Arwen Bunce is a qualitative research scientist at OCHIN. She is a medical anthropologist and founder and scientific lead of OCHIN’s Qualitative Research Core.
Arwen has a particular interest in the application of rigorous and innovative qualitative research methods to the study of health and health care systems. She has worked with historically marginalized communities domestically and abroad for over 20 years and is/has been co-investigator and qualitative lead on multiple equity-oriented NIH grants.
Previous areas of research include immigrant access to care in the U.S., support for HIV sero-discordant couples in India, the role of women in family planning decision-making in Guinea, self-rated health among the elderly, and social support for people with diabetes. More recently, her work has focused on the impact of technology on providing and receiving care in community health settings, with an emphasis on social/medical integration.
The flexibility, in-depth exploration, and openness to new ideas that are the hallmark of qualitative research benefit implementation research by providing a rich, nuanced understanding of the process under study. However, traditional qualitative approaches to data collection and analysis can be difficult to transfer to the realities of often fast-moving team-based research within the health care system, as well as burdensome to busy health care practitioners. Arwen has worked to adapt traditional anthropological methods to gathering and analyzing data to fit the needs of health services research in evolving health care systems and the realities of implementation research, both of which often involve numerous, geographically dispersed health care settings. She has led teams, taught clinical and informatics colleagues, and published on the real-world use of methods such as rapid qualitative assessment, ethnographic process evaluation, and realist evaluation in primary care/community settings. Her work has contributed to the development and use of rigorous, pragmatic, minimally disruptive approaches to investigating the complexities and interrelationships that underlie intervention outcomes. While primary care clinicians strive to provide person-centered care, there remains a multitude of unanswered questions about the best approaches to collecting, documenting, and acting on patient-specific contextual information, including social drivers of health. Arwen has designed and led the qualitative portions of multiple grants studying the interdependent factors that impact perception of and openness to routinized social risk screening in community health centers, as well as the feasibility, implementation, and use of EHR-based tools for supporting this work. This research has focused on using social risk screening to optimize the provision of contextualized, patient-centered care. Health information technology (HIT) is part of the complex sociotechnical interactions that form the daily work of health care. The study of the adoption and use of HIT thus requires consideration of the complexities of both health care and HIT, and how the two interact. Ethnography, with its emphasis on exploring the “how” and “why” behind quantitative results, can provide deep insight into the web of factors underlying study findings, improving their credibility and transferability. Arwen has been involved in a series of studies investigating the acceptability and use of clinical decision support (CDS), first as a member of a purely qualitative team studying the impact of CDS on providers and staff at community hospitals around the country, then branching out to consider the perspectives of those working to create and market the CDS, and finally leading the qualitative components of mixed methods research into CDS-based interventions in community health clinics. Her work has contributed to the ability to meaningfully incorporate the lived experience of relevant stakeholders (often clinicians and staff) into each step of the research process, increasing the integrity and usability of findings. How best to ensure adequate access to health care, particularly for vulnerable patients, has been the subject of much debate and experimentation over the years. An individual’s ability to access care for themselves and their family is influenced by a complex set of factors ranging from health care delivery system-level issues to patient-level factors. Arwen has worked on studies attempting to understand the role of immigration status in access to care, both from the immigrant perspective (interviews with immigrants from around the world and of all legal statuses, including undocumented) and from the standpoint of federal measurement and documentation of immigration status (exploring the methodological issues relating to definitions and assessment of legal status for the U.S. Census Bureau). In subsequent work, she provided qualitative methods expertise to research teams exploring the impact, from the perspective of the individuals and families, of programs designed to increase access to primary care for uninsured patients. Morbidity and mortality rates remain high in many resource-poor countries, despite ongoing attempts to address the issue(s). While reasons for these poor outcomes are multifaceted, one perspective that is often missing from well-intended programs is that of those whose behavior is targeted. As a qualitative research specialist with a large international health organization (Family Health International), Arwen worked closely with in- country teams to improve their qualitative data collection skills—how to ask open-ended questions and follow up appropriately, how to establish rapport while maintaining neutrality, how to approach sensitive topics with respect—with the goal of incorporating the perspective of those most intimately affected in the design, refinement and scale-up of health interventions. In this role, she also helped design the evaluations, created data collection guides and training materials, and often had primary responsibility for the qualitative analysis. In addition, she spent a year working with Doctors Without Border/MSF, where she was responsible for designing, conducting, analyzing and reporting on an evaluation of a five-year water and sanitation program; lessons learned were shared across the organization.
Qualitative methods in implementation and evaluation research
Impact of patients’ social risk on primary care provision
Ethnography of health information technology use in community health care settings
Investigating access to care from the patient, care team, and system perspectives
International health and program evaluation
OCHIN, Inc.
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