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Fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance

BACKGROUND: To evaluate the usefulness of the routine sonographic evaluation of the pattern of fluctuate portal velocity tracings and the hepatic veins for the diagnosis of arterioportal fistula (APF) and cardiogenic trans-sinusoidal shunting (CTS). MATERIALS AND METHODS. Color Doppler flow imaging...

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Autores principales: Meng, Qingxin, Lv, Lei, Yang, Bin, Fu, Ninghua, Lu, Guangming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita, Warsaw 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472948/
https://www.ncbi.nlm.nih.gov/pubmed/23077458
http://dx.doi.org/10.2478/v10019-012-0028-9
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author Meng, Qingxin
Lv, Lei
Yang, Bin
Fu, Ninghua
Lu, Guangming
author_facet Meng, Qingxin
Lv, Lei
Yang, Bin
Fu, Ninghua
Lu, Guangming
author_sort Meng, Qingxin
collection PubMed
description BACKGROUND: To evaluate the usefulness of the routine sonographic evaluation of the pattern of fluctuate portal velocity tracings and the hepatic veins for the diagnosis of arterioportal fistula (APF) and cardiogenic trans-sinusoidal shunting (CTS). MATERIALS AND METHODS. Color Doppler flow imaging and pulsed-wave Doppler (PW) examinations of the portal vein were performed in 282 subjects. The waveforms of the velocity tracings in the portal main trunk and its branches were determined to infer APF or CTS. Suspected cases of APFs or CTSs were always confirmed by echocardiography, contrast-enhanced ultrasound, computed tomography, or digital subtraction angiography findings. The portal maximum velocity (V(max)), minimum velocity(V(min)), V(max)/V(min), arterial peak systolic velocity and resistance index, and venous reverse and forward velocities were used to estimate their haemodynamics. RESULTS: The waveform of the velocity tracing for the draining portal vein of APF was typically arterial-like or diphase, as indicated by a systolic hepatofugal dwarf peak and a diastolic hepatopetal low flat shape. The flow in the affected portal vein was always hepatofugal in an intrahepatic patient, whereas a hepatopetal flow was observed in an extrahepatic APF patient. The waveform of the velocity tracing for the portal vein of CTS patients, especially its intrahepatic branches, showed a typical hump-like shape with or without a transitory hepatofugal tracing. The PW results displayed an increase in the retrograde phase of the hepatic venous flow with increased velocities in the two phases. CONCLUSIONS: Portal velocity tracings should be evaluated during routine detecting for APF or CTS, especially in patients with gastrointestinal upsets.
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spelling pubmed-34729482012-10-17 Fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance Meng, Qingxin Lv, Lei Yang, Bin Fu, Ninghua Lu, Guangming Radiol Oncol Research Article BACKGROUND: To evaluate the usefulness of the routine sonographic evaluation of the pattern of fluctuate portal velocity tracings and the hepatic veins for the diagnosis of arterioportal fistula (APF) and cardiogenic trans-sinusoidal shunting (CTS). MATERIALS AND METHODS. Color Doppler flow imaging and pulsed-wave Doppler (PW) examinations of the portal vein were performed in 282 subjects. The waveforms of the velocity tracings in the portal main trunk and its branches were determined to infer APF or CTS. Suspected cases of APFs or CTSs were always confirmed by echocardiography, contrast-enhanced ultrasound, computed tomography, or digital subtraction angiography findings. The portal maximum velocity (V(max)), minimum velocity(V(min)), V(max)/V(min), arterial peak systolic velocity and resistance index, and venous reverse and forward velocities were used to estimate their haemodynamics. RESULTS: The waveform of the velocity tracing for the draining portal vein of APF was typically arterial-like or diphase, as indicated by a systolic hepatofugal dwarf peak and a diastolic hepatopetal low flat shape. The flow in the affected portal vein was always hepatofugal in an intrahepatic patient, whereas a hepatopetal flow was observed in an extrahepatic APF patient. The waveform of the velocity tracing for the portal vein of CTS patients, especially its intrahepatic branches, showed a typical hump-like shape with or without a transitory hepatofugal tracing. The PW results displayed an increase in the retrograde phase of the hepatic venous flow with increased velocities in the two phases. CONCLUSIONS: Portal velocity tracings should be evaluated during routine detecting for APF or CTS, especially in patients with gastrointestinal upsets. Versita, Warsaw 2012-04-19 /pmc/articles/PMC3472948/ /pubmed/23077458 http://dx.doi.org/10.2478/v10019-012-0028-9 Text en Copyright © by Association of Radiology & Oncology http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Research Article
Meng, Qingxin
Lv, Lei
Yang, Bin
Fu, Ninghua
Lu, Guangming
Fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance
title Fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance
title_full Fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance
title_fullStr Fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance
title_full_unstemmed Fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance
title_short Fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance
title_sort fluctuating portal velocity tracing with rhythmicity: ultrasonic differential diagnosis and clinical significance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472948/
https://www.ncbi.nlm.nih.gov/pubmed/23077458
http://dx.doi.org/10.2478/v10019-012-0028-9
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