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Treatment of Irresectable Colorectal Liver Metastases by Combination of Liver Resection and Percutaneous Tumor Ablation: Mid-term Outcome. 肝切除联合经皮肿瘤消融治疗不可切除的结直肠癌肝转移:中期结果。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-06 DOI: 10.1055/a-2781-8926
Tanja Lokancevic, Sebastian Keil, Philipp Bruners, Sven Lang, Iakovos Amygdalos, Christiane K Kuhl, Peter Isfort, Emona Staudacher

Primary resection of liver metastases in colorectal cancer remains the leading curative approach. However, a small future liver remnant or central localization of metastases often prevent resectability. In such cases, combining resection with percutaneous ablation may offer a curative-intent treatment option. This study aims to evaluate the oncologic results and morbidity of this combined treatment.In this retrospective study, 21 patients with advanced colorectal liver metastases underwent a two-stage treatment consisting of planned incomplete resection and percutaneous ablation. Outcomes assessed included overall survival and intrahepatic progression-free survival. Main exclusion criteria were extrahepatic disease and ablation of metastases > 3 cm. Results are reported as medians with 95% confidence intervals and standard deviation.The median number of preoperative intrahepatic metastases was 5 [2-13]. Follow-up was available for 95% of patients, with a median follow-up of 21 months. Intra- und extrahepatic recurrences occurred in 81% (17/21). Median intrahepatic progression-free survival was 5 [0-44] months. Median overall survival was 36.5 [6.6-55] months, resulting in a 1-year survival rate of 91%. Twelve patients (57%) passed away. Technical success was achieved in 90%. Three major complications occurred, all of which were successfully treated.In patients with partially unresectable colorectal liver metastases, a two-stage approach combining resection and percutaneous ablation represents a potential curative-intent strategy, particularly when intraoperative ablation is not feasible. Despite high recurrence rates, OS was comparatively long relative to systemic therapy. Further studies are needed to explore treatment sequencing, perioperative therapies, and advanced ablation technologies for optimizing the concept. Ultimately, treatment must be individualized based on the patient's disease profile and institutional capabilities. · A two-stage approach combining resection and percutaneous ablation represents a potential curative-intent strategy in partially irresectable colorectal liver metastases.. · High recurrence rates occur, but overall survival remains comparatively long.. · Individualized, interdisciplinary treatment planning optimizes patient outcomes.. · Further research is needed on sequencing, perioperative strategies, and ablation technologies.. · Lokancevic T, Keil S, Bruners P et al. Treatment of Irresectable Colorectal Liver Metastases by Combination of Liver Resection and Percutaneous Tumor Ablation: Mid-term Outcome. Rofo 2026; DOI 10.1055/a-2781-8926.

原发性肝转移切除术仍然是结直肠癌的主要治疗方法。然而,小的肝脏残余或转移灶的中心定位往往阻止可切除性。在这种情况下,联合切除与经皮消融可能提供一种治愈意图的治疗选择。本研究旨在评估这种联合治疗的肿瘤学结果和发病率。在这项回顾性研究中,21例晚期结直肠肝转移患者接受了两期治疗,包括计划的不完全切除和经皮消融。评估的结果包括总生存期和肝内无进展生存期。主要的排除标准是肝外病变和转移灶消融≤3cm。结果以95%置信区间和标准差的中位数报告。术前肝内转移的中位数为5例[2-13]。95%的患者可随访,中位随访时间为21个月。肝内和肝外复发占81%(17/21)。中位肝内无进展生存期为5[0-44]个月。中位总生存期为36.5[6.6-55]个月,1年生存率为91%。12例患者(57%)死亡。技术成功率达90%。发生了三种主要并发症,均得到成功治疗。对于部分不可切除的结直肠肝转移患者,两期手术联合切除和经皮消融是一种潜在的治疗策略,特别是当术中消融不可行的情况下。尽管复发率高,但相对于全身治疗,OS的持续时间相对较长。需要进一步的研究来探索治疗顺序、围手术期治疗和先进的消融技术来优化这一概念。最终,治疗必须根据患者的疾病概况和机构能力进行个体化。·联合切除和经皮消融的两阶段方法代表了部分不可切除的结直肠癌肝转移的潜在治愈意图策略。·复发率高,但总体生存期相对较长。·个性化、跨学科的治疗计划可优化患者的治疗效果。·需要进一步研究测序、围手术期策略和消融技术。·Lokancevic T, Keil S, Bruners P等。肝切除联合经皮肿瘤消融治疗不可切除的结直肠癌肝转移:中期结果。Rofo 2026;DOI 10.1055 / - 2781 - 8926。
