Antiviral Therapy for a Postpartum Flare in Women with Chronic HBV Infection Shortens the ALT Recovery Time and Reduces Hepatitis Re-Flare Rates within 4 years
Background. Few studies explored whether anti-hepatitis B virus (HBV) therapy should be initiated during postpartum hepatitis flare. Aim. This study aimed to analyze the effect of anti-HBV therapy on postpartum hepatitis flare and evaluate the prognosis within 4 years postpartum. Methods. This retro...
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description | Background. Few studies explored whether anti-hepatitis B virus (HBV) therapy should be initiated during postpartum hepatitis flare. Aim. This study aimed to analyze the effect of anti-HBV therapy on postpartum hepatitis flare and evaluate the prognosis within 4 years postpartum. Methods. This retrospective study enrolled hepatitis B surface antigen (HBsAg)-positive and hepatitis B e antigen (HBeAg)-positive pregnant women with HBV DNA ≥ 106 IU/mL. A total of 152 pregnant women were included: 103 in the prophylactic anti-HBV therapy group (PT-G) and 49 in the non-prophylactic anti-HBV therapy group (NPT-G). The women with a postpartum flare were assigned to the anti-HBV therapy group (AT-G) and non-anti-HBV therapy group (NAT-G) to analyze the effect of postpartum anti-HBV therapy on hepatitis flare. Virological and biochemical parameters were assessed. Results. Taking postpartum 12 weeks as the cutoff point, the ALT recovered time for postpartum flare women is shorter in AT-G (n = 16, 42.1%) or PT-G (n = 23, 34.8%) than in NAT-G (n = 14, 23.0%; x2 = 4.067, P=0.044) or NPT-G (n = 4, 11.1%; x2 = 5.579, P=0.018). Taking postpartum 26 weeks as the cutoff point, the ALT recovered time is shorter in AT-G (n = 35, 57.3%) or PT-G (n = 44, 66.7%) than in NAT-G (n = 32, 84.2%; x2 = 7.707, P=0.006) or NPT-G (n = 16, 44.4%; x2 = 4.749, P=0.029). Postpartum flare recovery time was positively correlated with HBV DNA level at delivery [r = 0.223, P=0.025, 95%CI (0.022~0.41)]. The hepatitis re-flare rates within postpartum 4 years in AT-G (n = 3, 9.68%) is lower than that in NAT-G (n = 24, 45.4%; x2 = 14.003, P≤0.001). The HBeAg, HBsAg, HBV DNA, and ALT level at postpartum 4 years in AT-G were lower than that in NAT-G (P |
doi_str_mv | 10.1155/2022/4753267 |
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Few studies explored whether anti-hepatitis B virus (HBV) therapy should be initiated during postpartum hepatitis flare. Aim. This study aimed to analyze the effect of anti-HBV therapy on postpartum hepatitis flare and evaluate the prognosis within 4 years postpartum. Methods. This retrospective study enrolled hepatitis B surface antigen (HBsAg)-positive and hepatitis B e antigen (HBeAg)-positive pregnant women with HBV DNA ≥ 106 IU/mL. A total of 152 pregnant women were included: 103 in the prophylactic anti-HBV therapy group (PT-G) and 49 in the non-prophylactic anti-HBV therapy group (NPT-G). The women with a postpartum flare were assigned to the anti-HBV therapy group (AT-G) and non-anti-HBV therapy group (NAT-G) to analyze the effect of postpartum anti-HBV therapy on hepatitis flare. Virological and biochemical parameters were assessed. Results. Taking postpartum 12 weeks as the cutoff point, the ALT recovered time for postpartum flare women is shorter in AT-G (n = 16, 42.1%) or PT-G (n = 23, 34.8%) than in NAT-G (n = 14, 23.0%; x2 = 4.067, P=0.044) or NPT-G (n = 4, 11.1%; x2 = 5.579, P=0.018). Taking postpartum 26 weeks as the cutoff point, the ALT recovered time is shorter in AT-G (n = 35, 57.3%) or PT-G (n = 44, 66.7%) than in NAT-G (n = 32, 84.2%; x2 = 7.707, P=0.006) or NPT-G (n = 16, 44.4%; x2 = 