Síndrome Antifosfolípido: morbilidad y evolución de una cohorte de pacientes del Hospital Pablo Tobón Uribe de Medellín-Colombia

dc.contributor.authorFrancisco Vargas Grajales
dc.contributor.authorLuis Fernando Pinto Peñaranda
dc.contributor.authorJosé Fernando Molina Restrepo
dc.contributor.authorJosé Raúl Moreno Gómez
dc.contributor.authorRuth Eraso
dc.contributor.authorAndrés Tobón Ramírez
dc.contributor.authorPaola Ramírez
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T15:00:59Z
dc.date.available2026-03-22T15:00:59Z
dc.date.issued2006
dc.descriptionCitaciones: 12
dc.description.abstractObjetive: describe the clinical and laboratory characteristics in a cohort of patient with SAF and explore possible association between autoantibodies and clinical complications. Methods: this assay have been based in analytic study of transversal cohort in patients with a criterion of Sapporo of SAF. Results: a total of 62 patients are described, with a 83.9% of women and 16.1% of men. The patients were 28 years old at inclusion. The primary anthiphospholipid syndrome (PAPS) was observed in 32.3% of patients and the secondary anthiphospholipid syndrome (SAPS) were found in the 67.7% of patients. The patients with PAPS were older and have more fetal looses than SAPS. The risk of recurrence venous thrombosis was major than arterial thrombosis. Conclusions: anthiphospholipid syndrome have a big spectrum of clinicals manifestation afecting any organ. The association with autoinmune disease can create subgroups of this disease. Some differences were found between SAPS and PAPS in prognosis and clinical compromise.
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/49886
dc.language.isoes
dc.sourceUniversidad Privada Boliviana
dc.subjectMedicine
dc.subjectCohort
dc.subjectVenous thrombosis
dc.subjectInternal medicine
dc.subjectThrombosis
dc.subjectPediatrics
dc.titleSíndrome Antifosfolípido: morbilidad y evolución de una cohorte de pacientes del Hospital Pablo Tobón Uribe de Medellín-Colombia
dc.typearticle

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