AMSTAR2

AMSTAR2
  • 文章类型: Journal Article
    评估关于运动干预对轻度认知障碍(MCI)患者认知功能的meta分析文献的方法学质量及其结果指标的证据确定性,并为临床医生和研究人员提供更可靠的决策数据。
    通过PubMed检索运动干预对轻度认知障碍患者认知功能影响的Meta分析文献,科克伦图书馆,Embase,Scopus,物理治疗证据数据库和WebofScience,所有这些都有每个数据库的搜索周期框架,直到2024年6月1日。采用AMSTAR2量表评价纳入研究的方法学质量。
    包括17项荟萃分析。AMSTAR2量表评估结果显示,有一项中等质量的研究(5.55%),七项低质量研究(38.88%),和10项非常低质量的研究(55.55%)。方法上的缺陷包括未能编制计划和提供登记号,文献筛选,数据提取,未详细描述的排除原因,系统评估的实施过程不佳,以及未能描述纳入研究的资金来源或相关利益冲突。
    荟萃分析文献的总体方法学质量较低,证据的确定性很低。我们鼓励开展高质量的随机试验以产生更有力的证据。随后的系统评价可以综合这些证据,为未来的研究和临床指南提供信息。
    UNASSIGNED: To assess the methodological quality of meta-analytic literature on exercise interventions for cognitive function in patients with mild cognitive impairment (MCI) and the certainty of evidence for its outcome indicators, and to provide clinicians and researchers with more reliable data for making decisions.
    UNASSIGNED: Meta-analytic literature related to the effect of exercise intervention on cognitive function in patients with mild cognitive impairment was searched through PubMed, Cochrane Library, Embase, Scopus, Physiotherapy Evidence Database and Web of Science, all with a search period frame of each database until June 1, 2024. The AMSTAR2 scale was used to evaluate the methodological quality of the included studies.
    UNASSIGNED: Seventeen meta-analyses were included. The AMSTAR2 scale evaluation results showed that there was one medium-quality studies (5.55%), seven low-quality studies (38.88%), and 10 very low-quality studies (55.55%). Methodological deficiencies included failure to prepare a plan and provide a registration number, literature screening, data extraction, reasons for exclusion not described in detail, poor implementation process for systematic evaluation, and failure to describe the source of funding for the included studies or relevant conflicts of interest.
    UNASSIGNED: The overall methodological quality of the meta-analytic literature is low, and the certainty of evidence is low. We encourage the conduction of high-quality randomized trials to generate stronger evidence. Subsequent systematic reviews can then synthesize this evidence to inform future research and clinical guidelines.
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  • 文章类型: Systematic Review
    通过进行系统评价(SRs)概述,系统地总结当前证据,并确定太极拳治疗成人2型糖尿病(T2DM)的临床有效性和安全性。
    在2023年7月30日之前,进行了包含五个电子数据库的系统搜索,以基于有关太极拳治疗T2DM的随机对照试验(RCT)确定相关系统评价(SRs)。使用AMeaSurement工具评估系统评论(AMSTAR2)和系统评论中的偏倚风险(ROBIS)工具评估所包括SR的方法学质量。系统审查概述的首选报告项目(PRIO-harms)清单用于促进本概述中更平衡的利弊报告。校正后的覆盖面积(CCA)用于计算重叠的主要研究的程度。主要结局指标为糖化血红蛋白(HbA1c)和空腹血糖(FBG)。而次要结局包括与健康相关的质量指标.等级(建议等级,评估,发展,和评估)框架用于评估结果措施的证据质量。
    本概述中总共包括17个合格的SR。一位SR报告了负面结论,而其余16人报告了不同结局的阳性结果。共有4个SR报告了不良事件,缺席或轻微。大多数SR表现出严重低质量(15/17)和高偏见风险(14/17),如AMSTAR2和ROBIS所示,分别。CCA为12.14%,表明初级研究的高度重叠。使用GRADE方法评估了有关太极拳治疗T2DM的24个结局的135个结果的证据。其中大多数被评为非常低。
    太极拳有望成为成人T2DM患者的一种潜在有效且安全的生活方式干预措施。特别是在改善HbA1c方面,FBG,BMI,和整体生活质量(QoL)。然而,由于当前SRs中观察到的方法学缺陷以及基于GRADE的SRs质量较低,因此应谨慎解释这些结果。此外,迫切需要额外的精心设计,高质量的RCT和SRs,以建立关于太极拳在未来治疗T2DM的有效性的有力和确凿的证据。
    https://www.crd.约克。AC.英国/PROSPERO/,标识符CRD42019140988。
    UNASSIGNED: To systematically summarize current evidence and determine the clinical effectiveness and safety of Tai Chi for type 2 diabetes mellitus (T2DM) in adults by conducting an overview of systematic reviews (SRs).
