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What are the Goals of Alzheimer’s Treatment?

July 31, 2010

The primary goals of treatment for Alzheimer’s are to improve the quality of life for the person suffering and for his or her caregiver(s). Treatment typically comprises three interrelated approaches:

1.) Slowing the progression:
Treatment in most cases will involve methods of slowing cognitive decline and treating specific symptoms and/or co-occurring conditions with drug therapies.

2.) Managing the behavioral symptoms of Alzheimer’s:
There are many different strategies for doing this. Non-drug approaches, which should be tried first, are used by families and caregivers in consultation with social workers, nurses or support-group facilitators. Specific strategies that might be recommended for managing these symptoms include:

If non-drug approaches fail to adequately manage behavioral problems, talk to your physician about medications that may help. You’ll need to describe any behavioral problems to your doctor. You might want to use a journal to keep track of day-to-day changes in behavior and note when symptoms arise, what might precipitate them, and what, if anything, helps resolve them when they do arise.

Your doctor may recommend appropriate medications, depending on what the symptoms are, from a group of drugs generally referred to as “anti-agitation drugs”. The types of medications that might be used include antidepressants (if the patient has depression); anti-anxiety drugs (also called anxiolytics), anti-psychotic medications (some of which are also called neuroleptics); sedatives, and sleep medications. There are many different drugs within each of these classes of medication. Each acts in a somewhat different way and has different side effects, some of which may be severe. As a rule, doctors generally prescribe the lowest dose possible to alleviate symptoms and adjust the dosage as necessary.

3.) Support and education for the family and caregiver:
Caring for a person who has Alzheimer’s poses tremendous challenges, emotionally, physically and financially. Caregivers are subject to high levels of chronic stress, and caregiver burnout is a significant factor in the inability to continue caring for a person with Alzheimer’s at home.

Research shows that when families and caregivers are educated about Alzheimer’s disease and have the appropriate support, care of the person with Alzheimer’s is improved. There are many education and support programs available. Good programs can equip the caregiver with the skills and support necessary to care for a loved one at home and can significantly delay the time when placement in a nursing home becomes necessary. Taking advantage of these programs will improve not only the quality of life of the person with Alzheimer’s but also that of the family and caregivers.

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