Prospective comparison of transient elastography, point shear wave elastography, APRI and FIB‐4 for staging liver fibrosis in chronic viral hepatitis

Ultrasound‐based elastography and serum indexes have been individually validated as noninvasive methods for staging liver fibrosis in chronic viral hepatitis. We aimed to compare the accuracy of transient elastography (TE), shear wave elastography (SWE), aspartate aminotransferase to platelet index...

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Veröffentlicht in:Journal of viral hepatitis 2020-04, Vol.27 (4), p.437-448
Hauptverfasser: Udompap, Prowpanga, Sukonrut, Kamonthip, Suvannarerg, Voraparee, Pongpaibul, Ananya, Charatcharoenwitthaya, Phunchai
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container_end_page 448
container_issue 4
container_start_page 437
container_title Journal of viral hepatitis
container_volume 27
creator Udompap, Prowpanga
Sukonrut, Kamonthip
Suvannarerg, Voraparee
Pongpaibul, Ananya
Charatcharoenwitthaya, Phunchai
description Ultrasound‐based elastography and serum indexes have been individually validated as noninvasive methods for staging liver fibrosis in chronic viral hepatitis. We aimed to compare the accuracy of transient elastography (TE), shear wave elastography (SWE), aspartate aminotransferase to platelet index (APRI) and Fibrosis‐4 index (FIB‐4) with the METAVIR liver fibrosis staging in viral hepatitis patients. We enrolled 121 treatment‐naïve chronic hepatitis B and C monoinfected patients. All underwent liver biopsy had biochemistry tests and liver stiffness measurements by TE using M and XL probes followed by point SWE performed on the same day. The accuracy of each method for predicting different fibrosis stages was demonstrated as an area under the receiver operating characteristic (AUROC) curves. The AUROCs of TE using M and XL probes, SWE, APRI and FIB‐4 were 0.771, 0.761, 0.700, 0.698 and 0.697, respectively, for significant fibrosis; 0.974, 0.973, 0.929, 0.738 and 0.859, respectively, for advanced fibrosis; and 0.954, 0.949, 0.962, 0.765 and 0.962, respectively, for cirrhosis. TE using the M probe was comparable to the XL probe in detecting all fibrosis stages. TE was superior to SWE for assessing significant fibrosis and advanced fibrosis. For cirrhosis, the performances of TE, SWE and FIB‐4 were similar. APRI was least accurate in liver fibrosis staging. To conclude, for patients with viral hepatitis, TE using either M or XL probe is an effective noninvasive test for assessing liver fibrosis, particularly advanced fibrosis and cirrhosis, while SWE and FIB‐4 possess an excellent accuracy in predicting cirrhosis.
doi_str_mv 10.1111/jvh.13246
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We aimed to compare the accuracy of transient elastography (TE), shear wave elastography (SWE), aspartate aminotransferase to platelet index (APRI) and Fibrosis‐4 index (FIB‐4) with the METAVIR liver fibrosis staging in viral hepatitis patients. We enrolled 121 treatment‐naïve chronic hepatitis B and C monoinfected patients. All underwent liver biopsy had biochemistry tests and liver stiffness measurements by TE using M and XL probes followed by point SWE performed on the same day. The accuracy of each method for predicting different fibrosis stages was demonstrated as an area under the receiver operating characteristic (AUROC) curves. The AUROCs of TE using M and XL probes, SWE, APRI and FIB‐4 were 0.771, 0.761, 0.700, 0.698 and 0.697, respectively, for significant fibrosis; 0.974, 0.973, 0.929, 0.738 and 0.859, respectively, for advanced fibrosis; and 0.954, 0.949, 0.962, 0.765 and 0.962, respectively, for cirrhosis. TE using the M probe was comparable to the XL probe in detecting all fibrosis stages. TE was superior to SWE for assessing significant fibrosis and advanced fibrosis. For cirrhosis, the performances of TE, SWE and FIB‐4 were similar. APRI was least accurate in liver fibrosis staging. 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We aimed to compare the accuracy of transient elastography (TE), shear wave elastography (SWE), aspartate aminotransferase to platelet index (APRI) and Fibrosis‐4 index (FIB‐4) with the METAVIR liver fibrosis staging in viral hepatitis patients. We enrolled 121 treatment‐naïve chronic hepatitis B and C monoinfected patients. All underwent liver biopsy had biochemistry tests and liver stiffness measurements by TE using M and XL probes followed by point SWE performed on the same day. The accuracy of each method for predicting different fibrosis stages was demonstrated as an area under the receiver operating characteristic (AUROC) curves. The AUROCs of TE using M and XL probes, SWE, APRI and FIB‐4 were 0.771, 0.761, 0.700, 0.698 and 0.697, respectively, for significant fibrosis; 0.974, 0.973, 0.929, 0.738 and 0.859, respectively, for advanced fibrosis; and 0.954, 0.949, 0.962, 0.765 and 0.962, respectively, for cirrhosis. TE using the M probe was comparable to the XL probe in detecting all fibrosis stages. TE was superior to SWE for assessing significant fibrosis and advanced fibrosis. For cirrhosis, the performances of TE, SWE and FIB‐4 were similar. APRI was least accurate in liver fibrosis staging. To conclude, for patients with viral hepatitis, TE using either M or XL probe is an effective noninvasive test for assessing liver fibrosis, particularly advanced fibrosis and cirrhosis, while SWE and FIB‐4 possess an excellent accuracy in predicting cirrhosis.