network meta-analysis

网络荟萃分析
  • 文章类型: Letter
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  • 文章类型: Journal Article
    背景:网络荟萃分析旨在帮助临床医生就某些疾病的最有效治疗做出临床决定。颈部疼痛是多因素的,各种分类系统和治疗方案。在NMA的临床相关治疗节点中对患者进行分类和分组干预至关重要,但是这个过程定义不清。
    目的:我们的目标是在颈部疼痛分类和干预措施分组节点的专家之间达成共识,以便将来进行网络荟萃分析。
    方法:一项涉及全球颈痛专家的Delphi共识研究。
    方法:我们邀请了从2014年起发表的颈部疼痛临床实践指南的作者。德尔菲基线问卷是根据范围审查的结果制定的,包括四个分类项目和19个节点。要求参与者以7点的李克特量表或使用“是/否/不确定”的答案选项记录他们的协议水平。我们使用描述性分析来总结每个陈述的回答,并对自由文本评论进行内容分析。
    结果:总计,18/80专家(22.5%)同意参加一个或多个Delphi轮。我们需要三轮才能就颈部疼痛的两种分类达成共识:一种基于病因,另一种基于持续时间。此外,我们还就干预措施的分组达成了共识,包括每个节点的定义,节点数量减少到17。
    结论:根据这一共识,我们在临床上验证了两种颈部疼痛分类方法,并将保守治疗分为17个明确且临床相关的节点。
    BACKGROUND: A network meta-analysis aims to help clinicians make clinical decisions on the most effective treatment for a certain condition. Neck pain is multifactorial, with various classification systems and treatment options. Classifying patients and grouping interventions in clinically relevant treatment nodes for a NMA is essential, but this process is poorly defined.
    OBJECTIVE: Our aim is to obtain consensus among experts on neck pain classifications and the grouping of interventions into nodes for a future network meta-analysis.
    METHODS: A Delphi consensus study involving neck pain experts worldwide.
    METHODS: We invited authors of neck pain clinical practice guidelines published from 2014 onwards. The Delphi baseline questionnaire was developed based on the findings of a scoping review, including four items on classifications and 19 nodes. Participants were asked to record their level of agreement on a seven-point Likert scale or using Yes/No/Not sure answer options for the various statements. We used descriptive analysis to summarise the responses on each statement with content analysis of the free-text comments.
    RESULTS: In total, 18/80 experts (22.5%) agreed to participate in one or more Delphi rounds. We needed three rounds to reach consensus for two classification of neck pain: one based on aetiology and one on duration. In addition, we also reached consensus on the grouping of interventions, including a definition of each node, with the number of nodes reduced to 17.
    CONCLUSIONS: With this consensus we clinically validated two neck pain classifications and grouped conservative treatments into 17 well-defined and clinically relevant nodes.
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  • 文章类型: Letter
    近年来,几种新型药物已可用于治疗2型糖尿病(T2D)患者,如钠-葡萄糖协同转运蛋白-2抑制剂(SGLT-2i),泰西帕肽,这是双重葡萄糖依赖性促胰岛素多肽受体激动剂(GIPRA)/胰高血糖素样肽-1受体激动剂(GLP-1RA),还有Finerenone,一种非甾体盐皮质激素受体拮抗剂(MRA),可在(CKD)患者中赋予显着的肾脏和心血管益处。新药物有可能改善糖尿病患者的生活。然而,临床医生面临的挑战是了解与这些新的和新兴的治疗方案相关的益处和潜在风险.在这篇文章中,我们将讨论如何使用网络荟萃分析(NMA)来满足这一需求。
    In recent years, several novel agents have become available to treat individuals with type 2 diabetes (T2D), such as sodium-glucose cotransporter-2 inhibitors (SGLT-2i), tirzepatide, which is a dual glucose-dependent insulinotropic polypeptide receptor agonist (GIP RA)/glucagon-like peptide-1 receptor agonist (GLP-1 RA), and finerenone, a non-steroidal mineralocorticoid receptor antagonist (MRA) that confers significant renal and cardiovascular benefits in individuals with (CKD). New medications have the potential to improve the lives of individuals with diabetes. However, clinicians are challenged to understand the benefits and potential risks associated with these new and emerging treatment options. In this article, we discuss how use of network meta-analyses (NMA) can fill this need.
