Primary prevention

初级预防
  • 文章类型: Journal Article
    胃癌是全球癌症负担的重要贡献者。风险预测模型旨在根据当前和过去的信息来估计未来风险,并可用于胃癌人群筛查计划中的风险分层。这篇综述旨在探索现有模型的研究设计,以及方法,变量,和模型构建的性能。
    搜索了6个数据库,直到2023年11月4日,以确定适当的研究。遵循PRISMA扩展范围审查和Arksey和O\'Malley框架。数据源包括PubMed、Embase,WebofScience,CNKI,万方,VIP,重点对胃癌风险预测模型进行研究。
    共有29篇文章符合纳入标准,从中确定了28个符合分析标准的原始风险预测模型.对风险预测模型进行筛选,提取的数据包括研究特征,预测变量选择,模型构建方法和评价指标。模型的曲线下面积(AUC)范围为0.560至0.989,而C统计量在0.684至0.940之间变化。预测变量的个数主要集中在5~11个之间。最常见的前5个变量是年龄,幽门螺杆菌(Hp),癌前病变,胃蛋白酶原(PG),性别,和吸烟。年龄和Hp是最一致的变量。
    这篇综述增进了对当前胃癌风险预测研究及其未来方向的理解。研究结果为建立更准确的胃癌风险模型提供了有力的科学依据和技术支持。我们期望这些结论将为该领域的未来研究和临床实践指明道路,以协助胃癌的早期预防和治疗。
    UNASSIGNED: Gastric cancer is a significant contributor to the global cancer burden. Risk prediction models aim to estimate future risk based on current and past information, and can be utilized for risk stratification in population screening programs for gastric cancer. This review aims to explore the research design of existing models, as well as the methods, variables, and performance of model construction.
    UNASSIGNED: Six databases were searched through to November 4, 2023 to identify appropriate studies. PRISMA extension for scoping reviews and the Arksey and O\'Malley framework were followed. Data sources included PubMed, Embase, Web of Science, CNKI, Wanfang, and VIP, focusing on gastric cancer risk prediction model studies.
    UNASSIGNED: A total of 29 articles met the inclusion criteria, from which 28 original risk prediction models were identified that met the analysis criteria. The risk prediction model is screened, and the data extracted includes research characteristics, prediction variables selection, model construction methods and evaluation indicators. The area under the curve (AUC) of the models ranged from 0.560 to 0.989, while the C-statistics varied between 0.684 and 0.940. The number of predictor variables is mainly concentrated between 5 to 11. The top 5 most frequently included variables were age, helicobacter pylori (Hp), precancerous lesion, pepsinogen (PG), sex, and smoking. Age and Hp were the most consistently included variables.
    UNASSIGNED: This review enhances understanding of current gastric cancer risk prediction research and its future directions. The findings provide a strong scientific basis and technical support for developing more accurate gastric cancer risk models. We expect that these conclusions will point the way for future research and clinical practice in this area to assist in the early prevention and treatment of gastric cancer.
