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Evaluating and Improving Cancer Screening Process Quality in a Multilevel Context: The PROSPR II Consortium Design and Research Agenda.
Beaber, Elisabeth F; Kamineni, Aruna; Burnett-Hartman, Andrea N; Hixon, Brian; Kobrin, Sarah C; Li, Christopher I; Oliver, Malia; Rendle, Katharine A; Skinner, Celette Sugg; Todd, Kaitlin; Zheng, Yingye; Ziebell, Rebecca A; Breslau, Erica S; Chubak, Jessica; Corley, Douglas A; Greenlee, Robert T; Haas, Jennifer S; Halm, Ethan A; Honda, Stacey; Neslund-Dudas, Christine; Ritzwoller, Debra P; Schottinger, Joanne E; Tiro, Jasmin A; Vachani, Anil; Doria-Rose, V Paul.
  • Beaber EF; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Kamineni A; Kaiser Permanente Washington Health Research Institute, Seattle, Washington.
  • Burnett-Hartman AN; Institute for Health Research, Kaiser Permanente Colorado, Aurora, Colorado.
  • Hixon B; Institute for Health Research, Kaiser Permanente Colorado, Aurora, Colorado.
  • Kobrin SC; Division of Cancer Control and Population Sciences, NCI, Bethesda, Maryland.
  • Li CI; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Oliver M; Kaiser Permanente Washington Health Research Institute, Seattle, Washington.
  • Rendle KA; Departments of Family Medicine and Community Health and of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Skinner CS; Department of Population & Data Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Todd K; Simmons Comprehensive Cancer Center, Dallas, Texas.
  • Zheng Y; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Ziebell RA; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Breslau ES; Kaiser Permanente Washington Health Research Institute, Seattle, Washington.
  • Chubak J; Division of Cancer Control and Population Sciences, NCI, Bethesda, Maryland.
  • Corley DA; Kaiser Permanente Washington Health Research Institute, Seattle, Washington.
  • Greenlee RT; Division of Research, Kaiser Permanente Northern California, Oakland, California.
  • Haas JS; Center for Clinical Epidemiology & Population Health, Marshfield Clinic Research Institute, Marshfield, Wisconsin.
  • Halm EA; Division of General Internal Medicine, Massachusetts General Hospital, Boston, Massachusetts.
  • Honda S; Department of Medicine, Robert Wood Johnson Medical School, New Brunswick, New Jersey.
  • Neslund-Dudas C; Hawaii Permanente Medical Group, Kaiser Permanente Center for Integrated Health Care Research, Honolulu, Hawaii.
  • Ritzwoller DP; Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan.
  • Schottinger JE; Institute for Health Research, Kaiser Permanente Colorado, Aurora, Colorado.
  • Tiro JA; Kaiser Permanente Bernard J Tyson School of Medicine, Pasadena, California.
  • Vachani A; Department of Population & Data Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Doria-Rose VP; Simmons Comprehensive Cancer Center, Dallas, Texas.
Cancer Epidemiol Biomarkers Prev ; 31(8): 1521-1531, 2022 08 02.
Article in English | MEDLINE | ID: covidwho-1973969
ABSTRACT

BACKGROUND:

Cancer screening is a complex process involving multiple steps and levels of influence (e.g., patient, provider, facility, health care system, community, or neighborhood). We describe the design, methods, and research agenda of the Population-based Research to Optimize the Screening Process (PROSPR II) consortium. PROSPR II Research Centers (PRC), and the Coordinating Center aim to identify opportunities to improve screening processes and reduce disparities through investigation of factors affecting cervical, colorectal, and lung cancer screening in U.S. community health care settings.

METHODS:

We collected multilevel, longitudinal cervical, colorectal, and lung cancer screening process data from clinical and administrative sources on >9 million racially and ethnically diverse individuals across 10 heterogeneous health care systems with cohorts beginning January 1, 2010. To facilitate comparisons across organ types and highlight data breadth, we calculated frequencies of multilevel characteristics and volumes of screening and diagnostic tests/procedures and abnormalities.

RESULTS:

Variations in patient, provider, and facility characteristics reflected the PROSPR II health care systems and differing target populations. PRCs identified incident diagnoses of invasive cancers, in situ cancers, and precancers (invasive 372 cervical, 24,131 colorectal, 11,205 lung; in situ 911 colorectal, 32 lung; precancers 13,838 cervical, 554,499 colorectal).

CONCLUSIONS:

PROSPR II's research agenda aims to advance (i) conceptualization and measurement of the cancer screening process, its multilevel factors, and quality; (ii) knowledge of cancer disparities; and (iii) evaluation of the COVID-19 pandemic's initial impacts on cancer screening. We invite researchers to collaborate with PROSPR II investigators. IMPACT PROSPR II is a valuable data resource for cancer screening researchers.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Colorectal Neoplasms / COVID-19 / Lung Neoplasms Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Limits: Humans Language: English Journal: Cancer Epidemiol Biomarkers Prev Journal subject: Biochemistry / Epidemiology / Neoplasms Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Colorectal Neoplasms / COVID-19 / Lung Neoplasms Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Limits: Humans Language: English Journal: Cancer Epidemiol Biomarkers Prev Journal subject: Biochemistry / Epidemiology / Neoplasms Year: 2022 Document Type: Article