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Implementation of a curriculum on communicating diagnostic uncertainty for clerkship-level medical students: a pseudorandomized and controlled study. 实习医学生沟通诊断不确定性课程的实施:一项伪随机对照研究。
IF 2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-05-23 eCollection Date: 2025-08-01 DOI: 10.1515/dx-2025-0006
Neha Bansal Etherington, Casey N McQuade, Amar Kohli, Deborah DiNardo, Scott Rothenberger, Eliana Bonifacino

Objectives: Physicians rarely receive formal training on communicating diagnostic uncertainty to patients. Best practices in timing and educational strategies are not established. We aimed to develop, implement and assess a curriculum on communicating uncertainty for medical students.

Methods: This was a pseudorandomized and controlled study. Students on their Internal Medicine Clerkship during the study period from February to August 2023 were invited to participate and separated into control and intervention groups based on assigned rotation site. Students in the intervention group received a curriculum on communicating diagnostic uncertainty. All students completed a subscale of the Physicians' Reaction to Uncertainty Scale (PRUS) at the beginning of their clerkship and at the end of week 4 and an Objective Structured Clinical Examination (OSCE) at the end of week 4.

Results: Fifty-four students participated in the curriculum (29 intervention, 25 control). Intervention group students scored 2.13 points higher than control group students on their skills assessment (mean OSCE for intervention group=14.3, control group=12.17, p<0.001). PRUS increased in both groups, indicating improved tolerance of uncertainty, with no significant difference in change in PRUS between groups (mean change in PRUS for intervention group=2.68, control group=4.82, p=0.33). 97.7 % of students agreed that a curriculum on uncertainty should be included in their medical training.

Conclusions: Students who participated in a curriculum on communication of uncertainty demonstrated superior skills in communicating uncertainty during their OSCE. There was a significant increase in PRUS indicating decreased stress associated with uncertainty for all students. This may reflect high levels of baseline stress associated with starting a clerkship, maturation, exposure to cases, or role-modeling by the clinical team.

目的:医生很少接受与患者沟通诊断不确定性的正式培训。时间安排和教育策略方面的最佳做法尚未确立。我们的目的是开发、实施和评估医学生沟通不确定性的课程。方法:这是一项伪随机对照研究。邀请在2023年2月至8月期间在内科实习的学生参加,并根据轮换地点分为对照组和干预组。干预组的学生接受了关于沟通诊断不确定性的课程。所有学生在实习开始时和第4周结束时完成了医生不确定性反应量表(PRUS)的子量表,并在第4周结束时完成了客观结构化临床检查(OSCE)。结果:54名学生参加了课程,其中干预29名,对照组25名。干预组学生的技能评估得分比对照组学生高2.13分(干预组平均OSCE =14.3分,对照组=12.17分)。结论:参加不确定性沟通课程的学生在OSCE期间表现出更出色的不确定性沟通技能。PRUS的显著增加表明所有学生与不确定性相关的压力减少。这可能反映了高水平的基线压力与开始见习、成熟、接触病例或临床团队的角色塑造有关。
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引用次数: 0
Large language models for dermatological image interpretation - a comparative study. 用于皮肤病学图像解释的大型语言模型-比较研究。
IF 2.2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-05-23 DOI: 10.1515/dx-2025-0014
Lasse Cirkel, Fabian Lechner, Lukas Alexander Henk, Martin Krusche, Martin C Hirsch, Michael Hertl, Sebastian Kuhn, Johannes Knitza

Objectives: Interpreting skin findings can be challenging for both laypersons and clinicians. Large language models (LLMs) offer accessible decision support, yet their diagnostic capabilities for dermatological images remain underexplored. This study evaluated the diagnostic performance of LLMs based on image interpretation of common dermatological diseases.

Methods: A total of 500 dermatological images, encompassing four prevalent skin conditions (psoriasis, vitiligo, erysipelas and rosacea), were used to compare seven multimodal LLMs (GPT-4o, GPT-4o mini, Gemini 1.5 Pro, Gemini 1.5 Flash, Claude 3.5 Sonnet, Llama3.2 90B and 11B). A standardized prompt was used to generate one top diagnosis.