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  • 文章类型: Journal Article
    心血管疾病(CVD)是全球领先的健康问题,有效的初级预防战略对于减轻其影响至关重要。这篇综合综述研究了当前心血管疾病一级预防的风险评估策略,强调早期识别和干预对降低发病率的重要性。传统的危险因素,如高血压,高脂血症,吸烟,生活方式的选择与新兴因素一起讨论,包括遗传易感性和生物标志物。审查评估了各种风险评估工具和模型,比如弗雷明汉风险评分,动脉粥样硬化CVD风险计算器,QRISK,和雷诺兹风险评分,强调他们的方法,优势,和限制。此外,这篇评论探讨了生活方式的改变,包括饮食变化,身体活动,体重管理,戒烟,和药物干预措施,如他汀类药物和抗高血压药。对不同人群的特殊考虑,包括老年人,女人,那些有心血管疾病家族史的人,已解决。还讨论了心血管风险评估的未来方向,专注于技术进步和个性化医疗。这篇综述旨在通过对风险评估策略的全面分析,加强有效一级预防措施的实施,改善心血管健康结果。
    Cardiovascular disease (CVD) is a leading global health concern, and effective primary prevention strategies are essential to mitigate its impact. This comprehensive review examines current risk assessment strategies for primary prevention of CVD, emphasizing the importance of early identification and intervention to reduce disease incidence. Traditional risk factors such as hypertension, hyperlipidemia, smoking, and lifestyle choices are discussed alongside emerging factors, including genetic predispositions and biomarkers. The review evaluates various risk assessment tools and models, such as the Framingham risk score, atherosclerotic CVD risk calculator, QRISK, and Reynolds risk score, highlighting their methodologies, strengths, and limitations. Additionally, the review explores lifestyle modifications, including dietary changes, physical activity, weight management, smoking cessation, and pharmacological interventions like statins and antihypertensives. Special considerations for different populations, including the elderly, women, and those with a family history of CVD, are addressed. Future directions in cardiovascular risk assessment are also discussed, focusing on technological advancements and personalized medicine. This review aims to enhance the implementation of effective primary prevention measures and improve cardiovascular health outcomes by providing a thorough analysis of risk assessment strategies.
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  • 文章类型: Journal Article
    目的:一级预防策略对于减轻先天性心脏病(CHD)的全球负担至关重要;这需要对病因因素有充分的了解。我们旨在回顾CHD和产妇高龄之间的关联,肥胖,糖尿病,高血压,吸烟和饮酒,并评估关联的因果关系。
    方法:应用基于BradfordHill标准评分的因果评估系统对综述进行系统评价。
    方法:我们搜索了PubMed,Embase和Episteminokos(1990年1月至2023年4月)。
    方法:对原始流行病学研究的系统评价报告了一个或多个上述母体因素与随后后代的总体CHD(任何类型)之间的关联(相对风险)。
    方法:两名独立评审员选择了符合条件的评审,评估偏倚的风险,并分配因果关系的证据强度。
    结果:有强有力的证据表明,冠心病与产妇肥胖(孕前和孕早期)和预先存在的糖尿病之间存在因果关系(七个BradfordHill标准中有六个符合)。对于预先存在的高血压(强度和生物梯度未达到),和高龄(力量,一致性和生物梯度未达到),因果关系证据是适度的。妊娠期糖尿病因果关系的证据,妊娠期高血压,吸烟和饮酒较弱(力量,一致性,时间性和生物梯度未达到)。
    结论:可以通过更强的行动来减少CHD,以减少母亲肥胖和先前存在的糖尿病患病率。调查受到有限关注的环境暴露,如空气污染物和化学暴露,对进一步预防很重要。
    OBJECTIVE: Primary prevention strategies are critical to reduce the global burden of congenital heart defects (CHDs); this requires robust knowledge of causal agents. We aimed to review associations between CHDs and maternal advanced age, obesity, diabetes, hypertension, smoking and alcohol consumption and assess the causal nature of the associations.
    METHODS: Systematic review of reviews with application of a Bradford Hill criteria score-based causal assessment system.
    METHODS: We searched PubMed, Embase and Episteminokos (January 1990-April 2023).
    METHODS: Systematic reviews of original epidemiological studies reporting association (relative risk) between one or more of the above maternal factors and CHDs overall (any type) in subsequent offspring.
    METHODS: Two independent reviewers selected eligible reviews, assessed the risk of bias and assigned the strength of evidence for causality.
    RESULTS: There was strong evidence of a causal relationship between CHDs and maternal obesity (prepregnancy and early pregnancy) and pre-existing diabetes (six of seven Bradford Hill criteria met). For pre-existing hypertension (strength and biological gradient not met), and advanced age (strength, consistency and biological gradient not met), causal evidence was moderate. Evidence for the causal contribution of gestational diabetes, gestational hypertension, smoking and alcohol consumption was weak (strength, consistency, temporality and biological gradient not met).
