Recommendation

建议
  • 文章类型: Journal Article
    背景:肺炎支原体(M.肺炎)是儿童社区获得性肺炎的重要原因。自1968年以来,日本最初报道了对大环内酯类抗生素耐药的肺炎支原体菌株,大环内酯耐药肺炎支原体(MRMP)已在世界许多国家被证明,发病率不同。MRMP感染导致对大环内酯类抗生素的反应不佳,经常导致长时间的发烧,延长抗生素治疗,住院率增加,重症监护室入院,接受糖皮质激素或二线抗生素的患者比例明显更高。自2000年以来,MRMP的全球发病率逐渐上升,尤其是在东亚,对儿童肺炎支原体感染的治疗提出了严峻的挑战,引起了儿科医生的广泛关注。然而,关于儿童MRMP的诊断和治疗仍未达成全球共识.
    方法:我们组织了29名中国儿科肺病学和流行病学专家,撰写了世界上第一个关于小儿MRMP肺炎诊断和治疗的共识,基于证据收集。使用电子数据库进行证据搜索和审查,包括PubMed,Embase,WebofScience,CNKI,Medline,还有Cochrane图书馆.我们在术语“大环内酯抗性”中使用了变体,“肺炎支原体”,\"MP\",\"M.肺炎\“,\"肺炎\",\"MRMP\",“下呼吸道感染”,“肺炎支原体感染”,\"children\",和“儿科”。
    结果:流行病学,发病机制,临床表现,早期识别,实验室检查,抗生素使用原则,糖皮质激素和静脉注射免疫球蛋白的应用,并强调支气管镜检查的注意事项。现在,通过呼吸道标本中的聚合酶链反应和荧光探针技术,可以早期快速鉴定与MRMP相关的基因突变。尽管对大环内酯的耐药率仍然很高,幸运的是,肺炎支原体仍然对四环素和喹诺酮类药物等二线抗生素保持良好的体外敏感性,使它们成为由大环内酯类抗生素引起的初始治疗失败的患者的有效治疗选择。
    结论:这一共识,基于国际和国家科学证据,为儿童MRMP的诊断和治疗提供科学指导。迫切需要对儿童四环素和喹诺酮类药物进行进一步研究,以评估其对生长发育的影响。此外,制定抗生素轮换治疗策略对于降低MRMP菌株的患病率是必要的.
    BACKGROUND: Mycoplasma pneumoniae (M. pneumoniae) is a significant contributor to community-acquired pneumonia among children. Since 1968, when a strain of M. pneumoniae resistant to macrolide antibiotics was initially reported in Japan, macrolide-resistant M. pneumoniae (MRMP) has been documented in many countries worldwide, with varying incidence rates. MRMP infections lead to a poor response to macrolide antibiotics, frequently resulting in prolonged fever, extended antibiotic treatment, increased hospitalization, intensive care unit admissions, and a significantly higher proportion of patients receiving glucocorticoids or second-line antibiotics. Since 2000, the global incidence of MRMP has gradually increased, especially in East Asia, which has posed a serious challenge to the treatment of M. pneumoniae infections in children and attracted widespread attention from pediatricians. However, there is still no global consensus on the diagnosis and treatment of MRMP in children.
    METHODS: We organized 29 Chinese experts majoring in pediatric pulmonology and epidemiology to write the world\'s first consensus on the diagnosis and treatment of pediatric MRMP pneumonia, based on evidence collection. The evidence searches and reviews were conducted using electronic databases, including PubMed, Embase, Web of Science, CNKI, Medline, and the Cochrane Library. We used variations in terms for \"macrolide-resistant\", \"Mycoplasma pneumoniae\", \"MP\", \"M. pneumoniae\", \"pneumonia\", \"MRMP\", \"lower respiratory tract infection\", \"Mycoplasma pneumoniae infection\", \"children\", and \"pediatric\".
    RESULTS: Epidemiology, pathogenesis, clinical manifestations, early identification, laboratory examination, principles of antibiotic use, application of glucocorticoids and intravenous immunoglobulin, and precautions for bronchoscopy are highlighted. Early and rapid identification of gene mutations associated with MRMP is now available by polymerase chain reaction and fluorescent probe techniques in respiratory specimens. Although the resistance rate to macrolide remains high, it is fortunate that M. pneumoniae still maintains good in vitro sensitivity to second-line antibiotics such as tetracyclines and quinolones, making them an effective treatment option for patients with initial treatment failure caused by macrolide antibiotics.
