The American College of Physicians (ACP) and the American Academy of Family Physicians (AAFP) have issued a new guideline on current pharmacologic treatment of dementia. The guideline appears in the March 4, 2009, issue of Annals of Internal Medicine, ACP’s flagship journal, and is available online at www.annals.org.
A committee representing ACP and AAFP reviewed dementia literature for outcomes such as cognition, global function, behavior/mood, and quality of life/activities of daily living -- areas of importance to physicians treating patients. The committee found that high-quality scientific evidence was limited and so developed cautious recommendations:
1. Clinicians should base the decision to try therapy with the FDA approved drugs for dementia on an individualized assessment of the patient.
2. Clinicians should base the choice of drugs on tolerability, adverse effect profile, ease of use and cost of medication.
3. Further research is urgently needed to address gaps in knowledge about the clinical effectiveness of pharmacologic management of dementia.
Currently five drugs are approved by the FDA for dementia: four acetylcholinesterase inhibitors [donepezil (Aricept®), galantamine (Razadyne™, Reminyl™, Nivalin), rivastigmine (Exelon), and tacrine], and one neuropeptide-modifying agent [memantine (Mamenda®)]. These drugs do not cure dementia (there is no cure at this time) or repair brain damage. They may improve symptoms or slow down the disease. “Doctors, patients, and family care-givers desperately want information on how to treat this disease,” said Amir Qaseem, MD, PhD, MHA, Senior Medical Associate in the Clinical Programs and Quality of Care Department at ACP. “It is disheartening to find out that all we have to work with is these five drugs, and the evidence on these is scant. Consider that in 50 years, one in 45 Americans will suffer from Alzheimer’s disease. This is huge problem.”
The ACP-AAFP committee found that most of the existing studies focused on statistical significance of changes, but patients with dementia, caregivers, and physicians are more interested in clinically important improvement. “More research is warranted because the available evidence concerning these pharmaceuticals’ effects on quality of life is mixed and the clinical significance of many of the findings is questionable,” said Kenneth G. Schellhase, MD, MPH, an AAFP representative on the guideline committee. “In addition, the duration of existing trials was usually less than one year, providing insufficient information to determine the optimal length of treatment, and few trials compare one drug directly with another.”
In summary, no convincing evidence demonstrated that one therapeutic treatment is more effective than another, the committee concluded. The National Institutes of Health describes dementia as a group of symptoms caused by disorders that affect the brain. Dementia is not a specific disease. NIH says “people with dementia may not be able to think well enough to do normal activities, such as getting dressed or eating. They may lose their ability to solve problems or control their emotions. Their personalities may change. They may become agitated or see things that are not there.”
Two of the most common types of dementia, Alzheimer’s disease and vascular dementia, are covered by the ACP-AAFP guideline. ACP, through its Clinical Efficacy Assessment Subcommittee, has been developing guidelines since 1981. ACP guidelines have relied on evidence or clinical documentation rather than consensus or expert opinion. The guidelines grade the evidence recommendations using the American College of Physicians’ clinical practice guidelines grading system. ACP cautions that its clinical practice guidelines are guides only and may not apply to all patients and all clinical situations and are not intended to override clinicians' judgment. The AAFP’s clinical practice guidelines are designed to assist the clinician and patients in making decisions about appropriate health care for specific clinical circumstances. These evidence-based guidelines are often developed collaboratively between the AAFP’s Commission on Science and those of other specialty societies and the federal Agency for Healthcare Research and Quality.
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