Results: The highest overall accuracy was achieved by GPT-4o (67.8 %), followed by GPT-4o mini (63.8 %) and Llama3.2 11B (61.4 %). Accuracy varied considerably across conditions, with psoriasis with the highest mean LLM accuracy of 59.2 % and erysipelas demonstrating the lowest accuracy (33.4 %). 11.0 % of all images were misdiagnosed by all LLMs, whereas 11.6 % were correctly diagnosed by all models. Correct diagnoses by all LLMs were linked to clear, disease-specific features, such as sharply demarcated erythematous plaques in psoriasis. Llama3.2 90B was the only LLM to decline diagnosing images, particularly those involving intimate areas of the body.

Conclusions: LLM performance varied significantly, emphasizing the need for cautious usage. Notably, a free, locally hostable model correctly identified the top diagnosis for approximately two-thirds of all images, demonstrating the potential for safer, locally deployed LLMs. Advancements in model accuracy and the integration of clinical metadata could further enhance accessible and reliable clinical decision support systems.

目的:对外行人和临床医生来说,解释皮肤表现都是具有挑战性的。大型语言模型(llm)提供了可访问的决策支持,但其对皮肤病图像的诊断能力仍未得到充分开发。本研究基于常见皮肤病的图像解释评估LLMs的诊断性能。方法:采用包括银屑病、白癜风、丹痘和红斑痤疮在内的4种常见皮肤病的500张皮肤病图像,对7种多模式LLMs (gpt - 40、gpt - 40 mini、Gemini 1.5 Pro、Gemini 1.5 Flash、Claude 3.5 Sonnet、Llama3.2 90B和11B)进行比较。一个标准化的提示被用来生成一个顶级诊断。结果:gpt - 40的总体准确率最高(67.8% %),其次是gpt - 40 mini(63.8 %)和Llama3.2 11B(61.4 %)。准确度在不同情况下差异很大,牛皮癣的平均LLM准确度最高,为59.2% %,丹毒的准确度最低(33.4% %)。11.0 %的图像被所有llm误诊,而11.6 %的图像被所有模型正确诊断。所有llm的正确诊断都与明确的疾病特异性特征有关,例如银屑病中明显划分的红斑斑块。Llama3.2 90B是唯一一个拒绝诊断图像的LLM,尤其是那些涉及身体私密部位的图像。结论:LLM疗效差异显著,需谨慎使用。值得注意的是,一个免费的、本地托管的模型正确地识别了大约三分之二的图像的最高诊断,这表明了更安全的、本地部署的llm的潜力。模型准确性和临床元数据集成的进步可以进一步增强临床决策支持系统的可访问性和可靠性。
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引用次数: 0
Analytical performance and user-friendliness of four point-of-care measuring systems for monitoring prothrombin time international normalized ratio in the hands of the intended users. 在预期用户手中监测凝血酶原时间国际标准化比率的四个护理点测量系统的分析性能和用户友好性。
IF 2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-05-23 eCollection Date: 2025-08-01 DOI: 10.1515/dx-2025-0023
Dår Kristian Kur, Elisabet Eriksson Boija, Christine Morken, Sverre Sandberg, Anne Stavelin

Objectives: Scandinavian evaluation of laboratory equipment for point of care testing (SKUP) provides objective and supplier-independent information about analytical quality and user-friendliness of point-of-care (POC) measuring systems. The evaluation reports are freely available online and are valuable tools when selecting fit-for-purpose POC equipment. In this study, we present an overview of the performance of four POC measuring systems for monitoring prothrombin time international normalized ratio (INR) assessed against updated analytical performance specifications (APSs).

Methods: Primary healthcare centres (PHCCs) in Sweden and Norway did the practical work under real-life conditions. In each evaluation, 2-4 PHCCs participated with at least 40 patients on Warfarin treatment per site. Capillary samples were measured on the POC INR systems (qLabs Q3 Plus PT-INR Owren, Xprecia Stride, microINR or ProTime InRhythm), with venous samples analysed at hospital laboratories for comparison (STA-R Evolution or Sysmex CS5100). In the current study, APSs from SKUP, ISO 17593:2022, and CLSI POCT14-Ed2 were used. User-friendliness was assessed by addressing operational facilities, user-manual, time factors, and quality control.

