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Article
Electronic records, registries, and the development of "big data": crowd-sourcing quality toward knowledge.
Frontiers in oncology
  • Summer B Dewdney
  • Jason Lachance, Maine Medical Center
Document Type
Article
Publication Date
2-1-2016
Institution/Department
Obstetrics & Gynecology
Abstract

Despite many perceived advances in treatment over the past few decades, cancer continues to present a significant health burden, particularly to the aging US population. Forces including shrinking funding mechanisms, cost and quality concerns, as well as disappointing clinical outcomes have driven a surge of recent efforts into utilizing the technological innovation that has permeated other industries by leveraging large and complex data sets, so called "big data." In this review, we will review some of the history of oncology data collection, including the earliest data registries, as well as explore the future directions of this new brand of research while highlighting some of the more recent and promising efforts to harness the power of the electronic health record and the multitude of data co-located there, in an effort to improve individualized cancer-related outcomes in rapid real time.

Comments

Division of Gynecologic Oncology, Maine Medical Center, Portland ME, USA.

Citation Information
Summer B Dewdney and Jason Lachance. "Electronic records, registries, and the development of "big data": crowd-sourcing quality toward knowledge." Frontiers in oncology Vol. 6 (2016) p. 268 - 268 ISSN: 2234-943X
Available at: http://works.bepress.com/jason-lachance/1/