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  • 文章类型: Meta-Analysis
    背景:创伤后应激障碍(PTSD)是一种精神障碍,可以在个人经历诸如身体虐待之类的创伤事件后出现,性/关系暴力,战斗暴露,见证死亡,或重伤。本研究旨在基于网络荟萃分析(NMA)确定最适合治疗PTSD的药物。
    方法:六个数据库(OvidMedline,EMBase,中部,PsycINFO,奥维德健康和社会心理工具,和WebofScience)从开始到2022年9月6日进行了搜索。
    结果:共纳入了30篇文章,共5170名参与者。与安慰剂相比,活性药物包括奥氮平(SMD=-0.66,95%CI:-1.19至-0.13),利培酮(SMD=-0.23,95%CI:-0.42至-0.03),喹硫平(SMD=-0.49,95%CI:-0.93至-0.04),文拉法辛(SMD=-0.29,95%CI:-0.42至-0.16),舍曲林(SMD=-0.23,95%CI:-0.34至-0.11),帕罗西汀(SMD=-0.48,95%CI:-0.60至-0.36)和氟西汀(SMD=-0.27,95%CI:-0.42至-0.12),显著降低了临床医生给予的PTSD量表总评分.
    结论:这项研究的结果支持使用帕罗西汀,文拉法辛,喹硫平作为PTSD的一线治疗。此外,喹硫平被推荐用于患有创伤后应激障碍的患者,这些患者有过度觉醒和再体验障碍的症状。临床医生应根据PTSD症状的严重程度和其他情况开具药物,以制定针对该患者人群的最佳治疗策略。
    Post-traumatic stress disorder (PTSD) is a mental disorder that can emerge after an individual experiences a traumatic event such as physical abuse, sexual/relationship violence, combat exposure, witnessing death, or serious injury. This study aimed to identify the most suitable drugs for the management of PTSD based on a network meta-analysis (NMA).
    Six databases (Ovid Medline, EMBase, CENTRAL, PsycINFO, Ovid Health and Psychosocial Instruments, and Web of Science) were searched from inception to September 6, 2022.
    Thirty articles with a total of 5170 participants were included. Compared with placebo, active drugs including olanzapine (SMD = -0.66, 95% CI: -1.19 to -0.13), risperidone (SMD = -0.23, 95% CI: -0.42 to -0.03), quetiapine (SMD = -0.49, 95% CI: -0.93 to -0.04), venlafaxine (SMD = -0.29, 95% CI: -0.42 to -0.16), sertraline (SMD = -0.23, 95% CI: -0.34 to -0.11), paroxetine (SMD = -0.48, 95% CI: -0.60 to -0.36) and fluoxetine (SMD = -0.27, 95% CI: -0.42 to -0.12), significantly reduced the total clinician-administered PTSD scale score.
    The results of this study support the use of paroxetine, venlafaxine, and quetiapine as first-line treatment for PTSD. In addition, quetiapine is recommended for patients with PTSD affected by symptoms of hyperarousal and re-experience disorder. Clinicians should prescribe medications based on the severity of PTSD symptoms and other conditions to develop the best treatment strategy for this patient population.