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引用次数: 0
Correction: Wilhelm Conrad Röntgen's Strasbourg Years (1872-1879): W.C. Röntgen - Two Decades before the Discovery of X-rays (with GPX Track "Röntgen in Strasbourg"). 更正:威廉·康拉德Röntgen斯特拉斯堡年(1872-1879):W.C. Röntgen - x射线发现前二十年(GPX轨道“Röntgen在斯特拉斯堡”)。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-03 DOI: 10.1055/a-2795-5972
Jan Rabe, Uwe Busch, Marcel Michels, Heinz-Peter Schlemmer
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引用次数: 0
Performance of AI Approaches for COVID-19 Diagnosis Using Chest CT Scans: The Impact of Architecture and Dataset. 使用胸部CT扫描诊断COVID-19的AI方法的性能:架构和数据集的影响。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 Epub Date: 2025-04-29 DOI: 10.1055/a-2577-3928
Astha Jaiswal, Philipp Fervers, Fanyang Meng, Huimao Zhang, Dorottya Móré, Athanasios Giannakis, Jasmin Wailzer, Andreas Michael Bucher, David Maintz, Jonathan Kottlors, Rahil Shahzad, Thorsten Persigehl

AI is emerging as a promising tool for diagnosing COVID-19 based on chest CT scans. The aim of this study was the comparison of AI models for COVID-19 diagnosis. Therefore, we: (1) trained three distinct AI models for classifying COVID-19 and non-COVID-19 pneumonia (nCP) using a large, clinically relevant CT dataset, (2) evaluated the models' performance using an independent test set, and (3) compared the models both algorithmically and experimentally.In this multicenter multi-vendor study, we collected n=1591 chest CT scans of COVID-19 (n=762) and nCP (n=829) patients from China and Germany. In Germany, the data was collected from three RACOON sites. We trained and validated three COVID-19 AI models with different architectures: COVNet based on 2D-CNN, DeCoVnet based on 3D-CNN, and AD3D-MIL based on 3D-CNN with attention module. 991 CT scans were used for training the AI models using 5-fold cross-validation. 600 CT scans from 6 different centers were used for independent testing. The models' performance was evaluated using accuracy (Acc), sensitivity (Se), and specificity (Sp).The average validation accuracy of the COVNet, DeCoVnet, and AD3D-MIL models over the 5 folds was 80.9%, 82.0%, and 84.3%, respectively. On the independent test set with n=600 CT scans, COVNet yielded Acc=76.6%, Se=67.8%, Sp=85.7%; DeCoVnet provided Acc=75.1%, Se=61.2%, Sp=89.7%; and AD3D-MIL achieved Acc=73.9%, Se=57.7%, Sp=90.8%.The classification performance of the evaluated AI models is highly dependent on the training data rather than the architecture itself. Our results demonstrate a high specificity and moderate sensitivity. The AI classification models should not be used unsupervised but could potentially assist radiologists in COVID-19 and nCP identification. · This study compares AI approaches for diagnosing COVID-19 in chest CT scans, which is essential for further optimizing the delivery of healthcare and for pandemic preparedness.. · Our experiments using a multicenter, multi-vendor, diverse dataset show that the training data is the key factor in determining the diagnostic performance.. · The AI models should not be used unsupervised but as a tool to assist radiologists.. · Jaiswal A, Fervers P, Meng F et al. Performance of AI Approaches for COVID-19 Diagnosis Using Chest CT Scans: The Impact of Architecture and Dataset. Rofo 2026; 198: 185-198.