    CONCLUSIONS: This consensus, based on international and national scientific evidence, provides scientific guidance for the diagnosis and treatment of MRMP in children. Further studies on tetracycline and quinolone drugs in children are urgently needed to evaluate their effects on the growth and development. Additionally, developing an antibiotic rotation treatment strategy is necessary to reduce the prevalence of MRMP strains.
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  • 文章类型: Journal Article
    背景:最近的出版物强调需要更新的建议,以解决<2厘米肿瘤的根治性手术,诱导化疗,或局部晚期宫颈癌的免疫疗法,以及复发或转移性宫颈癌的全身治疗。目的:总结目前诊断的证据,治疗,和宫颈癌的随访并提供循证临床实践建议。方法:根据AGREEII标准开发,该指南根据卫生技术评估和关税系统标准对科学证据进行分类。建议根据发展小组的证据强度和共识水平进行分级。主要结果:(1)早期癌症:基质浸润和淋巴血管间隙受累(LVSI)从预处理活检确定候选手术,特别是简单的子宫切除术。(2)手术方式:不建议进行微创手术,除了T1A,LVSI阴性肿瘤,由于预期寿命的减少。(3)局部晚期癌症:同步放化疗(CCRT),然后进行近距离放射治疗(BRT)是基础治疗。低风险患者(少于两个转移淋巴结或FIGOIB2-II)可以在7天后考虑诱导化疗(ICT),然后进行CCRT和BRT。高风险患者(两个或更多转移性淋巴结或FIGOIIIA,IIIB,和IVA)受益于pembrolizumab与CCRT和维持治疗。(4)转移,持久性,和复发癌症:来自预处理活检的PD-L1状态可识别Pembrolizumab与可用的全身治疗的候选者,而三联疗法(阿替珠单抗/贝伐单抗/化疗)成为PD-L1非依赖性选择。结论:这些循证指南旨在通过基于个体风险因素的精确治疗策略来改善临床结果。预测因子,和疾病阶段。
    Background: Recent publications underscore the need for updated recommendations addressing less radical surgery for <2 cm tumors, induction chemotherapy, or immunotherapy for locally advanced stages of cervical cancer, as well as for the systemic therapy for recurrent or metastatic cervical cancer. Aim: To summarize the current evidence for the diagnosis, treatment, and follow-up of cervical cancer and provide evidence-based clinical practice recommendations. Methods: Developed according to AGREE II standards, the guidelines classify scientific evidence based on the Agency for Health Technology Assessment and Tariff System criteria. Recommendations are graded by evidence strength and consensus level from the development group. Key Results: (1) Early-Stage Cancer: Stromal invasion and lymphovascular space involvement (LVSI) from pretreatment biopsy identify candidates for surgery, particularly for simple hysterectomy. (2) Surgical Approach: Minimally invasive surgery is not recommended, except for T1A, LVSI-negative tumors, due to a reduction in life expectancy. (3) Locally Advanced Cancer: concurrent chemoradiation (CCRT) followed by brachytherapy (BRT) is the cornerstone treatment. Low-risk patients (fewer than two metastatic nodes or FIGO IB2-II) may consider induction chemotherapy (ICT) followed by CCRT and BRT after 7 days. High-risk patients (two or more metastatic nodes or FIGO IIIA, IIIB, and IVA) benefit from pembrolizumab with CCRT and maintenance therapy. (4) Metastatic, Persistent, and Recurrent Cancer: A PD-L1 status from pretreatment biopsy identifies candidates for Pembrolizumab with available systemic treatment, while triplet therapy (Atezolizumab/Bevacizumab/chemotherapy) becomes a PD-L1-independent option. Conclusions: These evidence-based guidelines aim to improve clinical outcomes through precise treatment strategies based on individual risk factors, predictors, and disease stages.
