dc.contributorPorras Ramírez, Alexandra
dc.contributorRico Mendoza, Franklin Alejandro
dc.contributorPeña Romero, Lilian Lizett [0000-0002-3968-8522]
dc.creatorPeña Romero, Lilian Lizett
dc.date.accessioned2022-08-02T21:22:05Z
dc.date.accessioned2023-06-05T14:31:39Z
dc.date.available2022-08-02T21:22:05Z
dc.date.available2023-06-05T14:31:39Z
dc.date.created2022-08-02T21:22:05Z
dc.date.issued2021
dc.identifierhttp://hdl.handle.net/20.500.12495/8582
dc.identifierinstname: Universidad El Bosque
dc.identifierreponame: Repositorio Institucional Universidad El Bosque
dc.identifierrepourl: https://repositorio.unbosque.edu.co
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/6638865
dc.description.abstractIntroduction: The Asian continent in 1972 was the first to recognize orphan diseases, followed by Europe and later America. In 2010 Colombia since the 1392 law, interdisciplinary work has been noted, however, it is not enough for global knowledge. Objective: To carry out a prevalence analysis, using databases that are freely accessible to the general public, comparing them with the reports made by the entities in charge of the management of the data for the capture, diagnosis and management of orphan diseases in Colombia. Materials and methods: a cross-sectional study was carried out using data cubes The Comprehensive Social Protection Information System (SISPRO) and the microdata of the National Administrative Department of Statistics (DANE), prevalences are estimated, a heat map and a Regression are performed Simple and multiple Poisson with robust variance, adjusted for sex, age, life cycle and region. Results: Information was collected from 2015 to 2018. 3014555 were people treated for one of the 319 diagnoses chosen. The most frequent disease was Viral Warts (14.4%). in females (58.9%), Bogotá (28%) and the Andean region (71%) had the highest. There is a 2.03 times chance for an older adult to have an orphan disease. The highest mortality rate was in the Andean region (0.12%). Discussion: The data obtained in this study differ from those published by the control entities. Conclusions: Quantitative and mixed research should be promoted, as well as a recoding of the diagnoses identified as orphan disease.
dc.languageeng
dc.publisherMaestría en Epidemiología
dc.publisherUniversidad El Bosque
dc.publisherFacultad de Medicina
dc.rightshttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rightsAcceso abierto
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.rightsAtribución-NoComercial-CompartirIgual 4.0 Internacional
dc.subjectEnfermedades huérfanas
dc.subjectCodificación
dc.subjectPrevalencia
dc.titleThe national recoding of orphan diseases: a proposal directed to health care


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