Josep Navarro-Manchón
Instituto Politécnico Nacional
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Featured researches published by Josep Navarro-Manchón.
Clinical Transplantation | 2011
Ignacio Sánchez-Lázaro; Luis Almenar; Luis Martínez-Dolz; Francisco Buendía-Fuentes; Jaime Agüero; Josep Navarro-Manchón; José-Luis Vicente; Antoinio Salvador
Sánchez‐Lázaro IJ, Almenar L, Martínez‐Dolz L, Buendía‐Fuentes F, Agüero J, Navarro‐Manchón J, Vicente J‐L, Salvador A. A prospective randomized study comparing cyclosporine versus tacrolimus combined with daclizumab, mycophenolate mofetil and steroids in heart transplantation. Clin Transplant 2011: 25: 606–613.
Revista Espanola De Cardiologia | 2010
Josep Navarro-Manchón; Luis Martínez-Dolz; Luis Almenar; José A. Moro; Esther Zorio; Rafael Raso; Francisco Buendía; Ignacio Sánchez-Lázaro; Jaime Agüero; Antonio Salvador
Introduccion y objetivos Uno de los problemas mas relevantes tras el trasplante cardiaco es el desarrollo de insuficiencia renal. La heterogeneidad en su definicion hace que la estimacion de su prevalencia sea variable. Por otro lado, su impacto en la mortalidad no ha sido suficientemente estudiado. El objetivo fue evaluar la relacion entre la tasa de filtracion glomerular al ano (TFG) y la mortalidad en el seguimiento. Metodos Se analizo la TFG de 316 pacientes vivos al ano del trasplante mediante la formula abreviada Modification of Diet in Renal Disease Study. Se clasificaron en tres grupos segun su TFG ( Resultados No hubo diferencias en el numero de rechazos ni infecciones durante el primer ano en los tres grupos. En el seguimiento medio (6,3 anos) fallecio el 74% de los pacientes con TFG Conclusiones La disfuncion grave de la funcion renal al ano es un predictor independiente de mortalidad por todas las causas a largo plazo en el paciente con trasplante cardiaco.
Revista Espanola De Cardiologia | 2010
Josep Navarro-Manchón; Luis Martínez-Dolz; Luis Almenar; José A. Moro; Esther Zorio; Rafael Raso; Francisco Buendía; Ignacio Sánchez-Lázaro; Jaime Agüero; Antonio Salvador
INTRODUCTION AND OBJECTIVES The development of renal failure is one of the most important problems after heart transplantation (HT), but the wide range of definitions means that estimates of its prevalence vary considerably. Furthermore, its impact on mortality has not been adequately studied. The objective was to investigate the relationship between the glomerular filtration rate (GFR) 1 year after transplantation and mortality during follow-up. METHODS The GFR was determined in 316 patients still living 1 year after transplantation using the abbreviated Modification of Diet in Renal Disease Study formula. Patients were divided into three groups according to GFR (i.e. <30, 30-59 and > or =60 mL/min per 1.73 m2) and pretransplant variables and rejection and infection rates within the first year were analyzed. The association between GFR at 1 year and mortality during follow-up was evaluated and reasons for the association were examined. RESULTS There was no difference in the number of rejections or infections in the first year between the three groups. During a mean follow-up period of 6.3 years, 74% of patients with a GFR <30 mL/min per 1.73 m2 died, compared with 24% and 30% of those with a GFR > or =60 and 30-59 mL/min per 1.73 m2, respectively. Survival analysis (i.e. Cox regression analysis) demonstrated a significant difference between patients with a GFR <30 mL/min per 1.73 m2 and other patients (P< .001). A very low GFR at 1 year was the only independent predictor that remained statistically significant on multivariate analysis (hazard ratio =2.87; 95% confidence interval, 1.52-5.41). CONCLUSIONS Severe renal dysfunction at 1 year was an independent predictor of long-term all-cause mortality in heart transplant patients.
