Evidence map›Paper›PMID 35162453›Full record

ArticleInternational journal of environmental research and public health2022

Lived Experience of Dementia in the New Zealand Indian Community: A Qualitative Study with Family Care Givers and People Living with Dementia.

Rita V Krishnamurthi, Ekta Singh Dahiya, Reshmi Bala, Gary Cheung, Susan Yates, Sarah Cullum

Open access · goldAbstract read
In one paragraph

Article in International journal of environmental research and public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 3 pooled it
2.4field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 3 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  9. Access and Use of Services by Caregivers of Older Adults: A Scoping Review of Cultural and Linguistic Diversity.Journal of applied gerontology : the official journal of the Southern Gerontological Society · 2023
    Article
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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

6 authors at 2 institutions in 1 country.

Rita V KrishnamurthiNational Institute for Stroke and Applied Neurosciences, Auckland University of Technology, Auckland 0627, New Zealand.
Ekta Singh DahiyaNational Institute for Stroke and Applied Neurosciences, Auckland University of Technology, Auckland 0627, New Zealand.
Reshmi BalaDepartment of Psychological Medicine, University of Auckland, Auckland 1142, New Zealand.
Gary CheungDepartment of Psychological Medicine, University of Auckland, Auckland 1142, New Zealand.ORCID 0000-0002-0239-9356
Susan YatesDepartment of Psychological Medicine, University of Auckland, Auckland 1142, New Zealand.
Sarah CullumDepartment of Psychological Medicine, University of Auckland, Auckland 1142, New Zealand.ORCID 0000-0003-0785-9101
University of Auckland · NZAuckland University of Technology · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, there are estimated to be 70,000 people living with dementia in Aotearoa, New Zealand (NZ). This figure is projected to more than double by 2040, but due to the more rapid growth of older age groups in non-European populations, prevalence will at least triple amongst the NZ Indian population. The impact of dementia in the NZ Indian community is currently unknown. The aim of this study was to explore the lived experiences of NZ Indians living with dementia and their caregivers. Ten caregivers (age range: 41-81) and five people living with mild dementia (age range: 65-77) were recruited from a hospital memory service and two not-for-profit community organisations in Auckland, Aotearoa, NZ. Semi-structured interviews were conducted by bilingual/bicultural researchers and transcribed for thematic analysis in the original languages. Dementia was predominantly thought of as being part of normal ageing. Getting a timely diagnosis was reported as difficult, with long waiting times. Cultural practices and religion played a large part in how both the diagnosis and ongoing care were managed. Caregivers expressed concerns about societal stigma and about managing their own health issues, but the majority also expressed a sense of duty in caring for their loved ones. Services were generally well-received, but gaps were identified in the provision of culturally appropriate services. Future health services should prioritise a timely diagnosis, and dementia care services should consider specific cultural needs to maximise uptake and benefit for Indian families living with dementia.

Indexed as

CaregiversDementiaAdultAgedAged, 80 and overHealth ServicesHumansMiddle AgedNew ZealandQualitative ResearchcaregiversdementiaIndian communityNew Zealandqualitative

Identifiers

PMID35162453
PMCPMC8834941
OpenAlexW4210491902

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.