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  • 文章类型: Journal Article
    目的:在两个网络meta分析(NMA)中评估冠状动脉血运重建和/或急性冠状动脉综合征后12个月内或之后所有可用的抗血栓治疗。
    结果:包括12个月内的43项(N=189.261)试验和12个月后的19项(N=139.086患者)试验用于疗效/安全性终点评估。在12个月内,替格瑞洛90mgbisindie(b.i.d.)(危险比[HR]0.66;95%置信区间[CI]:0.49-0.88),阿司匹林和替格瑞洛90mg(HR0.85;95CI:0.76-0.95),或者阿司匹林,氯吡格雷和利伐沙班2.5mgb.i.d.(HR0.66;95CI:0.51-0.86)是唯一与降低心血管死亡率相关的治疗方法。与阿司匹林和氯吡格雷相比,没有或具有更大的出血风险的第一和其他治疗方案,分别。超过12个月,无治疗策略降低死亡率;与阿司匹林相比;发现阿司匹林和氯吡格雷(HR0.68;95CI,0.55-0.85)或P2Y12抑制剂单药治疗(HR0.76;95CI,0.61-0.95)可最大程度地减少心肌梗死(MI),尤其是替格瑞洛90mg(HR0.54;95CI,0.32-0.92),和VKA的中风(HR,0.56;95CI,0.44-0.76)或阿司匹林和利伐沙班2.5mg(HR,0.58;95CI,0.44-0.76)。除P2Y12单药治疗外,所有治疗均增加出血,与阿司匹林相比。
    结论:在12个月内,替格瑞洛90mg单药治疗是唯一与死亡率降低相关的治疗,与阿司匹林和氯吡格雷相比,没有出血风险权衡。超过12个月,P2Y12单药治疗,尤其是替格瑞洛90毫克,与较低的MI相关,没有出血权衡;阿司匹林和利伐沙班2.5mg最有效地减少了卒中,具有比VKA更可接受的出血风险,与阿司匹林相比。注册网址:https://www。crd.约克。AC.uk/PROSPERO/;唯一标识符:CRD42021243985和CRD42021252398。
    To appraise all available antithrombotic treatments within or after 12 months following coronary revascularization and/or acute coronary syndrome in two network meta-analyses.
    Forty-three (N = 189 261 patients) trials within 12 months and 19 (N = 139 086 patients) trials beyond 12 months were included for efficacy/safety endpoints appraisal. Within 12 months, ticagrelor 90 mg bis in die (b.i.d.) [hazard ratio (HR), 0.66; 95% confidence interval (CI), 0.49-0.88], aspirin and ticagrelor 90 mg (HR, 0.85; 95% CI, 0.76-0.95), or aspirin, clopidogrel and rivaroxaban 2.5 mg b.i.d. (HR, 0.66; 95% CI, 0.51-0.86) were the only treatments associated with lower cardiovascular mortality, compared with aspirin and clopidogrel, without or with greater bleeding risk for the first and the other treatment options, respectively. Beyond 12 months, no strategy lowered mortality; compared with aspirin; the greatest reductions of myocardial infarction (MI) were found with aspirin and clopidogrel (HR, 0.68; 95% CI, 0.55-0.85) or P2Y12 inhibitor monotherapy (HR, 0.76; 95% CI: 0.61-0.95), especially ticagrelor 90 mg (HR, 0.54; 95% CI, 0.32-0.92), and of stroke with VKA (HR, 0.56; 95% CI, 0.44-0.76) or aspirin and rivaroxaban 2.5 mg (HR, 0.58; 95% CI, 0.44-0.76). All treatments increased bleeding except P2Y12 monotherapy, compared with aspirin.
    Within 12 months, ticagrelor 90 mg monotherapy was the only treatment associated with lower mortality, without bleeding risk trade-off compared with aspirin and clopidogrel. Beyond 12 months, P2Y12 monotherapy, especially ticagrelor 90 mg, was associated with lower MI without bleeding trade-off; aspirin and rivaroxaban 2.5 mg most effectively reduced stroke, with a more acceptable bleeding risk than VKA, compared with aspirin.Registration URL: https://www.crd.york.ac.uk/PROSPERO/; Unique identifiers: CRD42021243985 and CRD42021252398.
