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dc.creatorHernández Rodríguez, Juan Carloses
dc.creatorSendín‐Martín, Mercedeses
dc.creatorDurán Romero, Antonio Josées
dc.creatorOrtiz Álvarez, Juanes
dc.creatorConejo-Mir Sánchez, Juliánes
dc.creatorPereyra-Rodríguez, José-Juanes
dc.date.accessioned2024-07-09T07:53:05Z
dc.date.available2024-07-09T07:53:05Z
dc.date.issued2022
dc.identifier.citationHernández Rodríguez, J.C., Sendín‐Martín, M., Durán Romero, A.J., Ortiz Álvarez, J., Conejo-Mir Sánchez, J. y Pereyra-Rodríguez, J. (2022). Systemic sclerosis mortality trends in Spain from 1980 to 2019: age‐period‐cohort and Joinpoint analysis. Clinical and Experimental Dermatology (CED), 47 (11), 1943-1950. https://doi.org/10.1111/ced.15342.
dc.identifier.issn0307-6938es
dc.identifier.issn1365-2230es
dc.identifier.urihttps://hdl.handle.net/11441/161200
dc.description.abstractBackground: Systemic sclerosis (SSc) is an autoimmune chronic rheumatic disease with a high mortality rate, which continues to be a challenge for clinicians today. Aim: To assess changes in mortality trends in the Spanish SSc population between 1980 and 2019, taking into account the independent effects of sex, age, time period and birth cohort. Methods: SSc death records and mid-year population data were collected from the National Statistics Institute. Age-standardized mortality rates were calculated for the overall population and for each sex (male, female) and age group (5-year groups). Significant changes in mortality trends were identified by joinpoint regressions. An age-period-cohort (APC) analysis and potential years of life lost (PYLL) analysis were performed to identify the burden of SSc. Results: Age-standardized mortality rates due to SSc increased from 1.87 (95% CI 1.00-3.02) per 1 000 000 inhabitants between 1980 and 1984, to 2.47 (95% CI 1.74-3.02) per 1 000 000 inhabitants between 2015 and 2019. The relative risk of mortality fell in all groups in cohorts born after 1990. The PYLL rates showed a gradual rise for both sexes. Conclusion: There was an increase in overall SSc mortality in Spain during the 39 years evaluated, although there was a progressive drop for men.es
dc.formatapplication/pdfes
dc.format.extent8 p.es
dc.language.isoenges
dc.publisherOxford University Presses
dc.relation.ispartofClinical and Experimental Dermatology (CED), 47 (11), 1943-1950.
dc.subjectScleroderma systemices
dc.subjectSurvivales
dc.subjectMortalityes
dc.titleSystemic sclerosis mortality trends in Spain from 1980 to 2019: age‐period‐cohort and Joinpoint analysises
dc.typeinfo:eu-repo/semantics/articlees
dc.type.versioninfo:eu-repo/semantics/acceptedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicinaes
dc.relation.publisherversionhttps://academic.oup.com/ced/article-abstract/47/11/1943/6966131?redirectedFrom=fulltextes
dc.identifier.doi10.1111/ced.15342es
dc.journaltitleClinical and Experimental Dermatology (CED)es
dc.publication.volumen47es
dc.publication.issue11es
dc.publication.initialPage1943es
dc.publication.endPage1950es

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