European Journal of Medical Genetics | 2013
Oscar Campuzano; Mireia Alcalde; Paola Berne; Esther Zorio; Anna Iglesias; Josep Navarro-Manchón; Josep Brugada; Ramon Brugada
INTRODUCTION Arrhythmogenic right ventricular cardiomyopathy is an inherited disease characterized by a progressive myocardium fibrofatty replacement. This abnormality disrupts electrical transmission causing ventricular arrhythmias and sudden cardiac death. This genetic disease is transmitted mainly with an autosomal dominant pattern. Our aim was to identify the genetic defect responsible for the pathology in a Spanish family, and to perform its phenotype connotations. MATERIAL AND METHODS A total of 15 individuals in a three-generation Spanish family were screened after the sudden cardiac death of one family member. All they underwent a complete physical examination, 12-lead electrocardiogram, 2-dimensional echocardiography, magnetic resonance imaging, exercise stress test, 24-h Holter and genetic testing. RESULTS Autopsy revealed the presence of biventricular arrhythmogenic dysplasia in deceased member. Six family members showed clinical symptoms but only three of them fulfilled definite diagnostic criteria of the disease. Genetic analysis showed a novel nonsense genetic variation in nine family members. All family members with clinical symptoms carried the genetic variation. CONCLUSIONS Genetic testing in families affected by arrhythmogenic right ventricular cardiomyopathy helps to identify the genetic cause responsible for the disease. The incomplete penetrance and variable phenotypic expression highlights the need of comprehensive genetic analysis and further phenotype implications of genetics to clarify the pathophysiology of the disease.
Revista Espanola De Cardiologia | 2011
Josep Navarro-Manchón; Elena Rivero Fernández; Begoña Igual; Angeliki Asimaki; Petros Syrris; Joaquín Osca; Antonio Salvador; Esther Zorio
Left dominant arrhythmogenic cardiomyopathy (LDAC) exhibits characteristic phenotypic and genetic features which were found in the five Spanish family members described in this study. Triggered by a cold, a young man presented with a ventricular tachycardia of left ventricular origin and left ventricular late gadolinium enhancement. His resting ECG showed low potentials, delayed ventricular depolarization (inferior and V4-V6 leads) and atrioventricular conduction disturbances. His endomyocardial biopsy revealed myocyte loss with interstitial fibrosis. Despite the initial diagnosis of myocarditis, familial screening was pivotal in confirming the diagnosis of LDAC. A novel nonsense mutation in the desmoplakin gene (Q1866X) and the truncated protein which it produces were observed in skin samples.
Transplantation Proceedings | 2010
Josep Navarro-Manchón; L. Almenar Bonet; Luis Martínez-Dolz; Ignacio Sánchez-Lázaro; F. Buendía Fuentes; R. Raso Raso; J. Agüero Ramón-Llín; María Rodríguez-Serrano; E. Zorio Grima; A. Salvador Sanz
INTRODUCTION One of the most common, significant problems after heart transplantation (HT) is the development of renal dysfunction. In recent years, the glomerular filtration rate (GFR) has replaced the serum creatinine as the standard parameter for its determination. Our objective was to analyze which renal function parameter (creatinine or GFR) at 1 year after HT better classified patients who will die during follow-up. PATIENTS AND METHODS The study included 316 consecutive HT patients surviving at least 1 year after transplantation. Creatinine and GFR were determined by the Modification of Diet in Renal Disease Study (MDRD4) equation. Mortality during the follow-up was analyzed to compare both parameters using receiver operating characteristic curves. RESULTS Over a mean follow-up of 6±3 years, 97 patients died (30.7%). At 1 year after HT, the patients who succumbed displayed a significantly higher mean creatinine value (1.63±0.65 vs 1.41±0.64 mg/dL; P=.004) and a more decreased GFR (53.8 vs 60.8 mL/min/1.73 m2; P=.006). Both groups had the same area under the curve, 0.61 (95% confidence interval: 0.54-0.68; P=.002). CONCLUSION Among our population, GFR calculated by the abbreviated MDRD4 equation did not provide any additional prognostic value to serum creatinine at 1 year after HT to predict long-term mortality.