Results: Only microINR coagulometer met the APS for accuracy, while qLabs Q3 Plus PT-INR Owren and ProTime InRhythm met the repeatability criteria. Xprecia Stride scored highest on user-friendliness, whereas the other systems faced challenges with sample application and unclear error messages on the devices.

Conclusions: This study highlights the potential for improvements in POC INR measuring systems and underscores the importance of performing objective evaluations under real-life conditions.

目的:斯堪的纳维亚对护理点检测(SKUP)实验室设备的评估提供了关于护理点(POC)测量系统的分析质量和用户友好性的客观和独立于供应商的信息。评估报告可在网上免费获得,是选择适合用途的POC设备时的宝贵工具。在本研究中,我们概述了四种POC测量系统的性能,用于监测凝血酶原时间国际标准化比率(INR),并根据更新的分析性能规范(aps)进行评估。方法:瑞典和挪威的初级保健中心(phcc)在现实生活条件下进行了实际工作。在每次评估中,2-4个phcc参与,每个站点至少有40名患者接受华法林治疗。在POC INR系统(qLabs Q3 Plus PT-INR Owren, Xprecia Stride, microINR或ProTime InRhythm)上测量毛细血管样本,在医院实验室分析静脉样本进行比较(STA-R Evolution或Sysmex CS5100)。在本研究中,使用了来自SKUP、ISO 17593:2022和CLSI POCT14-Ed2的aps。通过处理操作设施、用户手册、时间因素和质量控制来评估用户友好性。结果:只有microINR凝血仪符合APS的准确性,而qLabs Q3 Plus PT-INR Owren和ProTime InRhythm符合重复性标准。Xprecia Stride在用户友好性方面得分最高,而其他系统则面临着应用程序示例和设备上错误信息不明确的挑战。结论:本研究强调了POC INR测量系统的改进潜力,并强调了在现实条件下进行客观评估的重要性。
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引用次数: 0
Benchmarking AI chatbots: assessing their accuracy in identifying hijacked medical journals. 对人工智能聊天机器人进行基准测试:评估其识别被劫持医学期刊的准确性。
IF 2.2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-05-22 DOI: 10.1515/dx-2025-0043
Mihály Hegedűs, Mehdi Dadkhah, Lóránt Dénes Dávid

Objectives: The challenges posed by questionable journals to academia are very real, and being able to detect hijacked journals would be valuable to the research community. Using an artificial intelligence (AI) chatbot may be a promising approach to early detection. The purpose of this research is to analyze and benchmark the performance of different AI chatbots in identifying hijacked medical journals.

Methods: This study utilized a dataset comprising 21 previously identified hijacked journals and 10 newly detected hijacked journals, alongside their respective legitimate versions. ChatGPT, Gemini, Copilot, DeepSeek, Qwen, Perplexity, and Claude were selected for benchmarking. Three question types were developed to assess AI chatbots' performance in providing information about hijacked journals, identifying hijacked websites, and verifying legitimate ones.

Results: The results show that current AI chatbots can provide general information about hijacked journals, but cannot reliably identify either real or hijacked journal titles. While Copilot performed better than others, it was not error-free.

Conclusions: Current AI chatbots are not yet reliable for detecting hijacked journals and may inadvertently promote them.