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  • 文章类型: Meta-Analysis
    未经评估:初级保健患者和临床医生可能更喜欢第二代抗抑郁药治疗重度抑郁症(MDD)的替代选择。
    UNASSIGNED:为了比较非药物治疗与第二代抗抑郁药作为急性MDD第一步干预措施的益处和危害,并比较首次尝试使用抗抑郁药后未缓解的患者的第二步治疗策略。
    UNASSIGNED:从1990年1月1日至2022年8月8日的几个电子数据库的英语研究,试验注册,灰色文献数据库,和参考列表,以确定未发表的研究。
    UNASSIGNED:2名研究者独立选择了至少6周持续时间的随机试验。
    未经评估:审稿人摘录了有关研究设计和实施的数据,参与者,干预措施,和结果。他们对研究偏差的风险和感兴趣结果的证据的确定性进行了双重评估。
    UNASSIGNED:65项随机试验符合纳入标准;未发现非随机研究的合格数据。荟萃分析和网络荟萃分析显示,大多数非药物治疗和抗抑郁药的益处与第一步治疗相似。与大多数其他治疗相比,抗抑郁药因不良事件而停药的风险更高。对于第二步疗法,不同的转换和增强策略提供了相似的症状缓解.大多数比较的证据的确定性较低;应谨慎解释调查结果。
    UNASSIGNED:许多研究存在方法学上的局限性或剂量不平等;发表偏倚可能影响了一些比较。在某些情况下,由于证据不足,无法得出结论。
    未经评估:尽管第一步和第二步MDD治疗的益处似乎相似,对于大多数比较,证据的确定性较低。临床医生和患者应关注具有最可靠证据的选择,并考虑不良事件概况和患者偏好。
    未经批准:美国医师学会。(PROSPERO:CRD42020204703)。
    Primary care patients and clinicians may prefer alternative options to second-generation antidepressants for major depressive disorder (MDD).
    To compare the benefits and harms of nonpharmacologic treatments with second-generation antidepressants as first-step interventions for acute MDD, and to compare second-step treatment strategies for patients who did not achieve remission after an initial attempt with antidepressants.
    English-language studies from several electronic databases from 1 January 1990 to 8 August 2022, trial registries, gray literature databases, and reference lists to identify unpublished research.
    2 investigators independently selected randomized trials of at least 6 weeks\' duration.
    Reviewers abstracted data about study design and conduct, participants, interventions, and outcomes. They dually rated the risk of bias of studies and the certainty of evidence for outcomes of interest.
    65 randomized trials met the inclusion criteria; eligible data from nonrandomized studies were not found. Meta-analyses and network meta-analyses indicated similar benefits of most nonpharmacologic treatments and antidepressants as first-step treatments. Antidepressants had higher risks for discontinuation because of adverse events than most other treatments. For second-step therapies, different switching and augmentation strategies provided similar symptomatic relief. The certainty of evidence for most comparisons is low; findings should be interpreted cautiously.
    Many studies had methodological limitations or dosing inequalities; publication bias might have affected some comparisons. In some cases, conclusions could not be drawn because of insufficient evidence.
    Although benefits seem to be similar among first- and second-step MDD treatments, the certainty of evidence is low for most comparisons. Clinicians and patients should focus on options with the most reliable evidence and take adverse event profiles and patient preferences into consideration.
    American College of Physicians. (PROSPERO: CRD42020204703).
