Department of Psychological Medicine, University of Otago, Christchurch, New Zealand
Centre for Adolescent Health, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
BMJ Open. 2023 Oct 27;13(10):e068733. doi: 10.1136/bmjopen-2022-068733.
A rise in premature mortality-defined here as death during the most productive years of life, between adolescence and middle adulthood (15-60 years)-is contributing to stalling life expectancy in high-income countries. Causes of mortality vary, but often include substance misuse, suicide, unintentional injury and non-communicable disease. The development of evidence-informed policy frameworks to guide new approaches to prevention require knowledge of early targets for intervention, and interactions between higher level drivers. Here, we aim to: (1) identify systematic reviews with or without meta-analyses focused on intervention targets for premature mortality (in which intervention targets are causes of mortality that can, at least hypothetically, be modified to reduce risk); (2) evaluate the review quality and risk of bias; (3) compare and evaluate each review's, and their relevant primary studies, findings to identify existing evidence gaps.
In May 2023, we searched electronic databases (MEDLINE, PubMed, Embase, Cochrane Library) for peer-reviewed papers published in the English language in the 12 years from 2012 to 2023 that examined intervention targets for mortality. Screening will narrow these papers to focus on systematic reviews with or without meta-analyses, and their primary papers. Our outcome is death between ages 15 and 60 years; with potential intervention targets measured prior to death. A MeaSurement Tool to Assess systematic Reviews (AMSTAR 2) will be used to assess quality and risk of bias within included systematic reviews. Results will be synthesised narratively due to anticipated heterogeneity between reviews and between primary studies contained within included reviews.
This review will synthesise findings from published systematic reviews and meta-analyses, and their primary reviewed studies, meaning ethics committee approval is not required. Our findings will inform cross-cohort consortium development, be published in a peer-reviewed journal, and be presented at national and international conferences.
CRD42022355861.
过早死亡(这里定义为生命最具生产力的时期,即青春期至中年(15-60 岁)之间的死亡)的增加正在导致高收入国家的预期寿命停滞不前。死亡原因各不相同,但通常包括药物滥用、自杀、意外伤害和非传染性疾病。制定基于证据的政策框架来指导预防新方法需要了解早期干预目标,以及更高层次驱动因素之间的相互作用。在这里,我们旨在:(1)确定针对过早死亡干预目标的系统评价(其中干预目标是死亡率的原因,至少可以假设可以通过改变这些原因来降低风险);(2)评估综述的质量和偏倚风险;(3)比较和评估每个综述及其相关主要研究的发现,以确定现有证据差距。
2023 年 5 月,我们在英语语言的 12 年时间内(2012 年至 2023 年)从电子数据库(MEDLINE、PubMed、Embase、Cochrane Library)中搜索了针对过早死亡干预目标的同行评审论文。筛选将缩小这些论文的范围,重点关注具有或不具有荟萃分析的系统评价及其主要论文。我们的结果是 15 至 60 岁之间的死亡;潜在的干预目标在死亡前进行测量。将使用评估系统评价的测量工具(AMSTAR 2)来评估纳入的系统评价中的质量和偏倚风险。由于综述之间以及纳入综述中的主要研究之间预计存在异质性,因此结果将以叙述性方式综合。
该综述将综合已发表的系统评价和荟萃分析及其主要综述研究的结果,这意味着不需要伦理委员会批准。我们的研究结果将为跨队列联盟的发展提供信息,发表在同行评议的期刊上,并在国家和国际会议上展示。
CRD42022355861。