    CONCLUSIONS: CHDs can be reduced with stronger action to reduce maternal obesity and pre-existing diabetes prevalence. Investigating environmental exposures that have received limited attention, such as air pollutants and chemical exposures, is important to further inform prevention.
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  • 文章类型: Journal Article
    目的:本范围审查旨在调查中东和北非(MENA)的医疗保健提供者(HCP)的知识,与经历过亲密伴侣暴力(IPV)的女性合作的态度和障碍。这篇综述旨在绘制可用的同行评审文献的广度,这些文献可能会为未来的教育培训计划提供信息。
    方法:范围审查。
    方法:范围审查包括截至2023年12月从PUBMED开始的研究,Medline,Cochrane,护理和相关健康文献的累积指数,PsycINFO和阿拉伯医学期刊。
    方法:选定的文章仅限于在MENA地区进行的文章,全文提供,没有日期限制。
    方法:从所有研究中提取数据,包括研究地点,出版年份,期刊类型,方法论,设计,参与者,知识,态度和障碍。通过将信息绘制到表格中,使用频率分析数据,计数和描述性内容分析。
    结果:在评论的1060篇文章中,29项符合条件的研究纳入本范围审查。27%的文章报告说,HCP缺乏关于IPV协议的知识。报告的主要态度是倾向于治疗提出的健康投诉并避免讨论IPV。最后,30%的文章报告说,HCPs缺乏培训是主要障碍。
    结论:我们的论文得出结论,在理解知识方面缺乏研究,MENA地区和IPV中HCP周围的态度和障碍。这一范围审查强调了进一步研究的必要性,对该地区的HCPs进行知情干预和培训。
    OBJECTIVE: This scoping review aims to survey healthcare providers (HCPs) in the Middle East and North Africa (MENA) about their knowledge, attitudes and barriers to working with women who have experienced intimate partner violence (IPV). This review aims to map the breadth of available peer-reviewed literature that may inform future educational training programmes.
    METHODS: Scoping review.
    METHODS: The scoping review included studies up to December 2023 from PUBMED, Medline, COCHRANE, Cumulative Index of Nursing and Allied Health Literature, PsycINFO and Arabic medical journals.
    METHODS: Selected articles were restricted to those carried out in the MENA region, available in full text and with no date restrictions.
    METHODS: Data were extracted from all studies to include research location, year of publication, type of journal, methodology, design, participants, knowledge, attitudes and barriers. By charting the information into a table, the data were analysed using frequency, counts and descriptive content analysis.
    RESULTS: Of the 1060 articles reviewed, 29 eligible studies were included in this scoping review. 27% of the articles reported HCPs\' lack of knowledge about IPV protocols. The dominant attitude reported was a preference to treat the presenting health complaint and avoid discussing IPV. Finally, 30% of articles reported HCPs\' lack of training as the main barrier.
    CONCLUSIONS: Our paper concluded that there is a lack of research in understanding the knowledge, attitudes and barriers surrounding HCPs in the MENA region and IPV. This scoping review highlights the need for further research, informed interventions and training for HCPs in the region.
