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Publicação:
Waiting DAAs list mortality impact in HCV cirrhotic patients

dc.contributor.authorSilva, Giovanni Faria [UNESP]
dc.contributor.authorde ANDRADE, Vanessa Gutierrez [UNESP]
dc.contributor.authorMoreira, Alecsandro [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2019-10-06T16:18:14Z
dc.date.available2019-10-06T16:18:14Z
dc.date.issued2018-10-01
dc.description.abstractBackground – The infection for the hepatitis C virus (HCV) is a leading cause of liver-related morbidity and mortality through its evolution to liver cirrhosis, end-stage liver complications and hepatocellular carcinoma. Currently, the new drugs for the HCV infection, based on direct antiviral agents, have changed the outcomes in this setting. Objective – To assess death incidence, during the wait for the treatment with the new drugs, and to analyze which independent variable (age, sex, ascite, HDA, albumin, α-fetoprotein, platelets and Meld score) had relation with death. Methods – Prospective study with cirrhotic patients by HCV. Inclusion: cirrhotic patients by hepatic biopsy (METAVIR), clinic or image, detectable RNA (HCV). Exclusion: Other stages of hepatic fibrosis and hepatocellular carcinoma. Descriptive statistic in continue variables. Fisher Exact and Kaplan Meier and Cox Regression Analysis to assess the association of variables studied with death. P<0.05. Results – A total of 129 patients were included. Of this, 73% were men. Mean age was 57.8±12.1, albumin of 3.5±0.6 mg/dL, platelets of 123.4±59.6 and Meld score of 10.59±3.56. The time of observation was 11.2±3.26 months, and the number of death 9/129 (6,9%). The Kaplan-Meier showed association between death with albumin lower than 2.9 (0.0006), MELD score higher than 15 (0.007) and α-fetoprotein higher than 40 ng/mL (<0.0001). Adjusted Cox Regression Analysis showed that α-fetoprotein higher than 40 ng/ml could be considered an independent risk for death. Conclusion – We conclude that, patients with advanced cirrhosis should be prioritized for treatment with direct antiviral agents.en
dc.description.affiliationUniversidade Estadual Paulista (UNESP) Faculdade de Medicina Departamento de Clínica Médica
dc.description.affiliationUnespUniversidade Estadual Paulista (UNESP) Faculdade de Medicina Departamento de Clínica Médica
dc.format.extent343-345
dc.identifierhttp://dx.doi.org/10.1590/s0004-2803.201800000-76
dc.identifier.citationArquivos de Gastroenterologia, v. 55, n. 4, p. 343-345, 2018.
dc.identifier.doi10.1590/s0004-2803.201800000-76
dc.identifier.fileS0004-28032018002400343.pdf
dc.identifier.issn1678-4219
dc.identifier.issn0004-2803
dc.identifier.scieloS0004-28032018002400343
dc.identifier.scopus2-s2.0-85061866313
dc.identifier.urihttp://hdl.handle.net/11449/188755
dc.language.isoeng
dc.relation.ispartofArquivos de Gastroenterologia
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectDrug therapy. Liver cirrhosis
dc.subjectHepacivirus. Liver cirrhosis
dc.subjectMortality
dc.titleWaiting DAAs list mortality impact in HCV cirrhotic patientsen
dc.titleImpacto da lista de espera para aads em pacientes cirróticos por VHCpt
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0001-6129-7045[1]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentClínica Médica - FMBpt

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