Results 21 to 30 of about 296,381 (341)

NoteChat: A Dataset of Synthetic Doctor-Patient Conversations Conditioned on Clinical Notes [PDF]

Findings of the Association for Computational Linguistics: ACL 2024, 2023
We introduce NoteChat, a novel cooperative multi-agent framework leveraging Large Language Models (LLMs) to generate patient-physician dialogues. NoteChat embodies the principle that an ensemble of role-specific LLMs, through structured role-play and strategic prompting, can perform their assigned roles more effectively.
arxiv   +1 more source

Researchers, patients, and other stakeholders’ perspectives on challenges to and strategies for engagement

Research Involvement and Engagement, 2020
Background There is growing interest in patient and stakeholder engagement in research, yet limited evidence about effective methods. Since 2012, the Patient-Centered Outcomes Research Institute (PCORI) has funded patient-centered comparative ...
Andrea Heckert, Laura P. Forsythe, Kristin L. Carman, Lori Frank, Rachel Hemphill, Emily A. Elstad, Laura Esmail, Julie Kennedy Lesch   +7 more
doaj   +1 more source

Correction to: Patient engagement in Canada: a scoping review of the ‘how’ and ‘what’ of patient engagement in health research

Health Research Policy and Systems, 2018
It has been highlighted that the original manuscript [1] contains a typesetting error in the surname of Virginia Vandall-Walker. This was incorrectly captured as Virgnia Vandall-Walker in the original manuscript which has since been updated.
Elizabeth Manafo, Lisa Petermann, Ping Mason-Lai, Virginia Vandall-Walker   +3 more
doaj   +1 more source

Development of the Engage with Impact Toolkit: A comprehensive resource to support the evaluation of patient, family and caregiver engagement in health systems

Health Expectations, 2023
Introduction Recent shifts in the patient, family and caregiver engagement field have focused greater attention on measurement and evaluation, including the impacts of engagement efforts.
Julia Abelson, Laura Tripp, Maggie MacNeil, Amy Lang, Carol Fancott, Rebecca Ganann, Marisa Granieri, Cathie Hofstetter, Bernice King, Betty‐Lou Kristy, Alies Maybee, Maureen Smith, Jeonghwa You, The Evaluating Patient Engagement Working Group   +13 more
doaj   +1 more source

Patient engagement in Canada: a scoping review of the ‘how’ and ‘what’ of patient engagement in health research

Health Research Policy and Systems, 2018
Background Over the last 10 years, patient engagement in health research has emerged as the next evolution in healthcare research. However, limited evidence about the clear role and scope of patient engagement in health research and a lack of evidence ...
Elizabeth Manafo, Lisa Petermann, Ping Mason-Lai, Virginia Vandall-Walker   +3 more
doaj   +1 more source

The Provincial Patient and Family Group (PFG) for Alberta Health Services Transforms How Care is Planned and Delivered: A Decade of Experience

Journal of Patient Experience, 2021
Although many health care organizations made significant headway in building relationships with patients and families at the point of care, there continues to be opportunities to partner with them at the system level.
Deanna Picklyk MSW, MBA (c), RSW, Shawn Volk BScN, Katharina Kovacs Burns MSc, MHSA, PhD   +2 more
doaj   +1 more source

Patient-centered benefit-risk analysis of transcatheter aortic valve replacement [version 3; peer review: 2 approved]

F1000Research, 2019
Background: Aortic stenosis (AS) treatments include surgical aortic valve replacement (SAVR) and transcatheter aortic valve replacement (TAVR). Choosing between SAVR and TAVR requires patients to trade-off  benefits and risks.
Kevin Marsh, Natalia Hawken, Ella Brookes, Carrie Kuehn, Barry Liden   +4 more
doaj   +1 more source

Patient-centered benefit-risk analysis of transcatheter aortic valve replacement [version 2; peer review: 2 approved]

F1000Research, 2019
Background: Aortic stenosis (AS) treatments include surgical aortic valve replacement (SAVR) and transcatheter aortic valve replacement (TAVR). Choosing between SAVR and TAVR requires patients to trade-off  benefits and risks.
Kevin Marsh, Natalia Hawken, Ella Brookes, Carrie Kuehn, Barry Liden   +4 more
doaj   +1 more source

Co-designing new tools for collecting, analysing and presenting patient experience data in NHS services: working in partnership with patients and carers

Research Involvement and Engagement, 2021
Plain English summary The way we collect and use patient experience data is important because of concern that patients and carers may be excluded by the limited ways it is currently done in NHS services.
Nicola Small, Bie Nio Ong, Annmarie Lewis, Dawn Allen, Nigel Bagshaw, Papreen Nahar, Caroline Sanders, the DEPEND team   +7 more
doaj   +1 more source

Demographic Characteristics Among Members of Patient Family Advisory Councils at a Pediatric Health System

Journal of Patient Experience, 2021
Patient Family Advisory Councils (PFACs) are groups of patients, families, and clinical health system leaders collaborating to improve the quality, safety, and experience of care.
Amanda Montalbano MD, MPH, FAAP, Sheryl Chadwick BS, DeeJo Miller BA, Kathryn Taff MBA, MHA, CPXP, Evelyn Donis De Miranda BHS, Kimberly Pina MPH, Andrea Bradley-Ewing MPA, MA   +6 more
doaj   +1 more source