Clinical decision-making

临床决策
  • 文章类型: Journal Article
    目的:系统评价和医学指南在临床实践中被广泛使用。然而,这些通常不是最新的,并且集中在普通患者身上.因此,我们的目标是评估一个指南附加组件,TherapySelector(TS),这是基于所有可用高质量研究的每月更新数据,分类为特定的患者概况。
    方法:我们在2015年至2020年期间,在接受直接作用抗病毒药物治疗的国际患者队列中评估了TS对丙型肝炎(HCV)的治疗。主要结果是接受HCVTS两种首选治疗方案之一的患者人数,基于最高水平的证据,治愈率,没有利巴韦林相关的不良反应,和治疗持续时间。
    结果:我们招募了567名患者。根据HCVTS,接受两种首选治疗方案之一治疗的患者数量介于27%(2015年)和60%(2020年;p<0.001)之间。大多数患者接受治疗持续时间较长(高达34%)和/或加用利巴韦林(高达14%)的方案。与实际治疗相比,当给予第一优选的TherapySelector选项时,对预期治愈率的影响是最小的(高1-6%)。
    结论:医学决策可以通过附加指南来优化;在HCV中,其使用似乎可以最大程度地减少不良反应和成本。使用这种附加功能可能会对治愈率欠佳的疾病产生更大的影响,高成本或不利影响,治疗方案依赖于特定的患者特征。
    OBJECTIVE: Systematic reviews and medical guidelines are widely used in clinical practice. However, these are often not up-to-date and focussed on the average patient. We therefore aimed to evaluate a guideline add-on, TherapySelector (TS), which is based on monthly updated data of all available high-quality studies, classified in specific patient profiles.
    METHODS: We evaluated the TS for the treatment of hepatitis C (HCV) in an international cohort of patients treated with direct-acting antivirals between 2015 and 2020. The primary outcome was the number of patients receiving one of the two preferred treatment options of the HCV TS, based on the highest level of evidence, cure rate, absence of ribavirin-associated adverse effects, and treatment duration.
    RESULTS: We enrolled 567 patients. The number of patients treated with one of the two preferred treatment options according to the HCV TS ranged between 27% (2015) and 60% (2020; p < 0.001). Most of the patients received a regimen with a longer treatment-duration (up to 34%) and/or addition of ribavirin (up to 14%). The effect on the expected cure-rate was minimal (1-6% higher) when the first preferred TherapySelector option was given compared to the actual treatment.
    CONCLUSIONS: Medical decision-making can be optimised by a guideline add-on; in HCV its use appears to minimise adverse effects and cost. The use of such an add-on might have a greater impact in diseases with suboptimal cure-rates, high costs or adverse effects, for which treatment options rely on specific patient characteristics.
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  • 文章类型: Journal Article
    背景:必须全面,正确地解释指南,以规范临床过程。然而,这一过程具有挑战性,需要口译员具有医学背景和资格。在这项研究中,评估了ChatGPT3.5回答与2019年重症急性胰腺炎指南相关的临床问题的准确性.
    结果:使用2019年重症急性胰腺炎指南进行了一项观察性研究。该研究比较了ChatGPT3.5在英语和汉语中的准确性,发现它在英语中(71%)比在汉语中(59%)更准确(P值:0.203)。此外,该研究评估了ChatGPT3.5回答简答题与真/假问题的准确性,发现它回答简答题(76%)比回答真/假问题(60%)更准确(P值:0.405).
    结论:对于重症急性胰腺炎的临床医生,ChatGPT3.5可能具有潜在价值。然而,临床决策不应过分依赖它。
    BACKGROUND: Guidelines must be interpreted comprehensively and correctly to standardize the clinical process. However, this process is challenging and requires interpreters to have a medical background and qualifications. In this study, the accuracy of ChatGPT3.5 in answering clinical questions related to the 2019 guidelines for severe acute pancreatitis was evaluated.
