Millions of people are living with dementia throughout the US and around the world. Dementia care has improved since the 1970s, with significant declines in previously common, yet harmful, practices such as mechanical restraining devices, forced feeding techniques, and overuse of antipsychotic medications. These harm-reducing advances are not sufficient, however. Many people still lack access to high-quality care and are not living as well as they might. Racial and ethnic minorities and other disadvantaged groups continue to experience deep and persistent inequities, such as lowerquality care in nursing homes and greater use of feeding tubes. 1,2 The COVID-19 pandemic has further exacerbated the social isolation, risk of abuse of older persons, and other challenges encountered by many persons living with dementia and their care partners and caregivers. 3 To move forward, dementia care needs to build on previous advances in harm reduction by also incorporating more focus on promoting well-being, respecting personhood, and supporting people's preferences, strengths, and abilities. Such an approach reframes aging to late life as a reward rather than something to dread.To help address this long-standing and urgent need to better support people living with dementia and their care partners and caregivers, there is also a need for evidence to guide effective action. The body of evidence on dementia care interventions, services, and supports is large and complex. A new report from the National Acad-emiesofSciences,Engineering,andMedicineassessesthis body of evidence, informs decision-making about which interventions should be broadly disseminated and implemented, and guides future actions and research. 4 The authoring committee's primary source of evidence was an Agency for Healthcare Research and Quality (AHRQ) systematic review of the available evidence on care interventions. 5 The committee also considered additional evidence and input, including perspectives from persons living with dementia, care partners, and caregivers. While the term caregiver is well known, the committee also uses the term care partner, which is preferred by some because it acknowledges the reciprocal contributions of and partnership between individuals.
An Urgent Need for Better Dementia CareAccording to recent estimates, between 3.7 and 5.8 million people are living with dementia in the United States, and between 37.8 and 51 million are living with dementia globally. 6,7 In a recent study of 646 persons living with dementia at home, every person reported at least 1 un-VIEWPOINT