目标:有问题的期刊给学术界带来的挑战是非常真实的,能够发现被劫持的期刊对研究界是有价值的。使用人工智能(AI)聊天机器人可能是一种很有前途的早期检测方法。本研究的目的是分析和基准测试不同的人工智能聊天机器人在识别被劫持的医学期刊方面的表现。方法:本研究利用了一个数据集,其中包括21种先前确定的被劫持期刊和10种新发现的被劫持期刊,以及它们各自的合法版本。选择ChatGPT、Gemini、Copilot、DeepSeek、Qwen、Perplexity和Claude进行基准测试。研究人员开发了三种问题类型来评估人工智能聊天机器人在提供被劫持期刊信息、识别被劫持网站和验证合法网站方面的表现。结果表明,目前的人工智能聊天机器人可以提供被劫持期刊的一般信息,但无法可靠地识别真实或被劫持的期刊标题。虽然“副驾驶”的表现要好于其他软件,但它并非没有错误。结论:目前的人工智能聊天机器人在检测被劫持期刊方面还不可靠,可能会无意中促进它们的发展。
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引用次数: 0
Creativity and diagnostic reasoning. 创造力和诊断推理。
IF 2.2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-05-06 DOI: 10.1515/dx-2025-0015
Sho Isoda, Taro Shimizu, Tadayuki Hashimoto, Masasi Hattori, Tomio Suzuki

Creativity is an important component of diagnostic reasoning, enabling the generation of novel and effective diagnostic hypotheses, in collaboration with abduction. The creative process not only fosters insight - critical for overcoming diagnostic challenges - but also enhances calibration by encouraging the exploration of alternative hypotheses. Insight, a key component of creativity, emerges when clinicians reconsider problems from fresh perspectives, breaking through diagnostic impasses. Similarly, calibration, essential for mitigating cognitive biases, promotes the generation and evaluation of alternative hypotheses. By fostering insight and calibration, creativity enhances precision and effectiveness of diagnostic reasoning. Leveraging insights from cognitive psychology to promote creativity can further elevate diagnostic reasoning, driving innovation and excellence in diagnosis. This article explores the pivotal role of creativity in diagnostic reasoning, its applications in diagnosis, approaches to nurture it, and its limitations, ultimately aiming to inspire innovation and excellence in the pursuit of diagnostic accuracy and patient care.

创造力是诊断推理的一个重要组成部分,它与溯因性协作,能够产生新颖有效的诊断假设。创造性的过程不仅培养了洞察力——这对克服诊断挑战至关重要——而且还通过鼓励探索替代假设来加强校准。洞察力是创造力的关键组成部分,当临床医生从新的角度重新考虑问题,突破诊断僵局时,洞察力就会出现。同样,校准对于减轻认知偏差至关重要,它促进了替代假设的产生和评估。通过培养洞察力和校准,创造力提高了诊断推理的准确性和有效性。利用认知心理学的见解来促进创造力,可以进一步提升诊断推理,推动诊断的创新和卓越。本文探讨了创造力在诊断推理中的关键作用,它在诊断中的应用,培养它的方法,以及它的局限性,最终旨在激发创新和卓越的追求诊断准确性和病人护理。
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引用次数: 0
Prenatal screening for genetic disorders: updated guidelines, proposed counseling, a holistic approach for primary health care providers in developing countries. 产前遗传病筛查:最新指南,建议咨询,发展中国家初级卫生保健提供者的整体方法。
IF 2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-04-16 eCollection Date: 2025-08-01 DOI: 10.1515/dx-2024-0137
Shailesh Pande, Vandana Bansal, Geetanjali Sachdeva

Prenatal screening (PNS) can be a very effective strategy for identifying the individuals at-risk of genetic disorders. In contrast to prenatal genetic tests, which are very expensive, require special set-ups and expertise, PNS can be of great help in reducing the burden of genetic disorders, especially in the Indian context. During the last 10 years, several advanced PNS tests utilizing new platforms, with comparatively more sensitivity and specificity, have emerged. PNS tests for chromosomal aneuploidies, microdeletion syndromes, hemoglobinopathies, neural tube defects etc. are available. However, primary health care providers need to be made more aware about the availability of different tests, the time point at which these need to be used, appropriateness of these tests to various presentations and interpretation of the result. They need to be periodically informed about the availability, limitations, sensitivity and specificity of different platforms for PNS. Further, there is a need to develop uniform, updated and practical guidelines on PNS and disseminate these to health care providers so as to benefit the mass population. This article compiles information on different types of PNS and prenatal diagnostic tests, commonly required for different genetic conditions. These recommendations may help clinicians and primary healthcare providers in PNS.