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  • 文章类型: Journal Article
    我们目前正处于动荡时期,随着许多新技术的出现,为塑造我们的日常生活开辟了新的可能性。特别是,在个性化人机交互领域,我们观察到很高的潜力,但也有挑战。在这篇文章中,我们探索越来越多的在线服务和工具不仅进一步促进了我们的生活,但也塑造了我们的生活和我们如何看待我们的环境。为此,我们采用个性化的“在线层”的隐喻,并展示了这些层如何与我们生活在现实世界的“人类层”中的生活交织在一起。
    We are currently in a period of upheaval, as many new technologies are emerging that open up new possibilities to shape our everyday lives. Particularly, within the field of Personalized Human-Computer Interaction we observe high potential, but also challenges. In this article, we explore how an increasing amount of online services and tools not only further facilitates our lives, but also shapes our lives and how we perceive our environments. For this purpose, we adopt the metaphor of personalized \'online layers\' and show how these layers are and will be interwoven with the lives that we live in the \'human layer\' of the real world.
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  • 文章类型: Journal Article
    背景:越来越多的国家已经引入了妊娠百日咳疫苗接种,以更好地保护婴儿在出生后的头几周免受疾病的侵害。然而,怀孕期间百日咳疫苗接种的最佳时机仍在争论中。
    方法:我们系统回顾了已发表的关于安全性的文献,妊娠百日咳疫苗的免疫原性和有效性与疫苗接种时间相关。搜索是使用PubMed进行的,MEDLINE和WebofScience,发表了1623篇文章,其中777个重复。筛查结果纳入了45份报告安全性的出版物(n=11),免疫原性(n=26)和/或有效性(n=9)。我们还根据推荐的疫苗接种时间,绘制了全球政府机构在怀孕期间百日咳的建议。
    结果:总体而言,选定的出版物未表明与妊娠期百日咳疫苗接种时间相关的安全性问题增加.免疫原性研究通常建议在孕晚期早期接种疫苗后在出生时提供最佳保护。很少有研究调查定性抗体特征,没有人研究母乳中的抗体滴度或与疫苗接种时间相关的细胞介导的免疫。有效性研究表明,与妊娠早期疫苗接种相比,妊娠晚期百日咳疫苗接种的疫苗有效性降低。全球,在58个国家发现了妊娠百日咳疫苗接种的一般建议,登记了多达22种不同的推荐计时。
    结论:妊娠期接种百日咳疫苗的时机似乎会影响免疫原性和疫苗的有效性,与妊娠早期疫苗接种相比,孕晚期百日咳疫苗接种在出生时具有最佳的免疫反应,并且与妊娠早期疫苗接种相比,孕晚期百日咳疫苗接种的疫苗效力降低.然而,不一致和缺乏的数据反映在全球妊娠百日咳疫苗接种的不同国家建议中.
    结论:妊娠百日咳疫苗接种旨在保护婴儿出生后的头几周。我们的审查表明,免疫原性和疫苗的有效性受到怀孕疫苗接种时间的影响。各国对妊娠百日咳疫苗接种的建议在世界范围内差异很大。
    BACKGROUND: Pertussis vaccination in pregnancy has been introduced in an increasing number of countries to better protect infants against the disease in their first weeks of life. The optimal timing of pertussis vaccination in pregnancy is however still under debate.
    METHODS: We systematically reviewed published literature on safety, immunogenicity and effectiveness of pertussis vaccination in pregnancy related to timing of vaccination. The search was conducted using PubMed, MEDLINE and Web of Science and yielded 1623 articles, thereof 777 duplicates. Screening resulted in the inclusion of 45 publications reporting on safety (n = 11), immunogenicity (n = 26) and/or effectiveness (n = 9). We also mapped pertussis recommendations in pregnancy by government institutions globally according to the recommended timing of vaccination.
    RESULTS: Overall, the selected publications did not indicate increased safety concerns associated with timing of pertussis vaccination in pregnancy. Immunogenicity studies often suggested optimal protection at birth after early third trimester vaccination. Few studies investigated qualitative antibody characteristics, and none investigated antibody titers in breastmilk or cellular-mediated immunity related to timing of vaccination. Effectiveness studies showed decreased vaccine effectiveness of late third trimester pertussis vaccination compared to vaccination earlier in pregnancy. Worldwide, a general recommendation for pertussis vaccination in pregnancy was found for 58 countries, with as many as 22 different recommended timings registered.
