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dc.contributor.advisorRodelo Ceballos, Joaquín-
dc.contributor.advisorMuñoz Vahos, Carlos Horacio-
dc.contributor.authorImbachí Salamanca, Alex Jhonier-
dc.contributor.authorRamírez Peralta, Andrés Felipe-
dc.date.accessioned2024-11-14T19:03:00Z-
dc.date.available2024-11-14T19:03:00Z-
dc.date.issued2024-
dc.identifier.urihttps://hdl.handle.net/10495/43487-
dc.description.abstractABSTRACT: Introduction: Vasculitis associated with antibodies against neutrophil cytoplasm (AAV) are rare diseases of autoimmune origin with local and/or systemic involvement, and a high rate of morbidity and mortality. There is little data on these diseases in Latin America and Colombia. Objectives: We describe the clinical characteristics, treatment, clinical outcomes and factors associated with all-cause mortality in patients diagnosed with AAV in Medellín, Colombia. Methods: An analytical observational study was designed to describe a retrospective cohort. Patients with diagnoses of granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), eosinophilic granulomatosis with polyangiitis (EGPA) and ANCA vasculitis limited to kidney (AAV-LR) who were hospitalized in two reference centers between 2014 and 2022 were included. The AAVs characteristics were compared, survival analyzes were performed and factors associated with all-cause mortality were searched. Results: Of 139 patients, the median age was 58 years (IQR 46-67). 51.5% were women. There were 71 patients (51.8%) with GPA, 42 (30.4%) with MPA, 14 (10.1%) with EGPA, and 11 (7.9%) with AAV-LR. Renal involvement was found in 101 (73.2%) with extra capillary glomerulonephritis in 63.9%. Antibodies against myeloperoxidase (anti-MPO) were the most common in 67.9% of patients. Mortality from any cause was 37.7%. The factors associated with higher mortality from any cause were an age at admission > 65 years (HR: 1.04 95% CI 1.01 - 1.06), pulmonary (HR: 2.32 95% CI 1.17 - 4.60) and gastrointestinal involvement (HR: 2.59 95% CI 1.09 - 6.14). Kaplan-Meier analyses showed lower survival in men, MPA, and those with renal and cardiovascular involvement. The most frequently used treatments were glucocorticoids and cyclophosphamide. Conclusions: In this AAV cohort, GPA was the most frequent phenotype, and the commonest antibody was anti-MPO. Higher mortality from any cause was documented compared to other cohorts.spa
dc.format.extent22 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.type.hasversioninfo:eu-repo/semantics/draftspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rightsAtribución-NoComercial-CompartirIgual 2.5 Colombia (CC BY-NC-SA 2.5 CO)*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/2.5/co/*
dc.titleCharacteristics and Clinical Outcomes of Patients with Vasculitis Associated with Antibodies Against Neutrophil Cytoplasm in two Hospitals in Medellín, Colombiaspa
dc.typeinfo:eu-repo/semantics/otherspa
oaire.versionhttp://purl.org/coar/version/c_b1a7d7d4d402bccespa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
thesis.degree.nameEspecialista en Reumatologíaspa
thesis.degree.levelEspecializaciónspa
thesis.degree.disciplineFacultad de Medicina. Especialización en Reumatologíaspa
thesis.degree.grantorUniversidad de Antioquiaspa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-sa/4.0/spa
dc.publisher.placeMedellín, Colombiaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_46ecspa
dc.type.redcolhttp://purl.org/redcol/resource_type/COtherspa
dc.type.localTesis/Trabajo de grado - Monografía - Especializaciónspa
dc.contributor.researcherVargas Camacho, Andrés Felipe-
dc.contributor.researcherEscobar Restrepo, Mauricio-
dc.contributor.researcherTaborda Murillo, Alejandra-
dc.contributor.researcherCalle Botero, Estefanía-
dc.subject.decsVasculitis asociada a anticuerpos citoplasmáticos antineutrófilos-
dc.subject.decsAnti-neutrophil cytoplasmic antibody-associated vasculitis-
dc.subject.decsAnticuerpos anticitoplasma de neutrófilos-
dc.subject.decsAntibodies, antineutrophil cytoplasmic-
dc.subject.decsGranulomatosis con poliangitis-
dc.subject.decsGranulomatosis with Polyangiitis-
dc.subject.decsPoliangitis microscópica-
dc.subject.decsMicroscopic polyangiitis-
dc.subject.decsSíndrome de Churg-Strauss-
dc.subject.decsChurg-Strauss syndrome-
dc.subject.decsGlomerulonefritis-
dc.subject.decsGlomerulonephritis-
dc.subject.decsMortalidad-
dc.subject.decsMortality-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D056648-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D019268-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D014890-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D055953-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D015267-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D005921-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D009026-
Aparece en las colecciones: Especializaciones de la Facultad de Medicina

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