expert consensus

专家共识
  • 文章类型: Journal Article
    重大创伤中心(MTC)护理与改善受伤患者的预后有关。英国的救护车服务和创伤网络目前使用一系列分诊工具来选择患者旁路到MTC。标准化的国家分诊工具可以提高分诊准确性,成本效益和决策的可重复性。
    我们进行了专家共识过程,以得出和开发一种主要的创伤分类工具,用于英国创伤网络。进行了基于网络的Delphi调查,以识别和确认主要创伤的候选分诊工具预测因子。召开了促进圆桌共识会议,以确认拟议的分类工具的目的,目标诊断阈值,范围,预期的人口和结构,以及个人分诊工具的预测因子和切点。举行了公众和患者参与(PPI)焦点小组,以确保分诊工具对服务用户的可接受性。
    Delphi调查就两个领域的9个分类变量达成共识,三轮后,从109个候选变量中提取。在协商一致会议期间对相关证据进行审查后,反复的讨论在分诊工具的以下方面达成了共识:参考标准,范围,目标诊断准确性和预期人群。包括生理学的三步工具,解剖损伤和临床判断领域,平行评估分诊变量,被推荐。分诊工具受到PPI焦点小组的好评。
    本文提出了一种新的专家共识得出的主要创伤分诊工具,具有明确的目的,范围,预期人口,结构,组成变量,变量定义和阈值。需要进行前瞻性评估以确定临床和成本效益,可接受性和可用性。
    UNASSIGNED: Major trauma centre (MTC) care has been associated with improved outcomes for injured patients. English ambulance services and trauma networks currently use a range of triage tools to select patients for bypass to MTCs. A standardised national triage tool may improve triage accuracy, cost-effectiveness and the reproducibility of decision-making.
    UNASSIGNED: We conducted an expert consensus process to derive and develop a major trauma triage tool for use in English trauma networks. A web-based Delphi survey was conducted to identify and confirm candidate triage tool predictors of major trauma. Facilitated roundtable consensus meetings were convened to confirm the proposed triage tool\'s purpose, target diagnostic threshold, scope, intended population and structure, as well as the individual triage tool predictors and cut points. Public and patient involvement (PPI) focus groups were held to ensure triage tool acceptability to service users.
    UNASSIGNED: The Delphi survey reached consensus on nine triage variables in two domains, from 109 candidate variables after three rounds. Following a review of the relevant evidence during the consensus meetings, iterative rounds of discussion achieved consensus on the following aspects of the triage tool: reference standard, scope, target diagnostic accuracy and intended population. A three-step tool comprising physiology, anatomical injury and clinical judgement domains, with triage variables assessed in parallel, was recommended. The triage tool was received favourably by PPI focus groups.
    UNASSIGNED: This paper presents a new expert consensus derived major trauma triage tool with defined purpose, scope, intended population, structure, constituent variables, variable definitions and thresholds. Prospective evaluation is required to determine clinical and cost-effectiveness, acceptability and usability.
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  • 文章类型: Journal Article
    异种移植的历史始于19世纪。经过几十年的调查,在全球范围内取得了重大突破和临床前里程碑。随着最近将转基因猪的肾脏和心脏移植到人类体内,这些开创性的成就引起了全世界的极大关注,希望异种移植可以缓解甚至解决器官短缺的问题。2022年1月20日,中国器官移植发展基金会召开了“历史,人类异种移植临床试验的现状和未来,“与会专家讨论了促进中国异种移植伦理和可持续发展的方法。作为专题讨论会的产物,达成了正式的共识,概述专家对科学的意见,监管,中国异种移植临床试验的伦理问题。
    The history of xenotransplantation started in the 19th century. After a few decades of investigation, significant breakthroughs and preclinical milestones have been achieved worldwide. With the recent transplantation of genetically modified porcine kidneys and heart into humans, these ground-breaking achievements have attracted great attention worldwide, in the hope that xenotransplantation might alleviate or even solve the problem of organ shortage. On January 20, 2022, the China Organ Transplantation Development Foundation convened a symposium on \"The History, Current Situation and Future of Human Xenotransplantation Clinical Trials,\" where ways to promote the ethical and sustainable development of xenotransplantation in China were discussed among the participating experts. A formal consensus was reached as the product of the symposium, outlining the expert opinions on scientific, regulatory, and ethical issues of clinical trials of xenotransplantation in China.