产前筛查(PNS)可以是一个非常有效的策略,以确定个人在遗传疾病的风险。产前基因检测非常昂贵,需要特殊的设备和专业知识,与此相反,PNS可以极大地帮助减轻遗传疾病的负担,特别是在印度情况下。在过去10年中,出现了几种利用新平台的先进的PNS测试,它们具有相对更高的灵敏度和特异性。可进行染色体非整倍体、微缺失综合征、血红蛋白病、神经管缺陷等的PNS检测。然而,初级卫生保健提供者需要更多地了解不同检测的可用性、需要使用这些检测的时间点、这些检测对各种形式的适当性以及对结果的解释。他们需要定期了解不同PNS平台的可用性、局限性、敏感性和特异性。此外,有必要制定统一的、最新的和实用的国家保健服务准则,并将这些准则分发给保健提供者,以使广大人民受益。本文汇编了不同类型的PNS和产前诊断测试的信息,通常需要不同的遗传条件。这些建议可能有助于临床医生和初级卫生保健提供者的PNS。
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引用次数: 0
Physicians' prism: illuminating history with structured expertise. 医生的棱镜:用结构化的专业知识照亮历史。
IF 2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-04-11 eCollection Date: 2025-08-01 DOI: 10.1515/dx-2025-0003
Taro Shimizu

Enhancing the resolution of patient history is crucial for accurate diagnosis and improving patient outcomes. This paper introduces the "GREAT PRISM" strategy, a framework to eliminate barriers to reconstructing comprehensive patient history. Grounded in Grid analysis, the analysis organizes patient information along temporal and symptomatic axes to achieve high-resolution narratives for reaching an accurate diagnosis. Techniques such as identifying missing information, uncovering hidden histories, and dissecting temporal patterns are explored. While emphasizing cognitive forcing strategies and practical applications, this method bridges the gap between traditional practices and modern diagnostic approaches, fostering precision in diagnostic excellence from the point-of-care perspective.

加强对患者病史的分析对于准确诊断和改善患者预后至关重要。本文介绍了“GREAT PRISM”策略,这是一个消除重建全面患者病史障碍的框架。该分析以网格分析为基础,沿着时间轴和症状轴组织患者信息,以实现准确诊断的高分辨率叙述。技术,如识别缺失的信息,揭示隐藏的历史,剖析时间模式进行了探索。在强调认知强迫策略和实际应用的同时,这种方法弥合了传统做法和现代诊断方法之间的差距,从护理点的角度促进了卓越诊断的准确性。
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引用次数: 0
A scoping review of fever of unknown origin with normal serum C-reactive protein. 血清c反应蛋白正常的不明原因发热的范围综述。
IF 2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-04-11 eCollection Date: 2025-08-01 DOI: 10.1515/dx-2024-0200
Yasuhiro Kano, Yukinori Harada, Toshinori Nishizawa, Taro Shimizu

Introduction: The differential diagnosis of fever of unknown origin (FUO) resembles that of inflammation of unknown origin (IUO), but the concept and differential diagnosis of FUO with no inflammatory laboratory evidence (FUO-NIL) are unknown. The aim was to propose the concept of FUO-NIL and explore its differential diagnosis.

Content: The present study is a scoping review of FUO-NIL, defined as FUO with normal serum C-reactive protein (CRP). The PubMed, Embase, CENTRAL, Web of Science, and Google Scholar databases were searched for relevant information. A study was considered eligible for enrolment if the final diagnosis was definitive and the CRP value was clearly noted as normal in each case. The data extracted included the patients' clinical information, final diagnosis, diagnostic tests performed, treatments, and outcomes.

Summary and outlook: The full text of 342 of 3,084 articles were reviewed, and 17 articles met the inclusion criteria. The review identified 19 cases that were eligible for quantitative analysis. The disease categories were infection (n=10, 52.6 %), malignancy (n=3, 15.8 %), non-infectious, inflammatory disease (n=4, 21.1 %), and miscellaneous (n=2, 10.5 %). A more specific differential diagnosis included intracellular fungal infection, tuberculosis, malignancy, systemic lupus erythematosus, granulomatous diseases, Fabry disease, hemophagocytic lymphohistiocytosis, and functional hyperthermia. FUO-NIL may have a unique differential diagnosis and have a different etiology from that of inflammatory FUO. In addition to the standard diagnostic work-up for FUO, tailored diagnostic strategies, including checking for a history of animal contact, the presence of hypohidrosis, and psychosocial stressors may be warranted in cases of FUO-NIL.