    UNASSIGNED: A systematic search encompassing five electronic databases was conducted until July 30, 2023, to identify relevant systematic reviews (SRs) based on randomized controlled trials (RCTs) concerning Tai Chi for T2DM. The methodological quality of the included SRs was assessed using the A MeaSurement Tool to Assess systematic Reviews (AMSTAR 2) and the Risk of Bias in Systematic Reviews (ROBIS) tool. The Preferred Reporting Items for Overview of Systematic Review (PRIO-harms) checklist was used to promote a more balanced reporting of benefits and harms in this overview. Corrected covered area (CCA) was used to calculate the degree of overlapping primary studies. Primary outcome measures were glycosylated hemoglobin (HbA1c) and fasting blood glucose (FBG), while secondary outcomes encompassed health-related quality measures. The GRADE (Grades of Recommendations, Assessment, Development, and Evaluation) framework was utilized to assess the quality of evidence for the outcome measures.
    UNASSIGNED: A total of 17 eligible SRs were included in this overview. One SR reported negative conclusions, while the remaining 16 reported positive ones on different outcomes. A total of 4 SRs reported adverse events, either absent or minor. Most of the SRs exhibited critically low quality (15/17) and a high risk of bias (14/17), as indicated by AMSTAR2 and ROBIS, respectively. The CCA was 12.14%, indicating a high degree of primary study overlapping. Evidence from 135 results for 24 outcomes concerning Tai Chi for T2DM was evaluated using the GRADE approach, most of which were rated very low.
    UNASSIGNED: Tai Chi shows promise as a potentially effective and safe lifestyle intervention for adults with T2DM, particularly in improving HbA1c, FBG, BMI, and overall quality of life (QoL). However, these results should be cautiously interpreted due to methodological flaws observed in the current SRs and the low quality of the SRs based on GRADE. Furthermore, there is a compelling need for additional well-designed, high-quality RCTs and SRs to establish robust and conclusive evidence regarding the efficacy of Tai Chi for managing T2DM in the future.
    UNASSIGNED: https://www.crd.york.ac.uk/PROSPERO/, identifier CRD 42019140988.
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  • 文章类型: Journal Article
    背景:本研究旨在评估慢性前列腺炎/慢性盆腔疼痛综合征(CP/CPPS)的系统评价/荟萃分析(SRs/MAs)的方法学质量,使用评估系统评价工具(AMSTAR2),并探讨潜在的影响因素。
    方法:PubMed,搜索EMBASE和Cochrane图书馆数据库以进行相关研究。AMSTAR2用于评估合格SRs/MA的方法学质量。使用卡方检验比较了SRs/MA的方法学特征之间的差异。在实验前,使用类内相关系数(ICC)来评估审阅者的一致性。多因素回归分析用于确定影响方法学质量的潜在因素。
    结果:共包括45个SRs/MA。经过AMSTAR2评估,45个SR/MA中只有两个(4.4%)是中等的,三个(6.7%)被评为低质量,其余40例(88.9%)被评为严重低质量。在AMSTAR2的16个项目中,项目3和项目10的遵守情况最差。项目4收到的“部分是”答复数量最多。单变量分析表明,不同大陆之间(P=0.027)以及预先注册的SR与未注册的SR之间的方法学质量存在显着差异(P=0.004)。然而,在多变量分析中,方法学质量与以下研究特征之间没有显着关联:出版年份,大陆,报告是否遵循系统审查的首选报告项目(PRISMA),预注册,资金支持,随机对照试验(RCT)登记,SR是否发布在Cochrane系统评论数据库(CDSR)中,以及是否进行荟萃分析。此外,基于介入SRs/MA的亚组分析显示,通过单变量和多变量分析,大陆与CP/CPPS的SRs/MA的方法学质量独立相关。
    结论:我们的研究表明,CP/CPPS的SRs/MA的方法学质量普遍较差。CP/CPPS的SRs/MA应采用AMSTAR2,以提高其方法学质量。
    This study aimed to assess the methodological quality of the systematic reviews/meta-analyses (SRs/MAs) of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) using A Measurement Tool to Assess systematic Reviews (AMSTAR2) and to explore the potential influencing factors.
