Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/18955
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorNACIF, Lucas Souto-
dc.contributor.authorPINHEIRO, Rafael Soares-
dc.contributor.authorPECORA, Rafael Antonio de Arruda-
dc.contributor.authorTANIGAWA, Ryan Yukimatsu-
dc.contributor.authorROCHA-SANTOS, Vinicius-
dc.contributor.authorANDRAUS, Wellington-
dc.contributor.authorALVES, Venancio Avancini Ferreira-
dc.contributor.authorD'ALBUQUERQUE, Luiz Carneiro-
dc.date.accessioned2017-04-07T15:11:45Z-
dc.date.available2017-04-07T15:11:45Z-
dc.date.issued2017-
dc.identifier.citationANNALS OF TRANSPLANTATION, v.22, p.9-16, 2017-
dc.identifier.issn1425-9524-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/18955-
dc.description.abstractBackground: Late acute rejection (LAR) differs in its clinical and histological presentation and management from early acute rejection. This clinical entity is not completely understood; thus, we aimed to identify significant prognostic factors that can influence post-transplant survival in LAR patients. The purpose of this study was to evaluate the incidence and post-transplant survival of patients from a single center with a focus on late acute rejection. Material/Methods: From January 2002 to June 2013, all liver biopsies from patients with rejection were scored using the Banff criteria. The groups were compared, and simple and multiple logistic regression and survival curves were created. Results: A total of 779 liver transplants were performed; 585 patients with no rejections and 194 patients with rejections were analyzed. The overall incidence of LAR was 6.7%, and there was a higher prevalence of early acute cellular rejection than LAR. The mean time to LAR was 564 days (median 214 days, range 91-2642). LAR had a more severe grade (35.3%) than early acute rejection (23.5%). The survival rates were similar between both modalities for the long-term period. Worse mortality rates were observed in liver re-transplantation (HR 4.77; p<0.0001); in hepatitis C virus patients with increased creatinine levels (HR 22.48; p=0.016); and in donors > 41 years of age (OR 2.1; p=0.047) in a long-term analysis of LAR. Conclusions: Liver re-transplantation, higher creatinine levels in hepatitis C virus patients, and donor age were predictors of mortality in this long-term analysis of late acute rejection in liver transplantation.-
dc.language.isoeng-
dc.publisherINT SCIENTIFIC LITERATURE, INC-
dc.relation.ispartofAnnals of Transplantation-
dc.rightsrestrictedAccess-
dc.subjectGraft Rejection-
dc.subjectGraft Survival-
dc.subjectLiver Transplantation-
dc.subjectLogistic Models-
dc.subjectSurvival Analysis-
dc.subject.otheracute cellular rejection-
dc.subject.otherrisk-
dc.subject.otherrecipients-
dc.subject.othersurvival-
dc.titleRe-Transplantation, Higher Creatinine Levels in Hepatitis C Virus Patients, and Donor Age Are Predictors of Mortality in Long-Term Analysis of Late Acute Rejection in Liver Transplantation-
dc.typearticle-
dc.rights.holderCopyright INT SCIENTIFIC LITERATURE, INC-
dc.identifier.doi10.12659/AOT.901010-
dc.identifier.pmid28070117-
dc.subject.wosSurgery-
dc.subject.wosTransplantation-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalPECORA, Rafael Antonio de Arruda:Univ Sao Paulo, Sch Med, Dept Gastroenterol, Liver & Gastrointestinal Transplant Div, Sao Paulo, SP, Brazil-
hcfmusp.description.beginpage9-
hcfmusp.description.endpage16-
hcfmusp.description.volume22-
hcfmusp.origemWOS-
hcfmusp.origem.id2-s2.0-85009785213-
hcfmusp.origem.idWOS:000395537300001-
hcfmusp.publisher.citySMITHTOWN-
hcfmusp.publisher.countryUSA-
hcfmusp.relation.referenceAkamatsu N, 2006, WORLD J GASTROENTERO, V12, P6674-
hcfmusp.relation.referenceFeng S, 2006, AM J TRANSPLANT, V6, P783, DOI 10.1111/j.1600-6143.2006.01242.x-
hcfmusp.relation.referenceFlorman S, 2004, CLIN TRANSPLANT, V18, P152, DOI 10.1046/j.1399-0012.2003.00139.x-
hcfmusp.relation.referenceJunge G, 2005, TRANSPLANT P, V37, P1716, DOI 10.1016/j.transproceed.2005.04.005-
hcfmusp.relation.referenceNACIF Lucas Souto, 2015, ABCD, arq. bras. cir. dig., V28, P212, DOI 10.1590/S0102-67202015000300017-
hcfmusp.relation.referenceNacif LS, 2014, CLINICS, V69, P745, DOI 10.6061/clinics/2014(11)07-
hcfmusp.relation.referenceNeil DAH, 2001, TRANSPLANT P, V33, P1525, DOI 10.1016/S0041-1345(00)02582-3-
hcfmusp.relation.referenceOzbilgin M, 2015, TRANSPL P, V47, P1474, DOI 10.1016/j.transproceed.2015.04.076-
hcfmusp.relation.referenceRamji A, 2002, LIVER TRANSPLANT, V8, P945, DOI 10.1053/jlts.2002.34969-
hcfmusp.relation.referenceSundaram SS, 2006, LIVER TRANSPLANT, V12, P58, DOI 10.1002/lt.20661-
hcfmusp.relation.referenceThurairajah PH, 2013, TRANSPLANTATION, V95, P955, DOI 10.1097/TP.0b013e3182845f6c-
hcfmusp.relation.referenceUemura T, 2008, CLIN TRANSPLANT, V22, P316, DOI 10.1111/j.1399-0012.2007.00788.x-
hcfmusp.relation.referenceWang GY, 2013, TRANSPL P, V45, P1198, DOI 10.1016/j.transproceed.2012.10.008-
hcfmusp.relation.referenceWiesner RH, 2006, AM J TRANSPLANT, V6, P1609, DOI 10.1111/j.1600-6143.2006.01382.x-
dc.description.indexMEDLINE-
hcfmusp.citation.scopus12-
hcfmusp.scopus.lastupdate2024-04-12-
Appears in Collections:

Artigos e Materiais de Revistas Científicas - FM/MGT
Departamento de Gastroenterologia - FM/MGT

Artigos e Materiais de Revistas Científicas - FM/MPT
Departamento de Patologia - FM/MPT

Artigos e Materiais de Revistas Científicas - HC/ICHC
Instituto Central - HC/ICHC

Artigos e Materiais de Revistas Científicas - LIM/14
LIM/14 - Laboratório de Investigação em Patologia Hepática

Artigos e Materiais de Revistas Científicas - LIM/37
LIM/37 - Laboratório de Transplante e Cirurgia de Fígado

Artigos e Materiais de Revistas Científicas - ODS/03
ODS/03 - Saúde e bem-estar


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