Reporting and representation of underserved groups in intervention studies for patients with multiple long-term conditions: a systematic review

IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Journal of the Royal Society of Medicine Pub Date : 2024-04-16 DOI:10.1177/01410768241233109
Zara Kayani, Andrew Willis, Shukrat O Salisu-Olatunji, Shavez Jeffers, Kamlesh Khunti, Ash Routen
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Abstract

ObjectivesGlobally, there is a growing number of people who are living with multiple long-term conditions (MLTCs). Due to complex management needs, it is imperative that research consists of participants who may benefit most from interventions. It is well documented that ethnic minority groups and lower socioeconomic status (SES) groups are at an increased risk of developing MLTCs. Therefore, the aim of this systematic review was to determine the level of reporting and representation of underserved groups (ethnic minority and low SES) in intervention studies addressing MLTCs.DesignSystematic review. Four databases including Cochrane Library, MEDLINE, CINAHL and Scopus were searched for intervention studies from North America or Europe published between January 1990 and July 2023.SettingHospital and community-based interventions. We included interventional studies focusing on improving MLTC-related outcomes.ParticipantsPatients with MLTCs.Main outcome measuresTotal number of studies reporting on ethnicity and SES. Number and proportion of studies reporting by ethnic/SES group.ResultsThirteen studies met the inclusion criteria. Only 4 of 13 studies (31%) recorded and reported ethnicity information. Of these four studies that reported on ethnicity, three studies consisted of primarily White participants. Ethnic minority groups were underrepresented, but one study included a majority of African American participants. Moreover, 12 of 13 studies (92%) reported on SES with income and educational level being the primary measures used. SES representation of higher deprivation groups was varied due to limited data.ConclusionsFor ethnicity, there was a lack of reporting, and ethnic minority groups were underrepresented in intervention studies. For SES, there was a high level of reporting but the proportion of study samples from across the spectrum of SES varied due to the variety of SES measures used. Findings highlight a need to improve the reporting and representation of ethnic minority groups and provide more detailed information for SES through using consistent measures (e.g. education, income and employment) to accurately determine the distribution of SES groups in intervention studies of people with MLTCs.
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针对多种长期病症患者的干预研究中服务不足群体的报告和代表性:系统综述
目标在全球范围内,患有多种长期疾病(MLTCs)的人越来越多。由于复杂的管理需求,研究必须包括可能从干预措施中获益最多的参与者。有资料表明,少数民族群体和社会经济地位(SES)较低的群体罹患多种长期病症的风险更高。因此,本系统性综述旨在确定在针对 MLTCs 的干预研究中,未得到充分服务的群体(少数民族和社会经济地位较低)的报告水平和代表性。我们在 Cochrane Library、MEDLINE、CINAHL 和 Scopus 等四个数据库中检索了 1990 年 1 月至 2023 年 7 月间发表的北美或欧洲干预研究。主要结果测量报告种族和社会经济地位的研究总数。结果13项研究符合纳入标准。13 项研究中只有 4 项(31%)记录并报告了种族信息。在这四项报告了种族信息的研究中,有三项研究的参与者主要是白人。少数族裔群体所占比例较低,但有一项研究的大多数参与者为非洲裔美国人。此外,13 项研究中有 12 项(92%)报告了社会经济地位,其中收入和教育水平是主要的衡量标准。结论 在种族方面,缺乏报告,少数族裔群体在干预研究中的代表性不足。在社会经济地位方面,报告水平较高,但由于所使用的社会经济地位衡量标准不同,来自不同社会经济地位群体的研究样本比例也各不相同。研究结果突出表明,有必要改进少数族裔群体的报告和代表性,并通过使用一致的测量方法(如教育、收入和就业)来提供更详细的社会经济地位信息,以准确确定多发性骨髓瘤患者干预研究中社会经济地位群体的分布情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.40
自引率
3.50%
发文量
107
审稿时长
6-12 weeks
期刊介绍: Since 1809, the Journal of the Royal Society of Medicine (JRSM) has been a trusted source of information in the medical field. Our publication covers a wide range of topics, including evidence-based reviews, original research papers, commentaries, and personal perspectives. As an independent scientific and educational journal, we strive to foster constructive discussions on vital clinical matters. While we are based in the UK, our articles address issues that are globally relevant and of interest to healthcare professionals worldwide.
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