Hepatitis C eradication with direct‐acting anti‐virals reduces the risk of variceal bleeding

Summary Background The real‐world, long‐term benefits of sustained virologic response (SVR) on the risk of variceal bleeding remain unclear. Aim To assess the association between DAA‐induced SVR and post‐treatment variceal bleeding Methods We identified patients who initiated DAA‐only anti‐viral tre...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2020-02, Vol.51 (3), p.364-373
Hauptverfasser: Moon, Andrew M., Green, Pamela K., Rockey, Don C., Berry, Kristin, Ioannou, George N.
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container_issue 3
container_start_page 364
container_title Alimentary pharmacology & therapeutics
container_volume 51
creator Moon, Andrew M.
Green, Pamela K.
Rockey, Don C.
Berry, Kristin
Ioannou, George N.
description Summary Background The real‐world, long‐term benefits of sustained virologic response (SVR) on the risk of variceal bleeding remain unclear. Aim To assess the association between DAA‐induced SVR and post‐treatment variceal bleeding Methods We identified patients who initiated DAA‐only anti‐viral treatments in the United States Veterans Affairs healthcare system from 2013 to 2015. We followed patients until 1 January 2019 for the development of gastro‐oesophageal variceal bleeding defined by diagnostic codes. We used multivariable Cox proportional hazards regression to assess the association between SVR and development of variceal bleeding, adjusting for potential confounders. Results Among 33 582 DAA‐treated patients, 549 (1.6%) developed variceal bleeding after treatment (mean follow‐up 3.1 years). Compared to no SVR, SVR was associated with a significantly lower incidence of variceal bleeding among all patients (0.46 vs 1.26 per 100 patient‐years, adjusted hazard ratio [AHR] 0.66, 95% CI 0.52‐0.83), among patients with pre‐treatment cirrhosis (1.55 vs 2.96 per 100 patient‐years, AHR 0.73, 95% CI 0.57‐0.93) and among patients without pre‐treatment cirrhosis (0.07 vs 0.29 per 100 patient‐years, AHR 0.33, 95% CI 0.17‐0.65). The risk of variceal bleeding after treatment was lower in those who achieved SVR vs no SVR among patients who had non‐bleeding varices (3.5 vs 4.9 per 100 patient‐years) or bleeding varices (12.9 vs 16.4 per 100 patient‐years) diagnosed before treatment, but these differences were not statistically significant in adjusted analyses. Conclusion DAA‐induced SVR is independently associated with a lower risk of variceal bleeding during long‐term follow‐up in patients with and without pre‐treatment cirrhosis. These findings demonstrate an important real‐world benefit of DAA treatment.
doi_str_mv 10.1111/apt.15586
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Aim To assess the association between DAA‐induced SVR and post‐treatment variceal bleeding Methods We identified patients who initiated DAA‐only anti‐viral treatments in the United States Veterans Affairs healthcare system from 2013 to 2015. We followed patients until 1 January 2019 for the development of gastro‐oesophageal variceal bleeding defined by diagnostic codes. We used multivariable Cox proportional hazards regression to assess the association between SVR and development of variceal bleeding, adjusting for potential confounders. Results Among 33 582 DAA‐treated patients, 549 (1.6%) developed variceal bleeding after treatment (mean follow‐up 3.1 years). Compared to no SVR, SVR was associated with a significantly lower incidence of variceal bleeding among all patients (0.46 vs 1.26 per 100 patient‐years, adjusted hazard ratio [AHR] 0.66, 95% CI 0.52‐0.83), among patients with pre‐treatment cirrhosis (1.55 vs 2.96 per 100 patient‐years, AHR 0.73, 95% CI 0.57‐0.93) and among patients without pre‐treatment cirrhosis (0.07 vs 0.29 per 100 patient‐years, AHR 0.33, 95% CI 0.17‐0.65). The risk of variceal bleeding after treatment was lower in those who achieved SVR vs no SVR among patients who had non‐bleeding varices (3.5 vs 4.9 per 100 patient‐years) or bleeding varices (12.9 vs 16.4 per 100 patient‐years) diagnosed before treatment, but these differences were not statistically significant in adjusted analyses. Conclusion DAA‐induced SVR is independently associated with a lower risk of variceal bleeding during long‐term follow‐up in patients with and without pre‐treatment cirrhosis. These findings demonstrate an important real‐world benefit of DAA treatment.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/apt.15586</identifier><identifier>PMID: 31773763</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adult ; Aged ; Antiviral Agents - therapeutic use ; Bleeding ; Cirrhosis ; Esophageal and Gastric Varices - complications ; Esophageal and Gastric Varices - drug therapy ; Esophageal and Gastric Varices - epidemiology ; Esophagus ; Female ; Follow-Up Studies ; Gastrointestinal Hemorrhage - epidemiology ; Gastrointestinal Hemorrhage - etiology ; Gastrointestinal Hemorrhage - prevention &amp; control ; Health hazards ; Hepatitis ; Hepatitis C ; Hepatitis C - complications ; Hepatitis C - drug therapy ; Hepatitis C - epidemiology ; Hepatitis C, Chronic - complications ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - epidemiology ; Humans ; Incidence ; Liver cirrhosis ; Liver Cirrhosis - complications ; Liver Cirrhosis - drug therapy ; Liver Cirrhosis - epidemiology ; Male ; Middle Aged ; Patients ; Remission Induction ; Risk Factors ; Statistical analysis ; Sustained Virologic Response ; United States - epidemiology ; Varicose Veins - complications ; Varicose Veins - drug therapy ; Varicose Veins - epidemiology ; Veterans - statistics &amp; numerical data</subject><ispartof>Alimentary pharmacology &amp; therapeutics, 2020-02, Vol.51 (3), p.364-373</ispartof><rights>2019 John Wiley &amp; Sons Ltd</rights><rights>2019 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2020 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3886-ac4836db915c4179d5c78ec6a1704c3a5030da9206dbaa37176854715f0760943</citedby><cites>FETCH-LOGICAL-c3886-ac4836db915c4179d5c78ec6a1704c3a5030da9206dbaa37176854715f0760943</cites><orcidid>0000-0003-1796-8977 ; 0000-0001-7163-2062</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fapt.15586$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fapt.15586$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27923,27924,45573,45574,46408,46832</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31773763$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moon, Andrew M.</creatorcontrib><creatorcontrib>Green, Pamela K.</creatorcontrib><creatorcontrib>Rockey, Don C.</creatorcontrib><creatorcontrib>Berry, Kristin</creatorcontrib><creatorcontrib>Ioannou, George N.</creatorcontrib><title>Hepatitis C eradication with direct‐acting anti‐virals reduces the risk of variceal bleeding</title><title>Alimentary pharmacology &amp; therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Summary Background The real‐world, long‐term benefits of sustained virologic response (SVR) on the risk of variceal bleeding remain unclear. Aim To assess the association between DAA‐induced SVR and post‐treatment variceal bleeding Methods We identified patients who initiated DAA‐only anti‐viral treatments in the United States Veterans Affairs healthcare system from 2013 to 2015. We followed patients until 1 January 2019 for the development of gastro‐oesophageal variceal bleeding defined by diagnostic codes. We used multivariable Cox proportional hazards regression to assess the association between SVR and development of variceal bleeding, adjusting for potential confounders. Results Among 33 582 DAA‐treated patients, 549 (1.6%) developed variceal bleeding after treatment (mean follow‐up 3.1 years). Compared to no SVR, SVR was associated with a significantly lower incidence of variceal bleeding among all patients (0.46 vs 1.26 per 100 patient‐years, adjusted hazard ratio [AHR] 0.66, 95% CI 0.52‐0.83), among patients with pre‐treatment cirrhosis (1.55 vs 2.96 per 100 patient‐years, AHR 0.73, 95% CI 0.57‐0.93) and among patients without pre‐treatment cirrhosis (0.07 vs 0.29 per 100 patient‐years, AHR 0.33, 95% CI 0.17‐0.65). The risk of variceal bleeding after treatment was lower in those who achieved SVR vs no SVR among patients who had non‐bleeding varices (3.5 vs 4.9 per 100 patient‐years) or bleeding varices (12.9 vs 16.4 per 100 patient‐years) diagnosed before treatment, but these differences were not statistically significant in adjusted analyses. Conclusion DAA‐induced SVR is independently associated with a lower risk of variceal bleeding during long‐term follow‐up in patients with and without pre‐treatment cirrhosis. These findings demonstrate an important real‐world benefit of DAA treatment.</description><subject>Adult</subject><subject>Aged</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Bleeding</subject><subject>Cirrhosis</subject><subject>Esophageal and Gastric Varices - complications</subject><subject>Esophageal and Gastric Varices - drug therapy</subject><subject>Esophageal and Gastric Varices - epidemiology</subject><subject>Esophagus</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastrointestinal Hemorrhage - epidemiology</subject><subject>Gastrointestinal Hemorrhage - etiology</subject><subject>Gastrointestinal Hemorrhage - prevention &amp; control</subject><subject>Health hazards</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Hepatitis C - complications</subject><subject>Hepatitis C - drug therapy</subject><subject>Hepatitis C - epidemiology</subject><subject>Hepatitis C, Chronic - complications</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - epidemiology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - complications</subject><subject>Liver Cirrhosis - drug therapy</subject><subject>Liver Cirrhosis - epidemiology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Patients</subject><subject>Remission Induction</subject><subject>Risk Factors</subject><subject>Statistical analysis</subject><subject>Sustained Virologic Response</subject><subject>United States - epidemiology</subject><subject>Varicose Veins - complications</subject><subject>Varicose Veins - drug therapy</subject><subject>Varicose Veins - epidemiology</subject><subject>Veterans - statistics &amp; 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Green, Pamela K. ; Rockey, Don C. ; Berry, Kristin ; Ioannou, George N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3886-ac4836db915c4179d5c78ec6a1704c3a5030da9206dbaa37176854715f0760943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Bleeding</topic><topic>Cirrhosis</topic><topic>Esophageal and Gastric Varices - complications</topic><topic>Esophageal and Gastric Varices - drug therapy</topic><topic>Esophageal and Gastric Varices - epidemiology</topic><topic>Esophagus</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastrointestinal Hemorrhage - epidemiology</topic><topic>Gastrointestinal Hemorrhage - etiology</topic><topic>Gastrointestinal Hemorrhage - prevention &amp; control</topic><topic>Health hazards</topic><topic>Hepatitis</topic><topic>Hepatitis C</topic><topic>Hepatitis C - complications</topic><topic>Hepatitis C - drug therapy</topic><topic>Hepatitis C - epidemiology</topic><topic>Hepatitis C, Chronic - complications</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - epidemiology</topic><topic>Humans</topic><topic>Incidence</topic><topic>Liver cirrhosis</topic><topic>Liver Cirrhosis - complications</topic><topic>Liver Cirrhosis - drug therapy</topic><topic>Liver Cirrhosis - epidemiology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Patients</topic><topic>Remission Induction</topic><topic>Risk Factors</topic><topic>Statistical analysis</topic><topic>Sustained Virologic Response</topic><topic>United States - epidemiology</topic><topic>Varicose Veins - complications</topic><topic>Varicose Veins - drug therapy</topic><topic>Varicose Veins - epidemiology</topic><topic>Veterans - statistics &amp; numerical data</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moon, Andrew M.</creatorcontrib><creatorcontrib>Green, Pamela K.</creatorcontrib><creatorcontrib>Rockey, Don C.</creatorcontrib><creatorcontrib>Berry, Kristin</creatorcontrib><creatorcontrib>Ioannou, George N.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moon, Andrew M.</au><au>Green, Pamela K.</au><au>Rockey, Don C.</au><au>Berry, Kristin</au><au>Ioannou, George N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis C eradication with direct‐acting anti‐virals reduces the risk of variceal bleeding</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2020-02</date><risdate>2020</risdate><volume>51</volume><issue>3</issue><spage>364</spage><epage>373</epage><pages>364-373</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>Summary Background The real‐world, long‐term benefits of sustained virologic response (SVR) on the risk of variceal bleeding remain unclear. Aim To assess the association between DAA‐induced SVR and post‐treatment variceal bleeding Methods We identified patients who initiated DAA‐only anti‐viral treatments in the United States Veterans Affairs healthcare system from 2013 to 2015. We followed patients until 1 January 2019 for the development of gastro‐oesophageal variceal bleeding defined by diagnostic codes. We used multivariable Cox proportional hazards regression to assess the association between SVR and development of variceal bleeding, adjusting for potential confounders. Results Among 33 582 DAA‐treated patients, 549 (1.6%) developed variceal bleeding after treatment (mean follow‐up 3.1 years). Compared to no SVR, SVR was associated with a significantly lower incidence of variceal bleeding among all patients (0.46 vs 1.26 per 100 patient‐years, adjusted hazard ratio [AHR] 0.66, 95% CI 0.52‐0.83), among patients with pre‐treatment cirrhosis (1.55 vs 2.96 per 100 patient‐years, AHR 0.73, 95% CI 0.57‐0.93) and among patients without pre‐treatment cirrhosis (0.07 vs 0.29 per 100 patient‐years, AHR 0.33, 95% CI 0.17‐0.65). The risk of variceal bleeding after treatment was lower in those who achieved SVR vs no SVR among patients who had non‐bleeding varices (3.5 vs 4.9 per 100 patient‐years) or bleeding varices (12.9 vs 16.4 per 100 patient‐years) diagnosed before treatment, but these differences were not statistically significant in adjusted analyses. Conclusion DAA‐induced SVR is independently associated with a lower risk of variceal bleeding during long‐term follow‐up in patients with and without pre‐treatment cirrhosis. These findings demonstrate an important real‐world benefit of DAA treatment.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31773763</pmid><doi>10.1111/apt.15586</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-1796-8977</orcidid><orcidid>https://orcid.org/0000-0001-7163-2062</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Antiviral Agents - therapeutic use
Bleeding
Cirrhosis
Esophageal and Gastric Varices - complications
Esophageal and Gastric Varices - drug therapy
Esophageal and Gastric Varices - epidemiology
Esophagus
Female
Follow-Up Studies
Gastrointestinal Hemorrhage - epidemiology
Gastrointestinal Hemorrhage - etiology
Gastrointestinal Hemorrhage - prevention & control
Health hazards
Hepatitis
Hepatitis C
Hepatitis C - complications
Hepatitis C - drug therapy
Hepatitis C - epidemiology
Hepatitis C, Chronic - complications
Hepatitis C, Chronic - drug therapy
Hepatitis C, Chronic - epidemiology
Humans
Incidence
Liver cirrhosis
Liver Cirrhosis - complications
Liver Cirrhosis - drug therapy
Liver Cirrhosis - epidemiology
Male
Middle Aged
Patients
Remission Induction
Risk Factors
Statistical analysis
Sustained Virologic Response
United States - epidemiology
Varicose Veins - complications
Varicose Veins - drug therapy
Varicose Veins - epidemiology
Veterans - statistics & numerical data
title Hepatitis C eradication with direct‐acting anti‐virals reduces the risk of variceal bleeding
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