It’s Not Always Easy: Cancer Survivorship Care in Primary Care Settings

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Abstract
By 2040, an anticipated 26.1 million people with a history of cancer will be part of the healthcare system. The purpose of this study was to explore Missouri-based non-oncology clinicians’ perspectives on caring for patients with a history of cancer to identify needs of rural-based clinicians to optimize their patients’ survivorship care. Using an interpretive qualitative descriptive approach, we conducted semi-structured interviews with 17 non-oncology clinicians. We encouraged clinicians to discuss their approach to caring for patients with a history of cancer and invited them to talk about what might help them increase their knowledge of survivorship care best practices. Through interpretive qualitative descriptive analysis methods including first level coding and constant comparison, we found there is consensus that cancer survivorship care is important; however, training that now guides our clinicians occurred mostly during residency, if at all. Clinicians relied on previous patient encounters and oncology notes combined with their patients’ personal account of treatment history to inform the best next steps. Clinicians expressed strong interest in having a simple protocol of their patient’s treatment with prompts of known long-term cancer treatment–related effects and a patient-centric follow-up monitoring schedule (mandatory vs recommended vs optional). Clinicians expressed interest in educational opportunities about cancer care and ability for curbside consults with oncologists. They consistently noted the limited resources available in rural areas and that rural patients may have different preferences and approaches to cancer survivorship. There is a clear opportunity to improve non-oncology clinicians’ knowledge of the needs of people with a history of cancer as well as their own knowledge base and self-efficacy, especially in rural settings.

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