    RESULTS: An observational study was conducted using the 2019 guidelines for severe acute pancreatitis. The study compared the accuracy of ChatGPT3.5 in English versus Chinese and found that it was more accurate in English (71%) than in Chinese (59%) (P value: 0.203). Additionally, the study assessed the accuracy of ChatGPT3.5 in answering short-answer questions versus true/false questions and found that it was more accurate in answering short-answer questions (76%) than in answering true/false questions (60%) (P value: 0.405).
    CONCLUSIONS: For clinicians managing severe acute pancreatitis, ChatGPT3.5 may have potential value. However, it should not be relied upon excessively for clinical decision making.
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  • 文章类型: Journal Article
    目的:在支持临床决策的新证据呈指数级增长的时期,结合选择这些证据的劳动密集型过程,需要一些方法来加快当前流程,以使医疗指南保持最新。这项研究评估了主动学习的性能和可行性,以支持在医学指南开发中选择相关出版物并研究嘈杂标签的作用。
    方法:我们使用了混合方法设计。对两名独立的临床医生手动文献选择过程进行了14次搜索评估。随后进行了一系列模拟,研究了随机阅读与使用基于主动学习的筛选优先级的性能。我们确定了难以找到的文件,并在反思对话中检查了标签。
    方法:使用Cohen的Kappa()评估评分者间的可靠性。为了评估主动学习的表现,我们使用了95%召回时保存的采样工作(WSS@95)和仅读取记录总数10%时发现的相关记录百分比(RRF@10)。我们使用平均发现时间(ATD)来检测具有潜在噪声标签的记录。最后,在与指南开发者的反思对话中讨论了标签的准确性。
    结果:临床医生手动标题摘要选择的平均值为0.50,基于5.021摘要,在-0.01和0.87之间变化。WSS@95的范围从基于临床医生选择的50.15%(SD=17.7)到基于研究方法学家选择的69.24%(SD=11.5)到基于最终全文纳入的75.76%(SD=12.2)。对于RRF@10观察到类似的模式,范围从48.31%(SD=23.3)到62.8%(SD=21.20)和65.58%(SD=23.25)。主动学习的性能随着较高的噪声而恶化。与最终全文选择相比,临床医生或研究方法学家的选择使WSS@95下降了25.61%和6.25%,分别。
    结论:虽然主动机器学习工具可以加速指南开发中的文献筛选过程,它们只能像人类评估者提供的输入一样工作。嘈杂的标签使机器学习变得嘈杂。
    OBJECTIVE: In a time of exponential growth of new evidence supporting clinical decision-making, combined with a labor-intensive process of selecting this evidence, methods are needed to speed up current processes to keep medical guidelines up-to-date. This study evaluated the performance and feasibility of active learning to support the selection of relevant publications within medical guideline development and to study the role of noisy labels.
    METHODS: We used a mixed-methods design. Two independent clinicians\' manual process of literature selection was evaluated for 14 searches. This was followed by a series of simulations investigating the performance of random reading versus using screening prioritization based on active learning. We identified hard-to-find papers and checked the labels in a reflective dialogue.
    METHODS: Inter-rater reliability was assessed using Cohen\'s Kappa (ĸ). To evaluate the performance of active learning, we used the Work Saved over Sampling at 95% recall (WSS@95) and percentage Relevant Records Found at reading only 10% of the total number of records (RRF@10). We used the average time to discovery (ATD) to detect records with potentially noisy labels. Finally, the accuracy of labeling was discussed in a reflective dialogue with guideline developers.
    RESULTS: Mean ĸ for manual title-abstract selection by clinicians was 0.50 and varied between - 0.01 and 0.87 based on 5.021 abstracts. WSS@95 ranged from 50.15% (SD = 17.7) based on selection by clinicians to 69.24% (SD = 11.5) based on the selection by research methodologist up to 75.76% (SD = 12.2) based on the final full-text inclusion. A similar pattern was seen for RRF@10, ranging from 48.31% (SD = 23.3) to 62.8% (SD = 21.20) and 65.58% (SD = 23.25). The performance of active learning deteriorates with higher noise. Compared with the final full-text selection, the selection made by clinicians or research methodologists deteriorated WSS@95 by 25.61% and 6.25%, respectively.
