Evidence map›Paper›PMID 30521532›Full record

ArticlePloS one2018

Non-professional caregiver burden is associated with the severity of patients' cognitive impairment.

Christopher M Black, Craig W Ritchie, Rezaul K Khandker, Robert Wood, Eddie Jones, Xiaohan Hu, Baishali M Ambegaonkar

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  13. Toward a broader concept of societal value: family spillovers in Alzheimer's disease.International journal of technology assessment in health care · 2021
    Article
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  15. Relation among Caregivers' Burden, Abuse and Behavioural Disorder in People with Dementia.International journal of environmental research and public health · 2021
    Article
  16. Review
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  18. Predictors of caregiver burden in patients with neurologic Wilson disease.The Journal of international medical research · 2020
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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 2 countries.

Christopher M BlackCenter for Observational and Real-World Evidence, Merck & Co., Inc., Kenilworth, New Jersey, United States of America.
Craig W RitchieCentre for Dementia Prevention, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Rezaul K KhandkerCenter for Observational and Real-World Evidence, Merck & Co., Inc., Kenilworth, New Jersey, United States of America.
Robert WoodAdelphi Real World, Macclesfield, United Kingdom.
Eddie JonesAdelphi Real World, Macclesfield, United Kingdom.ORCID 0000-0002-8602-4796
Xiaohan HuUniversity of Southern California, Los Angeles, California, United States of America.
Baishali M AmbegaonkarCenter for Observational and Real-World Evidence, Merck & Co., Inc., Kenilworth, New Jersey, United States of America.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USAdelphi Group (United Kingdom) · GBUniversity of Edinburgh · GBUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesTo analyse the relationship between caregiver burden and severity of patients' cognitive impairment.

designData were drawn from the cross-sectional 2015/2016 Adelphi Real World Dementia Disease-Specific Programme.

settingThis research was multi-national and studied physicians and their consulting patients with cognitive impairment.

participants1,201 caregivers completed self-assessment forms. MEASUREMENTS: Validated instruments of caregiver wellbeing and burden (EQ-5D-3L questionnaire, EQ-VAS, Zarit Burden Interview, and Work Productivity and Activity Impairment questionnaire) and number of caregiver hours were analysed by severity of patients' cognitive impairment, categorised according to the Mini-Mental State Examination. Data were analysed using Spearman's rank correlation coefficients and ordinary least squares regression models, to compare outcomes between caregivers of patients with prodromal, mild, moderate, and severe dementia.

resultsThe majority of caregivers were female (69.1%), lived with the patient they cared for (75.8%), and only approximately one third (28.3%) were in part- or full-time employment. There were statistically significant (p<0.001) increases in caregiver time (36.9 versus 108.6 hours per week for prodromal versus severe dementia, respectively) and measures of caregiver burden and health status (EQ-5D-3L, EQ-VAS, and Zarit Burden Interview) and increases in measures of work productivity and activity impairment with increasing severity of patients' disease.

conclusionThis study of real-world data confirmed an association between increased caregiver burden and severity of patients' cognitive impairment by analysis of a wide range of validated measures of caregiver burden. These findings suggest that maintaining patients in the earliest stages of their disease for as long as possible may potentially help to protect caregiver wellbeing, although further research is required to confirm this hypothesis.

Indexed as

CaregiversCognitive DysfunctionCost of IllnessHealth StatusSeverity of Illness IndexSurveys and QuestionnairesAgedFemaleHumansMaleMiddle AgedSex Factors

Identifiers

PMID30521532
PMCPMC6283568
OpenAlexW2903917028

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.