10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Specific agitation behaviours in dementia differentially contribute to aspects of caregiver burden

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          ABSTRACT

          Background

          Agitation is a common symptom in dementia and linked to caregiver burden, but both agitation and burden are multidimensional constructs. The current study sought to determine whether specific presentations of agitation differentially relate to aspects of caregiver burden.

          Methods

          Medical record data from an outpatient memory clinic were extracted for 609 persons with dementia, including caregiver‐reported burden and care recipient agitation.

          Results

          Exploratory factor analysis yielded three domains of agitation on the Cohen Mansfield Agitation Inventory (‘Physically Aggressive’, ‘Physically Non‐Aggressive’, ‘Verbally Agitated’) and four domains of burden on the Zarit Burden Interview (‘Impact on Life’, ‘Guilt/Uncertainty’, ‘Embarrassment/Frustration’, ‘Overwhelm’). Regression analyses demonstrated all domains of agitation positively predicted overall burden. Regarding specific aspects of burden, Physically Aggressive behaviours predicted Embarrassment/Frustration. Physically Non‐Aggressive behaviours predicted Impact on Life and Guilt/Uncertainty. Verbally Agitated behaviours predicted all burden dimensions.

          Conclusions

          Results suggest specific aspects of agitation may differentially contribute to facets of caregiver burden.

          Related collections

          Most cited references43

          • Record: found
          • Abstract: found
          • Article: not found

          The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment.

          To develop a 10-minute cognitive screening tool (Montreal Cognitive Assessment, MoCA) to assist first-line physicians in detection of mild cognitive impairment (MCI), a clinical state that often progresses to dementia. Validation study. A community clinic and an academic center. Ninety-four patients meeting MCI clinical criteria supported by psychometric measures, 93 patients with mild Alzheimer's disease (AD) (Mini-Mental State Examination (MMSE) score > or =17), and 90 healthy elderly controls (NC). The MoCA and MMSE were administered to all participants, and sensitivity and specificity of both measures were assessed for detection of MCI and mild AD. Using a cutoff score 26, the MMSE had a sensitivity of 18% to detect MCI, whereas the MoCA detected 90% of MCI subjects. In the mild AD group, the MMSE had a sensitivity of 78%, whereas the MoCA detected 100%. Specificity was excellent for both MMSE and MoCA (100% and 87%, respectively). MCI as an entity is evolving and somewhat controversial. The MoCA is a brief cognitive screening tool with high sensitivity and specificity for detecting MCI as currently conceptualized in patients performing in the normal range on the MMSE.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) Statement

              Routinely collected health data, obtained for administrative and clinical purposes without specific a priori research goals, are increasingly used for research. The rapid evolution and availability of these data have revealed issues not addressed by existing reporting guidelines, such as Strengthening the Reporting of Observational Studies in Epidemiology (STROBE). The REporting of studies Conducted using Observational Routinely collected health Data (RECORD) statement was created to fill these gaps. RECORD was created as an extension to the STROBE statement to address reporting items specific to observational studies using routinely collected health data. RECORD consists of a checklist of 13 items related to the title, abstract, introduction, methods, results, and discussion section of articles, and other information required for inclusion in such research reports. This document contains the checklist and explanatory and elaboration information to enhance the use of the checklist. Examples of good reporting for each RECORD checklist item are also included herein. This document, as well as the accompanying website and message board (http://www.record-statement.org), will enhance the implementation and understanding of RECORD. Through implementation of RECORD, authors, journals editors, and peer reviewers can encourage transparency of research reporting.
                Bookmark

                Author and article information

                Contributors
                mspitzna@kent.edu
                Journal
                Psychogeriatrics
                Psychogeriatrics
                10.1111/(ISSN)1479-8301
                PSYG
                Psychogeriatrics
                John Wiley & Sons Australia, Ltd (Melbourne )
                1346-3500
                1479-8301
                19 July 2022
                September 2022
                : 22
                : 5 ( doiID: 10.1111/psyg.v22.5 )
                : 688-698
                Affiliations
                [ 1 ] Department of Psychological Sciences Kent State University Kent Ohio USA
                [ 2 ] Department of Psychiatry Rhode Island Hospital Providence Rhode Island USA
                [ 3 ] Summa Health System Department of Geriatrics Akron Ohio USA
                Author notes
                [*] [* ] Correspondence: Mary Beth Spitznagel, PhD, Department of Psychological Sciences, Kent State University, 329 Kent Hall Addition, Kent, OH 44242. Email: mspitzna@ 123456kent.edu

                Author information
                https://orcid.org/0000-0002-1139-8670
                Article
                PSYG12871
                10.1111/psyg.12871
                9544824
                35853570
                bc70d660-87a1-48fb-badb-4c28cc457800
                © 2022 The Authors. Psychogeriatrics published by John Wiley & Sons Australia, Ltd on behalf of Japanese Psychogeriatric Society.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 26 May 2022
                : 09 March 2022
                : 06 June 2022
                Page count
                Figures: 0, Tables: 6, Pages: 11, Words: 6849
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                September 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.0 mode:remove_FC converted:07.10.2022

                agitation,caregiver burden,dementia
                agitation, caregiver burden, dementia

                Comments

                Comment on this article