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  • 文章类型: Journal Article
    研究结果与叶酸对中风一级预防的影响不一致。这项研究的目的是使用观察性研究和随机对照试验(RCTs)的数据来分析叶酸与中风一级预防之间的关系。
    在PubMed数据库中搜索了截至2024年6月出版的合格出版物,WebofScience和Embase。这项研究包括所有观察性研究和叶酸的RCT,以首次中风为报告终点。将相对风险(RR)和95%置信区间(CIs)合并在随机效应模型中,以评估叶酸对中风一级预防的影响。
    来自12个观察出版物和16个研究的结果,包括312320名参与者,联合探讨膳食叶酸摄入与卒中一级预防之间的关系。结果显示,高膳食叶酸摄入量与中风发生率降低17%相关(RR:0.83;95%CI:0.73-0.94)。在没有谷物强化的地区,膳食叶酸的作用更大(RR:0.80;95%CI:0.67-0.95)。来自12个随机对照试验的汇总结果,共有75,042名参与者,表明补充叶酸与卒中一级预防无关(RR:0.92;95%CI:0.80-1.05),但在没有谷物强化的地区补充叶酸是有效的(RR:0.78;95%CI:0.68-0.89)。
    我们的荟萃分析表明,膳食叶酸在中风一级预防中有效,仅在没有谷物强化的地区,补充叶酸对中风的一级预防有效。
    https://www.crd.约克。AC.uk/PROSPERO/#myprospro,标识符CRD42024516991。
    UNASSIGNED: Results from studies were inconsistent with regard to the effect of folic acid on the primary prevention of stroke. The aim of this study was to analyze the association between folic acid and the primary prevention of stroke using the data from observational studies and randomized controlled trials (RCTs).
    UNASSIGNED: Eligible publications published until June 2024 were searched in the database of PubMed, Web of Science and Embase. This study included all observational studies and RCTs of folic acid with first stroke as the reporting endpoints. Relative risks (RRs) and 95% confidence intervals (CIs) were pooled in the random-effects model to assess the effect of folic acid on the primary prevention of stroke.
    UNASSIGNED: Results from 12 observational publications with 16 research, including 312,320 participants, were combined to explore the association between dietary folic acid intake and the primary prevention of stroke. The results showed that high dietary folic acid intake was associated with a 17% reduction in stroke incidence (RR:0.83; 95% CI: 0.73-0.94), and the effect of dietary folic acid was greater in areas without grain fortification (RR:0.80; 95% CI: 0.67-0.95). The pooled results from 12 RCTs, totaling 75,042 participants, indicated that folic acid supplementation was not associated with the stroke primary prevention (RR:0.92; 95% CI: 0.80-1.05), but folic acid supplementation was effective in areas without grain fortification (RR:0.78; 95% CI: 0.68-0.89).
    UNASSIGNED: Our meta-analysis demonstrated that dietary folic acid is effective in stroke primary prevention, and folic acid supplementation is effective in stroke primary prevention only in areas without grain fortification.
    UNASSIGNED: https://www.crd.york.ac.uk/PROSPERO/#myprospero, identifier CRD42024516991.
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  • 文章类型: Systematic Review
    目的:他汀类药物广泛用于心血管疾病(CVD)预防;然而,相当比例的使用者因各种原因停止用药。这篇综述旨在确定他汀类药物治疗中断的患病率,其相关因素,以及停药后第一年内的不良心血管结局.
    方法:PubMed,EMBASE,ScienceDirect,Scopus,和GoogleScholar数据库从成立到2022年12月进行了系统搜索。还对相关文章的参考书目进行了手动搜索。包括定性数据综合研究,并评估方法学质量。
    结果:52项研究,主要是队列研究(n=38),纳入4277061名参与者.在开始他汀类药物的第一年内,他汀类药物停药的患病率为0.8%至70.5%。一级预防指征较高。经常与他汀类药物停药可能性增加相关的因素包括男性,非白人种族,吸烟状况,没有保险。相反,接受二级预防他汀类药物治疗的CVD患者和接受多重用药的患者停药的可能性较小.此外,在不同年龄类别中,年龄与他汀类药物停药的关系不同且不一致.5项研究报告了在开始治疗的第一年内他汀类药物停药的心血管风险,显示停药风险显著增加。包括全因死亡率(危险比:1.36-3.65)。
    结论:我们的研究结果表明,他汀类药物停药的患病率很高,停药后第一年内发生不良心血管结局的可能性增加。尽管在已发表的研究中差异很大。这篇综述强调了解决与他汀类药物停药相关的可改变危险因素的重要性,比如吸烟和缺乏保险。
    OBJECTIVE: Statins are widely prescribed for cardiovascular diseases (CVD) prevention; however, a significant proportion of users discontinue the medication for various reasons. This review aimed to determine the prevalence of statin therapy discontinuation, its associated factors, and adverse cardiovascular outcomes within the first year of discontinuation.
