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Correlation of optical coherence elastography with clinical evaluation of systemic sclerosis

机译:光学相干弹性成像与系统性硬化症临床评估的相关性

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摘要

Systemic sclerosis (SSc) is an autoimmune disorder with high mortality due to excessive accumulation of collagen inthe skin and internal organs. An accurate and early diagnosis is crucial to ensure effective treatment. Currently, themodified Rodnan skin score (mRSS) is the gold standard for evaluating dermal thickening during SSc onset andprogression. However, obtaining the mRSS can be time consuming, and the score has noticeable inter- and intraobservervariabilities. Optical coherence elastography (OCE) is an emerging technique for measuring soft tissuebiomechanical properties completely noninvasively. In this work, we demonstrate the first use of OCE combinedwith analysis of the OCT signal slope (OCTSS) for sclerosis detection in the dorsal forearm of 12 patients. Acomparison to clinical diagnoses including dermal thickness assessed by histology, mRSS, and site specific mRSS(SMRSS). Results of both optical assessments demonstrated high correlation (OCE: 0.78 and OCTSS: 0.65) withSMRSS as performed by an experienced physician. Importantly, the correlation of both proposed parameters withthe dermal thickness (OCTSS: r=0.78 and OCE: r=0.74) outperformed the SMRSS assessment (r=0.57),demonstrating the effectiveness of using OCT/OCE for monitoring the disease severity of SSc.
机译:系统性硬化症(SSc)是一种自身免疫性疾病,由于胶原蛋白在皮肤和内脏器官中的过度积聚而具有很高的死亡率。准确的早期诊断对于确保有效的治疗至关重要。目前,改良的Rodnan皮肤评分(mRSS)是评估SSc发作和进展期间皮肤增厚的金标准。但是,获取mRSS可能很耗时,并且评分在观察者之间和观察者内部\内部\内部都有明显的差异。光学相干弹性成像(OCE)是一种新兴的技术,可以完全无创地测量软组织\生物力学特性。在这项工作中,我们证明了OCE首次与OCT信号斜率分析(OCTSS)结合使用来检测12例患者前臂的硬化情况。与临床诊断比较,包括通过组织学,mRSS和部位特异性mRSS \ r \ n(SMRSS)评估的真皮厚度。两次光学评估的结果均表明,由经验丰富的医师进行的\ r \ nSMRSS具有较高的相关性(OCE:0.78和OCTSS:0.65)。重要的是,这两个建议参数与皮肤厚度(OCTSS:r = 0.78和OCE:r = 0.74)的相关性均胜过SMRSS评估(r = 0.57),这证明了使用OCT / OCE进行皮肤厚度测量的有效性监测SSc的疾病严重程度。

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  • 来源
    《Optical Elastography and Tissue Biomechanics VI》|2019年|1088004.1-1088004.8|共8页
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    Department of Biomedical Engineering, University of Houston, 3605 Cullen Boulevard, Houston, Texas 77204;

    Department of Biomedical Engineering, University of Houston, 3605 Cullen Boulevard, Houston, Texas 77204;

    Department of Biomedical Engineering, University of Houston, 3605 Cullen Boulevard, Houston, Texas 77204;

    Department of Biomedical Engineering, University of Houston, 3605 Cullen Boulevard, Houston, Texas 77204;

    Department of Biomedical Engineering, University of Houston, 3605 Cullen Boulevard, Houston, Texas 77204;

    Rheumatology and Clinical Immunogenetics, University of Texas Health Science Center at Houston, 7000 Fannin St., Houston, Texas 77030;

    Rheumatology and Clinical Immunogenetics, University of Texas Health Science Center at Houston, 7000 Fannin St., Houston, Texas 77030;

    Department of Biomedical Engineering, University of Houston, 3605 Cullen Boulevard, Houston, Texas 77204 Molecular Physiology and Biophysics, Baylor College of Medicine, One Baylor Plaza, Houston, USA, Texas 77584 klarin@uh.edu;

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