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  • 文章类型: Journal Article
    生活质量(QoL)评估是癌症护理不可或缺的一部分,然而,它们在提供支持幸存者的基本信息方面的有效性各不相同。本研究旨在从医疗保健专业人员的角度阐明结直肠癌幸存者QoL的关键指标,并评估与这些指标相关的现有QoL问卷。进行了两项研究:一项Delphi研究,以确定关键的QoL指标,并对适合结直肠癌幸存者的问卷进行范围审查。54名医疗保健专业人员参加了德尔福研究的第一轮,第二个是25。该研究确定了两个主要的QoL领域(生理和心理)和17个被认为最关键的子领域。此外,对12份问卷的审查显示了两种评估最重要一般领域的工具。研究结果强调了现有评估工具与医疗保健专业人员在结直肠癌幸存者工作中的临床优先事项之间的不一致。为了增强对幸存者QoL的支持,需要努力开发更符合临床实践中常规QoL评估要求的工具。
    Quality of life (QoL) assessments are integral to cancer care, yet their effectiveness in providing essential information for supporting survivors varies. This study aimed to elucidate key indicators of QoL among colorectal cancer survivors from the perspective of healthcare professionals, and to evaluate existing QoL questionnaires in relation to these indicators. Two studies were conducted: a Delphi study to identify key QoL indicators and a scoping review of questionnaires suitable for colorectal cancer survivors. Fifty-four healthcare professionals participated in the Delphi study\'s first round, with 25 in the second. The study identified two primary QoL domains (physical and psychological) and 17 subdomains deemed most critical. Additionally, a review of 12 questionnaires revealed two instruments assessing the most important general domains. The findings underscored a misalignment between existing assessment tools and healthcare professionals\' clinical priorities in working with colorectal cancer survivors. To enhance support for survivors\' QoL, efforts are needed to develop instruments that better align with the demands of routine QoL assessment in clinical practice.
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  • 文章类型: Journal Article
    精神分裂症患者(PWS)的护理通常由社区心理健康团队在门诊提供。然而,PWS经常需要住院治疗,因为广泛的临床,个人和/或社会情况。不幸的是,根据我们的知识,在PWS的出院决策过程中没有可用的指南来帮助精神科医生.该项目的目的是就PWS在急性住院精神病院后的出院标准达成专家共识。
    使用改良的Delphi方法,整个西班牙的42名精神科医生评估了有关此问题的四个感兴趣领域:临床症状学,治疗相关因素,出院后的后续保健单位,以及身体健康和监测。
    两轮后,在64份声明中,59份(92.2%)声明达成共识。在关于“临床症状学”的17项陈述中的3项(17.7%)和关于“出院后随访保健单位”的15项陈述中的2项(13.3%),没有达成共识;相比之下,所有关于“治疗相关因素”和“身体健康和监测”的陈述都达成了共识。共识结果强调了出院控制症状而不是入院时抑制症状的重要性,以及在选择抗精神病药物时的耐受性。
    尽管缺乏相关数据来指导PWS在急性住院精神病院住院后的出院,我们希望这种基于专家意见的共识可能有助于临床医生做出适当的决定.
    UNASSIGNED: The care of people with schizophrenia (PWS) is usually provided in an outpatient setting by community mental health teams. However, PWS frequently require inpatient treatment because of a wide array of clinical, personal and/or social situations. Unfortunately, to our knowledge, there are no guidelines available to help psychiatrists in the decision-making process on hospital discharge for PWS. The aim of this project was to develop an expert consensus on discharge criteria for PWS after their stay in an acute inpatient psychiatric unit.
    UNASSIGNED: Using a modified Delphi method a group of 42 psychiatrists throughout Spain evaluated four areas of interest regarding this issue: clinical symptomatology, treatment-related factors, follow-up health care units after discharge, and physical health and monitoring.
    UNASSIGNED: After two rounds, among the 64 statements, a consensus was reached for 59 (92.2%) statements. In three (17.7%) of the 17 statements on \'clinical symptomatology\' and 2 (13.3%) of the 15 statements on \'follow-up health care units after discharge\', a consensus was not reached; in contrast, a consensus was reached for all statements concerning \'treatment-related factors\' and those concerning \'physical health and monitoring\'. The consensus results highlight the importance for discharge of the control of symptoms rather than their suppression during admission and of tolerability in the selection of anantipsychotic.