    CONCLUSIONS: While active machine learning tools can accelerate the process of literature screening within guideline development, they can only work as well as the input given by human raters. Noisy labels make noisy machine learning.
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  • 文章类型: Journal Article
    目的:本研究的目的是使用报告循证实践教育干预和教学(GREET)清单评估循证医疗保健(EBHC)电子学习干预措施的报告,并探索与合规报告相关的因素。
    方法:方法学横断面研究。
    方法:根据早期系统评价中使用的标准,我们纳入了比较EBHC电子学习和任何其他形式的EBHC训练或不进行EBHC训练的研究.我们搜查了Medline,Embase,ERIC,CINAHL,中部,Scopus,WebofKnowledge,PsycInfo,ProQuest和最佳证据医学教育至2023年1月4日。标题筛选,摘要,全文文章和数据提取由两位作者独立完成.对于每一项研究,我们评估了17项GREET项目的依从性,并提取了可能预测因子的信息.对GREET核对表中的每个项目的报告是否充分,均以“是”(提供完整信息)进行判断,否(未提供任何信息),不清楚(当提供的信息不足时),或不适用,当项目显然与所描述的干预措施无关时(如项目8-关于教师的细节-在使用电子的研究中,自我节奏的干预,没有任何辅导)。研究对GREET清单的依从性以百分比和绝对数字表示。我们进行了单变量分析,以评估潜在的依从性预测因子与GREET检查表的关联。我们描述性地总结了结果。
    结果:我们纳入了40项研究,其中大多数评估电子学习或混合学习,主要涉及医学和其他医疗保健学生。没有一项研究完全报告了所有GREET项目。总的来说,每个研究满足的GREET项目的中位数(接受的是)为8个,每个研究满足的GREET项目的第三四分位数(Q3)为9个(min.4max.14).当我们使用Q3的项目满足的数量作为截止点,对GREET报告清单的依从性较差,40项研究中有7项(17.5%)报告清单的项目达到可接受水平(17项至少符合10项).没有一项研究报告了所有17项GREET项目。对于3个项目,80%的研究报告了良好的信息(这些项目收到的是):项目1(干预措施的简要描述),第4项(循证实践内容)和第6项(教育策略)。50%的纳入研究报告完整信息的项目(这些项目收到的是)包括:项目9(交付方式),项目11(时间表)和12(学习时间)。70%或更多的纳入研究没有提供信息的项目(这些项目没有收到)包括:项目7(激励措施)和项目13(适应;对于这两个项目,70%的研究没有收到)。项目14(教育干预措施的修改-95%的研究没有收到该项目的),项目16(确定教育干预中使用的材料和教育策略是否按原计划交付的任何过程-93%的研究没有获得该项目的结果)和17(根据时间表进行干预-100%的研究没有获得该项目的结果).2016年9月后发表的研究显示,9个报告项目略有改善。在逻辑回归模型中,使用第三季度的截止点(10分或以上),如果遵守其他准则(综合报告标准试验,加强流行病学观察研究的报告,等)是针对给定研究类型报告的(p=0.039),更多的研究作者使坚持GREET指导的几率增加了18%(p=0.037).
    结论:评估EBHC电子学习教育干预措施的研究仍然不符合GREET清单。使用其他报告准则增加了更好的GREET报告的可能性。期刊应呼吁在未来的EBHC教学研究中适当使用报告指南,以提高报告的透明度,减少不必要的研究重复,促进研究证据或结果的吸收。
    背景:开放科学框架(https://doi.org/10.17605/OSF。IO/V86FR)。
    OBJECTIVE: The objectives of this study are to assess reporting of evidence-based healthcare (EBHC) e-learning interventions using the Guideline for Reporting Evidence-based practice Educational interventions and Teaching (GREET) checklist and explore factors associated with compliant reporting.
