Improving the Use of Evidence-Based Heart Failure Therapies in the Outpatient Setting: The IMPROVE HF performance improvement registry
Evidence-based consensus treatment guidelines are available to assist physicians with the management of chronic heart failure (HF). Although it has been generally presumed that physicians incorporate these treatment guidelines into clinical practice, the actual assimilation of evidence-based strategies and guidelines has been demonstrated to be less than ideal. Studies of HF care show that treatment guidelines are slowly adopted and inconsistently applied and, thus, often fail to lead to improvements in patient care and outcomes. There are a number of ongoing, large, national quality improvement registries that are following the clinical care and outcomes of inpatient HF treatment. However, to date, there have been no similar quality improvement registries in the outpatient arena. The Registry to Improve the Use of Evidence-Based Heart Failure Therapies in the Outpatient Setting (IMPROVE HF) is the first large, comprehensive performance improvement registry designed to characterize the current outpatient management of systolic HF and assess the effect of practice-specific process improvement interventions consisting of education, specific clinical guidelines, reminder systems, benchmarked quality reports, and structured academic detailing on the use of evidence-based HF therapies. Seven performance measures to quantify the quality of outpatient HF care were explicitly developed by the IMPROVE HF Steering Committee. The primary objective is to observe, over the aggregate of IMPROVE HF practice sites, a relative ≥20% improvement in at least 2 of the 7 performance measures at 24 months, compared with baseline. Deidentified clinical data from the medical records of a planned 43
000 patients from 160 US cardiology practices will be included in this study.
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This registry is supported by Medtronic, Inc, Minneapolis, MN.
The IMPROVE HF registry and this study are sponsored by Medtronic, Inc. The IMPROVE HF registry was established by Medtronic, Inc, under the guidance of a steering committee of academic advisors, each of whom is an author on this manuscript. The financial disclosures of the IMPROVE HF steering committee members are given below. These academic advisors were intimately involved in the initial preparation and design of this registry. Medtronic, Inc, provided financial and material support for the IMPROVE HF registry. A contract research organization, Outcome Sciences, Inc (Cambridge, MA), independently performs the practice site chart abstractions for IMPROVE HF and is responsible for performing data checks, storing site-specific and aggregate data, as well as providing benchmarked quality of care reports to practice sites. The contract research organization receives funding from Medtronic, Inc. Identified, individual practice site data are not shared with either the steering committee or the sponsor. The authors had complete control and authority over the study design, the manuscript preparation, and the decision to submit this manuscript to the American Heart Journal for publication. The manuscript was submitted to Medtronic, Inc, prior to submission for publication.
PII: S0002-8703(07)00254-2
doi:10.1016/j.ahj.2007.03.030
© 2007 Published by Elsevier Inc.