    METHODS: The PubMed, EMBASE, ScienceDirect, SCOPUS, and Google Scholar databases were systematically searched from their inception to December 2022. Manual searches were also conducted on the bibliographies of relevant articles. Studies were included for qualitative data synthesis and assessed for methodological quality.
    RESULTS: Fifty-two studies, predominantly cohort studies (n = 38), involving 4 277 061 participants were included. The prevalence of statin discontinuation within the first year of statin initiation ranged from 0.8% to 70.5%, which was higher for primary prevention indications. Factors frequently associated with an increased likelihood of statin discontinuation included male sex, nonWhite ethnicity, smoking status, and being uninsured. Conversely, discontinuation was less likely in patients with CVD who received secondary prevention statin therapy and in patients with polypharmacy. Furthermore, age showed diverse and inconsistent relationships with statin discontinuation among various age categories. Five studies that reported the cardiovascular risk of statin discontinuation within the first year of initiation showed significantly increased risk of discontinuation, including all-cause mortality (hazard ratio: 1.36-3.65).
    CONCLUSIONS: Our findings indicate a high prevalence of statin discontinuation and an increased likelihood of adverse cardiovascular outcomes within the first year of discontinuation, despite wide variability across published studies. This review highlights the importance of addressing the modifiable risk factors associated with statin discontinuation, such as smoking and lack of insurance coverage.
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  • 文章类型: Journal Article
    关于他汀类药物用于老年人心血管疾病(CVD)一级预防的证据需要扩展和更新,旨在为临床实践提供进一步的指导。
    PubMed,EMBASE,搜索了Cochrane图书馆和WebofScience,以比较他汀类药物使用与老年人(年龄≥65岁)不使用他汀类药物进行CVD一级预防。主要结果是全因死亡率,CVD死亡率,冠心病(CHD)/心肌梗死(MI),卒中和总CV事件。在随机效应模型中,将每个相关结果的风险估计值合成为具有95%置信区间(95%CI)的风险比(HR)。
    纳入了12项符合条件的观察性研究(n=1,627,434)。汇总结果表明,他汀类药物的使用与全因死亡率的风险显着降低相关(HR:0.54,95%CI:0.46-0.63),CVD死亡率(HR:0.51,95%CI:0.39-0.65),冠心病/心肌梗死(HR:0.83,95%CI:0.69-1.00),卒中(HR:0.79,95%CI:0.68-0.92)和总CV事件(HR:0.75,95%CI:0.66-0.85).在较高的年龄(≥70岁,HR:0.56,95%CI:0.44-0.71;≥75岁,HR:0.70,95%CI:0.60-0.80;≥85岁,HR:0.85,95%CI:0.74-0.97),≥20%(HR:0.47,95%CI:0.35-0.62)和<20%糖尿病人群(HR:0.50,95%CI:0.40-0.64),和≥50%(HR:0.68,95%CI:0.59-0.79)和<50%高血压人群(HR:0.38,95%CI:0.16-0.88)。
    他汀类药物的使用占46%,49%,17%,全因死亡率风险降低21%和25%,CVD死亡率,CHD/MI,老年患者的卒中和总CV事件,分别。对于CVD一级预防,老年患者和≥75岁的个体也有显著的相关性。
    UNASSIGNED: Evidence on statin use for primary prevention of cardiovascular disease (CVD) in older people needs to be extended and updated, aiming to provide further guidance for clinical practice.
    UNASSIGNED: PubMed, EMBASE, Cochrane Library and Web of Science were searched for eligible observational studies comparing statin use vs. no-statin use for primary prevention of CVD in older people (age ≥ 65 years). The primary outcomes were all-cause mortality, CVD mortality, coronary heart disease (CHD)/myocardial infraction (MI), stroke and total CV events. Risk estimates of each relevant outcome were synthesized as a hazard ratio (HR) with 95% confidence interval (95% CI) using in the random-effects model.
