Selection of patients for large mailed fecal immunochemical test colorectal cancer screening outreach programs: A systematic review

Author:

Wang Andrew12ORCID,Lee Briton3,Patel Shreya4,Whitaker Evans5,Issaka Rachel B67,Somsouk Ma48

Affiliation:

1. David Geffen School of Medicine, University of California, Los Angeles, CA, USA

2. College of Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, CA, USA

3. Department of Medicine, New York University Langone Medical Center, New York, NY, USA

4. Division of Gastroenterology, University of California, San Francisco, CA, USA

5. University of California San Francisco Medical Library, University of California, San Francisco, CA, USA

6. Clinical Research and Public Health Science Divisions, Fred Hutchinson, Seattle, WA, USA

7. Division of Gastroenterology, University of Washington, Seattle, WA, USA

8. Center for Vulnerable Populations, University of California, San Francisco, CA, USA

Abstract

Objective Digital health care offers an opportunity to scale and personalize cancer screening programs, such as mailed outreach for colorectal cancer (CRC) screening. However, studies that describe the patient selection strategy and process for CRC screening are limited. Our objective was to evaluate implementation strategies for selecting patients for CRC screening programs in large health care systems. Methods We conducted a systematic review of 30 studies along with key informant surveys and interviews to describe programmatic implementation strategies for selecting patients for CRC screening. PubMed and Embase were searched since inception through December 2018, and hand searches were performed of the retrieved reference lists but none were incorporated ( n = 0). No language exclusions were applied. Results Common criteria for outreach exclusion included: being up-to-date with routine CRC screening ( n = 22), comorbidities ( n = 20), and personal history ( n = 22) or family history of cancer ( n = 9). Key informant surveys and interviews were performed ( n = 28) to understand data sources and practices for patient outreach selection, and found that 13 studies leveraged electronic medical care records, 10 studies leveraged a population registry (national, municipal, community, health), 4 studies required patient opt-in, and 1 study required primary care provider referral. Broad ranges in fecal immunochemical test completion were observed in community clinic ( n = 8, 31.0–59.6%), integrated health system ( n = 5, 21.2–82.7%), and national regional CRC screening programs ( n = 17, 23.0–64.7%). Six studies used technical codes, and four studies required patient self-reporting from a questionnaire to participate. Conclusion This systematic review provides health systems with the diverse outreach practices and technical tools to support efforts to automate patient selection for CRC screening outreach.

Funder

National Institutes of Health/National Cancer Institute

San Francisco Cancer (SF CAN) Initiative

Publisher

SAGE Publications

Subject

Public Health, Environmental and Occupational Health,Health Policy

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