Inicio
Resultado de la búsqueda
1 búsqueda de la palabra clave 'progression'
Clasificado(s) por (Año de edición descendente) Refinar búsqueda Genera el flujo rss de la búsqueda
Enlace permanente de la investigación
Clinical course of sepsis, severe sepsis, and septic shock in a cohort of infected patients from ten Colombian hospitals / Fabián Alberto Jaimes Barragán ; Gisela de la Rosa Echavez
Título : Clinical course of sepsis, severe sepsis, and septic shock in a cohort of infected patients from ten Colombian hospitals Tipo de documento : documento electrónico Autores : Fabián Alberto Jaimes Barragán, ; Gisela de la Rosa Echavez, Fecha de publicación : 2013 Títulos uniformes : BMC Infectious Diseases Idioma : Inglés (eng) Palabras clave : Severe sepsis septic shock progression GEE cox regression Resumen : Background: Sepsis has several clinical stages, and mortality rates are different for each stage. Our goal was to establish the evolution and the determinants of the progression of clinical stages, from infection to septic shock, over the first week, as well as their relationship to 7-day and 28-day mortality. Methods: This is a secondary analysis of a multicenter cohort of inpatients hospitalized in general wards or intensive care units (ICUs). The general estimating equations (GEE) model was used to estimate the risk of progression and the determinants of stages of infection over the first week. Cox regression with time-dependent covariates and fixed covariates was used to determine the factors related with 7-day and 28-day mortality, respectively. Results: In 2681 patients we show that progression to severe sepsis and septic shock increases with intraabdominal and respiratory sources of infection [OR = 1,32; 95%IC = 1,20-1,46 and OR = 1.21, 95%CI = 1,11-1,33 respectively], as well as according to Acute Physiology and Chronic Health Evaluation II (APACHE II) [OR = 1,03; 95%CI = 1,02-1,03]and Sequential Organ Failure Assessment (SOFA) [OR = 1,16; 95%CI = 1,14-1,17] scores. The variables related with first-week mortality were progression to severe sepsis [HR = 2,13; 95%CI = 1,13-4,03] and septic shock [HR = 3,00; 95%CI = 1,50-5.98], respiratory source of infection [HR = 1,76; 95%IC = 1,12-2,77], APACHE II [HR = 1,07; 95% CI = 1,04-1,10] and SOFA [HR = 1,09; 95%IC = 1,04-1,15] scores. Conclusions: Intraabdominal and respiratory sources of infection, independently of SOFA and APACHE II scores, increase the risk of clinical progression to more severe stages of sepsis; and these factors, together with progression of the infection itself, are the main determinants of 7-day and 28-day mortality. Mención de responsabilidad : Alba Luz León, Natalia Andrea Hoyos, Lena Isabel Barrera, Gisela De La Rosa, Rodolfo Dennis, Carmelo Dueñas, Marcela Granados, Dario Londoño, Ferney Alexander Rodríguez, Francisco José Molina, Guillermo Ortiz, Fabián Alberto Jaimes Referencia : BMC Infect Dis. 2013 Jul 24;13:345. DOI (Digital Object Identifier) : 10.1186/1471-2334-13-345 PMID : 23883312 Derechos de uso : CC BY En línea : https://bmcinfectdis.biomedcentral.com/articles/10.1186/1471-2334-13-345 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3690 Clinical course of sepsis, severe sepsis, and septic shock in a cohort of infected patients from ten Colombian hospitals [documento electrónico] / Fabián Alberto Jaimes Barragán, ; Gisela de la Rosa Echavez, . - 2013.
Obra : BMC Infectious Diseases
Idioma : Inglés (eng)
Palabras clave : Severe sepsis septic shock progression GEE cox regression Resumen : Background: Sepsis has several clinical stages, and mortality rates are different for each stage. Our goal was to establish the evolution and the determinants of the progression of clinical stages, from infection to septic shock, over the first week, as well as their relationship to 7-day and 28-day mortality. Methods: This is a secondary analysis of a multicenter cohort of inpatients hospitalized in general wards or intensive care units (ICUs). The general estimating equations (GEE) model was used to estimate the risk of progression and the determinants of stages of infection over the first week. Cox regression with time-dependent covariates and fixed covariates was used to determine the factors related with 7-day and 28-day mortality, respectively. Results: In 2681 patients we show that progression to severe sepsis and septic shock increases with intraabdominal and respiratory sources of infection [OR = 1,32; 95%IC = 1,20-1,46 and OR = 1.21, 95%CI = 1,11-1,33 respectively], as well as according to Acute Physiology and Chronic Health Evaluation II (APACHE II) [OR = 1,03; 95%CI = 1,02-1,03]and Sequential Organ Failure Assessment (SOFA) [OR = 1,16; 95%CI = 1,14-1,17] scores. The variables related with first-week mortality were progression to severe sepsis [HR = 2,13; 95%CI = 1,13-4,03] and septic shock [HR = 3,00; 95%CI = 1,50-5.98], respiratory source of infection [HR = 1,76; 95%IC = 1,12-2,77], APACHE II [HR = 1,07; 95% CI = 1,04-1,10] and SOFA [HR = 1,09; 95%IC = 1,04-1,15] scores. Conclusions: Intraabdominal and respiratory sources of infection, independently of SOFA and APACHE II scores, increase the risk of clinical progression to more severe stages of sepsis; and these factors, together with progression of the infection itself, are the main determinants of 7-day and 28-day mortality. Mención de responsabilidad : Alba Luz León, Natalia Andrea Hoyos, Lena Isabel Barrera, Gisela De La Rosa, Rodolfo Dennis, Carmelo Dueñas, Marcela Granados, Dario Londoño, Ferney Alexander Rodríguez, Francisco José Molina, Guillermo Ortiz, Fabián Alberto Jaimes Referencia : BMC Infect Dis. 2013 Jul 24;13:345. DOI (Digital Object Identifier) : 10.1186/1471-2334-13-345 PMID : 23883312 Derechos de uso : CC BY En línea : https://bmcinfectdis.biomedcentral.com/articles/10.1186/1471-2334-13-345 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3690 Reserva
Reservar este documentoEjemplares(1)
Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD000263 AC-2013-031 Archivo digital Producción Científica Artículos científicos Disponible Documentos electrónicos
2013-031.pdfAdobe Acrobat PDF