With
a growing elderly population and an increase in nursing home occupancy, it is
important we place more focus on how we treat pain in those with dementia. The
current systems for pain management are not always held to professional
standards and are sometimes not used at all in clinical settings. Pain
management is difficult in those with dementia because they are not always able
to communicate clearly and their actions are often mistaken as a “behavior”
rather than being in pain. It is also difficult for dementia patients to be
placed in hospice care, preventing them from the comfort care and end of life
medications often given to others with terminal illnesses. Our ethics topic
focuses on the facts and implications of current pain management in those with
dementia and what needs to be improved in the near future to provide the best
comfort care for those nearing the end of life.
It
is predicted that by 2025, nearly 115 million people will have dementia. Today,
only 11% of those in hospice programs have dementia, showing the major gap in
treatment plans between those with and without dementia. This is not only
because hospice programs require a diagnosis of death within six months, but
almost all pain assessment tools rely on self report as their only measurement.
People with advanced dementia lack the ability to communicate effectively and comprehend
complex questions, leaving it difficult for them to tell someone they are in
pain or where the pain is located. This often results in frustration of the
patient and acting out, a sign characterized as “behavior” by nursing staff and
often treated with antipsychotic medications rather than pain medications.
Talking about these issues is imperative. Vulnerable populations in healthcare,
especially those with mental illness, need others to advocate their rights for
them. We need to make sure these people are getting the best professional care
as possible even if they cannot communicate to us. written by students
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