    CONCLUSIONS: The timing of pertussis vaccination in pregnancy seems to impact immunogenicity and vaccine effectiveness, with optimal immune responses at birth suggested following early third trimester vaccination and reduced vaccine effectiveness of late third trimester pertussis vaccination suggested compared to vaccination earlier in pregnancy. However, inconsistent and lacking data are reflected in the divergent national recommendations for pertussis vaccination in pregnancy worldwide.
    CONCLUSIONS: Pertussis vaccination in pregnancy aims to protect infants in their first weeks of life. Our review suggests that immunogenicity and vaccine effectiveness are impacted by the timing of vaccination in pregnancy. National recommendations for pertussis vaccination in pregnancy vary widely worldwide.
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  • 文章类型: Journal Article
    过量的膳食糖摄入会增加不健康体重增加的风险,儿童心血管代谢的一个重要危险因素。为了加深我们对这种关系的理解,我们使用两种方法进行了叙述性审查。首先,研究检查膳食糖摄入量,它与心脏代谢健康的关联,遗传学对甜味感知和摄入的影响,综述了遗传学如何调节1.5-5岁学龄前儿童的膳食糖摄入和心脏代谢危险因素之间的关联。第二,收集和分析饮食中糖摄入量的方法学考虑因素,遗传信息,并提供幼儿心脏代谢健康的标记。我们对研究人员的主要建议包括:(1)关于糖摄入量和心脏代谢风险因素的进一步纵向研究是必要的,为学龄前儿童健康饮食的政策决定和指南提供信息。(2)在整个研究中需要糖定义的一致性,以帮助比较结果。(3)选择特定于每个研究的目的和糖定义的饮食收集工具。(4)限制饮食评估工具的主观性,因为这会影响研究结果的解释。(5)选择心脏代谢疾病的非侵入性生物标志物,直到澄清学龄前儿童可用生物标志物的优势和局限性。(6)选择考虑心脏代谢疾病的多基因性质的方法,例如基因组风险评分和全基因组关联研究,以评估遗传学如何调节饮食糖摄入量与心脏代谢风险之间的关系。这篇综述强调了潜在的建议,这些建议将支持研究环境,以帮助告知政策决策和健康饮食政策,以降低幼儿的心脏代谢风险。
    Excess dietary sugar intake increases the risk of unhealthy weight gain, an important cardiometabolic risk factor in children. To further our understanding of this relationship, we performed a narrative review using two approaches. First, research examining dietary sugar intake, its associations with cardiometabolic health, impact of genetics on sweet taste perception and intake, and how genetics moderates the association of dietary sugar intake and cardiometabolic risk factors in preschool-aged children 1.5-5 years old is reviewed. Second, methodological considerations for collecting and analyzing dietary intake of sugar, genetic information, and markers of cardiometabolic health among young children are provided. Our key recommendations include the following for researchers: (1) Further longitudinal research on sugar intake and cardiometabolic risk factors is warranted to inform policy decisions and guidelines for healthy eating in preschool-aged children. (2) Consistency in sugar definitions is needed across research studies to aid with comparisons of results. (3) Select dietary collection tools specific to each study\'s aim and sugar definition(s). (4) Limit subjectivity of dietary assessment tools as this impacts interpretation of study results. (5) Choose non-invasive biomarkers of cardiometabolic disease until the strengths and limitations of available biomarkers in preschool-aged children are clarified. (6) Select approaches that account for the polygenic nature of cardiometabolic disease such as genome risk scores and genome wide association studies to assess how genetics moderates the relationship between dietary sugar intake and cardiometabolic risk. This review highlights potential recommendations that will support a research environment to help inform policy decisions and healthy eating policies to reduce cardiometabolic risk in young children.
