Abstract

The diagnostic process for patients presenting with cognitive decline and suspected dementia is complex. Physicians face challenges distinguishing between normal aging, mild cognitive impairment, Alzheimer's disease, and other dementias. Although there is some evidence for improving attitudes towards the importance of prompt diagnosis, there is limited information describing how physicians approach this diagnostic challenge in practice. This was explored in the present study. Across-sectional survey of primary care and specialist physicians, in 5 European countries, Canada, and the United States, was conducted. Participants were asked about their use of cognitive screening tools and diagnostic technologies, as well as the rationales and barriers for use. In total, 1365 physicians participated in the survey, 63% of whom were specialists. Most physicians stated they use objective cognitive tools to aid the early detection of suspected mild cognitive impairment or Alzheimer's disease in patients. The Mini-Mental State Examination was the most common tool used for initial screening; respondents cited speed and ease of use but noted its lack of specificity. Cerebrospinal fluid biomarker and amyloid positron emission tomography tests, respectively, had been used by only 26% and 32% of physicians in the preceding 6 months, although patterns of use varied across countries. The most commonly cited reasons for not ordering such tests were invasiveness (for cerebrospinal fluid biomarker testing) and cost (for amyloid positron emission tomography imaging). Data reported by physicians reveal differences in the approaches to the diagnostics process in Alzheimer's. A higher proportion of primary care physicians in the United States are routinely incorporating cognitive assessment tools into annual visits, but this is due to country differences in clinical practice. The value of screening tools and regular use could be discussed further with physicians; however, lack of specificity associated with cognitive tools and the investment required from patients and the healthcare system are limiting factors.

Highlights

  • The diagnostic process for a person with suspected cognitive decline is complex

  • The study was a crosssectional survey of primary care and specialist physicians who were personally responsible for managing patients with dementia or cognitive decline in Canada, France, Germany, Italy, Spain, the UK, and the US

  • The two most common responses were ApoE4 carrier 42% of respondents and a family history of Alzheimer’s disease (AD) (39%). These responses were notably higher than other responses; the third most common responses were cognitive impairment that interferes with daily life and an atypical course. These findings suggest that decisions to use these biomarker tests may be more strongly influenced by genetic factors in comparison to other diagnostic decisions

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Summary

Introduction

The diagnostic process for a person with suspected cognitive decline is complex. Simple and specific diagnostic tests for dementing illnesses, such as Alzheimer’s disease (AD), are not yet available, and patients present with widely varying symptoms [1, 2]. The diagnosis of dementing illness in general and of specific forms of dementia in particular often depends on the exclusion of other possible causes of the patient’s symptoms. Because of this complexity and because of varying perceptions about the benefits of diagnosis, there is wide variation in the diagnostic process across different countries and across different healthcare providers [3,4,5]. Spouses have rated understanding what is wrong with their partners as being of high importance [10]

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