    UNASSIGNED: Although there is a lack of relevant data for guiding the discharge of PWS after hospitalization in an acute inpatient psychiatric unit, we expect that this consensus based on expert opinion may help clinicians to take appropriate decisions.
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  • 文章类型: English Abstract
    拔牙是口腔颌面外科中常见且广泛使用的治疗方法。微创拔牙可以减少患者的生理和心理创伤,并被广泛推荐作为一线临床治疗。但是目前尚无指南或共识来系统地介绍微创拔牙来指导临床实践。为了解决这个问题,这一共识,基于全面的文献综述和专家的临床经验,系统地总结了适应症,目标患者,和微创拔牙的禁忌症,该程序的总体工作流程(术前准备,手术步骤,术后管理,术后指导,药物,和后续行动),及其术后常见并发症,为该技术的临床应用提供全面指导。
    Tooth extraction is a common and widely employed therapeutic procedure in oral and maxillofacial surgery. Minimally invasive tooth extraction can reduce both physical and psychological trauma to the patients, and is widely recommended as a first-line clinical treatment. But currently no guidelines or consensus has been available to provide a systematic introduction of minimally invasive tooth extraction to guide the clinical practices. To address this issue, this consensus, based on a comprehensive literature review and clinical experiences of experts, systematically summarizes the indications, target patients, and contraindications of minimally invasive tooth extraction, the overall workflow of this procedure (preoperative preparation, surgical steps, postoperative management, postoperative instructions, medications, and follow-up), and its common postoperative complications to provide a comprehensive guidance for clinical application of this technique.
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  • 文章类型: Journal Article
    患者来源的类器官(PDO)已成为临床和转化研究的有希望的平台。临床结果与使用PDO来预测化疗和/或放疗的功效之间存在很强的相关性。规范解读,加强癌症精准医学领域的科学交流,我们重新审视基于PDO的药物敏感性试验(DST)的概念.我们提出了一种专家共识驱动的药物选择方法,旨在预测患者的反应。为了进一步标准化基于PDO的DST,我们提出了澄清和表征的指导方针。此外,我们确定了使用PDO时临床预测的几个主要挑战。
    Patient-derived organoids (PDOs) have emerged as a promising platform for clinical and translational studies. A strong correlation exists between clinical outcomes and the use of PDOs to predict the efficacy of chemotherapy and/or radiotherapy. To standardize interpretation and enhance scientific communication in the field of cancer precision medicine, we revisit the concept of PDO-based drug sensitivity testing (DST). We present an expert consensus-driven approach for medication selection aimed at predicting patient responses. To further standardize PDO-based DST, we propose guidelines for clarification and characterization. Additionally, we identify several major challenges in clinical prediction when utilizing PDOs.
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  • 文章类型: Journal Article
    中国一直在不断改进其监测方法和策略,以应对关键传染病(KID)。在2003年严重急性呼吸系统综合症流行之后,中国建立了传染病(ID)和突发公共卫生事件的综合报告制度。相对滞后的警告阈值,有限的警告信息,和过时的警告技术不足以满足对现代KID进行全面监控的需求。加强早期监测预警能力,增强公共卫生体系已成为当务之急,随着对预警阈值的需求不断增加,信息,和技术,得益于分子生物学的不断创新和发展,生物信息学,人工智能,以及其他识别和分析技术。由31名专家组成的小组推荐了针对KID(41种应报告疾病和新出现的ID)的第四代综合监测系统。该监测系统的目的是系统地监测人等宿主中KIDs的流行病学和致病性病原体,动物,和向量,以及相关的环境病原体。通过整合影响疫情传播的因素和风险评估,监视系统可以用来检测,预测,并提供早期预警,发展,变异,以及已知或新颖的KID的传播。此外,我们建议基于第四代监控系统进行全面的身份监控,以及数据集成的监测和预警平台和联合病原体检测技术系统。这一系列考虑是基于跨多个部门的系统和全面监测,尺寸,因素,以及数据集成和连接支持的病原体。这种专家共识将为各个领域的合作提供机会,并依靠跨学科应用来加强全面监测,预测,以及下一代身份监控的预警能力。这一专家共识将作为ID预防和控制以及其他相关活动的参考。
    China has been continuously improving its monitoring methods and strategies to address key infectious diseases (KIDs). After the severe acute respiratory syndrome epidemic in 2003, China established a comprehensive reporting system for infectious diseases (IDs) and public health emergencies. The relatively lagging warning thresholds, limited warning information, and outdated warning technology are insufficient to meet the needs of comprehensive monitoring for modern KIDs. Strengthening early monitoring and warning capabilities to enhance the public health system has become a top priority, with increasing demand for early warning thresholds, information, and techniques, thanks to constant innovation and development in molecular biology, bioinformatics, artificial intelligence, and other identification and analysis technologies. A panel of 31 experts has recommended a fourth-generation comprehensive surveillance