Only 1 in 10 older adults in a large national survey who were found to have cognitive impairment consistent with dementia reported a formal medical diagnosis of the condition.

Using data from the Health and Retirement Study to develop a nationally representative sample of roughly 6 million Americans age 65 or older, researchers at the University of Michigan, North Dakota State University, and Ohio University found that 91% of people with cognitive impairment consistent with dementia told questioners they did not have a formal medical diagnosis of Alzheimer’s disease or dementia.

“(The discrepancy) was higher than I was expecting,” says coauthor Sheria Robinson-Lane, assistant professor at the University of Michigan School of Nursing.

When proxy reporters (generally, family members) responded, the prevalence dropped from 91% to around 75%, which is still very significant, she says. While many people may have been diagnosed and remain unaware or forgot about their diagnosis, what’s concerning is that cognitive assessment, specifically dementia screening, isn’t routine during annual well visits for older adults.

COVID-19 gives these numbers heightened significance because people with dementia have higher risk for hospitalization and death following an infection, Robinson-Lane says. COVID-19 also causes long-standing neurological effects in some people, perhaps increasing risk for future dementia-related diagnoses.

“Now more than ever, these routine screenings and assessments are really critical,” she says. “I think it’s particularly important to have some baseline information available to providers of patients over 65.”

Coauthor Ryan McGrath, an assistant professor at North Dakota State University, suggests that the migration to telemedicine during the COVID-19 pandemic further underscores the importance of cognitive assessments.

“We recommend that health care providers screen for low cognitive functioning during routine health assessments when possible,” he says. “A telemedicine option may reduce clinic time and expand reach.”

The prevalence of not having reported a dementia-related diagnosis, despite being identified as living with a cognitive impairment consistent with dementia, differed by gender, education, and race.

People who identified as non-Hispanic Black had a higher estimated prevalence (93%) of no reported diagnosis, as did males (99.7%) compared to females (90.2%) The estimated prevalence of no reported diagnosis for non-high school graduates was about 93.5%, compared to 91% for those with at least a high school education.

“There is a large disparity in dementia-related treatment and diagnosis among Black older adults, who are often diagnosed much later in the disease trajectory compared to other racial and ethnic groups,” Robinson-Lane says.

Education is often a proxy for socioeconomic status, so throughout life, wealthier individuals have more access to resources that affect both risk and disease progression, she says. And, evidence suggests that education may influence cognitive testing performance.

The Medicare visit is supposed to include a cognitive screening, but it can be difficult to ascertain a cognitive concern in a 20-minute annual visit, she says. Adding a specific cognitive assessment can also take up visit time.

Often, Robinson-Lane hears from concerned family members who don’t know next steps, or the family member they’re concerned about wants to maintain independence and privacy, and doctors can’t share information without the patient’s consent.

She encourages open communication and reminds families that they can still share information with the loved one’s provider directly or through a nurse or medical assistant.

The study will appear in the Journal of Alzheimer’s Disease. Additional coauthors are from the University of Michigan, North Dakota State, and Ohio University.

Source: University of Michigan