    PubMed, EMBASE and Cochrane Library databases were searched for relevant studies. AMSTAR2 was used for evaluating the methodological quality of eligible SRs/MAs. Differences between methodological characteristics of SRs/MAs were compared using chi-square tests. The intra-class correlation coefficient (ICC) was used to assess reviewer agreement in the pre-experiment. Multivariate regression analysis was used to identify potential factors affecting methodological quality.
    A total of 45 SRs/MAs were included. After AMSTAR2 evaluation, only two (4.4%) of 45 SRs/MAs were moderate, three (6.7%) were rated as low quality, and the remainder 40 (88.9%) were rated as critically low quality. Among the 16 items of AMSTAR2, item 3 and item 10 had the poorest adherence. Item 4 received the most significant number of \"Partial Yes\" responses. Univariable analysis indicated that there were significant differences in methodological quality in SRs between different continents (P = 0.027) as well as between preregistered SRs and those that were not (P = 0.004). However, in multivariate analysis, there was no significant association between methodological quality and the following research characteristics: publication year, continent, whether reporting followed Preferred Reporting Items for Systematic Reviews (PRISMA), preregistration, funding support, randomized controlled trials (RCT) enrollment, whether SR was published in the Cochrane Database of Systematic Reviews (CDSR), and whether with meta-analysis. Additionally, subgroup analysis based on interventional SRs/MAs showed that continent was independently associated with the methodological quality of SRs/MAs of CP/CPPS via univariable and multivariate analysis.
    Our study demonstrates that the methodological quality of SRs/MAs of CP/CPPS was generally poor. SRs/MAs of CP/CPPS should adopt the AMSTAR2 to enhance their methodological quality.
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  • 文章类型: Journal Article
    未经评估:已经发表了许多系统评价,比较了全膝关节置换术(TKA)中接受后稳定型(PS)和交叉保留(CR)手术的患者的预后,但是有一些重叠和矛盾。本研究的目的是(1)对TKA中PS与CR的比较进行当前系统评价的概述,通过评估他们的方法论质量和偏见风险,(2)通过最佳证据提供建议。
    未经评估:对比较TKA中PS和CR的系统评价进行系统搜索,在2021年6月之前发布的是使用MEDLINE进行的,EMBASE,和Cochrane图书馆数据库。通过AMSTAR2工具和ROBIS工具评估纳入的系统评价的方法学质量和偏倚风险,分别。最佳证据的选择是根据Jadad决策算法进行的。
    UNASSIGNED:共有8篇系统综述符合纳入本研究的条件。Jadad决策算法建议应选择AMSTAR2得分最高的评论。根据ROBIS工具,有3篇评价偏倚风险低,5篇评价偏倚风险高.因此,Verra等人进行的一项系统评价。选择AMSTAR2评分最高且偏倚风险低的证据作为最佳证据.
    UASSIGNED:尽管目前的系统评价显示PS和CR在临床表现和功能结局方面存在一些统计学差异,目前的结果指标不能为进行PS或CR提供建议。选择假体的决定主要基于外科医生的偏好,指标和其他指标。
    UNASSIGNED: Numerous systematic reviews have been published comparing the outcomes of patients undergoing posterior stabilized (PS) versus cruciate-retaining (CR) procedures in total knee arthroplasty (TKA), but with some overlaps and contradictions. The objectives of this study were (1) to perform an overview of current systematic reviews comparing PS versus CR in TKA, by evaluating their methodological quality and risk of bias, and (2) to provide recommendations through the best evidence.
    UNASSIGNED: A systematic search of systematic reviews comparing PS and CR in TKA, published until June 2021 was conducted using the MEDLINE, EMBASE, and Cochrane Library databases. Included systematic reviews were assessed for methodological quality and risk of bias by the AMSTAR2 instrument and ROBIS tool, respectively. The choice of best evidence was conducted according to the Jadad decision algorithm.
    UNASSIGNED: A total of eight systematic reviews were eligible for inclusion in this study. The Jadad decision algorithm suggested that reviews with the highest AMSTAR2 scores should be selected. According to the ROBIS tool, there were three reviews with a low risk of bias and five with a high risk of bias. Consequently, one systematic review conducted by Verra et al. with the highest AMSTAR2 score and low risk of bias was selected as the best evidence.