system targeting KIDs (41 notifiable diseases and emerging IDs). The aim of this surveillance system is to systematically monitor the epidemiology and causal pathogens of KIDs in hosts such as humans, animals, and vectors, along with associated environmental pathogens. By integrating factors influencing epidemic spread and risk assessment, the surveillance system can serve to detect, predict, and provide early warnings for the occurrence, development, variation, and spread of known or novel KIDs. Moreover, we recommend comprehensive ID monitoring based on the fourth-generation surveillance system, along with a data-integrated monitoring and early warning platform and a consortium pathogen detection technology system. This series of considerations is based on systematic and comprehensive monitoring across multiple sectors, dimensions, factors, and pathogens that is supported by data integration and connectivity. This expert consensus will provides an opportunity for collaboration in various fields and relies on interdisciplinary application to enhance comprehensive monitoring, prediction, and early warning capabilities for the next generation of ID surveillance. This expert consensus will serve as a reference for ID prevention and control as well as other related activities.
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  • 文章类型: Journal Article
    经鼻加湿快速吹气换气(THRIVE)是一种安全的,有效,以及目前用于电惊厥治疗(ECT)的新技术。本研究旨在总结在ECT中使用THRIVE的临床实践,以帮助医生和机构实施ECT的最佳实践指南。因此,我们回顾了目前的文献,并就THRIVE在ECT的日常临床实践中的应用提出了共识.该共识提供了有关ECT中使用THRIVE的信息,包括它的安全性,有效性,程序,预防措施,特殊案件管理,以及在特殊人群中的应用。此外,它指导ECT中THRIVE的标准化使用。
    Transnasal humidified rapid-insufflation ventilatory exchange (THRIVE) is a safe, effective, and novel technique that is currently being used in electroconvulsive therapy (ECT). This study aimed to summarize the clinical practices of THRIVE use in ECT to aid physicians and institutions in implementing the best practice guidelines for ECT. Thus, we reviewed the current literature and presented our consensus on the application of THRIVE in ECT in daily clinical practice. This consensus provides information regarding THRIVE use in ECT, including its safety, effectiveness, procedures, precautions, special case management, and application in special populations. Moreover, it guides the standardized use of THRIVE in ECT.
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  • 文章类型: English Abstract
    Daytime hip arthroplasty refers to a medical procedure where a patient undergoes admission, surgery, and discharge all within a single day (24 hours). The establishment of daytime hip arthroplasty centers signifies a significant paradigm shift in the development model of modern hospitals. While numerous nationally accredited large medical institutions are undertaking daytime hip arthroplasty in various forms and scales, there remains a lack of standardized system processes and criteria. In this context, the National Clinical Research Center for Geriatric Disorders (Xiangya Hospital), Bone and Joint Specialty Committee of the China Ambulatory Surgery Alliance, Joint Surgery Branch of the Chinese Orthopedic Association, and Osteoarthritis Study Group of the Chinese Association of Orthopedic Surgeons have collaboratively organized experts in the relevant field domestically. Leveraging international experiences in daytime hip arthroplasty and integrating them with the clinical practices of well-established medical institutions conducting daytime surgeries in China, they have arrived at consensus recommendations. These recommendations cover the establishment of daytime hip arthroplasty centers, policies, procedures, and perioperative management. The ultimate goal is to provide reference points and guidance for the standardized implementation of daytime hip arthroplasty.
    日间髋关节置换手术是指接受髋关节置换手术患者在1 d(24 h)内完成入院、手术和出院的医疗模式。设置日间髋关节置换手术中心是适应现代医院发展模式的重大转变。全国已有部分大型医院以不同形式和规模开展了日间髋关节置换手术,但尚缺乏统一的制度规范和流程。在此背景下,国家老年疾病临床医学研究中心(湘雅医院)、中国日间手术合作联盟骨关节专业委员会、中华医学会骨科学分会关节外科学组和中国医师协会骨科医师分会骨关节炎学组联合组织国内相关领域专家,借鉴国际日间髋关节置换手术经验,结合国内开展日间手术的临床实践,从日间髋关节置换手术中心的设置、制度、流程以及围术期管理达成共识,旨在为规范化开展日间髋关节置换手术提供参考和指导。.
