Hung, Anna; Nalawade, Vinit; Shenoy, Devika A.; Moriarty, Frank; Ndai, Asinamai; Sloan, Caroline E.; Pavon, Juliessa; Hastings, Susan N.; Brookhart, Alan; Maciejewski, Matthew L.
doi: 10.1111/jgs.70395pmid: 41860759
doi: 10.1111/jgs.70370pmid: 41786645
Geriatricians have struggled to describe a complex and sometimes ambiguous professional identity. Unlike other medical specialties anchored in discrete organ systems, diagnostic and interventional technologies, or clearly defined clinical settings, geriatric medicine encompasses the care of a heterogeneous population of older adults with widely varying clinical needs, priorities, and trajectories relevant to function, multimorbidity, and complexity. This Special Article examines four distinct but overlapping perspectives on geriatrician identity—the complexivist, the healthful longevitist, the syndromist, and the contextualist. The complexivist perspective emphasizes expertise in managing multimorbidity, frailty, and the interplay of medical, functional, cognitive, and social challenges. The healthful longevitist reframes the discipline around extending healthspan, promoting resilience, and supporting healthy aging. The syndromist reflects a trend toward syndrome‐specific specialization, such as “brain health,” in some respects, paralleling subspecialty evolution in other fields. The contextualist highlights geriatricians who center their work within specific care settings or models of care, including home‐based primary care, skilled nursing facilities, PACE programs, ACE units, co‐management models of care with other specialties, and Age‐Friendly Health Systems. While each perspective offers valuable insights, none alone fully captures the breadth of geriatric medicine or resolves long‐standing tensions around recognition, prestige, and the profession's future. Debates over identity should not be viewed as divisive, but rather as essential to strengthening the profession. Continued examination of geriatrician identity is critical to ensuring that the specialty remains relevant, valued, and morally ambitious in the face of an aging population, major advances in geroscience and technology, and an evolving healthcare system.
Reuben, David B.; Chambliss, Allison B.; Katz, Bernard J.; López, Alejandra Sánchez; Hinman, Jason D.
doi: 10.1111/jgs.70384pmid: 41858054
With better understanding of the pathologic processes of Alzheimer's disease, diagnostic methods have been developed to focus on specific biomarkers of disease detectable on brain imaging, cerebral spinal fluid, and, more recently, plasma. Although these tests do not establish a diagnosis of dementia, which requires a clinical evaluation, they can more precisely identify whether Alzheimer's disease is a contributing cause. The recent FDA approval of two blood‐based biomarkers and the availability of others, including direct‐to‐consumer tests, has led to the potential for widespread use in primary and specialty care. However, the currently available blood‐based biomarkers are more highly correlated with amyloid brain PET scans, which are less specific for symptomatic Alzheimer's disease, than with p‐tau brain PET scans, which are strongly associated with changes in cognition. The value of a positive or negative blood‐based biomarker depends on the test characteristics (e.g., sensitivity and specificity) of the specific test as well as the prevalence of the disease in the population. Clinicians ordering blood‐based biomarkers must decide their value in the care of individual patients and be prepared to interpret the test results to their patients.
Hoque, Afshana; Cuthel, Allison; Grudzen, Corita R.; Shah, Manish N.; Brody, Abraham A.; Fleisher, Jori E.; DiMascio‐Donohue, Jennifer; McLain, Katelyn; Tun, Lin T.; Levine, Julia; Goldfeld, Keith S.; Chodosh, Joshua; , ; Abbate, Lauren; Anthopolos, Rebecca; Arbaje, Alicia; Bellolio, Fernanda; Berkowitz, Jonathan; Blome, Andrea;
Showing 1 to 10 of 17 Articles
doi: 10.1111/jgs.70394pmid: 41882986
Over 50% of persons living with dementia (PLWD) and their care partners (dyads) visit the emergency department (ED) every year. In the ED, healthcare professionals face complex challenges managing acute issues and symptoms of Alzheimer's disease and Alzheimer's disease–related dementias without provider training or in‐ED structures to ensure a successful discharge. While many of these visits are for conditions more suitable for ambulatory care, as many as 50% of PLWD discharged from the ED return within 30 days, suggesting opportunities to improve ED care, and discharge processes. Emergency Care Redesign (ECR) includes intentional workflows where physicians, nurses, and social workers engage in a team‐based approach with structured assessments to manage a myriad of potential psychosocial and behavioral issues contributing to the need for ED care. Three core components comprise this evidence‐based, efficient pragmatic intervention for PLWD and their care partners: (1) problem identification, (2) problem prioritization, and (3) provision of non‐pharmacologic solutions supported by community resources. Although these components are essential to provide optimal ED care and reduce revisits and other adverse outcomes, they require an embedded clinical decision support structure, focused training, and clear workflows. In this paper, we describe the ECR intervention as one of three being implemented in the cluster‐randomized multifactorial pragmatic trial, Emergency Departments LEading Transformation of Alzheimer's and Dementia Care (ED‐LEAD), designed to improve care for PLWD and their outcomes after discharge home within 15 health systems and 79 EDs across the United States.