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  • 文章类型: Journal Article
    西班牙风湿病学会(SER)汇集了大多数西班牙风湿病学家,在它为会员提供的众多服务中,有一个研究单位(RU)。该部门为SER成员提供临床和流行病学研究的方法学支持,协调和开展研究项目,设计和维护大型患者数据库,开发定性研究项目,并制作循证医学(EBM)文件。通过这最后的活动,SER的RU制定符合最苛刻方法学标准的风湿病学相关主题的临床实践指南和建议文件.本文的目的是描述SERUI遵循的管理流程和方法,以确定其EBM文档的主题以及如何执行和制定其指南和建议。
    The Spanish Society of Rheumatology (SER) brings together the majority of Spain\'s rheumatologists and, among the many services it offers its members, has a Research Unit (RU). This unit provides methodological support to SER members in clinical and epidemiological research, coordinates and carries out research projects, designs and maintains large patient databases, develops qualitative research projects and produces evidence-based medicine (EBM) documents. Through this last activity, the RU of the SER produces clinical practice guidelines and recommendation documents on topics relevant to rheumatology that meet the most demanding methodological standards. The aim of this article is to describe the management process and methodology followed by the UI of the SER to identify the topics of its EBM documents and how it executes and develops its guidelines and recommendations.
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  • 文章类型: Journal Article
    背景:人工智能(AI)在增强临床和行政医疗保健任务方面具有巨大潜力。然而,缓慢的采用和实施挑战凸显了需要考虑人类如何在更广泛的医疗保健社会技术系统中有效地与人工智能合作。
    目的:以重症监护病房(ICU)为例,我们比较了数据科学家和临床医生对人类和人工智能能力的最佳利用的评估,方法是确定合适的人类-人工智能团队,以安全和有意义地增强或自动化6项核心任务。目标是为政策制定者和医疗保健从业人员提供有关AI设计和实施的可行建议。
    方法:在这项多方法研究中,我们将6个ICU的系统任务分析与来自工业界和学术界的19名健康数据科学家和61名ICU临床医生(25名医生和36名护士)的国际Delphi调查相结合,以定义和评估最佳的人-AI合作水平(1级=无绩效收益;2级=AI增强人类绩效;3级=人类增强AI绩效;4级=AI无需人工投入).利益相关者团体还考虑了道德和社会影响。
    结果:两个利益相关者团体都选择了2级和3级人类-AI团队来完成ICU中6个核心任务中的4个。对于一项任务(监控),4级是首选的设计选择。对于患者互动的任务,数据科学家和临床医生都同意,由于医患关系和护患关系的重要性以及道德问题,无论技术可行性如何,都不应使用AI。人类人工智能设计选择依赖于可解释性,可预测性,以及对AI系统的控制。如果不满足这些条件,并且AI的性能低于人类水平的可靠性,建议将责任降低到1级,或将责任从人类最终用户转移出去。如果人工智能的性能达到或超过人类水平的可靠性,而这些条件不满足,应考虑转移到4级自动化,以确保安全和高效的人类-AI团队合作。
    结论:通过考虑社会技术系统并确定适当的人类-AI团队水平,我们的研究展示了在ICU和更广泛的医疗保健环境中提高AI使用安全性和有效性的潜力.监管措施应优先考虑可解释性,可预测性,并控制临床医生是否承担全部责任。必须仔细评估道德和社会影响,以确保人类和人工智能之间的有效合作。特别是考虑到生成人工智能的最新进展。
    BACKGROUND: Artificial intelligence (AI) holds immense potential for enhancing clinical and administrative health care tasks. However, slow adoption and implementation challenges highlight the need to consider how humans can effectively collaborate with AI within broader socio-technical systems in health care.
    OBJECTIVE: In the example of intensive care units (ICUs), we compare data scientists\' and clinicians\' assessments of the optimal utilization of human and AI capabilities by determining suitable levels of human-AI teaming for safely and meaningfully augmenting or automating 6 core tasks. The goal is to provide actionable recommendations for policy makers and health care practitioners regarding AI design and implementation.
    METHODS: In this multimethod study, we combine a systematic task analysis across 6 ICUs with an international Delphi survey involving 19 health data scientists from the industry and academia and 61 ICU clinicians (25 physicians and 36 nurses) to define and assess optimal levels of human-AI teaming (level 1=no performance benefits; level 2=AI augments human performance; level 3=humans augment AI performance; level 4=AI performs without human input). Stakeholder groups also considered ethical and social implications.
