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Dive into the research topics where Antonio Rivero Román is active.

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Featured researches published by Antonio Rivero Román.


American Journal of Transplantation | 2007

Pneumonia after lung transplantation in the RESITRA Cohort: a multicenter prospective study.

Manuela Aguilar-Guisado; J. Givaldá; P. Ussetti; Antonio Ramos; P. Morales; Marino Blanes; Germán Bou; J. De La Torre‐Cisneros; Antonio Rivero Román; J. M. Borro; R. Lama; José Miguel Cisneros

The aim of the present study is to evaluate the epidemiology, etiology and prognosis of pneumonia in lung transplant (LT) recipients. This is a prospective, multicenter study of a consecutive cohort of LT recipients in Spain. From September 2003 to November 2005, 85 episodes of pneumonia in 236 LT recipients were included (incidence 72 episodes per 100 LT/year). Bacterial pneumonia (82.7%) was more frequent than fungal (14%) and viral pneumonia (10.4%). The most frequent microorganisms in each etiological group were Pseudomonas aeruginosa (n = 14, 24.6%), CMV (n = 6, 10.4%) and Aspergillus spp. (n = 5, 8.8%). Incidence of Aspergillus spp. and CMV pneumonia is lower than previously reported, probably due to the spread of universal prophylaxis. Pneumonia caused by viruses appeared significantly later than pneumonia due to gram‐negative bacilli, fungi and those without known etiology (p < 0.01, p = 0.03 and p = 0.02, respectively). The routine use of ganciclovir has changed the natural history of CMV infection, so that pneumonia appears later, once prophylaxis is suspended. The probability of survival during the first year of follow‐up was significantly higher in the multivariate analysis in LT recipients who did not have a pneumonia episode compared with those that had at least one episode (p < 0.01).


Journal of Heart and Lung Transplantation | 2013

Prophylaxis with nebulized liposomal amphotericin B for Aspergillus infection in lung transplant patients does not cause changes in the lipid content of pulmonary surfactant

Víctor Monforte; Almudena López-Sánchez; Felipe Zurbano; Piedad Ussetti; Amparo Solé; Cristina Casals; José Cifrian; Alicia de Pablos; C. Bravo; Antonio Rivero Román

BACKGROUND Prophylaxis with inhaled liposomal amphotericin B has proven to be safe and effective for preventing infection due to Aspergillus spp in lung transplant recipients. However, the liposome contains a large quantity of phospholipids, and inhalation of these substances could potentially change the composition of pulmonary surfactant. The aim of this study was to determine the lipid composition of pulmonary surfactant in patients receiving inhaled liposomal amphotericin B prophylaxis. METHODS A prospective, open, controlled multicenter study was conducted in 2 groups: 19 lung transplant recipients who received regular prophylaxis with inhaled amphotericin B (study group) and 19 recipients who did not receive inhaled prophylaxis (control group). From both groups, 15 ml of the third aliquot of bronchoalveolar lavage fluid was obtained and phospholipid content determined in the active fraction of surfactant (large aggregates) and in the inactive fraction (small aggregates). Large aggregate cholesterol content was also determined. RESULTS Patient demographic data and characteristics were similar in the 2 groups. No between-group differences in median phospholipid content were found for large aggregates (study group, 0.4 [range, 0.18-1.9] μmol vs controls, 0.36 [range 2.15-0.12] μmol; p = 0.69) or small aggregates (study group, 0.23 [range, 0.1-0.58] μmol vs controls, 0.29 [range, 0.18-0.65] μmol; p = 0.33). The small aggregate-to-large aggregate phospholipid ratio, commonly used as a marker of alveolar injury, showed no differences between the groups (study group, 0.56 vs controls, 0.69; p = 0.28). Nor were there differences in the cholesterol content of large aggregates (study group, 0.04 μmol [range 0.01-0.1] vs controls, 0.04 μmol [range 0.02-0.27); p = 0.13). CONCLUSIONS These results seem to indicate that prophylaxis with nebulized liposomal amphotericin B does not cause changes in the lipid content of pulmonary surfactant.


