control). The multifaceted intervention includes: reminders, care algorithms, training of a case manager, audit and feedback reports, and distribution of educational materials to health care providers. The primary endpoint is the adherence to combined evidence-based therapies (statins, antiplatelet therapy and angiotensin converting enzyme inhibitors or angiotensin receptor blockers) at 12 months after the intervention period in patients without contra-indications for these medications. All analyses follow the intention-to-treat principle and take the cluster design into account using linear mixed logistic regression modeling. SUMMARY: If proven effective, this multifaceted intervention would have wide utility as a means of promoting optimal usage of evidence-based interventions for the management of high cardiovascular risk patients.

Full Text

Duke Authors

Cited Authors

  • Machline-Carrion, MJ; Soares, RM; Damiani, LP; Campos, VB; Sampaio, B; Yamashita, J; Fonseca, FH; Izar, MC; Amodeo, C; Pontes-Neto, OM; de Melo Barros, PG; Lopes, RD; Brandão da Silva, N; Guimarães, HP; Piegas, L; Stein, AT; Berwanger, O

Published Date

  • January 2019

Published In

Volume / Issue

  • 207 /

Start / End Page

  • 40 - 48

PubMed ID

  • 30415082

Pubmed Central ID

  • 30415082

Electronic International Standard Serial Number (EISSN)

  • 1097-6744

Digital Object Identifier (DOI)

  • 10.1016/j.ahj.2018.10.001


  • eng

Conference Location

  • United States