Revista Espanola De Cardiologia | 2018
F. Javier García-Fernández; José Luis Ibáñez Criado; Aurelio Quesada Dorador; Miguel Álvarez-López; Jesús Almendral; Concepción Alonso; Pau Alonso-Fernández; Nelson Alvaralenga; Luis Álvarez-Acosta; Ignasi Anguera; María Fe Arcocha; Miguel A. Arias; Antonio Asso; Alberto Barrera-Cordero; Gabriel Ballesteros; Juan Benezet-Mazuecos; Andrés Bodegas-Cañas; Josep Brugada; Claudia Cabadés Lucas Cano-Calabria; Eduardo Caballero-Dorta; Pilar Cabanas-Grandío; Sandra Cabrera; Victor Castro; Rocío Cózar; Ernesto Díaz-Infante; Manuel Doblado; Juliana Elices; María del Carmen Expósito-Pineda; Juan M. Fernández-Gómez; María Luisa Fidalgo
INTRODUCTION AND OBJECTIVES This report describes the findings of the 2017 Spanish Catheter Ablation Registry. METHODS Data collection was retrospective. A standardized questionnaire was completed by each of the participating centers. RESULTS A total of 15 284 ablation procedures were performed by 98 institutions (the highest number of ablations and institutions historically reported in this registry), with a mean of 156±126 and a median of 136 procedures per center. For the first time, the most frequently treated ablation target was atrial fibrillation (n=3457; 22.6%), followed by cavotricuspid isthmus (n=3449; 22.5%) and atrioventricular nodal re-entrant tachycardia (n=3429; 22.4%). The overall success rate was 87%. The rate of major complications was 2.6%, and the mortality rate was 0.09%. The percentage of procedures performed without fluoroscopic support increased to 6% of all ablations, and 2.3% of all ablations were performed in pediatric patients. CONCLUSIONS The Spanish Ablation Catheter Registry systematically and uninterruptedly collects data on the ablation procedures performed in Spain, revealing that both the number of ablations and the number of centers performing them has progressively increased, while maintaining a high success rate and a low percentage of complications.
Transplantation | 2010
Josep Navarro-Manchón; Luis Martínez-Dolz; Luis Almenar Bonet; Ignacio Sánchez-Lázaro; Rafael Raso; Esther Zorio Grima; Jaime Agüero Ramon-Llin; Francisco Buendía Fuentes; Juan-Miguel Sánchez-Gómez; Antonio Salvador Sanz
Revista Espanola De Cardiologia | 2011
Josep Navarro-Manchón; Elena Rivero Fernández; Begoña Igual; Angeliki Asimaki; Petros Syrris; Joaquín Osca; Antonio Salvador; Esther Zorio
Revista Espanola De Cardiologia | 2018
F. Javier García-Fernández; José Luis Ibáñez Criado; Aurelio Quesada Dorador; Miguel Álvarez-López; Jesús Almendral; Concepción Alonso; Pau Alonso-Fernández; Nelson Alvaralenga; Luis Álvarez-Acosta; Ignasi Anguera; María Fe Arcocha; Miguel A. Arias; Antonio Asso; Alberto Barrera-Cordero; Gabriel Ballesteros; Juan Benezet-Mazuecos; Andrés Bodegas-Cañas; Josep Brugada; Claudia Cabadés Lucas Cano-Calabria; Eduardo Caballero-Dorta; Pilar Cabanas-Grandío; Sandra Cabrera; Victor Castro; Rocío Cózar; Ernesto Díaz-Infante; Manuel Doblado; Juliana Elices; María del Carmen Expósito-Pineda; Juan M. Fernández-Gómez; María Luisa Fidalgo