    RESULTS: Both stakeholder groups chose level 2 and 3 human-AI teaming for 4 out of 6 core tasks in the ICU. For one task (monitoring), level 4 was the preferred design choice. For the task of patient interactions, both data scientists and clinicians agreed that AI should not be used regardless of technological feasibility due to the importance of the physician-patient and nurse-patient relationship and ethical concerns. Human-AI design choices rely on interpretability, predictability, and control over AI systems. If these conditions are not met and AI performs below human-level reliability, a reduction to level 1 or shifting accountability away from human end users is advised. If AI performs at or beyond human-level reliability and these conditions are not met, shifting to level 4 automation should be considered to ensure safe and efficient human-AI teaming.
    CONCLUSIONS: By considering the sociotechnical system and determining appropriate levels of human-AI teaming, our study showcases the potential for improving the safety and effectiveness of AI usage in ICUs and broader health care settings. Regulatory measures should prioritize interpretability, predictability, and control if clinicians hold full accountability. Ethical and social implications must be carefully evaluated to ensure effective collaboration between humans and AI, particularly considering the most recent advancements in generative AI.
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  • 文章类型: Journal Article
    背景:大型语言模型显示出改善放射学工作流程的希望,但是它们在结构化放射任务(例如报告和数据系统(RADS)分类)上的表现仍未得到探索。
    目的:本研究旨在评估3个大型语言模型聊天机器人-Claude-2、GPT-3.5和GPT-4-在放射学报告中分配RADS类别并评估不同提示策略的影响。
    方法:这项横断面研究使用30个放射学报告(每个RADS标准10个)比较了3个聊天机器人,使用3级提示策略:零射,几枪,和指南PDF信息提示。这些病例的基础是2018年肝脏影像学报告和数据系统(LI-RADS),2022年肺部CT(计算机断层扫描)筛查报告和数据系统(Lung-RADS)和卵巢附件报告和数据系统(O-RADS)磁共振成像,由董事会认证的放射科医生精心准备。每份报告都进行了6次评估。两名失明的评论者评估了聊天机器人在患者级RADS分类和总体评级方面的反应。使用Fleissκ评估了跨重复的协议。
    结果:克劳德-2在总体评分中获得了最高的准确性,其中少量提示和指南PDF(提示-2),在6次运行中获得57%(17/30)的平均准确率,在k-pass投票中获得50%(15/30)的准确率。没有及时的工程,所有聊天机器人都表现不佳。结构化示例提示(prompt-1)的引入提高了所有聊天机器人整体评分的准确性。提供prompt-2进一步改进了Claude-2的性能,GPT-4未复制的增强。TheinterrunagreementwassubstantialforClaude-2(k=0.66foroverallratingandk=0.69forRADScategorization),对于GPT-4来说是公平的(两者的k=0.39),对于GPT-3.5来说是公平的(总体评分k=0.21,RADS分类k=0.39)。与Lung-RADS版本2022和O-RADS相比,2018年的所有聊天机器人均显示出更高的准确性(P<0.05);在2018年LI-RADS版本中,使用prompt-2,Claude-2实现了75%(45/60)的最高总体评分准确性。
    结论:当配备结构化提示和指导PDF时,Claude-2显示了根据既定标准(如LI-RADS版本2018)将RADS类别分配给放射学病例的潜力。然而,当前一代的聊天机器人滞后于根据最新的RADS标准对案件进行准确分类。
    BACKGROUND: Large language models show promise for improving radiology workflows, but their performance on structured radiological tasks such as Reporting and Data Systems (RADS) categorization remains unexplored.
    OBJECTIVE: This study aims to evaluate 3 large language model chatbots-Claude-2, GPT-3.5, and GPT-4-on assigning RADS categories to radiology reports and assess the impact of different prompting strategies.
    METHODS: This cross-sectional study compared 3 chatbots using 30 radiology reports (10 per RADS criteria), using a 3-level prompting strategy: zero-shot, few-shot, and guideline PDF-informed prompts. The cases were grounded in Liver Imaging Reporting & Data System (LI-RADS) version 2018, Lung CT (computed tomography) Screening Reporting & Data System (Lung-RADS) version 2022, and Ovarian-Adnexal Reporting & Data System (O-RADS) magnetic resonance imaging, meticulously prepared by board-certified radiologists. Each report underwent 6 assessments. Two blinded reviewers assessed the chatbots\' response at patient-level RADS categorization and overall ratings. The agreement across repetitions was assessed using Fleiss κ.