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  • 文章类型: Journal Article
    随着多种免疫检查点抑制剂(ICIs)的批准,乳腺癌(BC)的免疫治疗取得了重大进展,特别是在早期和转移性三阴性乳腺癌(TNBC)设置。大多数指南都推荐免疫疗法作为BC的重要方法,然而,几个关键方面仍需要进一步澄清,包括适当的病人选择,治疗持续时间,优化的化疗伙伴,预测性生物标志物,以及对中国患者的具体考虑。
    (一)专家组成立:专家组由32名来自内科肿瘤等科室的专家组成,乳房手术,和病理学;(二)文献检索:主要在英文数据库(如PubMed,Embase,和Cochrane图书馆)和中文数据库(如中国国家知识基础设施,中国生物医药光盘,和万方数据库),搜索截止日期为2024年4月23日;(三)证据质量和推荐力度评估:根据中国临床肿瘤学会(CSCO)指南的证据类别和推荐水平对证据质量和推荐意见进行分级;(四)共识制定:2024年3月2日,通过在线共识会议,对共识内容进行了深入讨论,并征求所有专家的意见。
    共识会议提出了15项详细建议,为免疫治疗在BC管理中的临床应用提供更清晰的指导。核心建议如下:对于一线设置的早期II-III期TNBC和转移性TNBC(mTNBC),程序性细胞死亡蛋白1(PD-1)抑制剂可以考虑。然而,对于激素受体阳性/人表皮生长因子受体2阴性BC(HR/HER2-BC),HER2+BC,和mTNBC在后来的治疗中,缺乏支持使用免疫治疗的证据.
    这一共识提供了BC免疫治疗的全面概述,包括早期BC和晚期BC的免疫疗法,免疫相关不良事件(irAE)管理,免疫疗法的生物标志物,和未来的方向。协商一致意见将这些审议合并为15项基于证据的建议,作为临床医生更科学,更系统地管理免疫治疗的临床应用的实践指南。
    UNASSIGNED: Significant progress has been made in immunotherapy of breast cancer (BC) with the approval of multiple immune checkpoint inhibitors (ICIs), particularly in early and metastatic triple-negative breast cancer (TNBC) settings. Most guidelines have recommended immune therapy as the important approach in BC, yet several critical aspects still require further clarification, including proper patient selection, treatment duration, optimized chemotherapy partner, predictive biomarkers, and specific considerations for Chinese patients.
    UNASSIGNED: (I) Establishment of expert group: the expert group consists of 32 experts from departments such as medical oncology, breast surgery, and pathology; (II) literature search: mainly conducted in English databases (such as PubMed, Embase, and Cochrane Library) and Chinese databases (such as China National Knowledge Infrastructure, China Biology Medicine disc, and Wanfang Database), with a search cutoff date of April 23, 2024; (III) assessment of evidence quality and recommendation strength: evidence quality and recommendation opinions are graded based on the evidence category and recommendation level of the Chinese Society of Clinical Oncology (CSCO) guidelines; (IV) consensus formulation: on the March 2, 2024, through online consensus meeting, the consensus content is thoroughly discussed, and opinions from all experts are solicited.
    UNASSIGNED: The consensus meeting has resulted in 15 detailed recommendations, providing clearer guidance on the clinical application of immunotherapy in BC management. The core suggestions are as follows: for early-stage II-III TNBC and metastatic TNBC (mTNBC) in the first-line setting, programmed cell death protein 1 (PD-1) inhibitors can be considered. However, for hormone receptor-positive/human epidermal growth factor receptor 2-negative BC (HR+/HER2- BC), HER2+ BC, and mTNBC in later lines of therapy, evidence is lacking to support the use of immunotherapy.
    UNASSIGNED: This consensus provides a comprehensive overview of BC immunotherapy, including immunotherapy for early-stage BC and late-stage BC, immune related adverse event (irAE) management, biomarkers of immunotherapy, and future directions. The consensus consolidates these deliberations into 15 evidence-based recommendations, serving as a practical guide for clinicians to more scientifically and systematically manage the clinical application of immunotherapy.
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