Name: Linking Data for Health Services Research: A Framework and Instructional Guide (en Inglés)
Price: 100.03 PEN
Availability: InStock
Author: Human Services, U. S. Department of Heal ; And Quality, Agency for Healthcare Resea
ISBN: 9781505859430

portada Linking Data for Health Services Research: A Framework and Instructional Guide (en Inglés)

Formato

Libro Físico

Autor

U. S. Department of Heal Human Services

Agency for Healthcare Resea And Quality

Editorial

Createspace Independent Publishing Platform

Idioma

Inglés

N° páginas

Encuadernación

Tapa Blanda

Dimensiones

28.0 x 21.6 x 0.5 cm

Peso

0.22 kg.

ISBN13

9781505859430

Categorías

Investigación médica

Linking Data for Health Services Research: A Framework and Instructional Guide (en Inglés)

U. S. Department of Heal Human Services (Autor) · Agency for Healthcare Resea And Quality (Autor) · Createspace Independent Publishing Platform · Tapa Blanda

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Origen: Estados Unidos (Costos de importación incluídos en el precio)

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Reseña del libro "Linking Data for Health Services Research: A Framework and Instructional Guide (en Inglés)"

Health registries greatly enhance health services research, especially when linked with other data sources such as administrative claims. Recently, concerns about patient privacy and data security have produced policies such as the Health Insurance Portability and Accountability Act (HIPAA) that reduce the availability of sensitive identifying information. In this context, the development of effective record linkage approaches for varying scenarios of data availability is critical. This report presents a conceptual framework and instructional information that scientifically describe the strengths and limitations of different approaches to record linkage of registries to other data sources. The report defines the requirements for high-quality record linkage of registries to other data sources and describes the strengths and limitations of different approaches. By explaining the spectrum of activities involved, it serves as an instructional guide for researchers designing new CER studies using patient registries linked with other secondary data sources. Through this report, we provide an overview of linkage from registries to administrative claims, including considerations for researchers, data managers, information technology managers, and other stakeholders who are likely to be involved in the process of data linkage. We also apply the data linkage framework to a real-world problem and discuss the results.