4.749, P=0.029). Postpartum flare recovery time was positively correlated with HBV DNA level at delivery [r = 0.223, P=0.025, 95%CI (0.022~0.41)]. The hepatitis re-flare rates within postpartum 4 years in AT-G (n = 3, 9.68%) is lower than that in NAT-G (n = 24, 45.4%; x2 = 14.003, P≤0.001). The HBeAg, HBsAg, HBV DNA, and ALT level at postpartum 4 years in AT-G were lower than that in NAT-G (P<0.001). Conclusion. Anti-HBV therapy for postpartum hepatitis flare of women with chronic HBV could shorten the ALT recovery time and reduce hepatitis re-flare rates within 4 years of postpartum.</description><identifier>ISSN: 2291-2789</identifier><identifier>EISSN: 2291-2797</identifier><identifier>DOI: 10.1155/2022/4753267</identifier><identifier>PMID: 35770180</identifier><language>eng</language><publisher>Egypt: Hindawi</publisher><subject>Alanine Transaminase ; Antigens ; Antiviral Agents - therapeutic use ; Deoxyribonucleic acid ; DNA ; DNA, Viral ; Female ; Hepatitis B ; Hepatitis B e Antigens ; Hepatitis B Surface Antigens ; Hepatitis B virus ; Hepatitis B, Chronic - drug therapy ; Humans ; Infections ; Postpartum Period ; Pregnancy ; Retrospective Studies ; Symptom Flare Up</subject><ispartof>Canadian Journal of Gastroenterology and Hepatology, 2022, Vol.2022, p.4753267-9</ispartof><rights>Copyright © 2022 Min Quan et al.</rights><rights>Copyright © 2022 Min Quan et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2022 Min Quan et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c514t-7622d0f52fadec964088c1f5d7446d34e481ae46af8a3152a720773a145292cc3</citedby><cites>FETCH-LOGICAL-c514t-7622d0f52fadec964088c1f5d7446d34e481ae46af8a3152a720773a145292cc3</cites><orcidid>0000-0002-7547-0838 ; 0000-0002-9154-7049 ; 0000-0002-5692-8831 ; 0000-0002-9111-9669</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236834/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236834/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,877,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35770180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Fan, Yu-Chen</contributor><contributor>Yu-Chen Fan</contributor><creatorcontrib>Quan, Min</creatorcontrib><creatorcontrib>Liu, Cong</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Xing, Hui-Chun</creatorcontrib><title>Antiviral Therapy for a Postpartum Flare in Women with Chronic HBV Infection Shortens the ALT Recovery Time and Reduces Hepatitis Re-Flare Rates within 4 years</title><title>Canadian Journal of Gastroenterology and Hepatology</title><addtitle>Can J Gastroenterol Hepatol</addtitle><description>Background. Few studies explored whether anti-hepatitis B virus (HBV) therapy should be initiated during postpartum hepatitis flare. Aim. This study aimed to analyze the effect of anti-HBV therapy on postpartum hepatitis flare and evaluate the prognosis within 4 years postpartum. Methods. This retrospective study enrolled hepatitis B surface antigen (HBsAg)-positive and hepatitis B e antigen (HBeAg)-positive pregnant women with HBV DNA ≥ 106 IU/mL. A total of 152 pregnant women were included: 103 in the prophylactic anti-HBV therapy group (PT-G) and 49 in the non-prophylactic anti-HBV therapy group (NPT-G). The women with a postpartum flare were assigned to the anti-HBV therapy group (AT-G) and non-anti-HBV therapy group (NAT-G) to analyze the effect of postpartum anti-HBV therapy on hepatitis flare. Virological and biochemical parameters were assessed. Results. Taking postpartum 12 weeks as the cutoff point, the ALT recovered time for postpartum flare women is shorter in AT-G (n = 16, 42.1%) or PT-G (n = 23, 34.8%) than in NAT-G (n = 14, 23.0%; x2 = 4.067, P=0.044) or NPT-G (n = 4, 