Rofo-fortschritte Auf Dem Gebiet Der Rontgenstrahlen Und Der Bildgebenden Verfahren最新文献

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.

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.

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.

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.

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.

This study investigates the impact of echo time (TE) and repetition time (TR) on apparent diffusion coefficient (ADC) and diffusion-derived vessel density (DDVD) values. Spleen has longer T1 and T2 than the liver, and spleen has a T2 similar to most hepatocellular carcinomas.Liver and spleen diffusion MRI was conducted with six volunteers at 3.0 T with multiple sessions. When TE was changed with steps of TE=46 ms, 52 ms, 60 ms, 70 ms, and 80 ms, TR was fixed at 2000 ms. When TR was changed with steps of TR=200 ms, 300 ms, 500 ms, 1000 ms, and 2000 ms, TE was fixed at 46 ms. The b-values included 0, 1, 2, 10, and 600 s/mm². ADC was calculated with b=0 and b=600 s/mm² images. DDVD was the signal difference between on b=0 image and a very low b-value image (b=1, 2, 10 s/mm²). Thirty-five scans for each ADC data point and 23 scans for each DDVD data point were included.Following the increase in TE from 46ms to 80ms, the ADC value increased by 23.9% (median) for the liver and 18.2% (median) for the spleen, while the ADC_spleen/ADC_liver ratio was smaller when TE was longer. Following the increase in TR from 200ms to 2000 ms, the ADC value decreased by 4.8% (median) for the liver and 14.6% (median) for the spleen, while the ADC_spleen/ADC_liver ratio was smaller when TR was longer. Following the increase in TE from 46ms to 80ms, there was a decrease in the DDVD value. DDVD_spleen/DDVD_liver ratios were greater when TE was long. Following the increase in TR from 200ms to 2000ms, there was a biphasic change in the DDVD value. The DDVD values were highest when TR was 500ms, and DDVD_spleen/DDVD_liver ratios followed a mono-phasic decrease.TR and TE have very notable impact on the ADC and DDVD values of the liver and spleen. · An increase of TE and an increase of TR are both associated with a decreasing ADCspleen/ADCliver ratio.. · Longer TE is associated with an increased DDVDspleen/DDVDliver ratio.. · The lesion detectability and lesion-to-tissue contrast by ADC and DDVD maps may be amplified by optimizing TE and TR values.. · Xu FY, Wáng YXJ. The Impact of TE and TR on Apparent Diffusion Coefficient and Diffusion-derived Vessel Density Quantification: Studies of Healthy Liver and Spleen. Rofo 2026; DOI 10.1055/a-2777-6695.