2008
DOI: 10.1161/circoutcomes.108.801654
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The Cardiovascular Research Network

Abstract: The Cardiovascular Research Network represents a new paradigm in the approach to cardiovascular quality of care and outcomes research among community-based populations. Its unique ability to characterize longitudinally large, diverse populations will yield novel insights into contemporary disease and risk factor surveillance, management, outcomes, and costs. The Cardiovascular Research Network aims to become the national research partner of choice for efforts to improve the prevention, diagnosis, treatment, an… Show more

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Cited by 123 publications
(91 citation statements)
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“…These healthcare systems represent demographically and socioeconomically diverse community‐based populations in the specific geographic areas 11. Research divisions from these healthcare delivery systems each created site‐specific virtual data warehouses containing individual patient information from electronic medical records and administrative databases to promote interinstitutional research 10.…”
Section: Methodsmentioning
confidence: 99%
“…These healthcare systems represent demographically and socioeconomically diverse community‐based populations in the specific geographic areas 11. Research divisions from these healthcare delivery systems each created site‐specific virtual data warehouses containing individual patient information from electronic medical records and administrative databases to promote interinstitutional research 10.…”
Section: Methodsmentioning
confidence: 99%
“…Although new national and international registries of patients who are at risk for or experience AKI would be ideal to construct, the cost and time needed are probably prohibitive for providing short-term insights needed for current trial planning. Multiple data sources could be leveraged to inform clinical trial planning for selected AKI prevention and treatment populations (Table 2) (19)(20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30)(31)(32)(33)(34). Depending on the data source, insights into the likely proportion of eligible patients as well as preliminary outcome rates at different follow-up times would be available to assist in sample size and power calculations.…”
Section: Power and Sample Size Issuesmentioning
confidence: 99%
“…The following questions were addressed: All HMORN sites maintain a Virtual Data Warehouse (VDW) consisting of electronic medical record (EMR) and insurance claim data for their enrolled members. 24,25 Data on encounters, pharmacy fills, diagnoses, medical tests, and demographics are organized using the same definitions across sites and are quality checked locally. These data are matched to official regional mortality records using Social Security Numbers or patient names, birthdates, and demographic profiles.…”
Section: Introductionmentioning
confidence: 99%