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Self-Collection for Primary HPV Testing: Perspectives on Implementation From Federally Qualified Health Centers.
Le, Amanda; Rohweder, Catherine; Wheeler, Stephanie B; Lafata, Jennifer Elston; Teal, Randall; Giannone, Kara; Zaffino, MaryShell; Smith, Jennifer S.
Afiliación
  • Le A; Department of Public Health Leadership, Gillings School of Global Public Health, University of North Carolina at Chapel Hill.
  • Rohweder C; Center for Health Promotion and Disease Prevention, University of North Carolina at Chapel Hill.
  • Wheeler SB; Department of Health Policy and Management, Gillings School of Global Public Health, University of North Carolina at Chapel Hill.
  • Lafata JE; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill.
  • Teal R; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill.
  • Giannone K; Division of Pharmaceutical Outcomes and Policy, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill.
  • Zaffino M; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill.
  • Smith JS; Connected Health Applications and Interventions, University of North Carolina at Chapel Hill.
Prev Chronic Dis ; 20: E93, 2023 10 19.
Article en En | MEDLINE | ID: mdl-37857461
ABSTRACT

INTRODUCTION:

Primary testing for high-risk human papillomavirus (HPV) by self-collection could result in higher rates of cervical cancer screening. Federally qualified health centers (FQHCs) in the US serve a large proportion of women who have low income and no health insurance and are medically underserved - risk factors for being insufficiently screened for cervical cancer. Although the implementation of self-collection for HPV testing is not yet widespread, health care entities need to prepare for its eventual approval by the US Food and Drug Administration. We conducted focus groups and interviews among clinical and administrative staff and leadership to gather data on key logistical concerns that must be addressed before implementing self-collection for HPV testing in FQHCs.

METHODS:

We identified focus group and interview participants from 6 FQHCs in North Carolina. We conducted focus groups with clinical and administrative staff (N = 45) and semistructured interviews with chief executive officers, senior-level administrators, chief medical officers, and clinical data managers (N = 24). Transcripts were coded by using codebooks derived from research questions and notes taken during data collection. Themes emerged on implementation of self-collection for HPV testing. We applied the constructs from the Consolidated Framework for Implementation Research (CFIR) to themes to identify domains of potential barriers and facilitators to implementation.

RESULTS:

Clinical personnel reported that offering self-collection for HPV testing is acceptable and feasible and can increase cervical cancer screening rates. Uncertainties emerged about accuracy of results, workflow disruptions, financial implications, and effects on clinic quality measures.

CONCLUSION:

Implementing self-collection for HPV testing was considered feasible and acceptable by participants. However, important health service delivery considerations, including financial implications, must be addressed before integrating self-collection for HPV testing into the standard of care.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias del Cuello Uterino / Infecciones por Papillomavirus Límite: Female / Humans País/Región como asunto: America do norte Idioma: En Revista: Prev Chronic Dis Asunto de la revista: SAUDE PUBLICA Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias del Cuello Uterino / Infecciones por Papillomavirus Límite: Female / Humans País/Región como asunto: America do norte Idioma: En Revista: Prev Chronic Dis Asunto de la revista: SAUDE PUBLICA Año: 2023 Tipo del documento: Article