    METHODS: Methodological cross-sectional study.
    METHODS: Based on the criteria used in an earlier systematic review, we included studies comparing EBHC e-learning and any other form of EBHC training or no EBHC training. We searched Medline, Embase, ERIC, CINAHL, CENTRAL, SCOPUS, Web of Knowledge, PsycInfo, ProQuest and Best Evidence Medical Education up to 4 January 2023. Screening of titles, abstracts, full-text articles and data extraction was done independently by two authors. For each study, we assessed adherence to each of the 17 GREET items and extracted information on possible predictors. Adequacy of reporting for each item of the GREET checklist was judged with yes (provided complete information), no (provided no information), unclear (when insufficient information was provided), or not applicable, when the item was clearly of no relevance to the intervention described (such as for item 8-details about the instructors-in the studies which used electronic, self-paced intervention, without any tutoring). Studies\' adherence to the GREET checklist was presented as percentages and absolute numbers. We performed univariate analysis to assess the association of potential adherence predictors with the GREET checklist. We summarised results descriptively.
    RESULTS: We included 40 studies, the majority of which assessed e-learning or blended learning and mostly involved medical and other healthcare students. None of the studies fully reported all the GREET items. Overall, the median number of GREET items met (received yes) per study was 8 and third quartile (Q3) of GREET items met per study was 9 (min. 4 max. 14). When we used Q3 of the number of items met as cut-off point, adherence to the GREET reporting checklist was poor with 7 out of 40 studies (17.5%) reporting items of the checklist on acceptable level (adhered to at least 10 items out of 17). None of the studies reported on all 17 GREET items. For 3 items, 80% of included studies well reported information (received yes for these items): item 1 (brief description of intervention), item 4 (evidence-based practice content) and item 6 (educational strategies). Items for which 50% of included studies reported complete information (received yes for these items) included: item 9 (modes of delivery), item 11 (schedule) and 12 (time spent on learning). The items for which 70% or more of included studies did not provide information (received no for these items) included: item 7 (incentives) and item 13 (adaptations; for both items 70% of studies received no for them), item 14 (modifications of educational interventions-95% of studies received no for this item), item 16 (any processes to determine whether the materials and the educational strategies used in the educational intervention were delivered as originally planned-93% of studies received no for this item) and 17 (intervention delivery according to schedule-100% of studies received no for this item). Studies published after September 2016 showed slight improvements in nine reporting items. In the logistic regression models, using the cut-off point of Q3 (10 points or above) the odds of acceptable adherence to GREET guidelines were 7.5 times higher if adherence to other guideline (Consolidated Standards of Reporting Trials, Strengthening the Reporting of Observational Studies in Epidemiology, etc) was reported for a given study type (p=0.039), also higher number of study authors increased the odds of adherence to GREET guidance by 18% (p=0.037).
    CONCLUSIONS: Studies assessing educational interventions on EBHC e-learning still poorly adhere to the GREET checklist. Using other reporting guidelines increased the odds of better GREET reporting. Journals should call for the use of appropriate use of reporting guidelines of future studies on teaching EBHC to increase transparency of reporting, decrease unnecessary research duplication and facilitate uptake of research evidence or result.
    BACKGROUND: The Open Science Framework (https://doi.org/10.17605/OSF.IO/V86FR).
