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New or Worsening Symptoms and Signs in Community-Dwelling Persons with Dementia: Incidence and Relation to Use of Acute Medical Services

  • Autores: Philip D. Sloane, Christopher H. Schifeling, Anna Beeber, Kimberly Ward, David Reed, Lisa P. Gwyther, Bobbi Matchar, Sheryl Zimmerman
  • Localización: Journal of the American Geriatrics Society, ISSN 0002-8614, Vol. 65, Nº. 4, 2017, págs. 808-814
  • Idioma: inglés
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  • Resumen
    • Objectives To understand the range of symptoms that present to family caregivers of community-dwelling persons with Alzheimer's disease and related dementias (ADRD).

      Design Six-month longitudinal prospective study to identify the incidence of new or worsening symptoms and their association with acute care medical service use.

      Setting Community-based sample of volunteers from multiple states.

      Participants A total of 136 patient-caregiver dyads with a range of dementia severity.

      Measurements Forty four symptoms and signs common in older persons and/or persons with dementia; frequency of emergency department visits, hospitalizations, and death; and associations between reported symptoms and acute medical care.

      Results During a mean of 5.7 months’ follow-up, new or worsening organ-specific (90% of participants), nonspecific (89%), and behavioral (88%) symptoms were common, with the average caregiver reporting seven new or worsening symptoms. Most common were worsening confusion (74%), decreased activity (64%), agitation (57%), hallucinations/delusions (45%), voice and speaking problems (45%), not eating or drinking (44%), and stress/anxiety (41%). Hospitalization and emergency department use occurred respectively in 19% and 20% of participants, and were associated with organ-specific symptoms (OR 3.15, P = .02), less so with nonspecific symptoms (OR 2.27, P = .07), and very little with behavioral symptoms (OR 1.44, P = .38). Within each symptom category, certain symptoms were significantly associated with acute medical service use.

      Conclusion Family caregivers of persons with ADRD must respond to a variety of medical, nonspecific, and behavioral symptoms. The high incidence of new or worsening symptoms and of acute medical care use suggests a need to better target symptom evaluation and management in caregiver education.


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