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Can J Nurs Res. 2023 Dec;55(4):494-509. doi: 10.1177/08445621231159164. Epub 2023 Feb 27.
2
Genetic and genomic nursing competency among nurses in tertiary general hospitals and cancer hospitals in mainland China: a nationwide survey.中国内地三级综合医院和癌症医院护士的遗传和基因组护理能力:一项全国性调查。
BMJ Open. 2022 Dec 30;12(12):e066296. doi: 10.1136/bmjopen-2022-066296.
3
Leading Canadian Nurses into the Genomic Era of Healthcare.引领加拿大护士进入医疗保健的基因组时代。
Nurs Leadersh (Tor Ont). 2022 Jun;35(2):79-95. doi: 10.12927/cjnl.2022.26869.
4
Genomic research: The landscape for nursing.基因组研究:护理领域的现状
J Adv Nurs. 2022 Sep;78(9):e99-e100. doi: 10.1111/jan.15396. Epub 2022 Jul 27.
5
Issues associated with a hereditary risk of cancer: Knowledge, attitudes and practices of nurses in oncology settings.与癌症遗传风险相关的问题:肿瘤科室护士的知识、态度和行为
Can Oncol Nurs J. 2022 Apr 1;32(2):272-285. doi: 10.5737/23688076322272285. eCollection 2022 Spring.
6
Associations Between Medicaid Insurance, Biomarker Testing, and Outcomes in Patients With Advanced NSCLC.医疗补助保险、生物标志物检测与晚期非小细胞肺癌患者预后之间的关联
J Natl Compr Canc Netw. 2022 May;20(5):479-487.e2. doi: 10.6004/jnccn.2021.7083.
7
Health equity in the implementation of genomics and precision medicine: A public health imperative.实现基因组学和精准医学中的公平健康:公共卫生的当务之急。
Genet Med. 2022 Aug;24(8):1630-1639. doi: 10.1016/j.gim.2022.04.009. Epub 2022 Apr 28.
8
Precision Medicine Testing and Disparities in Health Care for Individuals With Non-Small Cell Lung Cancer: A Narrative Review.精准医疗检测与非小细胞肺癌患者医疗保健中的差异:叙事性综述。
Oncol Nurs Forum. 2022 May 1;49(3):257-272. doi: 10.1188/22.ONF.257-272.
9
Genomics and justice: mitigating the potential harms and inequities that arise from the implementation of genomics in medicine.基因组学与正义:减轻基因组学在医学应用中产生的潜在危害和不公平现象。
Hum Genet. 2022 May;141(5):1099-1107. doi: 10.1007/s00439-022-02453-w. Epub 2022 Apr 12.
10
Health economic evidence for the use of molecular biomarker tests in hematological malignancies: A systematic review.血液恶性肿瘤中应用分子生物标志物检测的健康经济学证据:系统评价。
Eur J Haematol. 2022 Jun;108(6):469-485. doi: 10.1111/ejh.13755. Epub 2022 Mar 2.

基于基因组学的护理策略与健康公平性:系统评价方案

Genomics-informed nursing strategies and health equity: A scoping review protocol.

机构信息

University of Victoria, School of Nursing, Director, Centre for Evidence informed Nursing and Health Care: JBI Centre of Excellence, Victoria, Canada.

Athabasca University, Chair, Ontario Cancer Research Ethics Board, Toronto, Canada.

出版信息

PLoS One. 2023 Dec 15;18(12):e0295914. doi: 10.1371/journal.pone.0295914. eCollection 2023.

DOI:10.1371/journal.pone.0295914
PMID:38100433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10723661/
Abstract

OBJECTIVE

The objective of this scoping review is to map the available evidence on strategies that nurses can use to facilitate genomics-informed healthcare to address health disparities.

INTRODUCTION

Advancements in genomics over the last two decades have led to an increase in the delivery of genomics-informed health care. Although the integration of genomics into health care services continues to enhance patient outcomes, access to genomic technologies is not equitable, exacerbating existing health disparities amongst certain populations. As the largest portion of the health workforce, nurses play a critical role in the delivery of equitable genomics-informed care. However, little is known about how nurses can help address health disparities within the context of genomics-informed health care. A review of the literature will provide the necessary foundation to identify promising practices, policy, and knowledge gaps for further areas of inquiry.

INCLUSION CRITERIA

We will include papers that explore strategies that nurses can undertake to facilitate genomics-informed care to address health disparities.

METHODS

This review will be conducted using JBI methodology for scoping reviews. We will search electronic databases including MEDLINE (OVID), EMBASE, Cochrane Library, PsychInfo, and CINAHL for quantitative and qualitative studies, systematic reviews and grey literature. Theses, books, and unavailable full-text papers will be excluded. The search will be limited to papers from 2013 and beyond. Two reviewers will screen titles and abstracts followed by full-text and disagreements will be resolved by a third reviewer. We will use a data extraction tool using Microsoft Excel and analyse data using descriptive statistics and conventional content analysis. Findings will be presented in the form of evidence tables and a narrative summary. We will report findings using the Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR).

DISCUSSION

Genomics will continue to transform all aspects of health care across the wellness continuum from prevention, assessment, diagnosis, management, treatment, and palliative care. The identification of nursing strategies to address health disparities will build the foundation for policy and practice to ensure that the integration of genomic technologies benefits everyone.

摘要

目的

本范围综述的目的是绘制现有证据,以了解护士可以用来促进以基因组信息为基础的医疗保健以解决健康差异的策略。

引言

在过去的二十年中,基因组学的进步导致了更多的以基因组信息为基础的医疗保健的提供。尽管将基因组学纳入医疗保健服务继续提高患者的治疗效果,但获得基因组技术并不公平,这加剧了某些人群中现有的健康差异。作为最大的医疗保健劳动力的一部分,护士在提供公平的以基因组信息为基础的护理方面发挥着至关重要的作用。然而,对于护士如何帮助解决以基因组信息为基础的医疗保健方面的健康差异,我们知之甚少。对文献的回顾将为确定有前途的实践、政策和知识差距提供必要的基础,以进一步进行调查。

纳入标准

我们将包括探讨护士可以采取的策略,以促进以基因组信息为基础的护理,以解决健康差异的论文。

方法

本综述将使用 JBI 方法进行范围综述。我们将搜索电子数据库,包括 MEDLINE(OVID)、EMBASE、Cochrane 图书馆、PsychInfo 和 CINAHL,以获取定量和定性研究、系统评价和灰色文献。将排除论文、书籍和无法获得全文的论文。搜索将限于 2013 年及以后的论文。两名审查员将筛选标题和摘要,然后进行全文筛选,如果出现分歧,将由第三名审查员解决。我们将使用 Microsoft Excel 的数据提取工具进行分析,并使用描述性统计和常规内容分析进行数据分析。研究结果将以证据表和叙述性摘要的形式呈现。我们将使用系统评价和荟萃分析扩展的首选报告项目(PRISMA-ScR)来报告发现。

讨论

基因组学将继续改变从预防、评估、诊断、管理、治疗和姑息治疗的整个健康保健连续体的所有方面。确定解决健康差异的护理策略将为政策和实践奠定基础,以确保基因组技术的整合使每个人受益。