Medicina Clinica | 2009

Estudio y tratamiento de las neumonías de adquisición comunitaria en adultos

Jerónimo Pachón; Juan de Dios Alcántara Bellón; Elisa Cordero Matía; Ángela Camacho Espejo; Carmen Lama Herrera; Antonio Rivero Román

El presente documento pretende ser una Guı́a práctica, de los cuidados, de los métodos de diagnóstico etiológico, del tratamiento y del seguimiento de los pacientes inmunocompetentes con neumonı́a adquirida en la comunidad (NAC), tanto en aquellos que se tratarán en su domicilio como en aquellos que necesitan tratamiento en régimen de hospitalización. Dado que se trata de que sea una Guı́a de uso real en la práctica clı́nica, no pretende ser una revisión de la extensa literatura médica existente sobre las NAC, ni sustituir las Guı́as de Práctica Clı́nica más prestigiosas sobre las NAC, a las que se remite al lector interesado en profundizar en los diferentes aspectos de éstas. En el presente documento se han actualizado aspectos relacionados con los factores de riesgo, la clı́nica, la susceptibilidad de determinados patógenos a los antimicrobianos, las reglas pronósticas y las recomendaciones sobre el tratamiento antimicrobiano en relación con las pruebas más importantes, a juicio de los autores, aparecidas en los últimos 5 años. Como método de elaboración de esta Guı́a se propuso un equipo compuesto por especialistas en Medicina Familiar y Comunitaria y en Medicina Interna, expertos en enfermedades infecciosas, todos éstos con experiencia y trabajos previos en la NAC y su tratamiento. Los borradores iniciales se discutieron en una sesión de trabajo con el fin de dar lugar al documento definitivo, el que se hizo accesible a través de las páginas web de la Sociedad Andaluza de Medicina Familiar y Comunitaria y de la Sociedad Andaluza de Enfermedades Infecciosas para su estudio por los miembros de ambas sociedades y el envı́o de sugerencias al coordinador del documento. Con las sugerencias recibidas, el


Archivos De Bronconeumologia | 2011

Normativa para la selección de pacientes candidatos a trasplante pulmonar

Antonio Rivero Román; P. Ussetti; Amparo Solé; Felipe Zurbano; José M. Borro; José M. Vaquero; Alicia de Pablo; Pilar Morales; Marina Blanco; Carlos Bravo; J. Cifrian; Mercedes de la Torre; Pablo Gámez; Rosalia Laporta; Víctor Monforte; Roberto Mons; Ángel Salvatierra; Francisco Santos; Joan Solé; Andrés Varela

The present guidelines have been prepared with the consensus of at least one representative of each of the hospitals with lung transplantation programs in Spain. In addition, prior to their publication, these guidelines have been reviewed by a group of prominent reviewers who are recognized for their professional experience in the field of lung transplantation. Within the following pages, the reader will find the selection criteria for lung transplantation candidates, when and how to remit a patient to a transplantation center and, lastly, when to add the patient to the waiting list. A level of evidence has been identified for the most relevant questions. Our intention is for this document to be a practical guide for pulmonologists who do not directly participate in lung transplantations but who should consider this treatment for their patients. Finally, these guidelines also propose an information form in order to compile in an organized manner the patient data of the potential candidate for lung transplantation, which are relevant in order to be able to make the best decisions possible.


American Journal of Transplantation | 2017

Epidemiology and immediate indirect effects of respiratory viruses in lung transplant recipients: a 5 year prospective study.

Maddalena Peghin; Hans H. Hirsch; Oscar Len; Gemma Codina; Cristina Berastegui; Berta Sáez; Juan Solé; Evelyn Cabral; Amparo Solé; Felipe Zurbano; Francisco López-Medrano; Antonio Rivero Román; Joan Gavaldà

