Conducting Patient-Oriented Research in Low-Income and Middle-Income Countries: A Scoping Review.

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Bukola Mary Ibitoye, Bernie Garrett, Manon Ranger, Jennifer Stinson
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引用次数: 1

Abstract

Background: Patient-oriented research involves extensive collaboration with patients, their families, caregivers, clinicians and other relevant stakeholders to identify and investigate problems and outcomes relevant to patients. Patient-oriented research can help develop effective patient-centred interventions. Patient-oriented research is an increasingly used approach in high-income countries, but it is unclear how patients are engaged in research in low-income and middle-income countries (LMICs).

Objectives: The aim of this scoping review was to explore how patient-oriented research is conducted in LMICs. The objectives were to determine the levels of involvement of patients in the research, how studies have impacted healthcare and patient outcomes in these countries, the reported benefits of patient-oriented research on the research process and the reported challenges of conducting patient-oriented research in LMICs.

Methods: A scoping review was conducted using the methodological framework suggested by Arksey and O'Malley and the Joanna Briggs Institute guidelines for conducting scoping reviews. The eligibility criteria were any healthcare research using any research design that involved patients of any age group in the research process. Six databases were searched from their inception till January 4, 2022: MEDLINE, Embase, Cumulated Index to Nursing and Allied Health Literature, PsychInfo, Cochrane Central Register of Controlled Trials and EBM Reviews. The reference lists of relevant articles and Google Scholar were combed as well. Data extraction was performed with a self-developed data extraction guide. The findings were narratively summarised.

Results: Thirteen articles were included in this scoping review, representing eight LMICs in Africa and Asia. The majority of studies (38%, n = 5) focused on patients living with human immunodeficiency virus. More than half of the studies (n = 8, 62%) were conducted in the adult population, 31% (n = 4) of the studies involved children and/or adolescents. For most of the studies (92%, n = 12), the participants served as consultants; for one study, the authors identified the participants as co-researchers. Across the studies, information regarding patient-oriented research activities was not consistently reported in the same manner (i.e. different locations in the article), with very limited information in some cases. None of the studies used a patient-oriented research framework and the majority did not report on how patient-oriented research impacted healthcare and patient outcomes. Patient-oriented research was beneficial in identifying relevant patients' needs and improving collaboration among stakeholders, but it also led to extended research timelines and increased financial costs for the researchers and patients.

Conclusions: Researchers in LMICs are incorporating patient-oriented research in their research; however, there is a need for improved reporting practices in published articles, and the use of frameworks to guide patient-oriented research in LMICs. In LMICs, patient-oriented research enhances collaboration across stakeholders and gives patients a sense of ownership over the interventions and research process. Future work should focus on developing contextually relevant conceptual frameworks and further studies should explore the impact of patient-oriented research on healthcare and patient outcomes in the LMIC context.

Abstract Image

在低收入和中等收入国家开展面向患者的研究:范围审查。
背景:以患者为导向的研究涉及与患者、其家属、护理人员、临床医生和其他相关利益相关者的广泛合作,以确定和调查与患者相关的问题和结果。以患者为导向的研究有助于制定有效的以患者为中心的干预措施。在高收入国家,以患者为导向的研究越来越多地被采用,但在低收入和中等收入国家,患者如何参与研究尚不清楚。目的:本综述的目的是探讨如何在中低收入国家开展以患者为导向的研究。目的是确定患者参与研究的程度、研究如何影响这些国家的医疗保健和患者结果、报告的以患者为导向的研究对研究过程的好处以及报告的在中低收入国家开展以患者为导向的研究的挑战。方法:使用Arksey和O'Malley以及乔安娜布里格斯研究所指导方针提出的方法框架进行范围审查。入选标准是任何医疗保健研究,使用任何研究设计,在研究过程中涉及任何年龄组的患者。从成立到2022年1月4日,检索了六个数据库:MEDLINE, Embase,护理和联合健康文献累积索引,PsychInfo, Cochrane中央对照试验注册库和EBM综述。并对相关文章和Google Scholar的参考书目进行了梳理。采用自行开发的数据提取指南进行数据提取。对调查结果作了叙述总结。结果:13篇文章被纳入这一范围综述,代表了非洲和亚洲的8个中低收入国家。大多数研究(38%,n = 5)集中于感染人类免疫缺陷病毒的患者。超过一半的研究(n = 8, 62%)是在成年人中进行的,31% (n = 4)的研究涉及儿童和/或青少年。在大多数研究中(92%,n = 12),参与者担任顾问;在一项研究中,作者将参与者确定为共同研究人员。在所有研究中,关于以患者为导向的研究活动的信息并没有以相同的方式一致地报告(即文章的不同位置),在某些情况下信息非常有限。没有一项研究使用以患者为导向的研究框架,大多数研究没有报告以患者为导向的研究如何影响医疗保健和患者结果。以患者为导向的研究有利于确定患者的相关需求和改善利益相关者之间的合作,但也导致研究时间延长,增加了研究人员和患者的财务成本。结论:中低收入国家的研究人员正在将以患者为导向的研究纳入其研究;然而,有必要改进发表文章的报告做法,并使用框架来指导中低收入国家面向患者的研究。在中低收入国家,以患者为导向的研究加强了各利益攸关方之间的合作,并使患者对干预措施和研究过程产生主人翁感。未来的工作应侧重于发展与情境相关的概念框架,进一步的研究应探讨以患者为导向的研究对低收入和中等收入国家医疗保健和患者结果的影响。
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来源期刊
Patient-Patient Centered Outcomes Research
Patient-Patient Centered Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
6.60
自引率
8.30%
发文量
44
审稿时长
>12 weeks
期刊介绍: The Patient provides a venue for scientifically rigorous, timely, and relevant research to promote the development, evaluation and implementation of therapies, technologies, and innovations that will enhance the patient experience. It is an international forum for research that advances and/or applies qualitative or quantitative methods to promote the generation, synthesis, or interpretation of evidence. The journal has specific interest in receiving original research, reviews and commentaries related to qualitative and mixed methods research, stated-preference methods, patient reported outcomes, and shared decision making. Advances in regulatory science, patient-focused drug development, patient-centered benefit-risk and health technology assessment will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in The Patient may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances. All manuscripts are subject to peer review by international experts.
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