    UNASSIGNED: Twelve eligible observational studies (n = 1,627,434) were enrolled. The pooled results suggested that statin use was associated with a significantly decreased risk of all-cause mortality (HR: 0.54, 95% CI: 0.46-0.63), CVD mortality (HR: 0.51, 95% CI: 0.39-0.65), CHD/MI (HR: 0.83, 95% CI: 0.69-1.00), stroke (HR: 0.79, 95% CI: 0.68-0.92) and total CV events (HR: 0.75, 95% CI: 0.66-0.85). The association in all-cause mortality still remained obvious at higher ages ( ≥ 70 years old, HR: 0.56, 95% CI: 0.44-0.71; ≥ 75 years old, HR: 0.70, 95% CI: 0.60-0.80; ≥ 85 years old, HR: 0.85, 95% CI: 0.74-0.97), ≥ 20% (HR: 0.47, 95% CI: 0.35-0.62) and < 20% diabetic populations (HR: 0.50, 95% CI: 0.40-0.64), and ≥ 50% (HR: 0.68, 95% CI: 0.59-0.79) and < 50% hypertensive populations (HR: 0.38, 95% CI: 0.16-0.88).
    UNASSIGNED: Statin use was related to a 46%, 49%, 17%, 21% and 25% risk reduction on all-cause mortality, CVD mortality, CHD/MI, stroke and total CV events in older patients, respectively. The significant association was also addressed in older patients and ≥ 75 years old individuals for CVD primary prevention.
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  • 文章类型: Systematic Review
    背景:抗凝血剂在高危癌症患者静脉血栓栓塞(VTE)一级预防中的作用已在先前的研究中得到证实;然而,对于Khorana评分≤2的癌症患者,常规使用血栓预防仍存在争议.本系统综述和荟萃分析旨在首次研究抗凝药预防在低至中度风险癌症患者中的作用。
    方法:PubMed,Scopus,谷歌学者,使用Mesh术语搜索和WebofScience数据库,以找到随机对照试验研究(RCT),该研究评估了截至2024年1月在低风险癌症患者中,针对安慰剂的血栓预防对VTE的影响.本系统综述是根据PRISMA指南进行的。使用I2检验评估研究之间的异质性。Egger的测试用于检查出版偏差。总的来说,21项研究纳入9985名参与者。
    结果:大多数研究具有高质量和低偏倚风险。汇总估计显示,与安慰剂相比,使用抗凝剂显着降低了VTE的风险(HR:0.53,95%CI:0.43,0.60,I2:8.1%)。基于抗凝剂类别的亚组分析表明,与安慰剂相比,直接口服抗凝剂(DOAC)(HR:0.46,95%CI:0.36,0.56,I2:8.5%)和低分子量肝素(LMWH)(HR:0.60,95%CI:0.51,70,I2:0%)均与VTE风险显着相关。对18项研究的汇总估计显示,大出血增加与抗凝预防之间没有显着关联。(HR:1.25,95%CI:0.96,1.54,I2:4%)。
    结论:与安慰剂相比,两种LMWH和DOAC的抗凝预防可能与低至中等风险癌症患者的VTE风险降低有关。DOAC与VTE风险的降低有关。抗凝预防与大出血的增加没有显着关系。
    BACKGROUND: The role of anticoagulants in the primary prevention of venous Thromboembolism(VTE) in high-risk cancer patients has been proven in previous studies; however, the routine use of thromboprophylaxis in cancer patients with Khorana score≤ 2 is still debated. This systematic review and meta-analysis aimed to investigate the role of prophylaxis with anticoagulants in cancer patients with low to moderate risk for first time.