The epidemiology of respiratory viruses (RVs) in lung transplant recipients (LTRs) and the relationship of RVs to lung function, acute rejection (AR) and opportunistic infections in these patients are not well known. We performed a prospective cohort study (2009–2014) by collecting nasopharyngeal swabs (NPSs) from asymptomatic LTRs during seasonal changes and from LTRs with upper respiratory tract infectious disease (URTID), lower respiratory tract infectious disease (LRTID) and AR. NPSs were analyzed by multiplex polymerase chain reaction. Overall, 1094 NPSs were collected from 98 patients with a 23.6% positivity rate and mean follow‐up of 3.4 years (interquartile range 2.5–4.0 years). Approximately half of URTIDs (47 of 97, 48.5%) and tracheobronchitis cases (22 of 56, 39.3%) were caused by picornavirus, whereas pneumonia was caused mainly by paramyxovirus (four of nine, 44.4%) and influenza (two of nine, 22.2%). In LTRs with LRTID, lung function changed significantly at 1 mo (p = 0.03) and 3 mo (p = 0.04). In a nested case–control analysis, AR was associated with RVs (hazard ratio [HR] 6.54), Pseudomonas aeruginosa was associated with LRTID (HR 8.54), and cytomegalovirus (CMV) replication or disease was associated with URTID (HR 2.53) in the previous 3 mo. There was no association between RVs and Aspergillus spp. colonization or infection (HR 0.71). In conclusion, we documented a high incidence of RV infections in LTRs. LRTID produced significant lung function abnormalities. Associations were observed between AR and RVs, between P. aeruginosa colonization or infection and LRTID, and between CMV replication or disease and URTID.


Transplant International | 2016

10 years of prophylaxis with nebulized liposomal amphotericin B and the changing epidemiology of Aspergillus spp. infection in lung transplantation.

M. Peghin; Monforte; María Teresa Martín-Gómez; Isabel Ruiz-Camps; C. Berastegui; Saez B; Riera J; Ussetti P; Solé J; Joan Gavaldà; Antonio Rivero Román

The aim of this study was to assess the outcome and tolerability of prophylactic nebulized liposomal amphotericin B (n‐LAB) in lung transplant recipients (LTR) and the changing epidemiology of Aspergillus spp. infection and colonization. We performed an observational study including consecutive LTR recipients (2003–2013) undergoing n‐LAB prophylaxis lifetime. A total of 412 patients were included (mean postoperative follow‐up 2.56 years; IQR 1.01–4.65). Fifty‐three (12.8%) patients developed 59 Aspergillus spp. infections, and 22 invasive aspergillosis (overall incidence 5.3%). Since 2009, person‐time incidence rates of Aspergillus spp. colonization and infection decreased (2003–2008, 0.19; 2009–2014, 0.09; P = 0.0007), but species with reduced susceptibility or resistance to amphotericin significantly increased (2003–2008, 38.1% vs 2009–2014, 58.1%; P = 0.039). Chronic lung allograft dysfunction (CLAD) was associated with Aspergillus spp. colonization and infection (HR 24.4, 95% CI 14.28–41.97; P = 0.00). Only 2.9% of patients presented adverse effects, and 1.7% required discontinuation. Long‐term administration of prophylaxis with n‐LAB has proved to be tolerable and can be used for preventing Aspergillus spp. infection in LTR. Over the last years, the incidence of Aspergillus spp. colonization and infection has decreased, but species with reduced amphotericin susceptibility or resistance are emerging. CLAD is associated with Aspergillus spp. colonization and infection.


Medicina Clinica | 2007

Variabilidad en la valoración del riesgo coronario en pacientes infectados por el virus de la inmunodeficiencia humana

Milagros García-Lázaro; Antonio Rivero Román; Ángela Camacho Espejo; Inés Pérez-Camacho; Clara Natera Kindelán; Juan José Castón Osorio; Julián de la Torre Cisneros