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  • 文章类型: Journal Article
    目的:Barrett食管(BE)是食管腺癌(EAC)的前体。内镜根除治疗(EET)可以有效根除BE和相关瘤形成,并且比监测内镜检查具有更大的危害和资源使用风险。本临床实践指南旨在通过为在BE和相关瘤形成中使用EET提供循证实践建议来告知临床医生和患者。
    方法:建议评估的分级,开发和评估框架用于评估证据并提出建议。小组根据临床医生和患者的重要性,优先考虑临床问题和结果,进行了证据审查,并使用证据到决策框架来制定关于在以下情况下对BE患者使用EET的建议:存在(1)高度发育不良,(2)低度发育不良,(3)无发育不良,(4)选择逐步内镜黏膜切除术(EMR)或局灶性EMR加消融,(5)内镜黏膜下剥离术与EMR的比较。临床建议基于理想和不良效果之间的平衡,患者价值观,成本,和健康公平考虑。
    结果:专家组同意在BE和相关瘤形成中使用EET的5项建议。根据现有证据,专家组提出了在有BE高度发育不良的患者中支持EET的强烈推荐和在无发育不良的BE中反对EET的有条件推荐.专家组提出了有条件的建议,支持EET用于BE低度发育不良;BE低度发育不良患者在降低食管癌死亡率方面对潜在危害的重视程度较高,对益处的重视程度较低(不确定),可以合理选择监测内镜检查。在有可见病变的患者中,有条件的建议支持局灶性EMR加消融,而不是逐步EMR.在进行切除的可见肿瘤性病变的患者中,根据病变特点,建议使用内镜黏膜切除术或内镜黏膜下剥离术.
    结论:本文件全面概述了EET在BE和相关瘤形成治疗中的适应症。还提供了有关实施EET的注意事项的指导。提供者应根据患者的偏好进行共享决策。强调了证据的局限性和差距,以指导未来的研究机会。
    Barrett\'s esophagus (BE) is the precursor to esophageal adenocarcinoma (EAC). Endoscopic eradication therapy (EET) can be effective in eradicating BE and related neoplasia and has greater risk of harms and resource use than surveillance endoscopy. This clinical practice guideline aims to inform clinicians and patients by providing evidence-based practice recommendations for the use of EET in BE and related neoplasia.
    The Grading of Recommendations Assessment, Development and Evaluation framework was used to assess evidence and make recommendations. The panel prioritized clinical questions and outcomes according to their importance for clinicians and patients, conducted an evidence review, and used the Evidence-to-Decision Framework to develop recommendations regarding the use of EET in patients with BE under the following scenarios: presence of (1) high-grade dysplasia, (2) low-grade dysplasia, (3) no dysplasia, and (4) choice of stepwise endoscopic mucosal resection (EMR) or focal EMR plus ablation, and (5) endoscopic submucosal dissection vs EMR. Clinical recommendations were based on the balance between desirable and undesirable effects, patient values, costs, and health equity considerations.
    The panel agreed on 5 recommendations for the use of EET in BE and related neoplasia. Based on the available evidence, the panel made a strong recommendation in favor of EET in patients with BE high-grade dysplasia and conditional recommendation against EET in BE without dysplasia. The panel made a conditional recommendation in favor of EET in BE low-grade dysplasia; patients with BE low-grade dysplasia who place a higher value on the potential harms and lower value on the benefits (which are uncertain) regarding reduction of esophageal cancer mortality could reasonably select surveillance endoscopy. In patients with visible lesions, a conditional recommendation was made in favor of focal EMR plus ablation over stepwise EMR. In patients with visible neoplastic lesions undergoing resection, the use of either endoscopic mucosal resection or endoscopic submucosal dissection was suggested based on lesion characteristics.
    This document provides a comprehensive outline of the indications for EET in the management of BE and related neoplasia. Guidance is also provided regarding the considerations surrounding implementation of EET. Providers should engage in shared decision making based on patient preferences. Limitations and gaps in the evidence are highlighted to guide future research opportunities.
