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Methylphenidate denied access to WHO's list of essential medicines for the third time. 哌甲酯第三次被拒绝使用世卫组织的基本药物清单。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-08 DOI: 10.1136/bmjebm-2025-114219
Ole Jakob Storebø, Henriette Edemann-Callesen, Johanne Pereira Ribeiro, Sophie Juul, Sabrina Katja Nestved, Helene Speyer, Andreas Hoff, Charlotte Lunde, Christian Gluud
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引用次数: 0
Using and distinguishing evidence from non-randomised studies of interventions. 使用和区分来自非随机干预研究的证据。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-07 DOI: 10.1136/bmjebm-2025-114125
Jamie Hartmann-Boyce, Nicola Lindson, Lisa Bero, Jo Dumville, Ella Flemyng, Barney Reeves, Peter Tugwell, David B Wilson, Hugh Sharma Waddington
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引用次数: 0
Evaluating the performance of maternal risk factors in predicting gestational diabetes mellitus: a systematic review and meta-analysis. 评估母体危险因素在预测妊娠期糖尿病中的表现:一项系统回顾和荟萃分析。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-23 DOI: 10.1136/bmjebm-2025-114065
Alemu Degu Ayele, Getnet Gedefaw Azeze, Beklau Kassie Alemu, Yao Wang, Chi Chiu Wang

Objective: To systematically consolidate the most consistently applicable risk factors and assess their predictive performance for gestational diabetes mellitus (GDM) prediction.

Design: Systematic review and meta-analysis.

Data sources: A comprehensive search included several databases (PubMed, Web of Science, Scopus, EMBASE via OVID and CINAHL) from inception to 30 October 2024.

Review: Methods prediction studies conducted in pregnant women during the first and second trimesters were included. Predictive parameters, including true positive, false positive, false negative and true negative values for each factor, were extracted from the 2×2 table. The Prediction model Risk Of Bias ASsessment Tool (PROBAST) was used to evaluate the risk of bias and the applicability of the included studies. A predictive meta-analysis was performed using Stata V.17. Variability was assessed through subgroup analysis.

Results: Seventy-seven eligible studies involving a total of 477 673 participants were included. Among these, 52 had an overall low risk of bias, and 65 demonstrated low concern regarding applicability. Common risk factors used to predict GDM included maternal age, body mass index (BMI), ethnicity, family history of diabetes mellitus (DM), previous GDM, previous macrosomia, multiparity, hypertensive disorders of pregnancy (HDP) and polycystic ovarian syndrome (PCOS). Among all factors, previous macrosomia showed the highest discriminatory power (area under the curve (AUC)=0.77), followed by previous GDM (AUC=0.73), PCOS (AUC=0.66), BMI (AUC=0.65), family history of DM (AUC=0.64), HDP (AUC=0.64), age over 30 (AUC=0.60), Asian ethnicity (AUC=0.59) and multiparity (AUC=0.56). A combination of age, BMI, family history of DM, previous GDM, ethnicity and multiparity achieved the highest AUC of 0.88, followed by the combination of age, BMI, family history of DM and previous GDM, with an AUC of 0.75.

Conclusions: Previous macrosomia and previous GDM are clinically essential risk factors with the highest discriminatory power, indicated by an AUC >0.7. Combining risk factors improves predictive performance, reaching an AUC of 0.88. Our findings highlight the need to enhance existing risk-based screening tools for early detection of GDM and to prevent its adverse pregnancy outcomes and future cardiometabolic risks.

Prospero registration number: CRD 42024598399.

