2020
DOI: 10.1136/bmjopen-2019-035360
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Barriers towards organ donor registration and consent among people of Indian origin living globally: a systematic review and integrative synthesis—protocol

Abstract: IntroductionThe need for organs is comparatively higher among people of Indian origin due to the higher prevalence of end-stage organ failure. In spite of the higher need, they have a lower number of organ donors. Studies have been carried out among people of Indian origin living globally to understand the reasons for the low donation rate, but there has been no systematic review that has integrated all of these studies to synthesise the current literature. Therefore, the purpose of this review is to examine t… Show more

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Cited by 5 publications
(4 citation statements)
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“…This systematic review’s protocol has been registered in PROSPERO (CRD42019155274) and also published. 18 …”
Section: Methodsmentioning
confidence: 99%
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“…This systematic review’s protocol has been registered in PROSPERO (CRD42019155274) and also published. 18 …”
Section: Methodsmentioning
confidence: 99%
“…The systematic review included studies with individuals of Indian origin living both within and outside India (ie, migrant/first/second generation), aged 18 years and above from varied settings. 18 Cross-sectional and qualitative study design were included as they were mostly employed to understand the barriers toward deceased organ donation. For all the databases, search strategy was restricted between 1 January 1994 (ie, the year when the first law towards organ donation was enacted in India) and 31 December 2021 (ie, a recent day before the submission) and was restricted only to studies published in English.…”
Section: Methodsmentioning
confidence: 99%
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“…Pilot studies which have sought to examine these aspects in relation to ODT have shown that "ethnicity" and/or "race" and/or "immigration background" do not operate in isolation but intersect with a range of other socioeconomic factors at the individual level, and with other factors at the interpersonal and societal level [13,14]. Therefore, to improve data comparability in Europe and to enable the effective development and subsequent implementation of interventions against inequities, there is a need for consensus on how these communities are conceptualized and what data should be collected when research is performed on these populations in ODT [6,8].…”
Section: Introductionmentioning
confidence: 99%