人工智能正在成为以胸部CT扫描为基础的新冠肺炎诊断工具。本研究的目的是比较新冠肺炎诊断的人工智能模型。因此,我们:(1)使用大型临床相关CT数据集训练了三种不同的AI模型,用于对COVID-19和非COVID-19肺炎(nCP)进行分类;(2)使用独立测试集评估模型的性能;(3)对模型进行算法和实验比较。在这项多中心、多供应商的研究中,我们收集了来自中国和德国的n=1591例COVID-19 (n=762)和nCP (n=829)患者的胸部CT扫描。在德国,数据是从浣熊的三个地点收集的。我们训练并验证了三种不同架构的COVID-19人工智能模型:基于2D-CNN的COVNet、基于3D-CNN的DeCoVnet和基于3D-CNN的AD3D-MIL。使用991次CT扫描对人工智能模型进行5倍交叉验证。来自6个不同中心的600个CT扫描被用于独立测试。通过准确性(Acc)、敏感性(Se)和特异性(Sp)来评估模型的性能。COVNet、DeCoVnet和AD3D-MIL模型在5倍范围内的平均验证准确率分别为80.9%、82.0%和84.3%。在n=600 CT扫描的独立测试集上,COVNet产生的Acc=76.6%, Se=67.8%, Sp=85.7%;DeCoVnet提供Acc=75.1%, Se=61.2%, Sp=89.7%;AD3D-MIL实现Acc=73.9%, Se=57.7%, Sp=90.8%。被评估的人工智能模型的分类性能高度依赖于训练数据,而不是架构本身。我们的结果显示高特异性和中等敏感性。人工智能分类模型不应在无人监督的情况下使用,但可能有助于放射科医生识别COVID-19和新型冠状病毒。·本研究比较了在胸部CT扫描中诊断COVID-19的人工智能方法,这对于进一步优化医疗服务和大流行防范至关重要。·我们使用多中心、多供应商、多样化数据集的实验表明,训练数据是决定诊断性能的关键因素。·人工智能模型不应在无人监督的情况下使用,而应作为辅助放射科医生的工具。·Jaiswal A, Fervers P, bbb90 F等。使用胸部CT扫描诊断COVID-19的AI方法的性能:架构和数据集的影响。Rofo 2025;DOI 10.1055 / - 2577 - 3928。
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引用次数: 0
Democratizing AI in Healthcare with Open Medical Inference (OMI): Protocols, Data Exchange, and AI Integration. 通过开放医疗推断(OMI)使医疗保健中的人工智能民主化:协议、数据交换和人工智能集成。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 Epub Date: 2025-09-29 DOI: 10.1055/a-2651-6653
Obioma Pelka, Stefan Sigle, Patrick Werner, Simon Tobias Schweizer, Alexa Iancu, Lucas Scherer, Nicolas Andreas Kamzol, Jan Horst Eil, Timo Apfelbacher, Dmitrii Seletkov, Tobias Susetzky, Matthias Stefan May, Andreas Michael Bucher, Christian Fegeler, Martin Boeker, Rickmer Braren, Hans-Ulrich Prokosch, Felix Nensa

The integration of artificial intelligence (AI) into healthcare is transforming clinical decision-making, patient outcomes, and workflows. AI inference, applying trained models to new data, is central to this evolution, with cloud-based infrastructures enabling scalable AI deployment. The Open Medical Inference (OMI) platform democratizes AI access through open protocols and standardized data formats for seamless, interoperable healthcare data exchange. By integrating standards like FHIR and DICOMweb, OMI ensures interoperability between healthcare institutions and AI services while fostering ethical AI use through a governance framework addressing privacy, transparency, and fairness.OMI's implementation is structured into work packages, each addressing technical and ethical aspects. These include expanding the Medical Informatics Initiative (MII) Core Dataset for medical imaging, developing infrastructure for AI inference, and creating an open-source DICOMweb adapter for legacy systems. Standardized data formats ensure interoperability, while the AI Governance Framework promotes trust and responsible AI use.The project aims to establish an interoperable AI network across healthcare institutions, connecting existing infrastructures and AI services to enhance clinical outcomes. · OMI develops open protocols and standardized data formats for seamless healthcare data exchange.. · Integration with FHIR and DICOMweb ensures interoperability between healthcare systems and AI services.. · A governance framework addresses privacy, transparency, and fairness in AI usage.. · Work packages focus on expanding datasets, creating infrastructure, and enabling legacy system integration.. · The project aims to create a scalable, secure, and interoperable AI network in healthcare.. · Pelka O, Sigle S, Werner P et al. Democratizing AI in Healthcare with Open Medical Inference (OMI): Protocols, Data Exchange, and AI Integration. Rofo 2026; 198: 173-184.