目的:系统整合最一致适用的危险因素并评价其对妊娠期糖尿病(GDM)的预测效果。设计:系统回顾和荟萃分析。数据来源:全面检索了从成立到2024年10月30日的几个数据库(PubMed, Web of Science, Scopus, EMBASE via OVID和CINAHL)。回顾:方法预测研究在妊娠早期和中期进行了纳入。从2×2表中提取预测参数,包括每个因素的真阳性、假阳性、假阴性和真阴性值。采用预测模型偏倚风险评估工具(PROBAST)对纳入研究的偏倚风险和适用性进行评估。使用Stata V.17进行预测荟萃分析。通过亚组分析评估变异性。结果:纳入77项符合条件的研究,共纳入477 673名受试者。其中,52个总体偏倚风险低,65个表现出对适用性的低关注。用于预测GDM的常见危险因素包括产妇年龄、体重指数(BMI)、种族、糖尿病家族史、既往GDM、既往巨大儿、多胎、妊娠高血压疾病(HDP)和多囊卵巢综合征(PCOS)。在所有因素中,既往巨大儿的区别程度最高(曲线下面积(AUC)=0.77),其次是既往GDM (AUC=0.73)、PCOS (AUC=0.66)、BMI (AUC=0.65)、DM家族史(AUC=0.64)、HDP (AUC=0.64)、30岁以上(AUC=0.60)、亚裔(AUC=0.59)和多胎(AUC=0.56)。年龄、BMI、糖尿病家族史、既往GDM、种族和多胎合并的AUC最高,为0.88,其次是年龄、BMI、糖尿病家族史和既往GDM, AUC为0.75。结论:既往巨大儿和既往GDM是临床必要的危险因素,其鉴别力最高,AUC为0.7。综合风险因素可提高预测性能,AUC达到0.88。我们的研究结果强调需要加强现有的基于风险的筛查工具,以早期发现GDM,并预防其不良妊娠结局和未来的心脏代谢风险。普洛斯彼罗注册号:CRD 42024598399。
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引用次数: 0
Reporting GUideline for Intervention DEscription in Rehabilitation (GUIDE-Rehab): a tool to open the 'black box' of rehabilitation complex interventions. 康复干预措施描述报告指南(GUIDE-Rehab):打开康复复杂干预措施“黑盒子”的工具。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-21 DOI: 10.1136/bmjebm-2025-113997
Stefano Negrini, Chiara Arienti, Susan Armijo-Olivo, Pierre Côté, Allen Walter Heinemann, Carlotte Kiekens, Dinesh Kumbhare, William Levack, Thorsten Meyer-Feil, John Whyte

In 2023, the World Health Assembly adopted a resolution to strengthen rehabilitation within health systems, calling for rehabilitation research. Within health, the term rehabilitation has multiple meanings, including a core strategy, a sector, a service and an intervention. The latter has been defined as complex and characterised as a 'black box', similar to complex interventions in other fields. The existing reporting guidelines are not sufficiently effective in describing interventions within the rehabilitation field. We developed the GUideline for Intervention DEscription in Rehabilitation (GUIDE-Rehab) to address these challenges.According to the Enhancing the QUAlity and Transparency Of health Research Network, we followed a Delphi process with multiple Consensus Meetings and piloting and used ACcurate COnsensus Reporting Document for reporting. The background research involved 21 papers. We based GUIDE-Rehab on the Rehabilitation Treatment Specification System, developed over 15 years of research to improve rehabilitation description; the definition of rehabilitation for research purposes; and the Template for Intervention Description and Replication reporting guideline. 68 representatives from global rehabilitation stakeholders (scientific societies, journals, evidence and methods groups), including individuals with lived experience of disability, from 26 countries across all continents and economies, participated. The piloting involved 17 chief editors, 7 research groups and participants from 10 scientific meetings.The complete version comprises 16 items, while the version for uncontrolled studies includes 13. The short version (10 items for text, 6 for appendix) helps reduce the manuscripts' length. The GUIDE-Rehab graphical illustration (nine items) facilitates the intervention description. GUIDE-Rehab will assist in the reporting of interventions in rehabilitation to enhance clinical research and support clinical implementation.

