Leveraging State Cancer Registries to Measure and Improve the Quality of Cancer Care: A Potential Strategy for California and Beyond

被引:25
作者
Hiatt, Robert A. [1 ]
Tai, Caroline G. [1 ]
Blayney, Douglas W. [2 ]
Deapen, Dennis [3 ]
Hogarth, Michael [4 ]
Kizer, Kenneth W. [5 ]
Lipscomb, Joseph [6 ]
Malin, Jennifer [7 ]
Phillips, Stephen K. [8 ]
Santa, John [9 ]
Schrag, Deborah [10 ]
机构
[1] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[2] Stanford Univ, Stanford Canc Inst, Stanford, CA 94305 USA
[3] Univ So Calif, Div Epidemiol, Prevent Med, Los Angeles, CA USA
[4] Univ Calif Davis, Dept Pathol & Lab Med, Sacramento, CA 95817 USA
[5] Univ Calif Davis, Inst Populat Hlth Improvement, Sacramento, CA 95817 USA
[6] Emory Univ, Winship Canc Inst, Rollins Sch Publ Hlth, Dept Hlth Policy & Management, Atlanta, GA 30322 USA
[7] WellPoint Inc, Oncol & Care Management, Thousand Oaks, CA USA
[8] Hooper Lundy & Bookman PC, San Francisco, CA USA
[9] Consumer Reports Hlth, Yonkers, NY USA
[10] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med, Boston, MA 02115 USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2015年 / 107卷 / 05期
关键词
COLORECTAL-CANCER; OUTCOMES;
D O I
10.1093/jnci/djv047
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite recent increased attention to healthcare performance and the burden of disease from cancer, measures of quality of cancer care are not readily available. In 2013, the California HealthCare Foundation convened an expert workgroup to explore the potential for leveraging data in the California Cancer Registry (CCR), one of the world's largest population-based cancer registries, for measuring and improving the quality of cancer care. The workgroup assessed current registry operations, the value to be gained by linking CCR data with health insurance claims or encounter data and clinical data contained in health system electronic health records, and potential barriers to these linkages. The workgroup concluded that: 1) The CCR mandate should be expanded to include use of its data for quality of cancer care measurement and public reporting; and 2) a system should be developed to support linkage of registry data with both claims data and provider electronic health record data.
引用
收藏
页数:7
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