人工智能(AI)与医疗保健的集成正在改变临床决策、患者结果和工作流程。人工智能推理,将训练好的模型应用于新数据,是这一演变的核心,基于云的基础设施支持可扩展的人工智能部署。开放医学推断(OMI)平台通过开放协议和标准化数据格式实现了人工智能访问的民主化,实现了无缝、可互操作的医疗保健数据交换。通过整合FHIR和DICOMweb等标准,OMI确保了医疗机构和人工智能服务之间的互操作性,同时通过解决隐私、透明度和公平性的治理框架促进人工智能的道德使用。OMI的实施分为几个工作包,每个工作包处理技术和道德方面的问题。其中包括扩展医学成像的医学信息学计划(MII)核心数据集,开发用于人工智能推理的基础设施,以及为遗留系统创建开源DICOMweb适配器。标准化数据格式确保互操作性,而人工智能治理框架促进信任和负责任的人工智能使用。该项目旨在在医疗机构之间建立一个可互操作的人工智能网络,连接现有的基础设施和人工智能服务,以提高临床效果。·OMI开发开放协议和标准化数据格式,实现医疗保健数据的无缝交换。·与FHIR和DICOMweb的集成确保了医疗保健系统和AI服务之间的互操作性。·治理框架解决人工智能使用中的隐私、透明度和公平性问题。·工作包侧重于扩展数据集、创建基础设施和实现遗留系统集成。·该项目旨在在医疗保健领域创建可扩展、安全且可互操作的人工智能网络。·Pelka O, Sigle S, Werner P等。通过开放医疗推断(OMI)使医疗保健中的人工智能民主化:协议、数据交换和人工智能集成。Rofo 2025;DOI 10.1055 / - 2651 - 6653。
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引用次数: 0
Extending the Age Range in Mammography Screening: A Benefit-Risk Assessment from a Radiation Protection Perspective. 扩大乳房x光检查的年龄范围:从辐射防护的角度进行获益-风险评估。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-02-01 Epub Date: 2025-08-28 DOI: 10.1055/a-2674-5744
Theresa Hunger, Elke Anna Nekolla, Eva Wanka-Pail, Katharina Stella Winter, Gunnar Brix

Mammography screening programs (MSP) are established for women age 50 to 69 years in Germany and Europe. Some of the studies that build the evidence base for these programs also included women who were younger or older than this target population. The aim of our study was to assess whether screening also provides more benefit than harm to women outside the originally defined age range of the German MSP.A systematic review and meta-analysis of randomized controlled trials (RCT) was performed to assess overall and breast cancer mortality in women older than 70 years and women under 50 years. Radiation-associated age-specific lifetime attributable risks (LAR) were estimated based on a modified risk model of the BEIR Committee using current cancer and lifetime data for a female German population.Two RCTs with 33,268 women age 70 years or older, and eight RCTs with 394,080 women age 39-49 years were included. The relative reduction in breast cancer mortality was 28% (risk ratio (RR) = 0.72; 95% confidence interval (CI): 0.54-0.95) and 18% (RR = 0.82; 95%-CI: 0.71-0.96), respectively. The proportion of overdiagnoses in older women is estimated at 19% and is higher than in younger women. Assuming biennial screening from below 50 to 69 years of age, the LAR decreases considerably with increasing age at start of screening, being 0.06%, 0.04%, and 0.025% when starting at 40, 45, or 50 years, respectively. The corresponding benefit-risk ratios are about 25, 35, and 45, respectively. Changing the upper screening age to 75 has little impact on the benefit-risk ratio.Extending the age limits in MSP to women starting from 45 years and up to 75 years is justified from the radiation perspective since the benefit substantially outweighs the radiation risk. Based on our report, the MSP has also been approved for women age 70 to 75 in Germany as of February 2024, while it is still pending for younger women. · Screening can reduce breast cancer mortality in women age 45-49 and 70-75.. · As a result, more women can benefit from mammography screening programs.. · The downside for older women is more overdiagnoses.. · Younger women face a higher radiation risk.. · Hunger T, Nekolla EA, Wanka-Pail E et al. Extending the Age Range in Mammography Screening: A Benefit-Risk Assessment from a Radiation Protection Perspective. Rofo 2026; 198: 164-172.