    UNASSIGNED: Although current systematic reviews demonstrated some statistical differences in clinical presentation and functional outcomes between PS and CR, the current outcome indicators cannot be taken to provide recommendations for undergoing PS or CR. The decision for prosthesis selection could be made mostly based on the surgeon\'s preference, indications and other indicators.
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  • 文章类型: Journal Article
    背景:艾迪注射液是中国食品药品监督管理局批准的中药注射剂之一,也是中国癌症治疗领域最具竞争力的产品。它由MylabrisPhalerata的提取物组成,黄芪,人参,和刺五加。
    目的:本概述旨在绘制艾迪注射液治疗癌症的系统评价(SRs)图,为临床实践和决策提供总结证据。
    方法:直到2020年12月,在七个数据库中搜索关于艾迪注射液用于癌症治疗的随机对照试验的SR和/或荟萃分析。六名作者成对独立确定的研究,收集的数据,并根据修订后的《多重系统评价》(AMSTAR2)和系统评价和荟萃分析首选报告项目(PRISMA)评估纳入研究的质量。叙事综合用于证据映射。
    结果:纳入艾迪注射液辅助治疗的52个SRs,涉及肺癌(20SR),肝癌(10),大肠癌(7),胃癌(6),淋巴瘤(2),乳腺癌(2),食管癌(1),卵巢癌(1),和不同癌症的混合(4)。除了一个专注于艾迪注射液的SR单独使用,其他SR评估了艾迪注射液与化疗的联合(43),放射治疗(4),或化学/放射学/靶向治疗(4)。艾迪注射液对存活显示出额外的有益作用(9),客观反应率(44),生活质量(42)和减少化疗/放疗的副作用(48)。使用AMSTAR2工具,两项审查被评估为低,其余评价为方法质量严重不足,主要是由于缺乏前瞻性注册.在搜索策略的报告中,PRISMA评估的报告质量不足(26,50.0%),附加分析(19,36.5%),和证据摘要(2,3.8%)。
    结论:已经评估了艾迪注射液对癌症生存的辅助有益作用,肿瘤反应,生活质量,减少化疗/放疗的副作用,主要集中在肺,肝癌和结直肠癌。方法和报告质量薄弱,今后需要改进。
    BACKGROUND: Aidi injection is one of the China Food and Drug Administration approved Chinese herbal injections and the most competitive product in cancer care in China. It is composed of the extracts from Mylabris Phalerata, Astragalus Membranaceus, Panax Ginseng, and Acanthopanax Senticosus.
    OBJECTIVE: This overview aims to map systematic reviews (SRs) of Aidi injection for cancer and provide a summarized evidence for clinical practice and decision making.
    METHODS: Seven databases were searched for SRs and/or meta-analyses of randomized controlled trials on Aidi injection for cancer care until December 2020. Six authors worked in pairs independently identified studies, collected data, and assessed the quality of included studies according to the revised Assessment of Multiple Systematic Reviews (AMSTAR 2) and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). A narrative synthesis was used for the evidence mapping.
    RESULTS: Fifty-two SRs on Aidi injection as adjuvant therapy were included, involving lung cancer (20 SRs), liver cancer (10), colorectal cancer (7), gastric cancer (6), lymphoma (2), breast cancer (2), esophageal cancer (1), ovary cancer (1), and a mix of different cancers (4). Except for one SR focusing on Aidi injection used alone, other SRs evaluated Aidi injection in combination with chemotherapy (43), radiotherapy (4), or chemo/radiology/targeting therapy (4). Aidi injection showed additional beneficial effects on survival (9), objective response rate (44), quality of life (42), and the reduction of side-effects from chemo/radiotherapy (48). Using AMSTAR 2 tool, two reviews were assessed as low and the rest as critically low methodological quality mainly due to the lack of prospective registration. The reporting quality was insufficient assessed with PRISMA in the reporting of search strategy (26, 50.0%), additional analysis (19, 36.5%), and the summary of evidence (2, 3.8%).
    CONCLUSIONS: Aidi injection has been evaluated for its adjuvant beneficial effects on cancer survival, tumor responses, quality of life, and reducing the side effects of chemo/radiotherapy, mainly focusing on lung, liver and colorectal cancer. The methodological and reporting quality are weak and need to be improved in the future.
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