    METHODS: PubMed, Scopus, Google Scholar, and Web of Science databases were searched with Mesh terms to find Randomized controlled trial studies (RCTs) that evaluated the effect of thromboprophylaxis against placebo on VTE up to January 2024 in low-risk cancer patients. This systematic review was conducted based on the PRISMA guidelines. Heterogeneity between studies was evaluated using the I2 test. Egger\'s test was used to check publication bias. In general, 21 studies with 9985 participants were included.
    RESULTS: The majority of studies had high quality and low risk of bias. The pooled estimate showed that using anticoagulants compared to placebo significantly reduces the risk of VTE (HR: 0.53, 95% CI: 0.43, 0.60, I2: 8.1%). Analysis of subgroups based on the class of anticoagulants showed that both direct oral anticoagulants (DOACs) (HR: 0.46, 95% CI: 0.36, 0.56, I2:8.5%) and Low molecular weight heparin (LMWH) (HR: 0.60, 95% CI: 0.51, 70, I2:0%) were significantly related to VTE risk compared to placebo. A pooled estimate of 18 studies did not show a significant association between increased major bleeding and anticoagulant prophylaxis. (HR: 1.25, 95% CI: 0.96, 1.54, I2: 4%).
    CONCLUSIONS: Anticoagulant prophylaxis with both classes of LMWHs and DOACs compared to placebo can be associated with a reduction in VTE risk in low-to-intermediate risk cancer patients. DOACs were associated with a greater reduction in VTE risk. Anticoagulant prophylaxis had no significant relationship with increased major bleeding.
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  • 文章类型: Journal Article
    背景:临床医生和患者经常面临继续或停用他汀类药物的决定。我们检查了停用他汀类药物与继续治疗相比对临床结局的影响(全因死亡率,心血管[CV]死亡率,CV事件,和生活质量)。
    方法:我们进行了系统评价。随机对照试验(RCT),队列研究,病例对照研究,在≥18岁人群中进行的准随机研究符合资格.我们搜索了MEDLINE,Embase,和科克伦中央登记处(始于2023年8月)。两名独立的审阅者进行筛选并提取数据。质量评估由一位作者进行,并由另一位作者验证。我们叙述性地总结了结果,对一部分研究进行了荟萃分析,并使用等级来评估证据的确定性。我们总结了≥75岁人群的发现。
    结果:我们检索了8369篇标题/摘要;来自36项研究的37篇报告符合资格。这包括35个非随机研究(n=1,708,684)和1个RCT(n=381)。在预期寿命<1年的人群中进行了1次RCT,显示60天死亡率可能没有差异(风险差异=3.5%,与继续治疗相比,他汀类药物停药的90%CI-3.5至10.5)。非随机研究在人群和环境方面有所不同,但一致表明,他汀类药物停药可能与相对增加的死亡风险相关(风险比(HR)1.92,95%CI1.52至2.44,九项研究),CV死亡率(HR1.63,95%CI1.27至2.10,五份报告),和CV事件(HR1.31,95%CI1.23至1.39,8份报告)。75岁以上人群的发现与主要结果一致。由于方法学上的限制,非随机研究的结果存在高度的不确定性。
    结论:根据一项RCT,停用他汀类药物似乎不会影响临终的短期死亡率。在这些人口之外,非随机研究的结果一致表明,他汀类药物停药可能与更差的结局相关,虽然这是不确定的。
    BACKGROUND: Clinicians and patients often face a decision to continue or discontinue statins. We examined the impact of discontinuation of statins compared with continuation on clinical outcomes (all-cause mortality, cardiovascular [CV] mortality, CV events, and quality of life).
    METHODS: We conducted a systematic review. Randomized controlled trials (RCTs), cohort studies, case-control studies, and quasi-randomized studies among people ≥18 years were eligible. We searched MEDLINE, Embase, and Cochrane Central Registry (inception to August 2023). Two independent reviewers performed screening and extracted data. Quality assessment was performed by one author and verified by another. We summarized results narratively, performed meta-analysis for a subset of studies, and used GRADE to assess certainty of evidence. We summarized findings in the subgroup of persons ≥75 years.
