Registries as a Knowledge-Development Tool

Research Report

Registries as a Knowledge-Development Tool

The Experience of Sweden and England
July 12, 2013

Abstract

Registries of patients with particular conditions or who have received a particular treatment have a long history and are widely used in many countries. This paper focuses on two kinds of registries for patients with diabetes and for those who have received a joint hip replacement in Sweden and England. These examples illustrate how registries can serve multiple purposes, including providing quality and safety feedback to providers and purchasers, generating planning data for health systems, evaluating guidelines, and performing outcomes research. While registries are not foreign to the United States, the completeness and accomplishments of Sweden and Englands registry system go well beyond the American experience, and show how more can be done to make use of these valuable tools.

Research Area: 

Centers

To reuse content from Urban Institute, visit copyright.com, search for the publications, choose from a list of licenses, and complete the transaction.