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Alan Campbell

Publications and source records attributed to Alan Campbell.

3 recordsLinked to original sources

Design and performance of the Fast Beam Condition Monitor for luminosity and background measurement at the CMS Experiment in LHC Run 3

The Fast Beam Condition Monitor (BCM1F) has been used at the CMS Experiment since the first LHC circulating beams in 2008. Originally meant as a beam-induced background monitor for fast beam losses detection, it showed a potential also for luminosity measurements in 2012 running, and has been used for luminosity measurements since the beginning of Run 2 data taking in 2015 as a part of the Beam Radiation, Instrumentation and Luminosity (BRIL) system. Over the years, the system has undergone various upgrades to the sensors, the front-end and back-end electronics, providing improvements in the precision of the measurements, that remain valid in the higher pileup conditions of LHC Run 3 (2022-2026). Based on the experience of all BCM1F Run 2 upgrades, the detector was completely rebuilt prior to LHC Run 3 using AC-coupled silicon-pad diodes and active cooling. This latest detector version exhibits excellent linearity with instantaneous luminosity and achieves nanosecond-level timing precision, enabling improved systematic corrections for luminosity and background measurements. This paper presents a detailed overview of the detector system for LHC Run 3, including the selection and qualification of sensors as well as a summary of the readout system. It also outlines the processing and calibration strategy for luminosity data, discussing operational hurdles and comparing BCM1F measurements to other CMS luminosity measurements to assess the system's performance as a luminometer. Lastly, the implications for the design of a future luminosity detector to be used in the envisioned HL-LHC upgrade are discussed.

physics.ins-det

Bidirectional human-AI collaboration in brain tumour assessments improves both expert human and AI agent performance

The benefits of artificial intelligence (AI) human partnerships-evaluating how AI agents enhance expert human performance-are increasingly studied. Though rarely evaluated in healthcare, an inverse approach is possible: AI benefiting from the support of an expert human agent. Here, we investigate both human-AI clinical partnership paradigms in the magnetic resonance imaging-guided characterisation of patients with brain tumours. We reveal that human-AI partnerships improve accuracy and metacognitive ability not only for radiologists supported by AI, but also for AI agents supported by radiologists. Moreover, the greatest patient benefit was evident with an AI agent supported by a human one. Synergistic improvements in agent accuracy, metacognitive performance, and inter-rater agreement suggest that AI can create more capable, confident, and consistent clinical agents, whether human or model-based. Our work suggests that the maximal value of AI in healthcare could emerge not from replacing human intelligence, but from AI agents that routinely leverage and amplify it.

cs.HC

Predicting brain tumour enhancement from non-contrast MR imaging with artificial intelligence: a multi-cohort retrospective diagnostic accuracy study

Brain tumour MRI typically requires both pre- and post-contrast imaging, but gadolinium is not always desirable (frequent follow-up, renal impairment, allergy, paediatric patients). We developed and validated a deep learning model to predict tumour contrast enhancement from non-contrast MRI alone. We assembled 11,089 brain MRI studies (2006-2024) from 10 datasets across four countries and three continents, spanning adult and paediatric populations with glioma, meningioma, metastases, and post-resection appearances. Three architectures were trained to detect and segment enhancing tumour from T1w, T2w and FLAIR alone. Performance was assessed in a 1,109-study held-out test set (primary endpoint: patient-level enhancement detection; secondary: voxel-level Dice). Eleven expert radiologists attempted the same task on a 564-case subset (100 cases each), blinded to history, prior imaging, and referral. The best model, nnU-Net, achieved 83.0% balanced accuracy (95% CI 79.1-87.2; sensitivity 91.5%, specificity 74.4%) for detection, with R2 = 0.859 for enhancement volume. Of enhancing cases, 76.8% reached Dice >= 0.3, 67.5% >= 0.5, and 50.2% >= 0.7. Under blinded conditions, radiologists' majority vote was lower (71.7% balanced accuracy; sensitivity 77.6%, specificity 65.8%). The proportion reaching Dice >= 0.3 varied by pathology (meningioma 93%, presurgical glioma 76%, metastases 74%, postoperative glioma 74%) and was lowest for paediatric cases (45%). Deep learning can identify contrast-enhancing brain tumours from non-contrast MRI. These models show promise as a triage or decision-support adjunct, such as in flagging studies likely to enhance so that contrast can be added to a non-contrast protocol, and may reduce gadolinium dependence in neuro-oncology imaging. Future work should optimise these models with radiologists.

eess.IV