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  • 文章类型: Journal Article
    背景:尽管有强有力的证据支持指南指导的药物治疗(GDMT)用于射血分数降低的心力衰竭患者(HFrEF),在临床实践中仍然缺乏处方率。
    方法:一项包含20例HFrEF患者临床样本的调查由127名心脏病专家和68名内部/家庭医学医师的国家样本回答。每个小插图都有4-5个调整GDMT的选项和不改变药物的选项。调查对象只能选择一个选项。为了进行分析,回答被分为感兴趣的答案。
    结果:心脏病学家比普通医学医师更容易改变GDMT(91.8%vs.82.0%;OR1.84[1.07-3.19];p=0.020)。心脏病学家更有可能使用β受体阻滞剂(46.3%vs.32.0%;OR2.38[1.18-4.81],p=0.016),血管紧张素受体阻滞剂/脑啡肽抑制剂(ARNI)(63.8%vs.48.1%;OR1.76[1.01-3.09],p=0.047),和肼屈嗪和硝酸异山梨酯(HYD/ISDN)(38.2%vs.23.7%;OR2.47[1.48-4.12],p<0.001)与普通医学医师相比。在启动血管紧张素转换酶抑制剂/血管紧张素受体阻滞剂(ACEi/ARBs)方面没有发现差异,启动盐皮质激素受体拮抗剂(MRA),钠-葡萄糖转运蛋白2(SGLT2)抑制剂,地高辛,或者伊伐布雷定.
    结论:我们的结果表明,心脏病专家比普通医学医生更有可能调整GDMT。未来对改善GDMT处方的关注应针对心脏病学家以外的提供者,以改善HFrEF患者的护理。
    BACKGROUND: Despite the strong evidence supporting guideline-directed medical therapy (GDMT) in patients with heart failure with reduced ejection fraction (HFrEF), prescription rates in clinical practice are still lacking.
    METHODS: A survey containing 20 clinical vignettes of patients with HFrEF was answered by a national sample of 127 cardiologists and 68 internal/family medicine physicians. Each vignette had 4-5 options for adjusting GDMT and the option to make no medication changes. Survey respondents could only select one option. For analysis, responses were dichotomized to the answer of interest.
    RESULTS: Cardiologists were more likely to make GDMT changes than general medicine physicians (91.8% vs. 82.0%; OR 1.84 [1.07-3.19]; p = 0.020). Cardiologists were more likely to initiate beta-blockers (46.3% vs. 32.0%; OR 2.38 [1.18-4.81], p = 0.016), angiotensin receptor blocker/neprilysin inhibitor (ARNI) (63.8% vs. 48.1%; OR 1.76 [1.01-3.09], p = 0.047), and hydralazine and isosorbide dinitrate (HYD/ISDN) (38.2% vs. 23.7%; OR 2.47 [1.48-4.12], p < 0.001) compared to general medicine physicians. No differences were found in initiating angiotensin-converting enzyme inhibitor/angiotensin receptor blocker (ACEi/ARBs), initiating mineralocorticoid receptor antagonist (MRA), sodium-glucose transporter protein 2 (SGLT2) inhibitors, digoxin, or ivabradine.
    CONCLUSIONS: Our results demonstrate cardiologists were more likely to adjust GDMT than general medicine physicians. Future focus on improving GDMT prescribing should target providers other than cardiologists to improve care in patients with HFrEF.
