Evidence map›Paper›PMID 37593781›Full record

ArticleJournal of evaluation in clinical practice2023

The needs of family caregivers of persons living with dementia cared for in primary care practices.

Michael Vetter, Karen Donelan, Sophia Guzikowski, Carie Michael, Christine S Ritchie, Christine Vogeli, Brent P Forester

Open access · hybridAbstract read
In one paragraph

Article in Journal of evaluation in clinical practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 2024 Alzheimer's disease facts and figures.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Michael VetterInstitute on Healthcare Systems, Heller School of Social Policy and Management, Brandeis University, Waltham, Massachusetts, USA.ORCID 0009-0003-9684-8128
Karen DonelanInstitute on Healthcare Systems, Heller School of Social Policy and Management, Brandeis University, Waltham, Massachusetts, USA.
Sophia GuzikowskiThe Mongan Institute, Health Policy Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Carie MichaelInstitute on Healthcare Systems, Heller School of Social Policy and Management, Brandeis University, Waltham, Massachusetts, USA.
Christine S RitchieDepartment of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Christine VogeliThe Mongan Institute, Health Policy Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Brent P ForesterDepartment of Psychiatry, Tufts University School of Medicine, Boston, Massachusetts, USA.
Brandeis University · USHarvard University · USMassachusetts General Hospital · USTufts University · US

Funding

Training Core (I)U54AG063546 · NIA · BROWN UNIVERSITY · PI Vincent Mor · 2019 to 2026
$125.9M
NIA NIH HHS U54 AG063546
6 · The paper itself

Abstract

rationaleThe informal caregivers who provide unpaid support for persons living with dementia (PLWD) are often unprepared to appropriately manage symptoms and navigate health services to support themselves or the PLWD.

aimTo understand informal caregivers' perceived capabilities of handling dementia symptomology and perceived support from providers.

methodsWe identified and surveyed caregivers of primary care patients in the Mass General Brigham health system. We included a self-efficacy questionnaire to assess caregivers' ability and confidence in access to dementia care, symptom management, and provider support.

resultsRespondents indicated that although their provider had knowledge of dementia and memory care, they were least likely to agree (39.2%) that their provider helped them with these challenging symptoms. Those who live with the care recipient were least likely to receive advice about common symptoms (43.6%) and to access community services (63.8%), and in general felt moderately knowledgeable about the progression of the disease (47.9%).

conclusionsThe findings imply that caregivers are aware of disease progression, dementia symptoms, and do not feel supported by their providers in managing care or accessing support services. There is opportunity to support informal caregivers in a primary care setting by appropriately uptraining providers in dementia care.

Indexed as

CaregiversDementiaHealth ServicesHumansPrimary Health Carecare deliverycaregiversdementiaprimary care

Identifiers

PMID37593781
PMCPMC10841202
OpenAlexW4385968470

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.