Rachel R Codden, Blessing S Ofori-Atta, Marjorie E Carter, Kimberly A Herget, Jennifer A Doherty, Anne C Kirchhoff, Morgan M Millar
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引用次数: 0
Abstract
Purpose: To identify clinical and sociodemographic factors associated with cancer-related pain among Utah cancer survivors 2-5 years after diagnosis.
Methods: Participants include 2232 Utah cancer survivors diagnosed with invasive cancers at ages 18 + who responded to a probability-based sample survey administered by the Utah Cancer Registry from 2018 to 2023. Participants self-reported cancer-related pain status and methods of pain control. We calculated counts and percentages and used logistic regression to identify sociodemographic and clinical factors associated with cancer-related pain. All analyses were weighted to account for complex survey sample design and age-adjusted to the Utah cancer survivor population.
Results: Twenty-two percent of survivors reported currently experiencing physical pain caused by their cancer or cancer treatment. Of those reporting pain, 24% reported their pain was not under control, 40% indicated their pain was under control with medication, and 36% reported it was under control without medication. The most frequently used pain control methods were nonopioid analgesics (49%) and physical activity (37%). In multivariable models, younger survivors, those either underweight or obese, survivors of breast cancer, and those facing material financial hardships were more likely to report cancer-related pain.
Conclusion: Twenty-two percent of Utah cancer survivors experienced pain related to their cancer or cancer treatment. For some, this pain is well managed, but approximately a quarter have uncontrolled pain.
Implications for cancer survivors: Cancer-related pain is not solely associated with clinical features, and the findings here can guide clinicians and researchers toward a better understanding of the needs of cancer survivors and tailor pain management treatments to this unique population.
期刊介绍:
Cancer survivorship is a worldwide concern. The aim of this multidisciplinary journal is to provide a global forum for new knowledge related to cancer survivorship. The journal publishes peer-reviewed papers relevant to improving the understanding, prevention, and management of the multiple areas related to cancer survivorship that can affect quality of care, access to care, longevity, and quality of life. It is a forum for research on humans (both laboratory and clinical), clinical studies, systematic and meta-analytic literature reviews, policy studies, and in rare situations case studies as long as they provide a new observation that should be followed up on to improve outcomes related to cancer survivors. Published articles represent a broad range of fields including oncology, primary care, physical medicine and rehabilitation, many other medical and nursing specialties, nursing, health services research, physical and occupational therapy, public health, behavioral medicine, psychology, social work, evidence-based policy, health economics, biobehavioral mechanisms, and qualitative analyses. The journal focuses exclusively on adult cancer survivors, young adult cancer survivors, and childhood cancer survivors who are young adults. Submissions must target those diagnosed with and treated for cancer.