在德国和欧洲,为50至69岁的女性建立了乳房x光检查项目(MSP)。为这些项目建立证据基础的一些研究还包括比目标人群年轻或年长的女性。我们研究的目的是评估筛查是否对德国MSP最初定义的年龄范围之外的女性也提供了更多的好处而不是伤害。对随机对照试验(RCT)进行了系统回顾和荟萃分析,以评估70岁以上妇女和50岁以下妇女的总体死亡率和乳腺癌死亡率。辐射相关的年龄特异性终生归因风险(LAR)是基于BEIR委员会的修正风险模型,使用德国女性人口的当前癌症和终生数据来估计的。两项随机对照试验纳入33,268名年龄在70岁及以上的女性,八项随机对照试验纳入394,080名年龄在39-49岁的女性。乳腺癌死亡率相对降低28%(风险比(RR) = 0.72;95%可信区间(CI): 0.54-0.95)和18% (RR = 0.82; 95% CI: 0.71-0.96)。据估计,老年妇女的过度诊断比例为19%,高于年轻妇女。假设从50岁以下到69岁进行两年一次的筛查,随着筛查开始年龄的增加,LAR显著下降,在40岁、45岁和50岁开始时分别为0.06%、0.04%和0.025%。相应的收益风险比分别约为25、35和45。将筛查年龄上限改为75岁对获益风险比影响不大。从辐射角度来看,将MSP的年龄限制从45岁扩大到75岁是合理的,因为其益处大大超过了辐射风险。根据我们的报告,截至2024年2月,德国还批准了70至75岁女性的MSP,而年轻女性的MSP仍在等待批准。·筛查可以降低45-49岁和70-75岁妇女的乳腺癌死亡率。·因此,更多的妇女可以从乳房x光检查项目中受益。老年妇女的缺点是更多的过度诊断。·年轻女性面临更高的辐射风险。·Hunger T, Nekolla EA, Wanka-Pail E等。扩大乳房x光检查的年龄范围:从辐射防护的角度进行获益-风险评估。Rofo 2025;DOI 10.1055 / - 2674 - 5744。
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引用次数: 0
Free-breathing non-contrast-enhanced flow-independent MR angiography using REACT: A prospective study for pediatric vessel assessment. 使用REACT的自由呼吸非对比增强不依赖血流的MR血管造影:一项用于儿童血管评估的前瞻性研究。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-01-30 DOI: 10.1055/a-2781-8861
Jakob Spogis, Ilias Tsiflikas, Christoph Katemann, Shuo Zhang, Masami Yoneyama, Juergen F Schaefer

To evaluate the non-contrast-enhanced relaxation-enhanced angiography without contrast (REACT) sequence for the assessment of extrathoracic vessels in pediatric patients compared to contrast-enhanced (CE), multiphasic magnetic resonance angiography (MRA).In this prospective, single-center study, pediatric patients referred for clinically indicated contrast-enhanced MRI of various extrathoracic body regions underwent additional free-breathing REACT and multiphasic, free-breathing CE-MRA at 1.5 T (Philips Ingenia). REACT was acquired using Cartesian k-space order, except in the abdomen, where it was acquired using a radial stack of stars k-space sampling (REACT VANE). The acquisition time was recorded. Image quality (Likert scale 1-5, with 5 being the best) and vessel diameter were evaluated by two independent readers in four predefined vessels in each body region. Furthermore, a quantitative analysis of SNR and CNR was performed.30 patients (age: 12.3 ± 4 years) successfully completed REACT and CE-MRA. The acquisition time for REACT was 2:49 ± 1:03 min, while abdominal REACT VANE required 4:51 ± 0:52 min. The CE-MRA acquisition time was 3:49 ± 1:03 min. The median image quality ratings were good to excellent (Likert scale 4-5) for both readers. No significant difference in the image quality ratings was found (p = 0.12 - 0.58). Interobserver agreement of image quality ratings of the two readers was moderate to substantial (Cohen's kappa REACT: 0.58, CE-MRA: 0.64). Vessel diameter measurements showed a strong correlation (r = 0.93) between REACT and CE-MRA with high intraclass correlation