BACKGROUND AND OBJECTIVE: Antiretroviral treatment of human immunodeficiency virus (HIV)-infected patients seems to increase the coronary risk (CR) in these patients. Adequate assessment of CR has significant implications for the management of these patients. Our objective was to compare 2 systems for assessing 10-year CR in HIV-infected patients. PATIENTS AND METHOD: CR was calculated in a prospective cohort of 205 HIV-infected patients using Framingham tables and REGICOR adapted tables. Prevalence of cardiovascular risk factors in these patients was evaluated. RESULTS: Mean age (standard deviation) was 41.4 (8.2) years. Most patients were taking antiretrovirals and had a good immunological status. Current smoking was reported by 77.1% of patients, while a history of dyslipidemia, hypertension, or diabetes was found in 29.3%, 7.3%, and 4.9% of patients, respectively. Lipodystrophy was seen in 41% of patients, abdominal obesity in 21.5%, and a sedentary lifestyle in 50.7% Mean values obtained were 6.55 (6.36) in the Framingham scale and 2.85 (2.31) in the REGICOR scale. A 10-year CR greater than 10% was found in 26 patients (12.9%) with the Framingham tables and in 4 patients (2.0%) with the REGICOR tables. The difference between both methods was significant (p < 0.001). CONCLUSIONS: Application of the Framingham tables to our cohort may overestimate the CR. Studies aimed at identifying the most adequate method for measuring CR in HIV-infected patients are required. Until such data are available, estimation of CR in these patients should be taken with caution.


Transplantation Reviews | 2015

Deep vein thrombosis and pulmonary embolism after solid organ transplantation: an unresolved problem.

Berta Sáez-Giménez; Cristina Berastegui; Karina Loor; Manuel López-Meseguer; Víctor Monforte; Carlos Bravo; Amparo Santamaría; Antonio Rivero Román

Venous thromboembolism (VTE) is a major complication after solid organ transplantation (SOT), with an incidence that ranges from 2 to 34%. Besides genetic risk factors such as inherited thrombophilia, other specific risk factors for VTE in SOT recipients include impairment of fibrinolysis produced by corticosteroids, in vitro procoagulant effects of calcineurin inhibitors, endothelial damage due to cytomegalovirus infection, and specific surgical factors. Prevention strategies have not been systematically studied. Therefore, it is mandatory for the international scientific community to conduct large, multicenter, randomized clinical trials to define strategies for the prevention of VTE in SOT recipients.


Transplant Infectious Disease | 2016

Epidemiology of invasive respiratory disease caused by emerging non‐Aspergillus molds in lung transplant recipients

M. Peghin; V. Monforte; María Teresa Martín-Gómez; Isabel Ruiz-Camps; C. Berastegui; Saez B; Riera J; Solé J; Joan Gavaldà; Antonio Rivero Román

Our aim was to assess the impact of positive cultures for non‐Aspergillus molds on the risk of progression to invasive fungal infection (IFI), and the effect of prophylactic nebulized liposomal amphotericin B (n‐LAB) on these pathogens.


Transplantation proceedings | 2013

Inhaled iloprost plus oral sildenafil in patients with severe pulmonary arterial hypertension delays the need for lung transplantation.

Manuel López-Meseguer; Cristina Berastegui; Víctor Monforte; C. Bravo; E. Domingo; Antonio Rivero Román

BACKGROUND Accepted treatment for severe pulmonary arterial hypertension (PAH) includes intravenous epoprostenol and lung transplantation (LT). Inhaled iloprost plus oral sildenafil (Ilo-Sil) is an alternative strategy that may also delay the need for LT. PATIENTS AND METHODS This was a long-term descriptive study in eight patients with PAH functional class (FC) IV with right heart failure, four of them potential candidates for LT, who were treated with Ilo-Sil as an alternative to epoprostenol. RESULTS At the start of the study, patients (seven women; mean age, 43.8 [range, 34-66] years) were in FC IV and unable to perform the 6-minute walk test. Mean cardiac index was 1.9 (range, 1.4-2.1) L/min/m(2). Treatment with Ilo-Sil provoked a rapid and sustained improvement; mean walking distance at 3 months was 322 ± 90 m and no patient remained in FC IV. Survival at 1 and 5 years was 100% and 75%, respectively. Of the four potential LT candidates, one underwent transplantation after 6.8 years and one died after 1.2 years. CONCLUSIONS These results suggest that therapy with Ilo-Sil represents an acceptable alternative in patients with severe and unstable PAH.

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Víctor Monforte

Autonomous University of Barcelona

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José López Aldeguer

Instituto de Salud Carlos III

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Carlos Bravo

Instituto de Salud Carlos III

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Cristina Berastegui

Instituto de Salud Carlos III

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Amparo Solé

Instituto Politécnico Nacional

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Antonio Antela

University of Santiago de Compostela

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Joan Gavaldà

Autonomous University of Barcelona

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