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1.
BMC Nephrol ; 22(1): 79, 2021 03 05.
Artículo en Inglés | MEDLINE | ID: mdl-33673808

RESUMEN

BACKGROUND: Whilst there are a number of publications comparing the relationship between body mass index (BMI) of kidney transplant recipients and graft/patient survival, no study has assessed this for a French patient cohort. METHODS: In this study, cause-specific Cox models were used to study patient and graft survival and several other time-to-event measures. Logistic regressions were performed to study surgical complications at 30 days post-transplantation as well as delayed graft function. RESULTS: Among the 4691 included patients, 747 patients were considered obese with a BMI level greater than 30 kg/m2. We observed a higher mortality for obese recipients (HR = 1.37, p = 0.0086) and higher risks of serious bacterial infections (HR = 1.24, p = 0.0006) and cardiac complications (HR = 1.45, p < 0.0001). We observed a trend towards death censored graft survival (HR = 1.22, p = 0.0666) and no significant increased risk of early surgical complications. CONCLUSIONS: We showed that obesity increased the risk of death and serious bacterial infections and cardiac complications in obese French kidney transplant recipients. Further epidemiologic studies aiming to compare obese recipients versus obese candidates remaining on dialysis are needed to improve the guidelines for obese patient transplant allocation.


Asunto(s)
Fallo Renal Crónico/complicaciones , Fallo Renal Crónico/cirugía , Trasplante de Riñón , Obesidad/complicaciones , Adulto , Anciano , Estudios de Cohortes , Femenino , Francia , Supervivencia de Injerto , Humanos , Masculino , Persona de Mediana Edad , Resultado del Tratamiento
2.
BMC Nephrol ; 20(1): 365, 2019 10 11.
Artículo en Inglés | MEDLINE | ID: mdl-31601177

RESUMEN

BACKGROUND: Kidney transplantation is considered to be the treatment of choice for people with end-stage renal disease (ESRD). However, due to the shortage of available organs and the increase in the ESRD prevalence in Europe, it is essential to improve transplantation outcomes by studying the related prognostic factors. Today, there is no European registry collecting data to perform such clinical epidemiology studies. MAIN BODY: Entitled EKiTE, for European cohort for Kidney Transplantation Epidemiology, this prospective and multicentric cohort includes patients from Spanish (Barcelona), Belgian (Leuven), Norwegian (Oslo) and French (Paris Necker, Lyon, Nantes, Nancy, Montpellier, Nice and Paris Saint Louis) transplantation centers and currently contains 13,394 adult recipients of kidney (only) transplantation from 2005 and updated annually. A large set of parameters collected from transplantation until graft failure or death with numbers of post-transplantation outcomes. The long-term follow-up and the collected data enable a wide range of possible survival and longitudinal analyses. CONCLUSION: EKiTE is a multicentric cohort aiming to better assess the natural history of the ESRD in European kidney transplant recipients and perform benchmarking of clinical practices. The data are available for clinical epidemiology studies and open for external investigators upon request to the scientific council. Short-term perspectives are to extend EKITE network to other European countries and collect additional parameters in respect of the common thesaurus.


Asunto(s)
Investigación Biomédica/tendencias , Bases de Datos Factuales/tendencias , Fallo Renal Crónico/epidemiología , Fallo Renal Crónico/cirugía , Trasplante de Riñón/tendencias , Investigación Biomédica Traslacional/tendencias , Investigación Biomédica/normas , Estudios de Cohortes , Bases de Datos Factuales/normas , Europa (Continente)/epidemiología , Estudios de Seguimiento , Supervivencia de Injerto/fisiología , Humanos , Colaboración Intersectorial , Estudios Prospectivos , Reproducibilidad de los Resultados , Investigación Biomédica Traslacional/normas
4.
Int J Clin Pharmacol Biopharm ; 17(5): 197-204, 1979 May.
Artículo en Inglés | MEDLINE | ID: mdl-468445

RESUMEN

Although the cardiotonic activity of gitoxin is known for almost half a century, this digitalis glycoside has never been used in therapy, due to its apparent lack of resorption after administration by oral route. Recent studies have demonstrated that the bioavailability of gitoxin could be upraised to 100% provided it be given as a hydroalcoholic solution. The present paper deals with the development of a solid dosage form (tablets) using a physical association of gitoxin and sodium escinate.


Asunto(s)
Digoxina/metabolismo , Adulto , Animales , Disponibilidad Biológica , Glicósidos Digitálicos/sangre , Digoxina/administración & dosificación , Perros , Escina/farmacología , Excipientes/administración & dosificación , Femenino , Humanos , Inyecciones Intravenosas , Isomerismo , Masculino , Persona de Mediana Edad , Solubilidad , Comprimidos
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