不明原因发热(FUO)的鉴别诊断与不明原因炎症(IUO)相似,但没有炎症实验室证据的FUO (FUO- nil)的概念和鉴别诊断尚不清楚。目的是提出FUO-NIL的概念并探讨其鉴别诊断。内容:本研究是对FUO- nil的范围综述,定义为血清c反应蛋白(CRP)正常的FUO。在PubMed、Embase、CENTRAL、Web of Science和谷歌Scholar数据库中搜索相关信息。如果最终诊断是明确的,并且每个病例的CRP值都明显正常,则认为该研究符合入组条件。提取的数据包括患者的临床信息、最终诊断、进行的诊断测试、治疗和结果。总结与展望:共审查3084篇文章中的342篇全文,其中17篇符合纳入标准。审查确定了19例符合定量分析条件的病例。疾病类型为感染(n=10, 52.6 %)、恶性(n=3, 15.8 %)、非感染性、炎症性疾病(n=4, 21.1 %)和杂症(n=2, 10.5 %)。更具体的鉴别诊断包括细胞内真菌感染、肺结核、恶性肿瘤、系统性红斑狼疮、肉芽肿性疾病、法布里病、噬血细胞淋巴组织细胞增多症和功能性热疗。FUO- nil可能具有独特的鉴别诊断,其病因与炎性FUO不同。除了对FUO的标准诊断检查外,对于FUO- nil病例,可能有必要采取量身定制的诊断策略,包括检查动物接触史、是否存在多汗症和社会心理压力源。
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引用次数: 0
Factors associated with positive findings of deep infection on computed tomography among patients with extremity cellulitis. 四肢蜂窝织炎患者计算机断层扫描深部感染阳性结果的相关因素。
IF 2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-04-11 eCollection Date: 2025-08-01 DOI: 10.1515/dx-2024-0156
Cynthia E Burke, Owen R Maley, Benjamin Mancini, Sahil Sardesai, Austin B Montgomery, Tonya S King, Donald J Flemming

Objectives: Cellulitis shares several clinical features with fulminant deep soft tissue infections, creating a diagnostic dilemma for which clinicians are increasingly using cross-sectional diagnostic imaging to resolve. However, the role of imaging in apparent cellulitis is poorly defined. In particular, the clinical utility of CT in extremity cellulitis is underexplored. The purpose of this study was to determine patient and clinical factors that increase likelihood for finding of deep infection on CT among patients with extremity cellulitis.

Methods: A retrospective observational study was performed of patients with cellulitis of the extremities who were examined with computed tomography from January 1, 2012 to December 31, 2021. Demographics, medical history, and clinical and laboratory characteristics were collected. The presence of positive findings on CT report was recorded. Repeated measures logistic regression was used to evaluate significant predictors of positive CT.

Results: There were 496 eligible patient encounters, and CT was positive for deep infection in 39 cases (7.9 %). Median patient age was 56 years of age, 58.1 % were male, and most patients had a history of diabetes mellitus, history of tobacco use, and/or obesity. Significant predictors for positive CT on multivariable analysis included gas on pre-CT radiographs, febrile leukopenic state, injection drug use, purulence on exam, and white blood cell count extremes. Elevated CRP was also a significant positive predictor on bivariate analysis.

Conclusions: Finding a deep infection on CT in a patient with extremity cellulitis is uncommon and is predominantly associated with a high-risk clinical picture, and/or with high index of suspicion based on pre-CT plain films. In the absence of these patient factors or compelling findings on radiographs, CT does not typically provide clinically actionable information for extremity cellulitis and should not be used as part of standard evaluation.

