Relationship between intersectionality and cancer inequalities: a scoping review protocol

被引:6
|
作者
de Mesa, Mar Estupinan Fdez [1 ]
Marcu, Afrodita [1 ]
Ream, Emma [1 ]
Whitaker, Katriina L. [1 ]
机构
[1] Univ Surrey, Sch Hlth S, Guildford, Surrey, England
来源
BMJ OPEN | 2023年 / 13卷 / 01期
关键词
PUBLIC HEALTH; Quality in health care; Health policy; EPIDEMIOLOGY; QUANTITATIVE INTERSECTIONALITY; CARE; CHALLENGES; IMPACT;
D O I
10.1136/bmjopen-2022-066637
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Persistent inequalities in cancer care and cancer outcomes exist within and between countries. However, the evidence pertaining to the root causes driving cancer inequalities is mixed. This may be explained by the inadequate attention paid to experiences of patients with cancer living at the intersection of multiple social categories (eg, social class, ethnicity). This is supported by the intersectionality framework. This framework offers an alternative lens through which to analyse and understand how these interlocking systems of oppression uniquely shape the experiences of patients with cancer and drive inequalities. In this protocol, we outline a scoping review that will systematically map what is known about the relationship between intersectionality and inequalities in care experience and cancer outcomes of patients with cancer; and to determine how the intersectionality framework has been applied in studies across the cancer care pathway and across countries. Methods and analysis This study will be guided by Arksey and O'Malley's, and Levac et al's frameworks for scoping reviews. We will identify and map the evidence on cancer inequalities and intersectionality from 1989 to present date. Electronic databases (EMBASE, PsychINFO, CINAHL, Medline, Web of Science, ProQuest) and a systematic search strategy using a combination of keywords and Boolean operators AND/OR will be used to identify relevant studies. Screening of eligible papers and data extraction will be conducted by two independent reviewers, and disagreements resolved by discussion with the research team. We will use an iterative process to data charting using a piloted form. Findings will be collated into a narrative report. Ethics and dissemination Ethical approval is not required since data used are from publicly available secondary sources. Findings will be disseminated through peer-reviewed journals, conferences and stakeholder meetings. Further, findings will inform the next phases of a multistage research project aimed at understanding inequalities among patients with breast cancer.
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页数:7
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