    RESULTS: Claude-2 achieved the highest accuracy in overall ratings with few-shot prompts and guideline PDFs (prompt-2), attaining 57% (17/30) average accuracy over 6 runs and 50% (15/30) accuracy with k-pass voting. Without prompt engineering, all chatbots performed poorly. The introduction of a structured exemplar prompt (prompt-1) increased the accuracy of overall ratings for all chatbots. Providing prompt-2 further improved Claude-2\'s performance, an enhancement not replicated by GPT-4. The interrun agreement was substantial for Claude-2 (k=0.66 for overall rating and k=0.69 for RADS categorization), fair for GPT-4 (k=0.39 for both), and fair for GPT-3.5 (k=0.21 for overall rating and k=0.39 for RADS categorization). All chatbots showed significantly higher accuracy with LI-RADS version 2018 than with Lung-RADS version 2022 and O-RADS (P<.05); with prompt-2, Claude-2 achieved the highest overall rating accuracy of 75% (45/60) in LI-RADS version 2018.
    CONCLUSIONS: When equipped with structured prompts and guideline PDFs, Claude-2 demonstrated potential in assigning RADS categories to radiology cases according to established criteria such as LI-RADS version 2018. However, the current generation of chatbots lags in accurately categorizing cases based on more recent RADS criteria.
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  • 文章类型: Journal Article
    锌,一种重要的微量元素,在体内的许多生理过程中具有重要意义。它参与了300多种酶促反应,代谢功能,基因表达的调节,凋亡和免疫调节,从而证明其在维护整体健康和福祉方面的重要作用。虽然锌缺乏与重大健康风险相关,过量的这种微量元素也会导致有害影响。根据世界卫生组织(WHO)每天6.7至15毫克是指饮食参考值。建议的每日摄入量过多可能会导致贫血等症状,中性粒细胞减少症和锌诱导的铜缺乏。欧洲食品安全局(EFSA)将可耐受的上限摄入量(UL)定义为每天25毫克。而美国食品和药物管理局(FDA)允许每天40毫克。这篇综述将总结有关UL计算和与锌相关的其他健康风险的当前知识。例如,锌的摄入不限于口服;其他途径,如吸入或局部应用,也可能造成锌中毒的风险。
    Zinc, a vital trace element, holds significant importance in numerous physiological processes within the body. It participates in over 300 enzymatic reactions, metabolic functions, regulation of gene expression, apoptosis and immune modulation, thereby demonstrating its essential role in maintaining overall health and well-being. While zinc deficiency is associated with significant health risks, an excess of this trace element can also lead to harmful effects. According to the World Health Organization (WHO), 6.7 to 15 mg per day are referred to be the dietary reference value. An excess of the recommended daily intake may result in symptoms such as anemia, neutropenia and zinc-induced copper deficiency. The European Food Safety Authority (EFSA) defines the tolerable upper intake level (UL) as 25 mg per day, whereas the Food and Drug Administration (FDA) allows 40 mg per day. This review will summarize the current knowledge regarding the calculation of UL and other health risks associated with zinc. For example, zinc intake is not limited to oral consumption; other routes, such as inhalation or topical application, may also pose risks of zinc intoxication.
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  • 文章类型: Journal Article
    准确的医疗建议对于确保最佳的患者护理至关重要,和错误信息可能导致错误的决定,潜在的有害健康结果。诸如OpenAI的GPT-4之类的大型语言模型(LLM)的出现激发了人们对其潜在医疗保健应用的兴趣,特别是在自动医疗咨询中。然而,严格的调查将他们的表现与人类专家进行比较仍然很少。
    这项研究旨在将GPT-4的医疗准确性与使用真实世界用户生成的查询提供医疗建议的人类专家进行比较,特别关注心脏病学。它还试图分析GPT-4和人类专家在特定问题类别中的表现,包括药物或药物信息和初步诊断。
    我们通过互联网门户收集了来自一般用户的251对心脏病学特定问题和来自人类专家的回答。GPT-4的任务是生成对相同问题的响应。三名独立心脏病专家(SL,JHK,和JJC)评估了人类专家和GPT-4提供的答案。使用计算机接口,每个评估者比较了这些对,并确定哪个答案更优越,他们定量地测量了问题的清晰度和复杂性以及回答的准确性和适当性,应用三级分级量表(低,中等,和高)。此外,我们进行了语言分析,使用字数和类型-标记比比较回答的长度和词汇多样性.