    RESULTS: We retrieved 8369 titles/abstracts; 37 reports from 36 studies were eligible. This comprised 35 non-randomized studies (n = 1,708,684) and 1 RCT (n = 381). The 1 RCT was conducted among persons with life expectancy <1 year and showed there is probably no difference in 60-day mortality (risk difference = 3.5%, 90% CI -3.5 to 10.5) for statin discontinuation compared with continuation. Non-randomized studies varied in terms of population and setting, but consistently suggested that statin discontinuation might be associated with a relative increased risk of mortality (hazard ratio (HR) 1.92, 95% CI 1.52 to 2.44, nine studies), CV mortality (HR 1.63, 95% CI 1.27 to 2.10, five reports), and CV events (HR 1.31, 95% CI 1.23 to 1.39, eight reports). Findings in people ≥75 years were consistent with main results. There was a high degree of uncertainty in findings from non-randomized studies due to methodological limitations.
    CONCLUSIONS: Statin discontinuation does not appear to affect short-term mortality near end-of-life based on one RCT. Outside of this population, findings from non-randomized studies consistently suggested statin discontinuation may be associated with worse outcomes, though this is uncertain.
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  • 文章类型: Journal Article
    目的:评估个体在绝经后妇女原发性骨折预防中骨质疏松GPG发展的观点。
    方法:我们对指南数据库和CPG开发组织网站进行了全面系统的搜索。使用AGREEII工具,我们评估了指南的质量,特别强调纳入患者,或开发过程中的代表。我们还研究了在建议层面是否考虑了女性的观点,并探讨了患者价值观和偏好与CPG质量之间的潜在关联。
    结果:我们共检索到491个合格的CPG,最终包括33个。大多数CPG是由科学协会开发的(63.6%),主要来自欧洲(39.4%)和北美(30.3%)。四分之一(24.2%)的指导方针明确包括个人发展的观点,十分之一(12.1%)的研究证据支持他们的建议。质量评估中平均得分最低的领域是适用性(42.4%),发展的严谨性(44.7%),和利益相关者参与(45.7%),根据我们的评估,61%被推荐使用。更高质量的指南更有可能将女性的观点纳入其发展中(平均差39.31,p=0.003)。
    结论:将妇女的观点纳入制定骨质疏松症初级骨折预防指南的过程中仍然不够。我们的发现呼吁指南开发人员改善这种情况,对于用户来说,和政策制定者要意识到这些限制,在此领域使用或实施指南时。
    OBJECTIVE: To assess the inclusion of individuals\' perspectives in the development of osteoporosis Clinical Practice Guidelines (CPGs) for primary fracture prevention in postmenopausal women.
    METHODS: We performed a comprehensive systematic search across guideline databases and (CPGs) developing organizations websites. Using the AGREE II tool, we assessed the quality of the guidelines, with particular emphasis on the inclusion of patients, or representatives in the development process. We also examined if women\'s perspectives were considered at the recommendations level and explored the potential association between the inclusion of patients\' values and preferences with the quality of the CPGs.
    RESULTS: We retrieved a total of 491 eligible CPGs, of which 33 were finally included. The majority of the CPGs were developed by scientific societies (63.6%), primarily from Europe (39.4%) and North America (30.3%). One in every four (24.2%) guidelines explicitly included individuals\' perspectives in their development, and one in ten (12.1%) included research evidence about this aspect to support their recommendations. The domains with the lowest mean scores in the quality assessment were applicability (42.4%), rigor of development (44.7%), and stakeholder involvement (45.7%), and 61% were recommended for use according to our assessment. Guidelines of higher quality were more likely to include women\'s perspective in their development (mean difference 39.31, P = .003).
    CONCLUSIONS: The incorporation of women\'s perspectives into the process of developing guidelines for primary fracture prevention in osteoporosis remains inadequate. Our findings serve as a call for guideline developers to improve this situation, and for users, and policymakers to be aware of these limitations, when using or implementing guidelines in this field.
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