2023年,世界卫生大会通过了一项加强卫生系统内康复的决议,呼吁开展康复研究。在卫生领域,康复一词有多重含义,包括一项核心战略、一个部门、一项服务和一项干预。后者被定义为复杂的,并被定性为“黑箱”,类似于其他领域的复杂干预。现有的报告准则在描述康复领域内的干预措施方面不够有效。为了应对这些挑战,我们制定了康复干预描述指南(GUIDE-Rehab)。根据提高卫生研究网络的质量和透明度,我们遵循了德尔福过程,包括多次共识会议和试点,并使用准确的共识报告文件进行报告。背景研究涉及21篇论文。我们以康复治疗规范系统为基础,开发了超过15年的研究,以改善康复描述;为研究目的而对康复的定义;以及干预措施描述和复制报告指南模板。来自各大洲和各经济体26个国家的全球康复利益攸关方(科学学会、期刊、证据和方法小组)的68名代表参加了会议,其中包括有残疾经历的个人。该试点项目涉及17位主编、7个研究小组和来自10个科学会议的与会者。完整版本包括16个项目,而非对照研究版本包括13个项目。简短的版本(正文10项,附录6项)有助于减少手稿的长度。指南-康复图解(九项)有助于干预措施的描述。康复指南将协助报告康复干预措施,以加强临床研究和支持临床实施。
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引用次数: 0
Environmental Lessons Learned and Applied (ELLA): a new framework for identifying, prioritising and implementing decarbonisation interventions in clinical care pathways. 环境经验教训和应用(ELLA):在临床护理途径中识别,优先考虑和实施脱碳干预的新框架。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-19 DOI: 10.1136/bmjebm-2025-113911
Joseph B John, William K Gray, Chantelle Rizan, Kristin J Konnyu, Forbes McGain, Manraj Phull, John Ford, Paula R Williamson, Edward Nickell, Kieran O'Flynn, Tim Briggs, John S McGrath

A multidisciplinary framework for designing rapidly deployable, scalable and context-specific decarbonisation interventions for clinical care has been developed within the National Health Service, devised at a care pathway level to identify modifiable emissions hotspots while addressing wider priority outcomes and implementation.

英国国家卫生服务体系(National Health Service)已经制定了一个多学科框架,用于为临床护理设计快速部署、可扩展和特定环境的脱碳干预措施,该框架在护理路径层面设计,以确定可修改的排放热点,同时解决更广泛的优先结果和实施问题。
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引用次数: 0
Ataluren for Duchenne: how politics and social pressure undermined evidence-based decisions. 杜兴的Ataluren:政治和社会压力如何破坏循证决策。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-13 DOI: 10.1136/bmjebm-2025-113995
Juan Erviti, Luis Carlos Saiz, Marta Gutiérrez-Valencia
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引用次数: 0
Regression to the mean: a primer for evidence-based medicine practitioners. 回归均值:循证医学从业者入门。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-13 DOI: 10.1136/bmjebm-2025-113948
Mohammad Hassan Murad, Neha Ramachandran, Lifeng Lin, Fan Li
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引用次数: 0
Less is more - but for whom? Evaluating patient reported outcomes in de-implementation. 少即是多——但对谁来说呢?评估患者报告的取消实施的结果。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-08 DOI: 10.1136/bmjebm-2025-113957
Eva Willemiek Verkerk, Paula Riganti
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引用次数: 0
Opportunities, challenges and risks of using artificial intelligence for evidence synthesis. 利用人工智能进行证据合成的机遇、挑战和风险。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-01 DOI: 10.1136/bmjebm-2024-113320
Waldemar Siemens, Erik von Elm, Harald Binder, Daniel Böhringer, Angelika Eisele-Metzger, Gerald Gartlehner, Piet Hanegraaf, Maria-Inti Metzendorf, Jacob-Jan Mosselman, Artur Nowak, Riaz Qureshi, James Thomas, Siw Waffenschmidt, Valérie Labonté, Joerg J Meerpohl
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引用次数: 0
AI in healthcare: an introduction for clinicians. 医疗保健中的人工智能:临床医生介绍。
IF 7.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-01 DOI: 10.1136/bmjebm-2024-112966
Ahmed Maiter, Samer Alabed, Genevera Allen, Fares Alahdab
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BMJ Evidence-Based Medicine
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