Sung-Liang Chen

Jieyun Bai, Zihao Zhou, Yitong Tang et al.

A substantial proportion (45\%) of maternal deaths, neonatal deaths, and stillbirths occur during the intrapartum phase, with a particularly high burden in low- and middle-income countries. Intrapartum biometry plays a critical role in monitoring labor progression; however, the routine use of ultrasound in resource-limited settings is hindered by a shortage of trained sonographers. To address this challenge, the Intrapartum Ultrasound Grand Challenge (IUGC), co-hosted with MICCAI 2024, was launched. The IUGC introduces a clinically oriented multi-task automatic measurement framework that integrates standard plane classification, fetal head-pubic symphysis segmentation, and biometry, enabling algorithms to exploit complementary task information for more accurate estimation. Furthermore, the challenge releases the largest multi-center intrapartum ultrasound video dataset to date, comprising 774 videos (68,106 frames) collected from three hospitals, providing a robust foundation for model training and evaluation. In this study, we present a comprehensive overview of the challenge design, review the submissions from eight participating teams, and analyze their methods from five perspectives: preprocessing, data augmentation, learning strategy, model architecture, and post-processing. In addition, we perform a systematic analysis of the benchmark results to identify key bottlenecks, explore potential solutions, and highlight open challenges for future research. Although encouraging performance has been achieved, our findings indicate that the field remains at an early stage, and further in-depth investigation is required before large-scale clinical deployment. All benchmark solutions and the complete dataset have been publicly released to facilitate reproducible research and promote continued advances in automatic intrapartum ultrasound biometry.

Da He, Jiasheng Zhou, Xiaoyu Shang et al.

As a hybrid imaging technology, photoacoustic microscopy (PAM) imaging suffers from noise due to the maximum permissible exposure of laser intensity, attenuation of ultrasound in the tissue, and the inherent noise of the transducer. De-noising is a post-processing method to reduce noise, and PAM image quality can be recovered. However, previous de-noising techniques usually heavily rely on mathematical priors as well as manually selected parameters, resulting in unsatisfactory and slow de-noising performance for different noisy images, which greatly hinders practical and clinical applications. In this work, we propose a deep learning-based method to remove complex noise from PAM images without mathematical priors and manual selection of settings for different input images. An attention enhanced generative adversarial network is used to extract image features and remove various noises. The proposed method is demonstrated on both synthetic and real datasets, including phantom (leaf veins) and in vivo (mouse ear blood vessels and zebrafish pigment) experiments. The results show that compared with previous PAM de-noising methods, our method exhibits good performance in recovering images qualitatively and quantitatively. In addition, the de-noising speed of 0.016 s is achieved for an image with $256\times256$ pixels. Our approach is effective and practical for the de-noising of PAM images.

Jiasheng Zhou, Da He, Xiaoyu Shang et al.

Photoacoustic microscopy (PAM) has been a promising biomedical imaging technology in recent years. However, the point-by-point scanning mechanism results in low-speed imaging, which limits the application of PAM. Reducing sampling density can naturally shorten image acquisition time, which is at the cost of image quality. In this work, we propose a method using convolutional neural networks (CNNs) to improve the quality of sparse PAM images, thereby speeding up image acquisition while keeping good image quality. The CNN model utilizes both squeeze-and-excitation blocks and residual blocks to achieve the enhancement, which is a mapping from a 1/4 or 1/16 low-sampling sparse PAM image to a latent fully-sampled image. The perceptual loss function is applied to keep the fidelity of images. The model is mainly trained and validated on PAM images of leaf veins. The experiments show the effectiveness of our proposed method, which significantly outperforms existing methods quantitatively and qualitatively. Our model is also tested using in vivo PAM images of blood vessels of mouse ears and eyes. The results show that the model can enhance the image quality of the sparse PAM image of blood vessels from several aspects, which may help fast PAM and facilitate its clinical applications.

Da He, De Cai, Jiasheng Zhou et al.

Fluorescence microscopy plays an important role in biomedical research. The depth-variant point spread function (PSF) of a fluorescence microscope produces low-quality images especially in the out-of-focus regions of thick specimens. Traditional deconvolution to restore the out-of-focus images is usually insufficient since a depth-invariant PSF is assumed. This article aims at handling fluorescence microscopy images by learning-based depth-variant PSF and reducing artifacts. We propose adaptive weighting depth-variant deconvolution (AWDVD) with defocus level prediction convolutional neural network (DelpNet) to restore the out-of-focus images. Depth-variant PSFs of image patches can be obtained by DelpNet and applied in the afterward deconvolution. AWDVD is adopted for a whole image which is patch-wise deconvolved and appropriately cropped before deconvolution. DelpNet achieves the accuracy of 98.2%, which outperforms the best-ever one using the same microscopy dataset. Image patches of 11 defocus levels after deconvolution are validated with maximum improvement in the peak signal-to-noise ratio and structural similarity index of 6.6 dB and 11%, respectively. The adaptive weighting of the patch-wise deconvolved image can eliminate patch boundary artifacts and improve deconvolved image quality. The proposed method can accurately estimate depth-variant PSF and effectively recover out-of-focus microscopy images. To our acknowledge, this is the first study of handling out-of-focus microscopy images using learning-based depth-variant PSF. Facing one of the most common blurs in fluorescence microscopy, the novel method provides a practical technology to improve the image quality.