11.1%; x2 = 5.579, P=0.018). Taking postpartum 26 weeks as the cutoff point, the ALT recovered time is shorter in AT-G (n = 35, 57.3%) or PT-G (n = 44, 66.7%) than in NAT-G (n = 32, 84.2%; x2 = 7.707, P=0.006) or NPT-G (n = 16, 44.4%; x2 = 4.749, P=0.029). Postpartum flare recovery time was positively correlated with HBV DNA level at delivery [r = 0.223, P=0.025, 95%CI (0.022~0.41)]. The hepatitis re-flare rates within postpartum 4 years in AT-G (n = 3, 9.68%) is lower than that in NAT-G (n = 24, 45.4%; x2 = 14.003, P≤0.001). The HBeAg, HBsAg, HBV DNA, and ALT level at postpartum 4 years in AT-G were lower than that in NAT-G (P<0.001). Conclusion. Anti-HBV therapy for postpartum hepatitis flare of women with chronic HBV could shorten the ALT recovery time and reduce hepatitis re-flare rates within 4 years of postpartum.</description><subject>Alanine Transaminase</subject><subject>Antigens</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA, Viral</subject><subject>Female</subject><subject>Hepatitis B</subject><subject>Hepatitis B e Antigens</subject><subject>Hepatitis B Surface Antigens</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B, Chronic - drug therapy</subject><subject>Humans</subject><subject>Infections</subject><subject>Postpartum Period</subject><subject>Pregnancy</subject><subject>Retrospective Studies</subject><subject>Symptom Flare Up</subject><issn>2291-2789</issn><issn>2291-2797</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>DOA</sourceid><recordid>eNp9ksGOUyEUhm-MxpmMs3NtSFxqHTjAhbsxGRvHNmmiGasuCQPcuTQtVKCd9Gl8VamtjbNxBTl8-Q4c_qZ5SfA7Qji_AgxwxQSn0IonzTlAR0YgOvH0tJfdWXOZ8wJjTIDzjsLz5oxyITCR-Lz5dR2K3_qkl2g-uKTXO9THhDT6EnNZ61Q2K3Sz1MkhH9CPuHIBPfgyoPGQYvAGTT58R9PQO1N8DOjrEFNxIaMyOHQ9m6NbZ-LWpR2a-5VDOthasRvjMpq4tS6--Fwro0OHW13qwV5fezG0czrlF82zXi-zuzyuF823m4_z8WQ0-_xpOr6ejQwnrIxEC2Bxz6HX1pmuZVhKQ3puBWOtpcwxSbRjre6lpoSDFoCFoJowDh0YQy-a6cFro16odfIrnXYqaq_-FGK6V3UY3iydkrilIKyVwhgGcCep6WwHVED9BNPy6np_cK03dytnjQulzveR9PFJ8IO6j1tVJa2krApeHwUp_ty4XNQiblKo71dQAYkpbnGl3h4ok2LOyfWnDgSrfTrUPh3qmI6Kv_r3Vif4bxYq8OYA1PFb_eD_r_sNydXBNQ</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Quan, Min</creator><creator>Liu, Cong</creator><creator>Li, Wei</creator><creator>Xing, Hui-Chun</creator><general>Hindawi</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7547-0838</orcidid><orcidid>https://orcid.org/0000-0002-9154-7049</orcidid><orcidid>https://orcid.org/0000-0002-5692-8831</orcidid><orcidid>https://orcid.org/0000-0002-9111-9669</orcidid></search><sort><creationdate>2022</creationdate><title>Antiviral Therapy for a Postpartum Flare in Women with Chronic HBV Infection Shortens the ALT Recovery Time and Reduces Hepatitis Re-Flare Rates within 4 years</title><author>Quan, Min ; Liu, Cong ; Li, Wei ; Xing, Hui-Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c514t-7622d0f52fadec964088c1f5d7446d34e481ae46af8a3152a720773a145292cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alanine Transaminase</topic><topic>Antigens</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA, Viral</topic><topic>Female</topic><topic>Hepatitis B</topic><topic>Hepatitis B e Antigens</topic><topic>Hepatitis B Surface Antigens</topic><topic>Hepatitis B virus</topic><topic>Hepatitis B, Chronic - drug therapy</topic><topic>Humans</topic><topic>Infections</topic><topic>Postpartum Period</topic><topic>Pregnancy</topic><topic>Retrospective Studies</topic><topic>Symptom Flare Up</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quan, Min</creatorcontrib><creatorcontrib>Liu, Cong</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Xing, Hui-Chun</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business & Current Affairs