TY - CHAP A1 - Rosbach, Emely A1 - Ammeling, Jonas A1 - Krügel, Sebastian A1 - Kießig, Angelika A1 - Fritz, Alexis A1 - Ganz, Jonathan A1 - Puget, Chloé A1 - Donovan, Taryn A1 - Klang, Andrea A1 - Köller, Maximilian C. A1 - Bolfa, Pompei A1 - Tecilla, Marco A1 - Denk, Daniela A1 - Kiupel, Matti A1 - Paraschou, Georgios A1 - Kok, Mun Keong A1 - Haake, Alexander F. H. A1 - de Krijger, Ronald R. A1 - Sonnen, Andreas F.-P. A1 - Kasantikul, Tanit A1 - Dorrestein, Gerry M. A1 - Smedley, Rebecca C. A1 - Stathonikos, Nikolas A1 - Uhl, Matthias A1 - Bertram, Christof A1 - Riener, Andreas A1 - Aubreville, Marc ED - Yamashita, Naomi ED - Evers, Vanessa ED - Yatani, Koji ED - Ding, Xianghua ED - Lee, Bongshin ED - Chetty, Marshini ED - Toups-Dugas, Phoebe T1 - "When Two Wrongs Don't Make a Right" - Examining Confirmation Bias and the Role of Time Pressure During Human-AI Collaboration in Computational Pathology T2 - CHI'25: Proceedings of the 2025 CHI Conference on Human Factors in Computing Systems N2 - Artificial intelligence (AI)-based decision support systems hold promise for enhancing diagnostic accuracy and efficiency in computational pathology. However, human-AI collaboration can introduce and amplify cognitive biases, like confirmation bias caused by false confirmation when erroneous human opinions are reinforced by inaccurate AI output. This bias may increase under time pressure, a ubiquitous factor in routine pathology, as it strains practitioners’ cognitive resources. We quantified confirmation bias triggered by AI-induced false confirmation and examined the role of time constraints in a web-based experiment, where trained pathology experts (n=28) estimated tumor cell percentages. Our results suggest that AI integration fuels confirmation bias, evidenced by a statistically significant positive linear-mixed-effects model coefficient linking AI recommendations mirroring flawed human judgment and alignment with system advice. Conversely, time pressure appeared to weaken this relationship. These findings highlight potential risks of AI in healthcare and aim to support the safe integration of clinical decision support systems. UR - https://doi.org/10.1145/3706598.3713319 Y1 - 2025 UR - https://doi.org/10.1145/3706598.3713319 UR - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:573-58797 SN - 979-8-4007-1394-1 PB - ACM CY - New York ER - TY - JOUR A1 - Ammeling, Jonas A1 - Ganz, Jonathan A1 - Wilm, Frauke A1 - Breininger, Katharina A1 - Aubreville, Marc T1 - Investigation of Class Separability within Object Detection Models in Histopathology JF - IEEE Transactions on Medical Imaging UR - https://doi.org/10.1109/TMI.2025.3560134 Y1 - 2025 UR - https://doi.org/10.1109/TMI.2025.3560134 SN - 0278-0062 SN - 1558-254X VL - 44 IS - 8 SP - 3162 EP - 3174 PB - IEEE CY - New York ER - TY - CHAP A1 - Rosbach, Emely A1 - Ganz, Jonathan A1 - Ammeling, Jonas A1 - Riener, Andreas A1 - Aubreville, Marc ED - Palm, Christoph ED - Breininger, Katharina ED - Deserno, Thomas Martin ED - Handels, Heinz ED - Maier, Andreas ED - Maier-Hein, Klaus H. ED - Tolxdorff, Thomas T1 - Automation Bias in AI-assisted Medical Decision-making under Time Pressure in Computational Pathology T2 - Bildverarbeitung für die Medizin 2025: Proceedings, German Conference on Medical Image Computing, Regensburg March 09–11, 2025 UR - https://doi.org/10.1007/978-3-658-47422-5_27 Y1 - 2025 UR - https://doi.org/10.1007/978-3-658-47422-5_27 SN - 978-3-658-47422-5 SP - 129 EP - 134 PB - Springer Vieweg CY - Wiesbaden ER - TY - CHAP A1 - Ganz, Jonathan A1 - Ammeling, Jonas A1 - Rosbach, Emely A1 - Lausser, Ludwig A1 - Bertram, Christof A1 - Breininger, Katharina A1 - Aubreville, Marc ED - Palm, Christoph