coefficients (REACT: 0.97, CE-MRA: 0.97). Quantitative analysis showed a higher venous SNR and higher arterial and venous CNR in REACT (p = 0.001-0.018).Given the good and comparable image quality, REACT can be useful in vascular imaging in children under free-breathing, while potentially eliminating the need for contrast agent injection. · MR angiography is widely used in pediatric imaging for vessel assessment.. · Contrast-enhanced MRA has limitations due to the use of gadolinium-based contrast agents.. · REACT is a novel contrast-free MRA technique performed during free breathing.. · REACT provides image quality comparable to contrast-enhanced free-breathing MRA.. · Spogis J, Tsiflikas I, Katemann C et al. Free-breathing non-contrast-enhanced flow-independent MR angiography using REACT: A prospective study for pediatric vessel assessment. Rofo 2026; 10.1055/a-2781-8861.

对比对比增强血管造影(CE)、多相磁共振血管造影(MRA)和非对比增强血管造影(REACT)序列对儿科患者胸外血管的评估。在这项前瞻性的单中心研究中,接受临床指示的不同胸外身体区域对比增强MRI检查的儿科患者在1.5 T时进行了额外的自由呼吸REACT和多相自由呼吸CE-MRA (Philips Ingenia)。REACT是使用笛卡尔k空间顺序获得的,除了在腹部,它是使用恒星k空间采样的径向堆栈(REACT VANE)获得的。记录采集时间。图像质量(Likert scale 1-5, 5为最佳)和血管直径由两个独立的阅读器在每个身体区域的四个预定义血管中进行评估。此外,还进行了信噪比和CNR的定量分析。30例患者(年龄:12.3±4岁)成功完成REACT和CE-MRA。REACT采集时间为2:49±1:03 min,腹部REACT VANE采集时间为4:51±0:52 min。CE-MRA采集时间为3:49±1:03 min。两位读者的图像质量评分中位数为好到优秀(李克特量表4-5)。两组图像质量评分差异无统计学意义(p = 0.12 - 0.58)。观察者之间对两名读者图像质量评级的一致性为中等至实质性(Cohen’s kappa REACT: 0.58, CE-MRA: 0.64)。血管直径测量结果显示REACT和CE-MRA之间有很强的相关性(r = 0.93),具有较高的类内相关系数(REACT: 0.97, CE-MRA: 0.97)。定量分析显示,反应组静脉SNR较高,动脉、静脉CNR较高(p = 0.001 ~ 0.018)。鉴于良好的图像质量,REACT可用于自由呼吸儿童的血管成像,同时可能消除注射造影剂的需要。·MR血管造影广泛应用于儿童血管评估成像。·由于使用基于钆的造影剂,对比增强MRA具有局限性。·REACT是一种在自由呼吸时进行的新型无对比MRA技术。·REACT提供的图像质量可与对比度增强的自由呼吸MRA媲美。·Spogis J, Tsiflikas I, Katemann C等。使用REACT的自由呼吸非对比增强不依赖血流的MR血管造影:一项用于儿童血管评估的前瞻性研究。Rofo 2026;10.1055 / - 2781 - 8861。
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引用次数: 0
Focused ultrasound-mediated drug delivery systems: a technological overview, possible musculoskeletal applications, and future directions. 聚焦超声介导的药物传递系统:技术概述,可能的肌肉骨骼应用和未来方向。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-01-30 DOI: 10.1055/a-2760-5392
Rebecca Sassi, Silvia Gazzotti, Maria Pilar Aparisi Gómez, Costanza Maria Donati, Alessio Giuseppe Morganti, Marc-André Weber, Pejman Ghanouni, Alessandro Napoli, Alberto Bazzocchi

Innovation in focused ultrasound (FUS) has led to new applications for treating musculoskeletal pathologies, including oncologic, infectious, and degenerative diseases. Focused ultrasound-mediated drug delivery is particularly interesting in fields in which high selectivity and localized action are needed to avoid unwanted side effects or therapy failure, for example with antineoplastic and antimicrobial drugs.For this paper, a literature search of the PubMed database was performed using the keywords "focused