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  • 文章类型: Journal Article
    网络荟萃分析(NMA)的概念已被引入物理治疗领域。然而,这些研究的报告标准指南尚未进行评估.在这次系统审查中,我们纳入了所有已发表的NMA物理疗法研究,这些研究比较了3种或3种以上干预措施的临床疗效,以评估物理疗法中的NMA是否表现出足够的报告建议.PubMed,EMBASE,WebofScience,并在2022年6月30日之前对Cochrane图书馆进行了搜索。在252篇确定的文章中,纳入19个NMA,包括805个随机对照试验。我们将首选报告项目应用于系统评价和荟萃分析(PRISMA)和PRISMA-NMA检查表,这是27项和32项报告标准指南评估工具,分别。议定书登记(68.4%),研究中存在偏倚的风险(63.2%),额外分析(57.9%),考虑到PRISMA指南,资金(31.6%)是有问题的项目。四项研究报告了所有五个新的NMA报告项目,15项(78.9%)未涉及PRISMA-NMA指南中的S1-5项.报告标准指南的中位数评分(四分位数范围)为27.0(25.8-28.0)。在培训研究人员时,应解决已发布的NMA的缺陷,应该鼓励他们应用PRISMA-NMA,作为评估NMA报告指南的公认工具是必需的。
    The concept of network meta-analyses (NMA) has been introduced to the field of physical therapy. However, the reporting standard guidelines of these studies have not been evaluated. In this systematic review, we included all published NMA physical therapy studies that compared the clinical efficacy of three or more interventions to evaluate whether NMAs in physical therapy exhibit adequate reporting recommendations. PubMed, EMBASE, Web of Science, and the Cochrane Library were searched up to 30 June 2022. Among the 252 identified articles, 19 NMAs including 805 randomized controlled trials were included. We applied both preferred reporting items for systematic reviews and meta-analysis (PRISMA) and PRISMA-NMA checklists, which are 27- and 32-item reporting standard guidelines assessment tools, respectively. Protocol registrations (68.4%), risk of bias across studies (63.2%), additional analysis (57.9%), and funding (31.6%) were problematic items considering the PRISMA guidelines. Four studies reported all five new NMA-reporting items, and 15 (78.9%) did not address items S1-5 from the PRISMA-NMA guidelines. The median score (interquartile range) of the reporting standard guidelines was 27.0 (25.8-28.0). The identified shortcomings of published NMAs should be addressed while training researchers, and they should be encouraged to apply PRISMA-NMA, as a recognized tool for assessing NMA reporting guidelines is required.
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  • 文章类型: Meta-Analysis
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  • 文章类型: Systematic Review
    胆总管结石在胆囊疾病患者中占相当比例。有几个管理选项,包括术前或术中内镜胰胆管造影(ERCP),和腹腔镜胆总管探查术(LCBDE)。
    为了发展证据,跨学科,欧洲关于在完整胆囊的情况下处理胆总管结石的建议,临床决定干预胆囊和胆总管结石。
    我们更新了LCBDE的系统评价和网络荟萃分析,术前,术中,和术后ERCP。我们使用等级和CINeMA方法形成了证据摘要,和一个普通外科医生小组,胃肠病学家,一名患者代表为GRADE证据决策框架的开发做出了贡献,该框架可在多种干预措施中进行选择。
    专家组就第一轮德尔福达成了一致共识。我们建议LCBDE术前,术中,或术后ERCP,当具有手术经验和专业知识时;术中ERCP超过LCBDE,术前或术后ERCP,当这在给定的医疗保健环境中在逻辑上是可行的;术前ERCP超过LCBDE或术后ERCP,术中ERCP不可行且LCBDE经验或专业知识不足(弱推荐)。证据摘要和决策辅助工具可在MAGICapp平台(https://app。magicapp.org/#/guideline/nJ5zyL)。
    我们制定了符合最新方法学标准的快速胆总管结石治疗指南。医疗保健专业人员和其他利益相关者可以使用它来告知临床和政策决定。
    IPGRP-2022CN170。
    Choledocholithiasis presents in a considerable proportion of patients with gallbladder disease. There are several management options, including preoperative or intraoperative endoscopic cholangiopancreatography (ERCP), and laparoscopic common bile duct exploration (LCBDE).
