Alzheimer’s disease (AD) prevalence rates in the United States are expected to triple over the next 50years, a consequence of the overall aging of the U.S. population. Because of the profound and far-reachingimpact of AD, this projected increase in prevalence is expected to pose a tremendous challenge. Alzheimer’s disease results in the cognitive and functional deterioration of the affected patient, and behavioral disturbancesfrequently accompany the disease. Furthermore, because of its progressive and debilitating nature,AD takes a dramatic emotional, physical, and financial toll on the patient’s primary caregiver. Nonetheless,despite the burden experienced by both patients and caregivers, strategies for minimizing the negative consequencesof AD are well characterized. Central to the successful management of AD is the prompt and accuratediagnosis of the disease, with current guidelines calling for a 2-tiered approach in which patients firstundergo screening using a brief cognitive assessment tool, followed by a comprehensive battery of physical,psychological, and neurologic tests if signs of possible cognitive impairment are evident upon screening.Once a conclusive diagnosis of AD has been made, the development of a disease management approach targetingthe needs of the patient and his or her caregiver becomes a primary concern. Pharmacologic interventionsmay play an important role in such approaches, as agents such as cholinesterase inhibitors and theN-methyl-D-aspartate receptor antagonist memantine have been associated with favorable outcomes for patientsand caregivers alike. However, in addition to the therapeutic benefits of these agents, associated sideeffects and potential drug-drug interactions must also factor into decisions regarding the pharmacologic treatmentof AD.
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