ultrasound" and "musculoskeletal applications".This review article presents an overview of the currently available technologies for focused ultrasound-mediated drug delivery and their possible musculoskeletal applications, along with a discussion of recent promising preclinical and clinical results. · Focused ultrasound is able to deliver drugs in a very selective way.. · Focused ultrasound-mediated hyperthermia may be promising for treating bone infections.. · Focused ultrasound-mediated drug delivery may also be an elegant method for treating bone cancer and arthritis.. · Sassi R, Gazzotti S, Aparisi Gómez MP et al. Focused ultrasound-mediated drug delivery systems: a technological overview, possible musculoskeletal applications, and future directions. Rofo 2025; DOI 10.1055/a-2760-5392.

聚焦超声(FUS)的创新导致了治疗肌肉骨骼病变的新应用,包括肿瘤、感染性和退行性疾病。聚焦超声介导的药物递送在需要高选择性和局部作用以避免不良副作用或治疗失败的领域尤其有趣,例如抗肿瘤和抗菌药物。本文使用关键词“聚焦超声”和“肌肉骨骼应用”对PubMed数据库进行文献检索。这篇综述文章概述了目前可用的聚焦超声介导药物递送技术及其可能的肌肉骨骼应用,并讨论了最近有希望的临床前和临床结果。聚焦超声能够以一种非常有选择性的方式输送药物。聚焦超声介导的热疗可能有望治疗骨感染。聚焦超声介导的药物递送也可能是治疗骨癌和关节炎的一种优雅方法。·Sassi R, Gazzotti S, Aparisi Gómez MP等。聚焦超声介导的药物传递系统:技术概述,可能的肌肉骨骼应用和未来方向。Rofo 2025;DOI 10.1055 / - 2760 - 5392。
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引用次数: 0
Paraligamentous Fat Necrosis Adjacent to the Falciform Ligament - A Rare Mimic of Acute Cholecystitis. 镰状韧带附近的韧带旁脂肪坏死-一种罕见的急性胆囊炎的模拟物。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-01-30 DOI: 10.1055/a-2779-7798
Maria Sophie Katz, Nina Pauline Haag, Christoph Mönninghoff, Jan Robert Kröger
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引用次数: 0
Inter- and intra-individual radiation dose variability in oncologic chest and abdominal computed tomography. 肿瘤胸部和腹部计算机断层扫描的个体间和个体内辐射剂量变异性。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-01-30 DOI: 10.1055/a-2786-2534
Arian Felix Moradians, Daniel Rosok, Raya Serger, Laura Valentina Klüner, Marcel Drews, Florian Behr, Luca Salhöfer, Denise Bos, Michael Forsting, Johannes Haubold, Marcel Klaus Opitz, Sebastian Zensen

Computed tomography (CT) plays a central role in oncologic imaging, yet repeated examinations contribute substantially to cumulative radiation exposure. This study aimed to evaluate inter- and intra-individual radiation dose variability in chest and abdominal CT and the impact of CT device model and protocol standardization.In this retrospective single-center study, 42441 CT scans from 4986 adult oncologic patients were analyzed. Dose metrics (CTDIvol, DLP, SSDE, effective dose) were extracted using automated dose monitoring. Inter- and intra-individual radiation dose variability was assessed across four CT device models and various protocol subtypes. Intra-individual radiation dose variability was calculated relative to the lowest dose per patient and compared across CT devices and protocol subtypes.Radiation dose varied substantially