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Fibrotic Liver Ultrasonic Imaging Diagnostic (FLUID) System

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Presentation on theme: "Fibrotic Liver Ultrasonic Imaging Diagnostic (FLUID) System"— Presentation transcript:

1 Fibrotic Liver Ultrasonic Imaging Diagnostic (FLUID) System
Student Researchers: Meredith Huszagh, Fahad Iqbal, Sara Keller, Lauren Severance, Patricia Twilley, Alison Williams BEAM Lab, Department of Biomedical Engineering, Vanderbilt University School of Engineering Mentor: Brett Byram PhD, Assistant Professor of Biomedical Engineering Background Design Approach Results Liver fibrosis: scarring of the liver tissue Due to liver damage and healing Progresses through 4 stages, ending in cirrhosis Liver cirrhosis causes more than 1 million deaths per year Conclusion Current Methods The gold standard is a liver biopsy, but this method produces a qualitative result, is expensive, and the process of retrieving a liver biopsy is painful for the patient and increases their risk of bleeding and infection. Non-invasive techniques also exist, but this imaging modalities are extremely complex and expensive and generally are not portable. Marketability Design Components Diagnosis Diet Dippers Non-Dippers Non-Dipper Ratio Healthy Low Salt 10 2 16.7% Normal Salt 13 4 23.5% High Salt 11 3 21.4% POTS 9 6 40.0% 38 29 43.3% 28.6% Acknowledgements Problem Statement References Ultrasound elastography is a promising new technique for the noninvasive diagnosis of liver fibrosis and cirrhosis. At the moment, however, this method is considered suboptimal, particularly in diagnosis of intermediate stages of the disease [2]. Recent progress in magnetic resonance and ultrasonic imaging has shown promise of an effective technique for diagnosis, but these methods are currently too expensive for implementation in most low resource environments. In addition, measurement sensitivity in the early stages of disease is a concern for these techniques [1]. The purpose of our work is to engineer a system consisting of an inexpensive, handheld, ultrasound­-based device and accompanying software for noninvasively assessing liver fibrosis and cirrhosis. Conclusion Hypovolemia, while a symptom of POTS, cannot be used as a predictor of the high incidence for non-dipping phenomenon seen in POTS patients. There was a decrease in the Non-Dipper Ratio for POTS patients due to diet from normal salt diet to high salt diet in the overall data. the difference wasn’t sufficient to be labeled significant during the ANOVA testing. For POTS patients data, the diet caused a significant change in the change in plasma volume. Future studies might consider the viability of a high salt diet as a treatment for POTS patient symptoms. Currently, the sample size is too small to be conducting variability tests. As more subjects get enrolled in the study, the statistical power shall increase and the ANOVA results should have more significance. Results Needs Assessment ANOVA statistical tests wrtr conducted on paired data from subjects who completed the study for both low and high salt diets: References In order to more efficiently diagnose liver fibrosis, we propose the development of an ultrasound-based system that: Is non-invasive to reduce patient discomfort Requires minimal training by the provider to eliminate need of designated ultrasound technician Is accessible to patients in low-resource environments Takes advantage of freely available software for data processing Uses a single-element as opposed to a multi-array transducer Quantitatively diagnoses stage of fibrosis progression (through correlation with tissue stiffness) in a way comparable to existing gold standard Characterizes risk of healthy tissue for becoming diseased Provides consistent and reliable measurements despite tissue inhomogeneity Reduces signal noise resulting from patient motion Utilizes a processor which decreases cost and increases portability Significant differences due to diagnosis were seen for: Plasma volume (p=0.0031) Change in plasma volume (p=3.45e-6) Blood volume (p=0.0034) Change in blood volume (p=1.41e-6) Red blood volume (p=0.0069) There were no significant differences due to dipping status for any blood volume parameter Significant differences due to diet were seen for: Plasma volume (p=0.0196) Change in plasma volume (p=0.0072) Change in blood volume (p=0.0299) Looking only at the POTS patient data, significant difference due to diet was seen for: Change in plasma volume (p= ) Bankir, Lise, Murielle Bochud, Marc Maillard, Pascal Bovet, Anne Gabriel, and Michel Burnier. “Nighttime Blood Pressure and Nocturnal Dipping Are Associated With Daytime Urinary Sodium Excretion in African Subjects.” Hypertension 51, no. 4 (April 1, 2008): 891–98. doi: /HYPERTENSIONAHA Diedrich, A., K. Sato, SR Raj, L. Diedrich, V. Weimann, D. Biaggioni, and D. Roberston. “Blood Volume Deficit and the Non-Dipping Phenomenon in Postural  Tachycardia Syndrome.” Clinical Autonomic Research 20 (2010): 292. Figueroa, Juan J., Darlene M. Bott-Kitslaar, Joaquin A. Mercado, Jeffrey R. Basford, Paola Sandroni, Win-Kuang Shen, David M. Sletten, et al. “Decreased Orthostatic Adrenergic Reactivity in Non-Dipping Postural Tachycardia Syndrome.” Autonomic Neuroscience: Basic & Clinical 185 (October 2014): 107–11. doi: /j.autneu Okamoto, L. E., A. Gamboa, C. Shibao, B. K. Black, A. Diedrich, S. R. Raj, D. Robertson, and I. Biaggioni. “Nocturnal Blood Pressure Dipping in the Hypertension of Autonomic Failure.” Hypertension 53 (February 2009): 363–69. doi: /HYPERTENSIONAHA Tikellis, Chris, Raelene J. Pickering., Tsorotes, Despina, et al. "Activation of the Renin-Angiotensin System Mediates the Effects of Dietary Salt Intake on Atherogenesis in the Apolipoprotein E Knockout Mouse." Hypertension 60 (2012): AHAJournals. Web. 1 Dec Acknowledgements Dr. Andre Diedrich (Vanderbilt University)


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