Patient registries in primary care: essential element for quality improvement

Mt Sinai J Med. Jul-Aug 2012;79(4):475-80. doi: 10.1002/msj.21328.

Abstract

Primary care in the United States has been in the midst of a transformation from a system based solely on individual office interactions to one that includes managing health at a population level. The chronic care model provides a robust framework for health systems to transform and restructure their delivery of care to one that is committed to delivering multidisciplinary quality care with a proactive approach. Patient and disease registries are the essential tools necessary to inform all elements of the chronic care model and guide practices though this transformation. Nationally as well as internationally, when used as part of a robust continuous quality-improvement program, registries have demonstrated to improve patient outcomes and reduce healthcare costs. Despite challenges practices may confront when initially developing a patient registry, it is evident that population management is now an important and integral component of a successful primary-care practice whose aim is to improve quality of patient care.

MeSH terms

  • Humans
  • Outcome and Process Assessment, Health Care
  • Primary Health Care / standards*
  • Quality Improvement*
  • Registries*
  • Sweden
  • United States