    GPT-4和人类专家在医疗准确性方面表现出可比的功效(132/251的“GPT-4更好”为52.6%,而119/251的“人类专家更好”为47.4%)。在准确度等级分类中,人类的高准确度应答高于GPT-4(50/237,21.1%vs30/238,12.6%),但低准确度应答的比例也更高(11/237,4.6%vs1/238,0.4%;P=.001).与人类专家相比,GPT-4的反应通常更长,并且使用的词汇量较少,可能增强一般用户的可理解性(句子计数:平均10.9,SD4.2与平均5.9,SD3.7;P<.001;类型令牌比:平均0.69,SD0.07与平均0.79,SD0.09;P<.001)。然而,人类专家在特定问题类别中的表现优于GPT-4,特别是那些与药物或药物信息和初步诊断有关的信息。这些发现强调了GPT-4在根据临床经验提供建议方面的局限性。
    GPT-4在自动医疗咨询中显示出了有希望的潜力,具有与人类专家相当的医疗准确性。然而,挑战仍然存在,尤其是在微妙的临床判断领域。LLM的未来改进可能需要整合特定的临床推理途径和监管机构,以确保安全使用。需要进一步的研究来了解LLM在各种医疗专业和条件下的全部潜力。
    UNASSIGNED: Accurate medical advice is paramount in ensuring optimal patient care, and misinformation can lead to misguided decisions with potentially detrimental health outcomes. The emergence of large language models (LLMs) such as OpenAI\'s GPT-4 has spurred interest in their potential health care applications, particularly in automated medical consultation. Yet, rigorous investigations comparing their performance to human experts remain sparse.
    UNASSIGNED: This study aims to compare the medical accuracy of GPT-4 with human experts in providing medical advice using real-world user-generated queries, with a specific focus on cardiology. It also sought to analyze the performance of GPT-4 and human experts in specific question categories, including drug or medication information and preliminary diagnoses.
    UNASSIGNED: We collected 251 pairs of cardiology-specific questions from general users and answers from human experts via an internet portal. GPT-4 was tasked with generating responses to the same questions. Three independent cardiologists (SL, JHK, and JJC) evaluated the answers provided by both human experts and GPT-4. Using a computer interface, each evaluator compared the pairs and determined which answer was superior, and they quantitatively measured the clarity and complexity of the questions as well as the accuracy and appropriateness of the responses, applying a 3-tiered grading scale (low, medium, and high). Furthermore, a linguistic analysis was conducted to compare the length and vocabulary diversity of the responses using word count and type-token ratio.
    UNASSIGNED: GPT-4 and human experts displayed comparable efficacy in medical accuracy (\"GPT-4 is better\" at 132/251, 52.6% vs \"Human expert is better\" at 119/251, 47.4%). In accuracy level categorization, humans had more high-accuracy responses than GPT-4 (50/237, 21.1% vs 30/238, 12.6%) but also a greater proportion of low-accuracy responses (11/237, 4.6% vs 1/238, 0.4%; P=.001). GPT-4 responses were generally longer and used a less diverse vocabulary than those of human experts, potentially enhancing their comprehensibility for general users (sentence count: mean 10.9, SD 4.2 vs mean 5.9, SD 3.7; P<.001; type-token ratio: mean 0.69, SD 0.07 vs mean 0.79, SD 0.09; P<.001). Nevertheless, human experts outperformed GPT-4 in specific question categories, notably those related to drug or medication information and preliminary diagnoses. These findings highlight the limitations of GPT-4 in providing advice based on clinical experience.
    UNASSIGNED: GPT-4 has shown promising potential in automated medical consultation, with comparable medical accuracy to human experts. However, challenges remain particularly in the realm of nuanced clinical judgment. Future improvements in LLMs may require the integration of specific clinical reasoning pathways and regulatory oversight for safe use. Further research is needed to understand the full potential of LLMs across various medical specialties and conditions.
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