Connecting the Dots

Ryerson, A. Blythe; Eheman, Christie; Styles, Timothy; Rycroft, Randi; Snyder, Claire

doi:10.1016/j.amepre.2015.08.026

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i

Connecting the Dots

12 2015
By Ryerson, A. Blythe ; Eheman, Christie ; Styles, Timothy ; ...
http://dx.doi.org/10.1016/j.amepre.2015.08.026
Source: Am J Prev Med. 49(0):S528-S535

[PDF-144.93 KB]

English

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Details:

Alternative Title:

Am J Prev Med
Personal Author:

Ryerson, A. Blythe ; Eheman, Christie ; Styles, Timothy ; Rycroft, Randi ; Snyder, Claire

Ryerson, A. Blythe ; Eheman, Christie ; Styles, Timothy ; Rycroft, Randi ; Snyder, Claire Less -
Description:

Cancer survivors, the medical community, public health professionals, researchers, and policymakers all need information about newly diagnosed cancer cases and deaths to better understand and address the disease burden. CDC collects cancer data on 96% of the U.S. population through the National Program of Cancer Registries. The National Program of Cancer Registries routinely collects data on all cancer occurrences, deaths, and the types of initial treatment received by the patients, and recently CDC has made advances in its cancer surveillance activities that have direct applicability to cancer survivorship research and care. This article examines CDC's innovative uses of the National Program of Cancer Registries infrastructure and data as a recruitment source for survivorship research studies and behavioral interventions; comparative effectiveness and patient-centered outcomes research; and the collection, consolidation, and dissemination of treatment summaries for cancer survivors and their providers. This paper also discusses long-term, idealistic plans for additional data linkages and sharing among public health, providers, and the cancer survivor through innovative concepts such as patient portals and rapid-learning health care.
Keywords:

[+]

Biomedical Research Centers For Disease Control And Prevention, U.S. Electronic Health Records Humans Information Dissemination Neoplasms Patient Care Planning Patient Outcome Assessment Patient Selection Public Health Registries Survivors United States
Source:

Am J Prev Med. 49(0):S528-S535
Pubmed ID:

26590648
Pubmed Central ID:

PMC4656128
Document Type:

Journal Article
Funding:

CC999999/Intramural CDC HHSUnited States/
Volume:

49
Issue:

0
Collection(s):

CDC Public Access
Main Document Checksum:

[+]

urn:sha256:2dbea39e65960efa0c521d818352a900b1eb4b463907ab4170d06fd8ed1221e9
Download URL:

https://stacks.cdc.gov/view/cdc/36217/cdc_36217_DS1.pdf
File Type:

nihms-724335.nxml

xml

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