By the end of this topic, the student should be able to:
One in five Canadians experiences chronic pain (Canadian Pain Task Force, 2019). Chronic pain is an individual experience that is affected by and affects all aspects of a person’s life and the lives of those who care for them.
NOTE: Pain is an individual, subjective experience and therefore pain management needs to take into account an individual’s experience of pain beyond the physical symptoms.
Health and social service providers need to address the social determinants of health that not only are related to the experience of pain but can also be barriers or facilitators in the successful management of pain.
An accepted model for understanding the assessment, prevention, and treatment of chronic pain is the biopsychosocial model. Health is understood to incorporate biological, psychological, and social factors, as shown below.
Ong, L. (n.d.). Health psychology. Perspectives Clinics. http://perspectivesclinic.com/health-psychology/
This model recognizes that multiple biological, psychological and social factors can be challenging or strengthening to a person’s health.
Pain is considered to be more than a biomedical phenomenon of the neurological expression of painful stimuli. Pain is a complex interaction of physiological, psychological, and social factors that influence the experience of pain. As such, pain is experienced differently by each individual because of the unique and dynamic interactions among those factors.
The biopsychosocial model of pain postulates that all aspects of a person’s life can affect and be affected by their experience of pain. Thus, a person’s experience of physical pain will be affected by their psychological status and their social experiences.
The impact of physical pain on psychosocial factors is illustrated by the following examples.
Pain that decreases a person’s ability to carry out activities of daily living such as dressing, feeding, hygiene, cooking, shopping, and so on, will Increase dependence on others.
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Disability because of pain creates a need for assistance from others and mobility aids.
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Fatigue or exhaustion resulting from pain impacts social participation.
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Pain may impact sexual arousal, which may alter intimate relationships.
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A person living with chronic pain may also be impacted on a social level. Examples include the following:
The impact of psychological pain may be evidenced in the following ways:
Caused by:
Spiritual well-being can be negatively affected by chronic pain. Spiritual suffering is commonly experienced by persons with significant or life-threatening illness and their families. The inability to clinically manage physical pain can be due, in part, to unmet emotional and spiritual needs.
NOTE: Spiritual distress is experienced in 25 percent of people receiving cancer treatment (Schultz et al., 2017).
Definition
A person experiencing spiritual distress may express concern with the meaning of life and death, question the meaning of suffering or of their own existence, verbalize inner conflict about beliefs, express anger towards God or other supreme being (however defined), or actively seek spiritual assistance (O’Toole, 2003).
As part of the assessment and intervention planning process, health and social service professionals must be aware that those who experience chronic pain might have feel diminished spiritual well-being, which can lead to increased substance use and form a repetitive downward cycle.
Pain can also negatively impact families and support people. For example, families of persons experiencing chronic pain and varying degrees of related disability may be required to take on new roles, responsibilities, and experiences such as:
Family members’ lives may be affected in many of the same ways as the person experiencing chronic pain:
Assessment and treatment for chronic pain, whether related to cancer or other causes, requires a comprehensive assessment of the family, friends, and support systems involved in the client’s life. Treatment and management plans should include interventions to reduce risk of poor outcomes such as:
Strengths should be identified and built upon in all intervention plans.
Canadian Pain Task Force. (2019). Chronic pain in Canada: Laying a foundation for action. Health Canada. https://www.canada.ca/content/dam/hc-sc/documents/corporate/about-health-canada/public-engagement/external-advisory-bodies/canadian-pain-task-force/report-2019/canadian-pain-task-force-June-2019-report-en.pdf
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Dueñas, M., Begoña, O., Salazar, A., Mico, J. A., & Failde, I. (2016). A review of chronic pain impact on patients, their social environment and the health care system. Journal of Pain Research, 9, 457–467.
Higgins, K. S., Birnie, K. A., Chambers, C. T., Wilson, A. C., Caes, L., Clark, A. J., Lynch, M., Stinson, J., & Campbell-Yeo, M. (2015). Offspring of parents with chronic pain: A systematic review and meta-analysis of pain, health, psychological, and family outcomes. Pain, 156(11), 2256–2266.
Knaster, P., Estlander, A.-M., Karlsson, H., Kaprio, J., & Kalso, E. (2016). Diagnosing depression in chronic pain patients: DSM-IV major depressive disorder vs. Beck Depression Inventory (BDI). PLoS One, 11(3), Article e0151982. https://doi.org/10.1371/journal.pone.0151982
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