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dc.contributor.authorCorma Gómez, Anai
dc.contributor.authorMorano, Luis
dc.contributor.authorRivero, Antonio
dc.contributor.authorTéllez, Francisco
dc.contributor.authorRíos, María José
dc.contributor.authorSantos, Marta
dc.contributor.authorSerrano, Miriam
dc.contributor.authorPalacios, Rosario
dc.contributor.authorMerino, Dolores
dc.contributor.authorReal, Luis Miguel
dc.contributor.authorDe los Santos Gil, Ignacio
dc.contributor.authorVera Méndez, Francisco Jesús
dc.contributor.authorGalindo, María José
dc.contributor.authorPineda, Juan A.
dc.date.accessioned2025-01-31T12:55:54Z
dc.date.available2025-01-31T12:55:54Z
dc.date.issued2020
dc.identifier.citationAnaïs Corma-Gómez, Juan Macías, Luis Morano, Antonio Rivero, Francisco Téllez, Maria José Ríos, Marta Santos, Miriam Serrano, Rosario Palacios, Dolores Merino, Luis Miguel Real, Ignacio De Los Santos, Francisco J Vera-Méndez, Maria José Galindo, Juan A Pineda, RIS-HEP13 and GEHEP 011 Study Groups , Liver Stiffness–Based Strategies Predict Absence of Variceal Bleeding in Cirrhotic Hepatitis C Virus–Infected Patients With and Without Human Immunodeficiency Virus Coinfection After Sustained Virological Response, Clinical Infectious Diseases, Volume 72, Issue 5, 1 March 2021, Pages e96–e102, https://doi.org/10.1093/cid/ciaa1726es
dc.identifier.urihttp://hdl.handle.net/10952/9061
dc.description.abstractBackground. In the setting of hepatitis C virus (HCV) active infection, liver stiffness (LS)–based strategies identify patients with low risk of developing esophageal variceal bleeding (VB) episodes, in whom unnecessary upper esophagogastroduodenoscopy (UGE) screening can be safely avoided. However, after sustained virological response (SVR), data on the accuracy of the criteria predicting this outcome in HCV-infected patients with cirrhosis, with or without human immunodeficiency virus (HIV) coinfection, are very limited. Methods. This was a multicenter prospective cohort study, where HCV-monoinfected patients and HIV/HCV-coinfected individuals were included if they had (1) SVR with direct-acting a antiviral–based therapy; (2) LS ≥9.5 kPa previous to treatment; and (3) LS measurement at the SVR time-point ≥14 kPa. Diagnostic accuracy of HEPAVIR, expanded Baveno VI, and HIV cirrhosis criteria, at the time of SVR, was evaluated. Missed VB episodes, negative predictive values (NPVs), and number of spared UGEs were specifically assessed. Results. Four hundred thirty-five patients were included, 284 (65%) coinfected with HIV. Seven (1.6%) patients developed a first episode of VB after SVR. In patients without a previous VB episode, HEPAVIR, expanded Baveno VI and HIV cirrhosis criteria achieved NPV for first VB episode after SVR of 99.5% (95% confidence interval [CI], 97.1%–100%), 100% (95% CI 97.8%–100%), and 100% (95% CI 98%–100%) while sparing 45%, 39%, and 44% of UGEs, respectively. When considering HIV coinfection, the performance of the 3 criteria was similar, both in HCV-monoinfected and HIV/HCV-coinfected individuals. Conclusions. After SVR, predictive LS-based strategies accurately identify HCV-infected patients, HIV coinfected or not, with low risk of developing VB during follow-up. In these specific patients, using HIV cirrhosis criteria maximize the number of spared UGEs while missing no VB episodees
dc.language.isoenes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectHCV infectiones
dc.subjectSustained virological responsees
dc.subjectDirect-acting antiviralses
dc.subjectLiver stiffnesses
dc.subjectVariceal bleedinges
dc.titleLiver Stiffness–Based Strategies Predict Absence of Variceal Bleeding in Cirrhotic Hepatitis C Virus–Infected Patients With and Without Human Immunodeficiency Virus Coinfection After Sustained Virological Responsees
dc.typejournal articlees
dc.rights.accessRightsopen accesses
dc.journal.titleClinical Infectious Diseaseses
dc.volume.number72es
dc.issue.number5es
dc.description.disciplineMedicinaes
dc.identifier.doi10.1093/cid/ciaa1726es
dc.description.facultyMedicinaes


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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