Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/119454
Campo DC Valoridioma
dc.contributor.authorDarwish Murad, Sarwaden_US
dc.contributor.authorPlessier, Aurelieen_US
dc.contributor.authorHernández Guerra, Manuelen_US
dc.contributor.authorFabris, Federicaen_US
dc.contributor.authorEapel, Chundamanilen_US
dc.contributor.authorBahr, Matthias J.en_US
dc.contributor.authorTrebicka, Jonelen_US
dc.contributor.authorMorard, Isabelleen_US
dc.contributor.authorLasser, Lucen_US
dc.contributor.authorHeller, Joergen_US
dc.contributor.authorHadengue, Antoineen_US
dc.contributor.authorLanglet, Phillippeen_US
dc.contributor.authorMiranda, Helenaen_US
dc.contributor.authorPrimignani, Massimoen_US
dc.contributor.authorElias, Elwynen_US
dc.contributor.authorLeebeek, Frank W.en_US
dc.contributor.authorRosendaal, Frits R.en_US
dc.contributor.authorGarcía Pagán, Juan Carlosen_US
dc.contributor.authorValla, Dominiqueen_US
dc.contributor.authorJanssen, Harry L. A.en_US
dc.contributor.authorMonescillo Francia, Alberto Fernandoen_US
dc.date.accessioned2022-11-28T18:17:14Z-
dc.date.available2022-11-28T18:17:14Z-
dc.date.issued2009en_US
dc.identifier.issn1539-3704en_US
dc.identifier.urihttp://hdl.handle.net/10553/119454-
dc.description.abstractBackground: The Budd–Chiari syndrome (BCS) is hepatic venous outflow obstruction. What is known about the syndrome is based on small studies of prevalent cases. Objective: To characterize the causes and treatment of incident BCS. Design: Consecutive case series of patients with incident BCS, enrolled from October 2003 to October 2005 and followed until May 2006. Setting: Academic and nonacademic hospitals in France, Spain, Italy, Great Britain, Germany, Belgium, the Netherlands, Portugal, and Switzerland. Patients: Persons older than 16 years with definite hepatic outflow obstruction diagnosed by imaging. Persons with hepatic outflow obstruction due to heart failure, sinusoidal obstruction syndrome, cancer, or liver transplantation were excluded. Measurements: Signs and symptoms; laboratory and imaging findings; diagnosis; treatment; and overall, transplantation-free, and intervention-free survival. Results: 163 incident cases of BCS were identified. Median follow-up was 17 months (range, 0.1 to 31 months). Most patients (84%) had at least 1 thrombotic risk factor, and many (46%) had more than 1; the most common was myeloproliferative disorders (49% of 103 tested patients). Patients were mainly treated with anticoagulation (140 patients [86%]), transjugular intrahepatic portosystemic shunting (56 patients [34%]), or liver transplantation (20 patients [12%]), and 80 patients (49%) were managed noninvasively. Only 3 patients underwent surgical shunting. The survival rate was 87% (95% CI, 82% to 93%) at 1 year and 82% (CI, 75% to 88%) at 2 years. Limitation: Treatment was not standardized across all centers, and data on important clinical variables were missing for some patients. Conclusion: Most patients with BCS have at least 1 thrombotic risk factor, and many have more than 1; myeloproliferative disorders are most common. One- and 2-year survival rates are good with contemporary management, which includes noninvasive therapies (anticoagulation and diuretics) and invasive techniques. Transjugular intrahepatic portosystemic shunting seems to have replaced surgical shunting as the most common invasive therapeutic procedure.en_US
dc.languageengen_US
dc.relation.ispartofAnnals of internal medicineen_US
dc.sourceAnnals of Internal Medicine [1539-3704], v. 51(3), pp. 167-175 (agosto 2009)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3205 Medicina internaen_US
dc.subject.otherAntibodiesen_US
dc.subject.otherAscitesen_US
dc.subject.otherBiopsyen_US
dc.subject.otherFactor V Leidenen_US
dc.subject.otherHospitalsen_US
dc.subject.otherLiveren_US
dc.subject.otherLiver transplantationen_US
dc.subject.otherMedical risk factorsen_US
dc.subject.otherProtein S deficiencyen_US
dc.subject.otherVeinsen_US
dc.titleEtiology, management, and outcome of the Budd-Chiari syndromeen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.7326/0003-4819-151-3-200908040-00004.en_US
dc.description.lastpage175en_US
dc.identifier.issue3-
dc.description.firstpage167en_US
dc.relation.volume51en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages9en_US
dc.utils.revisionen_US
dc.date.coverdateAgosto 2009en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-9490-4427-
crisitem.author.fullNameMonescillo Francia, Alberto Fernando-
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