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  • 文章类型: Journal Article
    目的:关于剖宫产期间和之后产后出血(PPH)的早期发现和第一反应处理策略,全球尚无共识。我们的研究旨在就剖宫产术中和术后PPH的早期发现和产科第一反应管理的循证方法达成国际专家共识。
    方法:系统评价和三阶段改良德尔菲专家共识。
    方法:国际。
    方法:由22名不同背景的PPH全球专家组成的小组,和性别,专业和地理平衡。
    方法:对剖宫产时PPH的早期发现和第一反应管理的策略达成一致或不一致。
    结果:专家同意相同的PPH定义应适用于阴道分娩和剖腹产。对于术中阶段,专家们一致认为,早期发现应通过定量失血测量来实现,辅以监测女性的血液动力学状态;一旦女性持续出血至少失去500毫升血液或当她表现出血液动力学不稳定的临床迹象时,应触发第一次反应,以先发生者为准。对于第一个回应,专家同意立即服用子宫内服和氨甲环酸,检查以确定病因和快速启动特定原因的反应。在术后阶段,专家们一致认为,剖腹产相关PPH应主要通过经常监测妇女的血流动力学状态和内出血的临床体征和症状来检测,通过定量或视觉估计进行累积失血评估来补充。确定术后第一反应需要个性化方法。
    结论:这些商定的拟议方法可以帮助改善剖宫产术中和术后阶段PPH的检测以及术中PPH的第一反应管理。确定如何最好地实施这些策略是关键的下一步。
    OBJECTIVE: There are no globally agreed on strategies on early detection and first response management of postpartum haemorrhage (PPH) during and after caesarean birth. Our study aimed to develop an international expert\'s consensus on evidence-based approaches for early detection and obstetric first response management of PPH intraoperatively and postoperatively in caesarean birth.
    METHODS: Systematic review and three-stage modified Delphi expert consensus.
    METHODS: International.
    METHODS: Panel of 22 global experts in PPH with diverse backgrounds, and gender, professional and geographic balance.
    METHODS: Agreement or disagreement on strategies for early detection and first response management of PPH at caesarean birth.
    RESULTS: Experts agreed that the same PPH definition should apply to both vaginal and caesarean birth. For the intraoperative phase, the experts agreed that early detection should be accomplished via quantitative blood loss measurement, complemented by monitoring the woman\'s haemodynamic status; and that first response should be triggered once the woman loses at least 500 mL of blood with continued bleeding or when she exhibits clinical signs of haemodynamic instability, whichever occurs first. For the first response, experts agreed on immediate administration of uterotonics and tranexamic acid, examination to determine aetiology and rapid initiation of cause-specific responses. In the postoperative phase, the experts agreed that caesarean birth-related PPH should be detected primarily via frequently monitoring the woman\'s haemodynamic status and clinical signs and symptoms of internal bleeding, supplemented by cumulative blood loss assessment performed quantitatively or by visual estimation. Postoperative first response was determined to require an individualised approach.
    CONCLUSIONS: These agreed on proposed approaches could help improve the detection of PPH in the intraoperative and postoperative phases of caesarean birth and the first response management of intraoperative PPH. Determining how best to implement these strategies is a critical next step.
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  • 文章类型: Journal Article
    目的:本研究旨在评估GPT-4在有或没有欧洲泌尿生殖系统放射学学会(ESUR)关于造影剂的指南背景下回答与造影剂相关的问题的可行性。总体目标是通过提供指南信息来确定上下文富集是否可以改善GPT-4在放射学中临床决策的答案。
    方法:一组64个问题,根据ESUR关于反映相关章节的造影剂的指南,在使用插件提供指南后,直接开发并提交给GPT-4。由经验丰富的放射科医师对信息质量和从指南中精确定位信息的准确性以及放射科住院医师对实用信息进行分级,使用李克特音阶。
    结果:GPT-4的性能在指南中得到了显着改善。没有准则,平均质量评分为3.98,在指南中增加至4.33(p=0036).在准确性方面,82.3%的答案与指南中的信息相符。效用得分也反映了该准则的显着改善,平均得分为4.1(无)和4.4(有)(p=0.008),Fleiss'Kappa为0.44。
    结论:GPT-4,在上下文中丰富了指南,在提供指南支持的建议方面表现出增强的能力。这种方法为实时临床决策支持提供了希望,使指导方针更具可操作性。然而,需要进一步改进,以最大限度地发挥大型语言模型(LLM)的潜力。需要解决固有的局限性。
    OBJECTIVE: This study aimed to assess the feasibility of GPT-4 for answering questions related to contrast media with and without the context of the European Society of Urogenital Radiology (ESUR) guideline on contrast agents. The overarching goal was to determine whether contextual enrichment by providing guideline information improves answers of GPT-4 for clinical decision-making in radiology.
