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Background and aims
Celiac disease with its endoscopic manifestation of villous atrophy is underdiagnosed worldwide. The application of artificial intelligence (AI) for the macroscopic detection of villous atrophy at routine esophagogastroduodenoscopy may improve diagnostic performance.
Methods
A dataset of 858 endoscopic images of 182 patients with villous atrophy and 846 images from 323 patients with normal duodenal mucosa was collected and used to train a ResNet 18 deep learning model to detect villous atrophy. An external data set was used to test the algorithm, in addition to six fellows and four board certified gastroenterologists. Fellows could consult the AI algorithm’s result during the test. From their consultation distribution, a stratification of test images into “easy” and “difficult” was performed and used for classified performance measurement.
Results
External validation of the AI algorithm yielded values of 90 %, 76 %, and 84 % for sensitivity, specificity, and accuracy, respectively. Fellows scored values of 63 %, 72 % and 67 %, while the corresponding values in experts were 72 %, 69 % and 71 %, respectively. AI consultation significantly improved all trainee performance statistics. While fellows and experts showed significantly lower performance for “difficult” images, the performance of the AI algorithm was stable.
Conclusion
In this study, an AI algorithm outperformed endoscopy fellows and experts in the detection of villous atrophy on endoscopic still images. AI decision support significantly improved the performance of non-expert endoscopists. The stable performance on “difficult” images suggests a further positive add-on effect in challenging cases.
Einleitung
Die sichere Detektion und Charakterisierung von Barrett-Ösophagus assoziierten Neoplasien (BERN) stellt selbst für erfahrene Endoskopiker eine Herausforderung dar.
Ziel
Ziel dieser Studie ist es, den Add-on Effekt eines künstlichen Intelligenz (KI) Systems (Barrett-Ampel) als Entscheidungsunterstüzungssystem für Endoskopiker ohne Expertise bei der Untersuchung von BERN zu evaluieren.
Material und Methodik
Zwölf Videos in „Weißlicht“ (WL), „narrow-band imaging“ (NBI) und „texture and color enhanced imaging“ (TXI) von histologisch bestätigten Barrett-Metaplasien oder BERN wurden von Experten und Untersuchern ohne Barrett-Expertise evaluiert. Die Probanden wurden dazu aufgefordert in den Videos auftauchende BERN zu identifizieren und gegebenenfalls die optimale Biopsiestelle zu markieren. Unser KI-System wurde demselben Test unterzogen, wobei dieses BERN in Echtzeit segmentierte und farblich von umliegendem Epithel differenzierte. Anschließend wurden den Probanden die Videos mit zusätzlicher KI-Unterstützung gezeigt. Basierend auf dieser neuen Information, wurden die Probanden zu einer Reevaluation ihrer initialen Beurteilung aufgefordert.
Ergebnisse
Die „Barrett-Ampel“ identifizierte unabhängig von den verwendeten Darstellungsmodi (WL, NBI, TXI) alle BERN. Zwei entzündlich veränderte Läsionen wurden fehlinterpretiert (Genauigkeit=75%). Während Experten vergleichbare Ergebnisse erzielten (Genauigkeit=70,8%), hatten Endoskopiker ohne Expertise bei der Beurteilung von Barrett-Metaplasien eine Genauigkeit von lediglich 58,3%. Wurden die nicht-Experten allerdings von unserem KI-System unterstützt, erreichten diese eine Genauigkeit von 75%.
Zusammenfassung
Unser KI-System hat das Potential als Entscheidungsunterstützungssystem bei der Differenzierung zwischen Barrett-Metaplasie und BERN zu fungieren und so Endoskopiker ohne entsprechende Expertise zu assistieren. Eine Limitation dieser Studie ist die niedrige Anzahl an eingeschlossenen Videos. Um die Ergebnisse dieser Studie zu bestätigen, müssen randomisierte kontrollierte klinische Studien durchgeführt werden.
Aims
Barrett´s esophagus related neoplasia (BERN) is difficult to detect and characterize during endoscopy, even for expert endoscopists. We aimed to assess the add-on effect of an Artificial Intelligence (AI) algorithm (Barrett-Ampel) as a decision support system (DSS) for non-expert endoscopists in the evaluation of Barrett’s esophagus (BE) and BERN.
Methods
Twelve videos with multimodal imaging white light (WL), narrow-band imaging (NBI), texture and color enhanced imaging (TXI) of histologically confirmed BE and BERN were assessed by expert and non-expert endoscopists. For each video, endoscopists were asked to identify the area of BERN and decide on the biopsy spot. Videos were assessed by the AI algorithm and regions of BERN were highlighted in real-time by a transparent overlay. Finally, endoscopists were shown the AI videos and asked to either confirm or change their initial decision based on the AI support.
Results
Barrett-Ampel correctly identified all areas of BERN, irrespective of the imaging modality (WL, NBI, TXI), but misinterpreted two inflammatory lesions (Accuracy=75%). Expert endoscopists had a similar performance (Accuracy=70,8%), while non-experts had an accuracy of 58.3%. When AI was implemented as a DSS, non-expert endoscopists improved their diagnostic accuracy to 75%.
Conclusions
AI may have the potential to support non-expert endoscopists in the assessment of videos of BE and BERN. Limitations of this study include the low number of videos used. Randomized clinical trials in a real-life setting should be performed to confirm these results.
Aims
VA is an endoscopic finding of celiac disease (CD), which can easily be missed if pretest probability is low. In this study, we aimed to develop an artificial intelligence (AI) algorithm for the detection of villous atrophy on endoscopic images.
Methods
858 images from 182 patients with VA and 846 images from 323 patients with normal duodenal mucosa were used for training and internal validation of an AI algorithm (ResNet18). A separate dataset was used for external validation, as well as determination of detection performance of experts, trainees and trainees with AI support. According to the AI consultation distribution, images were stratified into “easy” and “difficult”.
Results
Internal validation showed 82%, 85% and 84% for sensitivity, specificity and accuracy. External validation showed 90%, 76% and 84%. The algorithm was significantly more sensitive and accurate than trainees, trainees with AI support and experts in endoscopy. AI support in trainees was associated with significantly improved performance. While all endoscopists showed significantly lower detection for “difficult” images, AI performance remained stable.
Conclusions
The algorithm outperformed trainees and experts in sensitivity and accuracy for VA detection. The significant improvement with AI support suggests a potential clinical benefit. Stable performance of the algorithm in “easy” and “difficult” test images may indicate an advantage in macroscopically challenging cases.