目的:蜂窝织炎与暴发性深部软组织感染有几个共同的临床特征,造成了一个诊断困境,临床医生越来越多地使用横断面诊断成像来解决。然而,影像学在蜂窝织炎中的作用还不明确。特别是,CT在四肢蜂窝织炎中的临床应用尚未得到充分的探讨。本研究的目的是确定增加四肢蜂窝织炎患者CT上发现深部感染可能性的患者和临床因素。方法:回顾性观察研究2012年1月1日至2021年12月31日行计算机断层扫描的四肢蜂窝织炎患者。收集了人口统计学、病史、临床和实验室特征。记录CT报告阳性表现。采用重复测量逻辑回归评估CT阳性的显著预测因素。结果:入选病例496例,CT阳性39例(7.9% %)。患者年龄中位数为56岁,58.1% 为男性,大多数患者有糖尿病史、吸烟史和/或肥胖史。在多变量分析中,CT阳性的重要预测因素包括CT前x线片上的气体、发热性白细胞减少状态、注射药物使用、检查时脓性和白细胞计数极端。在双变量分析中,CRP升高也是显著的阳性预测因子。结论:在四肢蜂窝织炎患者的CT上发现深部感染是罕见的,主要与高危临床表现和/或基于CT前平片的高怀疑指数相关。在缺乏这些患者因素或x线片上令人信服的发现的情况下,CT通常不能为四肢蜂窝织炎提供临床可操作的信息,不应作为标准评估的一部分。
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引用次数: 0
Two decades of autopsy-detected diagnostic errors in Japan. 日本二十年的尸检诊断错误。
IF 2 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-04-11 eCollection Date: 2025-08-01 DOI: 10.1515/dx-2025-0013
Kohta Katayama, Tomoharu Suzuki, Maho Adachi-Katayama, Kenji Numata, Yuki Honda, Hiroyuki Nagano, Yuki Hiramatsu, Takashi Watari, Yasuharu Tokuda, Payal K Patel, Yoshiyuki Ohira

Objectives: Autopsy plays an essential role in detecting diagnostic errors and the findings from autopsies have the potential to reduce future errors. However, there are few reports from Japan on diagnostic errors based on autopsy diagnoses. This study aimed to detail diagnostic errors in autopsy reports in Japan.

Methods: This descriptive study utilized the case report abstract database of the Japanese Society of Internal Medicine chapter meetings. Autopsy cases from 2002 to 2022 were included. We defined diagnostic errors as discrepancies in the primary cause of death between autopsy and clinical diagnosis. Diagnostic error cases were also categorized according to the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD-10). To observe trends, a chi-square test was conducted by dividing the 20 years of data into four groups.

Results: Among 1,213 autopsied cases, diagnostic errors occurred in 435 cases (35.9 %; 95 % confidence interval, 33.2-38.6 %). The most frequent category of autopsy-detected diagnostic error cases was neoplasms (147, 33.8 %), followed by infections (131, 30.1 %), and cardiovascular diseases (49, 11.3 %). Over the 20 years, the incidence of diagnostic errors neither increased nor decreased.

Conclusions: Diagnostic errors detected in 35.8 % of autopsy cases in Japan. Autopsy is an important quality indicator for identifying diagnostic error.

目的:尸检在发现诊断错误中起着至关重要的作用,尸检的结果有可能减少未来的错误。然而,日本很少有基于尸检诊断的诊断错误的报道。本研究旨在详细分析日本尸检报告中的诊断错误。方法:采用日本内科学会分会会议病例报告摘要数据库进行描述性研究。包括2002年至2022年的尸检病例。我们将诊断错误定义为尸检和临床诊断之间主要死因的差异。还根据国际疾病和相关健康问题统计分类(ICD-10)第十次修订版对诊断错误病例进行分类。为了观察趋势,将20年的数据分为四组,进行卡方检验。结果:1213例尸检中,诊断错误435例(35.9 %;95 %置信区间,33.2-38.6 %)。最常见的尸检诊断错误类型是肿瘤(147例,33.8 %),其次是感染(131例,30.1 %)和心血管疾病(49例,11.3 %)。20年来,诊断错误的发生率既没有增加也没有减少。结论:在日本,35.8% %的尸检病例中检出诊断错误。尸检是鉴别诊断错误的重要质量指标。
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