    METHODS: A set of 64 questions, based on the ESUR guideline on contrast agents mirroring pertinent sections, was developed and posed to GPT-4 both directly and after providing the guideline using a plugin. Responses were graded by experienced radiologists for quality of information and accuracy in pinpointing information from the guideline as well as by radiology residents for utility, using Likert-scales.
    RESULTS: GPT-4\'s performance improved significantly with the guideline. Without the guideline, average quality rating was 3.98, which increased to 4.33 with the guideline (p = 0036). In terms of accuracy, 82.3% of answers matched the information from the guideline. Utility scores also reflected a significant improvement with the guideline, with average scores of 4.1 (without) and 4.4 (with) (p = 0.008) with a Fleiss´ Kappa of 0.44.
    CONCLUSIONS: GPT-4, when contextually enriched with a guideline, demonstrates enhanced capability in providing guideline-backed recommendations. This approach holds promise for real-time clinical decision-support, making guidelines more actionable. However, further refinements are necessary to maximize the potential of large language models (LLMs). Inherent limitations need to be addressed.
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  • 文章类型: Journal Article
    风险的综合评价,使用多个索引,对于肺动脉高压(PAH)提供可靠的预后信息和指导治疗是必要的。当前的ESC/ERS指南建议对事件(新诊断)患者使用三层模型,对PAH流行患者使用四层模型。四层模型是一种基本的风险分层工具,它依赖于在后续行动中必须考虑的指标的最小数据集。然而,在对中等风险类别的患者进行分类和管理时,仍然存在模糊和模糊的地方.对于这些患者来说,考虑因素应该包括右心成像,血流动力学,以及年龄等个人因素,性别,遗传概况,疾病类型,合并症,和肾功能。本报告的目的是介绍案例研究,特别关注最终被归类为中等风险的患者。我们的目标是强调在诊断领域遇到的挑战和复杂性,分类,以及对这些特定患者的治疗。
    A comprehensive evaluation of risk, using multiple indices, is necessary to provide reliable prognostic information and guide therapy in pulmonary arterial hypertension (PAH). The current ESC/ERS guidelines suggest using a three-strata model for incident (newly diagnosed) patients and a four-strata model for prevalent patients with PAH. The four-strata model serves as a fundamental risk-stratification tool and relies on a minimal dataset of indicators that must be considered during follow-up. Nevertheless, there are still areas of vagueness and ambiguity when classifying and managing patients in the intermediate-risk category. For these patients, considerations should include right heart imaging, hemodynamics, as well as individual factors such as age, sex, genetic profile, disease type, comorbidities, and kidney function. The aim of this report is to present case studies, with a specific focus on patients ultimately classified as intermediate risk. We aim to emphasize the challenges and complexities encountered in the realms of diagnosis, classification, and treatment for these particular patients.
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  • 文章类型: Journal Article
    个体和社会因素对于继发于脊髓损伤(SCI)的神经源性膀胱患者的临床决策很重要。这些因素包括护理人员的可用性,社会基础设施,和个人喜好,所有这些都可以驱动膀胱管理决策。这些因素在临床决策中可能会被忽视;因此,有必要在神经源性膀胱护理中引导和优先考虑患者的偏好和价值观,以促进个性化的膀胱管理选择.就本文而言,我们回顾了基于指南的护理和共同决策在有神经源性下尿路功能障碍的SCI人群中的作用.
    Individual and social factors are important for clinical decision-making in patients with neurogenic bladder secondary to spinal cord injury (SCI). These factors include the availability of caregivers, social infrastructure, and personal preferences, which all can drive bladder management decisions. These elements can be overlooked in clinical decision-making; therefore, there is a need to elicit and prioritize patient preferences and values into neurogenic bladder care to facilitate personalized bladder management choices. For the purposes of this article, we review the role of guideline-based care and shared decision-making in the SCI population with neurogenic lower urinary tract dysfunction.
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