</description><subject>Accuracy</subject><subject>Aspartate aminotransferase</subject><subject>Bile</subject><subject>Biopsy</subject><subject>Cirrhosis</subject><subject>diagnostic performance</subject><subject>Fibrosis</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>Liver</subject><subject>Liver cirrhosis</subject><subject>liver stiffness</subject><subject>noninvasive diagnosis</subject><subject>Probes</subject><subject>Ultrasound</subject><subject>viral hepatitis</subject><issn>1352-0504</issn><issn>1365-2893</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kc1q3DAQx0VoyVd7yAsUQS8N1Im-bR_T0DRbAg2l7dWMZWmtxSu5knfD3vIIueX98iRVumkhhQ4DI0a_-Y_EH6EjSk5ojtPFuj-hnAm1g_YpV7JgVc1fPJ4lK4gkYg8dpLQgJEOS7qI9Tsu6LgXZR_fXMaTR6MmtDdZhOUJ0KXgcLJ4i-OSMn7AZIE1hHmHsN-_xGFzupd5AxDeQx55fn11_nWHwHb6YfXi4vRPYhojTBHPn53jIayK2rs1bXcLOY93H4J3GaxdhwL0ZYXKTS6_QSwtDMq-f6iH6fvHx2_llcfXl0-z87KrQXHJVSAK0s0JKXndCAjPEQik1bXVlWw5VySUVwKhpS12qnKxujWLMaqM6Liw_RO-2umMMP1cmTc3SJW2GAbwJq9QwzqhSlaBVRt_-gy7CKvr8ukyVpZSqqmSmjreUzl9M0dhmjG4JcdNQ0jy61WS3mt9uZfbNk-KqXZruL_nHngycboEbN5jN_5Wazz8ut5K_AAdboVg</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Udompap, Prowpanga</creator><creator>Sukonrut, Kamonthip</creator><creator>Suvannarerg, Voraparee</creator><creator>Pongpaibul, Ananya</creator><creator>Charatcharoenwitthaya, Phunchai</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8334-0267</orcidid><orcidid>https://orcid.org/0000-0003-1022-7615</orcidid></search><sort><creationdate>202004</creationdate><title>Prospective comparison of transient elastography, point shear wave elastography, APRI and FIB‐4 for staging liver fibrosis in chronic viral hepatitis</title><author>Udompap, Prowpanga ; Sukonrut, Kamonthip ; Suvannarerg, Voraparee ; Pongpaibul, Ananya ; Charatcharoenwitthaya, Phunchai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-50a1df45539d45a2e0fa75c1bc8fb3a873514a21eb7c76c7629be622fce6d34f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Accuracy</topic><topic>Aspartate aminotransferase</topic><topic>Bile</topic><topic>Biopsy</topic><topic>Cirrhosis</topic><topic>diagnostic performance</topic><topic>Fibrosis</topic><topic>Hepatitis</topic><topic>Hepatitis B</topic><topic>Liver</topic><topic>Liver cirrhosis</topic><topic>liver stiffness</topic><topic>noninvasive diagnosis</topic><topic>Probes</topic><topic>Ultrasound</topic><topic>viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Udompap, Prowpanga</creatorcontrib><creatorcontrib>Sukonrut, Kamonthip</creatorcontrib><creatorcontrib>Suvannarerg, Voraparee</creatorcontrib><creatorcontrib>Pongpaibul, Ananya</creatorcontrib><creatorcontrib>Charatcharoenwitthaya, Phunchai</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of viral hepatitis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Udompap, Prowpanga</au><au>Sukonrut, Kamonthip</au><au>Suvannarerg, Voraparee</au><au>Pongpaibul, Ananya</au><au>Charatcharoenwitthaya, Phunchai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prospective comparison of transient elastography, point shear wave elastography, APRI and FIB‐4 for staging liver fibrosis in chronic viral hepatitis</atitle><jtitle>Journal of viral hepatitis</jtitle><addtitle>J Viral Hepat</addtitle><date>2020-04</date><risdate>2020</risdate><volume>27</volume><issue>4</issue><spage>437</spage><epage>448</epage><pages>437-448</pages><issn>1352-0504</issn><eissn>1365-2893</eissn><abstract>Ultrasound‐based elastography and serum indexes have been individually validated as noninvasive methods for staging liver fibrosis in chronic viral hepatitis. 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TE using the M probe was comparable to the XL probe in detecting all fibrosis stages. TE was superior to SWE for assessing significant fibrosis and advanced fibrosis. For cirrhosis, the performances of TE, SWE and FIB‐4 were similar. APRI was least accurate in liver fibrosis staging. To conclude, for patients with viral hepatitis, TE using either M or XL probe is an effective noninvasive test for assessing liver fibrosis, particularly advanced fibrosis and cirrhosis, while SWE and FIB‐4 possess an excellent accuracy in predicting cirrhosis.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31799740</pmid><doi>10.1111/jvh.13246</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-8334-0267</orcidid><orcidid>https://orcid.org/0000-0003-1022-7615</orcidid></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Accuracy
Aspartate aminotransferase
Bile
Biopsy
Cirrhosis
diagnostic performance
Fibrosis
Hepatitis
Hepatitis B
Liver
Liver cirrhosis
liver stiffness
noninvasive diagnosis
Probes
Ultrasound
viral hepatitis
title Prospective comparison of transient elastography, point shear wave elastography, APRI and FIB‐4 for staging liver fibrosis in chronic viral hepatitis
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