ED - Breininger, Katharina ED - Deserno, Thomas Martin ED - Handels, Heinz ED - Maier, Andreas ED - Maier-Hein, Klaus H. ED - Tolxdorff, Thomas T1 - Is Self-supervision Enough? BT - Benchmarking Foundation Models Against End-to-end Training for Mitotic Figure Classification T2 - Bildverarbeitung für die Medizin 2025: Proceedings, German Conference on Medical Image Computing, Regensburg March 09–11, 2025 UR - https://doi.org/10.1007/978-3-658-47422-5_15 Y1 - 2025 UR - https://doi.org/10.1007/978-3-658-47422-5_15 SN - 978-3-658-47422-5 SP - 63 EP - 68 PB - Springer Vieweg CY - Wiesbaden ER - TY - INPR A1 - Ammeling, Jonas A1 - Ganz, Jonathan A1 - Rosbach, Emely A1 - Lausser, Ludwig A1 - Bertram, Christof A1 - Breininger, Katharina A1 - Aubreville, Marc T1 - Benchmarking Foundation Models for Mitotic Figure Classification UR - https://doi.org/10.48550/arXiv.2508.04441 Y1 - 2025 UR - https://doi.org/10.48550/arXiv.2508.04441 PB - arXiv CY - Ithaca ER - TY - JOUR A1 - Puget, Chloé A1 - Ganz, Jonathan A1 - Bertram, Christof A1 - Conrad, Thomas A1 - Baeblich, Malte A1 - Voss, Anne A1 - Landmann, Katharina A1 - Haake, Alexander F. H. A1 - Spree, Andreas A1 - Hartung, Svenja A1 - Aeschlimann, Leonore A1 - Soto, Sara A1 - de Brot, Simone A1 - Dettwiler, Martina A1 - Aupperle-Lellbach, Heike A1 - Bolfa, Pompei A1 - Bartel, Alexander A1 - Kiupel, Matti A1 - Breininger, Katharina A1 - Aubreville, Marc A1 - Klopfleisch, Robert T1 - Artificial intelligence predicts c-KIT exon 11 genotype by phenotype in canine cutaneous mast cell tumors: Can human observers learn it? JF - Veterinary Pathology N2 - Canine cutaneous mast cell tumors (ccMCTs) are frequent neoplasms with variable biological behaviors. Internal tandem duplication mutations in c-KIT exon 11 (c-KIT-11-ITD) are associated with poor prognosis but predict therapeutic response to tyrosine kinase inhibitors. In a previous work, deep learning algorithms managed to predict the presence of c-KIT-11-ITD on digitalized hematoxylin and eosin-stained histological slides (whole-slide images, WSIs) in up to 87% of cases, suggesting the existence of morphological features characterizing ccMCTs carrying c-KIT-11-ITD. This 3-stage blinded study aimed to identify morphological features indicative of c-KIT-11-ITD and to evaluate the ability of human observers to learn this task. 17 untrained pathologists first classified 8 WSIs and 200 image patches (highly relevant for algorithmic classification) of ccMCTs as either positive or negative for c-KIT-11-ITD. Second, they self-trained to recognize c-KIT-11-ITD by looking at the same WSIs and patches correctly sorted. Third, pathologists classified 15 new WSIs and 200 new patches according to c-KIT-11-ITD status. In addition, participants reported microscopic features they considered relevant for their decision. Without training, participants correctly classified the c-KIT-11-ITD status of 63%–88% of WSIs and 43%–55% of patches. With self-training, 25%–38% of WSIs and 55%–56% of patches were correctly classified. High cellular pleomorphism, anisokaryosis, and sparse cytoplasmic granulation were commonly suggested as features associated with c-KIT-11-ITD-positive ccMCTs, none of which showed reliable predictivity in a follow-up study. The results indicate that transfer of algorithmic skills to the human observer is difficult. A c-KIT-11-ITD-specific morphological feature remains to be extracted from the artificial intelligence model. UR - https://doi.org/10.1177/03009858251380284 Y1 - 2025 UR - https://doi.org/10.1177/03009858251380284 UR - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:573-63841 SN - 1544-2217 VL - 63 IS - 2 SP - 369 EP - 379 PB - Sage CY - London ER -