between devices, with CTDIvol differences of up to 2.4-fold in chest CT (2.98-7.26 mGy) and 1.7-fold in abdominal CT (5.26-8.77 mGy). The median intra-individual radiation dose variability was 93.7% (IQR 19.8-142.0%) in non-contrast chest CT, 66.3% (31.1-105.4%) in contrast-enhanced chest CT, 19.8% (11.8-32.3%) in non-contrast abdominal CT, and 28.2% (16.6-41.0%) in contrast-enhanced abdominal CT. When consecutive scans were performed on the same scanner, intra-individual radiation dose variability decreased to 14.7% (IQR 8.1-33.1%), 18.1% (9.5-31.3%), 11.7% (7.8-19.8%), and 15.3% (8.3-24.7%), respectively, indicating substantial device-specific effects.Significant radiation dose variability persists in oncologic CT, both between and within patients, despite the use of standardized protocols. Device-adapted dose management and consistent device use may improve dose consistency, support optimization in oncologic imaging, and reduce radiation exposure. · Substantial radiation dose variability persists across CT devices despite protocol standardization.. · Intra-individual radiation dose variability is significant and highest in non-contrast chest CT.. · Consistent use of the same scanner reduces intra-individual radiation dose variability significantly.. · Internal diagnostic reference levels may improve radiation dose consistency and minimize exposure.. · Moradians AF, Rosok D, Serger R et al. Inter- and intra-individual radiation dose variability in oncologic chest and abdominal computed tomography. Rofo 2026; DOI 10.1055/a-2786-2534.

计算机断层扫描(CT)在肿瘤成像中起着核心作用,然而重复检查在很大程度上导致了累积辐射暴露。本研究旨在评估个体间和个体内胸部和腹部CT的辐射剂量变异性以及CT设备模型和方案标准化的影响。在这项回顾性单中心研究中,对4986名成年肿瘤患者的42441张CT扫描进行了分析。使用自动剂量监测提取剂量指标(CTDIvol, DLP, SSDE,有效剂量)。在四种CT设备模型和各种方案亚型中评估个体间和个体内辐射剂量变异性。相对于每位患者最低剂量计算个体内辐射剂量变异性,并比较不同CT设备和方案亚型。不同设备之间的辐射剂量差异很大,胸部CT (2.98-7.26 mGy)的CTDIvol差异高达2.4倍,腹部CT (5.26-8.77 mGy)的CTDIvol差异高达1.7倍。个体内辐射剂量变异中位数在胸部非对比CT为93.7% (IQR为19.8 ~ 142.0%),胸部增强CT为66.3% (IQR为31.1 ~ 105.4%),腹部非对比CT为19.8%(11.8 ~ 32.3%),腹部增强CT为28.2%(16.6 ~ 41.0%)。当在同一台扫描仪上进行连续扫描时,个体内辐射剂量变异性分别下降至14.7% (IQR 8.1-33.1%)、18.1%(9.5-31.3%)、11.7%(7.8-19.8%)和15.3%(8.3-24.7%),表明存在实质性的设备特异性效应。尽管使用了标准化的方案,但肿瘤CT在患者之间和患者内部仍然存在显著的辐射剂量差异。适应设备的剂量管理和一致的设备使用可以提高剂量一致性,支持肿瘤成像的优化,并减少辐射暴露。·尽管协议标准化,但在CT设备之间仍然存在大量辐射剂量差异。·个体内辐射剂量变异性显著且在胸部非对比CT中最高。·持续使用同一台扫描仪可显著降低个体内辐射剂量的可变性。·内部诊断参考水平可提高辐射剂量一致性并最大限度地减少照射。·Moradians AF, Rosok D, Serger R等。肿瘤胸部和腹部计算机断层扫描的个体间和个体内辐射剂量变异性。Rofo 2026;DOI 10.1055 / - 2786 - 2534。
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引用次数: 0
Cardiac computed tomography in patients with pacemakers. 心脏起搏器患者的计算机断层扫描。
IF 1.7 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2026-01-20 DOI: 10.1055/a-2771-3091
Niklas Deniz Frömmel, Stella Schütz, Abdelmajid Matoug
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引用次数: 0
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