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Understanding the Experiences of Patients With Pancreatic Cancer: Quantitative Analysis of the Pancreatic Cancer Action Network Patient Registry

Understanding the Experiences of Patients With Pancreatic Cancer: Quantitative Analysis of the Pancreatic Cancer Action Network Patient Registry

The majority (171/210, 81.4%) identified as White, and 11/210 (5.2%) of participants identified as being of Hispanic, Latino, or Spanish origin, and 7/210 (3.3%) identified as Black or African American. Of the 272 total participants, 102 (37.5%) were initially diagnosed with metastatic pancreatic cancer, 38 (14%) with locally advanced disease, 35 (12.9%) borderline resectable, and 75 (27.6%) had resectable pancreatic cancer at diagnosis.

Allison Rosenzweig, Sydney Rathjens, Kawther Abdilleh, Dennis Ladnier, Fatima Zelada-Arenas, Sudheer Doss, Lynn M Matrisian

J Particip Med 2025;17:e65046

Experiences Receiving and Delivering Virtual Health Care For Women: Qualitative Evidence Synthesis

Experiences Receiving and Delivering Virtual Health Care For Women: Qualitative Evidence Synthesis

Moreover, technology has been noted as a potential strategy to overcome insufficient communication between clinicians and Black women for key health issues, such as breast cancer risk [95]. Delivering high-quality virtual care requires the intentional consideration of determinants of health care, which apply to all patients but are more common or more impactful among women.

Karen M Goldstein, Sharron Rushton, Allison A Lewinski, Abigail Shapiro, Tiera Lanford-Davey, Jessica N Coleman, Neetu Chawla, Dhara B Patel, Katherine Van Loon, Megan Shepherd-Banigan, Catherine Sims, Sarah Cantrell, Susan Alton Dailey, Jennifer M Gierisch

J Med Internet Res 2025;27:e68314