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Automatic vertebral bodies detection of X-ray images using Invariant multiscale template matching

机译:使用不变多尺度模板匹配的自动椎体检测X射线图像

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Lower back pain and pathologies related to it are one of the most common results for a referral to a neurosurgical clinic in the developed and the developing world. Quantitative evaluation of these pathologies is a challenge. Image based measurements of angles/vertebral heights and disks could provide a potential quantitative biomarker for tracking and measuring these pathologies. Detection of vertebral bodies is a key element and is the focus of the current work. From the variety of medical imaging techniques, MRI and CT scans have been typically used for developing image segmentation methods. However, CT scans are known to give a large dose of x-rays, increasing cancer risk [8]. MRI can be substituted for CTs when the risk is high [8] but are difficult to obtain in smaller facilities due to cost and lack of expertise in the field [2]. X-rays provide another option with its ability to control the x-ray dosage, especially for young people, and its accessibility for smaller facilities. Hence, the ability to create quantitative biomarkers from x-ray data is especially valuable. Here, we develop a multiscale template matching, inspired by [9], to detect centers of vertebral bodies from x-ray data. The immediate application of such detection lies in developing quantitative biomarkers and in querying similar images in a database. Previously, shape similarity classification methods have been used to address this problem, but these are challenging to use in the presence of variation due to gross pathology and even subtle effects[1].
机译:与发达国家和发展中国家和发展中国家的神经外科诊所引用的最常见的疼痛和病理有关。对这些病理学的定量评估是挑战。基于图像的角度/椎体高度和盘的测量可以提供潜在的定量生物标志物,用于跟踪和测量这些病理学。椎体检测是关键元素,是当前工作的重点。从各种医学成像技术,MRI和CT扫描通常用于开发图像分段方法。然而,已知CT扫描用于给予大剂量的X射线,增加癌症风险[8]。当风险很高时,MRI可以代替CTS [8],但由于成本和缺乏领域的专业知识,难以在较小的设施中获得较小的设施[2]。 X射线提供了另一种选择,其能够控制X射线剂量,特别是对于年轻人,以及较小设施的可访问性。因此,从X射线数据创建定量生物标志物的能力尤其有价值。在这里,我们开发了一个由[9]的灵感的多尺度模板匹配,从X射线数据检测椎体的中心。这种检测的直接应用在于在数据库中求解定量生物标志物和查询类似的图像。以前,形状相似性分类方法已被用来解决这个问题,但这些问题是在存在变化的存在下挑战,因为由于病理粗糙,甚至细微效应[1]。

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