    To develop evidence-informed, interdisciplinary, European recommendations on the management of common bile duct stones in the context of intact gallbladder with a clinical decision to intervene to both the gallbladder and the common bile duct stones.
    We updated a systematic review and network meta-analysis of LCBDE, preoperative, intraoperative, and postoperative ERCP. We formed evidence summaries using the GRADE and the CINeMA methodology, and a panel of general surgeons, gastroenterologists, and a patient representative contributed to the development of a GRADE evidence-to-decision framework to select among multiple interventions.
    The panel reached unanimous consensus on the first Delphi round. We suggest LCBDE over preoperative, intraoperative, or postoperative ERCP, when surgical experience and expertise are available; intraoperative ERCP over LCBDE, preoperative or postoperative ERCP, when this is logistically feasible in a given healthcare setting; and preoperative ERCP over LCBDE or postoperative ERCP, when intraoperative ERCP is not feasible and there is insufficient experience or expertise with LCBDE (weak recommendation). The evidence summaries and decision aids are available on the platform MAGICapp ( https://app.magicapp.org/#/guideline/nJ5zyL ).
    We developed a rapid guideline on the management of common bile duct stones in line with latest methodological standards. It can be used by healthcare professionals and other stakeholders to inform clinical and policy decisions.
    IPGRP-2022CN170.
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  • 文章类型: Journal Article
    背景:成人GERD的外科治疗有几种选择。以前的指南和系统综述比较了完全胃底折叠术的效果与不同部分胃底折叠术技术的综合效果。
    目的:为了建立证据,值得信赖,关于使用总量的相关建议,成人GERD治疗的后部部分和前部部分胃底折叠。
    方法:我们进行了最新的系统评价,网络荟萃分析,使用GRADE和网络元分析方法的信心进行证据评估。一个国际,多学科外科医生小组,胃肠病学家,患者代表通过证据决策框架达成一致共识,在多种干预措施中进行选择,和Delphi程序来制定建议。该项目是在在线创作和出版平台(MAGICapp)中开发的,并由外部审计师监督。
    结果:我们建议成人GERD患者的后部部分胃底折叠术优于全部后部或前部90°胃底折叠术。我们建议前路>90°胃底折叠术作为替代方法,尽管相关比较证据有限(弱推荐).准则,有建议,用户友好格式的证据摘要和决策辅助工具也可以在MAGICapp中访问:https://app。magicapp.org/#/guideline/j20X4n。
    结论:该快速指南是根据最高方法学标准制定的,并提供了关于GERD手术治疗的循证建议。它提供用户友好的决策辅助工具,以告知医疗保健专业人员和患者的决策。
    There are several options for the surgical management of GERD in adults. Previous guidelines and systematic reviews have compared the effects of total fundoplication versus pooled effects of different techniques of partial fundoplication.
    To develop evidence-informed, trustworthy, pertinent recommendations on the use of total, posterior partial and anterior partial fundoplications for the management of GERD in adults.
    We performed an update systematic review, network meta-analysis, and evidence appraisal using the GRADE and the Confidence in Network Meta-Analysis methodologies. An international, multidisciplinary panel of surgeons, gastroenterologists, and a patient representative reached unanimous consensus through an evidence-to-decision framework to select among multiple interventions, and a Delphi process to formulate the recommendation. The project was developed in an online authoring and publication platform (MAGICapp), and was overseen by an external auditor.
    We suggest posterior partial fundoplication over total posterior or anterior 90° fundoplication in adult patients with GERD. We suggest anterior >90° fundoplication as an alternative, although relevant comparative evidence is limited (weak recommendation). The guideline, with recommendations, evidence summaries and decision aids in user friendly formats can also be accessed in MAGICapp: https://app.magicapp.org/#/guideline/j20X4n.
    This rapid guideline was developed in line with highest methodological standards and provides evidence-informed recommendations on the surgical management of GERD. It provides user-friendly decision aids to inform healthcare professionals\' and patients\' decision making.
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