Table 3.
Summary of studies about AI implementation in hysteroscopy. Sn, sensitivity; Sp, specificity; AUC—area under the curve; NK—not known; EH—endometrial hyperplasia; AH—atypical hyperplasia; EC—endometrial cancer; EP—endometrial polyps; SM—submucous myomas; FCM—Fuzzy C-Means.
Author, Year | Study Aim | Pati-ents n | Frames n | Pathologic Confirma-tion | AI Method | Dataset Method | Analysis Method | Catego-Ries | Performance Metrics % | ||
---|---|---|---|---|---|---|---|---|---|---|---|
Sn | Sp | AUC | |||||||||
Neofytou, M.S.; 2006, USA [50] |
Hysteroscopy image classification | 198 | 418 frames
|
No | Color– texture analysis methods | Frame annotation based on texture features (two different classifiers) | 10-fold cross validation (and leave-one-out method) | Normal vs. abnormal | 51–77 | 72–82 | NK |
Vlacho-kosta, 2013, Greece [51] |
Differentiating normal vs. uterine vs. endometrial cancer | 77 | NK Only number of patients per category |
Yes | DNN and FCM | Feature extraction related to vessel and texture structure | NK | Normal vs. patological | 71–93 | 71–91 | 91 |
Zhang, 2021, China [52] |
Differentiating benign (EH, EP, and SM) from premalignant/malignant lesions (AH and EC) | 454 | 1851 frames: EH = 509 AH = 222, EC = 280 EP = 615 SM = 225 |
Yes | VGGNet | Image-based frame labeling with preprocessing and retaining of region of interest and data augmentation | Train–test validation (50 images for each category in test set) | Part 1: EH vs. AH vs. EC vs. EP vs. SM; Part 2: benign vs. premalignant/malignant |
83 | 96 | 94 |
Takahashi, 2021, Japan [53] |
Differentiating malign vs. benign or normal findings | 177 | 411,800 frames
|
Yes | Xception, MobileNetV2 and EfficientNetB0 | Frame labeling in still images and video segments | Train–testvalidation | Malignant and others (uterine myoma, EP normal endometrium) |
92 | 89 | 90 |