Database</collection><collection>Canadian Business & Current Affairs Database (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Canadian Journal of Gastroenterology and Hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quan, Min</au><au>Liu, Cong</au><au>Li, Wei</au><au>Xing, Hui-Chun</au><au>Fan, Yu-Chen</au><au>Yu-Chen Fan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antiviral Therapy for a Postpartum Flare in Women with Chronic HBV Infection Shortens the ALT Recovery Time and Reduces Hepatitis Re-Flare Rates within 4 years</atitle><jtitle>Canadian Journal of Gastroenterology and Hepatology</jtitle><addtitle>Can J Gastroenterol Hepatol</addtitle><date>2022</date><risdate>2022</risdate><volume>2022</volume><spage>4753267</spage><epage>9</epage><pages>4753267-9</pages><issn>2291-2789</issn><eissn>2291-2797</eissn><abstract>Background. Few studies explored whether anti-hepatitis B virus (HBV) therapy should be initiated during postpartum hepatitis flare. Aim. This study aimed to analyze the effect of anti-HBV therapy on postpartum hepatitis flare and evaluate the prognosis within 4 years postpartum. Methods. This retrospective study enrolled hepatitis B surface antigen (HBsAg)-positive and hepatitis B e antigen (HBeAg)-positive pregnant women with HBV DNA ≥ 106 IU/mL. A total of 152 pregnant women were included: 103 in the prophylactic anti-HBV therapy group (PT-G) and 49 in the non-prophylactic anti-HBV therapy group (NPT-G). The women with a postpartum flare were assigned to the anti-HBV therapy group (AT-G) and non-anti-HBV therapy group (NAT-G) to analyze the effect of postpartum anti-HBV therapy on hepatitis flare. Virological and biochemical parameters were assessed. Results. Taking postpartum 12 weeks as the cutoff point, the ALT recovered time for postpartum flare women is shorter in AT-G (n = 16, 42.1%) or PT-G (n = 23, 34.8%) than in NAT-G (n = 14, 23.0%; x2 = 4.067, P=0.044) or NPT-G (n = 4, 11.1%; x2 = 5.579, P=0.018). Taking postpartum 26 weeks as the cutoff point, the ALT recovered time is shorter in AT-G (n = 35, 57.3%) or PT-G (n = 44, 66.7%) than in NAT-G (n = 32, 84.2%; x2 = 7.707, P=0.006) or NPT-G (n = 16, 44.4%; x2 = 4.749, P=0.029). Postpartum flare recovery time was positively correlated with HBV DNA level at delivery [r = 0.223, P=0.025, 95%CI (0.022~0.41)]. The hepatitis re-flare rates within postpartum 4 years in AT-G (n = 3, 9.68%) is lower than that in NAT-G (n = 24, 45.4%; x2 = 14.003, P≤0.001). The HBeAg, HBsAg, HBV DNA, and ALT level at postpartum 4 years in AT-G were lower than that in NAT-G (P<0.001). Conclusion. Anti-HBV therapy for postpartum hepatitis flare of women with chronic HBV could shorten the ALT recovery time and reduce hepatitis re-flare rates within 4 years of postpartum.</abstract><cop>Egypt</cop><pub>Hindawi</pub><pmid>35770180</pmid><doi>10.1155/2022/4753267</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7547-0838</orcidid><orcidid>https://orcid.org/0000-0002-9154-7049</orcidid><orcidid>https://orcid.org/0000-0002-5692-8831</orcidid><orcidid>https://orcid.org/0000-0002-9111-9669</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alanine Transaminase Antigens Antiviral Agents - therapeutic use Deoxyribonucleic acid DNA DNA, Viral Female Hepatitis B Hepatitis B e Antigens Hepatitis B Surface Antigens Hepatitis B virus Hepatitis B, Chronic - drug therapy Humans Infections Postpartum Period Pregnancy Retrospective Studies Symptom Flare Up |
title | Antiviral Therapy for a Postpartum Flare in Women with Chronic HBV Infection Shortens the ALT Recovery Time and Reduces Hepatitis Re-Flare Rates within 4 years |
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